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Aspergilose broncopulmonar alergica revisão do chest 2009
- 1. Allergic Bronchopulmonary Aspergillosis
Ritesh Agarwal
Chest 2009;135;805-826
DOI 10.1378/chest.08-2586
The online version of this article, along with updated information and
services can be found online on the World Wide Web at:
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Chest is the official journal of the American College of Chest
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Copyright2009by the American College of Chest Physicians, 3300
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ISSN:0012-3692
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- 2. CHEST Global Medicine
Allergic Bronchopulmonary
Aspergillosis*
Ritesh Agarwal, MD, DM, FCCP
Allergic bronchopulmonary aspergillosis (ABPA) is an immunologic pulmonary disorder caused
by hypersensitivity to Aspergillus fumigatus. Clinically, a patient presents with chronic asthma,
recurrent pulmonary infiltrates, and bronchiectasis. The population prevalence of ABPA is not
clearly known, but the prevalence in asthma clinics is reported to be around 13%. The disorder
needs to be detected before bronchiectasis has developed because the occurrence of bronchiec-
tasis is associated with poorer outcomes. Because many patients with ABPA may be minimally
symptomatic or asymptomatic, a high index of suspicion for ABPA should be maintained while
managing any patient with bronchial asthma whatever the severity or the level of control. This
underscores the need for routine screening of all patients with asthma with an Aspergillus skin
test. Finally, there is a need to update and revise the criteria for the diagnosis of ABPA. This
review summarizes the advances in the diagnosis and management of ABPA using a systematic
search methodology. (CHEST 2009; 135:805– 826)
Key words: allergic bronchopulmonary aspergillosis; Aspergillus; bronchial asthma; cystic fibrosis; prevalence
Abbreviations: AAS ϭ allergic Aspergillus sinusitis; ABPA ϭ allergic bronchopulmonary aspergillosis; ABPA-CB ϭ allergic
bronchopulmonary aspergillosus with central bronchiectasis; ABPA-CB-ORF ϭ allergic bronchopulmonary aspergillosus with
central bronchiectasis and other radiological findings; ABPA-S ϭ seropositive allergic bronchopulmonary aspergillosus;
AH ϭ Aspergillus hypersensitivity; CF ϭ cystic fibrosis; HRCT ϭ high-resolution CT; IL ϭ interleukin
A spergillus is aand 22% ofmold representing be-
tween 0.1%
ubiquitous
the total air spores
migatus clinically manifesting as chronic asthma, recur-
rent pulmonary infiltrates, and bronchiectasis.5–13 The
sampled.1 There are approximately 250 species of condition has immunologic features of immediate hy-
Aspergillus, but only a few are human pathogens.2,3 persensitivity (type I), antigen-antibody complexes
Depending on the host immunity and the organism (type III), and eosinophil-rich inflammatory cell
virulence, the respiratory diseases caused by As- responses (type IVb), based on the revised Gell and
pergillus are classified as saprophytic (aspergilloma), Coombs classification of immunologic hypersensitiv-
allergic (allergic Aspergillus sinusitis, allergic bron- ity.14,15 The disorder was first described by Hinson et
chopulmonary aspergillosis [ABPA], and hypersensitiv- al16 in 1952 in the United Kingdom. Occasionally,
ity pneumonias) and invasive (airway invasive aspergil- patients can develop a syndrome similar to ABPA,
losis, chronic necrotizing pulmonary aspergillosis, and but it is caused by fungi other than A fumigatus and
invasive aspergillosis).4 ABPA is an allergic pulmonary is called allergic bronchopulmonary mycosis.17 The
disorder caused by hypersensitivity to Aspergillus fu- prevalence of ABPA is believed to be about 1 to 2%
in patients with asthma and 2 to 15% in patients with
*From the Department of Pulmonary Medicine, Postgraduate cystic fibrosis (CF).13 The condition remains underdi-
Institute of Medical Education and Research, Chandigarh, India. agnosed in many countries with reports of mean diag-
The author has no conflicts of interest to disclose.
Manuscript submitted November 4, 2008; revision accepted nostic latency of even 10 years between the occurrence
November 20, 2008. of symptoms and the diagnosis.18 In the past two
Reproduction of this article is prohibited without written permission decades, there has been an increase in the number
from the American College of Chest Physicians (www.chestjournal.
org/misc/reprints.shtml). of cases of ABPA due to the heightened physician
Correspondence to: Ritesh Agarwal, MD, DM, FCCP, Assistant awareness and the widespread availability of sero-
Professor, Department of Pulmonary Medicine, Postgraduate logic assays.19 –23 This review provides a summary of
Institute of Medical Education and Research, Sector-12, Chandi-
garh 160012, India; e-mail: riteshpgi@gmail.com the advances in the field of ABPA. For the purpose of
DOI: 10.1378/chest.08-2586 this review, a systematic search of PubMed and Em-
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- 3. Table 1—Studies Describing the Prevalence of AH and/or ABPA in Patients with Bronchial Asthma Over the Last
Two Decades*
Type of Skin Criteria Used for Prevalence of AH Prevalence of ABPA
Study/Year Type of Study Test Type of Antigen Diagnosis of ABPA in Asthma (n/N) in Asthma (n/N)
Attapattu31/1991 Prospective Intradermal Commercial (Bencard Major (A/R/T/E/P) 58/134 8/134
Allergie; Munich, Minor (C)
Germany)
Eaton et al33/2000 Prospective Prick Commercial (Hollister- Major (A/R/T/E/P/ 47/255 9/35
Stier Laboratories) I/C/S)
Kumar and Gaur34/ Prospective Intradermal Locally prepared Major (A/R/T/E/P/ 47/200 32/200
2000 I/C/S)
Minor (C/S/B)
Al-Mobeireek et al20/ Prospective Prick Commercial (Soluprick; 12/53
2001 ALK Laboratories;
Wallingford, CT)
Maurya et al35/2005 Prospective Intradermal Locally prepared Major (A/R/T/E/P/ 30/105 8/105
I/C/S)
Minor (C/S)
Agarwal et al23/2007 Prospective Intradermal Commercial (Hollister- Major (A/R/T/E/P/ 291/755 155/755
Stier Laboratories) I/C/S)
Minor (S/B)
Prasad et al36/2008 Prospective Intradermal Not available Major (A/R/T/E/P/ 74/244 18/244
I/C/S)
Minor (C/S/B)
* Criteria for ABPA: Major (A ϭ asthma, R ϭ radiologic opacities, T ϭ immediate positive skin test, E ϭ eosinophilia, P ϭ precipitins to A
fumigatus, I ϭ IgE elevated, C ϭ central bronchiectasis, S ϭ specific IgG/IgE to A fumigatus); Minor (C ϭ sputum cultures of A fumigatus,
S ϭ type III skin test positivity, B ϭ brownish black mucus plugs).
Base was performed for relevant studies published from high in patients attending asthma clinics. Table 1
1952 to 2008. A total of 250 articles were reviewed for the summarizes the prevalence of ABPA in patients with
purpose of this article. asthma reported in various studies20,23,31–36 over the
last two decades. The prevalence of ABPA in pa-
Epidemiology of ABPA tients admitted with acute severe asthma is even
higher. In a recent study of 57 patients with acute
Aspergillus hypersensitivity (AH) is defined by the severe asthma admitted in the respiratory ICUs, we
presence of an immediate-type cutaneous hypersen- demonstrated the prevalence of AH and ABPA to be
sitivity to A fumigatus antigens, and it is the first step around 51% and 39%, respectively.37 The occurrence
in the development of ABPA.24 Only a minority of of AH and ABPA was significantly higher in patients
patients with AH develop the complete clinical with acute asthma compared to the outpatient bron-
picture of ABPA.25 The population prevalence of chial asthma (around 39% and 21%, respectively).23
ABPA in asthma, generally referred to as 1 to
2%,5,13,26,27 is based on the inference of only three
Pathogenesis of ABPA
studies (one peer-reviewed and two non–peer-re-
viewed studies).28,29 In the only peer-reviewed The susceptibility of asthmatic patients to develop
study,28 14 patients with allergic bronchopulmonary ABPA is not fully understood (Fig 1). Some authors
mycosis were identified from a total of 1,390 new have reported that exposure to large concentrations
referrals in a catchment area population of half a of spores of A fumigatus may cause ABPA.16,38 – 41
million, estimating a period prevalence of just above Environmental factors are not considered the main
1%. The other two non–peer-reviewed question- pathogenetic factors because not all asthmatics de-
naire-based studies suggested a maximum preva- velop ABPA despite being exposed to the same
lence of ABPA of 1% in the United States.29 In a environment. In a genetically predisposed individu-
recent metaanalysis,30 we demonstrated a prevalence al42–54 (Table 2), inhaled conidia of A fumigatus
of AH and ABPA in asthma of 28% and 12.9%, persist and germinate into hyphae with release of
respectively. The limitation noted in this review was antigens that compromise the mucociliary clearance,
that all the studies were performed in specialized stimulate and breach the airway epithelial barrier,
clinics and may not be representative of the general and activate the innate immunity of the lung.55–58
population. Thus the exact population prevalence of This leads to inflammatory cell influx and a resultant
ABPA remains speculative but is likely to be fairly early- and late-phase inflammatory reaction.59,60 The
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- 4. Figure 1. A line diagram depicting the pathogenesis of allergic bronchopulmonary aspergillosis. Th ϭ T-helper.
antigens are also processed presented to T-cells with Charcot-Leyden crystals, and inflammatory cells.
activation of Th2 CD4ϩ T-cell responses.42,61–63 The Th2 Scanty hyphae can often be demonstrated in the
cytokines (interleukin [IL]-4, IL-5, and IL-13) lead to total bronchiectatic cavities. The bronchial wall in ABPA
and A fumigatus-specific IgE synthesis, mast cell degran- is usually infiltrated by inflammatory cells, primarily
ulation, and promotion of a strong eosinophilic response. the eosinophils.65 The peribronchial parenchyma
This causes the characteristic pathology of ABPA. shows an inflammatory response with conspicuous
eosinophilia. Occasionally, fungal growth in the lung
Pathology of ABPA
parenchyma can occur in some patients with ABPA.66
The pathology of ABPA varies from patient to Patients can also demonstrate a pattern similar to that
patient, and in different areas of the lung in the same of bronchiolitis obliterans with organizing pneumo-
patient (Fig 2).64,65 Histologic examination reveals nia.67 Bronchocentric granulomatosis, the presence of
the presence of mucus, fibrin, Curschmann spirals, noncaseating granulomas containing eosinophils and
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- 5. Table 2—Genetic Factors Involved in the Pathogenesis is seen in 31 to 69% of patients.21,23,34 The symptoms
of ABPA* of hemoptysis, expectoration of brownish black mu-
HLA associations: presence of HLA DR-2 and absence of cus plugs, and history of pulmonary opacities in an
HLA-DQ2 sequences42,44,45 asthmatic patient suggests ABPA. Patients can oc-
IL-10 promoter polymorphisms49 casionally be asymptomatic, and the disorder is
Polymorphism at position 1,082 produces higher levels of IL-10 diagnosed on routine screening of asthmatic pa-
if 1082G allele is present and lower levels of IL-10 if the tients.22,23,33 Physical examination can be normal or
1082A allele is present
may reveal polyphonic wheeze. Clubbing is rare,
In patients with CF there is a relationship between the 1082GG
genotype with both Aspergillus colonization and ABPA seen in only 16% of patients. On auscultation, coarse
Surfactant protein A gene polymorphisms48,53 crackles can be heard in 15% of patients.23 Physical
A significantly higher frequency of the AGA allele (A1660G) of examination can also detect complications such as
SP-A2 found in patients with ABPA vs control subjects. pulmonary hypertension and/or respiratory failure.76
Coexistence of A1660G polymorphism with SP-A2 G1649C During exacerbations of ABPA, localized findings of
(Ala91Pro) found with 10-fold higher odds in patients with
ABPA. Patients with ABPA with GCT and AGG alleles
consolidation and atelectasis can occur that needs to
showed significantly higher levels of total IgE and percentage be differentiated from other conditions.
eosinophilia vs patients with ABPA with CCT and AGA
alleles48 Laboratory Findings
The T allele at T1492C and G allele at G1649C of SP-A2
observed at higher frequencies in ABPA patients than in Aspergillus Skin Test: The Aspergillus skin test is
controls. Also there is a higher frequency of the TT genotype performed using an A fumigatus antigen, either
at position1492 of SP-A2 than controls53 commercial (eg, Aspergillin; Hollister-Stier Labora-
There were no polymorphisms found in SP-A1 gene53 tories; Spokane, WA) or locally prepared. The test is
CFTR gene mutation:43,46,47 increased frequency of CFTR read every 15 min for 1 h, and then after 6 to 8 h.
mutations in patients with ABPA vs skin-prick test positive or
negative patients with bronchial asthma
The reactions are classified as type I if a wheal and
IL-15 polymorphisms:52 higher frequency of IL-15 ϩ 13689*A erythema developed within 1 min, reaches a maxi-
allele and A/A genotype mum after 10 to 20 min, and resolves within 1 to 2 h.
TNF-␣ polymorphisms:52 lower frequency of the TNF-␣ 308 * A/A A type III reaction is read after 6 h, and any amount
genotype of subcutaneous edema is considered a positive
Mannose-binding lectins:53 the intronic single nucleotide result. An immediate cutaneous hypersensitivity to A
polymorphism G1011A of mannose-binding lection seen with
increased frequency in patients with ABPA
fumigatus antigens is a characteristic finding of
IL-4 receptor polymorphisms:51 single nucleotide polymorphism of ABPA and represents the presence A fumigatus-
the extracellular IL-4R␣ ile75val observed in 80% of ABPA specific IgE antibodies, whereas a type III skin
patients reaction probably represents the immune complex
IL-13 polymorphisms:50 the arg110gln polymorphism found with hypersensitivity reaction, although its exact signifi-
increased frequency in ABPA and the combination of IL-4R␣
cance remains unclear. The test can be performed
ile75val/IL-13 arg110gln polymorphism found with an even
higher frequency using either a skin-prick test or intradermal injection
Toll-like receptor gene polymorphisms:54 susceptibility to ABPA with the latter being more sensitive.30,77,78 A skin-
was associated with allele C on T1237C (TLR9) prick test should be performed for Aspergillus skin
*HLA ϭ human leukocyte antigen; TNF ϭ tumor necrosis factor; testing, and if the results are negative should be
CFTR ϭ CF transmembrane conductance regulator. confirmed by an intradermal test.30 There is no
difference on the outcome of the test and the type of
antigen (locally prepared or commercial) used for
performance of the test.30
multinucleated giant cells centered on the airway, are
also seen.68,69 Rarely, invasive aspergillosis complicat- Total Serum IgE Levels: The total IgE level is the
ing the course of ABPA has also been described.70 –74 most useful test for diagnosis and follow-up of ABPA. A
normal serum IgE level excludes ABPA as the cause of
the patient’s current symptoms. The only situation
Clinical Features
where IgE levels can be normal in active ABPA is when
There is no gender predilection and majority of the the patient is already on glucocorticoid therapy for any
cases present in the third to fourth decade. A family reason and investigation for IgE levels has been con-
history of ABPA may be elicited occasionally.75 Table 3 ducted. After treatment with glucocorticoids, the se-
summarizes the clinical features of ABPA encoun- rum IgE levels decline, and a 35 to 50% decrease is
tered in three large series from our institute.19,21,23 taken as a criteria for remission.79 The serum IgE
Most present with low-grade fever, wheezing, bron- determination is also used for follow-up, and a doubling
chial hyperreactivity, hemoptysis, or productive of the patient’s baseline IgE levels indicates relapse of
cough. Expectoration of brownish black mucus plugs ABPA.80,81
808 Global Medicine
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- 6. Figure 2. Histopathologic findings in a patient with allergic bronchopulmonary aspergillosis. Top left, A:
photomicrograph showing bronchial lumen containing allergic mucin (hematoxylin-eosin, original ϫ100). Top
right, B: high-magnification photomicrograph of allergic mucin having variegated appearance, necrotic eosino-
phils, Charcot-Leyden crystals (thin arrow), and an occasional septate fungal hyphae indicated by a thick arrow
(hematoxylin-eosin, original ϫ200). Bottom left, C: photomicrograph showing eosinophilic pneumonia. There is
filling of the alveolar spaces by eosinophils admixed with variable number of macrophages (hematoxylin-eosin,
original ϫ200). Bottom right, D: photomicrograph showing bronchocentric granulomatosis. There is partial
replacement of bronchial epithelium by palisading histiocytes (hematoxylin-eosin, original ϫ100).
Serum IgE and IgG Antibodies Specific to A cutoff value of IgG/IgE more than twice the pooled
fumigatus: An elevated level of A fumigatus-specific serum samples from patients with AH can greatly
antibodies measured by fluorescent enzyme immuno- help in the differentiation of ABPA from other
assay is considered the hallmark of ABPA.22 A conditions.82
Table 3—Clinical Features Encountered in Three Large Case Series of ABPA Published From the Author’s
Institute*
Clinical Features Behera et al19/1994 Chakrabarti et al21/2002 Agarwal et al23/2007
Patients, No. 35 89 155
Male/female gender, No. 14/21 53/35 79/76
Mean age, yr 34.3 36.4 33.4
Mean duration of asthma, yr 11.1 12.1 8.9
History of asthma 94% 90% 100%
Expectoration of sputum plugs Not available 69% 46.5%
Mean eosinophil count, per L 1,264
AEC Ͼ 500/L, % 12/28 (43%) 100% 76.1%
Fleeting shadows 77% 74% 40%
History of intake of antituberculous drugs 34% 29% 44.5%
Skin test against Aspergillus
Type I 51% 85% 100%
Type III 25.7% 16.9% 83.2%
Mean IgE levels Not done Not done 6,434
Elevated IgE levels, % 100%
Aspergillus-specific IgE/IgG Not done Not done 100%
Serum precipitins against Aspergillus 77% 71.9% 86.5%
Central bronchiectasis 71% 69% 76.1%
*AEC ϭ absolute blood eosinophil count.
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- 7. Radiologic Investigations: A wide spectrum of have associated peripheral bronchiectasis.22,96 Mini-
radiographic appearances can occur in ABPA (Table mal bronchiectasis can also be seen in asthma,97,98
4). The chest radiographic findings of ABPA include but the findings of bronchiectasis affecting three or
transient or fixed pulmonary opacities (Fig 3), tram- more lobes, centrilobular nodules, and mucoid im-
line shadows, finger-in-glove opacities, and tooth- paction are highly suggestive of ABPA.99 The un-
paste shadows.83– 87 Findings noted on high-resolution common radiologic manifestations of ABPA include
CT (HRCT) include central bronchiectasis, mucoid miliary nodular opacities,100 perihilar opacities
impaction, mosaic attenuation, presence of centri- simulating hilar lymphadenopathy,84,101,102 pleural
lobular nodules, and tree-in-bud opacities (Fig effusions,103–105 and pulmonary masses.106 –111
4).88,89 High-attenuation mucoid impaction (mucus
visually denser than the paraspinal muscle) is a Serum Precipitins Against A fumigatus: The pre-
pathognomonic finding encountered in patients with cipitating IgG antibodies are elicited from crude
ABPA.23,90 –95 Central bronchiectasis with peripheral extracts of A fumigatus and can be demonstrated
tapering of bronchi on HRCT is believed to be a sine using the double gel diffusion technique.112,113 They
qua non for the diagnosis of ABPA. Bronchiectasis can also be present in other pulmonary disorders and
may not be present in all patients with ABPA, may be thus represent supportive not diagnostic evidence for
present in patients with CF without ABPA, and ABPA.112–114
almost 40% of the bronchiectatic segments can also
Peripheral Eosinophilia: A blood absolute eosino-
phil count Ͼ 1,000 cells/L is also a major criterion
for the diagnosis of ABPA. However, 53% of patients
Table 4 —Radiologic Findings Encountered in Patients
With ABPA
in our series22 had an absolute eosinophil count
Ͻ 1,000 cells/L, and thus a low eosinophil count
1. Chest radiographic findings does not exclude the diagnosis of ABPA.
Transient changes
Common Sputum Cultures for A fumigatus: Culture of A
Patchy areas of consolidation
Radiologic infiltrates: toothpaste and gloved finger shadows
fumigatus in the sputum is supportive but not diag-
due to mucoid impaction in dilated bronchi nostic of ABPA. The fungus can also be grown in
Collapse: lobar or segmental patients with other pulmonary diseases due to the
Uncommon ubiquitous nature of the fungi. We rarely perform
Bronchial wall thickening: tramline shadows sputum cultures for the diagnosis of ABPA.
Air-fluid levels from dilated central bronchi filled with fluid
Perihilar infiltrates simulating adenopathy
Massive consolidation: unilateral or bilateral
Pulmonary Function Tests: These tests help cate-
Small nodules gorize the severity of the lung disease but have no
Pleural effusions diagnostic value in ABPA and need not constitute
Permanent changes the basis for screening.22 The usual finding is an
Common obstructive defect of varying severity.115–117
Parallel-line shadows representing bronchial widening
Ring-shadows 1–2 cm in diameter representing dilated
bronchi en face Role of Specific Aspergillus Antigens: Patients with
Pulmonary fibrosis: fibrotic scarred upper lobes with ABPA are evaluated with crude extracts from As-
cavitation pergillus, which lack reproducibility and consistency,
Uncommon and they frequently cross-react with other anti-
Pleural thickening
gens.118 The advances in molecular techniques have
Mycetoma formation
Linear scars enabled detection and cloning of specific Aspergillus
2. HRCT findings antigens. The recombinant allergens Asp f1, Asp f2,
Common Asp f3, Asp f4, and Asp f6 have been evaluated for
Central bronchiectasis their diagnostic performance in serologic studies in
Mucus plugging with bronchoceles
asthmatic patients119 –122 and in patients with
Consolidation
Centrilobular nodules with tree-in-bud opacities CF121,123–125 Preliminary data suggest a promising
Bronchial wall thickening role of these antigens in the diagnosis of ABPA.
Areas of atelectasis Further studies are required before they can be
Mosaic perfusion with air trapping on expiration implemented in routine clinical practice.
Uncommon
High-attenuation mucus (finding most helpful in differential
diagnosis)
Diagnosis and Diagnostic Criteria
Pleural involvement The Rosenberg-Patterson criteria6,9 are most often
Randomly scattered nodular opacities
used for the diagnosis (Table 5). There are also a set
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- 8. Figure 3. Chest radiograph showing transient pulmonary opacities in the right lower lobe (left) in a
patient with allergic bronchopulmonary aspergillosis that have spontaneously disappeared (right).
of minimal diagnostic criteria for ABPA (Table ABPA.97–99 There are no cutoffs for total IgE levels
5).32,33 These criteria continue to be challenged and with many using 1,000 IU/mL,8,9,22,23,82,128 –130 and
modified because there is lack of evidence on the others using 1,000 ng/mL (equivalent to 417 IU/
number of criteria that should be present to make mL).5,27,33,34 The total IgE levels may also be ele-
the diagnosis. The differentiation of patients with vated in patients with AH without ABPA. As the
ABPA from patients with AH can also be problem- understanding of ABPA has evolved, it is clear that
atic. Serum precipitins to A fumigatus is present in patients with AH may present with less than the full
69 to 90% of patients with ABPA23,112,116,126,127 but complement of diagnostic criteria.131 Thus, a cutoff
also in 9% of asthmatics.112 Central bronchiectasis value of 1,000 ng/mL IgE will probably lead to an
can be seen in patients with asthma without overdiagnosis of ABPA.131 The use of A fumigatus-
Figure 4. HRCT images of different patients with allergic bronchopulmonary aspergillosis. Top right:
bilateral central bronchiectasis with centrilobular nodules and tree-in-bud opacities in the left lung. Top
left: bilateral central bronchiectasis with many mucus-filled bronchi. Bottom, left and right: images from
the same patient show high-attenuation mucoid impaction. Bottom right: the mucoid impaction in the
right lung is visually denser than the paraspinal skeletal muscle.
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- 9. Table 5—Criteria Used for the Diagnosis of ABPA systemic corticosteroids are essential to prevent irre-
6,9 versible damage.137 The natural course of ABPA can
Rosenberg-Patterson criteria
Major criteria (mnemonic ARTEPICS) be best understood if we recognize the two impor-
A ϭ Asthma tant classification schemes (Tables 6 and 7) of ABPA:
R ϭ Roentgenographic fleeting pulmonary opacities (1) classification of ABPA into five stages as de-
T ϭ Skin test positive for Aspergillus (type I reaction,
scribed by Patterson et al8, and (2) classification of
immediate cutaneous hyperreactivity)
E ϭ Eosinophilia ABPA into ABPA-S (seropositive ABPA) and ABPA-CB
P ϭ Precipitating antibodies (IgG) in serum (ABPA with central bronchiectasis) described by
I ϭ IgE in serum elevated (Ͼ 1,000 IU/mL) Greenberger et al.12
C ϭ Central bronchiectasis
S ϭ Serums A fumigatus-specific IgG and IgE (more than
twice the value of pooled serum samples from patients with Staging of ABPA: ABPA has been classified into
asthma who have Aspergillus hypersensitivity) five stages, but a patient does not necessarily
Minor criteria
Presence of Aspergillus in sputum progress from one stage to the other sequentially
Expectoration of brownish black mucus plugs (Table 6). Patients in stage I or III (depending on
Delayed skin reaction to Aspergillus antigen (type III whether or not the disorder has been previously
reaction) diagnosed) are generally symptomatic with radio-
The presence of six of eight major criteria makes the diagnosis
almost certain; the disease is further classified as ABPA-S or graphic infiltrates, raised IgE levels, and elevated A
ABPA-CB on the absence or presence of central fumigatus-specific IgG/IgE.23 With glucocorticoid
bronchiectasis, respectively therapy, there is clearing of radiographic opacities
Minimal diagnostic criteria for ABPA32 with a 35 to 50% decline in IgE levels by 6 weeks
Minimal ABPA-CB
Asthma that defines remission or stage II. The aim of
Immediate cutaneous hyperreactivity to Aspergillus antigens glucocorticoid therapy is not normalization of total
Central bronchiectasis IgE levels because the immunologic process goes in
Elevated IgE remission with just 35 to 50% decline in IgE levels,
Raised A fumigatus-specific IgG and IgE
Minimal ABPA-S and in many patients the IgE levels do not come to
Asthma down to normal values. The test needs to be often
Immediate cutaneous hyperreactivity to Aspergillus antigens repeated during therapy to determine the lowest
Transient pulmonary infiltrates on chest radiograph level for an individual patient that serves as the
Elevated IgE
Raised A fumigatus-specific IgG and IgE baseline for that particular patient. Treatment is
continued for 6 to 9 months, and if there are no
exacerbations over the next 3 months after stopping
specific IgE and IgG levels can help in confirming therapy, we label it as “complete remission.” Patients
the diagnosis of ABPA because values of IgG/IgE in complete remission are followed up by serial IgE
more than twice the pooled serum samples from levels every 6 months for the first year and then
patients with asthma are raised only in ABPA.113,132 annually. Even in patients with complete remission,
We currently use a cutoff value of 1,000 IU/mL for the IgE levels decline to normal in only a minority of
the diagnosis of ABPA.22,23 While investigating a patients,128,133 and the aim of glucocorticoid therapy
patient with asthma, we first perform an Aspergillus is not achievement of normal IgE levels.79 A com-
skin test. Once it is positive, the total serum IgE
plete remission does not imply a permanent remis-
levels are done.131 If the value is Ͼ 1,000 IU/mL, we
sion because exacerbations can occur several years
perform the other tests (Fig 5). If the value is
after remission.135 Almost 25 to 50% of the patients
between 500 and 1,000 IU/mL, the next step is analysis
have relapse/exacerbation of the disease, defined by
of A fumigatus-specific IgE and IgG antibodies. If the
doubling of the baseline IgE levels (stage III).8,9,22
levels are raised, the patient is followed up every 6 weeks
Patients in stage IV require oral glucocorticoids for
with total IgE levels. If the absolute value rises Ͼ 1,000
control of asthma (glucocorticoid-dependent asthma)
IU/mL or there is a rising trend with clinical deterioration,
or ABPA (glucocorticoid-dependent ABPA).10,22 Pa-
the treatment is started. If the value is between 500 and
tients in stage V are those with widespread bronchi-
1,000 IU/mL and IgE and IgG specific to A fumigatus are
ectasis and varying degrees of pulmonary dysfunc-
not raised, the patient is followed up with a yearly total
tion. We define patients in stage V if they have
IgE levels (Fig 5).
hypercapnic respiratory failure (Pao2 Ͻ 60 mm Hg
and Paco2 Ն 45 mm Hg) and/or cor pulmonale.
Natural History
Even in stage V ABPA, the disease can be clinically
The natural history of ABPA is not well character- as well as immunologically active requiring long-
ized.9,128,133–136 An early diagnosis and initiation of term glucocorticoid therapy.136,138
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- 10. Figure 5. Algorithm followed in the diagnostic workup for allergic bronchopulmonary aspergillosis in the author’s chest clinic.
Radiologic Classification of ABPA: ABPA is clas- and ABPA-CB-ORF (other radiologic findings)
sified as ABPA-S or ABPA-CB, respectively, de- (Table 7). Patients with ABPA-S probably repre-
pending on the absence or presence of bronchiec- sent the earliest stage of the disorder. It is be-
tasis or as ABPA-S (mild), ABPA-CB (moderate), lieved that patients with ABPA-S have a milder
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- 11. Table 6 —Stages of ABPA8,22
Stage Description Clinical Picture Radiologic Findings Immunologic Features
I Acute phase Usually symptomatic, Normal or presence of IgE Ͼ 1,000 IU/mL, raised
fever, weight loss, radiologic opacities specific IgG/IgE and
wheeze precipitins to A fumigatus
II Remission Asymptomatic Generally normal or significant Usually 35–50% decline in IgE
resolution of radiologic levels by 6 wk to 3 mo; we
opacities from the acute give additional label of
phase “complete remission” if the
patient did not have any
additional ABPA exacerbations
over the next 3 mo after
stopping steroid therapy
III Exacerbation Symptomatic as in acute Transient or fixed pulmonary Doubling of IgE levels from
phase opacities baseline
IV Glucocorticoid-dependent Symptomatic Transient or fixed pulmonary Two groups can be identified:
ABPA opacities one in whom IgE levels do not
rise but require steroids for
asthma control (glucocorticoid-
dependent asthma); the other
in whom steroids are required
to continually suppress the
disease activity (glucocorticoid-
dependent ABPA)
V End-stage (fibrotic) Symptomatic, findings of Evidence of bronchiectasis, Serum IgE levels and specific
ABPA fixed airway pulmonary fibrosis, immunoglobulins do not
obstruction, severe pulmonary hypertension become normal in most
pulmonary patients, and even these
dysfunction, type II patients can have frequent
respiratory failure, cor exacerbations
pulmonale
clinical course and less severe immunologic find- creases the probability of a smoother course of this
ings when compared to ABPA-CB based on the relapsing-remitting disorder.
inference of three studies (total of 124 pa-
tients).12,139,140 In the largest of these three studies Management
(76 patients), only the A fumigatus-specific IgG
levels were higher in patients with ABPA-CB The management of ABPA includes two important
compared to ABPA-S. Other immunologic param- aspects: institution of glucocorticoids to control the
eters were not significantly different between the immunologic activity and close monitoring for detec-
two groups.12 In our study of 126 patients, the tion of relapses. Another possible target is the use of
clinical, spirometric, and immunologic findings antifungal agents to attenuate the fungal burden
were not significantly different when classifying secondary to the fungal colonization in the airways.
ABPA into ABPA-S and ABPA-CB or as ABPA-S,
ABPA-CB, and ABPA-CB-ORF.22 Systemic Glucocorticoid Therapy: Oral corticoste-
However, the course of patients with ABPA-S is roids are the treatment of choice for ABPA. They not
likely to be less severe when compared to those with only suppress the immune hyperfunction but are also
ABPA-CB. In a multivariate analysis of 155 patients antiinflammatory. There are no data to guide the
with ABPA, we demonstrated that the severity of dose and duration of glucocorticoids, and different
bronchiectasis and presence of hyperattenuating regimens of glucocorticoids have been used (Table
mucoid impaction on HRCT-predicted relapses of 8). The use of lower doses of glucocorticoids was
ABPA and the severity of bronchiectasis was an associated with frequent relapses or corticosteroid
independent predictor of failure to achieve long- dependence (45%).9 We use a higher dosage of
term remission.23 Thus it may not be important to glucocorticoids for a longer duration and observed
stage the severity of ABPA based on the presence higher remission rates and a lower prevalence of
or absence of CB, but it remains prudent to glucocorticoid-dependent ABPA (13.5%).22 This
diagnose and treat ABPA early to prevent the raises the possibility of a higher dose and prolonged
development of bronchiectasis because it in- duration of corticosteroid therapy being associated
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- 12. Table 7—Radiologic Classification of ABPA* Table 8 —Treatment Protocols for the Management of
ABPA
Classification Features
Oral glucocorticoids
Greenberger et al 12
Regime 15
classification
Prednisolone, 0.5 mg/kg/d, for 1–2 wk, then on alternate days
ABPA-S All the diagnostic features of ABPA
for 6–8 wk. Then taper by 5–10 mg every 2 wk and
but no evidence of central
discontinue
bronchiectasis on HRCT.
Repeat the total serum IgE concentration and chest
Patients with ABPA-S may be
radiograph in 6 to 8 wk
classified as Patterson stages I to
Regime 222,113
IV. These patients may have
Prednisolone, 0.75 mg/kg, for 6 wk, 0.5 mg/kg for 6 wk, then
recurrent exacerbations and may
tapered by 5 mg every 6 wk to continue for a total duration
also be classified as stage III
of at least 6 to 12 mo. The total IgE levels are repeated
(ABPA-CB) All findings of ABPA including CB
every 6 to 8 wk for 1 yr to determine the baseline IgE
on HRCT. Patients with ABPA-
concentrations
CB may belong to any of the
Follow-up and monitoring
Patterson stages
The patients are followed up with a medical history and
Kumar140 classification
physical examination, chest radiograph, and measurement of
ABPA-S ABPA without CB
total IgE levels every 6 wk to demonstrate decline in IgE
ABPA-CB ABPA with CB
levels and clearing of the chest radiograph
ABPA-CB-ORF ABPA with CB other radiologic
A 35% decline in IgE level signifies satisfactory response to
features such as pulmonary
therapy. Doubling of the baseline IgE value can signify a
fibrosis, bleb, bullae,
silent ABPA exacerbation
pneumothorax, parenchymal
If the patient cannot be tapered off prednisolone, the disease
scarring, emphysematous change,
has evolved into stage IV. Management should be
multiple cyst, fibrocavitary
attempted with alternate-day prednisone with the least
lesions, aspergilloma, ground-
possible dose
glass appearance, collapse,
Monitor for adverse effects (eg, hypertension, secondary
mediastinal lymph node, pleural
diabetes)
effusion, and pleural thickening
Prophylaxis for osteoporosis: oral calcium and bisphosphonates
*Both the classification schemes believe that patients without CB and Oral itraconazole
ORF have serologically milder disease, but it has been shown that Dose: 200 mg bid for 16 wk then once a day for 16 wk
there is no difference in clinical, spirometric, and serological Indication: First relapse of ABPA or glucocorticoid-dependent
severity between patients with and without bronchiectasis (see text ABPA
for details). Follow-up and monitoring
Monitor for adverse effects (eg, nausea, vomiting, diarrhea,
and elevated liver enzymes)
with better outcomes. However, there are no direct
Monitor for drug–drug interactions
comparisons between the two regimens, and the Monitor clinical response based on clinical course,
selection is a matter of personal preference. The radiography, and total IgE levels
clinical effectiveness of steroid therapy is reflected
by marked decreases in the patient’s total serum IgE
levels (there seems to be no correlation between
serum levels of A fumigatus-specific IgE levels and agent, itraconazole.130,141,148 –160 Only two random-
disease activity141) along with symptom and radio- ized controlled studies (84 patients) have evaluated
graphic improvements. The goal of therapy is not to the role of itraconazole in ABPA.130,156 Pooled anal-
attempt normalization of IgE levels but to decrease ysis showed that itraconazole could significantly de-
the IgE levels by 35 to 50%, which leads to clinical crease the IgE levels by Ն 25% when compared to
and radiographic improvement. One should also placebo but did not cause significant improvement in
establish a stable serum level of total IgE to serve as lung function.161 A major limitation was that neither
a guide to future detection of relapse. of the studies reported long-term outcomes in
ABPA. Thus longer term trials are required before a
Inhaled Corticosteroids: Although small case stud- firm recommendation can be made for the use of
ies suggest some benefit of inhaled corticosteroids in itraconazole in ABPA. We currently use itraconazole
the management of ABPA,142–145 a double-blind mul- only after the first relapse of ABPA despite glucocor-
ticenter placebo-controlled trial in 32 patients sug- ticoid therapy or in patients with glucocorticoid-
gested no superiority over placebo.146 We use inhaled dependent ABPA (Table 8). In the limited numbers
corticosteroids only for the control of asthma once the of patients in whom we have used the drug, there
oral prednisolone dose is reduced to Ͻ 10 mg/day. was no observable advantage.22 Itraconazole not only
has numerous adverse effects,162 but it also inhibits
Oral Itraconazole: Ketoconazole has been tried in the metabolism of methylprednisolone (but not
the past147 and has been replaced by the less toxic prednisolone) with resultant increased frequency of
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- 13. Table 9 —Studies Describing Prevalence of AH and/or ABPA in Patients With CF
Study Year Nature of Study Patients, No. AH in CF ABPA* in CF Diagnosis of AH†
184
Mearns et al 1967 Prospective 86 28/86 Skin test
Allan et al185 1975 Prospective 30 11/30 Skin test
Silverman et al186 1978 Prospective 48 17 Skin test
Nelson et al187 1979 Prospective 46 18/46 5/46 Skin test
Laufer et al177 1984 Prospective 100 53/100 10/100 Skin test
Feanny et al188 1988 Prospective 117 18/117 12/117 Skin test
Schonheyder et al189 1988 Prospective 200 10/200
Zeaske et al190 1988 Prospective 75 44/75 10/75 Skin test
Knutsen et al176 1990 Prospective 73 18/73 9/73 Skin test
Nicolai et al179 1990 Prospective 148 58/148 Serology
Simmonds et al191 1990 Prospective 137 8/137
Hutcheson et al192 1991 Prospective 79 24/79 Skin test
el-Dahr et al193 1994 Prospective 147 30/147 22/147 Serology
Marchant et al194 1994 Retrospective 160 16/160 Skin test
Mroueh and Spock178 1994 Retrospective 236 38/87 15/236 Skin test
Becker et al181 1996 Prospective 53 15/51 1/53 Skin test
Hutcheson et al195 1996 Prospective 118 47/112 6/118 Skin test
Geller et al182 1999 Prospective 14,210 281/14,210
Nepomuceno et al153 1999 Retrospective 172 16/172
Cimon et al196 2000 Prospective 128 5/128
Mastella et al174 2000 Prospective 12,447 967/12,447
Taccetti et al197 2000 Prospective 3,089 191/3,089
Ritz et al180 2005 Prospective 160 20/160 11/160 Serology
Skov et al183 2005 Retrospective 277 13/277
Almeida et al198 2006 Prospective 32 11/32 2/32 Skin test
Kraemer et al173 2006 Prospective 122 16/122
Chotirmall et al199 2008 Prospective 50 6/50
Rapaka and Kolls200 2008 Retrospective 440 31/440
* ABPA: Studies have used different inclusion criteria for diagnosing ABPA. See text for further details.
† AH: Defined as immediate cutaneous hypersensitivity to Aspergillus antigen or a positive specific IgE in serum against A fumigatus
(radioallergosorbent test class Ն 2) and/or increased specific IgE in serum against rAsp f1 Ͼ 9.6 EU/mL, with normal values for rAsp f4 (Ͻ 8.4
EU/mL) and rAsp f6 (Ͻ 7.2 EU/mL)
steroid side effects including adrenal insufficiency.163 clude recurrent asthma exacerbations and, if
Adrenal suppression has also been reported with the untreated, the development of bronchiectasis with
concomitant use of itraconazole and inhaled budes- subsequent pulmonary hypertension and respiratory
onide.164,165 failure. In fact, this is the reason why routine screen-
ing is recommended in bronchial asthma to prevent
Other Therapies: There is a single patient case the complications just described.
report of ABPA treated with inhaled amphotericin
and budesonide.166 Similarly, there is another case ABPA in Special Situations
record on the use of omalizumab for the manage-
ABPA Complicating CF: The association of ABPA
ment of ABPA.167 One author has also used pulse
and CF was first reported in 1965.172 The occur-
doses of IV methylprednisolone for the treatment of
rence of ABPA in CF is associated with deterioration
severe ABPA.168 Recently, voriconazole has also
of lung function, higher rates of microbial coloniza-
been tried in the treatment of ABPA.169 –171
tion, pneumothorax, massive hemoptysis, and poorer
nutritional status.153,173,174 A key element in the
Differential Diagnosis and Complications
immunopathogenesis may be exposure to high levels
The disorder needs to be differentiated from the of Aspergillus allergens due to abnormal mucus
following conditions: Aspergillus hypersensitive properties.175 The recognition of ABPA in CF can be
bronchial asthma, pulmonary tuberculosis in en- difficult because ABPA shares many clinical charac-
demic areas, community-acquired pneumonia (espe- teristics with poorly controlled CF lung disease.
cially acute presentations), and other inflammatory Presence of wheezing, pulmonary infiltrates, bron-
pulmonary disorders such as eosinophilic pneumo- chiectasis, and mucus plugging are common mani-
nia, bronchocentric granulomatosis, and Churg- festations of CF-related pulmonary disease without
Strauss syndrome. The complications of ABPA in- ABPA. The prevalence of AH in patients with CF
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- 14. has been reported between 29% and 53%,176 –180 and prevalence of ABPA of 7.8% (95% confidence inter-
the prevalence of ABPA as 1 to 15%. Atopy seems to val, 5.8 to 10) using a random effects model [Figs 6
be an important risk factor for ABPA in CF, with and 7]. There was no uniformity in the diagnostic
ABPA observed in 22% of atopic patients but only criteria between different studies with varying crite-
2% of nonatopic patients.153,181–183 ria used for diagnosis of AH and ABPA. This fact has
To determine the prevalence of AH/ABPA in CF, also been previously reported in a questionnaire-
a systematic search was performed. The search based study, which revealed a considerable variabil-
yielded 28 studies (16 studies [1,391 patients] de- ity in the criteria used for the diagnosis of ABPA in
scribing the prevalence of AH in CF and 23 CF.201 Therefore, prospective reporting of cases with
studies [32,589 patients] describing the prevalence uniform criteria would be the only way to reliably
of ABPA in CF) that have described the preva- identify the true prevalence of ABPA in CF.
lence of AH and/or ABPA in patients with CF Although a high proportion of CF patients develop
(Table 9).153,173,174,176 –200 A proportion metaanalysis of sensitization to A fumigatus, many demonstrate a
these studies suggested the prevalence of AH in CF spontaneous decline in many immunologic parame-
of 34% (95% confidence interval, 27 to 41) and the ters, including IgE levels.192 The diagnosis of ABPA
Figure 6. Proportion metaanalysis showing the prevalence of Aspergillus hypersensitivity in patients with cystic fibrosis (random effects
model).
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- 15. Figure 7. Proportion metaanalysis showing the prevalence of allergic bronchopulmonary aspergillosis in patients with CF (random
effects model).
in CF should not be based solely on serology and data are available to formulate conclusive treatment
skin test results, and prolonged testing might be recommendations for ABPA in CF. The treatment
required to make a definite diagnosis (Table 10). The issues are further complicated because pulmonary
treatment of ABPA in CF is not very different from exacerbations in a patient with ABPA and CF could
that of ABPA in bronchial asthma, except minimal be related to ABPA or pulmonary infection, and
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- 16. Table 10 —Consensus Conference Proposed Diagnostic lung diseases like idiopathic bronchiectasis,209
and Screening Criteria for ABPA in CF202 post-tubercular bronchiectasis,210 bronchiectasis
Classic diagnostic criteria secondary to Kartagener syndrome,211 COPD,212
1. Acute or subacute clinical deterioration (cough, wheeze, and and in patients with chronic granulomatous dis-
other pulmonary symptoms) not explained by another etiology ease and hyper IgE syndrome.213 However, these
2. Serum total IgE levels Ͼ 1,000 IU/mL are case reports or small case studies, and larger
3. Immediate cutaneous reactivity to Aspergillus or presence of
observations are required to definitely establish an
serum IgE antibody to A fumigatus
4. Precipitating antibodies to A fumigatus or serum IgG antibody association.
to A fumigatus
5. New or recent abnormalities on chest radiograph or chest CT Coexistence of ABPA and Aspergilloma: The sero-
scan that have not cleared with antibiotics and standard logic findings of ABPA have also been reported in
physiotherapy
patients with aspergilloma214 –224 and chronic necro-
Minimal diagnostic criteria
1. Acute or subacute clinical deterioration (cough, wheeze, and tizing pulmonary aspergillosis.225 This ABPA-like
other pulmonary symptoms) not explained by another etiology syndrome probably represents a true hypersensitivity
2. Total serum IgE levels Ͼ 500 IU/mL. If total IgE level is 200– reaction consequent to the colonization of Aspergil-
500 IU/mL, repeat testing in 1–3 mo is recommended lus in long-standing pulmonary cavities and the
3. Immediate cutaneous reactivity to Aspergillus or presence of
continuous release of Aspergillus antigens that leads
serum IgE antibody to A fumigatus
4. One of the following: (1) precipitins to A fumigatus or to immunologic activation.214,215 Most patients show
demonstration of IgG antibody to A fumigatus; or (2) new or a brisk response to glucocorticoids.214 –217,224
recent abnormalities on chest radiography (on chest radiography
or chest CT scan that have not cleared with antibiotics and Allergic Bronchopulmonary Mycosis: Allergic
standard physiotherapy)
bronchopulmonary mycosis is the occurrence of an
Screening for ABPA in CF
1. Maintain a high level of suspicion for ABPA in patients with CF ABPA-like syndrome due to non-A fumigatus fungal
2. Determine the total serum IgE levels annually. If the total organisms. A variety of fungal agents (Table 11) have
serum IgE levels is Ͼ 500 IU/mL, perform A fumigatus skin test been reported to cause this syndrome, but the fre-
or use an IgE antibody to A fumigatus. If results are positive, quency is far less when compared to ABPA.218,226 –240
consider diagnosis on the basis of minimal criteria
3. If the total serum IgE levels is 200–500 IU/mL, repeat the
measurement if there is increased suspicion for ABPA and perform ABPA and Allergic Aspergillus Sinusitis: Allergic
further diagnostic tests (immediate skin test reactivity to A Aspergillus sinusitis (AAS) is a clinical entity in which
fumigatus, IgE antibody to A fumigatus, A fumigatus precipitins, or mucoid impaction akin to that of ABPA occurs in the
serum IgG antibody to A fumigatus, and chest radiography) paranasal sinuses.241 The pathogenesis is also similar
to ABPA and represents an allergic hypersensitivity
hence continuous assessment may be required over response to the presence of fungi within the sinus
months with repeat performance of all the serologic cavity.242 The patient is often asymptomatic or can
investigations for ABPA before a decision to treat an manifest with symptoms of nasal obstruction, rhinor-
individual case is made.202
ABPA Without Bronchial Asthma: ABPA may
Table 11—Fungi Implicated in the Causation of
occasionally develop in an individual without preex- Allergic Bronchopulmonary Mycosis
isting asthma. We have performed a systematic
MEDLINE search for the occurrence of ABPA Fungi Study/Year
without bronchial asthma.100 In total they included A niger Sharma et al218/1985
36 cases reported across the globe; two cases dem- Helminthosporium spp Dolan et al226/1970
onstrated bronchodilator reversibility,203 and one Penicillium spp Sahn and Lakshminarayan227/1973
Aspergillus ochraceus Novey and Wells228/1978
showed airway hyperresponsiveness to methacholine
Stemphylium spp Benatar et al229/1980
challenge.204 Most of the cases demonstrated hy- Aspergillus terreus Laham et al230/1981
persensitivity to A fumigatus, but three cases Drechslera spp McAleer et al231/1981
showed hypersensitivity to Helminthosporium,203 Torulopsis spp Patterson et al232/1982
and one case each to Aspergillus niger.205,206 Be- Mucor-like spp Patterson et al232/1982
Candida spp Akiyama et al234/1984
cause of the absence of bronchial asthma, these
Pseudallescheria spp Lake et al235/1990
cases are often mistaken initially for other pulmo- Bipolaris spp Lake et al236/1991
nary disorders like bronchogenic carcinoma206 –208 Curvularia spp Lake et al236/1991
or pulmonary tuberculosis.100 Schizophyllum spp Kamei et al237/1994
Fusarium spp Backman et al238/1995
ABPA Complicating Other Conditions: Occasion- Cladosporium spp Moreno-Ancillo et al239/1996
Saccharomyces spp Ogawa et al240/2004
ally ABPA has been reported to complicate other
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- 17. rhea, headache, and epistaxis. Occasionally, the 5 Greenberger PA. Allergic bronchopulmonary aspergillo-
allergic fungal sinusitis may extend into adjacent sis. J Allergy Clin Immunol 2002; 110:685– 692
6 Rosenberg M, Patterson R, Mintzer R, et al. Clinical and
spaces such as the orbit and manifest as propto-
immunologic criteria for the diagnosis of allergic broncho-
sis.243 Although in many patients with ABPA, pulmonary aspergillosis. Ann Intern Med 1977; 86:405– 414
sinusitis can often be radiologically demonstrated, 7 Greenberger PA, Patterson R, Ghory A, et al. Late sequelae
it may not be possible to confirm the diagnosis of of allergic bronchopulmonary aspergillosis. J Allergy Clin
AAS because many patients decline to undergo the Immunol 1980; 66:327–335
8 Patterson R, Greenberger PA, Radin RC, et al. Allergic
diagnostic procedures required to establish the
bronchopulmonary aspergillosis: staging as an aid to man-
diagnosis. We currently label the patients with agement. Ann Intern Med 1982; 96:286 –291
ABPA as having concomitant AAS if there is 9 Patterson R, Greenberger PA, Halwig JM, et al. Allergic
combination of hyperattenuating mucus and/or bronchopulmonary aspergillosis: natural history and classifi-
bony erosion on a paranasal CT scan. Treatment is cation of early disease by serologic and roentgenographic
studies. Arch Intern Med 1986; 146:916 –918
initiated for ABPA with patients receiving addi-
10 Patterson R, Greenberger PA, Lee TM, et al. Prolonged
tional intranasal glucocorticoids. If the symptoms evaluation of patients with corticosteroid-dependent asthma
persist or are troublesome, surgical management stage of allergic bronchopulmonary aspergillosis. J Allergy
may be required for the management of AAS. Clin Immunol 1987; 80:663– 668
11 Greenberger PA, Patterson R. Allergic bronchopulmonary
aspergillosis and the evaluation of the patient with asthma.
J Allergy Clin Immunol 1988; 81:646 – 650
Conclusions 12 Greenberger PA, Miller TP, Roberts M, et al. Allergic
bronchopulmonary aspergillosis in patients with and without
A high index of suspicion for ABPA should be evidence of bronchiectasis. Ann Allergy 1993; 70:333–338
maintained while managing any patient with bron- 13 Greenberger PA. Clinical aspects of allergic bronchopulmo-
chial asthma whatever the severity or the level of nary aspergillosis. Front Biosci 2003; 8:S119 –S127
14 Rajan TV. The Gell-Coombs classification of hypersensitivity
control. Host immunologic responses are central to
reactions: a re-interpretation. Trends Immunol 2003; 24:376 –
the pathogenesis, and they are the primary determi- 379
nants of the clinical, biologic, pathologic, and radio- 15 Geha RS, Sampson HA, Askenase PW, et al. Allergy and
logic features of this disorder. ABPA may precede hypersensitivity. In: Janeway CA, Travers P, Walport M, et al.
the clinical recognition of the disorder for many eds. Immunobiology. New York, NY: Garland, 2001; 517–556
16 Hinson KFW, Moon AJ, Plummer NS. Broncho-pulmonary
years or even decades, and it is often misdiagnosed as
aspergillosis; a review and a report of eight new cases.
a variety of pulmonary diseases. Because a patient Thorax 1952; 7:317–333
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chopulmonary aspergillosis is often made too late]. Med Klin
patients with Aspergillus hypersensitivity, further
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immunologic studies are warranted to diagnose 19 Behera D, Guleria R, Jindal SK, et al. Allergic bronchopul-
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in the natural history of this disease. 20 Al-Mobeireek AF, El-Rab M, Al-Hedaithy SS, et al. Allergic
bronchopulmonary mycosis in patients with asthma: period
ACKNOWLEDGMENT: The author wishes to thank Dr. Aman- prevalence at a university hospital in Saudi Arabia. Respir
jit Bal, Assistant Professor, Department of Histopathology, Med 2001; 95:341–347
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