The document lists various potential cutaneous manifestations associated with different medical conditions. It includes lists of skin findings related to acquired immunodeficiency syndrome, acromegaly, Addison's disease, alcoholism, recent aquatic activity, being an athlete, bone pain, cardiovascular disease, cataracts, chemotherapy, cirrhosis, cleft lip and/or palate, conditions exacerbated by or induced by cold, Cushing's disease, cystic fibrosis, deafness, diabetes mellitus, digital anomalies, and Down syndrome. Each condition's section provides examples of relevant skin findings and suggests further readings on the dermatological aspects of each condition.
5. 27The Past Medical History, Social History, and Review of Systems
Further reading:
Mailler-Savage EA, Adams BB (2006) Skin manifestations of running. J Am Acadâ˘
Dermatol 55(2):290â301
Bone Pain
Langerhans cell histiocytosisâ˘
Leukemiaâ˘
Lymphomaâ˘
Mastocytosisâ˘
Metastatic diseaseâ˘
MuckleâWells syndromeâ˘
Myelomaâ˘
Schnitzler syndromeâ˘
Scurvyâ˘
Sickle cell diseaseâ˘
Syphilisâ˘
Tuberculosisâ˘
Further reading:
de Koning HD, Bodar EJ, van der Meer JW et al (2007) Schnitzler syndrome. Beyondâ˘
the case reports: review and follow-up of 94 patients with an emphasis on prognosis
and treatment. Semin Arthritis Rheum 37(3):137â148
Cardiovascular Disease
Behçetâs diseaseâ˘
Carcinoid syndromeâ˘
Cardiofaciocutaneous syndromeâ˘
Carneyâs complexâ˘
Carvajal syndromeâ˘
Chagas diseaseâ˘
Cutis laxaâ˘
Dermatomyositisâ˘
7. 29The Past Medical History, Social History, and Review of Systems
Cataracts
Atopic dermatitis (Andogsky syndrome)â˘
Behçetâs diseaseâ˘
Cockayneâs syndromeâ˘
Diabetes mellitusâ˘
Down syndromeâ˘
Dyskeratosis congenitaâ˘
Ectodermal dysplasiasâ˘
Epidermal nevus syndromeâ˘
Fabryâs diseaseâ˘
HallermannâStreiff syndromeâ˘
Incontinentia pigmentiâ˘
Neurofibromatosis, type IIâ˘
Neutral lipid storage diseaseâ˘
Psoralen therapyâ˘
Rheumatoid arthritisâ˘
Refsumâs diseaseâ˘
RothmundâThomson syndromeâ˘
Sarcoidosisâ˘
Steroidsâ˘
Stickler syndromeâ˘
Syphilisâ˘
VogtâKoyanagiâHarada syndromeâ˘
Wernerâs diseaseâ˘
Wilsonâs diseaseâ˘
X-linked ichthyosisâ˘
X-linked-dominant chondrodysplasia punctataâ˘
Further reading:
Freiman A, Ting PT, Barankin B, Stanciu M, Rudnisky C (2006) Ophthalmologicâ˘
manifestations of cutaneous conditions. Ophthalmologica 220(5):281â240
8. 30 Chapter 2
Chemotherapy
Acneiform eruptionâ˘
Acral erythemaâ˘
Acral sclerosisâ˘
Anagen effluviumâ˘
Atrophic skinâ˘
Atrophic nailsâ˘
Flag signâ˘
Folliculitisâ˘
Inflamed seborrheic keratosesâ˘
Inflamed actinic keratosesâ˘
Injection site reactionsâ˘
Metastatic diseaseâ˘
Neutrophilic eccrine hidradenitisâ˘
Photosensitivityâ˘
Pruritusâ˘
Radiation enhancementâ˘
Radiation recallâ˘
Raynaudâs phenomenonâ˘
Hyperpigmentationâ˘
Stomatitisâ˘
Syringosquamous metaplasiaâ˘
Worsening of psoriasisâ˘
Further reading:
Lacouture M et al (2011) Adverse skin reactions to chemotherapeutic agents.â˘
Dermatol Ther 24(4):385â442
Cirrhosis (Including Primary Biliary Cirrhosis)
Caput medusaâ˘
Cirsoid aneurysmsâ˘
Gynecomastiaâ˘
Hyperpigmentation (PBC)â˘
9. 31The Past Medical History, Social History, and Review of Systems
Jaundiceâ˘
Muehrckeâs linesâ˘
Palmar erythemaâ˘
Pruritusâ˘
Purpura and ecchymoses (Vitamin K deficiency)â˘
Scleroderma/morphea (PBC)â˘
Sparse hairâ˘
Spider angiomasâ˘
Terryâs nailsâ˘
Xanthomas (PBC)â˘
Further reading:
Koulentaki M, Ioannidou D, Stefanidou M et al (2006) Dermatological manifestationsâ˘
in primary biliary cirrhosis (PBC) patients: a case control study. Am J Gastroenterol
101(3):541â546
Cleft Lip and/or Palate
4p syndromeâ˘
HayâWells syndromeâ˘
BeareâStevenson cutis gyrata syndromeâ˘
Branchio-oculo-facial syndromeâ˘
Cleft lip/palate â ectodermal dysplasia syndromeâ˘
Dermal melanocytosisâ˘
EEC syndromeâ˘
Encephaloceleâ˘
Nasal gliomaâ˘
Nailâpatella syndromeâ˘
Nevoid basal cell carcinoma syndromeâ˘
Oculocerebrocutaneous syndromeâ˘
Oralâfacialâdigital syndromeâ˘
Popliteal pterygium syndromeâ˘
RappâHodgkin syndromeâ˘
Robert syndromeâ˘
Van der Woude syndromeâ˘
10. 32 Chapter 2
Waardenburg syndrome, type 1 or 3â˘
WolfâHirschhorn syndromeâ˘
Further reading:
Steele JA, Hansen H, Arn P, Kwong PC (2005) Spectrum of phenotypic manifestationsâ˘
from a single point mutation of the p63 gene, including new cutaneous and
immunologic findings. Pediatr Dermatol 22(5):415â419
Cold Induced or Cold Exacerbated
Acrocyanosisâ˘
Asteatotic eczemaâ˘
Atopic dermatitisâ˘
Chilblains lupus erythematosusâ˘
Cold panniculitisâ˘
Cold urticariaâ˘
Cold-water foot immersionâ˘
Cryofibrinogenemiaâ˘
Cryoglobulinemiaâ˘
Cutis marmorataâ˘
Erythrokeratolysis hiemalisâ˘
Familial cold autoinflammatory syndromeâ˘
Frostbiteâ˘
Glomus tumorâ˘
Leiomyomaâ˘
Livedo reticularisâ˘
Perniosisâ˘
Raynaudâs phenomenonâ˘
Sclerema neonatorumâ˘
Subcutaneous fat necrosis of the newbornâ˘
Further reading:
Aksentijevich ID, Putnam C, Remmers EF et al (2007) The clinical continuum ofâ˘
cryopyrinopathies: novel CIAS1 mutations in North American patients and a new
cryopyrin model. Arthritis Rheum 56(4):1273â1285
11. 33The Past Medical History, Social History, and Review of Systems
Cushingâs Disease
Acneâ˘
Candidiasisâ˘
Dermatophytosisâ˘
Facial fullnessâ˘
Hirsutismâ˘
Lipoatrophy (arms and legs)â˘
Lipohypertrophy (especially upper back, abdomen)â˘
Poor wound healingâ˘
Purpuraâ˘
Skin fragilityâ˘
Striae distensaeâ˘
Tinea versicolorâ˘
Further reading:
Jabbour SA (2003) Cutaneous manifestations of endocrine disorders: a guide forâ˘
dermatologists. Am J Clin Dermatol 4(5):315â331
Cystic Fibrosis
Acrodermatitis enteropathicaâ˘
Aquagenic wrinkling of the palms and solesâ˘
Clubbingâ˘
Cutaneous vasculitisâ˘
Essential fatty acid deficiencyâ˘
Kwashiorkor-like eruptionâ˘
Phrynodermaâ˘
Xerosisâ˘
Further reading:
Katz KA, Yan AC, Turner ML (2005) Aquagenic wrinkling of the palms in patientsâ˘
with cystic fibrosis homozygous for the delta F508 CFTR mutation. Arch Dermatol
141(5):621â624
13. 35The Past Medical History, Social History, and Review of Systems
Xeroderma pigmentosumâ˘
ZiprkowskiâMargolis syndromeâ˘
Further reading:
Richard G, Brown N, Ishida-Yamamoto A, Krol A (2004) Expanding the phenotypicâ˘
spectrum of Cx26 disorders: BartâPumphrey syndrome is caused by a novel missense
mutation in GJB2. J Invest Dermatol 123(5):856â863
Diabetes Mellitus
Acanthosis nigricans (Fig.⢠2.1)
Acral gangreneâ˘
Acral erythemaâ˘
Bullosis diabeticorumâ˘
Candidiasisâ˘
Clear cell syringomaâ˘
Dermatophytosisâ˘
Diabetic bullaeâ˘
Diabetic dermopathyâ˘
Granuloma annulare (especially disseminated type)â˘
Erythrasmaâ˘
Fig. 2.1 Acral
acanthosis nigricans
14. 36 Chapter 2
Injection lipoatrophyâ˘
Mucormycosisâ˘
Necrobiosis lipoidicaâ˘
Neuropathic ulcersâ˘
Partial lipodystrophyâ˘
Perforating disordersâ˘
Pruritusâ˘
Rubeosisâ˘
Scleredema adultorumâ˘
Xerosisâ˘
Further reading:
Ahmed I, Goldstein B (2006) Diabetes mellitus. Clin Dermatol 24(4):237â246â˘
Digital Anomalies
AdamsâOliver syndromeâ˘
Apert syndromeâ˘
Cleft lip/palateâectodermal dysplasiaâ˘
EEC syndromeâ˘
Epidermal nevus syndromeâ˘
Focal dermal hypoplasiaâ˘
KlippelâTrenaunay syndromeâ˘
Limbâmammary syndromeâ˘
Nevoid basal cell carcinoma syndromeâ˘
Oculodentodigital syndromeâ˘
Oralâfacialâdigital syndromeâ˘
Popliteal pterygium syndromeâ˘
Proteus syndromeâ˘
Trichorhinophalangeal syndromeâ˘
Waardenburg syndrome, type 3â˘
Further reading:
Kalla G, Garg A (2002) Ectrodactyly. Indian J Dermatol Venereol Leprolâ˘
68(3):152â153
15. 37The Past Medical History, Social History, and Review of Systems
Down Syndrome
Alopecia areataâ˘
Brachycephalyâ˘
Brushfield spotsâ˘
Cheilitisâ˘
Collagenomasâ˘
Cutis marmorataâ˘
Dermatophyte infectionsâ˘
Elastosis perforans serpiginosaâ˘
Folliculitisâ˘
Ichthyosisâ˘
Immunodeficiencyâ˘
Leukemiaâ˘
Lichen simplex chronicusâ˘
Miliaâlike calcinosis cutisâ˘
Neonatal transient myeloproliferative disorderâ˘
Norwegian scabiesâ˘
Scrotal tongueâ˘
Seborrheic dermatitisâ˘
Single palmar creaseâ˘
Syringomasâ˘
Vitiligoâ˘
Further reading:
Daneshpazhooh M, Nazemi TM, Bigdeloo L, Yoosefi M (2007) Mucocutaneousâ˘
findings in 100 children with Down syndrome. Pediatr Dermatol 24(3):317â320
Dysphagia/Odynophagia
Behçetâs diseaseâ˘
Candidiasisâ˘
Darierâs diseaseâ˘
Dermatomyositisâ˘
16. 38 Chapter 2
Erosive lichen planusâ˘
Graft-vs-host diseaseâ˘
Herpes simplex virus infectionâ˘
HowellâEvans syndromeâ˘
Inflammatory bowel diseaseâ˘
Iron deficiency (PlummerâVinson syndrome)â˘
Oralâocularâgenital syndromeâ˘
Pemphigusâ˘
Sclerodermaâ˘
StevensâJohnson syndromeâ˘
Zosterâ˘
Further reading:
Espana A, Fernandez S, del Olmo J et al (2007) Ear, nose, and throat manifestations inâ˘
pemphigus vulgaris. Br J Dermatol 156(4):733â737
Eating Disorder
Acneâ˘
Acquired zinc deficiencyâ˘
Acral coldnessâ˘
Acrocyanosisâ˘
Aphthous stomatitisâ˘
Calluses on hands (Russellâs sign)â˘
Carotenemiaâ˘
Cheilitisâ˘
Dental cariesâ˘
Dermatomyositis-like syndrome (Ipecac)â˘
Dry hairâ˘
Ecchymoses from vitamin K deficiencyâ˘
Edemaâ˘
Emesis-related purpuraâ˘
Enamel erosionâ˘
Enlarged parotid glandsâ˘
17. 39The Past Medical History, Social History, and Review of Systems
Factitial dermatosesâ˘
Finger clubbingâ˘
Fixed drug eruption from phenolphthalein laxativeâ˘
Gum recessionâ˘
Interdigital intertrigoâ˘
Lanugo-like hairâ˘
Livedo reticularisâ˘
Loss of subcutaneous fatâ˘
Onychorrhexisâ˘
Paronychiaâ˘
Pellagraâ˘
Periungual erythemaâ˘
Perlecheâ˘
Perniosisâ˘
Petechiae and purpuraâ˘
Pitting edemaâ˘
Poor wound healingâ˘
Prurigo pigmentosaâ˘
Pruritusâ˘
Scurvyâ˘
Seborrheic dermatitisâ˘
Striae distensaeâ˘
Telogen effluviumâ˘
Trichotillomaniaâ˘
Xerosisâ˘
Further reading:
Strumia R (2005) Dermatologic signs in patients with eating disorders. Am J Clinâ˘
Dermatol 6(3):165â173
Epilepsy
Anticonvulsant reactionâ˘
Centrofacial lentiginosisâ˘
19. 41The Past Medical History, Social History, and Review of Systems
Hereditary hemorrhagic telangiectasiaâ˘
Kaposiâs sarcomaâ˘
Kawasaki diseaseâ˘
Maffucciâs syndromeâ˘
Malignant atrophic papulosisâ˘
MuirâTorre syndromeâ˘
PeutzâJeghers syndromeâ˘
Polyarteritis nodosaâ˘
Pseudoxanthoma elasticumâ˘
Scurvyâ˘
Ulcerative colitisâ˘
Vasculitisâ˘
Further reading:
Braverman IM (2003) Skin signs of gastrointestinal disease. Gastroenterologyâ˘
124(6):1595â1614
Gastrointestinal Neoplasia
Acanthosis nigricansâ˘
Arsenicismâ˘
Carcinoid syndromeâ˘
Cowdenâs diseaseâ˘
CronkhiteâCanada syndromeâ˘
Dermatitis herpetiformisâ˘
Dermatomyositisâ˘
Extramammary Pagetâs diseaseâ˘
Gardnerâs syndromeâ˘
Kaposiâs sarcomaâ˘
LeserâTrelat signâ˘
MuirâTorre syndromeâ˘
Necrolytic migratory erythemaâ˘
Neurofibromatosisâ˘
20. 42 Chapter 2
PeutzâJeghers syndromeâ˘
Sister Mary Joseph noduleâ˘
Tylosis (HowellâEvans syndrome)â˘
Further reading:
Braverman IM (2003) Skin signs of gastrointestinal disease. Gastroenterologyâ˘
124(6):1595â1614
Hemochromatosis
Alopeciaâ˘
Atrophyâ˘
Generalized hyperpigmentationâ˘
Ichthyosisâ˘
Koilonychiaâ˘
Leukonychiaâ˘
Onychonychiaâ˘
Palmar erythemaâ˘
Porphyria cutanea tardaâ˘
Spider telangiectasiasâ˘
⢠Vibrio vulnificus infection
Further reading:
Kostler E, Porst H, Wollina U (2005) Cutaneous manifestations of metabolic diseases:â˘
uncommon presentations. Clin Dermatol 23(5):457â464
Hemodialysis
Acquired perforating diseaseâ˘
Beta-2 microglobulin amyloidosisâ˘
Calciphylaxis/calcinosis cutisâ˘
Lindsayâs nails (half-and-half nails)â˘
Muehrckeâs linesâ˘
21. 43The Past Medical History, Social History, and Review of Systems
Nephrogenic fibrosing dermopathyâ˘
Pallorâ˘
Pruritusâ˘
Pseudoporphyriaâ˘
Uremic frostâ˘
Xerosis or ichthyosisâ˘
Further reading:
Udayakumar P, Balasubramanian S, Ramalingam KS et al (2006) Cutaneousâ˘
manifestations in patients with chronic renal failure on hemodialysis. Indian J
Dermatol Venereol Leprol 72(2):119â125
Hepatitis B or Hepatitis C Infection
Cutaneous small vessel vasculitisâ˘
Disseminated superficial porokeratosis (C)â˘
Erythema multiformeâ˘
Erythema nodosumâ˘
GianottiâCrosti syndrome (B)â˘
Lichen planus (C)â˘
Mixed essential cryoglobulinemia (C>B)â˘
Necrolytic acral erythema (C)â˘
Pigmented purpuric dermatosis (C)â˘
Polyarteritis nodosa (B>C)â˘
Porphyria cutanea tarda (C)â˘
Pruritusâ˘
Urticariaâ˘
Urticarial vasculitisâ˘
Xerostomiaâ˘
Further reading:
Bonkovsky HL, Mehta S (2001) Hepatitis C: a review and update. J Am Acadâ˘
Dermatol 44(2):159â182
23. 45The Past Medical History, Social History, and Review of Systems
Crusted scabiesâ˘
Cryptococcosisâ˘
Cutaneous lymphomaâ˘
Cutaneous pneumocystosisâ˘
Cytomegalovirusâ˘
Demodicidosisâ˘
Dermatophytosisâ˘
Deep fungal infectionâ˘
Drug eruptionâ˘
Ecthymaâ˘
Ecthyma gangrenosumâ˘
Eosinophilic folliculitisâ˘
Epidermodysplasia verruciformisâ˘
Erythema multiformeâ˘
Erythrodermaâ˘
Factitiousâ˘
Fungal folliculitisâ˘
Generalized pruritusâ˘
Granuloma annulareâ˘
Herpes simplex infectionâ˘
Herpes zosterâ˘
Histoplasmosisâ˘
HTLV-1 leukemia/lymphomaâ˘
Hyperpigmentationâ˘
Insect-bite reactionâ˘
Kaposiâs sarcomaâ˘
Kwashiorkorâ˘
Leishmaniasisâ˘
Lymphomaâ˘
Molluscum contagiosumâ˘
Necrotizing fasciitisâ˘
Non-Hodgkinâs lymphomaâ˘
Papular eruption of AIDSâ˘
Papular mucinosisâ˘
24. 46 Chapter 2
Papular urticariaâ˘
Penicilliosisâ˘
Perioral dermatitisâ˘
Photosensitive drug eruptionâ˘
Pityriasis rubra pilaris (type VI)â˘
Porphyria cutanea tardaâ˘
Post-inflammatory hyperpigmentationâ˘
Psoriasis (more severe)â˘
Reactive arthritis with urethritisâ˘
RED syndrome (see toxic shock syndrome)â˘
Rosaceaâ˘
Scabiesâ˘
Seborrheic dermatitisâ˘
Smooth muscle tumors (angioleiomyoma)â˘
Squamous cell carcinomaâ˘
StevensâJohnson syndromeâ˘
Toxic epidermal necrolysisâ˘
Verruca vulgarisâ˘
Verrucous carcinomaâ˘
Viral exanthemâ˘
Xerosisâ˘
Further reading:
Zancanaro PC, McGirt LY, Mamelak AJ et al (2006) Cutaneous manifestations of HIVâ˘
in the era of highly active antiretroviral therapy: an institutional urban clinic
experience. J Am Acad Dermatol 54(4):581â588
Hyperthyroidism
Alopecia areataâ˘
Hyperpigmentationâ˘
Koilonychiaâ˘
Onycholysisâ˘
Pemphigoid gestationisâ˘
Pretibial myxedemaâ˘
25. 47The Past Medical History, Social History, and Review of Systems
Pruritusâ˘
Thyroid acropachyâ˘
Urticariaâ˘
Vitiligoâ˘
Further reading:
Jabbour SA (2003) Cutaneous manifestations of endocrine disorders: a guide forâ˘
dermatologists. Am J Clin Dermatol 4(5):315â331
Hypothyroidism
Ascher syndromeâ˘
Carotenodermaâ˘
Chronic urticariaâ˘
Brittle hairâ˘
Easy bruisingâ˘
Eruptive and tuberous xanthomasâ˘
Hypohidrosisâ˘
Ichthyosisâ˘
Madarosisâ˘
Myxedemaâ˘
Onycholysisâ˘
Palmoplantar keratodermaâ˘
Vitiligoâ˘
Further reading:
Jabbour SA (2003) Cutaneous manifestations of endocrine disorders: a guide forâ˘
dermatologists. Am J Clin Dermatol 4(5):315â331
Immunosuppressed/Transplant Recipient
Actinic keratosisâ˘
Basal cell carcinomaâ˘
Candidiasisâ˘
Cryptococcosisâ˘
33. 55The Past Medical History, Social History, and Review of Systems
Scleromyxedemaâ˘
Subcorneal pustular dermatosisâ˘
Subepidermal bullous dermatosisâ˘
Sweetâs syndromeâ˘
Xanthoma disseminatumâ˘
Further reading:
Satta R, Casu G, Dore F, Longinotti M, Cottoni F (2003) Follicular spicules andâ˘
multiple ulcers: cutaneous manifestations of multiple myeloma. J Am Acad Dermatol
49(4):736â740
Multiple Endocrine Neoplasia, Type I
Adrenocortical tumorsâ˘
Angiofibromasâ˘
Cafe-au-lait maculesâ˘
Collagenomasâ˘
Confetti-like hypopigmentationâ˘
Gastrointestinal tumorsâ˘
Gingival papulesâ˘
Leiomyomasâ˘
Lipomasâ˘
Melanomaâ˘
Parathyroid adenomaâ˘
Pituitary adenomaâ˘
Further reading:
Jabbour SA, Davidovici BB, Wolf R (2006) Rare syndromes. Clin Dermatolâ˘
24(4):299â316
Multiple Endocrine Neoplasia, Type IIA
Lichen amyloidosisâ˘
Medullary thyroid carcinomaâ˘
34. 56 Chapter 2
Parathyroid hyperplasiaâ˘
Pheochromocytomaâ˘
Pruritusâ˘
Further reading:
Jabbour SA, Davidovici BB, Wolf R (2006) Rare syndromes. Clin Dermatolâ˘
24(4):299â316
Multiple Endocrine Neoplasia, Type IIB
Cafe-au-lait maculesâ˘
Elongated faciesâ˘
Marfanoid habitusâ˘
Medullary thyroid carcinomaâ˘
Mucosal neuromasâ˘
Pheochromocytomaâ˘
Further reading:
Jabbour SA, Davidovici BB, Wolf R (2006) Rare syndromes. Clin Dermatolâ˘
24(4):299â316
Obesity
Acanthosis nigricansâ˘
Acrochordonsâ˘
Adiposis dolorosaâ˘
Bacterial infectionsâ˘
Candidiasisâ˘
Dermatophytosisâ˘
Frictional hyperpigmentationâ˘
Goutâ˘
35. 57The Past Medical History, Social History, and Review of Systems
Hidradenitisâ˘
Hyperhidrosisâ˘
Intertrigoâ˘
Keratosis pilarisâ˘
Lipodermatosclerosisâ˘
Plantar hyperkeratosisâ˘
Pseudoacanthosis nigricansâ˘
Psoriasisâ˘
Stasis dermatitisâ˘
Striae distensaeâ˘
Venous insufficiency ulcersâ˘
Further reading:
Yosipovitch G, DeVore A, Dawn A (2007) Obesity and the skin: skin physiology andâ˘
skin manifestations of obesity. J Am Acad Dermatol 56(6):901â916
Pancreatic Disease
Cullenâs signâ˘
Familial melanomaâ˘
Glucagonoma syndromeâ˘
Jaundiceâ˘
Livedo reticularisâ˘
Metastatic diseaseâ˘
Migratory thrombophlebitis (Trousseauâs syndrome)â˘
Multiple endocrine neoplasiaâ˘
Panniculitisâ˘
Systemic lupus erythematosusâ˘
Turnerâs signâ˘
Xanthomas (hypertriglyceridemia)â˘
Further reading:
Kobayashi S, Yoshida M, Kitahara T et al (2007) Autoimmune pancreatitis as theâ˘
initial presentation of systemic lupus erythematosus. Lupus 16(2):133â136
36. 58 Chapter 2
POEMS Syndrome (CrowâFukase Syndrome)
Alopeciaâ˘
Cherry angiomasâ˘
Clubbingâ˘
Flushingâ˘
Glomeruloid hemangiomasâ˘
Hyperpigmentationâ˘
Hypertrichosisâ˘
Lymphadenopathyâ˘
Ichthyosisâ˘
Microvenular hemangiomasâ˘
Raynaudâs phenomenonâ˘
Sclerodermoid changesâ˘
Further reading:
Phillips JA, Dixon JE, Richardson JB et al (2006) Glomeruloid hemangioma leading toâ˘
a diagnosis of POEMS syndrome. J Am Acad Dermatol 55(1):149â152
Polyps, Intestinal
BannayanâRileyâRuvalcabaâ˘
BirtâHoggâDube syndromeâ˘
CronkhiteâCanada syndromeâ˘
Familial polyposisâ˘
Gardnerâs syndromeâ˘
MuirâTorre syndromeâ˘
Neurofibromatosisâ˘
PeutzâJeghers syndromeâ˘
Further reading:
Braverman IM (2003) Skin signs of gastrointestinal disease. Gastroenterologyâ˘
124(6):1595â1614
37. 59The Past Medical History, Social History, and Review of Systems
Pregnant
Acne vulgarisâ˘
Atopic dermatitis of pregnancyâ˘
Cholestasis of pregnancyâ˘
Darkening of neviâ˘
Diffuse hyperpigmentationâ˘
Erythema nodosumâ˘
Folliculitisâ˘
Impetigo herpetiformisâ˘
Melasmaâ˘
Palmar erythemaâ˘
Pemphigoid gestationisâ˘
Prurigo of pregnancyâ˘
Pruritic urticarial papules and plaques of pregnancyâ˘
Pyogenic granulomaâ˘
Spider telangiectasiasâ˘
Striae gravidarumâ˘
Urticariaâ˘
Varicositiesâ˘
Further reading:
Ambros-Rudolph CM (2006) Dermatoses of pregnancy. J Dtsch Dermatol Gesâ˘
4(9):748â759
Pulmonary Disease
Antitrypsin deficiency panniculitisâ˘
Arsenicismâ˘
Aspergillosisâ˘
Atopic dermatitisâ˘
BirtâHoggâDube syndromeâ˘
Blastomycosisâ˘
38. 60 Chapter 2
Chronic granulomatous diseaseâ˘
ChurgâStrauss syndromeâ˘
Coccidioidomycosisâ˘
CREST syndromeâ˘
Cystic fibrosisâ˘
Dermatomyositisâ˘
Hereditary hemorrhagic telangiectasiaâ˘
Histoplasmosisâ˘
Langerhans cell histiocytosisâ˘
Lymphomatoid granulomatosisâ˘
Mycoplasma infectionâ˘
Nocardiosisâ˘
Sarcoidosisâ˘
Sclerodermaâ˘
Sweetâs syndromeâ˘
Tuberculosisâ˘
Wegenerâs granulomatosisâ˘
Viral infectionâ˘
Tuberous sclerosusâ˘
Further reading:
Astudillo L, Sailler L, Launay F et al (2006) Pulmonary involvement in Sweetâsâ˘
syndrome: a case report and review of the literature. Int J Dermatol 45(6):677â680
Renal Disease
Alportâs syndromeâ˘
BirtâHoggâDube syndromeâ˘
Cholesterol emboli syndromeâ˘
Fabryâs diseaseâ˘
Goodpastureâs syndromeâ˘
HenochâSchĂśnlein purpuraâ˘
Hereditary leiomyomatosisâ˘
Myelomaâ˘
39. 61The Past Medical History, Social History, and Review of Systems
Nailâpatella syndromeâ˘
Neurofibromatosisâ˘
Oxalosisâ˘
Polyarteritis nodosaâ˘
Primary systemic amyloidosisâ˘
Pseudoporphyriaâ˘
Pseudoxanthoma elasticumâ˘
Renal cell carcinomaâ˘
Sarcoidosisâ˘
Sclerodermaâ˘
Small vessel vasculitisâ˘
Systemic lupus erythematosusâ˘
Tuberous sclerosusâ˘
Wegenerâs granulomatosisâ˘
Further reading:
Abdelbaqi-Salhab M, Shalhub S et al (2003) A current review of the cutaneousâ˘
manifestations of renal disease. J Cutan Pathol 30(9):527â538
Rheumatoid Arthritis
Accelerated rheumatoid nodulosisâ˘
Alopecia areataâ˘
Bullous pemphigoidâ˘
Bywaters lesionsâ˘
Cicatricial pemphigoidâ˘
Clubbingâ˘
Dermatitis herpetiformisâ˘
Digital pulp nodulesâ˘
Epidermolysis bullosa acquisitaâ˘
Erythema elevatum diutinumâ˘
Erythema multiformeâ˘
Erythema nodosumâ˘
Erythromelalgiaâ˘
40. 62 Chapter 2
Feltyâs syndromeâ˘
Hyperpigmentationâ˘
Interstitial granulomatous dermatitis with arthritisâ˘
Linear necrobiotic subcutaneous bandsâ˘
Localized hyperhidrosisâ˘
Mondorâs diseaseâ˘
Nail-fold telangiectasiaâ˘
Onychorrhexisâ˘
Palisaded neutrophilic and granulomatous dermatitisâ˘
Palmar erythemaâ˘
Pemphigusâ˘
Pyoderma gangrenosumâ˘
Reactive angioendotheliomatosisâ˘
Rheumatoid neutrophilic dermatitisâ˘
Rheumatoid nodulesâ˘
Rheumatoid vasculitisâ˘
Small vessel vasculitisâ˘
Splinter hemorrhagesâ˘
Subcorneal pustular dermatosisâ˘
Sweetâs syndromeâ˘
Transient macular erythemaâ˘
Urticariaâ˘
Vasculitisâ˘
Vitiligoâ˘
Yellow nail syndromeâ˘
Further reading:
Sayah A, English JC III (2005) Rheumatoid arthritis: a review of the cutaneousâ˘
manifestations. J Am Acad Dermatol 53(2):191â209
Sexually Promiscuous
Amebiasisâ˘
Candidiasisâ˘
41. 63The Past Medical History, Social History, and Review of Systems
Chancroidâ˘
⢠Chlamydia
Cytomegalovirusâ˘
Giardiasisâ˘
Gonorrheaâ˘
Granuloma inguinaleâ˘
Hepatitis A virusâ˘
Hepatitis B virusâ˘
Hepatitis C virusâ˘
Herpes simplex virusâ˘
Human herpes virus, type 8â˘
Human immunodeficiency virusâ˘
Human papillomavirus virusâ˘
Human T cell lymphotrophic virusâ˘
Lymphogranuloma venereumâ˘
Mobiluncus infectionâ˘
Molluscum contagiosumâ˘
Nongococcal urethritisâ˘
Pediculosis pubisâ˘
Scabiesâ˘
Syphilisâ˘
Trichomoniasisâ˘
Further reading:
Wang QQ, Mabey D, Peeling RW et al (2002) Validation of syndromic algorithm forâ˘
the management of genital ulcer diseases in China. Int J STD AIDS 13(7):469â474
SjĂśgren Syndrome
Amyloidosisâ˘
Annular erythemaâ˘
Benign hypergammaglobulinemic purpura of Waldenstromâ˘
Erythema multiforme-like lesionsâ˘
Erythema nodosumâ˘
45. 67The Past Medical History, Social History, and Review of Systems
Solar lentiginesâ˘
Squamous cell carcinomaâ˘
Stellate pseudoscarsâ˘
Telangiectasiaâ˘
Weathering nodulesâ˘
Venous lakeâ˘
Further reading:
Heras JA, Jimenez F, Soguero ML et al (2007) Bullous solar elastosis.â˘
Clin Exp Dermatol 32(3):272â274
Tick Bite
Babesiosisâ˘
Boutonneuse feverâ˘
Colorado tick feverâ˘
Human granulocytic anaplasmosisâ˘
Human monocytic ehrlichiosisâ˘
Lyme diseaseâ˘
Q feverâ˘
Fig. 2.5 Colloid
milium (Courtesy of
W. T. Massengale)
46. 68 Chapter 2
Rocky Mountain spotted feverâ˘
Southern tick-associated rash illnessâ˘
Tick-borne relapsing feverâ˘
Tularemiaâ˘
Further reading:
McGinley-Smith DE, Tsao SS (2003) Dermatoses from ticks. J Am Acad Dermatolâ˘
49(3):363â392
Turner Syndrome
Alopecia areataâ˘
Cardiovascular defectsâ˘
Cystic hygromaâ˘
Gonadal dysgenesisâ˘
Halo nevusâ˘
Keloidsâ˘
Lymphedemaâ˘
Multiple melanocytic neviâ˘
Renal malformationsâ˘
Short statureâ˘
Thyroid diseaseâ˘
Webbed neckâ˘
Widely spaced nipplesâ˘
Further reading:
Lowenstein EJ, Kim KH, Glick SA (2004) Turnerâs syndrome in dermatology.â˘
J Am Acad Dermatol 50(5):767â776
Virilization
Abnormal menstrual cycleâ˘
Acneâ˘
Androgenic alopeciaâ˘
Clitoral hypertrophyâ˘
47. 69The Past Medical History, Social History, and Review of Systems
Decreased breast sizeâ˘
Deep voiceâ˘
Hirsutismâ˘
Further reading:
Lee AT, Zane LT (2007) Dermatologic manifestations of polycystic ovary syndrome.â˘
Am J Clin Dermatol 8(4):201â219
X-Linked Dominant Inheritance Pattern
Albright hereditary osteodystrophyâ˘
Bazexâs syndromeâ˘
CHILD syndromeâ˘
Congenital generalized hypertrichosisâ˘
ConradiâHunermann syndromeâ˘
Goltz syndromeâ˘
Incontinentia pigmentiâ˘
Oralâfacialâdigital syndromeâ˘
X-Linked Recessive Inheritance Pattern
Anhidrotic ectodermal dysplasiaâ˘
Brutonâs agammaglobulinemiaâ˘
Chronic granulomatous diseaseâ˘
Crandallâs syndromeâ˘
Duncanâs syndromeâ˘
Dyskeratosis congenitaâ˘
Fabryâs diseaseâ˘
Hunter syndromeâ˘
Keratosis follicularis spinulosa decalvansâ˘
LeschâNyhan diseaseâ˘
Menkes kinky-hair diseaseâ˘
Severe combined immunodeficiencyâ˘
WiskottâAldrich syndromeâ˘
X-linked ichthyosisâ˘