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NEOPLASIA
Uncontrolled uncoordinated
 cell division non responsive
.to growth controls
:Benign            Malignant
   Well circumscribed,         Not well cirumscribed,
   Usually small in size,      Usually larger in size,
   Slow growing,               Fast growing,
   capsulated,                 non capsulated,
   Non-invasive                Invasive & Infiltrate
   No hge. and necrosis        He and necrosis.
   do not metastasize,         Metastasize.
   well differentiated,        poorly differentiated,
   suffix “oma” eg.            Suffix “Carcinoma” or
    Fibroma.                     “Sarcoma”
Signs of malignancy
Cellular
                             Nuclear
   Dysplasia (different
    from tissue of origin)      Large nuclei
   Disorganization             Hyperchromasia.
   Loss of polarity.           N/C ratio high.
   Pleomorphism                Pleomorphic nuclei.
    (variable in size and       Prominent nucleoli.
    shape)                      Frequent mitoses.
   Loss of cohesion.           Abnormal mitotic
   Presence of giant            figures.
    cells
Tumor Diagnosis
   History and Clinical examination
   Imaging - X-Ray, US, CT, MRI
   Biopsy –
    – Conventional histopathology: Paraffin sections stained with ordinary
      stains
    – Frozen sections: Intra-operativeexamination of frozen tissue
      sections.
    – Immunohistochemistry: Paraffin or frozen sections stained for
      markers.
   Cytology –
    – Exfoliative cytology : study of cells shedded in body fluids.
    – FNAB: Aspiration of cells from tumor masses.
   Tumor markers: Blood laboratory analysis
   Molecular Tech (DNA studies)
    – Gene re-arrangement studies ( in lymphoma)
    – DNA quantitation by image analaysis or flow cytometry.
Benign   Malignant
Slides of the week
Benign   Epithelial Tumours

 Squamous   cell papilloma.
 Adenoma intestine.
 Pericanalicular fibroadenoma.
 Intracanalicular fibroadenoma.
Papilloma
 Squamous cell papilloma(1)
.skin
Columnar cell papilloma(2)
as :Duct papilloma of breast
Squamous cell Papilloma
.Benign tumors of surface epithelium

 :Grossly
 Non capsulated, projectingvillous-like from
.the surface, sessile or pedunculated


:Microsciopically
 Vascularized connective tissue      core
.covered with proliferating epithelium

                                    .
                                   [-
Squamous cell papilloma
Squamous cell papilloma
Squamous cell papilloma
Squamous cell papilloma
Squamous cell papilloma
Duct Papilloma, Breast
Adenoma
.Benign tumor arising from columnar epithelium
Grossly: Capsulated, round or oval mass with a
.solid or cystic cut section
:Histological types
.: proliferating acini with stromaSimple adenoma(1)
: proliferating acini+Fibroadenoma(2)
 proliferatingstroma.( (Breast
: proliferating acini with dilatedCystadenoma(3)
 acini forming cysts.((Ovary
: cystadenoma withPapillary cystadenoma(4)
  the epithelial lining forming.papillae
Adenoma of intestine

  Benign tumour formed of 
 1-proliferating intestinal mucosal
  glands lined with columnar
  epithelial cells and slightly variable in
  size
 2- Glands separated by vascularized
  connective tissue stroma.
Adenomatous polyp - Colon
Familial Adenomatous Polyposis
Intestinal adenoma,Villous type
Adenoma
Adenoma
Fibroadenoma of the breast
* Mixed Tumour formed of  epithelial and stromal
elements
•Most common breast tumor in adolescent and young       adult
women (peak age = third decade).
• Higher incidence in black patients
• Well-circumscribed, freely movable (Breast mouse), non
painful mass
• Regress with age if left untreated (hormonal-dependent T).

•2 Types :
1- intracanalicular pattern. Compressed ducts
2-pericanalicular growth . Opened ducts .
Breast Fibroadenoma
Pericanalicular fibroadenoma
Tumor is capsulated
Tumor consists of:
1-  Opened proliferating breast ducts
  lined with an inner columnar and outer
 myoepithelial cells.
2- Ducts are separated by loose myxoid
 connective tissue stroma.
Pericanalicular fibroadenoma
Intracanalicular fibroadenoma
* Tumor is capsulated
•   Tumor consists of 
• 1- Compressed proliferating breast
  ducts that are lined with an inner
  columnar and outer myoepithelial
  cells.
• 2- Ducts are separated by  loose
  myxoid connective tissue stroma.
Intracanalicular Fibroadenoma
Slides of benign epithelium t.

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Slides of benign epithelium t.

  • 1. NEOPLASIA Uncontrolled uncoordinated cell division non responsive .to growth controls
  • 2. :Benign Malignant  Well circumscribed,  Not well cirumscribed,  Usually small in size,  Usually larger in size,  Slow growing,  Fast growing,  capsulated,  non capsulated,  Non-invasive  Invasive & Infiltrate  No hge. and necrosis  He and necrosis.  do not metastasize,  Metastasize.  well differentiated,  poorly differentiated,  suffix “oma” eg.  Suffix “Carcinoma” or Fibroma. “Sarcoma”
  • 3. Signs of malignancy Cellular Nuclear  Dysplasia (different from tissue of origin)  Large nuclei  Disorganization  Hyperchromasia.  Loss of polarity.  N/C ratio high.  Pleomorphism  Pleomorphic nuclei. (variable in size and  Prominent nucleoli. shape)  Frequent mitoses.  Loss of cohesion.  Abnormal mitotic  Presence of giant figures. cells
  • 4. Tumor Diagnosis  History and Clinical examination  Imaging - X-Ray, US, CT, MRI  Biopsy – – Conventional histopathology: Paraffin sections stained with ordinary stains – Frozen sections: Intra-operativeexamination of frozen tissue sections. – Immunohistochemistry: Paraffin or frozen sections stained for markers.  Cytology – – Exfoliative cytology : study of cells shedded in body fluids. – FNAB: Aspiration of cells from tumor masses.  Tumor markers: Blood laboratory analysis  Molecular Tech (DNA studies) – Gene re-arrangement studies ( in lymphoma) – DNA quantitation by image analaysis or flow cytometry.
  • 5. Benign Malignant
  • 6.
  • 7.
  • 8.
  • 9.
  • 10.
  • 11. Slides of the week Benign Epithelial Tumours  Squamous cell papilloma.  Adenoma intestine.  Pericanalicular fibroadenoma.  Intracanalicular fibroadenoma.
  • 12. Papilloma  Squamous cell papilloma(1) .skin Columnar cell papilloma(2) as :Duct papilloma of breast
  • 13. Squamous cell Papilloma .Benign tumors of surface epithelium :Grossly Non capsulated, projectingvillous-like from .the surface, sessile or pedunculated :Microsciopically Vascularized connective tissue core .covered with proliferating epithelium . [-
  • 20. Adenoma .Benign tumor arising from columnar epithelium Grossly: Capsulated, round or oval mass with a .solid or cystic cut section :Histological types .: proliferating acini with stromaSimple adenoma(1) : proliferating acini+Fibroadenoma(2) proliferatingstroma.( (Breast : proliferating acini with dilatedCystadenoma(3) acini forming cysts.((Ovary : cystadenoma withPapillary cystadenoma(4) the epithelial lining forming.papillae
  • 21. Adenoma of intestine  Benign tumour formed of   1-proliferating intestinal mucosal glands lined with columnar epithelial cells and slightly variable in size  2- Glands separated by vascularized connective tissue stroma.
  • 22.
  • 26.
  • 29. Fibroadenoma of the breast * Mixed Tumour formed of  epithelial and stromal elements •Most common breast tumor in adolescent and young adult women (peak age = third decade). • Higher incidence in black patients • Well-circumscribed, freely movable (Breast mouse), non painful mass • Regress with age if left untreated (hormonal-dependent T). •2 Types : 1- intracanalicular pattern. Compressed ducts 2-pericanalicular growth . Opened ducts .
  • 31. Pericanalicular fibroadenoma Tumor is capsulated Tumor consists of: 1-  Opened proliferating breast ducts  lined with an inner columnar and outer myoepithelial cells. 2- Ducts are separated by loose myxoid connective tissue stroma.
  • 33. Intracanalicular fibroadenoma * Tumor is capsulated • Tumor consists of  • 1- Compressed proliferating breast ducts that are lined with an inner columnar and outer myoepithelial cells. • 2- Ducts are separated by  loose myxoid connective tissue stroma.