Ovarian tumours
The article examines ovarian tumours including ovarian cancer.
An introduction to the ovary is in the ovary article, which also deals benign cysts.
What was labeled "ovarian cancer" in the past may really arise from fallopian tube.[1] The label tubo-ovarian cancer has been advocated to address this change. These tumours are dealt with in this article.
Clinical
Gynecologists use a scoring system to help decide which patients need surgery and estimate their pre-op risk of malignancy.
Risk of malignancy index
- Abbreviated RMI.
- There are two versions.[2]
Definition
Elements
Elements & points (RMI 2):[2]
- Ultrasound features.
- Significant findings: multilocular cyst, solid component, bilateral lesions, ascites, suspected intra-abdominal metastases (one finding=1 point, two or more findings=4 points).
- Menopause/pre-menopause status (menopausal=4 points, pre-menopausal=1 point).
- CA-125 (blood test) in U/ml.
Interpretation
- RMI > 200 -- predicts malignancy.
Classification
The Latta rule of fives
Can be divided as follows:[3][4]
- Surface epithelial tumours (most common).
- Sex cord stromal tumours (SCSTs).
- Germ cell tumours (GCTs).
- Metastatic tumours.
- Rare stuff that doesn't fit in any of the above (e.g. leiomyoma, angiosarcoma, ovarian small cell carcinoma of the hypercalcemic type).
Surface epithelial tumours:
- Serous carcinoma.
- High-grade serous carcinoma. †
- Low-grade serous carcinoma.
- Endometrioid carcinoma.
- Mucinous carcinoma.
- Clear cell carcinoma.
- Brenner tumour.
Note:
Sex cord stromal tumours:
- Granulosa cell tumour (adult type, juvenile type).
- Sertoli cell tumour.
- Leydig cell tumour.
- Fibroma.
- Thecoma.
- Dysgerminoma.
- Endodermal sinus tumour (yolk sac tumour).
- Embryonal carcinoma.
- Choriocarcinoma.
- Teratoma.
Common special tumours
Tumours associated with endometriosis:[8]
- Endometrioid.
- Clear cell carcinoma.
- Endocervical mucinous (AKA Seroumucinous type and Muellerian type).
Solid ovarian tumours
Simple version: basically anything sex cord stromal.
List:[9]
- Brenner tumour.
- SCSTs:
- Fibroma.
- Thecoma.
- Fibrothecoma.
- Leydig tumour.
- Sertoli cell tumour.
- Sertoli-Leydig tumour.
- Granulosa cell tumour.
- Granulosa-theca cell tumour.
A morphologic approach
Where is the tumour arising?
- Central location -- think GCTs and SCST.
- Surface of ovary -- think surface epithelial tumour.
- If no surface is apparent... possibly obliterated by tumour.
Spindle cell morphology?
- Consider sex cord stromal tumours.
Nests of cells?
- Consider Brenner tumour.
Gland-like structures?
- Endometrioid carcinoma.
- Granulosa cell tumour.
- Definition: cellular debris within gland lumen.[10]
- Characteristic of colorectal adenocarcinoma, may be absent in ovarian tumours -- limited value.[11]
Grading of ovarian cancer
- Silverberg grading system,[12] aka universal grading system.
- Based on pattern, cytologic atypia and mitotic rate.
- System somewhat similar to breast grading, which can be remembered as: TMN (tubular formation, mitotic rate, nuclear atypia).
Silverberg system
- Pattern:
- Glandular = 1.
- Papillary = 2.
- Solid = 3.
- Cytologic atypia:
- Slight = 1.
- Moderate = 2.
- Marked = 3.
- Mitoses (see note below):
- 0-9/(0.345 x10 mm^2) = 1.
- 10-24/(0.345 x10 mm^2) = 2.
- >=25/(0.345 x10 mm^2) = 3.
Composite score (pattern score + cytologic score + mitotic score):
- Grade I = 3-5.
- Grade II = 6-7.
- Grade III = 8-9.
Note:
- Most resident microscopes have an eyepiece diameter of 22 mm. Thus, the approximate field diameter is 0.55 mm (22 mm/40 X = 0.55 mm), at highest magnification, and the field area is 0.23758 mm^2 (pi*(0.55/2)^2=0.23758 mm^2).
- The number of HPFs should be adjusted if the area per field is different than 0.345 mm^2.
- If the field diameter is 0.55 mm and the sample area is 3.45 mm^2, this is equivalent to 14.52 HPFs (3.45 mm^2 / 0.23758 mm^2 = 14.52); thus, it would be appropriate to use 15 HPFs and the cut points above.
Predictive power of Silverberg grading
Good correlation with five year survival (rounded values):[13]
- Grade I = 90%.
- Grade II = 65%.
- Grade III = 40%.
Peritoneal implants
General
Applies only to:
Classification
There are two types:[14]
- Non-invasive implants.
- Subdivided into:
- Epithelial.
- Desmoplastic.
- Subdivided into:
- Invasive implants -- malignant cells within the stroma.
Notes:
- Invasive implants are significant clinically.
- Non-invasive implants have little clinical significance.
Microscopic
Non-invasive implant
Features (non-invasive implant epithelial-type):[15]
- Papillary proliferation on surface.
- +/-Smooth contoured invagination into:
- Submesothelium.
- Omental fat lobules.
- No "stromal response":
- Fibrosis.
- +/-Psammoma bodies.
Features (non-invasive implant desmoplastic-type):[15]
- Stromal reaction restricted to the:
- Serosal surface.
- Fibrous septae.
- +/-Psammoma bodies.
Note:
- No "destructive invasion".
- Irregular infiltration.
Invasive implant
Features (invasive implant):[15]
- Irregular infiltration of tumour into the submesothelial tissue - key feature - characterized by:
- +/-Solid nests.
- +/-Small glands +/- irregular "bridging" connections between glands - common.
- Nuclear atypia - common.
- +/-Psammoma bodies.
Stains
- Elastin stain:[14]
- Non-invasive implants are sit superficial to the peritoneal elastic lamina (PEL).
- Invasive implants are deep to the PEL.
Note:
- Elastin layer is not present in the omentum.
IHC
- Elastin stain.
Staging of ovarian cancer
- The CAP protocol talks of in the pelvis and outside the pelvis - pT2 versus pT3.
- Omental involvement is considered outside the pelvis; it is pT3.[16]
Surface epithelial tumours
Most common subtypes - in short:[17]
- Serous:
- Columnar cells.
- Cilia.
- Psammoma bodies.
- Papillae.
- Endometrioid:
- Tubular glands.
- Squamous differentiation (eosinophilic cytoplasm, well-defined cell borders, +/-keratin).
- Mucinous:
- Tall columnar cells with mucin.
- Glands with mucin.
Where to start when considering a malignant (epithelial) tumour of the ovary:
Features | Serous | Endometrioid | Mucinous |
---|---|---|---|
Histology | low grade: cilia, columnar cells, psammoma bodies, papillary arch.; high grade: marked nuclear pleomorphism, prominent red nucleoli, psammoma bodies | gland forming - esp. cribriforming, endometrium-like | mucinous glands, colon-like |
Differentiators | cilia, psammoma bodies | squamous metaplasia | mucin, often lack of necrosis |
Associations | atrophy | endometriosis, endometrial hyperplasia | (?) |
Typical age | usually 60s+ | 40-60 | varies (?) |
Grade | typically high grade | typically low grade | often low |
IHC | p53 +ve (diffuse), WT-1 +ve, CA-125 +ve, D2-40 +ve | WT-1 -ve | CK7 +ve, CK20 +ve (other tumours CK7 +ve, CK20 -ve) |
Main DDx | poorly diff. endometrioid | serous | metastatic tumour (usually GI) |
Serous tumours - overview
General
- Most common malignant ovarian tumour.
Classification
Based on features predictive of behaviour:[18]
- Benign.
- Borderline.
- May have pseudostratification of epithelial cells.
- "Usually, borderline if first impression is borderline."[19]
- Malignant.
- Cytologic atypia.
- +/-Papillae.
Microscopic
Features:[18]
- Tubal like epithelium:
- Ciliated.
- Columnar.
- Papillae.
- Psammoma bodies (concentric calcifications).
Note:
- In serous borderline tumours, micropapillae are thought to have significance -- assoc. with increased risk of distant recurrence[20][21][22] - though is disputed.[23]
- Psammoma bodies may be seen in endosalpingiosis.[24]
Serous carcinoma of the ovary
- AKA ovarian serous carcinoma.
Serous cystadenoma of the ovary
- AKA ovarian serous cystadenoma.
- Related to adenofibroma and serous cystadenofibroma.
Ovarian serous borderline tumour
- AKA serous borderline tumour of the ovary.
- AKA serous tumour of low malignant potential of the ovary, abbreviated SLMP.[25][26]
- AKA serous ovarian tumour of low malignant potential.[26]
General
- Usually benign.
- Require long term follow-up.
Microscopic
Features:[27]
- Cuboidal to columnar epithelium with mild to moderate atypia.
- No invasive.
- "Sparse" mitoses.
- +/-Psammoma bodies.
- +/-Micropapillary architecture - often described as a medusa head pattern.
DDx:
- Serous carcinoma of the ovary - focus a with stromal invasion >5mm (linear measurement) or > 10 mm2 (area).[27]
- Invasive cells are "pink", i.e. have abundant eosinophilic cytoplasm,[27]; also, cells usu. large (~2-3x size of non-invasive component), and typically have an enlarged nucleus (~2x non-invasive component).
- Clear cell carcinoma of the ovary - classically associated with endometriosis, have simpler, smaller papillae without branching.
Images:
Subclassification
Typical subdivided into:[29]
- Micropapillary serous borderline tumour.
- Typical serous borderline tumour (SBOT).
Mucinous tumours - overview
General
- Common.
- Tumours may be heterogenous; benign appearing epithelium may be beside clearly malignant epithelium.
- Good sampling of mucinous tumours, i.e. many blocks, is important to lessen the chance of undercalling them.
Subtypes
- Endocervical type.
- Less likely to be malignant.
- More common than malignant type.
- Intestinal type.
- More likely to be malignant.
- Goblet cells. (???)
- One large clear apical vacuole.
- If it doesn't look like intestine to you... it probably isn't.
- May vaguely resemble colorectal adenocarcinoma (hyperchromatic, columnar nuclei, nuclear pleomorphism).
- Image: [1]
Comparison of mucosa:
- Normal endocervical mucosa: endocervical mucosa (duke.edu).
- Normal gastric mucosa: gastric mucosa (WC).
Classification
- Benign. (Dx: mucinous cystadenoma or mucinous adenofibroma or mucinous cystadenofibroma)
- Single layer of cells.
- Borderline. (Dx: mucinous tumour of uncertain malignant potential or borderline mucinous tumour)
- Papillae.
- Malignant. (Dx: mucinous adenocarcinoma)
- Usually intestinal subtype.
Seromucinous borderline tumour of the ovary
General
- Rare.
- Associated with endometriosis.
Gross
- Mucin-filled cysts.
Image:
Microscopic
Features:
- Simple mucinous epithelium - endocervical type.[31]
- Tall columnar epithelium with apical pale cytoplasm.
- Simple serous epithelium - with cilia.
Mucinous cystadenoma of the ovary
- AKA ovarian mucinous cystadenoma.
Mucinous borderline tumour of the ovary
General
- Requires extensive sampling - to avoid missing an adenocarcinoma.
Note:
- The WHO prefers borderline over low malignant potential as the descriptor for these tumours.[33]
Classification
Subdivided into:[34]
- Intestinal type mucinous borderline tumour of the ovary ~ 90% of cases.
- Endocervical type mucinous borderline tumour of the ovary ~ 10% of cases.[35]
Gross
Intestinal type mucinous borderline tumour of the ovary and endocervical type mucinous borderline tumour of the ovary:
- Complex multiloculated mass with mucin.
- Often large - may > 30 cm.
Microscopic
Intestinal type mucinous borderline tumour of the ovary
Features:
- Mucinous differentiation:
- Tall columnar cells with apical mucin - usu. resembles gastric foveolar epithelium.
- Layering of epithelial cells (stratification).
- Must be <= 3 cells.[36]
- +/-Papillary infoldings.
- Projections into the cystic space.
- +/-Mild nuclear atypia.
- +/-Mitoses (focally).
Notes:
- Resembles a villous adenoma of the colon.[37]
- Borderline component must be >= 10% of the tumour.[37]
- Lesions with <10% borderline component are known as mucinous cystadenoma of the ovary with focal proliferation or mucinous cystadenoma of the ovary with focal atypia.
DDx:
- Mucinous adenocarcinoma of the ovary.
- Mucinous cystadenoma of the ovary.
- Mucinous cystadenoma of the ovary with focal proliferation.
Images:
- Ovarian MBT (webpathology.com).
- Ovarian mucinous borderline tumour and benign mucinous tumour (webpathology.com).
Endocervical type mucinous borderline tumour of the ovary
Features:[38]
- Cells with mucinous differentiation resembling endocervical epithelium:
- Tall columnar cells with grey apical mucin.
- Cells with eosinophilic cytoplasm - known as "pink cells".
- Ciliated cells.
- Neutrophils associated with the epithelium/mucin - common.[39]
Images:
- Endocervical type mucinous borderline tumour - low mag. (webpathology.com).
- Endocervical type mucinous borderline tumour - high mag. (webpathology.com).
Comparing intestinal versus endocervical
Feature | Intestinal | Endocervical |
---|---|---|
Primary mucin producing cell | clear - well-diff. component, eosinophilic (pink) | eosinophilic (pink), grey or clear |
Size | tall columnar (height:width >3:1) "champagne flute" | stubby columnar (height:width <3:1) |
Accompanying epithelial cells | +/-goblet cells | pink cells, ciliated cells |
Other cells | none | neutrophils (intraepithelial) - common |
Images | high mag. (webpathology.com) | low mag. (webpathology.com), high mag. (webpathology.com) |
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OVARY AND CYST, LEFT, OOPHORECTOMY: - MUCINOUS BORDERLINE TUMOUR, INTESTINAL TYPE, ARISING FROM A MUCINOUS CYSTADENOMA (INTESTINAL TYPE). - OVARIAN PARENCHYMA.
Mucinous adenocarcinoma of the ovary
General
- Malignant.
- May arise in endometriosis.[40]
- Poor response to chemotherapy vis-à-vis serous carcinoma.[41]
Gross
Features:
Microscopic
Features:
- Mucinous differentiation.
- Tall columnar cells in glands with apical mucin.
- May have an endocervical-like or intestinal-like appearance - see subtypes.
- Tall columnar cells in glands with apical mucin.
- Invasive morphology - one of the following:
- Back-to-back glands/confluent growth pattern.
- Desmoplastic stromal response.
- Cribriforming of glands.
- Malignant characteristics:
- +/-Nuclear atypia.
- +/-Necrosis.
- No cilia.
DDx:
Subtypes
- Endocervical type.
- Less likely to be malignant.
- More common than malignant type.
- Intestinal type.
- More likely to be malignant.
- +/-Goblet cells.
- One large clear apical vacuole.
- If it doesn't look like intestine to you... it probably isn't.
- May vaguely resemble colorectal adenocarcinoma (hyperchromatic, columnar nuclei, nuclear pleomorphism).
- Image: [2]
Comparison of mucosa:
- Normal endocervical mucosa: endocervical mucosa (duke.edu).
- Normal colonic mucosa: colonic type mucosa (WC).
IHC
- CK7 +ve.
- CK20 +ve.
Endometrioid carcinoma of the ovary
- AKA endometrioid ovarian carcinoma.
- AKA endometrioid adenocarcinoma of the ovary.
- AKA ovarian endometrioid adenocarcinoma.
Clear cell carcinoma of the ovary
- AKA ovarian clear cell adenocarcinoma, abbreviated OCCC.
- AKA ovarian clear cell carcinoma.
- AKA clear cell adenocarcinoma of the ovary.
Transitional cell carcinoma of the ovary
Brenner tumour
Germ cell tumours
These tumour are relatively uncommon, though are the most common grouping for young women.
Overview
- Dysgerminoma (most common).
- Female version of seminoma.
- Yolk sac tumour (endodermal sinus tumour).
- Embryonal carcinoma.
- Choriocarcinoma.
- Teratoma.
- Mixed GCT - 60% of GCTs are mixed.
- Common combinations:
- Teratoma + embryonal carcinoma + endodermal sinus tumour (yolk sac tumour) (TEE).
- Seminoma + embryonal (SE).
- Embryonal + teratoma (TE).
- Common combinations:
Mnemonic: SEE CT, S=Seminoma, Embryonal carcinoma, Endodermal Sinus Tumour, Choriocarcinoma, Teratoma.
Teratoma
- May be benign or malignant.
- Skin component only called "dermoid".
Dysgerminoma
General
Epidemiology:
- Most common GCT in females.
- Prognosis usually good.
Microscopic
Features:
- Fried egg appearance (clear cytoplasm, central nucleus).
- Nuclear membrane has "corners", i.e. is "squared-off" - or "polygonal".
- +/- Lymphocytes - often prominent.
- +/- Granulomata.
Dysgerminoma vs lymphoma:
- Dysgerminoma has "squared-off" nuclei,[44] i.e. the nuclei look are polygonal-shaped.
Gonadoblastoma
Details dealt with in the main article.
Microscopic
- Immature germ cells resembling Sertoli cells or granulosa cells.
- Cells with moderate cytoplasm is a trabecular or tubular architecture.
- Primitive germ cells resemble those of a dysgerminoma.
- Polygonal cells with a central nucleus, squared-off nuclear membrane and clear cytoplasm.
- +/-Calcification (very common).
Metastatic ovarian tumours
Generally
- Mostly Muellerian origin (uterus, fallopian tube) or pelvic peritoneum.
Extramuellerian metastatic tumours
DDx:
- Breast.
- Gastrointestinal (GI) tract.
- Pseudomyxoma peritonei, usu. appendiceal origin.
- Krukenberg tumour = signet ring cell cancer with mucin production of GI origin.
Microscopic
Features:
- Predominantly surface involvement and nodular at low power.
- Signet ring cells (suggestive of GI or breast primary).
- Lymphovascular invasion.
Image:
Mucinous carcinoma - GI tract metastasis vs. primary ovarian
Gross
Features favouring metastatic disease:[47]
- Bilaterality -- both ovaries involved.
- Small unilateral tumour size -- <10 cm = metastatic.
- >13 cm = primary ovarian.
IHC
Ovarian tumours:
- Dipeptidase 1 (DPEP1) +ve.[48]
- CK7 +ve.
Sex cord stromal tumours
General
- Most are unilateral.[49]
IHC
- Most are positive for alpha-inhibin.[49]
- Most are positive for calretinin -- considered more sensitive than alpha-inhibin.[50]
- Melan A +ve.
- CD99 +ve.
Memory device MAC = melan A, alpha-inhibin, calretinin.
Sex cord tumour with annular tubules
- Abbreviated SCTAT.
- NOT sex cord tumour with angulated tubules.
Juvenile granulosa cell tumour
Adult granulosa cell tumour
- AKA granulosa cell tumour.
- Should not be confused with granular cell tumour.
- Ideally, it should be called adult granulosa cell tumour to avoid confusion with juvenile granulosa cell tumour.
Fibroma-thecoma group
- Some say fibromas and thecomas are related,[51] while others believe they should be considered distinct entities.[52]
- A combination of a fibroma and a thecoma is known as a fibrothecoma.
Note:
- Some discourage the use of the term fibrothecoma and sugguest calling tumours in the fibroma-thecoma group fibroma unless there are lipid-laden cells and more than minimal alpha-inhibin positivity.[49]
Ovarian fibroma
Thecoma
Sertoli-Leydig cell tumour
- AKA androblastoma.
Hilus cell tumour
General
- Rare.[53]
- May cause virilization.
- Development of male (sexual) characteristics in a female.
- Arise from hilus cells.
Microscopic
Features - see Leydig cell tumour:
- Moderate eosinophilic cytoplasm.
- +/-Reinke crystalloids (cytoplasmic inclusions).
DDx:
- Hilus hyperplasia.
- Sertoli-Leydig tumour.
Benign
- Benign mesothelial inclusion cyst - may mimic a tumour.
See also
References
- ↑ Hirst, JE.; Gard, GB.; McIllroy, K.; Nevell, D.; Field, M. (Jul 2009). "High rates of occult fallopian tube cancer diagnosed at prophylactic bilateral salpingo-oophorectomy.". Int J Gynecol Cancer 19 (5): 826-9. doi:10.1111/IGC.0b013e3181a1b5dc. PMID 19574767.
- ↑ 2.0 2.1 URL: http://www.sign.ac.uk/guidelines/fulltext/75/section3.html. Accessed on: 16 September 2011.
- ↑ Cotran, Ramzi S.; Kumar, Vinay; Fausto, Nelson; Nelso Fausto; Robbins, Stanley L.; Abbas, Abul K. (2005). Robbins and Cotran pathologic basis of disease (7th ed.). St. Louis, Mo: Elsevier Saunders. pp. 1093. ISBN 0-7216-0187-1.
- ↑ LAE. 22 October 2009.
- ↑ Humphrey, Peter A; Dehner, Louis P; Pfeifer, John D (2008). The Washington Manual of Surgical Pathology (1st ed.). Lippincott Williams & Wilkins. pp. 401. ISBN 978-0781765275.
- ↑ Takeuchi, T.; Ohishi, Y.; Imamura, H.; Aman, M.; Shida, K.; Kobayashi, H.; Kato, K.; Oda, Y. (Jul 2013). "Ovarian transitional cell carcinoma represents a poorly differentiated form of high-grade serous or endometrioid adenocarcinoma.". Am J Surg Pathol 37 (7): 1091-9. doi:10.1097/PAS.0b013e3182834d41. PMID 23681072.
- ↑ Ali, RH.; Seidman, JD.; Luk, M.; Kalloger, S.; Gilks, CB. (Nov 2012). "Transitional cell carcinoma of the ovary is related to high-grade serous carcinoma and is distinct from malignant brenner tumor.". Int J Gynecol Pathol 31 (6): 499-506. doi:10.1097/PGP.0b013e31824d7445. PMID 23018212.
- ↑ LAE. 22 October 2009.
- ↑ NEED REF.
- ↑ http://www.cancer.gov/cancertopics/genetics-terms-alphalist/all#D. Accessed on: 14 September 2011.
- ↑ DeCostanzo DC, Elias JM, Chumas JC (July 1997). "Necrosis in 84 ovarian carcinomas: a morphologic study of primary versus metastatic colonic carcinoma with a selective immunohistochemical analysis of cytokeratin subtypes and carcinoembryonic antigen". Int. J. Gynecol. Pathol. 16 (3): 245–9. PMID 9421090.
- ↑ Silverberg SG (January 2000). "Histopathologic grading of ovarian carcinoma: a review and proposal". Int. J. Gynecol. Pathol. 19 (1): 7-15. PMID 10638449. http://meta.wkhealth.com/pt/pt-core/template-journal/lwwgateway/media/landingpage.htm?issn=0277-1691&volume=19&issue=1&spage=7.
- ↑ Sato Y, Shimamoto T, Amada S, Asada Y, Hayashi T (January 2003). "Prognostic value of histologic grading of ovarian carcinomas". Int. J. Gynecol. Pathol. 22 (1): 52-6. PMID 12496698. http://meta.wkhealth.com/pt/pt-core/template-journal/lwwgateway/media/landingpage.htm?issn=0277-1691&volume=22&issue=1&spage=52.
- ↑ 14.0 14.1 Stewart, CJ.; Brennan, BA.; Crook, ML.; Russell, P. (Sep 2007). "Value of elastin staining in the assessment of peritoneal implants associated with ovarian serous borderline tumours.". Histopathology 51 (3): 313-21. doi:10.1111/j.1365-2559.2007.02789.x. PMID 17727474.
- ↑ 15.0 15.1 15.2 Bell, DA.; Weinstock, MA.; Scully, RE. (Nov 1988). "Peritoneal implants of ovarian serous borderline tumors. Histologic features and prognosis.". Cancer 62 (10): 2212-22. PMID 3179935.
- ↑ URL: http://ovariancancer.about.com/od/testsdiagnosis/a/FIGO_stages.htm. Accessed on: 8 July 2013.
- ↑ Cotran, Ramzi S.; Kumar, Vinay; Fausto, Nelson; Nelso Fausto; Robbins, Stanley L.; Abbas, Abul K. (2005). Robbins and Cotran pathologic basis of disease (7th ed.). St. Louis, Mo: Elsevier Saunders. pp. 1096-7. ISBN 0-7216-0187-1.
- ↑ 18.0 18.1 Cotran, Ramzi S.; Kumar, Vinay; Fausto, Nelson; Nelso Fausto; Robbins, Stanley L.; Abbas, Abul K. (2005). Robbins and Cotran pathologic basis of disease (7th ed.). St. Louis, Mo: Elsevier Saunders. pp. 1096. ISBN 0-7216-0187-1.
- ↑ LAE. 19 February 2009.
- ↑ LAE. 19 February 2009.
- ↑ URL: http://www.ncbi.nlm.nih.gov/pubmed/15897738. Accessed on: 7 April 2011.
- ↑ Piura B, Rabinovich A, Yanai-Inbar I (2000). "Micropapillary serous carcinoma of the ovary: case report and review of literature". Eur. J. Gynaecol. Oncol. 21 (4): 374–6. PMID 11055486.
- ↑ Prat J, De Nictolis M (September 2002). "Serous borderline tumors of the ovary: a long-term follow-up study of 137 cases, including 18 with a micropapillary pattern and 20 with microinvasion". Am. J. Surg. Pathol. 26 (9): 1111-28. PMID 12218568. http://meta.wkhealth.com/pt/pt-core/template-journal/lwwgateway/media/landingpage.htm?issn=0147-5185&volume=26&issue=9&spage=1111.
- ↑ Hallman KB, Nahhas WA, Connelly PJ (September 1991). "Endosalpingiosis as a source of psammoma bodies in a Papanicolaou smear. A case report". J Reprod Med 36 (9): 675–8. PMID 1774734.
- ↑ Seidman, JD.; Kurman, RJ. (May 2000). "Ovarian serous borderline tumors: a critical review of the literature with emphasis on prognostic indicators.". Hum Pathol 31 (5): 539-57. PMID 10836293.
- ↑ 26.0 26.1 Dietel, M.; Hauptmann, S. (May 2000). "Serous tumors of low malignant potential of the ovary. 1. Diagnostic pathology.". Virchows Arch 436 (5): 403-12. PMID 10881733.
- ↑ 27.0 27.1 27.2 Nucci, Marisa R.; Oliva, Esther (2009). Gynecologic Pathology: A Volume in Foundations in Diagnostic Pathology Series (1st ed.). Churchill Livingstone. pp. 399. ISBN 978-0443069208.
- ↑ Burkholz, KJ.; Wood, BP.; Zuppan, C.. "Best cases from the AFIP: Borderline papillary serous tumor of the right ovary.". Radiographics 25 (6): 1689-92. doi:10.1148/rg.256055015. PMID 16284143.
- ↑ Park, JY.; Kim, DY.; Kim, JH.; Kim, YM.; Kim, KR.; Kim, YT.; Nam, JH. (Dec 2011). "Micropapillary pattern in serous borderline ovarian tumors: does it matter?". Gynecol Oncol 123 (3): 511-6. doi:10.1016/j.ygyno.2011.08.008. PMID 21917305.
- ↑ Shappell, HW.; Riopel, MA.; Smith Sehdev, AE.; Ronnett, BM.; Kurman, RJ. (Dec 2002). "Diagnostic criteria and behavior of ovarian seromucinous (endocervical-type mucinous and mixed cell-type) tumors: atypical proliferative (borderline) tumors, intraepithelial, microinvasive, and invasive carcinomas.". Am J Surg Pathol 26 (12): 1529-41. PMID 12459620.
- ↑ Shappell, HW.; Riopel, MA.; Smith Sehdev, AE.; Ronnett, BM.; Kurman, RJ. (Dec 2002). "Diagnostic criteria and behavior of ovarian seromucinous (endocervical-type mucinous and mixed cell-type) tumors: atypical proliferative (borderline) tumors, intraepithelial, microinvasive, and invasive carcinomas.". Am J Surg Pathol 26 (12): 1529-41. PMID 12459620.
- ↑ Khunamornpong, S.; Settakorn, J.; Sukpan, K.; Suprasert, P.; Siriaunkgul, S. (May 2011). "Mucinous tumor of low malignant potential (borderline or atypical proliferative tumor) of the ovary: a study of 171 cases with the assessment of intraepithelial carcinoma and microinvasion.". Int J Gynecol Pathol 30 (3): 218-30. doi:10.1097/PGP.0b013e3181fcf01a. PMID 21464732.
- ↑ Acs, G. (Jun 2005). "Serous and mucinous borderline (low malignant potential) tumors of the ovary.". Am J Clin Pathol 123 Suppl: S13-57. PMID 16100867.
- ↑ Rodriguez, IM.; Irving, JA.; Prat, J. (Oct 2004). "Endocervical-like mucinous borderline tumors of the ovary: a clinicopathologic analysis of 31 cases.". Am J Surg Pathol 28 (10): 1311-8. PMID 15371946.
- ↑ Nucci, Marisa R.; Oliva, Esther (2009). Gynecologic Pathology: A Volume in Foundations in Diagnostic Pathology Series (1st ed.). Churchill Livingstone. pp. 419. ISBN 978-0443069208.
- ↑ Nucci, Marisa R.; Oliva, Esther (2009). Gynecologic Pathology: A Volume in Foundations in Diagnostic Pathology Series (1st ed.). Churchill Livingstone. pp. 416. ISBN 978-0443069208.
- ↑ 37.0 37.1 Nucci, Marisa R.; Oliva, Esther (2009). Gynecologic Pathology: A Volume in Foundations in Diagnostic Pathology Series (1st ed.). Churchill Livingstone. pp. 416. ISBN 978-0443069208.
- ↑ Nucci, Marisa R.; Oliva, Esther (2009). Gynecologic Pathology: A Volume in Foundations in Diagnostic Pathology Series (1st ed.). Churchill Livingstone. pp. 420. ISBN 978-0443069208.
- ↑ URL: http://www.webpathology.com/image.asp?n=12&Case=526. Accessed on: 9 January 2013.
- ↑ Cotran, Ramzi S.; Kumar, Vinay; Fausto, Nelson; Nelso Fausto; Robbins, Stanley L.; Abbas, Abul K. (2005). Robbins and Cotran pathologic basis of disease (7th ed.). St. Louis, Mo: Elsevier Saunders. pp. 1097. ISBN 0-7216-0187-1.
- ↑ Shimada, M.; Kigawa, J.; Ohishi, Y.; Yasuda, M.; Suzuki, M.; Hiura, M.; Nishimura, R.; Tabata, T. et al. (Jun 2009). "Clinicopathological characteristics of mucinous adenocarcinoma of the ovary.". Gynecol Oncol 113 (3): 331-4. doi:10.1016/j.ygyno.2009.02.010. PMID 19275957.
- ↑ Offman, SL.; Longacre, TA. (Sep 2012). "Clear cell carcinoma of the female genital tract (not everything is as clear as it seems).". Adv Anat Pathol 19 (5): 296-312. doi:10.1097/PAP.0b013e31826663b1. PMID 22885379.
- ↑ Cotran, Ramzi S.; Kumar, Vinay; Fausto, Nelson; Nelso Fausto; Robbins, Stanley L.; Abbas, Abul K. (2005). Robbins and Cotran pathologic basis of disease (7th ed.). St. Louis, Mo: Elsevier Saunders. pp. 1101. ISBN 0-7216-0187-1.
- ↑ Baker P, Oliva E (July 2008). "A practical approach to intraoperative consultation in gynecological pathology". Int. J. Gynecol. Pathol. 27 (3): 353?65. doi:10.1097/PGP.0b013e31815c24fe. PMID 18580313.
- ↑ Cotran, Ramzi S.; Kumar, Vinay; Fausto, Nelson; Nelso Fausto; Robbins, Stanley L.; Abbas, Abul K. (2005). Robbins and Cotran pathologic basis of disease (7th ed.). St. Louis, Mo: Elsevier Saunders. pp. 1104. ISBN 0-7216-0187-1.
- ↑ URL: http://www.pathconsultddx.com/pathCon/diagnosis?pii=S1559-8675%2806%2970245-5. Accessed on: 8 April 2011.
- ↑ Yemelyanova, AV.; Vang, R.; Judson, K.; Wu, LS.; Ronnett, BM. (Jan 2008). "Distinction of primary and metastatic mucinous tumors involving the ovary: analysis of size and laterality data by primary site with reevaluation of an algorithm for tumor classification.". Am J Surg Pathol 32 (1): 128-38. doi:10.1097/PAS.0b013e3180690d2d. PMID 18162780.
- ↑ Okamoto, T.; Matsumura, N.; Mandai, M.; Oura, T.; Yamanishi, Y.; Horiuchi, A.; Hamanishi, J.; Baba, T. et al. (Feb 2011). "Distinguishing primary from secondary mucinous ovarian tumors: an algorithm using the novel marker DPEP1.". Mod Pathol 24 (2): 267-76. doi:10.1038/modpathol.2010.204. PMID 21076463.
- ↑ 49.0 49.1 49.2 Roth LM (July 2006). "Recent advances in the pathology and classification of ovarian sex cord-stromal tumors". Int. J. Gynecol. Pathol. 25 (3): 199–215. doi:10.1097/01.pgp.0000192271.22289.e6. PMID 16810055.
- ↑ Movahedi-Lankarani, S.; Kurman, RJ. (Nov 2002). "Calretinin, a more sensitive but less specific marker than alpha-inhibin for ovarian sex cord-stromal neoplasms: an immunohistochemical study of 215 cases.". Am J Surg Pathol 26 (11): 1477-83. PMID 12409724.
- ↑ http://www.pathologyoutlines.com/ovarytumor.html#fibroma
- ↑ Nocito AL, Sarancone S, Bacchi C, Tellez T (February 2008). "Ovarian thecoma: clinicopathological analysis of 50 cases". Ann Diagn Pathol 12 (1): 12–6. doi:10.1016/j.anndiagpath.2007.01.011. PMID 18164409.
- ↑ 53.0 53.1 Zafrakas, M.; Venizelos, ID.; Theodoridis, TD.; Zepiridis, L.; Agorastos, T.; Bontis, JN. (2009). "Virilizing ovarian hilus (Leydig) cell tumor with concurrent contralateral hilus cell hyperplasia: a rare diagnosis.". Eur J Gynaecol Oncol 30 (3): 338-40. PMID 19697637.