21KTJ Special Lecture - JSGYP
Transcript of 21KTJ Special Lecture - JSGYP
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Takako Kiyokawa, MDDepartment of Pathology, The Jikei University School
of Medicine, Tokyo, Japan
E-mail: [email protected]
The 21st Korea-Taiwan-Japan Joint Meeting for Gynecological Pathology Sendai, October 28, 2017
Special lecture
Peritoneal lesions
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Contents
1. Mesothelial lesions
2. Műllerian lesions
3. Mesenchymal tumors
4. Miscellaneous primary tumors
5. Secondary tumors
6. Other tumor-like lesions
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Contents
1. Mesothelial lesions
2. Műllerian lesions
3. Mesenchymal tumors
4. Miscellaneous primary tumors
5. Secondary tumors
6. Other tumor-like lesions
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Mesothelial lesions
Neoplasia
• Malignant mesothelioma
• Well-differentiated papillary mesothelioma
• Adenomatoid tumor
Non-neoplastic lesions
• Peritoneal inclusion cyst
• Mesothelial hyperplasia
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Malignant mesothelioma• Rare 7/1000,000 population
• M:F=7:3
• Increase of death of disease x3/20yrs
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Data by Ministry of welfare and labor of JApan
Total
Male
Female
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Peritoneal mesothelioma• 10% of all malig mesothelioma
• M:F=7:3 (Japanese mesothelioma registry) M:F=1.5:1 (Hillerdal G. Br J Dis Chest. 1983;77:321-343)
• Heavy asbestos exposure is a higher risk for development of peritoneal mesothelioma in men Asbestos exposure in brief period is a higher risk for plueral mesotheliomaAntman KH. Chest. 1993;103:373S-376S
• Half of the pts with no history of asbestos exposure
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Female peritoneal mesothelioma
Age:17-92(mean 47.4)yrs (n=75cases)
No association with asbestos exposure
Abdominal discomfort, distention, weight loss
Most cases are epithelioid type(tubular> papillary> solid, mixed)
Tumor cells: polygonal, cuboidal/low columnar, eosinophilic cytoplasm, mild to moderate nuclear atypia, mitoses may be infrequent
Minor foci may resemble WDPM
Baker PM, et al. Am J Clin Pathol. 2005;123:724-737.
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Malignant mesothelioma
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Female peritoneal mesotheliomaImmunohistochemistry
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Recommended Others
Positive calretinin CK7
WT-1 Pan CK
D2-40
CK5/6
Negative MOC-31 CEA
Ber-EP4 TTF-1
PAX8*
ER*, PgR*
Caludin 4
Loss of BAP 1 in only 50% of peritoneal mesothelioma
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Asbestos-Related Health Damage Relief System in Japan
• Act took effect on March 27, 2006• Provides relief benefit (medical care expenses) to
sufferers of the designated diseases and to the bereaved of those DOD
• Diseases covered by the benefits: The following diseases caused by asbestos
1)Mesothelioma
2)Malignant neoplasm of lung and bronchus
3)Asbestosis with heavy respiratory dysfunction
4)Diffuse pleural thickening with heavy respiratory dysfunction
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Results of female pts applied with peritoneal mesothelioma
Submission of pathology slides: 221 PtsMarch 31, 2006~ March 31, 2017
Certified
164 (74%)
Non-certified
51 (23%)
Others
6 (3%)
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Panel diagnosis in non-certified pts (51)March 31, 2006~ March 31, 2017
Gyn Malig
31(61%)
Non-Gyn Malig
15(29%)
Benign (10%)
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Well-differentiated papillary mesothelioma
• Gross: Papillary, well circumscribed tumor,0.1-2cm, 50% multiple
• Micro: papillary, wide fibrous stroma, bland nuclei, rare mitosis, inv<0.5cm
• dDx: malignant mesothelioma
• 23 -75 years (median, 47 y; mean, 48.6 y)
• No hx of asbestos exposure
• Incidental finding
• Favorable prognosisDaya D, et al. Cancer. 1990;65:292-296.Malpica A, et al. Am J Surg Pathol. 2012;36:117-127.
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Well-differentiated papillary mesothelioma
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Adenomatoid tumor
• Adults
• Incidental finding
• Benign
• Gross: Small, firm nodules
• Micro: cells with cytoplasmic vacuoles/eosinophilic abundant cytoplasm, bland round to oval nuclei, rare mitosis; anastomosing gland-like spaces>solid nests
• Immnohx: cytokeratin+, vimentin+, WT1+, calretinin, CK5/6, thrombomodulin+
• dDx: metastatic carcinoma
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Adenomatoid tumor
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Infarcted adenomatoid tumor
• Solitary solid mass 1.1-3.5cm
• Necrosis in the center of the tumor
• Proliferation of fibroblasts, myofibroblasts
• Tumor cells often arranged in a solid nest
( 4 males and one female-paratubal mass)
Skinnider BF, et al. Am J Surg Pathol 2004; 28: 77-83
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Peritoneal inclusion cyst
• Cyst-forming mesothelial proliferation
• Rare
• Women of reproductive age
• Unilocular>>>multilocular
• Multilocular cyst
up ∅20cm, ass w previous surgery, endometiosis, inflammatory process
• Most of them reactive rather than neoplastic
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Peritoneal inclusion cyst
• AKA
– Multilocular peritoneal inclusion cyst
– Mesothelial inclusion cyst
– Benign cystic mesothelioma*
– Multicystic mesothelioma*
* Not recommended (WHO2014)
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Peritoneal inclusion cyst
2cm
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Mesothelial hyperplasia
• Salpingitis, peritonitis, pelvic endometriosis, etc
• Grossly unidentifiable
• Stratification, papillary, enlarged mesothelial cells
• Mesothelial entrapment in the peritoneal stroma/ovarian stroma
• dDx : invasive carcinoma (adenocarcinoma), malignant mesothelioma
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18歳,女性卵巣内膜症性嚢胞
Entrapped hyperplastic mesothelial cells
in the endometrioticcyst
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Contents
1. Mesothelial lesions
2. Műllerian lesions
3. Mesenchymal tumors
4. Miscellaneous primary tumors
5. Secondary tumors
6. Other tumor-like lesions
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Műllerian-type neoplasia
• Serous carcinoma: high-grade>>>low-grade
• Serous borderline tumor
• Műllerian adenosarcoma
• Endometrioid stromal sarcoma
• Carcinosarcoma
• Endometrioid carcinoma
• Clear cell carcinoma
• Mucinous carcinoma
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High-grade serous carcinoma
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Classical criteria for peritoneal serous carcinoma
Carcinoma in the peritoneum
• Both ovaries are either normal in size or enlarged by a benign process
• The bulk of the tumor in the extrovarian sites is greater than on the ovarian surface
• Microscopically ovaries reveal
1) No tumor
2)Tumor confined to the surface epithelium 3)Tumor is <5x5mm in the ovarian substance
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Origin of “ovarian or peritoneal ” high-grade serous carcinoma
Traditional model
• No precursor lesion
• Arise from surface epithelial inclusion cyst
• Decision of primary site based on tumor volume
Paradigm shiftTubal origin
• Studies using RRSO in women with BRACA1/2 mutation
• Examination of fallopian tubes by SEE-FIM protocol, perspective studies
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Medeiros F, et al. Am J SurgPathol 30;230-236, 2006
fimbriated end of tube
Protocol for Sectioning and Extensively Examining the FIMbriated end (SEE-FIM)
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Serous intraepithelial carcinoma (STIC)
• Intraepithelial proliferation of atypical cells identical to HGSC in the tube
• 50-60%of extrauterine HGSC
• RRSO tubes of women with BRCA1/2 mutation
• >90% in fimbria
• Possible to spread to peritoneum and ovary
• Imhx: abberant expression of p53
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Criteria for peritoneal high-grade serous carcinoma 2014-
(WHO 2014)
• Carcinoma in the peritoneum
• Both ovaries and fallopian tubes are grossly and microscopically normal or enlarged only by a normal process
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Malignant tumors associated with endometriosis Extraova (%) Ova (%) Total(%)
Adenosarcoma 3 (33.3) 0 3 (8.3)
Clear cell Ca 4 (44.4) 9 (33.3) 13 (36.1)
Endom Ca 1 8 (29.7) 9 (23.1)
Serous Ca 1 5 (18.5) 6 (16.7)
Mucinous Ca 0 1 1
Serous BT 0 3 (11.1) 3 (8.3)
Mucinous BT 0 1 1
Total 9 (100) 27 (100) 36 (100)
Stern RC et al. Int J Gynecol Pathol, 2001, 20:133-9
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Adenosarcoma (arising in pelvic endometirosis)
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Adenosarcoma (arising in pelvic endometirosis)
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Non-neoplastic Műllerian lesions
• Endometriosis and its related lesions Endosalpingiosis, endocervicosis, Műllerianosis
• Ectopic decidua
• Endometriosis with pregnancy effect
• May mimic neoplastic process, both clinically and pathologically
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Endometriosis with decidual change:-white flat elevated lesion in the Douglas’ Pouch at c-section (preg38w)
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Contents
1. Mesothelial lesions
2. Műllerian lesions
3. Mesenchymal tumors
4. Miscellaneous primary tumors
5. Secondary tumors
6. Other tumor-like lesions
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Mesenchymal tumors
• Extra-gastrointestinal stromal tumor
• Solitary fibrous tumor
• Desmoid tumor (abdominal fibromatosis)
• Inflammatory myofibroblastic tumor
• Calcifying fibrous tumor
• Leiomyomatosis peritonealis disseminate
• Liposarcoma
• Others
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Solitary Fibrous Tumor
• Localized fibrous tumor with hemangio-pericytoma-like vascular pattern
• Originate from submesothelial fibroblast(CD34+)• Rare in the peritoneal cavity (usually in pleura)• Most with favorable prognosis; histology does
not predict malignant behavior• Doege-Potter syndrome
hypoglycemia (insulin-like GF 2)
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Desmoid tumor (abdominal fibromatosis)
• Invasive proliferation of fibroblastic spindle cells in the abdominal wall/cavity
• Adult; F>M
• Sporadic cases; familial adenomatous polyposis (10% of FAP), trisomy (#8,#20); 5q deletion
• Local rec; no distant metastasis
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40Desmoid tumor (abdominal fibromatosis)
2cm
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• Proliferation of myofibroblastic spindle cells with lymphoplasmacytic infiltrate
• Children, young adults
• Presentation: mass, fever, growth failure, weight loss, anemia, thrombocytosis, polyclonalhypergammaglabulinemia
• Imhx: SMA+, desmin+
• ALK gene rearrangement 60%
• Local rec; metastasis- histology cannot predict prognosisGynecologic Oncology Reports 12 (2015) :9–12
Inflammatory myofibroblastic tumor
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Calcifying fibrous tumor
• Fibrous tumor with calcification, well circumscribed, abundant collagen, lymphoplasmacytic infiltration
• Serosa of stomach, small intestine• Incidental finding• Young adults, adults
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Contents
1. Mesothelial lesions
2. Műllerian lesions
3. Mesenchymal tumors
4. Miscellaneous primary tumors
5. Secondary tumors
6. Other tumor-like lesions
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Desmoplastic small round cell tumor
• Malignant tumor of unknown origin
• Rare
• Adolescents, young adults (15-30yrs)
• Male >>Female (4:1)
• Abdominal and/or pelvic peritoneum• t(11;22)(p13;q12)⇒EWS-WT1 fusion protein• Poor prognosis (OS 50%)
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高Ca型小細胞癌 Desmoplastic small
round cell tumorDesmin CAM5.2
Desmoplastic small round cell tumor
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Peritoneal ependymoma• Prognosis• Imhx: some difference from CNS ependymoma
ER 100% (10% in CNS epen)PgR 80% (20% in CNS epen)CK7 80% (10% in CNS epen)GFAP 100% (100% in CNS)Am J Surg Pathol 2008;32:710–718
• Pathogenesis: controversial Metaplasia,? teratoma? Aberrant tissue?
• dDXserous carcinoma, malignant mesothelioma, gliomatosis peritonei
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Extra-CNS EpendymomaLiterature review
7 (54%)
2 (15%)
1 (7%)
1 (8%)
1 (8%)1 (8%) Location (n=13)
ovary
Paraovarian region
Liver
Mediastinum
Smal bowel
Peritoneum
Verdun TP, et al. Pathol Res Pract 2015; 211: 268-70
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Contents
1. Mesothelial lesions
2. Műllerian lesions
3. Mesenchymal tumors
4. Miscellaneous primary tumors
5. Secondary tumors
6. Other tumor-like lesions
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Secondary tumors
• Primary tumor: gyn, GI >>> pancreas, breast (lobular carcinoma)
• Peritoneal implant of ovarian serous borderline tumor
• Gliomatosis peritonei
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Peritoneal implant of ovarian serous borderline tumor
• Pts with ovarian serous borderline with peritoneal lesion
• WHO 2014-implant: formally called non-invasive implantfavorable prognosis
- low-grade serous carcinoma(LGSC): formally called non-invasive implantPoor prognosis
• …..invasive implant behave like LGSC they should be designated as such. All other implants that are non-invasive can be designated “implants” (WHO2014)
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Pseudomyxoma peritonei
• Clinical term :grossly evident peritoneal involvement by mucoid material due to peritoneal spread of mucinous neoplasm
• Origin: low-grade appendiceal mucinous neoplasia >>>mucinous component of ovarian mature cystic teratoma
• Histology: dissecting mucin with fibrosis
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Dissecting mucin with fibrosis with low-grade
mucinous tumor cells
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RE Scully et al. AFIP 3rd series, fascicle 23
Ronnett et al. AJSP1995; 19: 1390-1408
Mucinous ascitesw LG mucinous tumor cellsw HG mucinous tumor cells
Organizing mucinous fluidw LG mucinous tumor cellsw HG mucinous tumor cells
DPAMPMCA
Dissecting mucin with fibrosisw LG mucinous tumor cellsw HG mucinous tumor cells
DPAMPMCA
DPAM :Disseminated peritoneal adenomucinosis
PMCA: Peritoneal mucinous carcinomatosis
Peritoneal lesions with mucin: Pathology report
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Organizing mucinous fluid (with low-grade tumor cells)
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Gliomatosis peritonei
• Benign mature glial implants on the peritoneal surface
• Rare complication of ova immature/mature teratoma
• Good prognosis (Grade 0)
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Gliomatosis peritonei
Histogenesis• Peritoneal seeding of ovarian teratoma via
capsular rupture vs.
• Originate from peritoneal pluripotent cells stimulated by GF in ovarian tumor
(different genetic identity between peritoneal and ova tumor)
Am J Pathol 2001; 159: 51-55Hum Pathol 2004; 35: 685-688
with endometrisoisInt J Dev Biol 2012, 56:969-974Korean J Pathol 2013, 47:587-591
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Contents
1. Mesothelial lesions
2. Műllerian lesions
3. Mesenchymal tumors
4. Miscellaneous primary tumors
5. Secondary tumors
6. Other tumor-like lesions
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Sclerosing peritonitis a/w ovarian luteinized thecoma
• Reactive submesothelial mesenchymal proliferation; ascites; encases the small bowel to cause bowel obstraction
• Premenopausal pts (mean 28yrs)• Bil ova lesions ; No endocrine manifestation• No rec or spread of the ovarian lesion• Pts may die of sclerosing peritonitis• Ovarian lesion may be non-neoplastic nature:
entrapped follicles and normal structures within the lesions → ‘‘thecomatosis’’ ?
Am J Surg Pathol 2008,32:1273-90
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Peritoneal keratin granuloma
• Response to deposition of keratin derived from lesions in the female reproductive tract
- ovarian teratoma
- endometrial carcinoma with sq diff
- cervical Sq CC (bulky)
• may be confused with metastatic carcinoma