Comprehensive Clinicopathologic and Updated Immunohistochemical Characterization of Primary Ovarian Mucinous Carcinoma

Dina Bassiouny; Nadia Ismiil; Valerie Dubé; Guangming Han; Matthew Cesari; Fang I. Lu; Elzbieta Slodkowska; Carlos Parra-Herran; Hak Fai Chiu; Magda Naeim; Nim Li; Mahmoud Khalifa; Sharon Nofech-Mozes

doi:10.1177/1066896917752861

Comprehensive Clinicopathologic and Updated Immunohistochemical Characterization of Primary Ovarian Mucinous Carcinoma

Dina Bassiouny, Nadia Ismiil, Valerie Dubé, Guangming Han, Matthew Cesari, Fang I. Lu, Elzbieta Slodkowska, Carlos Parra-Herran, Hak Fai Chiu, Magda Naeim, Nim Li, Mahmoud Khalifa, Sharon Nofech-Mozes

Research output: Contribution to journal › Article › peer-review

9 Scopus citations

Abstract

The distinction of primary mucinous ovarian carcinoma (PMOC) from other primaries or secondaries is essential for selecting therapeutic options and prognostication. We aimed to characterize the immunohistochemical profile of 36 PMOCs using an extended immunohistochemical panel, with clinicopathologic features and outcome. PAX8 was negative in 30 (83.3%), and SATB2 was negative in 32/35. HNF1B, AMACR, and napsin-A were detected in 33 (91.7%), 35 (97.2%), and 0 (0%), respectively. MMR proteins and ARID1A were retained in 100%; PTEN was lost in 4 (11.1%). P53 was aberrant in 10 (27.8%); none overexpressed p16. HER2 was positive in 6/35 (17.1%). Most PMOCs had a favorable outcome. However, recurrence is usually fatal. The typical tumor profile was CK7+, CK20+/−, CDX2+/−, PAX8−, ER−, PgR−, and SATB2−. HER2 positivity suggests a possible target for therapy in advanced disease.

Original language	English (US)
Pages (from-to)	306-317
Number of pages	12
Journal	International Journal of Surgical Pathology
Volume	26
Issue number	4
DOIs	https://doi.org/10.1177/1066896917752861
State	Published - Jun 1 2018
Externally published	Yes

Keywords

HER2
HNF1b
PAX8
SATB2
immunohistochemistry
mucinous
napsin A
ovarian cancer

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Bassiouny, D., Ismiil, N., Dubé, V., Han, G., Cesari, M., Lu, F. I., Slodkowska, E., Parra-Herran, C., Chiu, H. F., Naeim, M., Li, N., Khalifa, M., & Nofech-Mozes, S. (2018). Comprehensive Clinicopathologic and Updated Immunohistochemical Characterization of Primary Ovarian Mucinous Carcinoma. International Journal of Surgical Pathology, 26(4), 306-317. https://doi.org/10.1177/1066896917752861

Comprehensive Clinicopathologic and Updated Immunohistochemical Characterization of Primary Ovarian Mucinous Carcinoma. / Bassiouny, Dina; Ismiil, Nadia; Dubé, Valerie; Han, Guangming; Cesari, Matthew; Lu, Fang I.; Slodkowska, Elzbieta; Parra-Herran, Carlos; Chiu, Hak Fai; Naeim, Magda; Li, Nim; Khalifa, Mahmoud; Nofech-Mozes, Sharon.

In: International Journal of Surgical Pathology, Vol. 26, No. 4, 01.06.2018, p. 306-317.

Research output: Contribution to journal › Article › peer-review

Bassiouny, D, Ismiil, N, Dubé, V, Han, G, Cesari, M, Lu, FI, Slodkowska, E, Parra-Herran, C, Chiu, HF, Naeim, M, Li, N, Khalifa, M & Nofech-Mozes, S 2018, 'Comprehensive Clinicopathologic and Updated Immunohistochemical Characterization of Primary Ovarian Mucinous Carcinoma', International Journal of Surgical Pathology, vol. 26, no. 4, pp. 306-317. https://doi.org/10.1177/1066896917752861

Bassiouny, Dina ; Ismiil, Nadia ; Dubé, Valerie ; Han, Guangming ; Cesari, Matthew ; Lu, Fang I. ; Slodkowska, Elzbieta ; Parra-Herran, Carlos ; Chiu, Hak Fai ; Naeim, Magda ; Li, Nim ; Khalifa, Mahmoud ; Nofech-Mozes, Sharon. / Comprehensive Clinicopathologic and Updated Immunohistochemical Characterization of Primary Ovarian Mucinous Carcinoma. In: International Journal of Surgical Pathology. 2018 ; Vol. 26, No. 4. pp. 306-317.

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abstract = "The distinction of primary mucinous ovarian carcinoma (PMOC) from other primaries or secondaries is essential for selecting therapeutic options and prognostication. We aimed to characterize the immunohistochemical profile of 36 PMOCs using an extended immunohistochemical panel, with clinicopathologic features and outcome. PAX8 was negative in 30 (83.3%), and SATB2 was negative in 32/35. HNF1B, AMACR, and napsin-A were detected in 33 (91.7%), 35 (97.2%), and 0 (0%), respectively. MMR proteins and ARID1A were retained in 100%; PTEN was lost in 4 (11.1%). P53 was aberrant in 10 (27.8%); none overexpressed p16. HER2 was positive in 6/35 (17.1%). Most PMOCs had a favorable outcome. However, recurrence is usually fatal. The typical tumor profile was CK7+, CK20+/−, CDX2+/−, PAX8−, ER−, PgR−, and SATB2−. HER2 positivity suggests a possible target for therapy in advanced disease.",

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