Small Cell Carcinoma of Ovary, Hypercalcemic Type (Malignant Rhabdoid Tumor of Ovary) with Loss of SMARCA4 (BRG1) Expression: Report of Two Cases

Small cell carcinoma of the ovary, hypercalcemic type (SCCOHT) / malignant rhabdoid tumor of the ovary (MRTO) is a rare tumor affecting young women. It is frequently misdiagnosed due to overlapping morphological and immunohistochemical features with many other ovarian tumors. The prognosis of the tu...

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Main Authors: Ayushi SAHAY, Katha KANTE, Santosh MENON, Jaya GHOSH, Rajendra A. KERKAR, Kedar K. DEODHAR
Format: Article
Language:English
Published: Federation of Turkish Pathology Societies 2020-09-01
Series:Türk Patoloji Dergisi
Subjects:
Online Access: http://www.turkjpath.org/pdf.php3?id=1914
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spelling doaj-246d8c6517e04c8da8a62214b85589c12020-11-25T03:42:27ZengFederation of Turkish Pathology SocietiesTürk Patoloji Dergisi1018-56151309-57302020-09-0136326126710.5146/tjpath.2020.01477Small Cell Carcinoma of Ovary, Hypercalcemic Type (Malignant Rhabdoid Tumor of Ovary) with Loss of SMARCA4 (BRG1) Expression: Report of Two CasesAyushi SAHAYKatha KANTESantosh MENONJaya GHOSHRajendra A. KERKARKedar K. DEODHARSmall cell carcinoma of the ovary, hypercalcemic type (SCCOHT) / malignant rhabdoid tumor of the ovary (MRTO) is a rare tumor affecting young women. It is frequently misdiagnosed due to overlapping morphological and immunohistochemical features with many other ovarian tumors. The prognosis of the tumors is very poor; hence an accurate diagnosis is of utmost importance. Recently, the loss of BRG1 protein by immunohistochemistry has been shown to be a useful diagnostic marker. We present here two cases of SSCOHT/MRTO, in young women 22 and 32 years of age, where several differential diagnoses were considered on morphology and immunohistochemistry but were confirmed as SCCOHT/MRTO by the demonstration of loss of BRG1. As the prognosis of SCCOHT is very dismal, and accurate diagnosis is of necessity, we recommend the inclusion of BRG1 immunohistochemistry in the diagnostic armamentarium of poorly differentiated ovarian tumors, particularly in young adults. http://www.turkjpath.org/pdf.php3?id=1914 small cell carcinoma ovaryrhabdoid tumor of ovarybrg1ovarian tumor
collection DOAJ
language English
format Article
sources DOAJ
author Ayushi SAHAY
Katha KANTE
Santosh MENON
Jaya GHOSH
Rajendra A. KERKAR
Kedar K. DEODHAR
spellingShingle Ayushi SAHAY
Katha KANTE
Santosh MENON
Jaya GHOSH
Rajendra A. KERKAR
Kedar K. DEODHAR
Small Cell Carcinoma of Ovary, Hypercalcemic Type (Malignant Rhabdoid Tumor of Ovary) with Loss of SMARCA4 (BRG1) Expression: Report of Two Cases
Türk Patoloji Dergisi
small cell carcinoma ovary
rhabdoid tumor of ovary
brg1
ovarian tumor
author_facet Ayushi SAHAY
Katha KANTE
Santosh MENON
Jaya GHOSH
Rajendra A. KERKAR
Kedar K. DEODHAR
author_sort Ayushi SAHAY
title Small Cell Carcinoma of Ovary, Hypercalcemic Type (Malignant Rhabdoid Tumor of Ovary) with Loss of SMARCA4 (BRG1) Expression: Report of Two Cases
title_short Small Cell Carcinoma of Ovary, Hypercalcemic Type (Malignant Rhabdoid Tumor of Ovary) with Loss of SMARCA4 (BRG1) Expression: Report of Two Cases
title_full Small Cell Carcinoma of Ovary, Hypercalcemic Type (Malignant Rhabdoid Tumor of Ovary) with Loss of SMARCA4 (BRG1) Expression: Report of Two Cases
title_fullStr Small Cell Carcinoma of Ovary, Hypercalcemic Type (Malignant Rhabdoid Tumor of Ovary) with Loss of SMARCA4 (BRG1) Expression: Report of Two Cases
title_full_unstemmed Small Cell Carcinoma of Ovary, Hypercalcemic Type (Malignant Rhabdoid Tumor of Ovary) with Loss of SMARCA4 (BRG1) Expression: Report of Two Cases
title_sort small cell carcinoma of ovary, hypercalcemic type (malignant rhabdoid tumor of ovary) with loss of smarca4 (brg1) expression: report of two cases
publisher Federation of Turkish Pathology Societies
series Türk Patoloji Dergisi
issn 1018-5615
1309-5730
publishDate 2020-09-01
description Small cell carcinoma of the ovary, hypercalcemic type (SCCOHT) / malignant rhabdoid tumor of the ovary (MRTO) is a rare tumor affecting young women. It is frequently misdiagnosed due to overlapping morphological and immunohistochemical features with many other ovarian tumors. The prognosis of the tumors is very poor; hence an accurate diagnosis is of utmost importance. Recently, the loss of BRG1 protein by immunohistochemistry has been shown to be a useful diagnostic marker. We present here two cases of SSCOHT/MRTO, in young women 22 and 32 years of age, where several differential diagnoses were considered on morphology and immunohistochemistry but were confirmed as SCCOHT/MRTO by the demonstration of loss of BRG1. As the prognosis of SCCOHT is very dismal, and accurate diagnosis is of necessity, we recommend the inclusion of BRG1 immunohistochemistry in the diagnostic armamentarium of poorly differentiated ovarian tumors, particularly in young adults.
topic small cell carcinoma ovary
rhabdoid tumor of ovary
brg1
ovarian tumor
url http://www.turkjpath.org/pdf.php3?id=1914
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