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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Federation of Turkish Pathology Societies
2020-09-01
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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
|
work_keys_str_mv |
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