Blastomatoid pulmonary carcinosarcoma: report of a case with a review of the literature

<p>Abstract</p> <p>Background</p> <p>Pulmonary carcinosarcoma is a biphasic tumour with an unfavourable prognosis. The differential diagnosis includes pulmonary blastoma and is often challenging.</p> <p>Case presentation</p> <p>We here describe a...

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Main Authors: Schaefer Inga-Marie, Sahlmann Carsten-Oliver, Overbeck Tobias, Schweyer Stefan, Menke Jan
Format: Article
Language:English
Published: BMC 2012-09-01
Series:BMC Cancer
Subjects:
Online Access:http://www.biomedcentral.com/1471-2407/12/424
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spelling doaj-ed9eaf3455b742e4b5c790c48afc1d172020-11-24T22:16:23ZengBMCBMC Cancer1471-24072012-09-0112142410.1186/1471-2407-12-424Blastomatoid pulmonary carcinosarcoma: report of a case with a review of the literatureSchaefer Inga-MarieSahlmann Carsten-OliverOverbeck TobiasSchweyer StefanMenke Jan<p>Abstract</p> <p>Background</p> <p>Pulmonary carcinosarcoma is a biphasic tumour with an unfavourable prognosis. The differential diagnosis includes pulmonary blastoma and is often challenging.</p> <p>Case presentation</p> <p>We here describe a case of blastomatoid pulmonary carcinosarcoma in a 58-year-old patient, who underwent surgical resection. Histopathological examination revealed immature glandular epithelium resembling high-grade fetal adenocarcinoma expressing epithelial markers and membranous beta-catenin, and blastomatoid spindle cells with partial rhabdomyosarcoma-like differentiation. Both elements expressed p53, MDM2, and cyclin-dependent kinase 4 (CDK4), but not thyroid-transcription factor 1 (TTF-1). Mutation analysis of <it>KRAS</it>, <it>EGFR</it>, and <it>beta-catenin</it> revealed no mutations. Comparative genomic hybridization detected +1q, +6p, +6q24qter, +8q, +11q12q14, +11q23qter, +12q12q21, +12q24qter, +17q, +20q, -5q14q23, -9p13pter, -13q21q21, and amplifications at 12q14q21, 15q24qter, 20q11q12.</p> <p>Conclusion</p> <p>The observed molecular and cytogenetic findings may provide additional tools for the differential diagnosis of biphasic pulmonary neoplasms. Furthermore, <it>TP53</it>, <it>MDM2</it>, <it>CDK4</it>, and <it>PTPN1</it> may be involved in tumourigenesis.</p> http://www.biomedcentral.com/1471-2407/12/424Lungbiphasic, Carcinosarcoma, Pulmonary blastoma, Comparative genomic hybridization
collection DOAJ
language English
format Article
sources DOAJ
author Schaefer Inga-Marie
Sahlmann Carsten-Oliver
Overbeck Tobias
Schweyer Stefan
Menke Jan
spellingShingle Schaefer Inga-Marie
Sahlmann Carsten-Oliver
Overbeck Tobias
Schweyer Stefan
Menke Jan
Blastomatoid pulmonary carcinosarcoma: report of a case with a review of the literature
BMC Cancer
Lung
biphasic, Carcinosarcoma, Pulmonary blastoma, Comparative genomic hybridization
author_facet Schaefer Inga-Marie
Sahlmann Carsten-Oliver
Overbeck Tobias
Schweyer Stefan
Menke Jan
author_sort Schaefer Inga-Marie
title Blastomatoid pulmonary carcinosarcoma: report of a case with a review of the literature
title_short Blastomatoid pulmonary carcinosarcoma: report of a case with a review of the literature
title_full Blastomatoid pulmonary carcinosarcoma: report of a case with a review of the literature
title_fullStr Blastomatoid pulmonary carcinosarcoma: report of a case with a review of the literature
title_full_unstemmed Blastomatoid pulmonary carcinosarcoma: report of a case with a review of the literature
title_sort blastomatoid pulmonary carcinosarcoma: report of a case with a review of the literature
publisher BMC
series BMC Cancer
issn 1471-2407
publishDate 2012-09-01
description <p>Abstract</p> <p>Background</p> <p>Pulmonary carcinosarcoma is a biphasic tumour with an unfavourable prognosis. The differential diagnosis includes pulmonary blastoma and is often challenging.</p> <p>Case presentation</p> <p>We here describe a case of blastomatoid pulmonary carcinosarcoma in a 58-year-old patient, who underwent surgical resection. Histopathological examination revealed immature glandular epithelium resembling high-grade fetal adenocarcinoma expressing epithelial markers and membranous beta-catenin, and blastomatoid spindle cells with partial rhabdomyosarcoma-like differentiation. Both elements expressed p53, MDM2, and cyclin-dependent kinase 4 (CDK4), but not thyroid-transcription factor 1 (TTF-1). Mutation analysis of <it>KRAS</it>, <it>EGFR</it>, and <it>beta-catenin</it> revealed no mutations. Comparative genomic hybridization detected +1q, +6p, +6q24qter, +8q, +11q12q14, +11q23qter, +12q12q21, +12q24qter, +17q, +20q, -5q14q23, -9p13pter, -13q21q21, and amplifications at 12q14q21, 15q24qter, 20q11q12.</p> <p>Conclusion</p> <p>The observed molecular and cytogenetic findings may provide additional tools for the differential diagnosis of biphasic pulmonary neoplasms. Furthermore, <it>TP53</it>, <it>MDM2</it>, <it>CDK4</it>, and <it>PTPN1</it> may be involved in tumourigenesis.</p>
topic Lung
biphasic, Carcinosarcoma, Pulmonary blastoma, Comparative genomic hybridization
url http://www.biomedcentral.com/1471-2407/12/424
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