Malignant Perivascular Epithelioid Cell Tumor of the Esophagus

Malignant perivascular epithelioid cell tumor (PEComa) is a rare tumor composed of hybrid tumor cells characterized by immunoreactivity for both melanocytic and smooth muscle markers. This paper describes the uncommon esophageal location of an 8 cm PEComa in a 75-year-old Caucasian man who was prese...

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Published inCase reports in pathology Vol. 2012; no. 2012; pp. 1 - 5
Main Authors Fassan, Matteo, Cassaro, Mauro, Vecchiato, Massimo, Clemente, Roberto, Pennelli, Gianmaria, Merigliano, Stefano, Altavilla, Giuseppe
Format Journal Article
LanguageEnglish
Published Cairo, Egypt Hindawi Puplishing Corporation 01.01.2012
Hindawi Publishing Corporation
Wiley
Subjects
Online AccessGet full text
ISSN2090-6781
2090-679X
2090-679X
DOI10.1155/2012/438505

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Abstract Malignant perivascular epithelioid cell tumor (PEComa) is a rare tumor composed of hybrid tumor cells characterized by immunoreactivity for both melanocytic and smooth muscle markers. This paper describes the uncommon esophageal location of an 8 cm PEComa in a 75-year-old Caucasian man who was presented with ingravescent dysphagia. Although PEComas arising within the gastrointestinal tract are exceptional findings, clinicians should not exclude this class of tumors in the diagnostic investigation of a bulky lesion of the esophageal wall.
AbstractList Malignant perivascular epithelioid cell tumor (PEComa) is a rare tumor composed of hybrid tumor cells characterized by immunoreactivity for both melanocytic and smooth muscle markers. This paper describes the uncommon esophageal location of an 8 cm PEComa in a 75-year-old Caucasian man who was presented with ingravescent dysphagia. Although PEComas arising within the gastrointestinal tract are exceptional findings, clinicians should not exclude this class of tumors in the diagnostic investigation of a bulky lesion of the esophageal wall.
Malignant perivascular epithelioid cell tumor (PEComa) is a rare tumor composed of hybrid tumor cells characterized by immunoreactivity for both melanocytic and smooth muscle markers. This paper describes the uncommon esophageal location of an 8 cm PEComa in a 75-year-old Caucasian man who was presented with ingravescent dysphagia. Although PEComas arising within the gastrointestinal tract are exceptional findings, clinicians should not exclude this class of tumors in the diagnostic investigation of a bulky lesion of the esophageal wall.Malignant perivascular epithelioid cell tumor (PEComa) is a rare tumor composed of hybrid tumor cells characterized by immunoreactivity for both melanocytic and smooth muscle markers. This paper describes the uncommon esophageal location of an 8 cm PEComa in a 75-year-old Caucasian man who was presented with ingravescent dysphagia. Although PEComas arising within the gastrointestinal tract are exceptional findings, clinicians should not exclude this class of tumors in the diagnostic investigation of a bulky lesion of the esophageal wall.
Author Vecchiato, Massimo
Pennelli, Gianmaria
Fassan, Matteo
Merigliano, Stefano
Cassaro, Mauro
Clemente, Roberto
Altavilla, Giuseppe
AuthorAffiliation 3 Surgery Unit, Department of Surgery, Oncology and Gastroenterology (DiSCOG), University of Padua, 35121 Padua, Italy
2 General Oncology Unit, Department of Surgery, Oncology and Gastroenterology (DiSCOG), University of Padua, 35121 Padua, Italy
1 Surgical Pathology and Cytopathology Unit, Department of Medicine (DIMED), University of Padua, 35121 Padua, Italy
AuthorAffiliation_xml – name: 2 General Oncology Unit, Department of Surgery, Oncology and Gastroenterology (DiSCOG), University of Padua, 35121 Padua, Italy
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10.1177/106689690000800112
10.1038/modpathol.3880351
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Snippet Malignant perivascular epithelioid cell tumor (PEComa) is a rare tumor composed of hybrid tumor cells characterized by immunoreactivity for both melanocytic...
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Title Malignant Perivascular Epithelioid Cell Tumor of the Esophagus
URI https://search.emarefa.net/detail/BIM-472355
https://dx.doi.org/10.1155/2012/438505
https://www.ncbi.nlm.nih.gov/pubmed/22957287
https://www.proquest.com/docview/1038595822
https://pubmed.ncbi.nlm.nih.gov/PMC3432343
https://doaj.org/article/808bcd0d151a47b2a236b6f87c272e5e
Volume 2012
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