Pseudomyogenic Hemangioendothelioma Involving the Esophagus: A Case Report

Herein, we describe the case of a 20-year-old woman who presented with dysphagia of 2 months’ duration associated with vomiting, moderate abdominal pain, decreased oral intake, and significant weight loss. During the past 3 years, the patient experienced intermittent mild abdominal pain with infr...

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Autores principales:	Abdul-Rahman Fadi Diab, Salam Saleh Daradkeh, Alaa Mohammed Hassouneh, Ali Mousa Alabbadi
Formato:	article
Lenguaje:	EN
Publicado:	Korean Society for Thoracic & Cardiovascular Surgery 2021
Materias:	hemangioendothelioma vascular neoplasms deglutition disorders esophageal neoplasms lymphadenopathy case report Medicine (General) R5-920
Acceso en línea:	https://doaj.org/article/cf9666765204496b9a517101789d5080
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spelling	oai:doaj.org-article:cf9666765204496b9a517101789d50802021-12-03T01:47:56ZPseudomyogenic Hemangioendothelioma Involving the Esophagus: A Case Report10.5090/jcs.20.1512765-16062765-1614https://doaj.org/article/cf9666765204496b9a517101789d50802021-12-01T00:00:00Zhttps://doaj.org/toc/2765-1606https://doaj.org/toc/2765-1614Herein, we describe the case of a 20-year-old woman who presented with dysphagia of 2 months’ duration associated with vomiting, moderate abdominal pain, decreased oral intake, and significant weight loss. During the past 3 years, the patient experienced intermittent mild abdominal pain with infrequent vomiting. Endoscopy at Jordan University Hospital showed a mass in the esophagus, and endoscopic biopsies were performed. The preliminary histopathological report excluded malignancy. Two days after endoscopy, the patient presented to the emergency department complaining of severely worsening pain and total dysphagia. The pain persisted despite intravenous paracetamol administration, which was concerning for esophageal perforation; therefore, an urgent surgical intervention was performed. The mass was removed surgically, along with a para-esophageal lymph node. The final histopathological results of the endoscopic and resected specimens supported the diagnosis of pseudomyogenic hemangioendothelioma (PMHE). This is the first case reporting esophageal involvement of PMHE.Abdul-Rahman Fadi DiabSalam Saleh DaradkehAlaa Mohammed HassounehAli Mousa AlabbadiKorean Society for Thoracic & Cardiovascular Surgeryarticlehemangioendotheliomavascular neoplasmsdeglutition disordersesophageal neoplasmslymphadenopathycase reportMedicine (General)R5-920ENJournal of Chest Surgery, Vol 54, Iss 6, Pp 524-527 (2021)
institution	DOAJ
collection	DOAJ
language	EN
topic	hemangioendothelioma vascular neoplasms deglutition disorders esophageal neoplasms lymphadenopathy case report Medicine (General) R5-920
spellingShingle	hemangioendothelioma vascular neoplasms deglutition disorders esophageal neoplasms lymphadenopathy case report Medicine (General) R5-920 Abdul-Rahman Fadi Diab Salam Saleh Daradkeh Alaa Mohammed Hassouneh Ali Mousa Alabbadi Pseudomyogenic Hemangioendothelioma Involving the Esophagus: A Case Report
description	Herein, we describe the case of a 20-year-old woman who presented with dysphagia of 2 months’ duration associated with vomiting, moderate abdominal pain, decreased oral intake, and significant weight loss. During the past 3 years, the patient experienced intermittent mild abdominal pain with infrequent vomiting. Endoscopy at Jordan University Hospital showed a mass in the esophagus, and endoscopic biopsies were performed. The preliminary histopathological report excluded malignancy. Two days after endoscopy, the patient presented to the emergency department complaining of severely worsening pain and total dysphagia. The pain persisted despite intravenous paracetamol administration, which was concerning for esophageal perforation; therefore, an urgent surgical intervention was performed. The mass was removed surgically, along with a para-esophageal lymph node. The final histopathological results of the endoscopic and resected specimens supported the diagnosis of pseudomyogenic hemangioendothelioma (PMHE). This is the first case reporting esophageal involvement of PMHE.
format	article
author	Abdul-Rahman Fadi Diab Salam Saleh Daradkeh Alaa Mohammed Hassouneh Ali Mousa Alabbadi
author_facet	Abdul-Rahman Fadi Diab Salam Saleh Daradkeh Alaa Mohammed Hassouneh Ali Mousa Alabbadi
author_sort	Abdul-Rahman Fadi Diab
title	Pseudomyogenic Hemangioendothelioma Involving the Esophagus: A Case Report
title_short	Pseudomyogenic Hemangioendothelioma Involving the Esophagus: A Case Report
title_full	Pseudomyogenic Hemangioendothelioma Involving the Esophagus: A Case Report
title_fullStr	Pseudomyogenic Hemangioendothelioma Involving the Esophagus: A Case Report
title_full_unstemmed	Pseudomyogenic Hemangioendothelioma Involving the Esophagus: A Case Report
title_sort	pseudomyogenic hemangioendothelioma involving the esophagus: a case report
publisher	Korean Society for Thoracic & Cardiovascular Surgery
publishDate	2021
url	https://doaj.org/article/cf9666765204496b9a517101789d5080
work_keys_str_mv	AT abdulrahmanfadidiab pseudomyogenichemangioendotheliomainvolvingtheesophagusacasereport AT salamsalehdaradkeh pseudomyogenichemangioendotheliomainvolvingtheesophagusacasereport AT alaamohammedhassouneh pseudomyogenichemangioendotheliomainvolvingtheesophagusacasereport AT alimousaalabbadi pseudomyogenichemangioendotheliomainvolvingtheesophagusacasereport
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Pseudomyogenic Hemangioendothelioma Involving the Esophagus: A Case Report

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