Loading…
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 in...
Saved in:
Published in: | Journal of chest surgery 2021, Vol.54 (6), p.524-527 |
---|---|
Main Authors: | , , , |
Format: | Article |
Language: | Korean |
Online Access: | Get full text |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
cited_by | |
---|---|
cites | |
container_end_page | 527 |
container_issue | 6 |
container_start_page | 524 |
container_title | Journal of chest surgery |
container_volume | 54 |
creator | Diab, Abdul-Rahman Fadi Daradkeh, Salam Saleh Hassouneh, Alaa Mohammed Alabbadi, Ali Mousa |
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 |
fullrecord | <record><control><sourceid>kisti</sourceid><recordid>TN_cdi_kisti_ndsl_JAKO202105650883320</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>JAKO202105650883320</sourcerecordid><originalsourceid>FETCH-kisti_ndsl_JAKO2021056508833203</originalsourceid><addsrcrecordid>eNqNikELgjAYQEcUJOV_2KWjsLk2pZuIYXUoorusXHM0N-lToX9fh-jc6T0eb4KCOBE8ooKupz8nYo5CAHMlnLFEpJQHaH8CNdS-fXmtnLnhUrXSaeOVq33fKGt8K_HOjd6Oxmn8SbgA3zVSD7DBGc4lKHxWnX_2SzS7Swsq_HKBVtvikpfRw0BvKleDrfbZ4RiTmBIuOElTxmLC_v3eQGI9JQ</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype></control><display><type>article</type><title>Pseudomyogenic Hemangioendothelioma Involving the Esophagus: A Case Report</title><source>PubMed Central Free</source><source>Directory of Open Access Journals</source><creator>Diab, Abdul-Rahman Fadi ; Daradkeh, Salam Saleh ; Hassouneh, Alaa Mohammed ; Alabbadi, Ali Mousa</creator><creatorcontrib>Diab, Abdul-Rahman Fadi ; Daradkeh, Salam Saleh ; Hassouneh, Alaa Mohammed ; Alabbadi, Ali Mousa</creatorcontrib><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.</description><identifier>ISSN: 2765-1606</identifier><identifier>EISSN: 2765-1614</identifier><language>kor</language><ispartof>Journal of chest surgery, 2021, Vol.54 (6), p.524-527</ispartof><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,314,780,784,885,4024</link.rule.ids></links><search><creatorcontrib>Diab, Abdul-Rahman Fadi</creatorcontrib><creatorcontrib>Daradkeh, Salam Saleh</creatorcontrib><creatorcontrib>Hassouneh, Alaa Mohammed</creatorcontrib><creatorcontrib>Alabbadi, Ali Mousa</creatorcontrib><title>Pseudomyogenic Hemangioendothelioma Involving the Esophagus: A Case Report</title><title>Journal of chest surgery</title><addtitle>Journal of chest surgery</addtitle><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.</description><issn>2765-1606</issn><issn>2765-1614</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2021</creationdate><recordtype>article</recordtype><recordid>eNqNikELgjAYQEcUJOV_2KWjsLk2pZuIYXUoorusXHM0N-lToX9fh-jc6T0eb4KCOBE8ooKupz8nYo5CAHMlnLFEpJQHaH8CNdS-fXmtnLnhUrXSaeOVq33fKGt8K_HOjd6Oxmn8SbgA3zVSD7DBGc4lKHxWnX_2SzS7Swsq_HKBVtvikpfRw0BvKleDrfbZ4RiTmBIuOElTxmLC_v3eQGI9JQ</recordid><startdate>2021</startdate><enddate>2021</enddate><creator>Diab, Abdul-Rahman Fadi</creator><creator>Daradkeh, Salam Saleh</creator><creator>Hassouneh, Alaa Mohammed</creator><creator>Alabbadi, Ali Mousa</creator><scope>JDI</scope></search><sort><creationdate>2021</creationdate><title>Pseudomyogenic Hemangioendothelioma Involving the Esophagus: A Case Report</title><author>Diab, Abdul-Rahman Fadi ; Daradkeh, Salam Saleh ; Hassouneh, Alaa Mohammed ; Alabbadi, Ali Mousa</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-kisti_ndsl_JAKO2021056508833203</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>kor</language><creationdate>2021</creationdate><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Diab, Abdul-Rahman Fadi</creatorcontrib><creatorcontrib>Daradkeh, Salam Saleh</creatorcontrib><creatorcontrib>Hassouneh, Alaa Mohammed</creatorcontrib><creatorcontrib>Alabbadi, Ali Mousa</creatorcontrib><collection>KoreaScience</collection><jtitle>Journal of chest surgery</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Diab, Abdul-Rahman Fadi</au><au>Daradkeh, Salam Saleh</au><au>Hassouneh, Alaa Mohammed</au><au>Alabbadi, Ali Mousa</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Pseudomyogenic Hemangioendothelioma Involving the Esophagus: A Case Report</atitle><jtitle>Journal of chest surgery</jtitle><addtitle>Journal of chest surgery</addtitle><date>2021</date><risdate>2021</risdate><volume>54</volume><issue>6</issue><spage>524</spage><epage>527</epage><pages>524-527</pages><issn>2765-1606</issn><eissn>2765-1614</eissn><abstract>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.</abstract><oa>free_for_read</oa></addata></record> |
fulltext | fulltext |
identifier | ISSN: 2765-1606 |
ispartof | Journal of chest surgery, 2021, Vol.54 (6), p.524-527 |
issn | 2765-1606 2765-1614 |
language | kor |
recordid | cdi_kisti_ndsl_JAKO202105650883320 |
source | PubMed Central Free; Directory of Open Access Journals |
title | Pseudomyogenic Hemangioendothelioma Involving the Esophagus: A Case Report |
url | http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-26T23%3A42%3A43IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-kisti&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Pseudomyogenic%20Hemangioendothelioma%20Involving%20the%20Esophagus:%20A%20Case%20Report&rft.jtitle=Journal%20of%20chest%20surgery&rft.au=Diab,%20Abdul-Rahman%20Fadi&rft.date=2021&rft.volume=54&rft.issue=6&rft.spage=524&rft.epage=527&rft.pages=524-527&rft.issn=2765-1606&rft.eissn=2765-1614&rft_id=info:doi/&rft_dat=%3Ckisti%3EJAKO202105650883320%3C/kisti%3E%3Cgrp_id%3Ecdi_FETCH-kisti_ndsl_JAKO2021056508833203%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_id=info:pmid/&rfr_iscdi=true |