[Primary pleural epithelioid hemangioendothelioma, an often-misdiagnosed rare tumor].
Hémangioendothéliome épithélioïde pleural, une tumeur rare de diagnostic difficile : à propos d’un cas et revue de la littérature.
Diagnosis
Epithelioid hemangioendothelioma
Ultrasound-guided biopsy
Journal
Revue des maladies respiratoires
ISSN: 1776-2588
Titre abrégé: Rev Mal Respir
Pays: France
ID NLM: 8408032
Informations de publication
Date de publication:
Apr 2022
Apr 2022
Historique:
received:
01
09
2021
accepted:
24
02
2022
pubmed:
10
5
2022
medline:
24
5
2022
entrez:
9
5
2022
Statut:
ppublish
Résumé
Epithelioid hemangioendothelioma (EHE) is a rare vascular tumor that develops in various organs. Primary pleural epithelioid hemangioendothelioma is an exceptional occurrence, with only forty cases reported in the literature. On account of its rarity, pleural EHE is difficult to diagnose. Differential diagnoses such as malignant pleural mesothelioma or lung carcinoma are often initially suspected. We herein describe the case of a 52-year-old man presenting with a primary pleural epithelioid hemangioendothelioma revealed by thoracic pain and having evolved for three months. Having reviewed the literature, we consider the clinical presentation and diagnosis modalities of this rare tumor. After an initial diagnosis of lung carcinoma, an ultrasound-guided biopsy was performed, confirming the diagnosis of pleural EHE in our patient. Ours is the first case of pleural EHE to be diagnosed with ultrasound-guided echography. Presentation of pleural EHE is often clinically and radiologically nonspecific. Most diagnoses are obtained by thoracoscopy, which allows for targeted biopsies and evacuation of pleural effusion. The diagnostic process for this rare tumor must be rigorous. Ultrasound-guided biopsy may be considered, provided that the lesions are accessible.
Identifiants
pubmed: 35534368
pii: S0761-8425(22)00137-1
doi: 10.1016/j.rmr.2022.03.005
pii:
doi:
Types de publication
Case Reports
Journal Article
Langues
fre
Sous-ensembles de citation
IM
Pagination
398-406Informations de copyright
Copyright © 2022 SPLF. Published by Elsevier Masson SAS. All rights reserved.