Open AccessRecurrent Haemoptysis Revealing Hughes-Stovin Syndrome
Author(s) -
N. Moussa,
Tasnim Znegui,
M. Snoussi,
R. Gargouri,
Z. Bahloul,
S. Abid,
S. Kammoun
Publication year - 2021
Publication title -
european journal of case reports in internal medicine
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.125
H-Index - 1
ISSN - 2284-2594
DOI - 10.12890/2021_002810
Subject(s) - etiology , medicine , disease , rare disease , pediatrics , intensive care medicine , pathology
Hughes-Stovin syndrome is a very rare condition with no defined diagnostic criteria. We present the case of a 26-year-old man who had haemoptysis revealing Hughes-Stovin syndrome. We will consider the aetiology, therapeutic and evolutionary aspects of this disease.