Unlabelled: 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.
Learning Points: Hughes-Stovin syndrome is a very rare disorder of unknown aetiology which can be fatal.It is considered a variant of Behcet's disease.Early diagnosis and treatment improve prognosis.
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http://dx.doi.org/10.12890/2021_002810 | DOI Listing |
Respirol Case Rep
December 2024
Department of Pulmonary Medicine St. John's National Academy of Health Sciences Bengaluru India.
Pulmonary artery aneurysmal rupture is a rare cause of massive hemoptysis. When the suspected origin of bleeding is the pulmonary artery, comprehensive evaluation is necessary to determine aetiology and guide appropriate management. Behçet's disease and Hughes-Stovin Syndrome (HSS) are important differentials to consider after infections and malignancy have been ruled out.
View Article and Find Full Text PDFJ Med Case Rep
December 2024
Student Research Committee, Shiraz University of Medical Sciences, Shiraz, Iran.
Vasc Endovascular Surg
February 2025
Nuclear and Energy Research Institute (IPEN), University of São Paulo, São Paulo, SP, Brazil.
Background: Pulmonary artery trunk aneurysm (PATA) is a rare and complex vascular anomaly characterized by the abnormal dilation of the initial portion of the pulmonary artery, posing significant diagnostic and therapeutic challenges.
Purpose: This clinical case report aims to describe the follow-up of a patient with PATA, emphasizing the role of imaging in diagnosis and monitoring, as well as discussing potential associations with other conditions.
Research Design: The study is designed as a clinical case report, detailing the longitudinal follow-up of a single patient with PATA.
Cureus
August 2024
Department of Diagnostic Radiology, College of Applied Medical Sciences, Taibah University, Al-Madinah Al-Munawwarah, SAU.
Behçet's syndrome (BS) is a rare chronic multisystemic inflammatory disorder of unknown etiopathogenesis. BS is classified as a vasculitis of variable vessel size, which can manifest in both arterial and venous blood vessels. BS commonly presents with mucocutaneous and ocular manifestations.
View Article and Find Full Text PDFEur Heart J Case Rep
August 2024
Internal Medicine Department, Ibn Sina University Hospital, Mohammed V University, 10100 Rabat, Morocco.
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