Hug(h)e(s') ears: an unusual presentation of antiphospholipid syndrome
نویسندگان
چکیده
منابع مشابه
An unusual case of Hughes-Stovin syndrome.
In 1959 HUGHES and STOVIN described a syndrome consisting of multiple pulmonary aneurysms and peripheral venous thrombosis. Since that time several cases of the Hughes-Stovin syndrome have been published. We present the case of a 25 yr old man who, in addition to the classical symptoms, had multiple aneurysms of the bronchial arteries, which were the cause of severe haemoptysis. An aneurysm of ...
متن کاملHughes-Stovin syndrome: an unusual cause of pulmonary artery aneurysms
Radiol Bras. 2016 Mai/Jun;49(3):199–204 202 http://dx.doi.org/10.1590/0100-3984.2015.0082 extraplexus nerve transfer techniques, the areas of activation mainly being located in the contralateral cortex. This study has some limitations. We presented the patient data only in comparison with those of a single control participant, rather than with a group of control, and both data sets were acquire...
متن کاملPrecocious Puberty: An Unusual Presentation of Hypothyroidism
Hypothyroidism is usually associated with delayed pubertal development but in rare occasions precocious puberty may ensue which is seen in cases of prolonged and untreated hypothyroidism. This is also called the Van Wyk Grumbach syndrome. Here we present 4 cases of precocious puberty due to hypothyroidism.
متن کاملThe Catastrophic Antiphospholipid Antibody Syndrome: An Unusual Presentation of Spontaneous Acute Intracranial Haemorrhage
Background: Catastrophic Antiphospholipid syndrome (CAPS) is a scarcely understood entity with a high mortality approaching 50%The rapid deterioration is triggered by a deadly cytokine storm, which is difficult to recognize and almost impossible to treat in time. Various regimens have been advocated, which include administration of monoclonal anti-phospholipid antibodies and pulses of high dose...
متن کاملAn Unusual Presentation of Granulomatosis with Polyangiitis
The granulomatosis with polyangiitis (GPA), formerly known as Wegener’s granulomatosis, is a pauci-immune vasculitis involving small- and medium-sized blood vessels. Classically, the patients inflicted with this disease present with a triad of necrotizing granulomatous inflammation of the respiratory tract, cutaneous necrotizing vasculitis, and glomerulonephritis (GN). The antinuclear (ANA) and...
متن کاملذخیره در منابع من
با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید
ژورنال
عنوان ژورنال: Annals of the Rheumatic Diseases
سال: 1999
ISSN: 0003-4967
DOI: 10.1136/ard.58.1.65