Mediastinal cyst: a case report (RCD code: VI)
نویسندگان
چکیده
منابع مشابه
Multiple mediastinal hydatic cyst: a case report.
Hydatid disease is a parasitic infection that is remains endemic in many countries, particularly the Middle East and Central Asia. Mediastinal hydatidosis is very rare (less than 0.1% of all hydatid disease cases) that have been only anecdotally in the literature. To the best of our knowledge only one case of multiple mediastineal hydatid cysts has been reported previously. We report the second...
متن کاملMediastinal hydatid cyst: a case report
INTRODUCTION Mediastinal localization of hydatidosis is very rare even in endemic areas. The diagnosis is based on typical clinical and radiological criteria. CASE PRESENTATION We report a case of a mediastinal location of hydatidosis in a 60-year-old Arab man admitted for chest pain. The chest radiograph showed a rounded and homogeneous opacity. Computed tomography showed a right mediastinal...
متن کاملMediastinal epidermoid cyst in an old man with recurrent pneumonia: A case report
Mediastinal epidermoid cyst is a rare condition that is considered as a congenital disorder. Various manifestations from asymptomatic cases to serious symptoms may be found in these patients. However, some cases may be diagnosed incidentally. Here, we report an old man with recurrent pneumonia who demonstrated symptoms of respiratory distress and chest pain. The high resolution computed tomogra...
متن کاملMultilocular Thymic Cyst Associated with Mediastinal Teratoma: A Case Report
Congenital cysts are typically unilocular and thin-walled to the point of translucency; careful histopathologic examination shows no evidence of inflammation. In contrast, acquired thymic cysts are usually multilocular, hence the commonly used term “multilocular thymic cyst (MTC).” These cysts have thick, fibrous walls, and histopathologic examination typically reveals significant inflammation ...
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ژورنال
عنوان ژورنال: Journal of Rare Cardiovascular Diseases
سال: 2015
ISSN: 2300-5505,2299-3711
DOI: 10.20418/jrcd.vol2no2.169