## Abstract Although cardiac tamponade is a known complication of malignancy, it is rarely the initial manifestation. We report a 46βyearβold male who presented with malignant cardiac tamponade 6 months prior to the definitive diagnosis of primary pericardial mesothelioma. A thorough literature sea
Pericardial effusion with cardiac tamponade as a cardiac manifestation of duchenne muscular dystrophy
β Scribed by Jainn-Jim Lin; Mao-Sheng Hwang; Shao-Hsuan Hsia; Hung-Tao Chung; Yu-Sheng Chang; Kuang-Lin Lin
- Publisher
- John Wiley and Sons
- Year
- 2009
- Tongue
- English
- Weight
- 158 KB
- Volume
- 40
- Category
- Article
- ISSN
- 0148-639X
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β¦ Synopsis
Abstract
Duchenne muscular dystrophy (DMD) is the most common hereditary neuromuscular disease in children. It is an Xβlinked hereditary dystrophinopathy due to the absence of dystrophin. Its onset is often in early childhood and presents with proximal distribution of weakness and a progressive course. Cardiac involvement in DMD is common, and its onset is usually after the age of 10 years. The most common cardiac manifestations are a dilated cardiomyopathy and cardiac arrhythmia. However, pericardial effusion with cardiac tamponade is a very rare cardiac complication of DMD. We report a boy with DMD who initially presented with progressive dyspnea and an enlarged cardiac silhouette on chest radiography who subsequently developed a large pericardial effusion with cardiac tamponade. Early recognition of pericardial effusion with cardiac tamponade is important for institution appropriate therapy. Muscle Nerve, 2009
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