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Adrenergic Myocarditis in Pheochromocytoma

机译:嗜铬细胞瘤中的肾上腺能心肌炎

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摘要

The clinical presentation of pheochromocytoma is variable and many biochemical and imaging methods have been suggested to improve the diagnostic accuracy of what has been termed "the great masquerader". This case-report is of a middle-aged woman with a non-specific clinical presentation suggesting acute coronary syndrome or subacute myocarditis. Cardiovascular magnetic resonance (CMR) at presentation showed myocardial edema and intramyocardial late gadolinium enhancement (LGE). An adrenal mass was seen, which was confirmed as pheochromocytoma and surgically removed. Our case shows evidence for acute adrenergic myocarditis, with resolution of both the edema and the LGE after surgical excision.
机译:嗜铬细胞瘤的临床表现是可变的,并且已经提出了许多生化和成像方法来提高所谓的“伟大的伪装者”的诊断准确性。该病例报告是一名中年妇女,具有非特异性临床表现,提示急性冠状动脉综合征或亚急性心肌炎。出席会议时的心血管磁共振(CMR)表现为心肌水肿和心肌内晚期late增强(LGE)。可见肾上腺肿块,证实为嗜铬细胞瘤并手术切除。我们的病例显示了急性肾上腺能动性心肌炎的证据,手术切除后水肿和LGE均得到缓解。

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