Giant cell myocarditis: an autoimmune disease?
Giant cell myocarditis: an autoimmune disease?
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巨细胞心肌炎:一种自身免疫性疾病?
DOI:
10.1016/0002-8703(88)90505-4
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发表时间:
1988
影响因子:
4.8
通讯作者:
J. Dupond
中科院分区:
文献类型:
--
作者:
P. Humbert;Rene Faryre;Dominique Fellman;Jean F Bassand;J. Dupond
Number 2 junction between the right atrium and the ventricle. The tumor had no stalk and completely obstructed the tricuspid valve, and invaded the ventricular septum and the pericardial surface. Most of the tumor was resected. Postoperatively, the patient received radiotherapy and chemotherapy. However, she became cachectic and died on June 7, 1985. Remnants of the tumor, with metastases to the pericardium, cerebrum, cerebellum, and both ovaries, were seen at autopsy.The most common variety of malignant cardiac tumors is angiosarcoma, which constitutes 7.3% to 13% of such tumors3p4 and is most commonly localized in the right atrium. A cardiac biopsy was performed in our patient because of th. e urgent need to confirm the diagnosis of right atria1 tumor and because cytologic examination of the pericardial effusion gave negative results. This biopsy yielded a histopathologic diagnosis of angiosarcoma of the right atrium. Results of ultrastructural study showed angiogenetic features in this tumor, as described by Yang et a1. 5 We have not been able to find previous reports on the diagnosis of cardiac tumors by cardiac biopsy. The prognosis of cardiac angiosarcoma is very poor. 6 If the diagnosis is made by biopsy early in the course of the disease, the most appropriate treatment can be selected and administered as soon as possible.