Primary malignant pericardial mesothelioma: a case report and review.
Primary malignant pericardial mesothelioma: a case report and review.
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原发性恶性心包间皮瘤：病例报告和回顾。
DOI：
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发表时间：
1994
期刊：
影响因子：
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通讯作者：
Kahn Dr
中科院分区：
文献类型：
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作者：
T. Kaul;Fields Bl;Kahn Dr
原发性恶性心包间皮瘤是一种罕见的肿瘤，病因不明。预后极差，因为一般迟发，无法完全根除它的手术和它的反应差，放疗或化疗。一个不寻常的情况下，心包间皮瘤提出的缩窄性心包炎的描述。本文对文献中报道的140例进行了全面的回顾，以帮助读者对这种罕见的病理性肿瘤的治疗和预后进行评估。
Primary malignant pericardial mesothelioma is a rare tumor of unknown etiology. The prognosis is extremely poor due to generally late presentation, inability to completely eradicate it surgically and its poor response to radiotherapy or chemotherapy. An unusual case of pericardial mesothelioma which presented as constrictive pericarditis is described. A comprehensive review of the 140 cases reported in the literature so far is presented to assist the readers in the management and prognosis of this rare, pathological tumor.