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一名儿童的原发性心脏黏液肉瘤

Primary cardiac myxosarcoma in a child.

作者信息

Mahar L J, Lie J T, Groover R V, Sweard J B, Puga F J, Feldt R H

出版信息

Mayo Clin Proc. 1979 Apr;54(4):261-6.

PMID:423607
Abstract

This is a detailed clinical and autopsy documentation of a rare entity--primary cardiac myxosarcoma in a 29-month-old girl. The patient had sudden onset of right hemiplegia and angiographic evidence of multiple occlusions of the left middle cerebral artery. Subsequent M-mode and sector echocardiography showed a mobile, pedunculated left atrial tumor, which was excised. No other tumor mass was noted at the time of surgical exploration, and postoperatively, the patient received a course of chemotherapy (vincristine, dactinomycin, and cyclophosphamide). After a temporary improvement in her condition, the patient died following several days of rapid deterioration; this was 3 months after the onset of symptoms. Autopsy showed that death was due to brainstem herniation secondary to massive infiltration of the brain by tumor, and there were also widespread systemic metastases.

摘要

这是一份关于一名29个月大女孩罕见疾病——原发性心脏黏液肉瘤的详细临床及尸检记录。患者突然出现右半身瘫痪,血管造影显示左大脑中动脉多处闭塞。随后的M型和扇形超声心动图显示左心房有一个可移动的带蒂肿瘤,该肿瘤被切除。手术探查时未发现其他肿瘤肿块,术后患者接受了一个疗程的化疗(长春新碱、放线菌素D和环磷酰胺)。患者病情暂时改善后,在症状出现3个月后,经过几天的快速恶化后死亡。尸检显示死亡原因是肿瘤大量浸润大脑继发脑干疝,并且还存在广泛的全身转移。

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