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心脏嗜铬细胞瘤:经铟-111奥曲肽扫描诊断后行切除术。

Cardiac pheochromocytoma: resection after diagnosis by 111-indium octreotide scan.

作者信息

Lin J C, Palafox B A, Jackson H A, Cohen A J, Gazzaniga A B

机构信息

Department of Surgery, Children's Hospital of Orange County, Orange, California, USA.

出版信息

Ann Thorac Surg. 1999 Feb;67(2):555-8. doi: 10.1016/s0003-4975(98)01291-0.

Abstract

Cardiac pheochromocytoma is an exceedingly rare and unusual clinical entity. Only 37 previous surgically treated adult patients were found in review of the surgical literature. We report the case of a 13-year-old boy who had a cardiac pheochromocytoma that was localized by the 111-indium diethylenetriamine pentaacetic acid octreotide scintigraphy scan and confirmed by magnetic resonance imaging after computed tomographic and B1-iodine-metaiodobenzylguanidine scans had failed. At operation, a 6-cm pheochromocytoma of the left atrium was found and successfully resected with reconstruction of the left atrium using autologous pericardium.

摘要

心脏嗜铬细胞瘤是一种极其罕见且特殊的临床病症。回顾外科文献发现,之前仅有37例接受手术治疗的成年患者。我们报告一例13岁男孩的病例,其心脏嗜铬细胞瘤通过铟-111二乙三胺五乙酸奥曲肽闪烁扫描定位,在计算机断层扫描和碘-131间碘苄胍扫描失败后,经磁共振成像得以确诊。手术中,发现左心房有一个6厘米的嗜铬细胞瘤,并成功切除,同时使用自体心包对左心房进行了重建。

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