Atrial myxoma occurring 15 years after subtotal resection of cerebellar hemangioblastoma - Case report

被引：2

作者：

Yanagawa, Youichi ^{[1
]}

Shimazaki, Hideyuki ^{[2
]}

Shima, Katsuji ^{[3
]}

Isoda, Susumu ^{[4
]}

Maehara, Tadaaki ^{[4
]}

机构：

[1] Natl Def Med Coll, Dept Traumatol & Crit Care Med, Tokorozawa, Saitama 3598513, Japan

[2] Natl Def Med Coll, Dept Lab Med, Tokorozawa, Saitama 3598513, Japan

[3] Natl Def Med Coll, Dept Neurosurg, Tokorozawa, Saitama 3598513, Japan

[4] Natl Def Med Coll, Div Surg 2, Tokorozawa, Saitama 3598513, Japan

来源：

NEUROLOGIA MEDICO-CHIRURGICA | 2008年 / 48卷 / 01期

关键词：

von Hippel-Lindau disease; hemangioblastoma; atrial myxoma;

D O I：

10.2176/nmc.48.37

中图分类号：

R74 [神经病学与精神病学];

学科分类号：

摘要：

A 51-year-old female, with a past medical history of resection of cerebellar hemangioblastoma, presented with an atrial tumor detected by sonography after undergoing a series of examinations for fever of unknown origin and subsequent symptoms of heart failure. After removing the atrial tumor, the histological findings demonstrated myxoma. Immunohistopathological study showed that the tumor cells in both the hemangioblastorna and the myxoma had strong cytoplasmic immunoreactivity for vascular endothelial growth factor. Hemangioblastoma associated with myxoma is extremely rare, and was probably a random occurrence in this case.

引用

页码：37 / 39

页数：3

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