Mediastinal Teratoma with Neuroendocrine Features in 34-Year-Old Male with Syncope

被引：1

作者：

Andrawes, Peter A. ^{[1
]}

Shariff, Masood A. ^{[2
]}

Chang, Qing ^{[3
]}

Kong, Fanyi ^{[3
]}

Rosell, Frank M. ^{[2
]}

机构：

[1] Staten Isl Univ Hosp, Dept Surg, Northwell Hlth Syst, 475 Seaview Ave, Staten Isl, NY 10305 USA

[2] Staten Isl Univ Hosp, Northwell Hlth Syst, Dept Cardiothorac Surg, Staten Isl, NY 10305 USA

[3] Staten Isl Univ Hosp, Northwell Hlth Syst, Dept Pathol, Staten Isl, NY 10305 USA

来源：

CASE REPORTS IN SURGERY | 2015年 / 2015卷

关键词：

D O I：

10.1155/2015/153959

中图分类号：

R61 [外科手术学];

学科分类号：

摘要：

Neuroendocrine tumors that arise in an extragonadal teratoma are extremely rare. Somatic-type malignancy, defined as any sarcoma, carcinoma, leukemia, or lymphoma developing in a germ cell tumor, occurs in approximately 2% of all germ cell tumors. Our case represents a mediastinal mass that was incidentally found in a patient with syncope. Surgical resection confirmed mature teratoma with neuroendocrine features.

引用

页数：5

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