Adrenal adenomatoid tumor.: A rare clinicopathological entity

被引:0
作者
Schadde, E
Meissner, M
Kroetz, M
Pickardt, C
Löhrs, U
Trupka, A
机构
[1] Tufts Univ New England Med Ctr, Dept Surg, Boston, MA 02111 USA
[2] Univ Munich, Klinikum Innenstadt, Chirurg Klin & Poliklin, D-80539 Munich, Germany
[3] Univ Munich, Inst Pathol, D-80539 Munich, Germany
[4] Univ Munich, Klinikum Innenstadt, Inst Radiol Diagnost, D-80539 Munich, Germany
[5] Univ Munich, Klinikum Innenstadt, Med Klin, D-80539 Munich, Germany
来源
CHIRURG | 2003年 / 74卷 / 03期
关键词
adenomatoid tumor; extragenital adenomatoid tumor; adrenal gland; mesothelial neoplasm;
D O I
10.1007/s00104-002-0611-5
中图分类号
R61 [外科手术学];
学科分类号
摘要
Adenomatoid tumors are uncommon, benign tumors of the genital tract which have also been reported to occur extragenitally. Case reports on adenomatoid tumors of the adrenal gland exist. Most of these are incidentally discovered at autopsy or after the resection of incidentalomas. We report on the case of a young man with epigastic pain and with the finding of a 4 cm heterogenous right adrenal mass on abdominal CT scan. After endocrine activity had been ruled out, an inactive, benign adrenal tumor was suspected and laparoscopic right adrenalectomy performed. The specimen was found to be an adenomatoid tumor. We discuss the differential diagnosis and the possible embryological origin of these tumors. The feature of 'local invasive ability' does not imply malignancy. All cases discovered surgically and at autopsy have been benign. Local resection seems to be the appropriate therapy.
引用
收藏
页码:248 / 252
页数:5
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