DIAGNOSTIC AND THERAPEUTIC PROBLEMS IN MULTICENTRIC RENAL ANGIOMYOLIPOMA

被引：44

作者：

TALLARIGO, C ^{[1
]}

BALDASSARRE, R ^{[1
]}

BIANCHI, G ^{[1
]}

COMUNALE, L ^{[1
]}

OLIVO, G ^{[1
]}

PEA, M ^{[1
]}

BONETTI, F ^{[1
]}

MARTIGNONI, G ^{[1
]}

ZAMBONI, G ^{[1
]}

MOBILIO, G ^{[1
]}

机构：

[1] OSPED CIVILE,DIV UROL,LEGNAGO,ITALY

来源：

JOURNAL OF UROLOGY | 1992年 / 148卷 / 06期

关键词：

ANGIOMA; SCLEROSING; LIPOMA; TUBEROUS SCLEROSIS; KIDNEY NEOPLASMS; IMMUNOHISTOCHEMISTRY;

D O I：

10.1016/S0022-5347(17)37057-X

中图分类号：

R5 [内科学]; R69 [泌尿科学（泌尿生殖系疾病）];

学科分类号：

1002 ; 100201 ;

摘要：

Multicentric renal angiomyolipoma is a rare form of benign tumor. However, its effective incidence as evaluated in autopsy studies may be as high as 8%. There are 2 main types of renal angiomyolipoma, that is isolated forms and those associated with other diseases, such as phakomatosis, polycystic kidneys and fibromuscular dysplasia. The tumor may also display malignant behavior with local invasiveness and regional lymph node involvement. However, the clinical course is benign and multicentricity is important for prognosis. Histopathological diagnosis often is difficult. Immunohistochemical analysis of surgical specimens using a panel of monoclonal antibodies, including HMB-45 and actin, enabled us to make a definitive diagnosis in 3 cases of multicentric renal angiomyolipoma.

引用

页码：1880 / 1884

页数：5

共 33 条

[1] TUBEROUS SCLEROSIS WITH ANGIOMYOLIPOMA AND METASTASIZED HYPERNEPHROMA [J].