Epithelioid angiomyolipoma mimicking adrenal cortical carcinoma: A diagnostic pitfall

被引：5

作者：

Komarowska, Hanna ^{[1
]}

Bednarek-Rajewska, Katarzyna ^{[2
]}

Kanski, Marcin ^{[3
]}

Janicka-Jedyska, Malgorzata ^{[2
]}

Gut, Pawel ^{[1
]}

Ruchala, Marek ^{[1
]}

机构：

[1] Poznan Univ Med Sci, Dept Endocrinol Metab & Internal Med, PL-60355 Poznan, Poland

[2] Poznan Univ Med Sci, Dept Clin Pathomorphol, PL-60355 Poznan, Poland

[3] Poznan Univ Med Sci, Dept Geriatr Med & Gerontol, PL-60355 Poznan, Poland

来源：

ONCOLOGY LETTERS | 2015年 / 10卷 / 04期

关键词：

epithelioid angiomyolipoma; adrenal cortical carcinoma; histopathological diagnosis; ADRENOCORTICAL CARCINOMA; RENAL ANGIOMYOLIPOMA; MANAGEMENT; KIDNEY; CANCER;

D O I：

10.3892/ol.2015.3543

中图分类号：

R73 [肿瘤学];

学科分类号：

100214 ;

摘要：

Epithelioid angiomyolipoma (EAML) is a rare mesenchymal neoplasmic variant of angiomyolipoma characterized by aggressive growth and unpredictable outcome. Cases of local recurrence and distant metastasis have been described. The histopathological diagnosis may be difficult, as EAML often mimics other neoplasms. This is the case report of a 39-year-old male patient with EAML, which was initially diagnosed as adrenal cortical carcinoma, due to the lack of cooperation between clinicians and pathologists.

引用

页码：2130 / 2134

页数：5

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