Alatassi Houda, Sahoo Sunati
Division of Cytopathology, Department of Pathology, University of Louisville, Louisville, Kentucky 40202, USA.
Diagn Cytopathol. 2009 Mar;37(3):192-4. doi: 10.1002/dc.20979.
Angiomyolipoma (AML) is a uncommon benign neoplasm of the liver with cyto- and histologic features similar to the more commonly encountered renal AML. Tumors composed predominantly of epithelioid cells have been referred to as epithelioid AML. Because most liver lesions are first evaluated by fine-needle aspiration biopsy (FNAB), it is important to distinguish this variant of AML from more common hepatic neoplasms such as hepatocellular carcinoma (HCC) or metastatic tumors. Rare reports of epithelioid AML of the liver diagnosed by FNAB are in the literature. Here, we describe the cytologic findings of a unique case of epithelioid AML with numerous giant cells.
血管平滑肌脂肪瘤(AML)是一种罕见的肝脏良性肿瘤,其细胞和组织学特征与更常见的肾AML相似。主要由上皮样细胞组成的肿瘤被称为上皮样AML。由于大多数肝脏病变首先通过细针穿刺活检(FNAB)进行评估,因此将这种AML变体与更常见的肝脏肿瘤如肝细胞癌(HCC)或转移性肿瘤区分开来很重要。文献中有关于通过FNAB诊断肝脏上皮样AML的罕见报道。在此,我们描述了一例具有大量巨细胞的独特上皮样AML病例的细胞学发现。