Meir Karen, Maly Alexander, Doviner Victoria, Gross Eitan, Weintraub Michael, Rabin Lionel, Pappo Orit
Department of Pathology, Hadassah-Hebrew University Medical Center, Jerusalem, Israel.
Pediatr Dev Pathol. 2009 May-Jun;12(3):233-6. doi: 10.2350/08-03-0437.1.
Nested stromal-epithelial tumor (NSET) of the liver is an extremely rare primary hepatic tumor with uncertain malignant potential. To date, only 11 cases have been described. We describe the case of a 2 1/2-year-old girl with an incidental liver mass. The mass was discovered on follow-up abdominal imaging for asymptomatic hydronephrosis diagnosed on antenatal ultrasound. Needle biopsy showed a mixed stromal and epithelial process in a nested pattern, with foci of ossification and no significant pleomorphism or necrosis. The nest cells stained with WT-1, cytokeratin 18, and CD56. Ossifying stromal epithelial tumor of the liver was strongly suspected. The findings were confirmed in the subsequent partial hepatectomy specimen. To our knowledge, this is the 12th case of NSET in the English-language literature and the 3rd case of NSET associated with genitourinary system abnormalities. Possible associations with dysregulated WT-1 expression are discussed.
肝脏巢状间质-上皮肿瘤(NSET)是一种极为罕见的原发性肝脏肿瘤,其恶性潜能尚不明确。迄今为止,仅报道过11例。我们报告了一名2岁半女童偶然发现肝脏肿块的病例。该肿块是在对产前超声诊断为无症状肾积水进行腹部影像学随访时发现的。针吸活检显示为巢状的混合性间质和上皮病变,有骨化灶,无明显多形性或坏死。巢状细胞WT-1、细胞角蛋白18和CD56染色阳性。强烈怀疑为肝脏骨化性间质上皮肿瘤。后续的部分肝切除标本证实了这些发现。据我们所知,这是英文文献中第12例NSET病例,也是第3例与泌尿生殖系统异常相关的NSET病例。文中讨论了与WT-1表达失调可能存在的关联。