Department of Hepatic and Gastrointestinal Pathology, Armed Forces Institute of Pathology, 6825 16th Street, N.W., Building 54, Washington, DC 20306-6000, USA.
Am J Surg Pathol. 2009 Jul;33(7):976-83. doi: 10.1097/PAS.0b013e31819c1ab3.
There is a rare primary liver tumor that has been reported as "ossifying stromal-epithelial tumor" (3 cases), "desmoplastic nested spindle cell tumor" (4 cases), and "nested stromal-epithelial tumor" (6 cases). Herein we report 9 cases of this tumor, including 3 previously reported, from the files of the Armed Forces Institute of Pathology. All tumors were discovered incidentally in patients between 2 and 33 years of age. Four had a history of calcified hepatic nodules since childhood (ages 4 to 10 y). One had Cushing syndrome that abated after excision. Eight patients had a partial hepatectomy and 1 underwent liver transplantation. The tumors ranged from 5.5 to 20 cm and had a characteristic histologic appearance with irregular, sharply circumscribed nests and islands of bland-appearing spindled to focally epithelioid cells, surrounded by a cellular desmoplastic stroma. The tumor nests had focal psammoma-like calcifications with or without ossification. Immunohistochemistry demonstrated at least focal positivity for keratin cocktail AE1/AE3/LP34 in all 9 cases, and Wilms tumor suppressor gene (7/7) with variable staining for other epithelial (except keratins 7 and 20), neural, and mesenchymal markers. None of the tumors was positive for Ewing sarcoma-primitive neuroectodermal tumors, desmoplastic small round cell tumor, and SYT-SSX fusion transcript. Follow-up revealed that 1 patient had 2 local recurrences successfully treated by radiofrequency ablation. The patient who underwent liver transplantation died of postoperative complications. Six patients were alive and well up to 22 years after surgery. We propose the name "calcifying nested stromal and epithelial tumor" for this rare but distinctive clinicopathologic entity of uncertain histogenesis. On the basis of currently available information, this tumor is best considered a low-grade malignancy.
有一种罕见的原发性肝肿瘤,曾被报道为“骨化性间质-上皮性肿瘤”(3 例)、“促结缔组织增生性巢状梭形细胞肿瘤”(4 例)和“巢状间质-上皮性肿瘤”(6 例)。在此,我们从武装部队病理研究所的档案中报告了 9 例这种肿瘤,其中包括 3 例以前报道过的病例。所有肿瘤均为偶然发现于 2 至 33 岁的患者。其中 4 例有自儿童时期(4 至 10 岁)以来钙化性肝结节的病史。1 例患有库欣综合征,切除后缓解。8 例患者行部分肝切除术,1 例患者行肝移植术。肿瘤大小为 5.5 至 20cm,具有特征性的组织学表现,可见不规则、界限分明的巢状和岛屿状的温和梭形至局灶性上皮样细胞,周围为细胞性促结缔组织增生性基质。肿瘤巢可有局灶性沙粒体样钙化,伴或不伴骨化。免疫组织化学染色显示,9 例肿瘤均至少局灶性表达角蛋白鸡尾酒 AE1/AE3/LP34(9/9),7/7 例肿瘤表达 Wilms 肿瘤抑制基因,其他上皮(角蛋白 7 和 20 除外)、神经和间叶标记物的染色呈可变阳性。所有肿瘤均不表达尤文肉瘤-原始神经外胚层肿瘤、促结缔组织增生性小圆细胞肿瘤和 SYT-SSX 融合转录本。随访显示,1 例患者的 2 处局部复发经射频消融治疗后成功治疗。行肝移植术的患者因术后并发症死亡。6 例患者在手术后 22 年的随访期间存活且状况良好。我们提出了“钙化性巢状间质和上皮性肿瘤”这一名称,用于这一罕见但具有独特临床病理特征的实体,其组织发生尚不确定。根据目前的信息,该肿瘤最好被认为是一种低度恶性肿瘤。