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肝外胆管树巨细胞瘤:4例临床病理研究并与伴有破骨细胞样巨细胞的间变性梭形细胞和巨细胞癌相比较

Giant cell tumor of the extrahepatic biliary tree: a clinicopathologic study of 4 cases and comparison with anaplastic spindle and giant cell carcinoma with osteoclast-like giant cells.

作者信息

Albores-Saavedra Jorge, Grider Douglas J, Wu Jianhua, Henson Donald E, Goodman Zachary D

机构信息

Department of Pathology, Louisiana State University Health Sciences Center, Shreveport, LA, USA.

出版信息

Am J Surg Pathol. 2006 Apr;30(4):495-500. doi: 10.1097/00000478-200604000-00010.

Abstract

We report four previously undescribed primary giant cell tumors of the extrahepatic biliary tree and morphologically compare them with 10 anaplastic spindle and giant cell carcinomas with osteoclast-like giant cells of the gallbladder. Two giant cell tumors were located in the distal common bile duct; one in the cystic duct and one in the gallbladder. The 3 patients with bile duct tumors were male, and the only patient with a gallbladder tumor was a female. The age of the patients ranged from 45 to 60 years with an average of 55 years. The patients with bile duct tumors presented with biliary obstruction, and the patient with a gallbladder tumor presented with symptoms of cholelithiasis and a gallbladder mass. Histologically, the tumors were similar to giant cell tumors of bone. They consisted of a mixture of mononuclear and multinucleated osteoclast-like giant cells. The mononuclear cells showed no atypical features, and their nuclei were similar to those of the multinucleated giant cells. CD163 immunoreactivity was restricted to the mononuclear cells, whereas CD68 and HAM 56 labeled only the multinucleated osteoclast-like giant cells. The mononuclear cells were EMA-positive but did not express cytokeratins. Follow-up showed that 3 patients were alive and disease-free 3.7 to 7 years after surgery. The anaplastic spindle and giant cell carcinomas contained a fewer number of osteoclast-like giant cells, and their mononuclear cells showed considerable variation in size and shape, marked cytologic atypia, and numerous mitotic figures. They were focally cytokeratin positive (AE1/AE3; CAM 5.2) and did not label with CD163, CD68, and HAM 56. The benign osteoclast-like giant cells showed immunoreactivity for CD68 and HAM 56 but were negative for CD163 and cytokeratins. Giant cell tumors of the extrahepatic biliary tree are benign true histiocytic neoplasms that should be distinguished from the highly lethal anaplastic spindle and giant cell carcinomas with osteoclast-like giant cells by detailed cytologic analysis and immunohistochemical stains for CD163, CD68, HAM 56, and cytokeratins.

摘要

我们报告了4例先前未描述过的肝外胆管原发性巨细胞瘤,并在形态学上将它们与10例胆囊间变性梭形和巨细胞癌(伴有破骨细胞样巨细胞)进行比较。2例巨细胞瘤位于胆总管远端;1例位于胆囊管,1例位于胆囊。3例胆管肿瘤患者为男性,唯一1例胆囊肿瘤患者为女性。患者年龄在45至60岁之间,平均55岁。胆管肿瘤患者表现为胆管梗阻,胆囊肿瘤患者表现为胆石症症状和胆囊肿块。组织学上,肿瘤类似于骨巨细胞瘤。它们由单核和多核破骨细胞样巨细胞混合组成。单核细胞无非典型特征,其细胞核与多核巨细胞的细胞核相似。CD163免疫反应性仅限于单核细胞,而CD68和HAM 56仅标记多核破骨细胞样巨细胞。单核细胞EMA阳性,但不表达细胞角蛋白。随访显示,3例患者术后3.7至7年存活且无疾病。间变性梭形和巨细胞癌含有较少数量的破骨细胞样巨细胞,其单核细胞在大小和形状上有相当大的差异,有明显的细胞学异型性和大量有丝分裂象。它们局灶性细胞角蛋白阳性(AE1/AE3;CAM 5.2),不被CD163、CD68和HAM 56标记。良性破骨细胞样巨细胞对CD68和HAM 56有免疫反应性,但对CD163和细胞角蛋白呈阴性。肝外胆管巨细胞瘤是良性真性组织细胞肿瘤,应通过详细的细胞学分析以及CD163、CD68、HAM 56和细胞角蛋白的免疫组化染色与具有破骨细胞样巨细胞的高度致死性间变性梭形和巨细胞癌相鉴别。

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