Molberg K H, Heffess C, Delgado R, Albores-Saavedra J
Department of Pathology, University of Texas Southwestern Medical Center, Dallas 75235-9072, USA.
Cancer. 1998 Apr 1;82(7):1279-87. doi: 10.1002/(sici)1097-0142(19980401)82:7<1279::aid-cncr10>3.0.co;2-3.
Undifferentiated carcinomas with osteoclast-like giant cells are rare pancreatic and periampulary neoplasms that morphologically mimic giant cell tumor of bone. Despite numerous publications based primarily on single case reports, the terminology, histogenesis, and biologic behavior of these tumors remain controversial.
The authors studied one periampullary and nine pancreatic neoplasms of this type. Immunohistochemistry was performed on nine of the cases and clinical follow-up data was obtained in eight.
The neoplasms were large (average 9 cm), partially or completely multicystic, and hemorrhagic. Histologically, they were composed predominantly of ovoid or spindle-shaped bland mononuclear cells and evenly spaced osteoclast-like giant cells. However, three neoplasms had foci in which the nuclear pleomorphism of the mononuclear cells approached that observed in anaplastic spindle and giant cell carcinomas. Other histologic features included phagocytosis of the mononuclear cells by the osteoclast-like giant cells (in 7 of 10 cases), osteoid or bone formation (in 3 of 10 cases), and chondroid differentiation (in 1 of 10 cases). Four neoplasms had foci of conventional adenocarcinoma and two arose in preexisting mucinous cystic neoplasms of the pancreas. The mononuclear cells were positive for epithelial markers in six of nine tumors tested (cytokeratins AE-1, AE-3, Cam 5.2, and/or epithelial membrane antigen). They were negative for the histiocytic markers (CD-68, lysozyme) in all nine cases tested. In contrast, the osteoclast-like giant cells were positive for CD-68 in all nine cases, positive for lysozyme in four cases, and negative for cytokeratins (AE-1, AE-3, and Cam 5.2) in all nine cases. p53 stained the mononuclear tumor cells in three cases and MIB-1 stained the mononuclear tumor cells in four cases, but the osteoclast-like giant cells did not stain with either antibody in all nine cases tested. Most of the patients died of disease within 1 year of diagnosis; only 1 patient was alive and disease free 14 years after surgical excision.
The association of these tumors with conventional adenocarcinoma or mucinous cystic neoplasms, the histologic features, and the immunohistochemical profile supports an epithelial phenotype for the mononuclear cells and a reactive histiocytic lineage for the nonneoplastic osteoclast-like giant cells. These neoplasms, which are better classified as undifferentiated carcinomas, follow an aggressive clinical course; most patients die of disease within 1 year.
伴有破骨细胞样巨细胞的未分化癌是罕见的胰腺和壶腹周围肿瘤,在形态学上类似于骨巨细胞瘤。尽管有大量主要基于单病例报告的文献,但这些肿瘤的术语、组织发生和生物学行为仍存在争议。
作者研究了1例壶腹周围和9例胰腺的此类肿瘤。对其中9例进行了免疫组织化学检查,并获得了8例的临床随访数据。
肿瘤体积较大(平均9厘米),部分或完全呈多囊性,伴有出血。组织学上,它们主要由卵圆形或梭形的温和单核细胞和间隔均匀的破骨细胞样巨细胞组成。然而,3例肿瘤存在单核细胞核异型性接近间变性梭形和巨细胞癌所见的区域。其他组织学特征包括破骨细胞样巨细胞对单核细胞的吞噬作用(10例中的7例)、类骨质或骨形成(10例中的3例)以及软骨样分化(10例中的1例)。4例肿瘤存在传统腺癌灶,2例起源于胰腺先前存在的黏液性囊性肿瘤。在检测的9例肿瘤中,6例的单核细胞上皮标志物呈阳性(细胞角蛋白AE-1、AE-3、Cam 5.2和/或上皮膜抗原)。在检测的所有9例中,它们的组织细胞标志物(CD-68、溶菌酶)均为阴性。相比之下,9例中的破骨细胞样巨细胞CD-68均为阳性,4例溶菌酶阳性,9例中的细胞角蛋白(AE-1、AE-3和Cam 5.2)均为阴性。3例中p53染色单核肿瘤细胞,4例中MIB-1染色单核肿瘤细胞,但在检测的所有9例中,破骨细胞样巨细胞均未被这两种抗体染色。大多数患者在诊断后1年内死于疾病;仅1例患者在手术切除14年后存活且无疾病。
这些肿瘤与传统腺癌或黏液性囊性肿瘤的关联、组织学特征以及免疫组化谱支持单核细胞的上皮表型和非肿瘤性破骨细胞样巨细胞的反应性组织细胞谱系。这些肿瘤更好地归类为未分化癌,临床病程侵袭性强;大多数患者在1年内死于疾病。