Jundt G, Remberger K, Roessner A, Schulz A, Bohndorf K
German Cancer Research Center (DKFZ), Heidelberg, FRG.
Pathol Res Pract. 1995 Mar;191(2):112-20. doi: 10.1016/S0344-0338(11)80560-1.
The clinical and histological data of twenty-three cases of adamantinomas of the long bone collected by the Working Group on Bone Tumors at the DKFZ/FRG are reported including immunohistochemical observations in twenty-one of the cases. Females and males between 5 and 67 years (mean, 25.4 years) were affected equally (11/12). All adamantinomas were positive for cytokeratins often in coexpression with vimentin, at least focally. Although exhibiting varying histological patterns, no correlation between histology and clinical course was seen. However, sex and mode of initial therapy seem to influence an unfavorable clinical outcome. All three decreased patients were males receiving marginal or delayed surgery. This underlines the low-grade malignant character of adamantinoma. To assure the histological diagnosis pathologists should employ immunohistochemistry for demonstrating the sometimes sparse epithelial cell nests when radiology is suggestive for adamantinoma. Correct diagnosis should lead to resection with wide surgical margins.
德国癌症研究中心/联邦德国骨肿瘤工作组收集的23例长骨造釉细胞瘤的临床和组织学数据被报道,其中21例有免疫组化观察结果。年龄在5至67岁(平均25.4岁)的女性和男性受影响程度相同(11/12)。所有造釉细胞瘤的细胞角蛋白均呈阳性,且常与波形蛋白共表达,至少局灶性如此。尽管组织学模式各异,但未发现组织学与临床病程之间存在相关性。然而,性别和初始治疗方式似乎会影响不良的临床结果。所有三名病情恶化的患者均为男性,接受的是边缘性或延迟性手术。这突出了造釉细胞瘤的低度恶性特征。为确保组织学诊断,当放射学提示为造釉细胞瘤时,病理学家应采用免疫组化来显示有时稀疏的上皮细胞巢。正确的诊断应导致进行广泛手术切缘的切除。