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Bcl-2和PTHLH免疫组织化学在临床病理背景下诊断外周型软骨肉瘤中的应用。

The use of Bcl-2 and PTHLH immunohistochemistry in the diagnosis of peripheral chondrosarcoma in a clinicopathological setting.

作者信息

Hameetman Liesbeth, Kok Petra, Eilers Paul H C, Cleton-Jansen Anne-Marie, Hogendoorn Pancras C W, Bovée Judith V M G

机构信息

Department of Pathology, Leiden University Medical Centre, L1-Q, PO Box 9600, 2300 RC, Leiden, The Netherlands.

出版信息

Virchows Arch. 2005 Apr;446(4):430-7. doi: 10.1007/s00428-005-1208-4. Epub 2005 Mar 3.

DOI:10.1007/s00428-005-1208-4
PMID:15744499
Abstract

Distinguishing osteochondroma from low-grade secondary peripheral chondrosarcoma can be difficult. In osteochondroma, growth-signalling pathways are thought to be downregulated through exostosin (EXT) inactivation. A previous pilot study focusing on expression of putative EXT downstream effectors indicated that progression of osteochondroma towards grade I chondrosarcoma was characterised by upregulation of Bcl-2 and parathyroid hormone-like hormone (PTHLH). We investigated their use as diagnostic markers in a large nationwide series of 71 osteochondromas and 34 chondrosarcomas. Bcl-2 immunohistochemistry proved to be a valuable diagnostic tool: scoring negative in 95% (specificity) of the osteochondromas and positive in 57% (sensitivity) of the chondrosarcomas, reaching a positive predictive value of 84% and negative predictive value of 82%. Positivity was not related to age, hereditary status, gender or thickness of the cartilage cap. Presence of internal controls and verification using mRNA in situ hybridisation strengthened the reliability of the immunohistochemical staining. PTHLH showed more variable staining, being positive in osteochondromas from females or adolescent males, suggesting age- and gender-dependent expression. Thus, in cases where the distinction between osteochondroma and chondrosarcoma is difficult, Bcl-2 is a valuable diagnostic marker for malignancy, regardless of tumour size, patient gender or age, and this can be extended with PTHLH for non-adolescent male patients.

摘要

区分骨软骨瘤和低级别继发性外周软骨肉瘤可能具有挑战性。在骨软骨瘤中,生长信号通路被认为通过外生骨疣蛋白(EXT)失活而受到下调。一项先前聚焦于假定的EXT下游效应分子表达的初步研究表明,骨软骨瘤向I级软骨肉瘤进展的特征是Bcl-2和甲状旁腺激素样激素(PTHLH)上调。我们在一项涵盖全国范围的大型研究中,对71例骨软骨瘤和34例软骨肉瘤进行研究,以探究它们作为诊断标志物的效用。Bcl-2免疫组化被证明是一种有价值的诊断工具:在95%(特异性)的骨软骨瘤中呈阴性,在57%(敏感性)的软骨肉瘤中呈阳性,阳性预测值达84%,阴性预测值达82%。阳性与年龄、遗传状态、性别或软骨帽厚度无关。内部对照的存在以及使用mRNA原位杂交进行验证增强了免疫组化染色的可靠性。PTHLH染色变化更大,在女性或青春期男性的骨软骨瘤中呈阳性,提示其表达存在年龄和性别依赖性。因此,在难以区分骨软骨瘤和软骨肉瘤的病例中,无论肿瘤大小、患者性别或年龄,Bcl-2都是恶性肿瘤的一种有价值的诊断标志物,对于非青春期男性患者,可结合PTHLH进行诊断。

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Parathyroid hormone-related Peptide expression in cartilaginous tumors.甲状旁腺激素相关肽在软骨肿瘤中的表达
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