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皮肤T细胞淋巴瘤的骨骼表现

Skeletal manifestations in cutaneous T-cell lymphomas.

作者信息

Brigham B A, Bunn P A, Horton J E, Schechter G P, Wahl L M, Bradley E C, Dunnick N R, Matthews M J

出版信息

Arch Dermatol. 1982 Jul;118(7):461-7.

PMID:6979976
Abstract

The clinical course of three patients with cutaneous T-cell lymphoma (CTCL) in whom skeletal disease developed is presented and the literature on skeletal involvement in these disorders is reviewed. Three separate types of skeletal manifestations occurred: (1) osteolytic lesions, (2) osteoblastic lesions, and (3) diffuse osteoporosis. Hypercalcemia was present in two cases. Tumor cells from two patients in short-term culture secreted osteoclast-activating factor(s). Both of these patients had pathologic evidence of osteoclast activation in bone sections. Thus, the tumor cells in certain patients with CTCL may derive from a monoclonal proliferation of a T-cell subset capable of producing humoral bone-resorbing factor(s) similar to those demonstrated in cultures of mitogen- and antigen-activated normal lymphocytes. Since skeletal lesions are unusual, it would follow that other T-cell subsets account for pathologic cell proliferation in most patients with CTCL.

摘要

本文报告了3例皮肤T细胞淋巴瘤(CTCL)患者出现骨骼病变的临床病程,并对这些疾病中骨骼受累的文献进行了综述。出现了三种不同类型的骨骼表现:(1)溶骨性病变,(2)成骨性病变,(3)弥漫性骨质疏松。2例患者出现高钙血症。2例患者的肿瘤细胞在短期培养中分泌破骨细胞激活因子。这2例患者在骨切片中均有破骨细胞激活的病理证据。因此,某些CTCL患者的肿瘤细胞可能来源于能够产生与丝裂原和抗原激活的正常淋巴细胞培养物中所显示的类似体液性骨吸收因子的T细胞亚群的单克隆增殖。由于骨骼病变并不常见,因此可以推断,在大多数CTCL患者中,其他T细胞亚群是病理性细胞增殖的原因。

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