Martí R M, Campo E, Bosch F, Palou J, Estrach T
Department of Dermatology, Hospital Clínic i Provincial de Barcelona, Barcelona, Spain.
J Cutan Pathol. 2001 May;28(5):256-64. doi: 10.1034/j.1600-0560.2001.028005256.x.
Cutaneous lymphocyte-associated antigen (CLA) is a lymphocyte homing receptor selectively expressed by T cells of the cutaneous immune system and their malignant counterpart, that is to say, cutaneous T-cell lymphomas. However it is absent in the vast mayority of other T-cell malignancies and B-cell lineage lymphomas irrespective on primary tumor site.
Expression of CLA was investigated on six cases of mantle cell lymphoma (MCL) which differed in their histopathological subtype (typical or blastic) and their tendency to infiltrate skin and/or central nervous system (CNS).
CLA immunostaining on neoplastic cells was only observed in a 61-year-old female suffering from a lymphoblastoid MCL which clinically presented with specific skin lesions and further developped CNS disease. In this patient, coexpression of CLA with MCL markers (CD20 and CD5) was confirmed by conventional immunohistochemistry and double immunofluorescence studies.
To our knowledge, CLA immunoreactivity on B-cell lymphomas has not beeen previously reported. The expression of this skin-related adhesion molecule on malignant MCL cells could explain the clinical behavior of our case which presented and relapsed with cutaneous lesions. However, CLA seems not to be a MCL marker nor a CNS-related adhesion molecule. The authors review the clinical and histopathological characteristics of MCL-specific skin lesions and their diagnostic clues based on cell morphology, immunohistochemistry and molecular investigations.
皮肤淋巴细胞相关抗原(CLA)是一种淋巴细胞归巢受体,由皮肤免疫系统的T细胞及其恶性对应物(即皮肤T细胞淋巴瘤)选择性表达。然而,无论原发性肿瘤部位如何,绝大多数其他T细胞恶性肿瘤和B细胞系淋巴瘤中均不存在CLA。
研究了6例套细胞淋巴瘤(MCL)中CLA的表达情况,这些病例在组织病理学亚型(典型或母细胞样)以及浸润皮肤和/或中枢神经系统(CNS)的倾向方面存在差异。
仅在一名61岁患有淋巴母细胞样MCL的女性患者的肿瘤细胞中观察到CLA免疫染色,该患者临床上出现特异性皮肤病变并进一步发展为CNS疾病。在该患者中,通过传统免疫组织化学和双重免疫荧光研究证实了CLA与MCL标志物(CD20和CD5)的共表达。
据我们所知,先前尚未报道过B细胞淋巴瘤上的CLA免疫反应性。这种与皮肤相关的黏附分子在恶性MCL细胞上的表达可以解释我们病例出现皮肤病变并复发的临床行为。然而,CLA似乎既不是MCL标志物,也不是与CNS相关的黏附分子。作者基于细胞形态学、免疫组织化学和分子研究,回顾了MCL特异性皮肤病变的临床和组织病理学特征及其诊断线索。