Primary MALT Type Skin Lymphoma—Is ‘Wait and See’ a Possible Strategy?

F. Delli, T. Zaraboukas, I. Mandekou‐Lefaki
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引用次数: 3

Abstract

Primary cutaneous lymphomas are the second most common site of extranodal non-Hodgkin lymphoma. A specifically type named extranodal marginal zone B-cell lymphomas are indolent low-grade neoplasma. We report a case of a 42-year-old white man with multiple subcutaneous tumors located on the trunk and neck. The histopathological exam showed a non-epidermotropic, dense lymphocytic infiltrate. Histologic, immunohistochemical and cytologenetic analysis diagnosed primary cutaneous B-cell lymphoma MALT type. Investigation for other extranodal MALT lymphoma gastrointestinal tract, lung, salivary and thyroid glands was negative. The patient refused radiotherapy, but he accepted every 6 months close follow-up. Over a seven years period, we noticed a progressively disappearance of the skin lesions. The necessity of aggressive treatment of this disease with excellent prognosis is discussed. The treatment necessity of primary cutaneous B-cell lymphoma MALT type is discussed.
原发性MALT型皮肤淋巴瘤:“观望”是一种可能的策略吗?
原发性皮肤淋巴瘤是结外非霍奇金淋巴瘤的第二常见部位。结外边缘区b细胞淋巴瘤是一种惰性低级别肿瘤。我们报告一例42岁的白人男性与多个皮下肿瘤位于躯干和颈部。组织病理学检查显示非表皮性,密集的淋巴细胞浸润。组织学,免疫组织化学和细胞遗传学分析诊断原发性皮肤b细胞淋巴瘤MALT型。其他结外MALT淋巴瘤胃肠道、肺、唾液腺和甲状腺检查均为阴性。患者拒绝放疗,但接受每6个月的密切随访。在七年的时间里,我们注意到皮肤损伤逐渐消失。讨论了积极治疗这种预后良好的疾病的必要性。探讨原发性皮肤b细胞淋巴瘤MALT型治疗的必要性。
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