Fan Peiyuan, Nong Lin, Sun Jingru, Liu Xiaoqing, Kadin Marshall E, Li Ting, Tu Ping, Wang Yang
Department of Dermatology and Venerology, Peking University First Hospital, Beijing, China.
Department of Pathology, Peking University First Hospital, Beijing, China.
J Cutan Pathol. 2017 Jul;44(7):616-619. doi: 10.1111/cup.12933. Epub 2017 May 5.
Chronic lymphedema predisposes to develop malignant cutaneous tumors, including angiosarcoma, Kaposi's sarcoma and B-cell lymphoma. T-cell malignancy has rarely been associated with chronic lymph stasis. Here, we report a case of primary cutaneous anaplastic large cell lymphoma (pcALCL) with lymphatic spread associated with chronic lymphedema. The patient is a 56-year-old man who received orchiectomy and right inguinal lymphadenectomy for malignant seminoma 10 years ago, which led to prominent lymphedema of the right leg. He developed extensive skin nodules on the lymphedematous area for 3 months. Histopathology findings confirmed a diagnosis of pcALCL, which is a subtype of cutaneous T-cell lymphoma characterized by the presence of CD30+ T cells. Intralymphatic infiltration of malignant cells is prominent. The pathogenesis of intralymphatic cutaneous anaplastic large cell lymphoma is largely unknown. Our case suggests that chronic lymphedema resulted in persistent CD4+ T-cell inflammation, which then may contribute to the development of pcALCL.
慢性淋巴水肿易引发恶性皮肤肿瘤,包括血管肉瘤、卡波西肉瘤和B细胞淋巴瘤。T细胞恶性肿瘤很少与慢性淋巴淤滞相关。在此,我们报告一例伴有淋巴扩散的原发性皮肤间变性大细胞淋巴瘤(pcALCL)病例,该病例与慢性淋巴水肿有关。患者为一名56岁男性,10年前因恶性精原细胞瘤接受了睾丸切除术和右腹股沟淋巴结切除术,导致右腿出现明显的淋巴水肿。他在淋巴水肿区域出现广泛的皮肤结节3个月。组织病理学检查结果确诊为pcALCL,这是皮肤T细胞淋巴瘤的一种亚型,其特征为存在CD30+ T细胞。恶性细胞的淋巴管内浸润明显。淋巴管内皮肤间变性大细胞淋巴瘤的发病机制在很大程度上尚不清楚。我们的病例表明,慢性淋巴水肿导致持续性CD4+ T细胞炎症,进而可能促使pcALCL的发生。