Ginoux Emmanuelle, Julia Fanny, Balme Brigitte, Thomas Luc, Dalle Stéphane
Emmanuelle Ginoux, Fanny Julia, Luc Thomas, Stéphane Dalle, Department of Dermatology, Centre Hospitalier Lyon-Sud, Hospices Civils de Lyon, 69002 Lyon, France.
World J Clin Cases. 2015 Aug 16;3(8):727-31. doi: 10.12998/wjcc.v3.i8.727.
To study dermatological manifestation of T-lymphoblastic lymphoma and to help clinicians in the diagnosis, we report here the case of a 75-year-old patient who presented with violaceous nodules acquired during the last 4 wk and affecting the scalp and right arm. The diagnosis of systemic lymphoma was suggested upon the appearance of cutaneous tumors, palpable lymph nodes and general symptoms including asthenia and weight-loss. The pathology features: positive immunostaining for CD3 and terminal deoxynucleotidyl transferase (TdT) and staging, led us to the final diagnosis of T-lymphoblastic lymphoma (T-LBL) with cutaneous involvement. He received a CHOP regimen as first-line treatment. Unfortunately, the patient relapsed and died 8 mo after the treatment initiation. T-LBL may be diagnosed by skin lesions. Additional immunostaining including TdT and experienced histopathologists are needed to correctly classify this aggressive disease and discuss the correct management including bone-marrow transplantation where appropriate.
为研究T淋巴母细胞淋巴瘤的皮肤表现并协助临床医生进行诊断,我们在此报告一例75岁患者的病例,该患者在过去4周内出现了紫罗兰色结节,累及头皮和右臂。皮肤肿瘤、可触及的淋巴结以及包括乏力和体重减轻在内的全身症状出现后,提示了系统性淋巴瘤的诊断。病理特征、CD3和末端脱氧核苷酸转移酶(TdT)免疫染色阳性以及分期,使我们最终诊断为伴有皮肤受累的T淋巴母细胞淋巴瘤(T-LBL)。他接受了CHOP方案作为一线治疗。不幸的是,患者在治疗开始后8个月复发并死亡。T-LBL可通过皮肤病变进行诊断。需要包括TdT在内的额外免疫染色以及经验丰富的组织病理学家来正确分类这种侵袭性疾病,并讨论正确的治疗方法,包括在适当情况下进行骨髓移植。