Primary Cutaneous Large B Cell Lymphoma, Leg Type: Good Evolution of A Particular Location

Lahlou A, E. S, B. H, Mernissi Fz
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Abstract

Primary cutaneous B-cell lymphomas are a heterogeneous group of rare clonal B-cell lymphoproliferative disorders with distinct clinicopathological features compared with nodal counterparts [1]. Primary cutaneous diffuse large B-cell lymphoma-leg type (PCLBCL-LT) is a rare subtype which constitutes only 4% [2]. They have a predilection to the leg (72%), advanced age of onset (mean age, 76 years), high Bcl-2 expression (85%) and frequent relapses with extracutaneous dissemination [10-20%]. We report a case we report the case of a young patient of 39 years old who consulted for a hummocky tumor in the back whose histology was in favor of lymphoma B-type leg, with good response to rituximab combined with doxorubicin, cyclophosphamide, vincristine, and prednison (R-CHOP).
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原发性皮肤大B细胞淋巴瘤,腿部型:特定部位的良好进化
原发性皮肤b细胞淋巴瘤是一种异质性的罕见克隆性b细胞淋巴增生性疾病,与淋巴结性b细胞淋巴瘤相比,具有不同的临床病理特征[1]。原发性皮肤弥漫性大b细胞淋巴瘤腿部型(PCLBCL-LT)是一种罕见的亚型,仅占4%[2]。他们倾向于腿部(72%),发病年龄较晚(平均年龄76岁),Bcl-2高表达(85%),经常复发并皮外传播[10-20%]。我们报告一例39岁的年轻患者,因背部隆起性肿瘤就诊,其组织学倾向于b型腿部淋巴瘤,利妥昔单抗联合阿霉素、环磷酰胺、长春新碱和prednison (R-CHOP)疗效良好。
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