Institute of Pathology, Medical Faculty Mannheim, University of Heidelberg, Theodor-Kutzer-Ufer 1-3, 68167 Mannheim, Germany.
Diagn Pathol. 2012 Apr 12;7:38. doi: 10.1186/1746-1596-7-38.
Primary involvement of skeletal muscle is a very rare event in ALK-1 positive anaplastic large cell lymphoma (ALCL). We describe a case of a 10-year old boy presenting with a three week history of pain and a palpable firm swelling at the dorsal aspect of the left thigh. Histological examination of the lesion revealed a tumoral and diffuse polymorphic infiltration of the muscle by large lymphoid cells. Tumor cells displayed eccentric, lobulated "horse shoe" or "kidney-shape" nuclei. The cells showed immunohistochemical positivity for CD30, ALK-1, CD2, CD3, CD7, CD8, and Perforin. Fluorescence in situ hybridization analysis revealed a characteristic rearrangement of the ALK-1 gene in 2p23 leading to the diagnosis of ALK-1 positive ALCL. Chemotherapy according to the ALCL-99-NHL-BFM protocol was initiated and resulted in a complete remission after two cycles. This case illustrates the unusual presentation of a pediatric ALCL in soft tissue with a good response to chemotherapy.
ALK-1 阳性间变性大细胞淋巴瘤(ALCL)中骨骼肌肉的原发性受累非常罕见。我们描述了一例 10 岁男孩的病例,他因左大腿背部疼痛和可触及的坚实肿胀而就诊,病史为 3 周。病变的组织学检查显示肿瘤和弥漫性多形性浸润肌肉的大淋巴细胞。肿瘤细胞显示偏心、分叶的“马蹄铁”或“肾形”核。细胞对 CD30、ALK-1、CD2、CD3、CD7、CD8 和穿孔素表现出免疫组织化学阳性。荧光原位杂交分析显示 2p23 中 ALK-1 基因的特征重排,导致诊断为 ALK-1 阳性 ALCL。根据 ALCL-99-NHL-BFM 方案开始化疗,两个周期后完全缓解。该病例说明了儿科 ALCL 在软组织中罕见的表现,对化疗有良好的反应。