Rossbach Hans-Christoph, Chamizo Wilfredo, Dumont Doris P, Barbosa Jerry L, Sutcliffe Maxine J
Divisions of Pediatric Hematology/Oncology, All Children's Hospital, University of South Florida, St. Petersburg, USA.
J Pediatr Hematol Oncol. 2002 Feb;24(2):154-7. doi: 10.1097/00043426-200202000-00020.
The authors report a child younger than age 15 years with a rare hepatosplenic gamma/delta T-cell lymphoma, which is highly aggressive and primarily seen in young men. A 9-year-old girl presented with thrombocytopenia and hepatosplenomegaly. Bone marrow analysis revealed a metastatic pleomorphic lymphoma of peripheral T-cell phenotype, with rearrangement of the T-cell receptor gamma/delta and expression of CD3 and CD16/56. Instead of the previously reported primary, nonrandom, chromosomal abnormalities, isochromosome 7q and trisomy 8, this patient had four copies each of chromosome 7q, including isochromosome 7[i(7)(q10)] and der(21)t(7;21), as well as chromosome 8. This entity needs to be considered in women and children with lymphoma. Conventional therapy appears to be inadequate for cure.
作者报告了一名15岁以下患有罕见肝脾γ/δ T细胞淋巴瘤的儿童,该肿瘤具有高度侵袭性,主要见于年轻男性。一名9岁女孩出现血小板减少和肝脾肿大。骨髓分析显示为外周T细胞表型的转移性多形性淋巴瘤,伴有T细胞受体γ/δ重排以及CD3和CD16/56表达。该患者并非如先前报道的那样存在原发性、非随机的染色体异常,即7号染色体等臂和8号染色体三体,而是每条7号染色体有四个拷贝,包括7号染色体等臂[i(7)(q10)]和der(21)t(7;21),以及8号染色体。对于患有淋巴瘤的女性和儿童,需要考虑这种疾病。传统治疗似乎不足以治愈。