Kaplinsky C, Toren A, Neumann Y, Mandel M, Kenet G, Sharon N, Rechavi G, Biniaminov M, Rubanov V, Rosenthal E, Rosner E, Mark Z, Amariglio N, Brok-Simoni F
Department of Pediatric Hemato-Oncology, Chaim Sheba Medical Center, Tel-Hashomer, Israel.
Med Pediatr Oncol. 1997 Feb;28(2):132-5. doi: 10.1002/(sici)1096-911x(199702)28:2<132::aid-mpo7>3.0.co;2-l.
Central nervous system (CNS) involvement in Ki-1/CD30 lymphoma is extremely rare, in contrast to the frequent involvement in other types of pediatric non-Hodgkin's lymphoma. No mechanism has yet been proposed to explain the sparing of the blood brain barrier in Ki-1/lymphoma. We present a 2-year-old boy who was admitted to the Department of Pediatric Hemato-Oncology due to lethargy, progressive breathing difficulties, massive diffuse lymphadenopathy, hepatosplenomegaly, and ichthyosis-like skin involvement with epidermolysis. A lymph node biopsy was compatible with Ki-1/CD30 anaplastic large cell lymphoma (ALCL). Bone marrow aspirate and biopsy demonstrated reactive hyperplasia. Cytogenetic analysis displayed hyperdiploid cells with 1p(-) in most cells. Cerebrospinal fluid examination showed pleocytosis with CD30+ cells. Possible mechanisms which could enable CNS involvement in this unusual case are discussed.
与其他类型的儿童非霍奇金淋巴瘤常累及中枢神经系统(CNS)不同,Ki-1/CD30淋巴瘤累及CNS极为罕见。目前尚未提出任何机制来解释Ki-1/淋巴瘤为何未累及血脑屏障。我们报告一名2岁男孩,因嗜睡、进行性呼吸困难、大量弥漫性淋巴结肿大、肝脾肿大以及类似鱼鳞病样皮肤受累伴表皮松解而入住儿科血液肿瘤学部门。淋巴结活检结果符合Ki-1/CD30间变性大细胞淋巴瘤(ALCL)。骨髓穿刺和活检显示为反应性增生。细胞遗传学分析显示大多数细胞为超二倍体细胞且伴有1p(-)。脑脊液检查显示细胞增多且存在CD30+细胞。本文讨论了在这一罕见病例中可能导致CNS受累的机制。