Tasso M, Esquembre C, Blanco E, Moscardó C, Niveiro M, Payá A
Division of Pediatric Oncology, Hospital General Universitario de Alicante, Alicante, Spain.
Pediatr Blood Cancer. 2006 Oct 15;47(5):612-5. doi: 10.1002/pbc.20668.
Sinus histiocytosis with massive lymphadenopathy (SHML) or Rosai-Dorfman disease (RDD) is a rare but well-defined histiocytic proliferative disorder of unknown etiology that usually presents with cervical lymphadenopathy, fever, leukocytosis, and hypergammaglobulinemia in an otherwise healthy child. Although many patients undergo spontaneous remission, a subset of patients with systemic disease has a more serious course. For those patients with a poor outcome, steroids and chemotherapeutic agents such as etoposide or 6-mercaptopurine plus low dose methotrexate have been used. We present a child with a massive cervical lymphadenopathy treated with 2-chlorodeoxyadenosine (2-CdA, cladribine) after other approaches failed.
伴巨大淋巴结病的窦性组织细胞增生症(SHML)或罗萨伊-多夫曼病(RDD)是一种病因不明的罕见但明确的组织细胞增生性疾病,通常在健康儿童中表现为颈部淋巴结病、发热、白细胞增多和高球蛋白血症。虽然许多患者会自发缓解,但一部分全身性疾病患者病程更为严重。对于那些预后不良的患者,已使用类固醇和化疗药物,如依托泊苷或6-巯基嘌呤加低剂量甲氨蝶呤。我们报告一名颈部巨大淋巴结病患儿,在其他治疗方法失败后接受了2-氯脱氧腺苷(2-CdA,克拉屈滨)治疗。