El Kohen A, Planquart X, Al Hamany Z, Bienvenu L, Kzadri M, Herman D
Department of Otorhinolaryngology and Maxillofacial Surgery, Avicenne's Hospital, Faculty of Medicine and University Hospital of Rabat, Rabat, Morocco.
Int J Pediatr Otorhinolaryngol. 2001 Dec 1;61(3):243-7. doi: 10.1016/s0165-5876(01)00523-7.
Sinus histiocytosis with massive lymphadenopathy or Destombes-Rosai-Dorfman's syndrome is a rare benign disease of unknown etiology, usually seen in younger patients. The cases reported concerned a 15-month old Caucasian boy and an 8 year old black boy with unilateral cervical enlargement, occasional fever and without any extranodal involvement. Diagnosis was performed by superficial lymph node biopsy. No immunodeficiency was found. The patients received no therapy and a complete spontaneous resolution was seen after a few months in the two cases. The clinical presentation, histologic characteristics, pathogenesis and treatment of the Destombes-Rosai-Dorfman's syndrome are discussed.
伴巨大淋巴结病的窦性组织细胞增生症或德斯顿布-罗萨伊-多夫曼综合征是一种病因不明的罕见良性疾病,多见于年轻患者。报告的病例为一名15个月大的白种男孩和一名8岁的黑种男孩,均有单侧颈部肿大,偶尔发热,且无任何结外受累情况。通过浅表淋巴结活检进行诊断。未发现免疫缺陷。两名患者均未接受治疗,数月后均完全自发缓解。本文讨论了德斯顿布-罗萨伊-多夫曼综合征的临床表现、组织学特征、发病机制及治疗。