Jabali Y, Smrcka V, Pradna J
Department of Pediatrics, Regional Hospital, Ceske Budejovice, Czech Republic.
Int J Surg Pathol. 2005 Jul;13(3):285-9. doi: 10.1177/106689690501300311.
Sinus histiocytosis with massive lymphadenopathy (SHML), also known as Rosai-Dorfman disease (RDD), is a rare clinicopathologic entity of unknown etiology. The majority of patients do not require treatment, demonstrating spontaneous resolution or stable disease. However, in some cases the disorder runs a progressive course and/or threatens vital structures and functions, which dictates some form of intervention. It is not clear what constitutes the best approach for those cases. We report on a girl with an extensive and progressive form of the disease who was cured with combination chemotherapy, showing no evidence of recurrence after a follow-up of 5.5 years.
伴有巨大淋巴结病的窦组织细胞增生症(SHML),也称为罗萨伊-多夫曼病(RDD),是一种病因不明的罕见临床病理实体。大多数患者无需治疗,可自行缓解或病情稳定。然而,在某些情况下,该疾病呈进行性发展和/或危及重要结构和功能,这就需要某种形式的干预。目前尚不清楚对于这些病例哪种方法是最佳的。我们报告了一名患有广泛进展型该疾病的女孩,她通过联合化疗治愈,在5.5年的随访中未发现复发迹象。