Maheshwari Anu, Seth Anju, Choudhury Monisha, Aggarwal Varun, Patra Bijoy, Aggarwal Shilpi, Mukherjee Sharmila B, Aneja Satinder
Department of Pediatrics, Lady Hardinge Medical College, New Delhi, India.
J Pediatr Hematol Oncol. 2009 Mar;31(3):200-2. doi: 10.1097/MPH.0b013e31818e5369.
Rosai-Dorfman disease (RDD), originally described as sinus histiocytosis with massive lymphadenopathy, is a rare histiocytic proliferative disorder with a distinctive microscopic appearance. Formerly thought to be a disease process limited to lymph nodes, RDD has now been reported in many organ systems like bone, skin and soft tissue, central nervous system, eye and orbit, and upper respiratory tract. Here we report a case of RDD with hepatic involvement, which is even more rare.
罗萨伊-多夫曼病(RDD)最初被描述为伴有巨大淋巴结病的窦性组织细胞增多症,是一种罕见的组织细胞增生性疾病,具有独特的微观表现。RDD以前被认为是一种仅限于淋巴结的疾病过程,现在已在许多器官系统中被报道,如骨骼、皮肤和软组织、中枢神经系统、眼和眼眶以及上呼吸道。在此,我们报告一例累及肝脏的RDD病例,这更为罕见。