Rajasekharan Chandrasekharan, Ratheesh Narayanan Santhanavally, Nandinidevi Rajan, Parvathy Rajasekharan
Department of Internal Medicine, Medical College Hospital, Thiruvananthapuram, Kerala, India.
BMJ Case Rep. 2012 Sep 21;2012:bcr2012006723. doi: 10.1136/bcr-2012-006723.
A 14-year-old boy was referred to us with a history of progressive painless massive symmetrical cervical lymphadenopathy, provisionally diagnosed as lymphoma. Multiple biopsies were needed, and confirmed the diagnosis of Rosai Dorfman disease (RDD), which is a very rare benign condition. Sinus histiocytosis with massive lymphadenopathy, also known as RDD, manifests as bulky lymphadenopathy in children and young adults. Extranodal sites such as the skin, upper airways, gastrointestinal tract and central nervous system can be involved. There is a characteristic pattern of lymphoid proliferation with a thick fibrous capsule, distention of lymphoid sinuses, accumulation of plasma cells and proliferation of large, often atypical, histiocytes showing emperipolesis is characteristic. The disease is considered to be benign and usually self-limited. We emphasise the need for doing a repeat lymphnode biopsy even if the prior histopathology is suggestive of reactive lypmhnode hyperplasia in every case of persisting lymphadenopathy.
一名14岁男孩因进行性无痛性双侧颈部对称性巨大淋巴结肿大前来我院就诊,初步诊断为淋巴瘤。需要进行多次活检,最终确诊为罗萨伊-多夫曼病(RDD),这是一种非常罕见的良性疾病。伴有巨大淋巴结病的窦性组织细胞增生症,也称为RDD,在儿童和年轻人中表现为巨大淋巴结肿大。皮肤、上呼吸道、胃肠道和中枢神经系统等结外部位也可能受累。其具有特征性的淋巴样增生模式,有厚的纤维包膜、淋巴窦扩张、浆细胞积聚以及大量通常为非典型的组织细胞增生并呈现吞噬现象。该疾病被认为是良性的,通常具有自限性。我们强调,对于每一例持续性淋巴结肿大病例,即使先前的组织病理学提示为反应性淋巴结增生,也有必要再次进行淋巴结活检。