儿童罗塞-多尔夫曼病的异常部位:来自三级保健儿科血液肿瘤中心的5年经验。

Janani Arul, Riya Kataria, Varsha Kolli, Arunan Murali, Gramani Arumugam Vasugi, Arathi Srinivasan
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引用次数: 1

摘要

Rosai-Dorfman病(RDD)是一种罕见的组织细胞疾病,通常表现为大面积淋巴结病变。累及淋巴结外部位、骨和淋巴结如纵隔是罕见的。本文分析了近5年来我院儿科血液肿瘤科收治的3例淋巴结外RDD的临床资料。结外RDD(上颌窦、鼻咽病灶及外耳道)经组织病理学及正电子发射断层扫描诊断。他们用类固醇治疗,但难以治愈,因此需要补救性化疗。目前,他们三人都已完全康复。结节外RDD诊断困难,组织病理学和影像学起重要作用。在这里,我们提出了三个病例,其中两个是类固醇难治性的,他们接受了补救性化疗并完全缓解。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Unusual sites of Rosai-Dorfman disease in children: 5 years experience from tertiary care paediatric haemato-oncology centre.

Unusual sites of Rosai-Dorfman disease in children: 5 years experience from tertiary care paediatric haemato-oncology centre.

Rosai-Dorfman disease (RDD) is a rare histiocytic disorder, usually presenting with massive lymphadenopathy. The involvement of extra nodal sites, bone and nodal sites like mediastinum are rare. Clinical data of three cases of extra nodal RDD who were admitted in our paediatric haemato-oncology unit were analysed in the last 5 years. The extra nodal RDD (maxillary sinus, nasal pharyngeal focus, and external auditory meatus) were diagnosed based on histopathology and positron emission tomography scan. They were treated with steroids but were refractory hence requiring salvage chemotherapy. Currently all three of them are in complete remission. Extra nodal RDD is difficult to diagnose, histopathology and radiology play an important role. Here, we present three cases, of which two were steroid-refractory which were treated with salvage chemotherapy and are in complete remission.

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