Rosai-Dorfman病(窦性组织细胞增多症伴大量淋巴结病):个人观察和文献复习

Q4 Medicine
A. Rudneva, D. Abramov, A. S. Sharlay, Y. Likar, I. N. Vorozhtsov, N. Myakova
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引用次数: 0

摘要

Rosai-Dorfman病(RDD)是一种罕见的组织细胞疾病,发生在任何年龄,几乎可以影响任何器官和组织,没有病理症状,只能通过组织学检查确诊。本文描述了通过多步骤的手术治疗和化疗,成功治疗了淋巴结、鼻咽、皮下组织、脾脏和骨骼受累的儿童RDD。本文对文献进行了回顾,包括对RDD患者的检查和治疗的建议。患者的父母同意在科学研究和出版物中使用这些信息,包括孩子的照片。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Rosai–Dorfman disease (sinus histiocytosis with massive lymphadenopathy): personal observations and literature review
Rosai–Dorfman disease (RDD) is a rare histiocytic disorder, which occurs at any age, can affect almost any organs and tissues, does not have pathognomonic symptoms and could be confirmed only by histological examination of the affected tissue. The article describes the successful treatment of a child with RDD with lymph nodes, nasopharynx, subcutaneous tissue, spleen and bones involvement, by multistep surgical treatment and chemotherapy. A review of the literature is provided, including recommendations for the examination and treatment of patients with RDD. The patient's parents agreed to use the information, including the child's photo, in scientific research and publications.
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来源期刊
Pediatric Hematology/Oncology and Immunopathology
Pediatric Hematology/Oncology and Immunopathology Medicine-Pediatrics, Perinatology and Child Health
CiteScore
0.40
自引率
0.00%
发文量
49
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