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2
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本文引用的文献

1
Rosai-Dorfman Disease: A Rare Clinicopathological Presentation and Review of the Literature.罗萨达-多夫曼病:一种罕见的临床病理表现及文献复习。
Head Neck Pathol. 2021 Mar;15(1):352-360. doi: 10.1007/s12105-020-01183-7. Epub 2020 Jun 5.
2
Rosai-Dorfman Disease: Self-Resolving Unilateral Lymphadenopathy and a Brief Review of Literature.罗萨伊-多夫曼病:自行消退的单侧淋巴结病及文献综述
Case Rep Oncol Med. 2018 Sep 16;2018:4869680. doi: 10.1155/2018/4869680. eCollection 2018.
3
Pediatric Cervical Lymphadenopathy.小儿颈淋巴结病
Pediatr Rev. 2018 Sep;39(9):433-443. doi: 10.1542/pir.2017-0249.
4
Rosai-Dorfman disease (RDD) in the paraglottic space: report of a case and review of literature.声门旁间隙的罗萨伊-多夫曼病(RDD):一例报告并文献复习
Int J Clin Exp Pathol. 2015 Oct 1;8(10):13532-8. eCollection 2015.
5
Rosai-Dorfman disease: tumor biology, clinical features, pathology, and treatment.罗萨伊-多夫曼病:肿瘤生物学、临床特征、病理学及治疗
Cancer Control. 2014 Oct;21(4):322-7. doi: 10.1177/107327481402100408.
6
Rosai-Dorfman disease with spontaneous resolution: case report of a child.伴自发缓解的罗萨伊-多夫曼病:一例儿童病例报告
Rev Bras Hematol Hemoter. 2011;33(4):312-4. doi: 10.5581/1516-8484.20110083.
7
High prevalence of BRAF V600E mutations in Erdheim-Chester disease but not in other non-Langerhans cell histiocytoses.Erdheim-Chester 病中 BRAF V600E 突变的高发生率,但非朗格汉斯细胞组织细胞增生症。
Blood. 2012 Sep 27;120(13):2700-3. doi: 10.1182/blood-2012-05-430140. Epub 2012 Aug 9.
8
Factors associated with recurrence and therapeutic strategies for sinonasal Rosai-Dorfman disease.与鼻窦 Rosai-Dorfman 病复发相关的因素及治疗策略。
Head Neck. 2012 Oct;34(10):1504-13. doi: 10.1002/hed.21832. Epub 2011 Aug 4.
9
Treatment of sinus histiocytosis with massive lymphadenopathy (Rosai-Dorfman disease): report of a case and literature review.巨大淋巴结病性窦组织细胞增生症(罗萨伊-多夫曼病)的治疗:1例报告及文献复习
Am J Hematol. 2002 Jan;69(1):67-71. doi: 10.1002/ajh.10008.
10
[Adenitis with lipid excess, in children or young adults, seen in the Antilles and in Mali. (4 cases)].[脂质过多性腺炎,见于安的列斯群岛和马里的儿童或年轻人。(4例)]
Bull Soc Pathol Exot Filiales. 1965 Nov-Dec;58(6):1169-75.

罗萨伊-多夫曼病:一种表现为单侧颈部肿胀的罕见疾病。

Rosai-Dorfmann Disease: A Rare Disease Presenting as a Unilateral Neck Swelling.

作者信息

John Stanley, Goel Tanubha

机构信息

Department of Otorhinolaryngology, Dr. B R Ambedkar Medical College and Hospital, Kadugondanahalli, Bangalore, Karnataka 560045 India.

出版信息

Indian J Otolaryngol Head Neck Surg. 2024 Feb;76(1):1260-1263. doi: 10.1007/s12070-023-04254-7. Epub 2023 Oct 11.

DOI:10.1007/s12070-023-04254-7
PMID:38440436
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10908954/
Abstract

Rosai-Dorfman disease (RDD) is a rare histiocytic proliferative disorder of unknown etiology. Usually it presents with massive painless cervical lymph node enlargement. Histologically, it shows proliferation of distinctive histiocytic cells that demonstrate emperipolesis in the background of a mixed inflammatory infiltrates. Immunohistochemically, the cells are positive for markers such as CD68 and S100. A 14-year-old boy presented with painless right sided cervical lymphadenopathy without any systemic and other ear, nose, and throat manifestations. The biopsy report of the lymph node showed infiltration of sheets of histiocytes showing emperipolesis with areas of fibrosis and hyalinisation. The sinus histiocytes were strongly positive for S-100 protein. RDD must be considered in the differential diagnosis of massive or multiple lymphadenopathies.

摘要

罗萨伊-多夫曼病(RDD)是一种病因不明的罕见组织细胞增生性疾病。通常表现为颈部淋巴结无痛性肿大。组织学上,它显示出独特的组织细胞增生,这些细胞在混合性炎症浸润背景下呈现吞噬现象。免疫组织化学检查显示,这些细胞对CD68和S100等标志物呈阳性。一名14岁男孩出现右侧颈部无痛性淋巴结病,无任何全身及其他耳鼻喉症状。淋巴结活检报告显示成片的组织细胞浸润,可见吞噬现象,并伴有纤维化和玻璃样变区域。窦组织细胞S-100蛋白呈强阳性。在鉴别诊断巨大或多发淋巴结病时必须考虑罗萨伊-多夫曼病。