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婴儿期全身性淋巴结病;病例报告。

Generalized lymphadenopathy in infancy; a case report.

作者信息

Setareh Mamishi, Zahra Movahedi, Vahid Mohammadzadeh, Farah Sabouni

机构信息

Pediatric Infectious Diseases Research Center, Tehran University of Medical Sciences, Tehran, Iran ; Department of Pediatrics, Tehran University of Medical Sciences, Tehran, Iran.

出版信息

Iran J Pediatr. 2013 Feb;23(1):105-8.

Abstract

BACKGROUND

Rosai-Dorfman disease (RDD) is a rare disease of histiocytic cells, a cause of benign cervical lymphadenopathy (LAP) and massive generalized lymph node enlargement in children and adults. There are also some reports on involvement of other human body organs with or without LAP.

CASE PRESENTATION

A 7-month-old infant with chief complaint of generalized massive LAP was referred to our center. RDD was diagnosed according to clinical manifestations and confirmed through histopathologic and immunoreactivity study on the obtained sample by cervical lymph node biopsy.

CONCLUSION

RDD is not a malignant illness and lymph node enlargement most often decreases in its size happens without special treatment.

摘要

背景

罗萨伊-多夫曼病(RDD)是一种组织细胞罕见病,是儿童和成人良性颈部淋巴结病(LAP)及广泛性全身淋巴结肿大的病因。也有一些关于其他人体器官受累伴或不伴LAP的报道。

病例报告

一名以广泛性巨大LAP为主诉的7个月大婴儿被转诊至我院。根据临床表现诊断为RDD,并通过对颈部淋巴结活检获取的样本进行组织病理学和免疫反应性研究得以确诊。

结论

RDD并非恶性疾病,淋巴结肿大通常无需特殊治疗即可自行缩小。

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