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罗萨伊-多夫曼病的细胞形态学与组织学相关性:来自印度南部一家三级转诊中心的15年研究。

Cytomorphology and Histology Correlation of Rosai-Dorfman Disease: A 15-Year Study from a Tertiary Referral Centre in South India.

作者信息

Hussain Abid, Tandon Ashwani, Prayaga Aruna K, Paul Tara Roshni, Narendra Anukonda M V R

机构信息

Department of Pathology, Nizam's Institute of Medical Sciences, Hyderabad, India.

出版信息

Acta Cytol. 2017;61(1):55-61. doi: 10.1159/000449460. Epub 2016 Sep 28.

Abstract

OBJECTIVES

Rosai-Dorfman disease (RDD) is an uncommon, benign histiocytic disorder of unknown etiology, typically presenting in young adulthood. We highlight the cytomorphology of RDD and correlate it with the histopathology.

STUDY DESIGN

All cases diagnosed as RDD on fine-needle aspiration cytology between January 2001 and June 2015 were included. Clinical details were obtained from medical records. The cytology smears were reviewed along with the histopathology and immunohistochemistry, wherever available.

RESULTS

The study included 10 cases ranging in age from 11 to 68 years (median 29). There was a male predominance with a male:female ratio of 1.5:1. The patients commonly presented with bilateral cervical lymphadenopathy. Extranodal involvement was seen in 2 cases in the nose and mandible, respectively. Of these 10 cases, 8 were later biopsied. The cytological features included numerous crescentic histiocytes, emperipolesis, reactive lymphocytes and plasma cells. A histological diagnosis of RDD was made in 7 out of 8 cases, and 1 was diagnosed as Hodgkin lymphoma.

CONCLUSION

FNA represents an efficient, minimally invasive, cost-effective and reliable technique for the diagnosis of RDD and may obviate the need for further biopsy. However, the disease has close differential diagnoses, including Langerhans cell histiocytosis, granulomatous lesions, and Hodgkin lymphoma. Hence, it must be remembered that there can be pitfalls when the diagnosis is made by cytology alone.

摘要

目的

罗萨伊-多夫曼病(RDD)是一种病因不明的罕见良性组织细胞疾病,通常在青年期发病。我们着重介绍RDD的细胞形态学,并将其与组织病理学相关联。

研究设计

纳入2001年1月至2015年6月间经细针穿刺细胞学诊断为RDD的所有病例。从病历中获取临床细节。如有可能,对细胞学涂片以及组织病理学和免疫组织化学检查结果进行回顾。

结果

该研究包括10例患者,年龄在11至68岁之间(中位数为29岁)。男性占优势,男女比例为1.5:1。患者通常表现为双侧颈部淋巴结肿大。分别有2例在鼻部和下颌骨出现结外受累。这10例患者中,8例后来接受了活检。细胞学特征包括大量新月形组织细胞、血细胞吞噬现象、反应性淋巴细胞和浆细胞。8例中有7例经组织学诊断为RDD,1例诊断为霍奇金淋巴瘤。

结论

细针穿刺抽吸术是诊断RDD的一种有效、微创、经济且可靠的技术,可能无需进一步活检。然而,该疾病有相近的鉴别诊断,包括朗格汉斯细胞组织细胞增多症、肉芽肿性病变和霍奇金淋巴瘤。因此,必须记住仅通过细胞学进行诊断时可能存在陷阱。

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