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菊池富士本病的细针穿刺细胞学检查

Fine-needle aspiration cytology of Kikuchi Fujimoto disease.

作者信息

Hasan Mehboob, Zaheer Sufian, Sofi Lateef Ahmed, Parvez Anjum

机构信息

Department of Pathology, Jawaharlal Nehru Medical College and Hospital, Aligarh Muslim University, Aligarh, India.

出版信息

J Cytol. 2009 Jan;26(1):43-5. doi: 10.4103/0970-9371.54870.

Abstract

Kikuchi disease (KD) is an enigmatous, self-limiting, rarely fatal, disease of young females. The self-limiting disorder usually occurs in Asian women in their late 20s or early 30s. Typically it runs a benign course and appears to resolve spontaneously one to six months after definitive diagnosis. We report a 27 years old lady presenting with cervical lymphadenopathy. Fine needle aspiration cytology of the node clinched the diagnosis revealing crescentic histiocytes, plasmacytoid monocytes, extracellular (karyorrhectic) debris and necrosis. The diagnosis was subsequently confirmed by histopathology.

摘要

菊池病(KD)是一种病因不明、自限性、极少致命的年轻女性疾病。这种自限性疾病通常发生在28岁晚期或30岁早期的亚洲女性身上。通常病程呈良性,在明确诊断后1至6个月似乎会自发缓解。我们报告一位27岁出现颈部淋巴结病的女性。对该淋巴结进行细针穿刺细胞学检查确诊,发现有新月形组织细胞、浆细胞样单核细胞、细胞外(核碎裂)碎片和坏死。随后通过组织病理学证实了诊断。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bd98/3167992/2faf499158b4/JCytol-26-43-g001.jpg

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