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菊池淋巴结炎的细针穿刺表现。

The fine needle aspiration appearances of Kikuchi's lymphadenitis.

作者信息

Osborn M, Aqel N, Levine T S

机构信息

Department of Cellular Pathology, Northwick Park Hospital, North West London Hospitals NHS Trust, Harrow, UK.

出版信息

Cytopathology. 2009 Feb;20(1):36-43. doi: 10.1111/j.1365-2303.2007.00491.x. Epub 2007 Oct 4.

Abstract

OBJECTIVE

To describe the fine needle aspiration cytological appearances of Kikuchi's lymphadenitis.

METHODS

Cytological review with histological correlation of all cases of Kikuchi's disease (KD) in which there had been an antecedent fine needle aspirate of the involved lymph node prior to lymph node excision between 2001 and 2006.

RESULTS

Twelve cases of KD were identified in which cytological and histological material was available. In eight cases the original prospective diagnosis of necrotizing non-granulomatous lymphadenitis consistent with KD had been suggested on the lymph node aspirate. Review of these cytological samples identified abundant extra- and intracellular apoptotic debris - the latter embedded in the cytoplasm of crescentic and phagocytic macrophages, set in a background reactive lymphoid population. Three of 12 cases were initially reported as in keeping with nonspecific reactive lymphadenopathy. Review identified intracellular apoptotic debris but no conspicuous extracellular nuclear debris. One case had originally been reported as possible non-Hodgkin's lymphoma. Histological review of the excised lymph nodes in all 12 cases showed the classical appearances of KD.

CONCLUSION

The accurate diagnosis of KD on fine needle aspiration is possible given correct clinical data, an adequately sampled and well-prepared specimen in which the characteristic intra- and extracellular apoptotic nuclear debris with admixed crescentic macrophages are identified on a reactive lymphoid background.

摘要

目的

描述菊池淋巴结炎的细针穿刺细胞学表现。

方法

对2001年至2006年间所有菊池病(KD)病例进行细胞学回顾,并与组织学进行相关性分析,这些病例在淋巴结切除术前均对受累淋巴结进行过细针抽吸。

结果

共确定12例KD病例,有细胞学和组织学资料。8例病例在淋巴结抽吸物中最初前瞻性诊断为与KD一致的坏死性非肉芽肿性淋巴结炎。对这些细胞学样本进行回顾发现有大量细胞内外凋亡碎片——后者嵌入新月形和吞噬性巨噬细胞的细胞质中,背景为反应性淋巴细胞群。12例中有3例最初报告符合非特异性反应性淋巴结病。回顾发现有细胞内凋亡碎片,但无明显的细胞外核碎片。1例最初报告可能为非霍奇金淋巴瘤。对所有12例切除淋巴结的组织学回顾均显示出KD的典型表现。

结论

在有正确临床资料的情况下,通过细针穿刺对KD进行准确诊断是可能的,标本取样充分且制备良好,在反应性淋巴细胞背景上可识别出特征性的细胞内和细胞外凋亡核碎片以及混合的新月形巨噬细胞。

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