肾上腺外副神经节瘤和嗜铬细胞瘤细胞学诊断的误区:一家三级医疗中心的经验。

IF 1 4区 医学 Q4 MEDICAL LABORATORY TECHNOLOGY Diagnostic Cytopathology Pub Date : 2024-08-17 DOI:10.1002/dc.25390
Raktim Mukherjee, Soumya Dey, Farjana Khatun, Firdous Wasim Sk, Oindrila Das, Debansu Sarkar, Krishnendu Maiti, Uttara Chatterjee
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引用次数: 0

摘要

背景:由于成像技术和生化检查的改进,嗜铬细胞瘤和肾上腺外副神经节瘤日益受到关注。有关肾上腺和肾上腺外副神经节瘤细胞学检查结果的文献很少:我们对 16 例细胞学标本进行了为期 3 年的回顾性研究,这些标本的组织学诊断结果为嗜铬细胞瘤或副神经节瘤:共研究了 16 份细胞学标本。结果:共研究了 16 份细胞学标本,其中 9 例为肾上腺 SOL,7 例为肾上腺外病变。年龄介于 12 岁至 60 岁之间,大部分细胞涂片为细胞涂片(87.5%)。涂片由小的细胞团和分散的浆细胞组成,细胞核偏心,含有盐和胡椒染色质以及中等至大量颗粒状细胞质。其中一个病例出现了模仿 Zellballen 模式的大细胞簇。除三例病例的明显异核现象给诊断带来困难外,其他病例的异核现象均为轻度至中度。所有病例的背景均为出血性,但有两例病例还伴有坏死性炎症背景。所有病例均缺乏有丝分裂活动,细胞质细腻,细胞边界不清。经常发现裸椭圆形核。核沟或细胞质空泡缺失。在 16 个病例中,有 12 个病例的最初细胞学诊断与最终组织学诊断相关,总体诊断准确率为 75%。4例误诊病例具有一些不典型的细胞学特征,如明显的无核、坏死性炎症背景和突出的核小体:在此,我们强调了一些有助于副神经节瘤细胞学诊断的细胞学特征。出血背景与浆细胞形态、颗粒状胞质、裸核和无有丝分裂是有用的线索。
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Pitfalls in Cytological Diagnosis of Extra Adrenal Paraganglioma and Pheochromocytoma: Experience From a Tertiary Care Center.

Background: Pheochromocytoma and extra-adrenal paragangliomas increasingly coming into light nowadays because of improved imaging techniques and biochemical investigations. There is sparse literature available regarding cytological findings of adrenal and extra-adrenal paragangliomas.

Material and methods: We studied 16 cytological specimens retrospectively over a period of 3 years, where subsequent histological diagnosis of phaeochromocytoma or paraganglioma was available.

Results: A total of 16 cytology specimens were studied. Nine patients had adrenal SOLs and seven patients had extra-adrenal lesions. Age range was 12 to 60 years Majority of the cytology smears were cellular (87.5%). The smears were composed of small clusters as well as dispersed plasmacytoid cells with eccentric nuclei containing salt and pepper chromatin and moderate to abundant granular cytoplasm. Large cellular clusters mimicking the Zellballen pattern was present in one case. Anisonucleosis was mild to moderate, except in three cases where marked anisonucleosis posed diagnostic challenges. The background was hemorrhagic in all cases, however, two cases in addition had necroinflammatory background. All cases lacked mitotic activity and cytoplasm was delicate with indistinct cell borders. Bare oval nuclei were a frequent finding. Nuclear grooves or cytoplasmic vacuoles were absent. In 12 out of 16 cases, the initial cytological diagnosis correlated with final histological diagnosis, with an overall diagnostic accuracy of 75%. Four misdiagnosed cases had some atypical cytological features like marked anisonucleosis, necroinflammatory background, and presence of prominent nucleoli.

Conclusion: Here we have highlighted some of the distinguishing cytological features that can help in cytological diagnosis of paragangliomas. Hemorrhagic background with plasmacytoid morphology, granular cytoplasm, naked nuclei, and absence of mitosis are useful clues.

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来源期刊
Diagnostic Cytopathology
Diagnostic Cytopathology 医学-病理学
CiteScore
2.60
自引率
7.70%
发文量
163
审稿时长
3-6 weeks
期刊介绍: Diagnostic Cytopathology is intended to provide a forum for the exchange of information in the field of cytopathology, with special emphasis on the practical, clinical aspects of the discipline. The editors invite original scientific articles, as well as special review articles, feature articles, and letters to the editor, from laboratory professionals engaged in the practice of cytopathology. Manuscripts are accepted for publication on the basis of scientific merit, practical significance, and suitability for publication in a journal dedicated to this discipline. Original articles can be considered only with the understanding that they have never been published before and that they have not been submitted for simultaneous review to another publication.
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