淋巴结坏死及其鉴别诊断:网状纤维素染色法的应用。

IF 3.4 3区 医学 Q1 PATHOLOGY Virchows Archiv Pub Date : 2024-07-01 Epub Date: 2023-07-01 DOI:10.1007/s00428-023-03588-5
Shan-Chi Yu, Han-Ho Chen, Pin-Yu Lin
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引用次数: 0

摘要

本研究旨在加强对坏死淋巴结标本的组织病理学诊断。病历回顾显示,导致淋巴结坏死最常见的原因是菊地病(33%)、肉芽肿性炎症(25%)、转移瘤(17%)和淋巴瘤(12%)。对 333 份标本中的坏死组织进行的组织学分析表明,四种疾病之间存在显著差异。菊池病的坏死组织呈无定形、高细胞性,并表现为核分裂和充血。肉芽肿性炎症表现为无定形的坏死组织,呈结节状。转移瘤的形态各异,因癌症类型而异。淋巴瘤表现为广泛坏死,伴有鬼细胞、充血和气泡。不同疾病的网织红蛋白染色模式也不尽相同。菊池病和淋巴瘤的坏死组织中保留了网状纤维网,与存活组织相似。肉芽肿性炎症和转移瘤坏死组织中的网状纤维网被破坏。基于这些发现,组织学特征和网状纤维素染色模式可帮助诊断坏死淋巴结标本中的菊地病、肉芽肿性炎症、转移瘤和淋巴瘤。
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Necrosis in lymph nodes and their differential diagnoses: application of reticulin staining.

This study aimed to enhance the histopathological diagnosis of necrotic lymph node specimens. A chart review was conducted, revealing that the most common causes of lymph node necrosis were Kikuchi disease (33%), granulomatous inflammation (25%), metastasis (17%), and lymphomas (12%). Histological analysis of necrotic tissue in 333 specimens demonstrated significant differences between the four diseases. The necrotic tissue of Kikuchi disease was amorphous, and hypercellular, and exhibited karyorrhexis and congestion. Granulomatous inflammation presented amorphous necrotic tissue with a nodular-like pattern. Metastasis exhibited heterogeneous morphology that varied between cancer types. Lymphomas displayed extensive necrosis with ghost cells, congestion, and bubbles. Reticulin staining patterns also differed between diseases. Kikuchi disease and lymphomas exhibited preserved reticular fiber networks in the necrotic tissue, resembling the viable tissue. Granulomatous inflammation and metastasis showed disrupted reticular fiber networks in the necrotic tissue. Based on these findings, histological features and reticulin staining patterns can aid in diagnosing Kikuchi disease, granulomatous inflammation, metastasis, and lymphomas in necrotic lymph node specimens.

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来源期刊
Virchows Archiv
Virchows Archiv 医学-病理学
CiteScore
7.40
自引率
2.90%
发文量
204
审稿时长
4-8 weeks
期刊介绍: Manuscripts of original studies reinforcing the evidence base of modern diagnostic pathology, using immunocytochemical, molecular and ultrastructural techniques, will be welcomed. In addition, papers on critical evaluation of diagnostic criteria but also broadsheets and guidelines with a solid evidence base will be considered. Consideration will also be given to reports of work in other fields relevant to the understanding of human pathology as well as manuscripts on the application of new methods and techniques in pathology. Submission of purely experimental articles is discouraged but manuscripts on experimental work applicable to diagnostic pathology are welcomed. Biomarker studies are welcomed but need to abide by strict rules (e.g. REMARK) of adequate sample size and relevant marker choice. Single marker studies on limited patient series without validated application will as a rule not be considered. Case reports will only be considered when they provide substantial new information with an impact on understanding disease or diagnostic practice.
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