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恶性肿瘤的黄瘤样炎性病变模仿物:来自印度农村的一项临床病理研究。

Xanthogranulomatus inflammatory lesion mimicker of malignancy: A clinicopathological study from rural India.

作者信息

Krishna Mani, Dayal Seema

机构信息

Department of Pathology, Uttar Pradesh University of Medical Sciences, Saifai, Etawah (U.P), India.

出版信息

North Clin Istanb. 2021 Oct 6;8(5):485-492. doi: 10.14744/nci.2021.04317. eCollection 2021.

Abstract

OBJECTIVE

Xanthogranulomatus inflammation is an uncommon variant of chronic inflammation and a well-established pathological entity involving various organs and systems. It may be associated with infection and obstruction, defective lipid transport, immunological disturbances, and often confused as a malignant neoplasm. The confirmative diagnosis is made on histopathology.

METHODS

This is a retrospective study conducted from January 2008 to April 2020 on histopathologically diagnosed xanthogranulomatus lesions. All the relevant available data regarding age, sex, and organ involvement were collected from histopathology lab records. The macroscopic and microscopic evaluation of cases was also done. This study was aimed to determine the significance of histopathology in the diagnosis of xanthogranulomatus lesions, revealing pathological changes, and clinicopathological correlation.

RESULTS

In the current study, there were 93 cases of xanthogranulomatus inflammatory lesion. Gall bladder was frequently involved 70 (75.27%), followed by 5 (5.37%) kidney, gastrointestinal Tract 6 (3 [3.23%] cases in colon and 3 [3.23%] in appendix, respectively), and others. The maximum number of cases was in the age group of 31-40 years with 24 (25.80%) cases. The female to male sex ratio was 2.3:1.

CONCLUSION

Awareness and knowledge of xanthogranulomatus inflammatory lesion is significant to the pathologist and surgeon to prevent extensive surgery. This lesion often mimics as malignancy and confirmatory diagnosis is made on histopathology. Thus, every excised specimen must be examined histopathologically to diagnose and rule out differential.

摘要

目的

黄色肉芽肿性炎症是一种罕见的慢性炎症变体,是一种公认的涉及多个器官和系统的病理实体。它可能与感染和梗阻、脂质转运缺陷、免疫紊乱有关,且常被误诊为恶性肿瘤。确诊依靠组织病理学检查。

方法

这是一项回顾性研究,对2008年1月至2020年4月间经组织病理学诊断为黄色肉芽肿性病变的病例进行研究。从组织病理学实验室记录中收集所有关于年龄、性别和器官受累的相关可用数据。对病例进行了大体和显微镜评估。本研究旨在确定组织病理学在黄色肉芽肿性病变诊断中的意义,揭示病理变化,并进行临床病理相关性分析。

结果

在本研究中,有93例黄色肉芽肿性炎症病变。胆囊最常受累,有70例(75.27%),其次是肾脏5例(5.37%),胃肠道6例(结肠3例[3.23%],阑尾3例[3.23%]),以及其他部位。病例数最多的年龄组为31 - 40岁,有24例(25.80%)。男女比例为2.3:1。

结论

了解黄色肉芽肿性炎症病变对病理学家和外科医生预防广泛手术具有重要意义。这种病变常类似恶性肿瘤,确诊依靠组织病理学检查。因此,每个切除标本都必须进行组织病理学检查以诊断并排除鉴别诊断。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dac7/8630717/6993f5b1cc02/NCI-8-485-g001.jpg

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