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浆细胞性龈炎的临床病理及免疫组化分析——一项回顾性研究

Clinicopathological and immunohistochemical analysis of plasma cell gingivitis- A retrospective study.

作者信息

Gupta Vandana, Kaur Harpreet, Yadav Vikender Singh, Kala Sunny, Mishra Deepika

机构信息

Centre for Dental Education and Research, Division of Periodontics, All India Institute of Medical Sciences, New Delhi, India.

Department of Oral Pathology and Microbiology, Centre for Dental Education and Research, All India Institute of Medical Sciences, New Delhi, India.

出版信息

J Indian Soc Periodontol. 2022 Sep-Oct;26(5):434-439. doi: 10.4103/jisp.jisp_67_21. Epub 2022 Sep 1.

DOI:10.4103/jisp.jisp_67_21
PMID:36339381
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9626791/
Abstract

BACKGROUND

This study aims to describe the demographics and clinicopathological characteristics of the cases of plasma cell gingivitis (PCG) reported in our institute, supported by a review of pertinent literature. Further, we investigated the role of the cluster of differentiation CD138, Ki67, CD56, and CD117 immunoexpression in the differential diagnosis of PCG from plasma cell dyscrasias.

MATERIALS AND METHODS

All histopathologically confirmed cases of PCG, whose relevant details could be obtained, were included in this study. They were subjected to panel of immunohistochemical markers to exclude plasma cell malignancies. Further, published English literature for PCG since 1970-2020 was reviewed.

RESULTS

Nine histopathologically confirmed cases of PCG, were retrieved from the archives of our department. The cases comprised 3 males and 6 females with their ages ranging between 14 and 82 years. The plasma cells exhibited equivocal reactivity for kappa and lambda; and immunonegativity for CD56, CD117 with low Ki67 proliferation index. Published literature in English showed 43 cases of PCG were predominantly female; the diffuse involvement of maxilla and mandible was a common finding.

CONCLUSION

In addition to kappa lambda reactivity, an immunoprofile of CD138, Ki67, CD56, and CD117 may be used as a diagnostic adjunct to exclude malignant plasma cell lesions in confusing cases.

摘要

背景

本研究旨在描述我院报告的浆细胞性龈炎(PCG)病例的人口统计学和临床病理特征,并辅以相关文献综述。此外,我们研究了分化簇CD138、Ki67、CD56和CD117免疫表达在PCG与浆细胞发育异常的鉴别诊断中的作用。

材料与方法

本研究纳入所有经组织病理学确诊且能获取相关细节的PCG病例。对其进行一组免疫组化标记物检测以排除浆细胞恶性肿瘤。此外,回顾了1970年至2020年以来发表的关于PCG的英文文献。

结果

从我院病理档案中检索到9例经组织病理学确诊的PCG病例。这些病例包括3名男性和6名女性,年龄在14岁至82岁之间。浆细胞对κ和λ表现出不明确的反应性;对CD56、CD117呈免疫阴性,Ki67增殖指数较低。英文发表文献显示43例PCG病例以女性为主;上颌骨和下颌骨的弥漫性受累是常见表现。

结论

除κλ反应性外,CD138、Ki67、CD56和CD117的免疫表型可作为诊断辅助手段,用于在疑难病例中排除恶性浆细胞病变。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/19c1/9626791/84597ba2cb03/JISP-26-434-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/19c1/9626791/11dd36fc9869/JISP-26-434-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/19c1/9626791/1b87b9aaa033/JISP-26-434-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/19c1/9626791/84597ba2cb03/JISP-26-434-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/19c1/9626791/11dd36fc9869/JISP-26-434-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/19c1/9626791/1b87b9aaa033/JISP-26-434-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/19c1/9626791/84597ba2cb03/JISP-26-434-g003.jpg

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本文引用的文献

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Plasma Cell Gingivitis Mimicking Granulomatous Disease: A Diagnostic Dilemma.浆细胞性龈炎酷似肉芽肿性疾病:诊断困境。
Clin Adv Periodontics. 2021 Dec;11(4):220-224. doi: 10.1002/cap.10108. Epub 2020 Jun 24.
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Plasma-Cell Gingivitis a Challenge to the Oral Physician.浆细胞性龈炎:口腔医生面临的一项挑战
Contemp Clin Dent. 2019 Jul-Sep;10(3):565-570. doi: 10.4103/ccd.ccd_776_18.
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Interdisciplinary assessment and management of a patient with a fibrous gingival enlargement of unknown origin: A case report.一例不明原因纤维性牙龈增生患者的多学科评估与管理:病例报告
Clin Case Rep. 2019 Dec 12;8(1):159-165. doi: 10.1002/ccr3.2605. eCollection 2020 Jan.
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A Rare Case of Plasma Cell Gingivitis with Cheilitis.一例罕见的浆细胞性龈炎伴唇炎病例。
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