罗素体宫颈炎:一例报告和文献回顾突出诊断缺陷

IF 0.7 Q4 OBSTETRICS & GYNECOLOGY
Lalani De Silva , Kaumadi Udeshika , Sinha De Silva , Priyani Amarathunga
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引用次数: 0

摘要

罗素体在各种炎症和肿瘤条件下被观察到,尽管它们在女性生殖道中的存在是罕见的,罗素体宫颈炎的记录病例不到10例。本病例报告似乎是第一个罗素体宫颈炎确定在怀孕期间。一名28岁的妇女,在怀孕20周时,在宫颈环切术中偶然发现息肉后,接受了宫颈息肉切除术。病理检查显示一炎性宫颈息肉,以浆细胞浸润为主。大多数浆细胞含有胞浆内罗素小体,少量有莫特细胞。免疫组化染色证实了浆细胞浸润的多克隆性。本报告强调了与罗素体宫颈炎相关的诊断挑战,因为它的罕见性和组织学上与其他炎症和肿瘤条件相似。回顾文献显示,少数报告的病例在育龄期间呈现非肿瘤过程,随访顺利。本报告有助于罗素体宫颈炎的有限知识,特别是在怀孕的背景下。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Russell body cervicitis: A case report and literature review highlighting diagnostic pitfalls
Russell bodies have been observed in various inflammatory and neoplastic conditions, although their presence in the female genital tract is rare, with fewer than ten documented cases of Russell body cervicitis. This case report appears to be the first of Russell body cervicitis identified during pregnancy. A 28-year-old woman, at 20 weeks of gestation, underwent a cervical polypectomy after a polyp was detected incidentally during a cervical cerclage procedure. Pathological examination revealed an inflamed endocervical polyp with predominant plasma cell infiltrate. Most of the plasma cells contained intracytoplasmic Russell bodies and there were some Mott cells. Immunohistochemical stains confirmed the polyclonal nature of the plasma cell infiltrate.
This report highlights the diagnostic challenges associated with Russell body cervicitis, given its rarity and histological resemblance to other inflammatory and neoplastic conditions. A review of the literature reveals that the few reported cases presented as a non-neoplastic process during reproductive age, with an uneventful follow-up. This report contributes to the limited knowledge of Russell body cervicitis, particularly in the context of pregnancy.
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来源期刊
Case Reports in Women's Health
Case Reports in Women's Health Medicine-Obstetrics and Gynecology
CiteScore
2.10
自引率
0.00%
发文量
89
审稿时长
7 days
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