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45例浆细胞性龈炎的临床病理特征及预后

Clinico-Pathological Profile and Outcomes of 45 Cases of Plasma Cell Gingivitis.

作者信息

Leuci Stefania, Coppola Noemi, Adamo Nicola, Bizzoca Maria Eleonora, Russo Daniela, Spagnuolo Gianrico, Lo Muzio Lorenzo, Mignogna Michele Davide

机构信息

Department of Neurosciences, Reproductive and Odontostomatological Sciences, Oral Medicine Unit, University of Naples Federico II, 80131 Naples, Italy.

Department of Clinical and Experimental Medicine, University of Foggia, 71122 Foggia, Italy.

出版信息

J Clin Med. 2021 Feb 18;10(4):830. doi: 10.3390/jcm10040830.

Abstract

Plasma cell gingivitis (PCG) is an infrequent inflammatory disease of the gingiva of unknown etiology, characterized by a dense polyclonal proliferation of plasma cells in the connective tissue. The aim of this study was to present a case series of patients affected by PCG, analyzing demographic, clinical, histopathological, and therapeutic data. A group of 36 females and 9 males with a mean age of 60.3 years was evaluated. Clinically, 25 cases were bullous, a clinical phenotype never reported to date, 4 erythematous, 4 keratotic, 4 verruciform, and 3 ulcerative. On histological examination, pure polyclonal plasma cell infiltrate was detected in 20 specimens, while in 25 specimens it was associated with a mixed infiltrate. The first-line therapy consisted of oral hygiene and topical corticosteroids in all patients. In 25 patients, doxycycline and sulfasalazine were added; in 10 of these patients, the disease persisted, and it was necessary to resort to systemic steroids. This study presented the clinico-pathological profile and outcomes of a case series of PCG. This could be an aid for clinicians to be aware of the heterogeneous clinical phenotype and of the possible pure bullous phenotype of PCG. Further studies are needed to improve the knowledge about this disorder.

摘要

浆细胞性龈炎(PCG)是一种病因不明的罕见牙龈炎症性疾病,其特征为结缔组织中浆细胞的密集多克隆增殖。本研究的目的是呈现一组受PCG影响患者的病例系列,分析人口统计学、临床、组织病理学和治疗数据。评估了一组36名女性和9名男性,平均年龄为60.3岁。临床上,25例为大疱性,这是迄今为止从未报道过的临床表型,4例为红斑性,4例为角化性,4例为疣状,3例为溃疡性。组织学检查显示,20份标本中检测到单纯多克隆浆细胞浸润,而25份标本中其与混合浸润相关。所有患者的一线治疗包括口腔卫生和局部使用皮质类固醇。25例患者加用了强力霉素和柳氮磺胺吡啶;其中10例患者病情持续,有必要采用全身用类固醇。本研究呈现了PCG病例系列的临床病理特征和结果。这有助于临床医生了解PCG的异质性临床表型以及可能的单纯大疱性表型。需要进一步研究以增进对这种疾病的认识。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6d3d/7922699/0a281dd7b12f/jcm-10-00830-g001.jpg

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