Lymphangioma Circumscriptum - A Rare Cause of Gingival Enlargement: A Case Report and Review of Literature.

IF 1.5 Q3 DENTISTRY, ORAL SURGERY & MEDICINE Clinical, Cosmetic and Investigational Dentistry Pub Date : 2022-07-11 eCollection Date: 2022-01-01 DOI:10.2147/CCIDE.S367281
Arun Sadasivan, Roshni Ramesh
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Abstract

Background: Lymphangiomas or microcystic lymphatic malformations (MLM) are hamartomatous formations that occur due to the proliferation of lymphatic vessels. They commonly manifest in the head and neck region with only a few cases reported within the oral cavity. Lymphangioma circumscriptum in the gingiva is a rare condition which presents as asymptomatic pebbly gingival enlargement. They are characterized by lesions that are microscopic thin-walled cysts. Histopathologically, they show multiple dilated lymphatic channels which are lined by endothelial cells. The lumen is filled with lymphatic fluid, red blood cells, and other inflammatory cells. These are dispersed within connective tissue stroma. Multiple modalities of treatment have been reported, including surgical excision, laser therapy, and sclerotherapy.

Case presentation: This paper reports a rare case of multiple lymphangiomas of the gingiva in a 21-year-old female patient. The clinical picture, surgical treatment, histologic features, and immunohistochemistry [IHC] findings are presented. The histologic findings of lymphangioma were confirmed with IHC being positive for lymphatic marker D2-40. The patient was followed up for a period of 2 years, with no recurrence noted.

Conclusion: Lymphangiomas or microcystic lymphatic malformations presenting as a gingival enlargement are a rare occurrence. Therefore, lymphangiomas may also be considered in the differential diagnosis of gingival enlargements.

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环状淋巴管瘤--牙龈增生的罕见原因:病例报告和文献综述。
背景:淋巴管瘤或微囊性淋巴畸形(MLM)是由于淋巴管增生而形成的肉瘤。淋巴管瘤通常发生在头颈部,只有少数病例发生在口腔。牙龈淋巴管瘤(Lymphangioma circumscriptum)是一种罕见的病症,表现为无症状的鹅卵石状牙龈增生。其特征是病变为显微镜下的薄壁囊肿。从组织病理学角度看,它们表现为多条扩张的淋巴管,内衬为内皮细胞。管腔内充满淋巴液、红细胞和其他炎性细胞。这些细胞分散在结缔组织基质中。已有多种治疗方法的报道,包括手术切除、激光治疗和硬化剂注射:本文报告了一例罕见的牙龈多发性淋巴管瘤病例,患者为 21 岁女性。本文介绍了该病例的临床表现、手术治疗、组织学特征和免疫组化[IHC]结果。淋巴管瘤的组织学结果经 IHC 证实为淋巴标记物 D2-40 阳性。对患者进行了为期两年的随访,未发现复发:淋巴管瘤或微囊性淋巴畸形表现为牙龈肿大的情况非常罕见。因此,在牙龈肿大的鉴别诊断中也应考虑淋巴管瘤。
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来源期刊
CiteScore
3.90
自引率
5.60%
发文量
43
审稿时长
16 weeks
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