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伴有巨细胞纤维瘤的黑素斑

Melanotic Macule in Conjunction with a Giant Cell Fibroma.

作者信息

Seitz Samantha D, Dinh Thanhphuong N, Yoon Thomas Yh

机构信息

Department of Restorative Dentistry, Lake Erie College of Osteopathic Medicine, School of Dental Medicine, Bradenton Florida, USA.

Department of Periodontology, Lake Erie College of Osteopathic Medicine, School of Dental Medicine, Bradenton, Florida, USA, Phone: +9414051506, e-mail:

出版信息

J Contemp Dent Pract. 2017 Oct 1;18(10):981-985. doi: 10.5005/jp-journals-10024-2160.

Abstract

INTRODUCTION

The aim of this study is to describe a case of a melanotic macule found in conjunction with a giant cell fibroma (GCF). For oral pigmented lesions without an identifiable etiologic factor, critical factors in determining the differential diagnosis are clinical history, symmetry, and uniformity of the lesions. Potential differential diagnosis includes racial pigmentation, endocrine disturbance, Peutz-Jeghers syndrome, trauma, hemochromatosis, oral malignant melanoma, or idiopathic etiology and melanotic macules. Melanotic macules are the most common solitary pigmented melanocytic lesions in the oral mucosa, corresponding to 86.1% of melanocytic lesions of the mouth. Giant cell fibromas are reactive connective tissue lesions in the oral cavity. They were first described as a distinct entity in 1974 by Weathers and Callihan and make up around 5 to 10% of all oral mucosa fibrous lesions. They are commonly mistaken for other growths, such as pyogenic granuloma and fibroma, and diagnosis is accurately based on its distinctive histopathology. This article presents the clinicopathologic findings of a 15-year-old Hispanic male presenting for biopsy of a melanotic macule on the mandibular anterior buccal gingiva. Histologic evaluation of the specimen revealed that the lesion also contained a GCF. Pathologic lesions of the mouth should be carefully diagnosed. Conventionally, histologic evaluation is the gold standard to produce a final diagnosis. As evidenced in this article, multiple lesions may exist in a site and may be mistakenly diagnosed as a single entity.

CLINICAL SIGNIFICANCE

While each lesion has been reported individually, in reviewing the literature, no cases were reported in which both histopathologic findings of GCF and melanotic macule were present within the same lesion.

摘要

引言

本研究旨在描述一例与巨细胞纤维瘤(GCF)同时出现的黑素斑病例。对于无明确病因的口腔色素沉着病变,确定鉴别诊断的关键因素是临床病史、病变的对称性和均匀性。潜在的鉴别诊断包括种族色素沉着、内分泌紊乱、黑斑息肉综合征、创伤、血色素沉着症、口腔恶性黑色素瘤或特发性病因及黑素斑。黑素斑是口腔黏膜中最常见的孤立性色素沉着黑素细胞病变,占口腔黑素细胞病变的86.1%。巨细胞纤维瘤是口腔内的反应性结缔组织病变。它们于1974年由韦瑟斯和卡利汉首次描述为一种独特的实体,占所有口腔黏膜纤维性病变的5%至10%左右。它们常被误诊为其他肿物,如化脓性肉芽肿和纤维瘤,准确的诊断基于其独特的组织病理学。本文介绍了一名15岁西班牙裔男性下颌前颊侧牙龈黑素斑活检的临床病理结果。对标本的组织学评估显示病变还包含一个巨细胞纤维瘤。口腔的病理性病变应仔细诊断。传统上,组织学评估是做出最终诊断的金标准。如本文所示,一个部位可能存在多种病变,可能被误诊为单一实体。

临床意义

虽然每种病变都有单独报道,但在回顾文献时,未发现同一病变中同时存在巨细胞纤维瘤和黑素斑组织病理学表现的病例。

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