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下颌骨中央性巨细胞肉芽肿型和小梁状幼年骨化性纤维瘤型杂交瘤:口腔内罕见病变,并对其发病机制进行复习。

Hybrid tumor of central giant cell granuloma and trabecular juvenile ossifying fibroma of the mandible: A rare event in the oral cavity with a review on pathogenesis.

机构信息

Department of Oral Pathology, Government College of Dentistry, Indore, Madhya Pradesh, India.

Department of Oral Pathology, Index Institute of Dental Sciences, Indore, Madhya Pradesh, India.

出版信息

Indian J Pathol Microbiol. 2024 Jul 1;67(3):638-640. doi: 10.4103/ijpm.ijpm_623_22. Epub 2023 Jul 10.

Abstract

Hybrid tumors are rare lesions having features of multiple diseases in one lesion. A hybrid tumor of central giant cell granuloma (CGCG) and central ossifying fibroma (COF) shows the presence of microscopically large areas with CGCG character and large areas with COF features inside a single clinical lesion, separated by a transition zone. A rare type of COF is juvenile ossifying fibroma (JOF)-trabecular variant in the mandible. We present a unique and rare case of a hybrid tumor of the CGCG-JOF-trabecular variant in the mandible of a 14-year-old female which initially diagnosed with CGCG. The ambiguous pathogenesis of hybrid tumors and giant cells is reviewed. The goal of this article is to highlight the importance of careful clinical, radiological, and histopathological examination of each case to prevent misdiagnoses and recurrences. Similar and other cases must be reported in order to better understand the interrelationship between these hybrid lesions and their biological behavior.

摘要

混合瘤是一种罕见的病变,在一个病变中具有多种疾病的特征。中央巨细胞瘤(CGCG)和中央骨化性纤维瘤(COF)的混合瘤表现为在单个临床病变中存在具有 CGCG 特征的显微镜下大片区域和具有 COF 特征的大片区域,由过渡区隔开。下颌骨中 COF 的一种罕见类型是青少年骨化性纤维瘤(JOF)-小梁变体。我们报告了一例下颌骨 CGCG-JOF-小梁变体混合瘤的罕见病例,该患者最初被诊断为 CGCG。回顾了混合瘤和巨细胞瘤的模糊发病机制。本文的目的是强调仔细检查每个病例的临床、放射学和组织病理学的重要性,以防止误诊和复发。为了更好地理解这些混合病变及其生物学行为之间的相互关系,必须报告类似和其他病例。

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