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cherubism:两名兄弟姐妹的锥形束计算机断层扫描结果

Cherubism: Cone-Beam Computed Tomography Findings in Two Siblings.

作者信息

Mohod Swapnil, Dadgal Komal V

机构信息

Oral Medicine and Radiology, Sharad Pawar Dental College and Hospital, Datta Meghe Institue of Higher Education and Research, Wardha, IND.

出版信息

Cureus. 2024 Feb 19;16(2):e54465. doi: 10.7759/cureus.54465. eCollection 2024 Feb.

Abstract

Cherubism is an uncommon, multilocular cystic condition of the jaws. This autosomal dominant, nonneoplastic, fibro-osseous condition of the jaws affects children and is self-limiting. Clinically, it shows up as an expansion or distortion of the jaw together with an unnatural teeth alignment. In their most severe forms, these deformations might cause phonation difficulties, decreased pharynx lumen, visual issues, and psychological effects. This case report describes a case report of two siblings involving the maxilla and the mandible presenting with a painless bilateral symmetrical enlargement. Cherubism is a hereditary condition characterized by nonneoplastic bone lesions that damage the jaws. Surgery should be used to resolve any functional or aesthetically problematic issues. Typically, the surgical procedure is postponed until after puberty.

摘要

cherubism是一种罕见的颌骨多房囊性病变。这种常染色体显性遗传的、非肿瘤性的颌骨纤维-骨病变影响儿童,且具有自限性。临床上,表现为颌骨膨胀或变形以及牙齿排列不自然。在最严重的情况下,这些畸形可能导致发声困难、咽腔缩小、视觉问题和心理影响。本病例报告描述了两例涉及上颌骨和下颌骨的兄弟姐妹病例,表现为无痛性双侧对称性肿大。cherubism是一种遗传性疾病,其特征是损害颌骨的非肿瘤性骨病变。应采用手术解决任何功能或美学方面的问题。通常,手术会推迟到青春期后进行。

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