进行性面肌萎缩累及下颌骨和牙齿:1例报告

IF 2.4 3区 医学 Q2 DENTISTRY, ORAL SURGERY & MEDICINE Oral Surgery Oral Medicine Oral Pathology Oral Radiology Pub Date : 2025-03-01 Epub Date: 2025-02-04 DOI:10.1016/j.oooo.2024.11.025
Dr. Marta C.L. Somaschini , Dr. Tina Meisami , Dr. Susanne E. Perschbacher
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引用次数: 0

摘要

本病例报告描述了一位19岁男性进行性面瘫(PHA)患者,也被称为Parry-Romberg综合征,这是一种罕见的疾病,其特征是面部硬组织和软组织逐渐萎缩,原因不明。患者寻求矫正面部不对称,自童年以来一直是进行性的。临床检查显示右下半部脸比左半部脸小。无线状硬皮病。患者无外伤史。颧区和外耳正常。颅面锥束计算机断层扫描用于术前计划,并提交口腔颌面放射学审查。放射学检查显示右下颌骨发育不全,但颞下颌关节结构正常。牙齿异常也被注意到,包括根吸收和缺失的下颌前磨牙在患侧。右侧面部软组织严重萎缩,特别是在联合/副淋巴区附近。鉴别诊断PHA的诊断需要排除单侧面部发育不全的其他原因,包括特发性或创伤性下颌发育不全和眼-耳-椎谱。正常的颞下颌关节结构和严重的面部软组织萎缩以及儿童期进行性改变的历史有利于PHA的诊断。根据临床表现和影像学表现,诊断为PHA。治疗计划包括下颌角和体植入手术,以解决面部不对称,第二步计划进行脂肪移植,以解决软组织缺损。结论本病例报告显示了PHA的特点,包括很少报道的下颌骨骨和牙的变化。诊断依赖于影像学排除和临床检查的结合。治疗包括骨和软组织缺陷的矫正,以帮助减轻这种情况对审美和功能的影响。
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Mandibular osseous and dental involvement in progressive hemifacial atrophy: a case report

Clinical Presentation

This case report describes a 19-year-old male patient with progressive hemifacial atrophy (PHA), also known as Parry-Romberg syndrome, a rare condition characterized by gradual atrophy of facial hard and soft tissues of unknown etiology. The patient sought consultation to correct facial asymmetry, which had been progressive since childhood. Clinical examination revealed a smaller right lower half of the face compared with the left. There was no linear scleroderma present. The patient had no history of trauma. The malar region and external ear were normal. A craniofacial cone beam computed tomography scan was acquired for presurgical planning and submitted for oral and maxillofacial radiology review. Radiologic examination revealed hypoplasia of the right body of the mandible but normal temporomandibular joint structures. Dental abnormalities also were noted, including root resorption and a missing mandibular premolar on the affected side. There was severe atrophy of the facial soft tissues on the right, particularly near the symphyseal/parasymphyseal area.

Differential Diagnosis

Diagnosis of PHA requires ruling out other causes of unilateral facial hypoplasia including idiopathic or trauma-induced mandibular hypoplasia and oculo-auricular-vertebral spectrum. The normal temporomandibular joint structures and severe atrophy of the facial soft tissues with a history of progressive changes during childhood favor a diagnosis of PHA.

Diagnosis and Management

On the basis of the clinical presentation and radiographic findings, a diagnosis of PHA was made. The management plan included onlay mandibular angle and body implant surgery to address the facial asymmetry, with a second step planned for fat grafting to address the soft tissue deficiency.

Conclusion

This case report presents features of PHA including rarely-reported osseous and dental changes in the mandible. The diagnosis relies on a combination of radiographic exclusions and clinical examination. Management involves correction of osseous and soft tissue defects to help mitigate the aesthetic and functional impact of this condition.
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来源期刊
Oral Surgery Oral Medicine Oral Pathology Oral Radiology
Oral Surgery Oral Medicine Oral Pathology Oral Radiology DENTISTRY, ORAL SURGERY & MEDICINE-
CiteScore
3.80
自引率
6.90%
发文量
1217
审稿时长
2-4 weeks
期刊介绍: Oral Surgery, Oral Medicine, Oral Pathology and Oral Radiology is required reading for anyone in the fields of oral surgery, oral medicine, oral pathology, oral radiology or advanced general practice dentistry. It is the only major dental journal that provides a practical and complete overview of the medical and surgical techniques of dental practice in four areas. Topics covered include such current issues as dental implants, treatment of HIV-infected patients, and evaluation and treatment of TMJ disorders. The official publication for nine societies, the Journal is recommended for initial purchase in the Brandon Hill study, Selected List of Books and Journals for the Small Medical Library.
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