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Combined cutaneous findings with segmental odontomaxillary dysplasia: Review of the literature and proposal of a new clinical classification

机译:结合皮肤发现与节段性上颌骨不典型增生:文献综述和新的临床分类建议

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摘要

Segmental odontomaxillary dysplasia is characterized by variability of its clinical and radiological features, and may mimic other fibro-osseous lesions. We describe the case of a segmental odontomaxillary dysplasia in a 12-year-old male comprising of dermal, gingival, bony, and dental abnormalities. He presented with left midfacial diffuse hyperkeratotic erythematous lesion, ipsilateral hypopigmentation of upper lip with indistinct vermilion border, left-sided facial swelling, unilateral maxillary enlargement and ipsilateral failure of eruption of permanent teeth. Radiographic imaging showed abnormal bony trabeculation, impacted and missing teeth. Histopathologic findings showed characteristic features of segmental odontomaxillary dysplasia. We herein report a case of this rare unusual anomaly, review the literature, and propose a new clinical classification based on the limited number of previously reported cases in an attempt to categorize the clinical variants of the condition which might be helpful when treatment options are to be considered. Clinicians should be aware of its presence when encountering patients presenting with a facial cutaneous lesion especially when it is associated with facial asymmetry and unresponsive to treatment.
机译:节段性牙颌上颌发育不良的特征是其临床和放射学特征的变化,并且可能模仿其他纤维骨病变。我们描述了由皮肤,牙龈,骨和牙齿畸形组成的12岁男性的分段上颌骨发育不良的情况。他表现为左面中部弥漫性过度角化性红斑病变,上唇同侧色素沉着,朱红边界不清晰,左侧面部肿胀,单侧上颌骨肿胀以及同侧恒牙萌发失败。影像学检查显示骨小梁异常,牙齿受累和缺失。组织病理学发现显示节段性上颌骨发育不良的特征。我们在此报告这种罕见的异常异常的情况,回顾文献,并基于有限数量的先前报道的病例提出新的临床分类,以试图对疾病的临床变异进行分类,这可能在治疗选择方面有所帮助。被考虑。当遇到患者出现面部皮肤病变时,尤其是与面部不对称相关且对治疗无反应的患者时,临床医生应意识到其存在。

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