Angiero Francesca, Farronato Giampietro, Benedicenti Stefano, Vinci Raffaele, Farronato Davide, Magistro Sarah, Stefani Michele
University of Milan Biccoca, Italy.
Cranio. 2009 Jan;27(1):24-32. doi: 10.1179/crn.2009.005.
Condylar hyperplasia is a rare disorder characterized by an increased volume of the condyle, ramus, and mandibular body leading to facial asymmetry. We present three cases of condylar hyperplasia: two women and one man, age range 27 to 34. Clinically, all three patients showed a deviation of the mandible to the opposite side and a protruded position of the chin, hypertrophy of the lower border of the mandible, combined with an elongation of the mandibular ramus, open-bite on the deformed side, and cross-bite on the opposite side. In all three cases, scintigraphy showed an increased uptake. Radiography and CT scanning confirmed the clinical diagnosis and patients were subjected to surgery, comprising high condylectomy on the affected side with access in the pre-tragus area. The surgical piece sent to the Institute of Pathological Anatomy for histological examination revealed a nonuniform picture, in terms of both the depth of cartilage islands and the thickness of the fibrous layer covering the joint surface. Common to all three cases, however, was the apparent evolution of fibrous tissue to cartilage, and of this to compact bone tissue. At two-four years, all cases have maintained a good occlusal response. The asymmetric deformity of the mandible resulting from the rare condition of hemimandibular hyperplasia is presented and the clinical, histopathological and therapeutic aspects discussed.
髁突增生是一种罕见的疾病,其特征为髁突、下颌支和下颌体体积增大,导致面部不对称。我们报告三例髁突增生病例:两名女性和一名男性,年龄在27至34岁之间。临床上,所有三名患者均表现出下颌向对侧偏斜、下巴前突、下颌下缘肥厚,同时伴有下颌支伸长、患侧开牙合以及对侧反牙合。在所有三例病例中,闪烁扫描显示摄取增加。X线摄影和CT扫描证实了临床诊断,患者接受了手术,包括在患侧进行高位髁突切除术,手术入路为耳屏前区域。送检至病理解剖研究所进行组织学检查的手术标本显示,在软骨岛深度和覆盖关节面的纤维层厚度方面,呈现出不均匀的图像。然而,所有三例病例的共同之处在于,纤维组织明显演变为软骨,进而演变为致密骨组织。在两到四年的时间里,所有病例均保持了良好的咬合反应。本文介绍了由半侧下颌骨增生这种罕见病症导致的下颌骨不对称畸形,并讨论了其临床、组织病理学和治疗方面的情况。