Mukhopadhyay Santanu, Chattopadhyay Abira, Bhattacharya Raja, Roy Ushapati
Department of Pedodontics and Preventive Dentistry, Dr. R Ahmed Dental College and Hospital, Kolkata, West Bengal, India.
J Indian Soc Pedod Prev Dent. 2016 Apr-Jun;34(2):180-4. doi: 10.4103/0970-4388.180450.
Gorham's disease or vanishing bone disease is a rare, progressive musculoskeletal disorder characterized by resorption of bone matrix, and later replaced by fibrous connective tissue. The disease has no specific predilection for age, gender, or race. The most common sites of involvement are the shoulder and pelvic bones. To date, nearly 50 cases of Gorham's disease with maxillofacial involvement have been reported in the literature. The etiology of Gorham's disease is not known, clinical features are variable, and prognosis is generally good unless vital structures are involved. Due to the rarity of the condition, no definite treatment protocol exists for this disorder. Here, we described a pediatric case of Gorham's disease with mandibular involvement.
戈勒姆病或骨质消失症是一种罕见的进行性肌肉骨骼疾病,其特征是骨基质吸收,随后被纤维结缔组织替代。该疾病在年龄、性别或种族方面没有特定的偏好。最常受累的部位是肩部和骨盆骨。迄今为止,文献中已报道了近50例累及颌面的戈勒姆病病例。戈勒姆病的病因尚不清楚,临床特征多变,除非重要结构受累,否则预后一般良好。由于该病罕见,目前尚无针对该疾病的确切治疗方案。在此,我们描述了一例累及下颌骨的儿童戈勒姆病病例。