Institute of Human Genetics, Soroka Medical Center, Faculty of Health Sciences, Ben Gurion University of Negev, Beer Sheva, Israel.
J Craniomaxillofac Surg. 2013 Mar;41(2):e39-41. doi: 10.1016/j.jcms.2012.07.008. Epub 2012 Aug 2.
Congenital insensitivity to pain with anhidrosis (CIPA) is a rare hereditary sensory and autonomic neuropathy (HSAN) characterized by pain, self-mutilating behaviour, anhidrosis and recurrent hyperthermia. CIPA has a multisystem involvement, including fractures of the extremities with slow healing, immunologic abnormalities, and a chronic inflammatory state. The mandible is reported to have a higher incidence of osteomyelitis, though mandibular fracture among CIPA patients, is very rare, with to our knowledge no reports in children. A case of pathological fracture of the mandible in a 6-year-old child with CIPA treated by ORIF is reported. In contrast to the slow healing reported in long bones, the mandible healed very quickly, possibly indicating that the osteoporotic mandible in this group of patients is different from that seen in the elderly. Furthermore, the standard ORIF technique can be safely used in this rare group.
先天性无痛无汗症(CIPA)是一种罕见的遗传性感觉和自主神经病(HSAN),其特征为疼痛、自残行为、无汗和反复发热。CIPA 多系统受累,包括四肢骨折愈合缓慢、免疫异常和慢性炎症状态。据报道,下颌骨的骨髓炎发病率更高,尽管 CIPA 患者的下颌骨骨折非常罕见,但据我们所知,儿童中尚无报道。报告了一例 CIPA 患儿经 ORIF 治疗的下颌骨病理性骨折。与长骨报道的愈合缓慢不同,下颌骨愈合非常快,这可能表明该组患者的骨质疏松下颌骨与老年人不同。此外,标准的 ORIF 技术可安全用于这一罕见人群。