Oral and Maxillofacial Surgery, Birmingham Children's Hospital NHS Foundation Trust, Birmingham, UK
Oral and Maxillofacial Surgery, Queen Elizabeth Hospital Birmingham, Birmingham, UK.
BMJ Case Rep. 2022 May 12;15(5):e246789. doi: 10.1136/bcr-2021-246789.
Osteosclerotic metaphyseal dysplasia (OMD) is an extremely rare form of osteopetrosis, which bears significant clinical similarities to dysosteosclerosis (DSS). We aim to present a rare case of OMD with mandibular swelling and osteomyelitis infection including diagnosis journey as well as management in 7-year-old patient. Literature review completed for OMD cases. Case report investigative methods include genetic testing, CT facial bones and MRI scan, orthopantogram and bone biopsies. An initial suspected diagnosis of DSS with chronic osteomyelitis was made. However, following genetic testing, a diagnosis of OMD was confirmed. Our patient underwent a surgical debulking procedure and antibiotic treatment. Less than 10 patients with this condition have been reported within the international literature. There is a wide range of presentation. OMD, DSS and osteomyelitis are all within a similar spectrum of bone conditions. Our understanding, regarding OMD, remains limited and, hence, further research is required to elucidate a thorough clinical picture.
骨硬化性干骺端发育不良(OMD)是一种极为罕见的骨质硬化症,其临床表现与骨发育不良(DSS)有显著相似之处。我们旨在介绍一例 7 岁患儿的下颌肿胀和骨髓炎感染的 OMD 罕见病例,包括诊断过程和治疗方法。我们对 OMD 病例进行了文献回顾。病例报告的研究方法包括基因检测、面部 CT 骨骼和 MRI 扫描、全景片和骨活检。最初怀疑为 DSS 合并慢性骨髓炎。然而,经过基因检测,确诊为 OMD。我们的患者接受了手术去瘤和抗生素治疗。国际文献中报道的此类病例不足 10 例。其临床表现多样。OMD、DSS 和骨髓炎都属于相似的骨骼疾病范畴。我们对 OMD 的认识仍然有限,因此需要进一步研究以阐明其全面的临床表现。