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1
Osteosclerotic metaphyseal dysplasia, dysosteosclerosis or osteomyelitis? Paediatric case presentation with associated mandibular swelling and a review of the literature.骨硬化性干骺端发育不良、骨硬化症或骨髓炎?伴有下颌肿胀的儿科病例报告并文献复习。
BMJ Case Rep. 2022 May 12;15(5):e246789. doi: 10.1136/bcr-2021-246789.
2
Osteosclerotic metaphyseal dysplasia with extensive interstitial pulmonary lesions: a case report and literature review.伴有广泛间质性肺病变的骨硬化性干骺端发育异常:一例报告及文献复习
Skeletal Radiol. 2015 Oct;44(10):1529-33. doi: 10.1007/s00256-015-2190-9. Epub 2015 Jun 18.
3
An extremely rare case: osteosclerotic metaphyseal dysplasia.一个极其罕见的病例:骨硬化性干骺端发育异常。
Genet Couns. 2013;24(1):69-74.
4
Osteomyelitis of the mandible in a patient with dysosteosclerosis. Report of a case.骨硬化发育异常患者的下颌骨骨髓炎。病例报告。
Oral Surg Oral Med Oral Pathol. 1991 Feb;71(2):144-7. doi: 10.1016/0030-4220(91)90455-l.
5
Osteopetrosis: Gene-based nosology and significance Dysosteosclerosis.骨硬化症:基于基因的疾病分类学及意义 骨发育异常性骨硬化症
Bone. 2023 Feb;167:116615. doi: 10.1016/j.bone.2022.116615. Epub 2022 Nov 17.
6
[Osteomyelitis of the mandible and dysosteosclerosis].[下颌骨骨髓炎与骨发育异常性骨硬化症]
Arch Pediatr. 2015 Nov;22(11):1154-6. doi: 10.1016/j.arcped.2015.08.005. Epub 2015 Sep 26.
7
Case Report: Osteosclerotic metaphyseal dysplasia with optic nerve involvement and progressive osteonecrosis of the jaw due to a novel LRRK1 mutation.病例报告:LRRK1 基因突变导致伴有视神经受累的硬化性干骺端发育不良和进行性下颌骨坏死。
Front Endocrinol (Lausanne). 2023 Oct 18;14:1258340. doi: 10.3389/fendo.2023.1258340. eCollection 2023.
8
Mandibular osteomyelitis and multiple skeletal complications in Albers-Schönberg disease.阿尔伯斯-尚伯格病中的下颌骨骨髓炎及多种骨骼并发症
Singapore Med J. 2008 Sep;49(9):e229-33.
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Bell's palsy with facial bone involvement: A rare presentation of chronic nonbacterial osteomyelitis with literature review.伴有面骨受累的贝尔麻痹:慢性非细菌性骨髓炎的一种罕见表现并文献复习
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10
[Acute progressive primary chronic osteomyelitis in the mandibular bone in childhood - A case report].[儿童下颌骨急性进行性原发性慢性骨髓炎——一例报告]
Swiss Dent J. 2015;125(1):31-43. doi: 10.61872/sdj-2015-01-03.

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Chronic Diffuse Sclerosing Osteomyelitis of the Mandible: The Use of Bisphosphonates as a Treatment for a Rare and Challenging Condition.下颌骨慢性弥漫性硬化性骨髓炎:双膦酸盐在一种罕见且具有挑战性疾病治疗中的应用。
Medicina (Kaunas). 2024 May 30;60(6):917. doi: 10.3390/medicina60060917.
2
Osteosclerotic Metaphyseal Dysplasia Due to a Likely Pathogenic LRRK1 Variant as a Cause of Recurrent Long Bone Fractures.由于可能致病的LRRK1变异导致的骨硬化性干骺端发育异常作为复发性长骨骨折的原因
JBMR Plus. 2023 Jun 28;7(8):e10755. doi: 10.1002/jbm4.10755. eCollection 2023 Aug.

本文引用的文献

1
Assessing the optimal imaging modality in the diagnosis of jaw osteomyelitis. A meta-analysis.评估颌骨骨髓炎诊断的最佳影像学方式。一项荟萃分析。
Br J Oral Maxillofac Surg. 2021 Nov;59(9):982-992. doi: 10.1016/j.bjoms.2020.11.012. Epub 2020 Nov 27.
2
Adult Osteosclerotic Metaphyseal Dysplasia With Progressive Osteonecrosis of the Jaws and Abnormal Bone Resorption Pattern Due to a LRRK1 Splice Site Mutation.因LRRK1剪接位点突变导致的成人骨硬化性干骺端发育异常伴颌骨进行性骨坏死及异常骨吸收模式
J Bone Miner Res. 2020 Jul;35(7):1322-1332. doi: 10.1002/jbmr.3995. Epub 2020 Mar 19.
3
Identification of a novel LRRK1 mutation in a family with osteosclerotic metaphyseal dysplasia.在一个患有骨硬化性干骺端发育异常的家族中鉴定出一种新的LRRK1突变。
J Hum Genet. 2017 Mar;62(3):437-441. doi: 10.1038/jhg.2016.136. Epub 2016 Nov 10.
4
The imaging of osteomyelitis.骨髓炎的影像学检查
Quant Imaging Med Surg. 2016 Apr;6(2):184-98. doi: 10.21037/qims.2016.04.01.
5
Identification of biallelic LRRK1 mutations in osteosclerotic metaphyseal dysplasia and evidence for locus heterogeneity.骨硬化性干骺端发育异常中双等位基因LRRK1突变的鉴定及基因座异质性证据
J Med Genet. 2016 Aug;53(8):568-74. doi: 10.1136/jmedgenet-2016-103756. Epub 2016 Apr 7.
6
Osteosclerotic metaphyseal dysplasia with extensive interstitial pulmonary lesions: a case report and literature review.伴有广泛间质性肺病变的骨硬化性干骺端发育异常:一例报告及文献复习
Skeletal Radiol. 2015 Oct;44(10):1529-33. doi: 10.1007/s00256-015-2190-9. Epub 2015 Jun 18.
7
Acute osteomyelitis in children.儿童急性骨髓炎
N Engl J Med. 2014 Apr 3;370(14):1365-6. doi: 10.1056/NEJMc1402234.
8
A case report of dysosteosclerosis observed from the prenatal period.产前观察到的骨硬化发育异常病例报告。
Clin Pediatr Endocrinol. 2010 Jul;19(3):57-62. doi: 10.1297/cpe.19.57. Epub 2010 Aug 31.
9
An extremely rare case: osteosclerotic metaphyseal dysplasia.一个极其罕见的病例:骨硬化性干骺端发育异常。
Genet Couns. 2013;24(1):69-74.
10
Surgical management of primary chronic osteomyelitis of the jaws in children: a prospective analysis of five cases and review of the literature.儿童颌骨原发性慢性骨髓炎的外科治疗:5例前瞻性分析及文献复习
Oral Maxillofac Surg. 2011 Mar;15(1):41-50. doi: 10.1007/s10006-010-0248-3. Epub 2010 Oct 27.

骨硬化性干骺端发育不良、骨硬化症或骨髓炎?伴有下颌肿胀的儿科病例报告并文献复习。

Osteosclerotic metaphyseal dysplasia, dysosteosclerosis or osteomyelitis? Paediatric case presentation with associated mandibular swelling and a review of the literature.

机构信息

Oral and Maxillofacial Surgery, Birmingham Children's Hospital NHS Foundation Trust, Birmingham, UK

Oral and Maxillofacial Surgery, Queen Elizabeth Hospital Birmingham, Birmingham, UK.

出版信息

BMJ Case Rep. 2022 May 12;15(5):e246789. doi: 10.1136/bcr-2021-246789.

DOI:10.1136/bcr-2021-246789
PMID:35550322
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9109017/
Abstract

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.

摘要

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。