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本文引用的文献

1
Pycnodysostosis. A report of 3 clinical cases.致密性成骨不全症。3例临床病例报告。
Med Oral Patol Oral Cir Bucal. 2008 Oct 1;13(10):E633-5.
2
Molecular analysis and characterization of nine novel CTSK mutations in twelve patients affected by pycnodysostosis. Mutation in brief #961. Online.12例致密性骨发育不全患者中9种新型CTSK突变的分子分析与特征。简要突变#961。在线版。
Hum Mutat. 2007 May;28(5):524. doi: 10.1002/humu.9490.
3
Osteoclast diseases and dental abnormalities.破骨细胞疾病与牙齿异常。
Arch Oral Biol. 2005 Feb;50(2):115-22. doi: 10.1016/j.archoralbio.2004.11.016. Epub 2005 Jan 18.
4
Decreased bone turnover and deterioration of bone structure in two cases of pycnodysostosis.两例致密性骨发育不全患者的骨转换降低及骨结构破坏
J Clin Endocrinol Metab. 2004 Apr;89(4):1538-47. doi: 10.1210/jc.2003-031055.
5
Maxillofacial alterations in a family with pycnodysostosis.患有致密性骨发育不全症的一个家族中的颌面改变。
Med Oral. 2000 May-Jul;5(3):169-176.
6
Pycnodysostosis: clinical, radiologic, and endocrine evaluation and linear growth after growth hormone therapy.致密性成骨不全症：生长激素治疗后的临床、放射学及内分泌评估与线性生长
Metabolism. 2001 Aug;50(8):905-11. doi: 10.1053/meta.2001.24924.
7
Pyknodysostosis--a report of two cases with a brief review of the literature.致密性骨发育不全——两例报告并文献简要回顾
Int J Oral Maxillofac Surg. 2000 Dec;29(6):439-42.
8
Osteomyelitis of the jaws in pycnodysostosis.致密性骨发育不全症中的颌骨骨髓炎
Int J Oral Maxillofac Surg. 1987 Oct;16(5):615-9. doi: 10.1016/s0901-5027(87)80116-9.
9
Bilateral osteomyelitis of the mandible in pycnodysostosis. A case report.致密性骨发育不全症中的双侧下颌骨骨髓炎。病例报告。
Int J Oral Maxillofac Surg. 1991 Apr;20(2):71-2. doi: 10.1016/s0901-5027(05)80709-x.

致密性骨发育不全中的骨髓炎——2例临床病例报告

Osteomyelitis in pycnodysostosis - report of 2 clinical cases.

作者信息

S Rohit, B Praveen Reddy, B Sreedevi, Prakash Sandeep

机构信息

Reader, Department of Oral and Maxillofacial Surgery, Rajarajeswari Dental College and Hospital , Bangalore, India .

Professor & Head, Department of Oral and Maxillofacial Surgery, Government Dental College, RIMS , Imphal, India .

出版信息

J Clin Diagn Res. 2015 Jan;9(1):ZD15-7. doi: 10.7860/JCDR/2015/10114.5461. Epub 2015 Jan 1.

DOI:10.7860/JCDR/2015/10114.5461
PMID:25738091
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4347182/
Abstract

Pycnodysostosis is a rare craniofacial syndrome characterized by dwarfism, cranial anomalies, diffuse osteosclerosis where multiple fracture of long bones and osteomyelitis of jaw are frequent complications. This clinical entity was first described in 1962 by Maroteaux and Lamy. This article presents two clinical cases of pycnodysostosis with their clinical and radiological characteristics.

摘要

致密性成骨不全症是一种罕见的颅面综合征，其特征为侏儒症、颅骨异常、弥漫性骨硬化，长骨多发骨折和颌骨骨髓炎是常见并发症。这种临床病症于1962年由马罗泰克斯和拉米首次描述。本文介绍了两例致密性成骨不全症的临床病例及其临床和放射学特征。