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Engelmann's disease of bone--a systemic disorder?

作者信息

Crisp A J, Brenton D P

出版信息

Ann Rheum Dis. 1982 Apr;41(2):183-8. doi: 10.1136/ard.41.2.183.

DOI:10.1136/ard.41.2.183
PMID:7073346
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1000905/
Abstract

A patient with Engelmann's disease of bone (progressive diaphyseal dysplasia) also suffered from Raynaud's phenomenon, multiple nail fold infarcts, anaemia, leucopenia, hepatosplenomegaly, and a raised erythrocyte sedimentation rate. Her mother, who also had this inherited bone disease, was known to have Raynaud's phenomenon, necrotising vasculitis, and digital gangrene. Review of other published cases of Engelmann's disease indicates that some of these features are not uncommon. It is argued that Engelmann's disease is not primarily a metabolic bone disease but may be a systemic disorder which might be included within the spectrum of the inflammatory connective tissue diseases. The beneficial effects of steroid treatment on both skeletal and systemic features are compatible with this view.

摘要
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/844b/1000905/16b0cd884402/annrheumd00109-0086-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/844b/1000905/aae269e5ac3a/annrheumd00109-0084-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/844b/1000905/5c1400e25ffa/annrheumd00109-0085-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/844b/1000905/e5f96d1e7781/annrheumd00109-0085-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/844b/1000905/7d473d3c1439/annrheumd00109-0086-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/844b/1000905/16b0cd884402/annrheumd00109-0086-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/844b/1000905/aae269e5ac3a/annrheumd00109-0084-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/844b/1000905/5c1400e25ffa/annrheumd00109-0085-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/844b/1000905/e5f96d1e7781/annrheumd00109-0085-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/844b/1000905/7d473d3c1439/annrheumd00109-0086-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/844b/1000905/16b0cd884402/annrheumd00109-0086-b.jpg

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本文引用的文献

1
Corticosteroids in the treatment of Engelmann's disease: progressive diaphyseal dysplasia.
Pediatrics. 1970 Oct;46(4):523-31.
2
Camurati-Engelmann disease. Genetics and clinical manifestations with a review of the literature.卡姆拉蒂-恩格尔曼病。遗传学与临床表现并文献综述
J Med Genet. 1972 Mar;9(1):73-85. doi: 10.1136/jmg.9.1.73.
3
Clinical and biochemical studies in Engelmann's disease (progressive diaphyseal dysplasia).
Q J Med. 1977 Apr;46(182):273-94.
高骨量的遗传结构。
Front Endocrinol (Lausanne). 2020 Oct 29;11:595653. doi: 10.3389/fendo.2020.595653. eCollection 2020.
4
Seropositive Rheumatoid Arthritis with Very Unusual X-ray Findings.血清阳性类风湿关节炎伴非常不寻常的X线表现。
Eur J Case Rep Intern Med. 2018 Jul 26;5(7):000883. doi: 10.12890/2018_000883. eCollection 2018.
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Discrepancy between bone density and bone material strength index in three siblings with Camurati-Engelmann disease.三兄妹的骨密度和骨材料强度指数存在差异,患有 Camurati-Engelmann 病。
Osteoporos Int. 2017 Dec;28(12):3489-3493. doi: 10.1007/s00198-017-4198-6. Epub 2017 Aug 25.
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Friend or foe: high bone mineral density on routine bone density scanning, a review of causes and management.友敌之间:常规骨密度扫描中骨密度增高,原因和处理方法综述。
Rheumatology (Oxford). 2013 Jun;52(6):968-85. doi: 10.1093/rheumatology/ket007. Epub 2013 Feb 27.
7
Camurati-Engelmann disease: unique variant featuring a novel mutation in TGFβ1 encoding transforming growth factor beta 1 and a missense change in TNFSF11 encoding RANK ligand.卡姆鲁蒂-恩格尔曼病:一种独特的变异型,其特征在于 TGFβ1 编码转化生长因子β 1 的新突变和 TNFSF11 编码 RANK 配体的错义变化。
J Bone Miner Res. 2011 May;26(5):920-33. doi: 10.1002/jbmr.283.
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Ghosal type hemato-diaphyseal dysplasia: a rare variety of Engelmann's disease.
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Camurati-Engelmann disease: review of the clinical, radiological, and molecular data of 24 families and implications for diagnosis and treatment.卡姆拉蒂-恩格尔曼病:24个家族的临床、放射学及分子数据回顾以及对诊断和治疗的意义
J Med Genet. 2006 Jan;43(1):1-11. doi: 10.1136/jmg.2005.033522. Epub 2005 May 13.
10
Genetic mapping of the Camurati-Engelmann disease locus to chromosome 19q13.1-q13.3.卡姆拉蒂-恩格尔曼病基因座定位于19号染色体q13.1-q13.3区域。
Am J Hum Genet. 2000 Jan;66(1):143-7. doi: 10.1086/302728.