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特发性家族性肢端骨质溶解症:骨组织形态计量学研究及黑吉二氏综合征文献综述

Idiopathic familial acroosteolysis: histomorphometric study of bone and literature review of the Hajdu-Cheney syndrome.

作者信息

Udell J, Schumacher H R, Kaplan F, Fallon M D

出版信息

Arthritis Rheum. 1986 Aug;29(8):1032-8. doi: 10.1002/art.1780290815.

DOI:10.1002/art.1780290815
PMID:3527178
Abstract

We describe a 27-year-old man with familial acroosteolysis involving 9 fingers. Bone biopsy of an affected digit showed osteolysis with no tetracycline deposition, rare osteoclasts, increased vascularity, and numerous mast cells. In contrast, the iliac crest bone showed active bone remodeling and normal double-tetracycline labeling. We believe mast cells deserve further study as possible factors in this form of localized osteolysis.

摘要

我们描述了一名27岁患有家族性肢端骨质溶解症累及9根手指的男性。对一根受累手指进行骨活检显示骨质溶解,无四环素沉积,破骨细胞罕见,血管增多,且有大量肥大细胞。相比之下,髂嵴骨显示有活跃的骨重塑和正常的双四环素标记。我们认为肥大细胞作为这种局限性骨质溶解症的可能因素值得进一步研究。

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Idiopathic familial acroosteolysis: histomorphometric study of bone and literature review of the Hajdu-Cheney syndrome.特发性家族性肢端骨质溶解症:骨组织形态计量学研究及黑吉二氏综合征文献综述
Arthritis Rheum. 1986 Aug;29(8):1032-8. doi: 10.1002/art.1780290815.
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Hereditary osteodysplasia with acro-osteolysis. (The Hajdu-Cheney syndrome).伴有肢端骨质溶解的遗传性骨发育异常(哈伊杜-切尼综合征)。
Am J Med. 1978 Oct;65(4):627-36. doi: 10.1016/0002-9343(78)90851-3.
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Severe osteoporosis in familial Hajdu-Cheney syndrome: progression of acro-osteolysis and osteoporosis during long-term follow-up.家族性哈伊杜-切尼综合征中的严重骨质疏松症:长期随访期间肢端骨质溶解和骨质疏松症的进展
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A genetic acro-osteolysis syndrome. A Hajdu-Cheney syndrome.一种遗传性肢端骨质溶解综合征。一种哈伊杜-切尼综合征。
Acta Rhumatol Belg. 1978 Jan-Jun;2(1-2):45-51.
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High turnover osteoporosis in acro-osteolysis (Hajdu-Cheney syndrome).肢端骨质溶解症(哈伊杜-切尼综合征)中的高转换型骨质疏松症。
J Endocrinol Invest. 1990 Mar;13(3):251-5. doi: 10.1007/BF03349553.
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[Hajdu-Cheney Syndrome: a case of acroosteolysis].[哈伊杜-切尼综合征:一例肢端骨质溶解症]
Acta Reumatol Port. 2007 Apr-Jun;32(2):169-74.
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Hajdu--Cheney syndrome: evolution of phenotype and clinical problems.哈伊杜-切尼综合征:表型演变与临床问题
Am J Med Genet. 2001 May 15;100(4):292-310. doi: 10.1002/1096-8628(20010515)100:4<292::aid-ajmg1308>3.0.co;2-4.
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[Idiopathic osteolysis (Hajdu-Cheney) (author's transl)].特发性骨质溶解症(哈伊杜-切尼综合征)(作者译)
Rofo. 1978 Jan;128(1):75-9.
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The acro-osteolysis (Hadju-Cheney) syndrome. Review of the literature and report of a case.肢端骨质溶解(哈朱-切尼)综合征。文献综述及一例病例报告。
J Periodontol. 1984 Apr;55(4):224-9. doi: 10.1902/jop.1984.55.4.224.
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Sporadic idiopathic acroosteolysis with cranio-skeletal dysplasis, polycystic kidneys and glomerulonephritis. A case of the Hajdu-Cheney syndrome.伴有颅骨骼发育异常、多囊肾和肾小球肾炎的散发性特发性肢端骨质溶解症。一例哈伊杜-切尼综合征病例。
Pediatr Radiol. 1977 Sep 1;6(2):116-20. doi: 10.1007/BF00973535.

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