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Hemochromatosis and femoral head aseptic osteonecrosis: a nonfortuitous association?

作者信息

Rollot Florence, Wechsler Bertrand, du Boutin Le Thi Huong, De Gennes Christian, Amoura Zahir, Hachulla Eric, Piette Jean-Charles

机构信息

Department of Internal Medicine, Pitie-Salpetriere Hospital, Paris, France.

出版信息

J Rheumatol. 2005 Feb;32(2):376-8.

PMID:15693103
Abstract

Chondrocalcinosis, chronic pseudo-osteoarthritis arthropathy, and osteoporosis are classic osteoarticular complications of hemochromatosis (HC). Within HC, femoral head aseptic osteonecrosis (FHAO) is not notified in textbooks. We describe 3 cases of FHAO occurring in this setting in 3 patients homozygous for the C282Y mutation on HFE gene who had no other risk factors for FHAO. FHAO was diagnosed 9 years before (Case 1), concomitantly with (Case 3), or 9 years after HC (Case 2). In one case, FHAO occurred although phlebotomies were regularly carried out. There are scarce data available in the literature on HC and FHAO. Our observations suggest FHAO may be an indicator for HC, and iron balance should be determined before considering FHAO as idiopathic. Thus phlebotomy may not be protective against the occurrence of FHAO. Studies are needed to determine the prevalence of HC in consecutive patients with FHAO.

摘要

相似文献

1
Hemochromatosis and femoral head aseptic osteonecrosis: a nonfortuitous association?
J Rheumatol. 2005 Feb;32(2):376-8.
2
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N Engl J Med. 2008 Jan 17;358(3):221-30. doi: 10.1056/NEJMoa073286.
3
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Isr Med Assoc J. 2004 Jan;6(1):30-3.
4
HLA haplotype A*03-B*07 in hemochromatosis probands with HFE C282Y homozygosity: frequency disparity in men and women and lack of association with severity of iron overload.HFE基因C282Y纯合子的血色素沉着症先证者中的HLA单倍型A*03 - B*07:男性和女性中的频率差异以及与铁过载严重程度缺乏关联
Blood Cells Mol Dis. 2005 Jan-Feb;34(1):38-47. doi: 10.1016/j.bcmd.2004.08.022.
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[Molecular genetic diagnostics and screening of hereditary hemochromatosis].[遗传性血色素沉着症的分子遗传学诊断与筛查]
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6
[Mutations in the HFE gene in patients with rheumatic diseases].
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7
Transferrin receptor-2 gene and non-C282Y homozygous patients with hemochromatosis.转铁蛋白受体-2基因与非C282Y纯合子血色素沉着症患者
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年龄相关的铁蛋白升高和 HFE C282Y 突变是男性症状性膝骨关节炎的危险因素:一项纵向队列研究。
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Hereditary hemochromatosis: a neglected diagnosis in orthopedics: a series of 7 patients with ankle arthritis, and a review of the literature.遗传性血色素沉着症:骨科领域被忽视的诊断:7例踝关节关节炎患者系列病例及文献综述
Acta Orthop. 2009 Jun;80(3):371-4. doi: 10.3109/17453670903035583.