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一名患有遗传性低磷性佝偻病的25岁男性双侧股骨颈假关节。

Bilateral pseudarthrosis of the femoral neck in a 25-year-old male with hereditary hypophosphatemic rickets.

作者信息

Anthonissen Joris, Ossendorf Christian, Vetter Thomas, Habermann Björn, Rommens Pol M

机构信息

Department of Orthopaedics and Traumatology, University Medical Center, Johannes Gutenberg University of Mainz, Langenbeckstraße 1, 55131 Mainz, Germany.

出版信息

Case Rep Orthop. 2014;2014:312712. doi: 10.1155/2014/312712. Epub 2014 May 15.

DOI:10.1155/2014/312712
PMID:24955267
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4052474/
Abstract

Hereditary hypophosphatemic rickets (HHR) is a rare disorder of renal phosphate wasting and the most common form of heritable rickets. Here, we report a case of an active 25-year-old male with HHR showing atraumatic bilateral femoral neck pseudarthrosis after 4 years of consecutive knee pain. A conservative therapy was administered, taking into account both the risks of surgical treatment and the little impairment even in the sport activities which the patient experienced.

摘要

遗传性低磷性佝偻病（HHR）是一种罕见的肾性磷酸盐消耗性疾病，也是遗传性佝偻病最常见的形式。在此，我们报告一例25岁患有HHR的活跃男性病例，该患者在连续4年膝关节疼痛后出现双侧股骨颈无创伤性假关节。考虑到手术治疗的风险以及患者在体育活动中所经历的轻微损伤，我们给予了保守治疗。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1fbf/4052474/ef2ba6bce49c/CRIOR2014-312712.003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1fbf/4052474/dae409b9efdb/CRIOR2014-312712.001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1fbf/4052474/d4eb062ca4ad/CRIOR2014-312712.002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1fbf/4052474/ef2ba6bce49c/CRIOR2014-312712.003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1fbf/4052474/dae409b9efdb/CRIOR2014-312712.001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1fbf/4052474/d4eb062ca4ad/CRIOR2014-312712.002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1fbf/4052474/ef2ba6bce49c/CRIOR2014-312712.003.jpg

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本文引用的文献

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