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一名年轻患者的特发性二水焦磷酸钙晶体沉积病合并隆突性骨肥厚综合征病例。

An idiopathic case of calcium pyrophosphate dihydrate crystal deposition disease with crowned dens syndrome in a young patient.

作者信息

Unlu Zeliha, Tarhan Serdar, Ozmen Eylem Mete

机构信息

Department of Physical Medicine and Rehabilitation, Celal Bayar University, Medical Faculty, Manisa, Turkey.

出版信息

South Med J. 2009 Sep;102(9):949-51. doi: 10.1097/SMJ.0b013e3181b08c26.

Abstract

Calcium pyrophosphate dihydrate (CPPD) crystal deposition disease is rare in patients under the age of 40 in the absence of metabolic or familial predisposition. A high incidence of involvement of the transverse ligament of the atlas in CPPD deposition disease was reported. However, involvement of the craniocervical junction is rarely symptomatic. We report a rare case in a young male with severe idiopathic CPPD crystal deposition disease, including crowned dens syndrome in the cervical spine.

摘要

在没有代谢或家族易感性的情况下,40岁以下的患者很少发生二水焦磷酸钙(CPPD)晶体沉积病。据报道,CPPD沉积病中寰椎横韧带受累的发生率较高。然而,颅颈交界区受累很少有症状。我们报告了一例年轻男性严重特发性CPPD晶体沉积病的罕见病例,包括颈椎的齿突冠征综合征。

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