Unlu Zeliha, Tarhan Serdar, Ozmen Eylem Mete
Department of Physical Medicine and Rehabilitation, Celal Bayar University, Medical Faculty, Manisa, Turkey.
South Med J. 2009 Sep;102(9):949-51. doi: 10.1097/SMJ.0b013e3181b08c26.
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.
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。