[进行性骨化性纤维发育不良：病例报告]
[Fibrodysplasia ossificans progressiva: case report].
作者信息
Puszczewicz Mariusz, Kołczewska Aleksandra, Zimmermann-Górska Irena, Majewski Dominik, Ogrodowicz Agnieszka
机构信息
Katedra i Klinika Reumatologiczno-Rehabilitacyjna i Chorób Wewnetrznych, Uniwersytet Medyczny im. Karola Marcinkowskiego, Pozna6i.
出版信息
Pol Arch Med Wewn. 2007 Jan-Feb;117(1-2):53-6.
Fibrodysplasia ossificans progressiva (FOP) is a rare genetic disease characterized by widespread soft tissue ossification and congenital stigmata of the extremities. We report the case of a 33-year-old woman with clinical and radiological features of FOP. She was born with bilateral hallux valgus and at the age of 10 presented swelling and ossification of the left scapula. During the course of the disease numerous crises were observed. In this patient authors noticed FOP exacerbation after a surgical operation.
进行性骨化性纤维发育不良（FOP）是一种罕见的遗传性疾病，其特征为广泛的软组织骨化和肢体先天性畸形。我们报告一例具有FOP临床和放射学特征的33岁女性病例。她出生时患有双侧拇外翻，10岁时出现左肩胛骨肿胀和骨化。在疾病过程中观察到多次病情发作。在该患者中，作者注意到手术后FOP病情加重。
Zotero 插件