Gupta Nitin, Pruthi Ankur, Kumar Suneel, Verma Ritu, Belho Ethel Shangne
Department of Nuclear Medicine and PET/CT, Mahajan Imaging Centre, Sir Ganga Ram Hospital, New Delhi, India.
Department of Nuclear Medicine, Manipal Hospital, New Delhi, India.
Indian J Nucl Med. 2019 Jul-Sep;34(3):209-212. doi: 10.4103/ijnm.IJNM_57_19.
Fibrodysplasia ossificans progressiva is a rare genetic disease believed to occur in approximately 1 in 2 million people worldwide and is characterized by progressive extraosseous ossification over the course of a lifetime in an inevitable and unpredictable episodic manner, with most patients being confined to a wheelchair by the third decade of life and requiring life-long care. The extraosseous calcification involves ligaments, tendons, muscles, and connective tissue leading to severe restriction of movements. Another hallmark of this condition is abnormal great toes. The diagnosis is often made on clinical and radiological examination, but Technetium-99m methylene diphosphonate (Tc-99m MDP) bone scan is usually indicated to determine the extent of the disease. We hereby present a case series comprising of four patients suffering from this debilitating illness who underwent Tc99m MDP bone scan for initial diagnosis and localizing sites of heterotopic ossification.
进行性骨化性纤维发育不良是一种罕见的遗传性疾病,据信全球约每200万人中就有1人患病,其特征是在一生中以不可避免且不可预测的发作方式进行性地在骨外形成骨组织,大多数患者在30岁时就需要依靠轮椅行动,并需要终身护理。骨外钙化累及韧带、肌腱、肌肉和结缔组织,导致严重的活动受限。这种疾病的另一个特征是大脚趾异常。诊断通常通过临床和放射学检查做出,但通常需要进行锝-99m亚甲基二膦酸盐(Tc-99m MDP)骨扫描以确定疾病的范围。我们在此呈现一个病例系列,包括四名患有这种使人衰弱疾病的患者,他们接受了Tc99m MDP骨扫描以进行初步诊断并确定异位骨化的部位。