Casari S, Rossi V, Varenna M, Gasparini M, Parafioriti A, Failoni S, Sinigaglia L
Department of Rheumatology, Pini Institute, Milan, Italy.
Clin Exp Rheumatol. 2003 Jul-Aug;21(4):493-6.
A case of tumor-induced osteomalacia in a 35-year-old woman suffering from severe bone pain and muscle weakness is described. This uncommon disease is characterized by a reduced serum phosphorus level with elevated urinary phosphate excretion, normocalcemia, high serum bone alkaline phosphatase and a deficiency of 1,25 dihydroxyvitamin D3. The tumors responsible for oncogenic osteomalacia are usually small, benign and commonly located in bone or soft tissues of the head and the limbs, so the diagnosis can often be difficult. In this case a 111In-pentetreotide scintigraphy was able to detect a hemangiopericytoma located in the right mascellar sinus. Removal of the tumor resulted in the reversal of clinical and biochemical abnormalities.
本文描述了一名35岁女性患肿瘤性骨软化症的病例,该患者伴有严重骨痛和肌肉无力。这种罕见疾病的特征是血清磷水平降低、尿磷排泄增加、血钙正常、血清骨碱性磷酸酶升高以及1,25-二羟维生素D3缺乏。导致致癌性骨软化症的肿瘤通常较小,为良性,常见于头和四肢的骨骼或软组织中,因此诊断往往困难。在该病例中,111铟-喷替酸奥曲肽闪烁扫描能够检测到位于右泪囊窦的血管外皮细胞瘤。切除肿瘤后,临床和生化异常得以逆转。