Artul Suheil, Bowirrat Abdalla, Yassin Mustafa, Armaly Zaher
EMMS Nazareth, The Nazareth Hospital, Faculty of Medicine Bar-Ilan, Galilee University, 16100 Nazareth, Israel.
Case Rep Oncol Med. 2013;2013:909150. doi: 10.1155/2013/909150. Epub 2013 Aug 19.
Brown tumors are rare focal giant cell lesions of the bone caused by primary hyperparathyroidism (HPT). Brown tumor was reported in 1891; it presents as the end-stage findings of HPT. Common involvements are skull and pelvic girdle. We describe a case of 46-year-old female hemodialysis patient, with secondary HPT in whom multiple masses lesions of the left maxillary sinus and frontal bone were radiologically suspected to be brown tumor. This unusual manifestation of secondary HPT can be expected to occur with increased longevity of patients with renal failure and illustrates the need to include brown tumor in the differential diagnosis.
棕色瘤是由原发性甲状旁腺功能亢进(HPT)引起的罕见的骨局灶性巨细胞病变。棕色瘤于1891年被报道;它表现为HPT的终末期表现。常见受累部位是颅骨和骨盆带。我们描述了一例46岁的女性血液透析患者,患有继发性HPT,其左上颌窦和额骨的多个肿块病变在放射学上怀疑为棕色瘤。随着肾衰竭患者寿命的延长,继发性HPT的这种不寻常表现可能会出现,这说明在鉴别诊断中需要考虑棕色瘤。