Ruggeri Rosaria M, Calamoneri Emanuele, Russo Antonia, Sindoni Alessandro, Mondello Baldassarre, Monaco Maurizio, Rosa Michele A, Baldari Sergio, Benvenga Salvatore, Campennì Alfredo, Trimarchi Francesco
Department of Clinical Experimental Medicine and Pharmacology, University of Messina, Messina, Italy.
ScientificWorldJournal. 2010 May 4;10:799-805. doi: 10.1100/tsw.2010.86.
A 63-year-old woman presented to the Orthopedic Unit of our hospital complaining of right hip pain of 6 months' duration associated with a worsening limp. Her past medical history included chronic renal insufficiency. Physical examination revealed deep pain in the iliac region and severe restriction of the right hip's articular function in the maximum degrees of range of motion. X-rays and CT scan detected an osteolytic and expansive lesion of the right supra-acetabular region with structural reabsorption of the right iliac wing. 99mTc-MDP whole-body bone scan showed an abnormal uptake in the right iliac region. Bone biopsy revealed an osteolytic lesion with multinucleated giant cells, indicating a brown tumor. Serum intact PTH was elevated (1020 pg/ml; normal values, 12-62 pg/ml), but her serum calcium was normal (total=9.4 mg/dl, nv 8.5-10.5; ionized=5.0 mg/dl, nv 4.2-5.4) due to the coexistence of chronic renal failure. 99mTc-MIBI scintigraphy revealed a single focus of sestamibi accumulation in the left retrosternal location, which turned out to be an intrathoracic parathyroid adenoma at surgical exploration. After surgical removal of the parathyroid adenoma, PTH levels decreased to 212 pg/ml. Three months after parathyroidectomy, the imaging studies showed complete recovery of the osteolytic lesion, thus avoiding any orthopedic surgery. This case is noteworthy because (1) primary hyperparathyroidism was not suspected due to the normocalcemia, likely attributable to the coexistence of chronic renal failure; and (2) it was associated with a brown tumor of unusual location (right supra-acetabular region).
一名63岁女性因右髋部疼痛6个月并伴有跛行加重,前来我院骨科就诊。她既往有慢性肾功能不全病史。体格检查发现髂区深部疼痛,右髋关节在最大活动度时关节功能严重受限。X线和CT扫描发现右髋臼上区有溶骨性、膨胀性病变,右侧髂骨翼有结构吸收。99mTc-MDP全身骨扫描显示右髂区摄取异常。骨活检显示有溶骨性病变及多核巨细胞,提示为棕色瘤。血清完整甲状旁腺激素(PTH)升高(1020 pg/ml;正常值为12 - 62 pg/ml),但由于并存慢性肾衰竭,其血清钙正常(总钙=9.4 mg/dl,正常范围8.5 - 10.5;离子钙=5.0 mg/dl,正常范围4.2 - 5.4)。99mTc-MIBI闪烁显像显示胸骨后左侧有一个单一的锝-甲氧基异丁基异腈(MIBI)聚集灶,手术探查发现是胸内甲状旁腺腺瘤。手术切除甲状旁腺腺瘤后,PTH水平降至212 pg/ml。甲状旁腺切除术后3个月,影像学检查显示溶骨性病变完全恢复。从而避免了任何骨科手术。该病例值得注意,原因如下:(1)由于血钙正常,最初未怀疑原发性甲状旁腺功能亢进,这可能归因于并存慢性肾衰竭;(2)它与一个位置不寻常的棕色瘤(右髋臼上区)相关。