Miyakoshi Masashi, Kamoi Kyuzi, Takano Toru, Nishihara Mamiko, Kawashima Tadashi, Sudo Norihito, Togashi Ken-Ichi, Emura Iwao, Williams Dillwyn
Department of Medicine, Nagaoka Red Cross Hospital, Niigata, Japan.
Endocr J. 2007 Apr;54(2):205-10. doi: 10.1507/endocrj.k05-175. Epub 2007 Jan 22.
We encountered an unusual case of hyperparathyroidism with both hemosiderin deposits on the ribs and low intensity on T2-weighted magnetic resonance imaging (MRI) caused by a parathyroid adenoma with multiple brown tumors that mimicked metastatic bone tumor due to false positive results on computed tomography (CT) and Tc-99m sestamibi (MIBI) imaging. The patient, a middle-aged woman, had very high serum levels of calcium (14.1 mg/dl), alkaline phosphatase (9,369 IU/l) and intact-PTH (12,400 pg/ml), and a large tumor (2.5 cm in diameter) in the lower portion of the left lobe of the thyroid. Plain X-ray revealed a soft tumor in the left chest wall. On CT scan, there were multiple destructive masses in the ribs, including large intramedullary masses on both 3rd ribs. On MIBI scintigraphy, there was strong late uptake in the lower portion of the left cervical region, both 3rd ribs, and the left 7th, 8th, and 10th ribs. T2-weighted image MRI scans showed that both 3rd ribs had a low intensity with hemosiderin deposits. These findings suggested that the patient had hyperparathyroidism with multiple bone metastases due to carcinoma of the parathyroid gland. However, on pathology, the resected tumor of lower portion of the left lobe of thyroid was diagnosed as a parathyroid adenoma, and the tumors of the left 3rd and 7th ribs, as well as the right 2nd rib, were shown to be brown tumors. After resection, the patient's serum levels of calcium, alkaline phosphatase, and intact-PTH normalized. At 1.5-years follow-up, CT, MIBI, and MRI scans showed no abnormal findings. It is necessary to determine whether MRI can be used to distinguish between brown tumors and metastases caused by carcinoma of the parathyroid gland.
我们遇到了一例不寻常的甲状旁腺功能亢进病例,该患者肋骨有含铁血黄素沉积,且甲状旁腺腺瘤伴多发棕色瘤在T2加权磁共振成像(MRI)上呈低信号强度,因计算机断层扫描(CT)和锝-99m甲氧基异丁基异腈(MIBI)成像出现假阳性结果,酷似转移性骨肿瘤。患者为中年女性,血清钙(14.1mg/dl)、碱性磷酸酶(9369IU/l)和完整甲状旁腺激素(12400pg/ml)水平极高,甲状腺左叶下部有一个大肿瘤(直径2.5cm)。X线平片显示左胸壁有一个软组织肿瘤。CT扫描显示肋骨有多个破坏性肿块,包括双侧第3肋骨的大髓内肿块。MIBI闪烁显像显示左颈部下部、双侧第3肋骨以及左第7、8、10肋骨有强烈的延迟摄取。T2加权图像MRI扫描显示双侧第3肋骨呈低信号强度并有含铁血黄素沉积。这些发现提示该患者患有甲状旁腺癌伴多发骨转移。然而,病理检查显示,切除的甲状腺左叶下部肿瘤被诊断为甲状旁腺腺瘤,左第3和7肋骨以及右第2肋骨的肿瘤为棕色瘤。切除术后,患者的血清钙、碱性磷酸酶和完整甲状旁腺激素水平恢复正常。随访1.5年时,CT、MIBI和MRI扫描均未发现异常。有必要确定MRI是否可用于区分甲状旁腺癌引起的棕色瘤和转移瘤。