Localization in primary hyperparathyroidism.

Piyush Aggarwal, Vinisha Gunasekaran, Ashwani Sood, Bhagwant Rai Mittal
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Abstract

Primary hyperparathyroidism is the main cause of hypercalcemia, resulting predominantly from parathyroid adenomas followed by hyperplasia. Diagnosis relies on clinical and biochemical parameters. Accurate pre-operative localization is mandatory for better surgical outcome. Various non-invasive imaging modalities includes cervical ultrasound, radionuclide scintigraphy with 99mTc-Methoxyisobutyl isonitrile combined with SPECT/CT, 4DCT, MRI and 18F-Choline PET/CT. Functional imaging has shown higher accuracy in localization especially in ectopic parathyroid adenomas and persistent or recurrent hyperparathyroidism. Combined ultrasound and 99mTc-MIBI has shown high sensitivity and specificity than individual imaging modality. 18F-Choline PET/CT has better diagnostic performance in identifying parathyroid hyperplasia and multiple adenomas. In patients with equivocal findings and concurrent thyroid nodular diseases, 18F-Choline PET/MRI and 4DCT helps in better characterization of lesion. Intraoperative probe guided surgery facilitates targeted and minimally invasive surgery resulting in better surgical outcome. More specific radiopharmaceuticals for parathyroid imaging need to be developed to reduce false positive results.

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原发性甲状旁腺功能亢进的定位。
原发性甲状旁腺功能亢进是高钙血症的主要原因,主要由甲状旁腺瘤引起,然后是增生。诊断依赖于临床和生化参数。准确的术前定位是提高手术效果的必要条件。各种非侵入性成像方式包括宫颈超声、99mtc -甲氧基异丁基异腈放射核素显像联合SPECT/CT、4DCT、MRI和18f -胆碱PET/CT。功能成像显示定位的准确性较高,特别是在异位甲状旁腺腺瘤和持续或复发的甲状旁腺功能亢进。超声联合99mTc-MIBI比单独成像方式具有更高的灵敏度和特异性。18f -胆碱PET/CT对甲状旁腺增生及多发腺瘤有较好的诊断价值。在表现不明确并伴有甲状腺结节性疾病的患者中,18f -胆碱PET/MRI和4DCT有助于更好地表征病变。术中探针引导手术有利于手术的靶向性和微创性,手术效果较好。为了减少假阳性结果,需要开发更多针对甲状旁腺成像的特异性放射性药物。
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Adolescent primary hyperparathyroidism. Localization in primary hyperparathyroidism. Parathyroid carcinoma: New insights. Pre-clinical phaeochromocytoma and paraganglioma models: Cell lines, animal models, and a human primary culture model. Recent discoveries of Sino-Caucasian differences in the genetics of phaeochromocytomas and paragangliomas.
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