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dc.contributor.author Panuwat Wongwattana th_TH
dc.contributor.author Pannipa Wiriyaamornchai th_TH
dc.date.accessioned 2022-03-28T05:31:36Z
dc.date.available 2022-03-28T05:31:36Z
dc.date.issued 2021
dc.identifier.uri https://ir.swu.ac.th/jspui/handle/123456789/19377
dc.description.abstract Parathyroid carcinoma is a very rare cancer, accounting for 0.5% to 5% of all causes of primary hyperparathyroidism. Parathyroid carcinoma has an equal frequency of occurrence in both genders, usually in the fifth decade of life. Preoperative diagnosis of parathyroid carcinoma is difficult due to a lack of clinical findings, laboratory results, or radiological characteristics specific to the disease. Though, parathyroid carcinoma patients usually present with severe hypercalcemia at the time of diagnosis. Complete en-bloc resection is the mainstay of the treatment. The adjuvant therapy such as radiotherapy or chemotherapy has not shown effective in the treatment of parathyroid carcinoma. th_TH
dc.description.uri http://www.jmatonline.com/index.php/jmat/article/view/13161
dc.language.iso en th_TH
dc.subject Parathyroid th_TH
dc.subject Carcinoma th_TH
dc.subject Neoplasm th_TH
dc.subject Hyperparathyroidism th_TH
dc.subject Parathyroid glands th_TH
dc.title Parathyroid Carcinoma th_TH
dc.type Article th_TH
dc.identifier.bibliograpycitation J Med Assoc Thai 2021;104(Suppl.3): S83-90 th_TH


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