Please use this identifier to cite or link to this item: https://ir.swu.ac.th/jspui/handle/123456789/19377
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dc.contributor.authorPanuwat Wongwattanath_TH
dc.contributor.authorPannipa Wiriyaamornchaith_TH
dc.date.accessioned2022-03-28T05:31:36Z-
dc.date.available2022-03-28T05:31:36Z-
dc.date.issued2021-
dc.identifier.urihttps://ir.swu.ac.th/jspui/handle/123456789/19377-
dc.description.abstractParathyroid 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.urihttp://www.jmatonline.com/index.php/jmat/article/view/13161-
dc.language.isoenth_TH
dc.subjectParathyroidth_TH
dc.subjectCarcinomath_TH
dc.subjectNeoplasmth_TH
dc.subjectHyperparathyroidismth_TH
dc.subjectParathyroid glandsth_TH
dc.titleParathyroid Carcinomath_TH
dc.typeArticleth_TH
dc.identifier.bibliograpycitationJ Med Assoc Thai 2021;104(Suppl.3): S83-90th_TH
Appears in Collections:Med-Journal Articles

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