Publication:
Parathyroid Carcinoma

dc.contributor.authorPanuwat Wongwattana
dc.contributor.authorPannipa Wiriyaamornchai
dc.contributor.orgunitคณะแพทยศาสตร์
dc.date.accessioned2022-03-28T05:31:36Z
dc.date.available2022-03-28T05:31:36Z
dc.date.issued2021
dc.date.issuedBE2564
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.
dc.description.urihttp://www.jmatonline.com/index.php/jmat/article/view/13161
dc.format.mimetypeapplication/pdf
dc.identifier.citationJ Med Assoc Thai 2021;104(Suppl.3): S83-90
dc.identifier.urihttps://hdl.handle.net/20.500.14740/8882
dc.language.isoeng
dc.rightsผลงานนี้เผยแพร่ภายใต้ สัญญาอนุญาตครีเอทีฟคอมมอนส์แบบ แสดงที่มา-ไม่ใช้เพื่อการค้า-ไม่ดัดแปลง 4.0 (CC BY-NC-ND 4.0)
dc.rights.holderมหาวิทยาลัยศรีนครินทรวิโรฒ
dc.subject.otherParathyroid
dc.subject.otherCarcinoma
dc.subject.otherNeoplasm
dc.subject.otherHyperparathyroidism
dc.subject.otherParathyroid glands
dc.titleParathyroid Carcinoma
dc.typeArticle
dcterms.accessRightsopen access
dspace.entity.typePublication

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