Clinical Outcomes of the Germline <i>RET</i> M918T Pathogenic Variant in Hereditary Medullary Thyroid Carcinoma: A Systematic Review and Meta-Analysis. [PDF]
Medicina (Kaunas)Jongthawin J +6 more
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Magnitude of Survival Benefit Associated With Tyrosine Kinase Inhibitors in Advanced Thyroid Carcinoma: A Systematic Review and Meta-Analysis Incorporating Updated Long-Term Evidence From SELECT (Lenvatinib) and COSMIC-311 (Cabozantinib) Trials. [PDF]
World J OncolRoy P +3 more
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Is Calcitonin at 6-12 Months an Appropriate Criterion to Define Cure in Medullary Thyroid Carcinoma? [PDF]
World J SurgRos-Madrid I +6 more
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Muir-Torre Syndrome Associated With a Cryptic Intronic MSH2 Variant Identified via Whole-Genome Sequencing: A Case Report. [PDF]
Pathol IntNoda K +13 more
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Medullary thyroid carcinoma with cervical metastasis following anterior cervical disc replacement: a case report. [PDF]
J Med Case RepHoward MD, Humayun Y.
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Medullary thyroid cancer is a rare neoplasm that arises from the parafollicular C cells. It occurs in a sporadic form, or less commonly as a hereditary form, as part of multiple endocrine neoplasia syndromes types 2A and 2B. The RET proto-oncogene is currently the primary factor that is implicated in the hereditary forms of this neoplasm. The knowledge
Gary L, Clayman, Tarek S, el-Baradie
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Patients with clinically evident medullary thyroid cancer should have a total extracapsular thyroidectomy with bilateral central neck dissection and an ipsilateral prophylactic or therapeutic modified (functional) radical neck dissection when the primary tumor is greater than 1 cm and when the central neck nodes are positive.
E, Kebebew, O H, Clark
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