Current Approaches to Primary Therapy for Papillary and Follicular Thyroid Cancer

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ID: 294617
2001
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Abstract
Patient variables Age Ͻ15 yr or Ͼ45 yr Age 15-45 yr Male sex Female sex Family history of thyroid cancer No family history of thyroid cancer Tumor variables Tumor Ͼ4 cm in diameter Tumor Ͻ4 cm in diameter Bilateral disease Unilateral disease Extrathyroidal extension No extrathyroidal extension Vascular Invasion (both papillary and follicular thyroid cancer) Absence of vascular invasion Cervical, or mediastinal lymph node metastases No lymph node metastases Certain tumor subtypes: Hu ¨rthle cell, tall cell, columnar cell, diffuse sclerosis, insular variants Encapsulated papillary thyroid carcinoma, papillary microcarcinoma, cystic papillary thyroid carcinoma Marked nuclear atypia, tumor necrosis, and vascular invasion (i.e.histologic grade) Absence of nuclear atypia, tumor necrosis, and vascular invasion Tumors or metastases that concentrate radioiodine poorly or not at all Tumors or metastases that concentrate radioiodine well Distant metastases No distant metastases Modified from the NCCN guidelines for the diagnosis and treatment of thyroid cancer (3, 6).
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openalex_W2091923260 Use this key to autocite in the manuscript while using SciMatic Manuscript Manager or Thesis Manager
Authors Ernest L. Mazzaferri, Richard T. Kloos
Journal the journal of clinical endocrinology & metabolism
Year 2001
DOI
10.1210/jcem.86.4.7407
URL
https://academic.oup.com/jcem/article-pdf/86/4/1447/9164405/jcem1447.pdf
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