(connections to ovarian cancer noted) Genetic Predisposition to Endocrine Tumors: Diagnosis, Surveillance and Challenges in Care Ovarian Cancer and Us OVARIAN CANCER and US Ovarian Cancer and Us

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Thursday, September 22, 2016

(connections to ovarian cancer noted) Genetic Predisposition to Endocrine Tumors: Diagnosis, Surveillance and Challenges in Care



Note: examples of (some) highlighted syndromes connected to ovarian cancer

abstract

  In this review, we describe the main endocrine tumor manifestations found in familial cancer syndromes in an organ-based approach

Abbreviations:
ACC (Adrenocortical carcinoma), BWS (Beckwith-Wiedemann syndrome), CHRPE (Congenital Hypertrophy of the Retinal Pigment Epithelium), CMV (Cribiform morullar variant of thyroid cancer), DTC (Differentiated thyroid cancer), ELST (Endolymphatic Sac Tumor), FAP (Familial Adenomatous Polyposis), FMTC (Familial Medullary Thyroid Cancer), GIST (Gastrointestinal Stromal Tumor), HPGL (Hereditary Paraganglioma Syndrome), HLRCC (Hereditary Leiomyomatosis and Renal Cell Cancer), LFS (Li-Fraumeni Syndrome), MEN1 (Multiple Endocrine Neoplasia type 1), MEN2 (Multiple Endocrine Neoplasia type 2), MNG (Multinodular Goiter), MNST (Malignant Nervesheath Tumor), MTC (Medullary Thyroid Carcinoma), NET (Neuroendocrine Tumor), NF1 (Neurofibromatosis type 1), NGS (Next Generation Sequencing), PCC (Pheochromocytoma), PGL (Paraganglioma), pHPT (Primary Hyperparathyroidism), PHTS (PTEN Hamartoma Tumor Syndrome), PPB (Pleuropulmonary Blastoma), RCC (Renal Cell Cancer), SDHx (Succinate Dehydrogenase Subunit (A,B,C,D,AF2)), SLCT (Sertoli Leydig Cell Tumor), VHL (von Hippel-Lindau Disease)

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