Search Results - "WAGUESPACK, Steven G"
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Beyond the “3 Ps”: A critical appraisal of the non-endocrine manifestations of multiple endocrine neoplasia type 1
Published in Frontiers in endocrinology (Lausanne) (17-10-2022)“…Multiple endocrine neoplasia type 1 (MEN1), an autosomal-dominantly inherited tumor syndrome, is classically defined by tumors arising from the “3 Ps”:…”
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Thyroid Sequelae of Pediatric Cancer Therapy
Published in Hormone research in paediatrics (01-01-2019)“…The hypothalamic-pituitary-thyroid axis is a common site of unintended, acquired disease either during or after the treatment of cancer. Children treated with…”
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Revised American Thyroid Association guidelines for the management of medullary thyroid carcinoma
Published in Thyroid (New York, N.Y.) (01-06-2015)“…The American Thyroid Association appointed a Task Force of experts to revise the original Medullary Thyroid Carcinoma: Management Guidelines of the American…”
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A comprehensive review on MEN2B
Published in Endocrine-related cancer (01-02-2018)“…MEN2B is a very rare autosomal dominant hereditary tumor syndrome associated with medullary thyroid carcinoma (MTC) in 100% cases, pheochromocytoma in 50%…”
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Risk of Neoplasia in Pediatric Patients Receiving Growth Hormone Therapy—A Report From the Pediatric Endocrine Society Drug and Therapeutics Committee
Published in The journal of clinical endocrinology and metabolism (01-06-2015)“…Context: GH and IGF-1 have been shown to affect tumor growth in vitro and in some animal models. This report summarizes the available evidence on whether GH…”
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Adrenocortical carcinoma: clinical outcomes and prognosis of 330 patients at a tertiary care center
Published in European journal of endocrinology (01-12-2013)“…ObjectiveAdrenocortical carcinoma (ACC) is a rare malignancy with a poor prognosis. Herein, we describe the clinical features and outcomes for a large series…”
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Guidelines for surveillance of patients with von Hippel‐Lindau disease: Consensus statement of the International VHL Surveillance Guidelines Consortium and VHL Alliance
Published in Cancer (01-10-2023)“…Von Hippel‐Lindau disease is a rare inherited cancer‐predisposition syndrome. The authors report the updated recommendations for the multiorgan surveillance…”
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Immune checkpoint inhibitor related hypophysitis: diagnostic criteria and recovery patterns
Published in Endocrine-related cancer (01-07-2021)“…Data on the diagnosis, natural course and management of immune checkpoint inhibitor (ICI)-related hypophysitis (irH) are limited. We propose this study to…”
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The Characterization of Pheochromocytoma and Its Impact on Overall Survival in Multiple Endocrine Neoplasia Type 2
Published in The journal of clinical endocrinology and metabolism (01-11-2013)“…Context: Pheochromocytoma (PHEO) occurs in 50% of patients with multiple endocrine neoplasia type 2 (MEN2). It is unknown if the presence of PHEO is associated…”
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Efficacy of pembrolizumab in patients with pituitary carcinoma: report of four cases from a phase II study
Published in Journal for immunotherapy of cancer (01-12-2020)“…Pituitary carcinoma is an aggressive tumor characterized by metastatic spread beyond the sellar region. Symptoms can be debilitating due to hormonal excess and…”
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Pediatric, Adolescent, and Young Adult Thyroid Carcinoma Harbors Frequent and Diverse Targetable Genomic Alterations, Including Kinase Fusions
Published in The oncologist (Dayton, Ohio) (01-03-2017)“…Background Thyroid carcinoma, which is rare in pediatric patients (age 0–18 years) but more common in adolescent and young adult (AYA) patients (age 15–39…”
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Genetic profiling as a clinical tool in advanced parathyroid carcinoma
Published in Journal of cancer research and clinical oncology (01-08-2019)“…Context Parathyroid carcinoma (PC) is a rare endocrine malignancy with no approved systemic therapies for unresectable locally invasive or distant metastatic…”
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Management of medullary thyroid carcinoma and MEN2 syndromes in childhood
Published in Nature reviews. Endocrinology (01-10-2011)“…Medullary thyroid carcinoma is a rare endocrine malignancy that, when diagnosed during childhood, is almost always associated with multiple endocrine neoplasia…”
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Pediatric thyroid cancer guidelines: challenges in stratifying care based on limited data
Published in European thyroid journal (01-12-2022)“…The 2022 European Thyroid Association Guidelines for the management of pediatric thyroid nodules and differentiated thyroid carcinoma (1) were developed by a…”
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Analytical and Clinical Validation of Expressed Variants and Fusions From the Whole Transcriptome of Thyroid FNA Samples
Published in Frontiers in endocrinology (Lausanne) (11-09-2019)“…Introduction: The Afirma® Xpression Atlas (XA) detects gene variants and fusions in thyroid nodule FNA samples from a curated panel of 511 genes using…”
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Steroid Cell Ovarian Tumor in a Case of von Hippel-Lindau Disease: Demonstrating Lipid Content of the Mass with MR Imaging
Published in Magnetic Resonance in Medical Sciences (01-01-2019)Get full text
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Initial management and follow-up of differentiated thyroid cancer in children
Published in Journal of the National Comprehensive Cancer Network (01-11-2010)“…Children with differentiated thyroid cancer (DTC) often present with metastatic disease and have a high risk for recurrence, but rarely die of the disease…”
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Thyroid Dysfunction and Thyroid Cancer in Childhood Cancer Survivors: Prevalence, Surveillance and Management
Published in Frontiers of hormone research (2021)“…Childhood cancer survivors (CCS) are at increased risk of developing thyroid disorders during follow-up. Radiation therapy to a field that includes the thyroid…”
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Feasibility and outcome of re-irradiation in the treatment of multiply recurrent pituitary adenomas
Published in Pituitary (01-12-2014)“…Purpose This study evaluates the toxicity and outcomes of re-irradiation to the sella for pituitary adenomas. Methods Patients diagnosed with a pituitary…”
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Recent Therapeutic Advances in Pituitary Carcinoma
Published in Journal of Immunotherapy and Precision Oncology (01-05-2023)“…Pituitary carcinoma (PC) is a rare, aggressive malignancy that comprises 0.1-0.2% of all pituitary tumors. PC is defined anatomically as a pituitary tumor that…”
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