Search Results - "Castinetti, Frederic"
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Radiation techniques in aggressive pituitary tumours and carcinomas
Published in Reviews in endocrine & metabolic disorders (01-06-2020)“…Defining the role of radiation techniques in treatment of aggressive pituitary tumours and carcinomas is a difficult task: indeed, studies reported in the…”
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Aggressive pituitary tumours and pituitary carcinomas
Published in Nature reviews. Endocrinology (01-11-2021)“…Although usually benign, anterior pituitary tumours occasionally exhibit aggressive behaviour, with invasion of surrounding tissues, rapid growth, resistance…”
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Long-term follow-up of ipilimumab-induced hypophysitis, a common adverse event of the anti-CTLA-4 antibody in melanoma
Published in European journal of endocrinology (01-02-2015)“…ObjectiveFew data are published on the long-term follow-up of ipilimumab-induced hypophysitis, a cytotoxic T-lymphocyte antigen 4 antibody. We characterized…”
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Genetics, diagnosis, management and future directions of research of phaeochromocytoma and paraganglioma: a position statement and consensus of the Working Group on Endocrine Hypertension of the European Society of Hypertension
Published in Journal of hypertension (01-08-2020)“…Phaeochromocytoma and paraganglioma (PPGL) are chromaffin cell tumours that require timely diagnosis because of their potentially serious cardiovascular and…”
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Temozolomide treatment can improve overall survival in aggressive pituitary tumors and pituitary carcinomas
Published in European journal of endocrinology (01-06-2017)“…Objectives Only few retrospective studies have reported an efficacy rate of temozolomide (TMZ) in pituitary tumors (PT), all around 50%. However, the long-term…”
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Challenges in molecular diagnosis of multiple endocrine neoplasia
Published in Frontiers in endocrinology (Lausanne) (27-09-2024)“…Multiple endocrine neoplasia (MEN) is a group of rare genetic diseases characterized by the occurrence of multiple tumors of the endocrine system in the same…”
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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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Real-life clinical impact of a five-tiered classification of pituitary tumors
Published in European journal of endocrinology (01-12-2022)“…Introduction Usually benign, pituitary tumors (PT) can be invasive and aggressive with a propensity to progress and/or recur. Trouillas’s clinicopathological…”
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Complications Related to Endoscopic Endonasal Transsphenoidal Approach for Nonfunctioning Pituitary Macroadenomas in 300 Consecutive Patients
Published in World neurosurgery (01-05-2016)“…Abstract Objective The study aimed to analyze complications of endoscopic transsphenoidal surgery (ETS) for nonfunctioning pituitary adenomas (NFPAs). Methods…”
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Familial hypocalciuric hypercalcemia: the challenge of diagnosis
Published in Endocrine (01-02-2022)Get full text
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Management of clinically non-functioning pituitary adenoma
Published in Annales d'endocrinologie (01-07-2015)“…Abstract Clinically NFPA is currently the preferred term for designing all the pituitary adenomas which are not hormonally active (in other words, not…”
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Outcome of non-functioning ACTH pituitary tumors: silent does not mean indolent
Published in Pituitary (01-10-2024)“…Introduction Silent corticotroph tumors (siACTH) represent a rare entity of pituitary tumors (PT), usually more aggressive than other PT. Few predictor factors…”
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Surgical indications for pituitary tumors during pregnancy: a literature review
Published in Pituitary (01-04-2020)“…Purpose Surgical indications for pituitary tumors during pregnancy are rare, and are derived from a balance between expected benefits, particularly for…”
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MEN2-related pheochromocytoma: current state of knowledge, specific characteristics in MEN2B, and perspectives
Published in Endocrine (01-09-2020)“…Multiple endocrine neoplasia type 2 (MEN2) is a rare hereditary syndrome due to mutations of the proto-oncogene REarranged during Transfection (RET), defined…”
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HCG-responsive aldosteronoma with transient secretion during pregnancy confirmed through HCG-stimulated adrenal venous sampling
Published in Frontiers in endocrinology (Lausanne) (28-02-2023)“…Primary aldosteronism can be regulated by the ectopic expression of G-protein coupled receptors in aldosteronomas or bilateral hyperplasias. We report a rare…”
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Deficient anterior pituitary with common variable immune deficiency (DAVID syndrome): a new case and literature reports
Published in Journal of neuroendocrinology (01-06-2023)“…Deficient anterior pituitary with common variable immune deficiency (DAVID) syndrome is a rare condition characterized by adrenocorticotropic hormone (ACTH)…”
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Germinal defects of SDHx genes in patients with isolated pituitary adenoma
Published in European journal of endocrinology (01-10-2020)“…Background: The ‘3PAs’ syndrome, associating pituitary adenoma (PA) and pheochromocytoma/paraganglioma (PPGL), is sometimes associated with mutations in…”
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Pheochromocytoma surgery without systematic preoperative pharmacological preparation: insights from a referral tertiary center experience
Published in Surgical endoscopy (01-02-2021)“…Background Despite significant advances in imaging and genetics, as well as surgical and anesthetic innovations, morbidity in pheochromocytoma surgery remains…”
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Heterozygous variants in SIX3 and POU1F1 cause pituitary hormone deficiency in mouse and man
Published in Human molecular genetics (13-01-2023)“…Congenital hypopituitarism is a genetically heterogeneous condition that is part of a spectrum disorder that can include holoprosencephaly. Heterozygous…”
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