New therapies for patients with multiple endocrine neoplasia type 1 |
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Authors: | Aurore Geslot Magaly Vialon Philippe Caron Solange Grunenwald Delphine Vezzosi |
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Affiliation: | 1. Institut CardioMet, Toulouse, France;2. Service d’endocrinologie, hôpital Larrey, 24, chemin de Pouvourville, 31029 Toulouse cedex 9, France;1. Département d’Endocrinologie, Diabète, CHU de Montpellier, Université de Montpellier, Montpellier, France;2. Département d’Endocrinologie, Diabète, Nutrition Inserm 1411, CHU de Montpellier, Université de Montpellier, Montpellier, France;1. Department of Endocrinology, Queen Mary University of London, E1 4NS London, United Kingdom;2. Department of Endocrinology, Saint-Bartholomew''s Hospital, EC1A 7BE London, United Kingdom;3. Department of Cardiology, University Hospitals Birmingham NHS Foundation Trust, B15 2GW Birmingham, United Kingdom;4. Institute of Cardiovascular Sciences, University of Birmingham, B15 2TT Birmingham, United Kingdom;2. Department of endocrine surgery, Hôpital Lyon Sud, 165, rue du grand Revoyet, 69495 Pierre-Bénite, France;3. Inserm U1290, Research on Healthcare Performance Lab (RESHAPE), Université Claude-Bernard Lyon 1, domaine Rockefeller, 8, avenue Rockefeller, 69003 Lyon, France |
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Abstract: | In 1953, for the first time, Paul Wermer described a family presenting endocrine gland neoplasms over several generations. The transmission was autosomal dominant and the penetrance was high. Forty years later in 1997, the multiple endocrine neoplasia type 1 (MEN1) gene was sequenced, thus enabling diagnosis and early optimal treatment. Patients carrying the MEN1 gene present endocrine but also non-endocrine tumors. Parathyroid, pancreatic and pituitary impairment are the three main types of endocrine involvement. The present article details therapeutic management of hyperparathyroidism, neuroendocrine pancreatic tumors and pituitary adenomas in patients carrying the MEN1 gene. Significant therapeutic progress has in fact been made in the last few years. As concerns the parathyroid glands, screening of family members and regular monitoring of affected subjects now raise the question of early management of parathyroid lesions and optimal timing of parathyroid surgery. As concerns the duodenum-pancreas, proton-pump inhibitors are able to control gastrin-secreting syndrome, reducing mortality in MEN1 patients. Mortality in MEN1 patients is no longer mainly secondary to uncontrolled hormonal secretion but to metastatic (mainly pancreatic) disease progression. Tumor risk requires regular monitoring of morphological assessment, leading to iterative pancreatic surgery in a large number of patients. Finally, pituitary adenomas in MEN1 patients are traditionally described as aggressive, invasive and resistant to medical treatment. However, regular pituitary screening showed them to be in fact infra-centimetric and non-secreting in the majority of patients. Consequently, it is necessary to regularly monitor MEN1 patients, with regular clinical, biological and morphological work-up. Several studies showed that this regular monitoring impairs quality of life. Building a relationship of trust between patients and care provider is therefore essential. It enables the patient to be referred for psychological or psychiatric care in difficult times, providing long-term support and preventing any breakdown in continuity of care. |
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Keywords: | Multiple endocrine neoplasia type 1 Primary hyperparathyroidism Duodenopancreatic neuroendocrine tumor Pituitary adenoma Néoplasie endocrinienne multiple de type 1 Hyperparathyroïdie primaire Tumeur neuroendocrine duodéno-pancréatique Adénome hypophysaire |
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