multiple endocrine neoplasia type 1
Multiple endocrine neoplasia type 1
... Multiple Endocrine Neoplasia type 1 (MEN1) is a rare autosomal dominant hereditary cancer syndrome presented mostly by tumours of the parathyroids, endocrine pancreas and ...
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Multiple Endocrine Neoplasia Type 1 with Multiple Leiomyomas Linked to a Novel Mutation in the MEN1 Gene
... Multiple endocrine neoplasia type 1 (MEN1) is an auto- somal dominantly inherited ...with multiple leiomyomas in ...with multiple leiomyomas, parathyroid adenoma, ...
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Diagnosis and Management of Multiple Endocrine Neoplasia Type 1 (MEN1)
... 1. Chandrasekharappa SC, Guru SC, Manickam P, Olufemi SE, Collins FS, Emmert-Buck MR, Debelenko LV, Zhuang Z, Lubensky IA, Liotta LA, Crabtree JS, Wang Y, Roe BA, Weisemann J, Boguski MS, Agarwal SK, Kester MB, ...
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Non functioning Pancreatic Neuroendocrine Tumor in a Patient with Multiple Endocrine Neoplasia Type 1 Syndrome: Case Report
... with Multiple Endocrine Neoplasia Type 1 Syndrome in the same patient, the literature shows 80 to 100% ...three endocrine sites: the parathyroid glands, the pancreatic islet and ...
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Fast growing pancreatic neuroendocrine carcinoma in a patient with multiple endocrine neoplasia type 1: a case report
... Multiple endocrine neoplasia type 1 syndrome (MEN1) is an inherited tumor syndrome, which is typically charac- terized by tumors of the parathyroid glands, the pancreas and the ...
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Clinical presentation and management of primary ovarian neuroendocrine tumor in multiple endocrine neoplasia type 1
... Multiple endocrine neoplasia type 1 (MEN1) is an autosomal dominant condition characterized by parathyroid, anterior pituitary and enteropancreatic endocrine cell ...
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Concomitant existence of pheochromocytoma in a patient with multiple endocrine neoplasia type 1
... 2. Chandrasekharappa SC, Guru SC, Manickam P, Olufemi SE, Collins FS, Emmert-Buck MR, Debelenko LV, Zhuang Z, Lubensky IA, Liotta LA, Crabtree JS, Wang Y, Roe BA, Weisemann J, Boguski MS, Agarwal SK, Kester MB, Kim YS, ...
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Predictive testing for multiple endocrine neoplasia type 1 using DNA polymorphisms
... Multiple endocrine neoplasia type 1 (MEN1) is an autosomal dominantly inherited predisposition to neoplastic lesions of the parathyroids, pancreas, and the ...
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Treatment-resistant pediatric giant prolactinoma and multiple endocrine neoplasia type 1
... Pituitary adenomas account for <3 % of all childhood intracranial tumors with an estimated incidence of 0.1 cases/million/year [1, 2]. Prolactin (PRL)-secreting tumors alone account for 50-70 % of pituitary ...
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'Quality in, quality out', a stepwise approach to evidence-based medicine for rare diseases promoted by multiple endocrine neoplasia type 1
... is multiple endocrine neoplasia type 1 (MEN1), which is an autosomal dominant endocrine tumor syndrome with an estimated occurrence rate of 2–3 per ...by multiple ...
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Multiple endocrine neoplasia type 1 presenting with concurrent insulinoma and prolactinoma in early-adolescence
... In pediatrics, hypoglycemia most commonly presents in infants and toddlers. Presentation in early adolescence is unusual, but can be due to ingestions including hypoglycemic agents or ethanol or hormonal causes, such as ...
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Multiple endocrine neoplasia type 1: clinical correlates of MEN1 gene methylation
... Multiple Endocrine Neoplasia Type 1 (MEN 1) has marked severity variation between individuals with the same ...Tasman 1 MEN 1 kindred carrying a common splice site ...
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Intertumor heterogeneity in 60 pancreatic neuroendocrine tumors associated with multiple endocrine neoplasia type 1
... The procedures currently discussed are either resection or follow-up. Lopez et al. have recommended surgical treatment for NF-PNENs in MEN-1 with a size between 10 and 20 mm, should rapid progression – defined by ...
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Molecular cytogenetic analysis applied to multiple endocrine neoplasia type 1 and colorectal carcinogenesis
... Pituitary tumours are usually recognised during the fourth decade of life and detected by elevated hormone levels or excess tumour mass. The most common tumour is chromophobe adenoma, a non functioning tumour, usually ...
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Molecular genetic analysis of chromosome 11q13; localisation of the multiple endocrine neoplasia type 1 gene
... one endocrine gland (Thakker and Ponder, ...f multiple endocrine neoplasia, namely type 1 and type 2, and each form is characterised by the development of tumours within ...
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No evidence of adverse fertility and pregnancy outcomes in patients with unrecognised and untreated multiple endocrine neoplasia type 1
... Tasman 1 MEN 1 kindred spanning six generations from 1825-1990 there was no adverse impact of MEN 1 on fertility, stillbirth rate or apparent miscarriage ...MEN 1 was not recognised or treated ...
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Bilateral adrenocortical carcinoma in a patient with multiple endocrine neoplasia type 1 (MEN1) and a novel mutation in the MEN1 gene
... adrenal neoplasia is of important clinical significance, close bio- chemical and radiologic follow-up is ...and endocrine-inactive with low malignant potential ...
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Multiple endocrine neoplasia type 1: extensive analysis of a large database of Florentine patients
... mutation type and/or mutated gene region were analysed by chi-squared test, assuming a positive significance with p < ...haplo- type, absence of an identified mutation, and mutations located in all the ...
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<p>Medullary Thyroid Carcinoma in a Patient with MEN 1 Syndrome. Case Report and Literature Review</p>
... Multiple endocrine neoplasia type 1 (MEN 1) is a hereditary syndrome characterized by hyperplastic and neoplastic dis- orders mainly affecting the parathyroid, anterior pituitary ...
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Gastrinoma and neurofibromatosis type 2: the first case report and review of the literature
... Case presentation: This report refers to an Italian 69 year old woman with neurofibromatosis type 2 and a pancreatic gastrinoma. In the past she had encephalic meningiomas, a tongue schwannoma and bilateral ...
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