Patients With MEN1 Are at an Increased Risk for Venous Thromboembolism

Abstract Background Multiple endocrine neoplasia type 1 (MEN1) is a rare inherited disorder predisposing the development of multiple functional and nonfunctional neuroendocrine tumors (NETs). Only uncommon MEN1-associated functional NETs such as glucagonomas (

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Bibliographic Details
Published in:The journal of clinical endocrinology and metabolism 2021-02, Vol.106 (2), p.e460-e468
Main Authors: Lee, Maya E, Ortega-Sustache, Yashira M, Agarwal, Sunita K, Tepede, Aisha, Welch, James, Mandl, Adel, Bansal, Rashika, Tirosh, Amit, Piaggi, Paolo, Cochran, Craig, Simonds, William F, Weinstein, Lee S, Blau, Jenny E
Format: Article
Language:English
Subjects:
Adolescent
Adult
Aged
Aged, 80 and over
Anticoagulants
Anticoagulants (Medicine)
Anticoagulants - therapeutic use
Aspirin
Clinical s
Development and progression
Embolism
Enoxaparin
Female
Gene mutations
Genetic aspects
Health aspects
Hematology
History, 20th Century
History, 21st Century
Humans
Incidence
Male
Middle Aged
Multiple endocrine neoplasia
Multiple Endocrine Neoplasia Type 1 - complications
Multiple Endocrine Neoplasia Type 1 - drug therapy
Multiple Endocrine Neoplasia Type 1 - epidemiology
Neuroendocrine tumors
Pancreatic cancer
Patients
Population Surveillance
Prevalence
Pulmonary embolism
Retrospective Studies
Risk Factors
Thromboembolism
Tumors
Type 2 diabetes
United States - epidemiology
Venous Thromboembolism - epidemiology
Venous Thromboembolism - etiology
Venous Thromboembolism - prevention & control
Young Adult
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Description
Summary:Abstract Background Multiple endocrine neoplasia type 1 (MEN1) is a rare inherited disorder predisposing the development of multiple functional and nonfunctional neuroendocrine tumors (NETs). Only uncommon MEN1-associated functional NETs such as glucagonomas (
ISSN:0021-972X
1945-7197
DOI:10.1210/clinem/dgaa501