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Three systematic reviews and a meta-analysis - treatments for MEN1 associated endocrine tumours

Abstract:

Background: Multiple endocrine neoplasia type 1 (MEN1) is a rare hereditary disorder characterised by the combined occurrence of parathyroid, pancreatic, and pituitary tumours. Current treatments are based on very low-quality evidence. Our aims were to determine treatment outcomes in patients with MEN1 for: subtotal parathyroidectomy versus less than subtotal parathyroidectomy for primary hyperparathyroidism (Q1); surgery versus active surveillance for non-functioning panc...

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Publication status:
Published
Peer review status:
Peer reviewed

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Publisher copy:
10.1016/S2213-8587(25)00118-4

Authors


More by this author
Institution:
University of Oxford
Division:
MSD
Department:
RDM
Role:
Author
ORCID:
0000-0003-1439-1834
More by this author
Institution:
University of Oxford
Division:
MSD
Department:
RDM
Sub department:
RDM OCDEM
Role:
Author
ORCID:
0000-0002-0764-8681


Publisher:
Elsevier
Journal:
Lancet Diabetes & Endocrinology More from this journal
Publication date:
2025-06-13
Acceptance date:
2025-04-15
DOI:
EISSN:
2213-8595
ISSN:
2213-8587


Language:
English
Pubs id:
2119651
Local pid:
pubs:2119651
Deposit date:
2025-04-24

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