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. 2017 May/Jun;46(5):589-594.
doi: 10.1097/MPA.0000000000000825.

Treatment of Pancreatic Neuroendocrine Tumors in Multiple Endocrine Neoplasia Type 1: Some Clarity But Continued Controversy

Robert T Jensen  1 , Jeffrey A Norton
Affiliations

Treatment of Pancreatic Neuroendocrine Tumors in Multiple Endocrine Neoplasia Type 1: Some Clarity But Continued Controversy

Robert T Jensen et al. Pancreas. 2017 May/Jun.
No abstract available

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Conflict of interest statement

Disclosure: The authors declare no conflict of interest or funding

Figures

Fig. 1
Fig. 1
Time course of the changes in the reported causes of death in various series of MEN1 patients. This figures is modified from to include data on the recent effect of thymic carcinoids on survival. Data are from–
See this image and copyright information in PMC

References

    1. Jensen RT, Berna MJ, Bingham MD, et al. Inherited pancreatic endocrine tumor syndromes: advances in molecular pathogenesis, diagnosis, management and controversies. Cancer. 2008;113(7 suppl):1807–1843. - PMC - PubMed
    1. Norton JA, Krampitz G, Jensen RT. Multiple Endocrine Neoplasia: Genetics and Clinical Management. Surg Oncol Clin N Am. 2015;24:795–832. - PMC - PubMed
    1. Vezzosi D, Cardot-Bauters C, Bouscaren N, et al. Long-term results of the surgical management of insulinoma patients with MEN1: a Groupe d’etude des Tumeurs Endocrines (GTE) retrospective study. Eur J Endocrinol. 2015;172:309–319. - PubMed
    1. Ballard HS, Frame B, Harstock RT. Familial endocrine adenoma-peptic ulcer disease. Medicine (Baltimore) 1964;43:481–515. - PubMed
    1. Lamers CB. Familial multiple endocrine neoplasia type I (Wermer’s syndrome) Neth J Med. 1978;21:270–274. - PubMed

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