Lung adenocarcinoma and adrenocortical carcinoma in a patient with multiple endocrine neoplasia type 1

Multiple endocrine neoplasia type 1 (MEN1) is an autosomal dominant disorder caused by heterozygous germline mutations in the tumor suppressor gene MEN1, which encodes a nuclear protein, menin. MEN1 is characterized by the combined occurrence of tumors involving the pituitary gland, pancreatic islet...

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Vydáno v:Respir Med Case Rep
Hlavní autoři: Ohara, Nobumasa, Kaneko, Masanori, Ikeda, Masahiro, Ishizaki, Fumio, Suzuki, Kazuya, Maruyama, Ryo, Komeyama, Takeshi, Sato, Kazuhiro, Togashi, Kenichi, Usuda, Hiroyuki, Yamazaki, Yuto, Sasano, Hironobu, Kaneko, Kenzo, Kamoi, Kyuzi
Médium: Artigo
Jazyk:Inglês
Vydáno: Elsevier 2016
Témata:
Case Report
On-line přístup:https://ncbi.nlm.nih.gov/pmc/articles/PMC5219631/
https://ncbi.nlm.nih.gov/pubmed/28070481
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.rmcr.2016.12.002
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