Duodenal Rare Neuroendocrine Tumor: Clinicopathological Characteristics of Patients with Gangliocytic Paraganglioma

Gangliocytic paraganglioma (GP) has been regarded as a rare benign tumor that commonly arises from the second part of the duodenum. As GP does not exhibit either prominent mitotic activity or Ki-67 immunoreactivity, it is often misdiagnosed as neuroendocrine tumor (NET) G1. However, the prognosis mi...

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Vydáno v:Gastroenterol Res Pract
Hlavní autoři: Okubo, Yoichiro, Yokose, Tomoyuki, Motohashi, Osamu, Miyagi, Yohei, Yoshioka, Emi, Suzuki, Masaki, Washimi, Kota, Kawachi, Kae, Nito, Madoka, Nemoto, Tetsuo, Shibuya, Kazutoshi, Kameda, Yoichi
Médium: Artigo
Jazyk:Inglês
Vydáno: Hindawi Publishing Corporation 2016
Témata:
Review Article
On-line přístup:https://ncbi.nlm.nih.gov/pmc/articles/PMC5209618/
https://ncbi.nlm.nih.gov/pubmed/28096810
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1155/2016/5257312
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