WordNet

of or relating to the stomach and intestines; "a gastrointestinal disorder" (同)GI
a small tumor (benign or malignant) arising from the mucosa of the gastrointestinal tract; usually associated with excessive secretion of serotonin

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MEN1 c.825‑1G>A mutation in a family with multiple endocrine neoplasia type 1: A case report.

Ning Z1, Wang O1, Meng X1, Xing X1, Xia W1, Jiang Y1, Li M1, Xu Y2.
Molecular medicine reports.Mol Med Rep.2015 Oct;12(4):6152-6. doi: 10.3892/mmr.2015.4138. Epub 2015 Jul 29.
Multiple endocrine neoplasia type 1 (MEN1) is an autosomal dominant disease characterized by combined occurrence of tumors and hyperplasia in tissues including the parathyroid, gastrointestinal endocrine tissue and anterior pituitary. Heterozygous germline mutation of the tumor suppressor gene MEN1
PMID 26239674

Role of computed tomography angiography in detection and staging of small bowel carcinoid tumors.

Bonekamp D1, Raman SP1, Horton KM1, Fishman EK1.
World journal of radiology.World J Radiol.2015 Sep 28;7(9):220-35. doi: 10.4329/wjr.v7.i9.220.
Small-bowel carcinoid tumors are the most common form (42%) of gastrointestinal carcinoids, which by themselves comprise 70% of neuroendocrine tumors. Although primary small bowel neoplasms are overall rare (3%-6% of all gastrointestinal neoplasms), carcinoids still represent the second most common
PMID 26435774

Mariniello A1, Bodei L2, Tinelli C3, Baio SM2, Gilardi L2, Colandrea M2, Papi S2, Valmadre G4, Fazio N5, Galetta D6, Paganelli G7, Grana CM2.
European journal of nuclear medicine and molecular imaging.Eur J Nucl Med Mol Imaging.2015 Sep 21. [Epub ahead of print]
PURPOSE: Peptide receptor radionuclide therapy (PRRT) for the treatment of neuroendocrine tumours (NET) has been explored for almost two decades, but there are still few trials that have exclusively investigated well-differentiated and moderately differentiated NET arising from the respiratory tree.
PMID 26392198

宮川明祐,石橋啓如,高科亜弓,石垣和祥,岩井優,阿部宏美,片桐智子,坂口賀基,松島知広,田村寿英,小又誠一,窪田学,鈴木良夫,中村朗,糸林詠,紫村治久,志村謙次
Nippon Shokakibyo Gakkai Zasshi 111(1), 105-114, 2014
59歳男性．黒色便を契機に上部消化管内視鏡検査を施行．噴門部直下に潰瘍をともなう隆起性病変を認め，生検で腺癌と診断された．急速に増大し，肝転移も認めたが，出血管理目的に胃全摘術を施行した結果，骨肉腫への分化をともなう真性癌肉腫と診断された．S-1/CDDP併用療法は無効であったがCPT-11/MMC併用療法を3コース施行し，部分奏効を得た．同レジメンが骨肉腫への分化をともなう胃癌肉腫に有効であった …
NAID 130003383337

高住美香,石幡良一,紺野直紀,渡辺研也,高野真,猪狩弘之,内海康文,村島正泰,引地拓人,小原勝敏,大平弘正
日本消化器内視鏡学会雑誌 55(3), 450-458, 2013
69歳，男性．市民検診にて胃の隆起性病変を指摘され，精査加療目的に当科を受診した．内視鏡検査では胃体上部大弯後壁側に上皮性変化を伴う3cm大の亜有茎性腫瘍を認め，早期胃癌と考えESDを施行した．病理組織にて胃癌とカルチノイドが同一病変内に併存している所見を認め，背景粘膜には非腫瘍性内分泌小胞巣が認められた．さらに本例では，胃体部粘膜の萎縮，高ガストリン血症，抗胃壁細胞抗体陽性を認めA型胃炎と診断し …
NAID 130003375266