Molecular Biology of Gastrointestinal Stromal Tumor (GIST)

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Gastrointestinal stromal tumor (GIST).

Gastrointestinal stromal tumors (GISTs) may be defined as morphologically spindle cell, epithelioid, or occasionally pleomorphic mesenchymal tumours of the gastrointestinal tract that usually express the KIT protein and harbour mutation of a gene that encodes for a type III receptor tyrosine kinase (either KIT or PDGFRA). In Caucasian populations their annual incidence is 10 to 15 cases per mil...

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Primary omental Gastrointestinal stromal tumor (GIST)

BACKGROUND We report herein a rare case of primary omental gastrointestinal stromal tumor (GIST). CASE PRESENTATION A 65 year-old man was referred to our hospital with a huge abdominal mass occupying the entire left upper abdomen as shown by sonography. On computed tomography (CT), this appeared as a heterogeneous low-density mass with faint enhancement. Abdominal angiography revealed that th...

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Gastrointestinal stromal tumor (GIST) with liver metastases

Approximately 40% to 50% of gastrointestinal stromal tumor (GIST) patients will have recurrence or metastases after resection of the primary lesion, and the most common affected sites will be liver and peritoneum. Imatinib has been considered as the first-line therapy of metastatic GIST. Surgery for metastases is proposed when possible. Furthermore, there are controversies concerning hepatic re...

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Gastrointestinal bleeding and intussusception due to gastrointestinal stromal tumor (GIST).

BACKGROUND Small bowel tumors comprise 25% of gastrointestinal (GI) neoplasms, of which only between 0.2 and 1% correspond to gastrointestinal stromal tumors (GIST). GI bleeding is the most common presentation of GIST, being responsible in 1% of the cases. This type of neoplasm can also be the origin of an intussusception, which is an infrequent process during adult age, representing only 5% of...

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ژورنال

عنوان ژورنال: Nihon Gekakei Rengo Gakkaishi (Journal of Japanese College of Surgeons)

سال: 2004

ISSN: 0385-7883,1882-9112

DOI: 10.4030/jjcs1979.29.2_158