Journals / Turkish Journal of Gastroenterology / 2007 / Cilt: 18 - Sayı: 1

Papiller renal hücreli kanser ve gastrointestinal stromal tümör birlikteliği

Coexistence of papillary renal cell carcinoma and gastrointestinal stromal tumor in a case

Pages
47–49
DOI
—
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AI Summary & Key Takeaways

AI Insight
⚡ TL;DR(Too Long; Didn't Read)

In this paper, we present the appearance and growth of papillary renal cell carcinoma in a patient receiving Gleevec therapy for gastrointestinal stromal tumor

📌 3 Key Takeaways

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Objective & Hypothesis:Gastrointestinal stromal tumors are rare causes of gastrointestinal bleeding.
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Key Findings & Data:In most cases, these tumors are localized in the stomach and small intestine, more rarely in the esophagus and colon.
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Conclusion & Impact:In this paper, we present the appearance and growth of papillary renal cell carcinoma in a patient receiving Gleevec therapy for gastrointestinal stromal tumor
🔬Design:Research Article
📍Scope:Comprehensive Sample
⚙️Variables:Karsinom · renal hücreli · Nefrektomi

Abstract

Gastrointestinal stromal tumors are rare causes of gastrointestinal bleeding. In most cases, these tumors are localized in the stomach and small intestine, more rarely in the esophagus and colon. Papillary renal cell carcinoma and gastrointestinal stromal tumor may occur as recurrent familial tumors related to mutations in the protooncogenes, c-MET and c-KIT, both of which are tyrosine kinase receptor molecules. However, these two tumors can sometimes occur simultaneously in sporadic cases. Some authors blame imatinib mesylate (Gleevec), which is traditionally used in gastrointestinal stromal tumor therapy, as the etiological factor in certain secondary tumors, especially papillary renal cell cancer. In this paper, we present the appearance and growth of papillary renal cell carcinoma in a patient receiving Gleevec therapy for gastrointestinal stromal tumor

Özet

Gastrointestinal stromal tümörler sindirim sisteminin nadir görülen tümörleridir ve sıklıkla mide veya incebarsaktan, nadiren ise özefagus ve kolondan köken alırlar. Bu tümörler birer reseptör tirozin kinaz molekülü olan c-MET ve c-KIT protoonkogenlerinde meydana gelen mutasyonlar sonucu papiller renal hücreli kanser ile birlikte ailesel kanserler şeklinde karşımıza çıkabilmektedirler. Ancak bazen bu iki tümör sporadik vakalar olarak bir arada bulunabilmektedir ve bu durum bazı yazarlarca gastrointestinal stromal tümör tedavisinde kullanılan imatinib mesylate (gleveec)’ın sekonder tümörlere özellikle de papiller renal hücreli kansere yol açma potansiyeline bağlanmı ştır. Biz bu yazımızda metastatik gastrointestinal tümörü olan bir hastanın bu dönemde ortaya çıkıp gleevec tedavisi sı- rasında ilerleme gösteren papiller renal hücreli kanser ile birlikteliğ ini sunmaktayız.

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Cite This Article

REŞORLU, B., BALTACI, S., REŞORLU, M., KANKAYA, D., SAVAŞ, B. (2007). Papiller renal hücreli kanser ve gastrointestinal stromal tümör birlikteliği. Turkish Journal of Gastroenterology, Cilt: 18 - Sayı: 1, 47–49. https://ajindex.com/articles/409965

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