Journals / İstanbul Kuzey Klinikleri / 2015 / Cilt: 2 - Sayı: 2

A rare malignancy in a patient with neurofibromatosis: gastric adenocarcinoma

Pages
162–164
Publication Date
2022-10-18
DOI
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AI Summary & Key Takeaways

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

In this case report we aim to present a patient with neurofibromatosis operated due to gastric adenocarcinoma.

📌 3 Key Takeaways

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Objective & Hypothesis:Neurofibromatosis is an autosomal dominant disease that is characterized by cutaneous hyperpigmentation and multiple neurofibromas and often accompanied by localized peripheral and central neural tumors.
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Key Findings & Data:Gastrointestinal involvement is seen in 25% of the cases.
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Conclusion & Impact:In this case report we aim to present a patient with neurofibromatosis operated due to gastric adenocarcinoma.
🔬Design:Research Article
📍Scope:Comprehensive Sample
⚙️Variables:Domain Parameters

Abstract

Neurofibromatosis is an autosomal dominant disease that is characterized by cutaneous hyperpigmentation and multiple neurofibromas and often accompanied by localized peripheral and central neural tumors. Gastrointestinal involvement is seen in 25% of the cases. Gastrointestinal stromal tumors, pancreatic and duodenal neuroendocrine tumors are the most common tumors in patients with neurofibromatosis. Neurofibromatosis and gastric adenocarcinoma constitute an extremely rare combination. In this case report we aim to present a patient with neurofibromatosis operated due to gastric adenocarcinoma.

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Cite This Article

BARUT, B., OZDEMİR, F., HARPUTLUOGLU, M., ISİK, B., INCE, V. (2022). A rare malignancy in a patient with neurofibromatosis: gastric adenocarcinoma. İstanbul Kuzey Klinikleri, Cilt: 2 - Sayı: 2, 162–164. https://ajindex.com/articles/551691

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References (7)

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