Journals / Ulusal Cerrahi Dergisi / 2006 / Cilt: 22 - Sayı: 4

Intra-abdominal lymphangiomyomatosis

İntraabdominal lenfanjiomyiyomatoz

Pages
150–152
DOI
—
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AI Summary & Key Takeaways

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

Extrapulmonary LAM is quite rare.

📌 3 Key Takeaways

🎯
Objective & Hypothesis:Lymphangiomyomatosis (LAM) is a rare idiopathic disease characterized by hamartomatous smooth muscle proliferation of the lymph nodes, lymphatics, blood vessels as well as airways within the lung, mediastinum and abdomen.
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Key Findings & Data:Lymphangiomyomatosis (LAM) is a rare idiopathic disease characterized by hamartomatous smooth muscle proliferation of the lymph nodes, lymphatics, blood vessels as well as airways within the lung, mediastinum and abdomen.
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Conclusion & Impact:Extrapulmonary LAM is quite rare.
🔬Design:Research Article
📍Scope:Comprehensive Sample
⚙️Variables:Domain Parameters

Abstract

Lymphangiomyomatosis (LAM) is a rare idiopathic disease characterized by hamartomatous smooth muscle proliferation of the lymph nodes, lymphatics, blood vessels as well as airways within the lung, mediastinum and abdomen. Extrapulmonary LAM is quite rare.

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Cite This Article

TÜRKELİ, V., ŞENGÜL, N., ŞENOCAK, E., ERKOL, H. (2006). Intra-abdominal lymphangiomyomatosis. Ulusal Cerrahi Dergisi, Cilt: 22 - Sayı: 4, 150–152. https://ajindex.com/articles/325732

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