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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
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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