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

İntraabdominal lenfanjiomyiyomatoz

Intra-abdominal lymphangiomyomatosis

Vildan TÜRKELİ
Neriman ŞENGÜL
Efsun ŞENOCAK
Hayri ERKOL
Sayfa
150–152
DOI
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Yapay Zeka Hızlı Bakış & Çıkarımlar

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⚡ TL;DR(1 Cümlede Hızlı Çıkarım)

Extrapulmonary LAM is quite rare.

📌 3 Maddede Bu Makale

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Amaç & Hipotez: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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Temel Bulgular & Veri: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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Sonuç & Katkı:Extrapulmonary LAM is quite rare.
🔬Tür:Araştırma Makalesi
📍Kapsam:Genişletilmiş Akademik Örneklem
⚙️Değişkenler:Alan Parametreleri

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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Bu Makaleye Atıf Yap

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

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Kaynakça (10)

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