Hoehn T, William M, McPhaden A R, Stannigel H, Mayatepek E, Wadsworth R M
Neonatology and Paediatric Intensive Care Medicine, Dept of General Paediatrics, Heinrich-Heine-University, Moorenstr. 5, D-40225 Düsseldorf, Germany.
Eur Respir J. 2006 Jun;27(6):1311-5. doi: 10.1183/09031936.06.00082705.
Abnormal growth and development of lymphatic pulmonary structures leads to severe hypoxia in congenital pulmonary lymphangiectasis (CPL). This case study aims to determine the cellular source and topographical distribution of the nitric oxide synthases in CPL. It studies the post mortem tissue of a term newborn with the clinical course and histological findings of CPL and three controls without pulmonary pathology. It was found that endothelial cells of pulmonary arteries and lymphatic structures stained significantly more for endothelial nitric oxide synthase protein in the CPL patient compared to the controls. The authors conclude that synthesis of endothelial nitric oxide synthase is upregulated in vascular and lymphatic endothelial cells in congenital pulmonary lymphangiectasis.
先天性肺淋巴管扩张症(CPL)中肺淋巴结构的异常生长和发育会导致严重缺氧。本病例研究旨在确定CPL中一氧化氮合酶的细胞来源和拓扑分布。它研究了一名足月儿的尸检组织,该患儿具有CPL的临床病程和组织学表现,并与三名无肺部病理的对照者进行了比较。结果发现,与对照组相比,CPL患者肺动脉和淋巴结构的内皮细胞中内皮型一氧化氮合酶蛋白的染色明显更多。作者得出结论,先天性肺淋巴管扩张症中血管和淋巴管内皮细胞的内皮型一氧化氮合酶合成上调。