Diaphragmatic hernia pathophysiology
Diaphragmatic hernia Main page |
Diagnosis |
---|
Treatment |
Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1];Associate Editor(s)-in-Chief: Ahmed Younes M.B.B.CH [2]
Overview
Pathophysiology
- The herniated viscera decrease the area needed by the lung to develop appropriately.[1]
- According to the degree of herniation, the degree of pulmonary hypoplasia is determined.
- The herniated viscera impairs the development of the bronchial tree.
- As a consequence, the alveoli development is also slowed.[2]
- The development of the pulmonary artery tree is halted too resulting in excessive masculinization of the arteries.
- The increased pulmonary pressure leads to increased pressure on the right ventricle leading to the development of a right to left shunt.
- As most of the cases of diaphragmatic hernias are unilateral, the pulmonary hypoplasia is also usually unilateral, but it can be bilateral if the mediastinum is pushed by a massive unilateral hernia.
- The abnormal alveolar development can lead to hypoxemia leading to pulmonary vasoconstriction which aggravates the condition.
References
- ↑ Langham MR, Kays DW, Ledbetter DJ, Frentzen B, Sanford LL, Richards DS (1996). "Congenital diaphragmatic hernia. Epidemiology and outcome". Clin Perinatol. 23 (4): 671–88. PMID 8982563.
- ↑ Keijzer R, Puri P (2010). "Congenital diaphragmatic hernia". Semin. Pediatr. Surg. 19 (3): 180–5. doi:10.1053/j.sempedsurg.2010.03.001. PMID 20610190.