Congenital Diaphragmatic Hernia

التفاصيل البيبلوغرافية
العنوان: Congenital Diaphragmatic Hernia
المؤلفون: Mattioli G., Palo F.
المساهمون: Mattioli G., Mattioli, G., Palo, F.
بيانات النشر: Springer International Publishing
سنة النشر: 2021
المجموعة: Università degli Studi di Genova: CINECA IRIS
مصطلحات موضوعية: Bochdalek hernia, CDH, Diaphragmatic hernia, ECMO, hypoplastic lung, Morgagni hernia
الوصف: Congenital diaphragmatic hernia occurs in 1–5/10,000 live births. It is characterized by a defect in the separation of the thoracic cavity from the abdominal cavity due to incomplete development of the diaphragm. It follows the herniation of abdominal viscera at the thoracic level with hypoplasia of the lung ipsilateral to the hernia. The pre-and postoperative management of the patient is very complex. Contrary to what happened in the past, surgical treatment does not necessarily have to be urgent but only under stable clinical conditions, except in special cases. The postoperative survival rate is 70–80%, up to 90% in some structures and in particular for CDH not associated with other anomalies.
نوع الوثيقة: book part
وصف الملف: ELETTRONICO
اللغة: English
Relation: info:eu-repo/semantics/altIdentifier/isbn/978-3-030-74667-4; info:eu-repo/semantics/altIdentifier/isbn/978-3-030-74668-1; ispartofbook:Thoracic Surgery in Pediatric Patients; firstpage:175; lastpage:181; numberofpages:7; https://hdl.handle.net/11567/1138615; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-85161142626
DOI: 10.1007/978-3-030-74668-1_18
الاتاحة: https://hdl.handle.net/11567/1138615
https://doi.org/10.1007/978-3-030-74668-1_18
رقم الانضمام: edsbas.D0DC4067
قاعدة البيانات: BASE
الوصف
DOI:10.1007/978-3-030-74668-1_18