Zobrazeno 1 - 10
of 452
pro vyhledávání: '"congenital chylothorax"'
Autor:
Amel Ben Hamad, Chiraz Regaieg, Manel Charfi, Nadia Kolsi, Amira Bouraoui, Nedia Hamida, Afef Ben Thabet, Abdellatif Gargouri
Publikováno v:
Iranian Journal of Neonatology, Vol 15, Iss 1, Pp 55-62 (2024)
Background: Congenital Chylothorax (CC) is a rare condition, which is defined as an accumulation of the chyle in the pleural cavity;moreover, it is associated with significant morbidities, including respiratory distress, malnutrition, immunodeficienc
Externí odkaz:
https://doaj.org/article/8dbdf7d6067e4cad90f2897633fc9e56
Publikováno v:
Journal of Cardiothoracic Surgery, Vol 17, Iss 1, Pp 1-6 (2022)
Abstract Objective Congenital chylothorax (CC) is an uncommon congenital disease. The objective of this study was to analyze the clinical features, treatment, and outcome of infants with CC in a Chinese tertiary medical center. Methods CC was defined
Externí odkaz:
https://doaj.org/article/591f98ca37de45e794b40c8028e71a91
Akademický článek
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Autor:
Michaela Höck, Alexander Höller, Marlene Hammerl, Karina Wechselberger, Jakob Krösslhuber, Ursula Kiechl-Kohlendorfer, Sabine Scholl-Bürgi, Daniela Karall
Publikováno v:
Italian Journal of Pediatrics, Vol 47, Iss 1, Pp 1-7 (2021)
Abstract Background Congenital chylothorax (CC) is a rare but potentially life-threatening condition in newborns. It is defined as an accumulation of chyle in the pleural cavity. The few publications regarding medical management and therapeutic dieta
Externí odkaz:
https://doaj.org/article/2a473f198c3f4029955d4690c40b987c
Autor:
Andreea Vidru, Alexandra Cozinov, Cristina Dumitru, Andreea Avramescu, Veronica Marcu, Andra Pîrnuță, Alexandra Bouariu, Anca Panaitescu
Publikováno v:
Romanian Journal of Pediatrics, Vol 69, Iss 4, Pp 323-326 (2020)
Superior vena cava (SVC) agenesis or total congenital absence of superior vena cava is a very rare vascular anomaly, mainly asymptomatic throughout neonatal period. We present a case of bilateral total congenital absence of superior vena cava and tho
Externí odkaz:
https://doaj.org/article/b9942ae9ce7743f585e9b2afb0401f3d
Publikováno v:
Biomedicine Hub, Vol 5, Iss 3, Pp 66-70 (2020)
Etilefrine, a sympathomimetic agent, is reportedly effective against postoperative chylothorax. However, its effectiveness in treating congenital chylothorax was unknown. We report herein a case of refractory congenital chylothorax treated with etile
Externí odkaz:
https://doaj.org/article/02b1d1ac319d4c44a245d89881aa3aea
Publikováno v:
Frontiers in Pediatrics, Vol 9 (2021)
Background: Idiopathic congenital chylothorax is a rare but serious disease. Advancement in perinatal care and the renovated treatment modalities have brought about significant improvement in patient outcome.Objective: To describe the clinical course
Externí odkaz:
https://doaj.org/article/95900badc34f4826944b71725c5b09ca
Publikováno v:
American Journal of Perinatology Reports, Vol 10, Iss 04, Pp e403-e407 (2020)
Introduction Congenital complete atrioventricular block (CCAVB) associated with congenital chylothorax is a rare finding that has been reported in only one case in the literature. We report here the case of an infant with CCAVB complicated by congeni
Externí odkaz:
https://doaj.org/article/11a28dd94636447d911d805a5f9c2838
Publikováno v:
Journal of Neonatal Surgery, Vol 9 (2020)
Externí odkaz:
https://doaj.org/article/36d90429b6d14b8aacb56d036870d051
Publikováno v:
Iranian Journal of Neonatology, Vol 9, Iss 3, Pp 83-87 (2018)
Background: Oculo-palato-cerebral syndrome is an extremely rare condition characterized by various features, including low-birth weight, microcephaly, cerebral atrophy, mild-to-severe developmental delay, cleft palate, persistent hyperplastic primary
Externí odkaz:
https://doaj.org/article/0b52d4f977c3455ead7f91904a7ab914