Zobrazeno 1 - 10
of 145
pro vyhledávání: '"Pýcha K"'
Publikováno v:
European Journal of Pediatric Surgery Reports
European Journal of Pediatric Surgery Reports, Vol 05, Iss 01, Pp e51-e54 (2017)
European Journal of Pediatric Surgery Reports, Vol 05, Iss 01, Pp e51-e54 (2017)
Background Delayed surgery after stabilization of infants with congenital diaphragmatic hernia (CDH) is an accepted strategy. However, the evidence favoring delayed versus immediate surgical repair is limited. We present an extremely rare case of a v
Autor:
Koutecký J, K. Svojgr, Radvanský J, Kodetová D, Jeřábková, Smelhaus, Malinová B, Kodet R, Pýcha K, M. Zitková, Churáčková M, Snajdauf J, Malis J, Cyprová S, Starý J
Publikováno v:
Klinicka onkologie. 26:336-342
INTRODUCTION Nephroblastoma (Wilms tumor - WT) is the most common solid tumor of kidney in children. We present treatment development of WT at the Department of Pediatric Hematology and Oncology, Charles University in Prague, 2nd Faculty of Medicine
Autor:
Ladislav Krofta, Jaroslav Feyereisl, Jiří Vojtěch, Pýcha K, Zbyněk Straňák, Michal Rygl, L.A. Haak, Luboš Hašlík
Publikováno v:
The journal of maternal-fetalneonatal medicine : the official journal of the European Association of Perinatal Medicine, the Federation of Asia and Oceania Perinatal Societies, the International Society of Perinatal Obstetricians. 30(1)
Respiratory morbidity in congenital diaphragmatic hernia (CDH) is associated with high mortality and adverse outcome. Accurate prenatal diagnosis is essential for prognosis and potential treatment in utero. The aim was to evaluate the prenatal ultras
Publikováno v:
European Journal of Pediatric Surgery. 9:416-419
Papillary cystic and solid tumor of the pancreas (PCSTP), so-called Frantz tumor, is a very rare tumor in children. Only 62 cases, 57 girls and 5 boys, have been reported in children since 1959. The tumor presents usually as a slowly growing abdomina
Autor:
Tláskal T, Jachym Kucera, Jan Janota, Jan Miletin, Pýcha K, V. Čunát, Zbyněk Straňák, P. Velebil, Melichar J
Publikováno v:
Pediatric Surgery International. 21:684-686
The occurrence of coexisting congenital diaphragmatic hernia (CDH) and esophageal atresia (EA) with distal tracheoesophageal fistula (TEF) is extremely rare and is considered highly lethal. The combination of CDH with EA/TEF and truncus arteriosus co
Publikováno v:
The American Journal of Surgical Pathology. 18:837-842
We present a case of juxtaglomerular cell tumor (JCT) in a 10-year-old boy. The child suffered from severe hypertension that returned to normal following the tumor resection. The diagnosis of JCT was supported by electron-microscopic findings of typi
Autor:
Stejskalová E, Jarosová M, Malis J, Sumerauer D, Urbánková H, Lenka Krsková, Pýcha K, Schovanec J, Balcárková J, Smelhaus V, Kodetová D, Starý J
Publikováno v:
Europe PubMed Central
We present the results of a cytogenetic and molecular cytogenetic analysis of a series of patients with bone and soft tissue tumors. PATIENTS ANDMETHODS: We analyzed a cohort of 26 patients with Ewing sarcoma/PNET, 15 patients with rhabdomyosarcoma,
Autor:
Pýcha K, O. Petrů, Radan Keil, J. Kalousová, Jiří Šnajdauf, A. Kučera, Vladimir Mixa, Michal Rygl, Z. Hříbal
Publikováno v:
European journal of pediatric surgery : official journal of Austrian Association of Pediatric Surgery ... [et al] = Zeitschrift fur Kinderchirurgie. 17(5)
Introduction: Les traumatismes pancreatiques majeurs ou compliques chez l'enfant sont rares et leurs traitements demeurent discutes. Le but de cette etude est d'evaluer notre experience avec a la fois la chirurgie precoce et tardive dans ces cas pedi
Publikováno v:
Europe PubMed Central
To evaluate some perinatal and neonatal risk factors of occurrence of necrotising enterocolitis (NEC) and the current possibilities of treatment.A retrospective data analysis.Mother and Child Care Institute, Prague.The clinical course in 28 neonates
Publikováno v:
Europe PubMed Central
The authors present their experience with the reconstruction of the diaphragm with a synthetic polytetrafluoroethylene patch in a group of 66 neonates with a congenital diaphragmatic hernia. After preoperative stabilization 53 neonates (80%) were ope