Displaying all 9 publications

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  1. Raa H, As R, Tp G, A S
    J Neonatal Surg, 2016 04 10;5(2):19.
    PMID: 27123403
    Spontaneous gastric perforation is a rare entity in neonates. We report a case of spontaneous gastric perforation in a neonate operated for in-utero rupture of omphalocele.
    Matched MeSH terms: Hernia, Umbilical
  2. Yeo TC
    Med J Malaysia, 1986 Dec;41(4):352-5.
    PMID: 3670160
    Two cases of enteroumbilical fistula presenting in the neonatal period are reported. Both developed complications which required surgical intervention. A brief discussion on clinical features and management follows.
    Matched MeSH terms: Hernia, Umbilical/surgery
  3. Zurina Zainudin, Farah Inaz Syed Abdullah, Hong, Neoh Siew, Mughni Bahari, Irene Cheah Guat Sim
    MyJurnal
    Focal eventration involving the posterior segment of the
    hemidiaphragm is a rare congenital anomaly. We report of a 10-
    day-old infant who presented with significant respiratory
    insufficiency and failure to show any responses to standard
    treatment. The diagnosis of focal eventration of the diaphragm
    was not anticipated until ultrasonographic examination revealed
    the defect. Diaphragmatic plication resulted in complete
    resolution of symptoms. A high level clinical awareness is
    crucial as a relatively simple surgical procedure could avert long
    term life-threatening complications.
    Matched MeSH terms: Hernia, Umbilical
  4. Mohamed Faisal, A.H., Tan, H.L., Andrea, B.Y.L.
    MyJurnal
    Eventration of the diaphragm is caused by weakened musculature of the diaphragm. This can occur in one or
    both hemidiaphragms. Symptoms may be minimal and it is usually detected incidentally on chest radiograph
    which would show an elevation of the diaphragm. We report and discuss a case of eventration of right
    diaphragm in a patient presented with a lobulated lung mass on chest radiograph.
    Matched MeSH terms: Hernia, Umbilical
  5. Thambi Dorai CR
    Pediatr Surg Int, 2000;16(1-2):128-9.
    PMID: 10663861
    A neonate with umbilical evagination of the bladder (UEB) and omphalocele minor (OM) is reported. The findings in this case support the origin of the urachus from the upper end of the cloaca rather than the allantois. The frequent occurrence of OM with urachal anomalies, including UEB, suggests an embryological association between the two conditions.
    Matched MeSH terms: Hernia, Umbilical/pathology*
  6. Thambidorai CR, Arief H, Noor Afidah MS
    Singapore Med J, 2009 Dec;50(12):e412-4.
    PMID: 20087543
    Localised dilatation of a segment of the intestine without any macroscopically-identifiable cause is rare, and has been reported in association with omphalocoele in only 14 children up to 2006. In most of these cases, the segmental intestinal dilatation (SID) was either diagnosed incidentally, or due to presentation with partial or complete intestinal obstruction. We report, for the first time, a 37-week-old neonate with bowel perforation in SID associated with omphalocoele. In our case, a long thin vessel that resembled the mesodiverticular vessel of a Meckel's diverticulum was present in the dilated segment, supporting the view that SID and Meckel's diverticulum may be embryologically related.
    Matched MeSH terms: Hernia, Umbilical/complications
  7. Lim WK, Leong MC, Samion H
    Ann Pediatr Cardiol, 2016 5 24;9(2):183-5.
    PMID: 27212859 DOI: 10.4103/0974-2069.173549
    A 1.7 kg infant with obstructed supracardiac total anomalous pulmonary venous drainage (TAPVD) presented with severe pulmonary hypertension secondary to vertical vein obstruction. The child, in addition, had a large omphalocele that was being managed conservatively. The combination of low weight, unoperated omphalocele, and severe pulmonary hypertension made corrective cardiac surgery very high-risk. Therefore, transcatheter stenting of the stenotic vertical vein, as a bridge to corrective surgery was carried out. The procedure was carried out through the right internal jugular vein (RIJ). The stenotic segment of the vertical vein was stented using a coronary stent. After procedure, the child was discharged well to the referred hospital for weight gain and spontaneous epithelialization of the omphalocele. Stenting of the vertical vein through the internal jugular vein can be considered in very small neonates as a bridge to repair obstructed supracardiac total anomalous venous drainage.
    Matched MeSH terms: Hernia, Umbilical
  8. Wong AR, Ibrahim H, Van Rostenberghe H, Ishak Z, Radzi MJ
    J Paediatr Child Health, 2000 Dec;36(6):609-10.
    PMID: 11115044
    We present an unusual neonatal fungal infection, Hansenula anomala in a very low birthweight infant who underwent abdominal surgery for an omphalocele. Despite treatment with adequate doses of amphotericin B, the yeast continued to grow from the blood culture, and was only eradicated with the use of oral ketoconazole.
    Matched MeSH terms: Hernia, Umbilical/surgery
  9. Wong TL, Baki MM, Ishak S, See GB
    Int J Pediatr Otorhinolaryngol, 2018 Nov;114:134-137.
    PMID: 30262351 DOI: 10.1016/j.ijporl.2018.08.037
    We report a bizarre case of accessory larynx in an infant with OEIS syndrome (omphalocele, cloacal exstrophy, imperforated anus & spinal defects). This is the first reported case in literature of a duplicate accessory larynx which is a mirror image of the true larynx. A congenital duplication of the larynx is a rare anomaly and can present in various forms. In this case, the infant presented with recurrent lung infection and inability to wean off oxygen. Scope revealed severe laryngomalacia in addition to the accessory larynx. Hence, supraglottoplasty was done with aim to resolve the lung and airway problem.
    Matched MeSH terms: Hernia, Umbilical/complications*
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