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1.
Pediatr Surg Int ; 28(6): 645-8, 2012 Jun.
Article in English | MEDLINE | ID: mdl-22207458

ABSTRACT

Skip segment Hirschprung's disease (SSHD) is an uncommon variant of Hirschprung's disease where normal intestine is interspersed proximally and distally by abnormal, aganglionated intestine. These segmental changes have no well-defined embryological explanation. We present a case of SSHD in the small bowel and concomitant perforated Meckel's diverticulum, with review of the literature relevant to SSHD.


Subject(s)
Hirschsprung Disease/complications , Hirschsprung Disease/diagnosis , Intestinal Perforation/etiology , Meckel Diverticulum/etiology , Hirschsprung Disease/pathology , Humans , Infant, Newborn , Male
2.
Thorax ; 66(2): 140-3, 2011 Feb.
Article in English | MEDLINE | ID: mdl-21160087

ABSTRACT

BACKGROUND: Gastro-oesophageal reflux is common in children with cystic fibrosis (CF) and is thought to be associated with pulmonary aspiration of gastric contents. The measurement of pepsin in bronchoalveolar lavage (BAL) fluid has recently been suggested to be a reliable indicator of aspiration. The prevalence of pulmonary aspiration in a group of children with CF was assessed and its association with lung inflammation investigated. METHODS: This was a cross-sectional case-control study. BAL fluid was collected from individuals with CF (n=31) and healthy controls (n=7). Interleukin-8 (IL-8), pepsin, neutrophil numbers and neutrophil elastase activity levels were measured in all samples. Clinical, microbiological and lung function data were collected from medical notes. RESULTS: The pepsin concentration in BAL fluid was higher in the CF group than in controls (mean (SD) 24.4 (27.4) ng/ml vs 4.3 (4.0) ng/ml, p=0.03). Those with CF who had raised pepsin concentrations had higher levels of IL-8 in the BAL fluid than those with a concentration comparable to controls (3.7 (2.7) ng/ml vs 1.4 (0.9) ng/ml, p=0.004). Within the CF group there was a moderate positive correlation between pepsin concentration and IL-8 in BAL fluid (r=0.48, p=0.04). There was no association between BAL fluid pepsin concentrations and age, sex, body mass index z score, forced expiratory volume in 1 s or Pseudomonas aeruginosa colonisation status. CONCLUSIONS: Many children with CF have increased levels of pepsin in the BAL fluid compared with normal controls. Increased pepsin levels were associated with higher IL-8 concentrations in BAL fluid. These data suggest that aspiration of gastric contents occurs in a subset of patients with CF and is associated with more pronounced lung inflammation.


Subject(s)
Bronchoalveolar Lavage Fluid/chemistry , Cystic Fibrosis/metabolism , Interleukin-8/analysis , Pepsin A/analysis , Adolescent , Biomarkers/analysis , Case-Control Studies , Child , Child, Preschool , Cystic Fibrosis/complications , Female , Humans , Infant , Male , Respiratory Aspiration/diagnosis , Respiratory Aspiration/etiology
3.
Pediatr Surg Int ; 25(1): 77-81, 2009 Jan.
Article in English | MEDLINE | ID: mdl-19002694

ABSTRACT

PURPOSE: In exomphalos major (EM), closure of the defect in the abdominal wall presents a challenge. The aim of this study is to evaluate a single centre experience of EM. MATERIALS: A 15-year retrospective case-note review; data presented as median (range). RESULTS: Fourteen infants (7 female) were born with EM: birth weight 2.9 (1.2-3.8) kg, gestational age 38 (31-39) weeks. One infant died in utero and one within the first hour of life. Severe pulmonary hypoplasia was present in 7/13 (54%), and there was a mortality of 6/13 (46%) live births. Infants were treated non-operatively primarily. Two infants underwent early surgery: one infant, born with a ruptured sac, had a surgical silo constructed on day 1 and closure on day 8, while a second infant had partial closure (skin only) on day 11. Ten infants had application of silver sulphadiazine to the sac 2-3 times per week. Enteral feeds were established soon after birth. They were discharged from hospital to allow granulation. Ventral hernia closure was performed on a subsequent admission. CONCLUSIONS: Exomphalos major can be successfully treated non-operatively, allowing immediate enteral feeding and early discharge while granulation takes place. In this series, exomphalos major has an incidence of 1 in 26,000, mortality is 46% and severe pulmonary hypoplasia is present in 54% of infants.


Subject(s)
Hernia, Umbilical/mortality , Hernia, Umbilical/therapy , Anti-Infective Agents, Local/therapeutic use , Bandages , Enteral Nutrition , Female , Fetal Death , Humans , Infant, Newborn , Ireland/epidemiology , Length of Stay/statistics & numerical data , Lung/abnormalities , Male , Pregnancy , Retrospective Studies , Silver Sulfadiazine/therapeutic use
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