RESUMO
Omphalocele minor is often associated with the presence of other anomalies compared to that of omphalocele major. The occurrence of intestinal atresia is seldom associated with omphalocele minor. Prompt diagnosis and intervention can prevent morbidity and mortality. Following is a rare case report of combination of omphalocele minor and intestinal atresia with strangulation of the proximal bowel.
RESUMO
Background: Hernia of the umbilical cord is a rare clinical entity which presents with hernia of the small bowel into the proximal part of the umbilical cord. This is sporadically associated with other congenital malformations. This is usually poorly identified and mistakenly termed as 'omphalocele minor. Inadvertent clamping of the cord in these cases leads to iatrogenic bowel wall injury. The aim of this study is to present a spectrum of cases presenting with umbilical cord hernia in a tertiary care Govt medical college, along with demography, intra operative findings, associated malformations and postoperative outcome and 1 year follow up.Methods: This is an ambispective study on neonates who attended the Outpatient Department (OPD) or Emergency department. The babies were evaluated by age, birth weight, gender, any gross clinical malformation. They were also evaluated intraoperatively for any associated anomalies. Post-surgery the babies were followed up until 2 years of age in pediatric surgery OPD of the same institute and outcome was recorded.Results: Out of 90 babies, 88 babies (97.77%) had body weight more than 2.5 kg, and rest 2(2.22%) had bodyweight of 1.5kg and 1.8 kg. Regarding content of contents of umbilical cord hernia, out of 87 patients, 43 patients (49.42%) had ileal loop as, 32 patients (36.78%) had ileum with Meckel's diverticulum, 6 patients (6.39%) had cecum with appendix.Conclusions: Most of this study cases had ileal loops as content of the hernial sacs, and 36.78% cases had Meckel's diverticulum associated, which is a remnant of Vitello intestinal duct. Prompt identification of the condition and early intervention and adequate post-natal care are affective to prevent long term morbidity.
RESUMO
As hérnias perineais primárias resultam de um defeito no assoalho pélvico que permite a passagem de conteúdo abdominal para a região pelve-perineal. É uma enfermidade rara, tendo sido descritos menos de cem casos até hoje. Apresentamos o caso de uma paciente jovem com queixa recente de tumoração glútea dolorosa que, mesmo após o exame físico e tomográfico, não teve sua etiologia esclarecida. Foi então submetida à ressecção cirúrgica da lesão via perineal, quando se confirmou tratar-se de saco herniário isquiorretal esquerdo transpondo defeito no músculo elevador do ânus. Evoluiu sem intercorrências no pósoperatório e sem indícios de recidiva.
Primary perineal hernias result from a defect in the pelvic floor. It is a rare disease, having been described less than one hundred cases until today. We present a case of a young patient with recent complaint of painful gluteal tumor that even after the physical examination and CT did not clarified its etiology. She was submitted to a perineal resection of the lesion that confirmed being a hernia. She is going well without recurrence.