Meconium peritonitis: Prenatal diagnosis of a rare entity and postnatal management.
نویسندگان
چکیده
The aims of this study were to review our therapy and outcome for meconium peritonitis (MP) patients, and to clarify predictors of postoperative morbidity and mortality. We retrospectively reviewed a total 15 patients with MP who received surgical intervention at our institute from December 1990 to November 2012. Diagnosis of MP was confirmed by operative findings. We analyzed the relationship between outcome and patients' factors including patients' characteristics, prenatal diagnosis, type of MP, general condition, and surgical procedure. There was no relationship between outcome and the following factors: gender, gestational age, body weight at birth, delivery type, Apgar score, prenatal diagnosis, types and causes of MP, and surgical procedure. However, the preoperative presence of circulation deficiency and serum CRP values were statistically significant predictors of outcome in our MP patients. Prenatal diagnosis is essential for the first step of perinatal therapy for MP. Surgical strategy should be selected according to the information of prenatal diagnosis. Early surgical procedures to reduce systemic and abdominal inflammation just after birth may improve the outcome of severe MP cases.
منابع مشابه
A Rare Case of Meconium Periorchitis Diagnosed in Utero
Meconium periorchitis is a rare disorder caused by fetal meconium peritonitis, with subsequent passage of meconium into the scrotum via a patent processus vaginalis. To date, clinical significance of meconium periorchitis for the prenatal diagnosis of meconium peritonitis and prediction for postnatal surgery remains to be determined. We present a clinical course of a fetus presenting with mecon...
متن کاملPostnatal Treatment in Antenatally Diagnosed Meconium Peritonitis.
Meconium peritonitis is a rare prenatal disease with an increased rate of morbidity and mortality in the neonatal period. Distinctive features revealed by prenatal and postnatal ultrasoundmay be present: abdominal calcifications, ascites, polyhydramnios, meconium pseudocyst, echogenic mass and dilated bowel or intestinal obstruction. Establishing clear postnatal treatment and prognosis is diffi...
متن کاملPrenatal diagnosis and postnatal management of meconium peritonitis.
BACKGROUND Meconium peritonitis (MP) is a rare prenatal condition that leads to substantial neonatal morbidity and mortality. PATIENTS AND METHODS All patients between 1998 and 2006 referred for prenatal diagnosis were retrospectively analyzed for diagnosis of MP. Prenatal ultrasound findings were compared with postnatal etiology, intraoperative findings, and postnatal outcome of the patients...
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The management of a case of antenatally diagnosed meconium peritonitis (MP) due to intrauterine intestinal perforation secondary to bowel atresia is reported. The literature is reviewed with reference to the significance and outcome of antenatally diagnosed MP.
متن کامل“The Nitty Gritty of it All”: Meconium Periorchitis
Meconium periorchitis is a bizarre albeit rare extraabdominal sequel of fetal meconium peritonitis; ensuing the passage of meconium into the scrotum via a patent processus vaginalis. We hereby present the case of a 20 day old male neonate with the sonographic, peroperative and histopathological correlates of Meconium Periorchitis. The scrotal meconium being predestined for calcification and res...
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ورودعنوان ژورنال:
- Intractable & rare diseases research
دوره 4 2 شماره
صفحات -
تاریخ انتشار 2015