VACTERL Association Complicated with Right-sided Congenital Diaphragmatic Hernia

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VACTERL Association Complicated with Right-sided Congenital Diaphragmatic Hernia.

We describe a neonate with VACTERL association and right-sided congenital diaphragmatic hernia (CDH). Such coexistence is rare. The lack of symptoms during the early neonatal period, the absence of bowel loops herniated into the right thoracic cavity, and an unfinished surgery led to clinical and radiological diagnostic difficulties. Respiratory distress occurred when the patient was 2 months o...

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Congenital Right-sided Diaphragmatic Hernia

Right-sided congenital diaphragmatic hernia has in the past been considered to be incompatible with life. Even as recently as 1925 Hedblom stated that 75 per cent. of all cases of congenital diaphragmatic hernia die before the age of one month. With modem advances in technique death is now in most cases avoidable, and must be blamed on failure to diagnose correctly. Mis-diagnosis is so much the...

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A Rare Association of Right-sided Congenital Diaphragmatic Hernia and Encephalocele: A Case Report

Background: This is a case report regarding a 2051-gram female newborn affected by right-sided congenital diaphragmatic hernia (CDH) presenting with encephalocele in the occipital region. Case report: The newborn was delivered by a 38-year-old mother from Darmian city, a rural district located in South Khorasan province, Iran. Co...

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Right-Sided Congenital Diaphragmatic Hernia and Myelomeningocele: A Rare Association.

Congenital diaphragmatic hernia (CDH) is a rare birth defect with a prevalence of < 0.5 per 1,000 live births. Majority of these defects are left-sided as most studies suggest that frequency of right-sided CDH was 10% of the total. The association of CDH with myelomeningocele (MMC) is extremely rare; as in Sweed's study of 116 consecutive cases of CDH, the incidence of associated MMC with CDH w...

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Hepatic pulmonary fusion: a rare association of right-sided congenital diaphragmatic hernia

Hepatic pulmonary fusion is a rare association of rightsided congenital diaphragmatic hernia. The repair and reduction in this case depends on the extent of fusion to the lungs and the associated mediastinal structures [1]. This case has thumb and index finger syndactyly and multiple clefts in vertebrae besides hepatic pulmonary fusion which makes it unique, the first of its kind. This is a cas...

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ژورنال

عنوان ژورنال: Pediatrics & Neonatology

سال: 2016

ISSN: 1875-9572

DOI: 10.1016/j.pedneo.2013.10.004