Gene/Protein Disease Symptom Drug Enzyme Compound
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Query: UMLS:C0019270 (hernia)
 15,856 document(s) hit in 31,850,051 MEDLINE articles (0.00 seconds)

An autopsy of a six-hour-old term neonate, who died during surgery for repair of a left diaphragmatic hernia, revealed an infantile hemangioendothelioma type I arising in a heterotopic lobe of liver in the left thorax. The upper pole of the tumor was attached by fibrovascular tissue to the lower lobe of the left hypoplastic lung. A pedicle attached to the lower pole of the heterotopic liver pierced through the diaphragm to the left lobe of the normal liver. This case is an example of an unusual association of congenital malformation and putative neoplasm.
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PMID:Infantile hemangioendothelioma of heterotopic intrathoracic liver associated with diaphragmatic hernia. 359 93

An unusual case of a neonate with absent pericardium, left-sided diaphragmatic hernia, and hepatic hemangioendothelioma is described. The posterolateral diaphragmatic hernia was successfully repaired, and agenesis of the pericardium did not interfere with cardiac function postoperatively. The hepatic tumour was a coincidental radiological finding, while liver function and the biochemical profile were normal. We also present a review of the literature on congenital absence of the pericardium and conclude that all cases should be screened for cardiac and hepatic anomalies.
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PMID:Congenital absence of the pericardium associated with congenital diaphragmatic hernia and hepatic hemangioendothelioma: case report and review of the literature. 1585 62

Diaphragmatic hernia is a rare complication following pediatric LT. Here, four children who developed right-sided posteromedial diaphragmatic hernias after LT are reported. The primary disease was biliary atresia in two patients, hemangioendothelioma in one, and angiosarcoma in one patient. All of the patients underwent living-donor LT using a left lateral graft. The patients presented with abdominal and/or pulmonary signs and symptoms. The diaphragmatic hernias were diagnosed at 28 days to seven months post-transplant by standard radiographs or chest CT. The defects were located at the posteromedial aspect of the diaphragm and were closed by primary closure. After diaphragm repair, the post-operative course was unremarkable and there were no recurrences. Thermal or mechanical injuries to the bare area, especially in cases of excessive adhesion between the liver and diaphragm after Kasai operation, were the possible causes of the posteromedial diaphragmatic hernia after pediatric LT.
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PMID:Posteromedial diaphragmatic hernia following pediatric liver transplantation. 2123 8