pubmed-article:16691304 | rdf:type | pubmed:Citation | lld:pubmed |
pubmed-article:16691304 | lifeskim:mentions | umls-concept:C0027651 | lld:lifeskim |
pubmed-article:16691304 | lifeskim:mentions | umls-concept:C0030274 | lld:lifeskim |
pubmed-article:16691304 | lifeskim:mentions | umls-concept:C0030305 | lld:lifeskim |
pubmed-article:16691304 | pubmed:issue | 5 | lld:pubmed |
pubmed-article:16691304 | pubmed:dateCreated | 2006-5-12 | lld:pubmed |
pubmed-article:16691304 | pubmed:abstractText | Eosinophilic pancreatitis (EP) is a rare disease. It typically occurs in the setting of either eosinophilic gastroenteritis or the hypereosinophilic syndrome. Isolated eosinophilic infiltration of the pancreas is less common. EP usually presents as a pancreatic tumour with abdominal pain and/or obstructive jaundice. The diagnosis is often not made until after pancreatic resection under suspicion of a pancreatic tumour. The case of a 14-year-old boy whose initial presentation was suggestive of a pancreatic tumour is reported. Radiological evaluation revealed a pancreatic mass suggestive of a pancreatic tumour obstructing the duodenum and common bile duct. The patient underwent surgery and a gastrojejunal anostomosis, tube cholecystostomy and biopsy were performed with no postoperative complications. The diagnosis of EP was established after surgical biopsy. The biopsy specimen revealed prominent eosinophilic infiltration. Serum immunoglobulin E levels were elevated. The patient was treated with oral prednisolone (40 mg/day). After two months of oral steroid therapy, clinical manifestations rapidly improved and peripheral eosinophilia subsided. Computed tomography scan revealed remission of the pancreatic mass-like lesion. | lld:pubmed |
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pubmed-article:16691304 | pubmed:language | eng | lld:pubmed |
pubmed-article:16691304 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:16691304 | pubmed:citationSubset | IM | lld:pubmed |
pubmed-article:16691304 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:16691304 | pubmed:status | MEDLINE | lld:pubmed |
pubmed-article:16691304 | pubmed:month | May | lld:pubmed |
pubmed-article:16691304 | pubmed:issn | 0835-7900 | lld:pubmed |
pubmed-article:16691304 | pubmed:author | pubmed-author:FoyH MHM | lld:pubmed |
pubmed-article:16691304 | pubmed:author | pubmed-author:CobanogluUmit... | lld:pubmed |
pubmed-article:16691304 | pubmed:author | pubmed-author:ImamogluMusta... | lld:pubmed |
pubmed-article:16691304 | pubmed:issnType | Print | lld:pubmed |
pubmed-article:16691304 | pubmed:volume | 20 | lld:pubmed |
pubmed-article:16691304 | pubmed:owner | NLM | lld:pubmed |
pubmed-article:16691304 | pubmed:authorsComplete | Y | lld:pubmed |
pubmed-article:16691304 | pubmed:pagination | 361-4 | lld:pubmed |
pubmed-article:16691304 | pubmed:dateRevised | 2009-11-18 | lld:pubmed |
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pubmed-article:16691304 | pubmed:year | 2006 | lld:pubmed |
pubmed-article:16691304 | pubmed:articleTitle | Eosinophilic pancreatitis mimicking pancreatic neoplasia. | lld:pubmed |
pubmed-article:16691304 | pubmed:affiliation | Department of Pediatric Surgery, Karadeniz Technical University, Trabzon, Turkey. dralicay@yahoo.com | lld:pubmed |
pubmed-article:16691304 | pubmed:publicationType | Journal Article | lld:pubmed |
pubmed-article:16691304 | pubmed:publicationType | Case Reports | lld:pubmed |