- Case Report
- A case of hereditary pancreatitis with a N29I mutation in the cationic trypsinogen gene
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Jee Youn Shin, Dae Sung Oh, Jeong Min Rheu, Jeong Ok Shim, Ji Sook Park, Jae Sung Ko, Jeong Kee Seo
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Clin Exp Pediatr. 2006;49(10):1111-1115. Published online October 15, 2006
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Hereditary pancreatitis is an autosomal dominant disease characterized by recurrent episodes of pancreatitis, often beginning in childhood, with a positive family history involving at least two other affected family members with no known other precipitating factors. Most forms of hereditary pancreatitis are caused by one of two common mutations, i.e., R122H in exon 3 and N29I in exon 2 of... |
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- Original Article
- A Case of Pancreatoblastoma with Metastasis of the Liver.
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Dae Sung Oh, Yong Won Paik, Jae Sun Park, Kyung Hyun Choi, Man Ha Huh
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Clin Exp Pediatr. 1990;33(5):684-689. Published online May 31, 1990
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We experenced a case of pancreatoblastoma in a 6 years old Korean male who was admmited to
the pediatric department because of an abdominal mass and pathologically diagnosed following
surgical removal.
Microscopically, the resected mass was composed of small sized tumor cells arranged in glandular
or acini structure with multifoci of squamoid corpuscle. Extensive hemorrhagic necrosis was another
feature. Ultrastructucturally, two types of cells, dark... |
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