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Peutz-Jegher syndrome (PJS) is a rare, autosomal-dominant disorder characterized by hamartomatous polyps in any part of the alimentary tract, and almost always associated with intestinal polyposis and mucocutaneous pigmentation (1). Rarely, solitary PJP arise inpatients without other features of PJS. A review of the English literature revealed only 6 published cases since 1989. Here, we would l...
Pigmentation of lips in Peutz-Jeghers syndrome. Development of cancer is related to both environmental carcinogens and genetic predisposition. Though the risk of a common cancer occurring in relatives ofan affected person is generally low, familial aggregations that cannot be explained by environmental factors alone exist in some O neoplasms, such as breast and ovarian cancers and melanomas. In...
entity and is usually associated with polyposis syndromes such as familial polyposis coli, Cowden syndrome, Peutz Jegher syndrome, and Cronkhite-Canada syndrome (1, 2). A few reports have described a gastric hamartoma without polyposis coli (3-5). It is often overlooked due to its clinical insignificance and small size. We report a case of an unusually large sized, fat-containing gastric hamart...
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