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10.4103/1947-2714.153928

http://scihub22266oqcxt.onion/10.4103/1947-2714.153928
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C4382768!4382768!25839006
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suck abstract from ncbi

pmid25839006      N+Am+J+Med+Sci 2015 ; 7 (3): 125-8
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  • Hereditary Hemorrhagic Telangiectasia #MMPMID25839006
  • Kamath N; Bhatia S; Singh H; Shetty A; Shetty S
  • N Am J Med Sci 2015[Mar]; 7 (3): 125-8 PMID25839006show ga
  • Background:: Hereditary hemorrhagic telangiectasia (HHT) is an autosomal dominant disorder, which affects various internal organs and has a tendency for bleeding. It has a classic triad of mucocutaneous telangiectasias, recurrent hemorrhages and positive familial history of first-degree relative. Epistaxis or gastrointestinal telangiectasia can be fatal in a small number of cases. Case Report:: A 44-year-old woman came with complaints of recurrent episodes of hematemesis and epistaxis. Patient had a family history of similar complaints. Patient underwent esophagogastroduodenoscopy (EGD), which revealed telangiectasia in the stomach. Imaging of the abdomen showed features suggestive of arteriovenous shunting. Conclusion:: HHT can remain undiagnosed for a long time, and is rarely being reported in the literature with management needing a multidisciplinary approach with early inputs from a gastroenterologist.
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