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10.1155/2016/3212947 http://scihub22266oqcxt.onion/10.1155/2016/3212947 C5078661!5078661!27807449     free     free     free Deprecated: Implicit conversion from float 217.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534       Case+Rep+Med 2016 ; 2016 (ä): ä Nephropedia Template TP {{tp|p=27807449|t=2016. Splenic Involvement in Hereditary Hemorrhagic Telangiectasia |pdf=|usr=}}{{27807449}} gab.com Text Splenic Involvement in Hereditary Hemorrhagic Telangiectasia JO: Case Rep Med http://www.kidney.de/pget.php?&tw=1&pmid=27807449 #FOAvip A 33-year-old man who presented with prolonged epigastric pain was referred to our hospital. He had experienced recurrent epistaxis and had a family history of hereditary hemorrhagic telangiectasia. Computed tomography and magnetic resonance imaging revealed splenomegaly and a 9?cm hypervascular mass in his spleen. Computed tomography also showed a pulmonary arteriovenous malformation and heterogeneous enhancement of the liver parenchyma, suggesting the presence of arteriosystemic shunts and telangiectases. Based on these findings, the patient was definitely diagnosed with hereditary hemorrhagic telangiectasia according to Curaçao criteria. He underwent splenectomy, and his symptoms disappeared after surgery. Pathological examination of the resected specimen revealed that the hypervascular lesion of the spleen was not a tumor but was composed of abnormal vessels associated with hereditary hemorrhagic telangiectasia. Symptomatic splenic involvement may be a rare manifestation of hereditary hemorrhagic telangiectasia but can be revealed by imaging modalities. Twit Text FOAVip Splenic Involvement in Hereditary Hemorrhagic Telangiectasia ????Case Rep Med http://www.kidney.de/pget.php?&tw=1&pmid=27807449 #FOAvip Twit Text # Free Paper on # # # # # LINK http://www.kidney.de/pget.php?&tw=1&pmid=27807449 #FOAvip English Wikipedia <ref>{{Cite pmid|27807449}}</ref> Splenic Involvement in Hereditary Hemorrhagic Telangiectasia #MMPMID27807449 Takamatsu S; Sato K; Kato S; Nagano H; Ohtsukasa S; Kawachi Y Case Rep Med 2016[]; 2016 (ä): ä PMID27807449show ga A 33-year-old man who presented with prolonged epigastric pain was referred to our hospital. He had experienced recurrent epistaxis and had a family history of hereditary hemorrhagic telangiectasia. Computed tomography and magnetic resonance imaging revealed splenomegaly and a 9?cm hypervascular mass in his spleen. Computed tomography also showed a pulmonary arteriovenous malformation and heterogeneous enhancement of the liver parenchyma, suggesting the presence of arteriosystemic shunts and telangiectases. Based on these findings, the patient was definitely diagnosed with hereditary hemorrhagic telangiectasia according to Curaçao criteria. He underwent splenectomy, and his symptoms disappeared after surgery. Pathological examination of the resected specimen revealed that the hypervascular lesion of the spleen was not a tumor but was composed of abnormal vessels associated with hereditary hemorrhagic telangiectasia. Symptomatic splenic involvement may be a rare manifestation of hereditary hemorrhagic telangiectasia but can be revealed by imaging modalities. äSplenic Involvement in Hereditary Hemorrhagic Telangiectasia (epmc).pdf DeepDyve Pubget Overpricing