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10.1097/MD.0000000000011153 http://scihub22266oqcxt.onion/10.1097/MD.0000000000011153 C6039685!6039685!29952963     free     free     free Deprecated: Implicit conversion from float 231.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Deprecated: Implicit conversion from float 231.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Deprecated: Implicit conversion from float 231.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Deprecated: Implicit conversion from float 231.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Deprecated: Implicit conversion from float 231.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Deprecated: Implicit conversion from float 231.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Deprecated: Implicit conversion from float 265.2 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534       Medicine+(Baltimore) 2018 ; 97 (26): ä Nephropedia Template TP {{tp|p=29952963|t=2018. Behçet disease associated with gastrointestinal amyloidosis manifested as hematochezia: A case report |pdf=|usr=}}{{29952963}} gab.com Text Behçet disease associated with gastrointestinal amyloidosis manifested as hematochezia: A case report JO: Medicine (Baltimore) http://www.kidney.de/pget.php?&tw=1&pmid=29952963 #FOAvip Rationale:: Behçet disease (BD) is an inflammatory disorder characterized by recurrent oral aphthous ulcers, genital ulcers, ocular lesions, and skin lesions. Complication of amyloidosis in patients with BD is rare. Here, we report a case of BD with immunoglobulin light chain (AL)-amyloidosis manifested as hematochezia. Patient concerns:: A 61-year-old man developed sudden hematochezia due to bleeding from multiple small colonic ulcers; AL-amyloid deposition was found on immunohistochemical examination of biopsy specimen of colonic ulcer. Systemic investigation revealed cardiac disfunction with cardiomegaly and progressive renal dysfunction, which indicated the presence of systemic AL-amyloidosis. Diagnoses:: Based on the findings of colonic ulcers with cardiac and renal involvement, a diagnosis of systemic AL-amyloidosis complicated by incomplete BD was established. Interventions:: He was treated with increased dose of oral prednisolone (20?mg/day), colchicine and mesalazine, because he was reluctant to receive aggressive chemotherapy (melphalan and dexamethasone) or autologous stem cell transplantation. Outcomes:: Colonic ulcers completely diminished after treatment, however, he died because of severe urinary tract infection and progressive renal failure after one year of gastrointestinal (GI) manifestations. Lessons:: Our case shows that patients with BD may have GI manifestations due not only to entero-BD but also due to GI amyloidosis. Twit Text FOAVip Behçet disease associated with gastrointestinal amyloidosis manifested as hematochezia: A case report ????Medicine (Baltimore) http://www.kidney.de/pget.php?&tw=1&pmid=29952963 #FOAvip Twit Text # Free Paper on # # # # # LINK http://www.kidney.de/pget.php?&tw=1&pmid=29952963 #FOAvip English Wikipedia <ref>{{Cite pmid|29952963}}</ref> Behçet disease associated with gastrointestinal amyloidosis manifested as hematochezia: A case report #MMPMID29952963 Sato S; Yashiro M; Matsuoka N; Kawana S; Asano T; Kobayashi H; Tasaki K; Watanabe H; Hashimoto Y; Migita K Medicine (Baltimore) 2018[Jun]; 97 (26): ä PMID29952963show ga Rationale:: Behçet disease (BD) is an inflammatory disorder characterized by recurrent oral aphthous ulcers, genital ulcers, ocular lesions, and skin lesions. Complication of amyloidosis in patients with BD is rare. Here, we report a case of BD with immunoglobulin light chain (AL)-amyloidosis manifested as hematochezia. Patient concerns:: A 61-year-old man developed sudden hematochezia due to bleeding from multiple small colonic ulcers; AL-amyloid deposition was found on immunohistochemical examination of biopsy specimen of colonic ulcer. Systemic investigation revealed cardiac disfunction with cardiomegaly and progressive renal dysfunction, which indicated the presence of systemic AL-amyloidosis. Diagnoses:: Based on the findings of colonic ulcers with cardiac and renal involvement, a diagnosis of systemic AL-amyloidosis complicated by incomplete BD was established. Interventions:: He was treated with increased dose of oral prednisolone (20?mg/day), colchicine and mesalazine, because he was reluctant to receive aggressive chemotherapy (melphalan and dexamethasone) or autologous stem cell transplantation. Outcomes:: Colonic ulcers completely diminished after treatment, however, he died because of severe urinary tract infection and progressive renal failure after one year of gastrointestinal (GI) manifestations. Lessons:: Our case shows that patients with BD may have GI manifestations due not only to entero-BD but also due to GI amyloidosis. äBehçet disease associated with gastrointestinal amyloidosis manifested(epmc).pdf DeepDyve Pubget Overpricing