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10.12998/wjcc.v5.i2.35 http://scihub22266oqcxt.onion/10.12998/wjcc.v5.i2.35 C5314258!5314258!28255545     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       World+J+Clin+Cases 2017 ; 5 (2): 35-9 Nephropedia Template TP {{tp|p=28255545|t=2017. Fatality in Kikuchi-Fujimoto disease: A rare phenomenon |pdf=|usr=}}{{28255545}} gab.com Text Fatality in Kikuchi-Fujimoto disease: A rare phenomenon JO: World J Clin Cases http://www.kidney.de/pget.php?&tw=1&pmid=28255545 #FOAvip Kikuchi-Fujimoto disease (KFD), also known as histiocytic necrotizing lymphadenitis, is an uncommon condition, typically characterized by lymphadenopathy and fevers. It usually has a benign course; however, it may progress to fatality in extremely rare occasions. The diagnosis is made via lymph node biopsy and histopathology. Our patient was a young female who presented with shortness of breath, fever, and malaise. Physical examination revealed significant cervical and axillary lymphadenopathy. Chest X-ray displayed multilobar pneumonia. She required intubation and mechanical ventilation for progressive respiratory distress. Histopathology of lymph nodes demonstrated variable involvement of patchy areas of necrosis within the paracortex composed of karyorrhectic debris with abundant histiocytes consistent with KFD. After initial stabilization, the patient?s condition quickly deteriorated with acute anemia, thrombocytopenia and elevated prothrombin time, partial prothrombin time, and D-dimer levels. Disseminated intravascular coagulopathy (DIC) ensued resulting in the patient?s fatality. DIC in KFD is not well understood, but it is an important cause of mortality in patients with aggressive disease. Twit Text FOAVip Fatality in Kikuchi-Fujimoto disease: A rare phenomenon ????World J Clin Cases http://www.kidney.de/pget.php?&tw=1&pmid=28255545 #FOAvip Twit Text # Free Paper on # # # # # LINK http://www.kidney.de/pget.php?&tw=1&pmid=28255545 #FOAvip English Wikipedia <ref>{{Cite pmid|28255545}}</ref> Fatality in Kikuchi-Fujimoto disease: A rare phenomenon #MMPMID28255545 Barbat B; Jhaj R; Khurram D World J Clin Cases 2017[Feb]; 5 (2): 35-9 PMID28255545show ga Kikuchi-Fujimoto disease (KFD), also known as histiocytic necrotizing lymphadenitis, is an uncommon condition, typically characterized by lymphadenopathy and fevers. It usually has a benign course; however, it may progress to fatality in extremely rare occasions. The diagnosis is made via lymph node biopsy and histopathology. Our patient was a young female who presented with shortness of breath, fever, and malaise. Physical examination revealed significant cervical and axillary lymphadenopathy. Chest X-ray displayed multilobar pneumonia. She required intubation and mechanical ventilation for progressive respiratory distress. Histopathology of lymph nodes demonstrated variable involvement of patchy areas of necrosis within the paracortex composed of karyorrhectic debris with abundant histiocytes consistent with KFD. After initial stabilization, the patient?s condition quickly deteriorated with acute anemia, thrombocytopenia and elevated prothrombin time, partial prothrombin time, and D-dimer levels. Disseminated intravascular coagulopathy (DIC) ensued resulting in the patient?s fatality. DIC in KFD is not well understood, but it is an important cause of mortality in patients with aggressive disease. äFatality in Kikuchi-Fujimoto disease: A rare phenomenon (epmc).pdf DeepDyve Pubget Overpricing