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http://scihub22266oqcxt.onion/ C5337772!5337772!28293057     free     free     free Warning: file_get_contents(https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&id=28293057&cmd=llinks): Failed to open stream: HTTP request failed! HTTP/1.1 429 Too Many Requests in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 215 Deprecated: Implicit conversion from float 211.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Deprecated: Implicit conversion from float 211.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Deprecated: Implicit conversion from float 211.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534       Iran+J+Med+Sci 2017 ; 42 (1): 94-7 Nephropedia Template TP {{tp|p=28293057|t=2017. Kikuchi-Fujimoto Disease: A Rare Presentation with Localized Iliac Lymphadenitis |pdf=|usr=}}{{28293057}} gab.com Text Kikuchi-Fujimoto Disease: A Rare Presentation with Localized Iliac Lymphadenitis JO: Iran J Med Sci http://www.kidney.de/pget.php?&tw=1&pmid=28293057 #FOAvip Kikuchi-Fujimoto disease (KFD) is a benign, self-limiting disease characterized by histiocytic necrotising lymphadenitis. Though several viral agents or an autoimmune etiology has been proposed as causative, the exact cause remains unknown. It has a female predilection and most commonly seen among young Asian people. Patients usually present with a febrile illness and the presence of lymphadenopathy may provide a clue to diagnosis. The most common site of lymphadenopathy is cervical lymph nodes while intra-abdominal involvement is uncommon. Cases of KFD presenting with intra-abdominal lymphadenopathy have been reported to occur with equal frequency in both sexes. Abdominal tuberculosis, non-Hodgkin?s lymphoma, and systemic lupus erythematosus are close differential diagnoses for this type of presentation. Treatment is mostly supportive as the disease usually resolves spontaneously; steroids are only required in severe cases. We report a 32-year-old male patient of intra-abdominal lymphadenitis that presented as fever of unknown origin (FUO) and diagnosed by excisional biopsy as a case of KFD. Twit Text FOAVip Kikuchi-Fujimoto Disease: A Rare Presentation with Localized Iliac Lymphadenitis ????Iran J Med Sci http://www.kidney.de/pget.php?&tw=1&pmid=28293057 #FOAvip Twit Text # Free Paper on # # # # # LINK http://www.kidney.de/pget.php?&tw=1&pmid=28293057 #FOAvip English Wikipedia <ref>{{Cite pmid|28293057}}</ref> Kikuchi-Fujimoto Disease: A Rare Presentation with Localized Iliac Lymphadenitis #MMPMID28293057 Anikhindi SA; Arora A; Dhawan S; Bansal N; Sharma P; Singla V; Kumar A Iran J Med Sci 2017[Jan]; 42 (1): 94-7 PMID28293057show ga Kikuchi-Fujimoto disease (KFD) is a benign, self-limiting disease characterized by histiocytic necrotising lymphadenitis. Though several viral agents or an autoimmune etiology has been proposed as causative, the exact cause remains unknown. It has a female predilection and most commonly seen among young Asian people. Patients usually present with a febrile illness and the presence of lymphadenopathy may provide a clue to diagnosis. The most common site of lymphadenopathy is cervical lymph nodes while intra-abdominal involvement is uncommon. Cases of KFD presenting with intra-abdominal lymphadenopathy have been reported to occur with equal frequency in both sexes. Abdominal tuberculosis, non-Hodgkin?s lymphoma, and systemic lupus erythematosus are close differential diagnoses for this type of presentation. Treatment is mostly supportive as the disease usually resolves spontaneously; steroids are only required in severe cases. We report a 32-year-old male patient of intra-abdominal lymphadenitis that presented as fever of unknown origin (FUO) and diagnosed by excisional biopsy as a case of KFD. äKikuchi-Fujimoto Disease: A Rare Presentation with Localized Iliac Lym(epmc).pdf DeepDyve Pubget Overpricing