| Literature DB >> 32295999 |
Tatsunori Shizuku1, Keiji Matsui1, Shinya Yagi2, Shogo Iwabuchi1.
Abstract
TEMPI syndrome, a disease entity comprising telangiectasia, erythrocytosis with high erythropoietin, monoclonal gammopathy, perinephric fluid collection, and intrapulmonary shunting, was first described by Sykes et al. in 2011. To our knowledge, only 15 cases have been reported worldwide, none of which were in Japan. We herein report a 47-year-old man who had intractable ascites for 2 and a half years and was referred to our department for a peritoneovenous shunt. In addition to ascites, he had telangiectasia, high erythropoietin, monoclonal gammopathy, and perinephric fluid collection. Thus, this is the first case of TEMPI syndrome in Japan.Entities:
Keywords: TEMPI syndrome; erythrocytosis; monoclonal gammopathy; perinephric fluid collection
Year: 2020 PMID: 32295999 DOI: 10.2169/internalmedicine.3547-19
Source DB: PubMed Journal: Intern Med ISSN: 0918-2918 Impact factor: 1.271