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10.1016/j.anndiagpath.2020.151530

http://scihub22266oqcxt.onion/10.1016/j.anndiagpath.2020.151530
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32387855!7182529!32387855
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suck abstract from ncbi


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pmid32387855      Ann+Diagn+Pathol 2020 ; 46 (ä): 151530
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  • Analysis of complement deposition and viral RNA in placentas of COVID-19 patients #MMPMID32387855
  • Mulvey JJ; Magro CM; Ma LX; Nuovo GJ; Baergen RN
  • Ann Diagn Pathol 2020[Jun]; 46 (ä): 151530 PMID32387855show ga
  • COVID-19, the disease caused by the novel Coronavirus, SARS-CoV-2, is increasingly being recognized as a systemic thrombotic and microvascular injury syndrome that may have its roots in complement activation. We had the opportunity to study the placental pathology of five full-term births to COVID-19 patients. All five exhibited histology indicative of fetal vascular malperfusion characterized by focal avascular villi and thrombi in larger fetal vessels. Vascular complement deposition in the placentas was not abnormal, and staining for viral RNA and viral spike protein was negative. While all cases resulted in healthy, term deliveries, these findings indicate the systemic nature of COVID-19 infection. The finding of vascular thrombosis without complement deposition may reflect the systemic nature of COVID-19's procoagulant effects unrelated to systemic complement activation.
  • |Betacoronavirus/*genetics[MESH]
  • |COVID-19[MESH]
  • |Coronavirus Infections/complications/*virology[MESH]
  • |Female[MESH]
  • |Humans[MESH]
  • |Pandemics[MESH]
  • |Placenta/*virology[MESH]
  • |Pneumonia, Viral/complications/*virology[MESH]
  • |Pregnancy[MESH]
  • |RNA, Viral/*genetics[MESH]
  • |SARS-CoV-2[MESH]


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