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10.1111/bjd.19415

http://scihub22266oqcxt.onion/10.1111/bjd.19415
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32779733!7405151!32779733
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suck abstract from ncbi


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pmid32779733      Br+J+Dermatol 2021 ; 184 (1): 141-150
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  • The differing pathophysiologies that underlie COVID-19-associated perniosis and thrombotic retiform purpura: a case series #MMPMID32779733
  • Magro CM; Mulvey JJ; Laurence J; Sanders S; Crowson AN; Grossman M; Harp J; Nuovo G
  • Br J Dermatol 2021[Jan]; 184 (1): 141-150 PMID32779733show ga
  • BACKGROUND: There are two distinctive acral manifestations of COVID-19 embodying disparate clinical phenotypes. One is perniosis occurring in mildly symptomatic patients, typically children and young adults; the second is the thrombotic retiform purpura of critically ill adults with COVID-19. OBJECTIVES: To compare the clinical and pathological profiles of these two different cutaneous manifestations of COVID-19. METHODS: We compared the light microscopic, phenotypic, cytokine and SARS-CoV-2 protein and RNA profiles of COVID-19-associated perniosis with that of thrombotic retiform purpura in critical patients with COVID-19. RESULTS: Biopsies of COVID-19-associated perniosis exhibited vasocentric and eccrinotropic T-cell- and monocyte-derived CD11c(+) , CD14(+) and CD123(+) dendritic cell infiltrates. Both COVID-associated and idiopathic perniosis showed striking expression of the type I interferon-inducible myxovirus resistance protein A (MXA), an established marker for type I interferon signalling in tissue. SARS-CoV-2 RNA, interleukin-6 and caspase 3 were minimally expressed and confined to mononuclear inflammatory cells. The biopsies from livedo/retiform purpura showed pauci-inflammatory vascular thrombosis without any MXA decoration. Blood vessels exhibited extensive complement deposition with endothelial cell localization of SARS-CoV-2 protein, interleukin-6 and caspase 3; SARS-CoV-2 RNA was not seen. CONCLUSIONS: COVID-19-associated perniosis represents a virally triggered exaggerated immune reaction with significant type I interferon signaling. This is important to SARS-CoV-2 eradication and has implications in regards to a more generalized highly inflammatory response. We hypothesize that in the thrombotic retiform purpura of critically ill patients with COVID-19, the vascular thrombosis in the skin and other organ systems is associated with a minimal interferon response. This allows excessive viral replication with release of viral proteins that localize to extrapulmonary endothelium and trigger extensive complement activation.
  • |Adolescent[MESH]
  • |Age Factors[MESH]
  • |Aged[MESH]
  • |Biopsy[MESH]
  • |COVID-19/*complications/diagnosis/immunology/virology[MESH]
  • |Caspase 3/immunology/metabolism[MESH]
  • |Chilblains/*diagnosis/immunology/pathology[MESH]
  • |Diagnosis, Differential[MESH]
  • |Female[MESH]
  • |Foot[MESH]
  • |Hand[MESH]
  • |Humans[MESH]
  • |Interferon Type I/immunology/metabolism[MESH]
  • |Interleukin-6/immunology/metabolism[MESH]
  • |Livedo Reticularis/*diagnosis/immunology/pathology/virology[MESH]
  • |Male[MESH]
  • |Middle Aged[MESH]
  • |Myxovirus Resistance Proteins/analysis/metabolism[MESH]
  • |Purpura/*diagnosis/immunology/pathology/virology[MESH]
  • |RNA, Viral/isolation & purification[MESH]
  • |SARS-CoV-2/genetics/*immunology/isolation & purification[MESH]
  • |Severity of Illness Index[MESH]
  • |Skin/immunology/pathology/virology[MESH]


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