SARS‐CoV‐2 endothelial infection causes COVID‐19 chilblains: histopathological, immunohistochemical and ultrastructural study of seven paediatric cases

Summary Background Chilblains (‘COVID toes’) are being seen with increasing frequency in children and young adults during the COVID‐19 pandemic. Detailed histopathological descriptions of COVID‐19 chilblains have not been reported, and causality of SARS‐CoV‐2 has not yet been established. Objectives...

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Veröffentlicht in:British journal of dermatology (1951) 2020-10, Vol.183 (4), p.729-737
Hauptverfasser: Colmenero, I., Santonja, C., Alonso‐Riaño, M., Noguera‐Morel, L., Hernández‐Martín, A., Andina, D., Wiesner, T., Rodríguez‐Peralto, J.L., Requena, L., Torrelo, A.
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container_end_page 737
container_issue 4
container_start_page 729
container_title British journal of dermatology (1951)
container_volume 183
creator Colmenero, I.
Santonja, C.
Alonso‐Riaño, M.
Noguera‐Morel, L.
Hernández‐Martín, A.
Andina, D.
Wiesner, T.
Rodríguez‐Peralto, J.L.
Requena, L.
Torrelo, A.
description Summary Background Chilblains (‘COVID toes’) are being seen with increasing frequency in children and young adults during the COVID‐19 pandemic. Detailed histopathological descriptions of COVID‐19 chilblains have not been reported, and causality of SARS‐CoV‐2 has not yet been established. Objectives To describe the histopathological features of COVID‐19 chilblains and to explore the presence of SARS‐CoV‐2 in the tissue. Methods We examined skin biopsies from seven paediatric patients presenting with chilblains during the COVID‐19 pandemic. Immunohistochemistry for SARS‐CoV‐2 was performed in all cases and electron microscopy in one. Results Histopathology showed variable degrees of lymphocytic vasculitis ranging from endothelial swelling and endotheliitis to fibrinoid necrosis and thrombosis. Purpura, superficial and deep perivascular lymphocytic inflammation with perieccrine accentuation, oedema, and mild vacuolar interface damage were also seen. SARS‐CoV‐2 immunohistochemistry was positive in endothelial cells and epithelial cells of eccrine glands. Coronavirus particles were found in the cytoplasm of endothelial cells on electron microscopy. Conclusions Although the clinical and histopathological features were similar to other forms of chilblains, the presence of viral particles in the endothelium and the histological evidence of vascular damage support a causal relation of the lesions with SARS‐CoV‐2. Endothelial damage induced by the virus could be the key mechanism in the pathogenesis of COVID‐19 chilblains and perhaps also in a group of patients severely affected by COVID‐19 presenting with features of microangiopathic damage. What is already known about this topic? Despite the high number of cases of chilblains seen during the COVID‐19 pandemic, a definite causative role for SARS‐CoV‐2 has not yet been proven. Different pathogenetic hypotheses have been proposed, including coagulation anomalies, interferon release and external factors. What does this study add? The demonstration of SARS‐CoV‐2 in endothelial cells of skin biopsies by immunohistochemistry and electron microscopy confirms that these lesions are part of the spectrum of COVID‐19. Virus‐induced vascular damage and secondary ischaemia could explain the pathophysiology of COVID‐19 chilblains. Our findings support the hypothesis that widespread endothelial infection by SARS‐CoV‐2 could have a pathogenetic role in the severe forms of COVID‐19. Linked Comment: Wetter. Br J Dermatol 2020; 183:
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Detailed histopathological descriptions of COVID‐19 chilblains have not been reported, and causality of SARS‐CoV‐2 has not yet been established. Objectives To describe the histopathological features of COVID‐19 chilblains and to explore the presence of SARS‐CoV‐2 in the tissue. Methods We examined skin biopsies from seven paediatric patients presenting with chilblains during the COVID‐19 pandemic. Immunohistochemistry for SARS‐CoV‐2 was performed in all cases and electron microscopy in one. Results Histopathology showed variable degrees of lymphocytic vasculitis ranging from endothelial swelling and endotheliitis to fibrinoid necrosis and thrombosis. Purpura, superficial and deep perivascular lymphocytic inflammation with perieccrine accentuation, oedema, and mild vacuolar interface damage were also seen. SARS‐CoV‐2 immunohistochemistry was positive in endothelial cells and epithelial cells of eccrine glands. Coronavirus particles were found in the cytoplasm of endothelial cells on electron microscopy. Conclusions Although the clinical and histopathological features were similar to other forms of chilblains, the presence of viral particles in the endothelium and the histological evidence of vascular damage support a causal relation of the lesions with SARS‐CoV‐2. Endothelial damage induced by the virus could be the key mechanism in the pathogenesis of COVID‐19 chilblains and perhaps also in a group of patients severely affected by COVID‐19 presenting with features of microangiopathic damage. What is already known about this topic? Despite the high number of cases of chilblains seen during the COVID‐19 pandemic, a definite causative role for SARS‐CoV‐2 has not yet been proven. Different pathogenetic hypotheses have been proposed, including coagulation anomalies, interferon release and external factors. What does this study add? The demonstration of SARS‐CoV‐2 in endothelial cells of skin biopsies by immunohistochemistry and electron microscopy confirms that these lesions are part of the spectrum of COVID‐19. Virus‐induced vascular damage and secondary ischaemia could explain the pathophysiology of COVID‐19 chilblains. Our findings support the hypothesis that widespread endothelial infection by SARS‐CoV‐2 could have a pathogenetic role in the severe forms of COVID‐19. Linked Comment: Wetter. Br J Dermatol 2020; 183:611. Linked Comment: Wetter. Br J Dermatol 2020; 183:611. Plain language summary available online</description><identifier>ISSN: 0007-0963</identifier><identifier>EISSN: 1365-2133</identifier><identifier>DOI: 10.1111/bjd.19327</identifier><identifier>PMID: 32562567</identifier><language>eng</language><publisher>England: Oxford University Press</publisher><subject>Betacoronavirus - isolation &amp; purification ; Betacoronavirus - pathogenicity ; Biopsy ; Chilblains - pathology ; Chilblains - virology ; Child ; Coronavirus Infections - complications ; Coronavirus Infections - pathology ; Coronavirus Infections - virology ; Coronaviruses ; COVID-19 ; Cytoplasm ; Edema ; Electron microscopy ; Endothelial cells ; Endothelial Cells - pathology ; Endothelial Cells - ultrastructure ; Endothelial Cells - virology ; Endothelium ; Endothelium, Vascular - pathology ; Endothelium, Vascular - virology ; Epithelial cells ; Glands ; Histopathology ; Humans ; Immunohistochemistry ; Interferon ; Ischemia ; Microscopy ; Microscopy, Electron ; Original ; Paediatric Dermatology ; Pandemics ; Pediatrics ; Pneumonia, Viral - complications ; Pneumonia, Viral - pathology ; Pneumonia, Viral - virology ; Purpura ; SARS-CoV-2 ; Severe acute respiratory syndrome coronavirus 2 ; Skin - blood supply ; Skin - pathology ; Skin - virology ; Skin Diseases - pathology ; Skin Diseases - virology ; Thrombosis ; Vasculitis ; Vasculitis - pathology ; Vasculitis - virology ; Young adults</subject><ispartof>British journal of dermatology (1951), 2020-10, Vol.183 (4), p.729-737</ispartof><rights>2020 British Association of Dermatologists</rights><rights>2020 British Association of Dermatologists.</rights><rights>Copyright © 2020 British Association of Dermatologists</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4437-5862d0c5a5df5d762b127b4a159b68a0507b96e3bcdc843ff7c94d5186ba40453</citedby><cites>FETCH-LOGICAL-c4437-5862d0c5a5df5d762b127b4a159b68a0507b96e3bcdc843ff7c94d5186ba40453</cites><orcidid>0000-0001-5694-8536 ; 0000-0002-5400-0693 ; 0000-0001-5877-2992 ; 0000-0002-1045-4810 ; 0000-0002-5940-6916 ; 0000-0001-6859-187X ; 0000-0001-7260-8718</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1111%2Fbjd.19327$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1111%2Fbjd.19327$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>230,314,776,780,881,1411,27903,27904,45553,45554</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/32562567$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Colmenero, I.</creatorcontrib><creatorcontrib>Santonja, C.</creatorcontrib><creatorcontrib>Alonso‐Riaño, M.</creatorcontrib><creatorcontrib>Noguera‐Morel, L.</creatorcontrib><creatorcontrib>Hernández‐Martín, A.</creatorcontrib><creatorcontrib>Andina, D.</creatorcontrib><creatorcontrib>Wiesner, T.</creatorcontrib><creatorcontrib>Rodríguez‐Peralto, J.L.</creatorcontrib><creatorcontrib>Requena, L.</creatorcontrib><creatorcontrib>Torrelo, A.</creatorcontrib><title>SARS‐CoV‐2 endothelial infection causes COVID‐19 chilblains: histopathological, immunohistochemical and ultrastructural study of seven paediatric cases</title><title>British journal of dermatology (1951)</title><addtitle>Br J Dermatol</addtitle><description>Summary Background Chilblains (‘COVID toes’) are being seen with increasing frequency in children and young adults during the COVID‐19 pandemic. Detailed histopathological descriptions of COVID‐19 chilblains have not been reported, and causality of SARS‐CoV‐2 has not yet been established. Objectives To describe the histopathological features of COVID‐19 chilblains and to explore the presence of SARS‐CoV‐2 in the tissue. Methods We examined skin biopsies from seven paediatric patients presenting with chilblains during the COVID‐19 pandemic. Immunohistochemistry for SARS‐CoV‐2 was performed in all cases and electron microscopy in one. Results Histopathology showed variable degrees of lymphocytic vasculitis ranging from endothelial swelling and endotheliitis to fibrinoid necrosis and thrombosis. Purpura, superficial and deep perivascular lymphocytic inflammation with perieccrine accentuation, oedema, and mild vacuolar interface damage were also seen. SARS‐CoV‐2 immunohistochemistry was positive in endothelial cells and epithelial cells of eccrine glands. Coronavirus particles were found in the cytoplasm of endothelial cells on electron microscopy. Conclusions Although the clinical and histopathological features were similar to other forms of chilblains, the presence of viral particles in the endothelium and the histological evidence of vascular damage support a causal relation of the lesions with SARS‐CoV‐2. Endothelial damage induced by the virus could be the key mechanism in the pathogenesis of COVID‐19 chilblains and perhaps also in a group of patients severely affected by COVID‐19 presenting with features of microangiopathic damage. What is already known about this topic? Despite the high number of cases of chilblains seen during the COVID‐19 pandemic, a definite causative role for SARS‐CoV‐2 has not yet been proven. Different pathogenetic hypotheses have been proposed, including coagulation anomalies, interferon release and external factors. What does this study add? The demonstration of SARS‐CoV‐2 in endothelial cells of skin biopsies by immunohistochemistry and electron microscopy confirms that these lesions are part of the spectrum of COVID‐19. Virus‐induced vascular damage and secondary ischaemia could explain the pathophysiology of COVID‐19 chilblains. Our findings support the hypothesis that widespread endothelial infection by SARS‐CoV‐2 could have a pathogenetic role in the severe forms of COVID‐19. Linked Comment: Wetter. Br J Dermatol 2020; 183:611. Linked Comment: Wetter. Br J Dermatol 2020; 183:611. Plain language summary available online</description><subject>Betacoronavirus - isolation &amp; purification</subject><subject>Betacoronavirus - pathogenicity</subject><subject>Biopsy</subject><subject>Chilblains - pathology</subject><subject>Chilblains - virology</subject><subject>Child</subject><subject>Coronavirus Infections - complications</subject><subject>Coronavirus Infections - pathology</subject><subject>Coronavirus Infections - virology</subject><subject>Coronaviruses</subject><subject>COVID-19</subject><subject>Cytoplasm</subject><subject>Edema</subject><subject>Electron microscopy</subject><subject>Endothelial cells</subject><subject>Endothelial Cells - pathology</subject><subject>Endothelial Cells - ultrastructure</subject><subject>Endothelial Cells - virology</subject><subject>Endothelium</subject><subject>Endothelium, Vascular - pathology</subject><subject>Endothelium, Vascular - virology</subject><subject>Epithelial cells</subject><subject>Glands</subject><subject>Histopathology</subject><subject>Humans</subject><subject>Immunohistochemistry</subject><subject>Interferon</subject><subject>Ischemia</subject><subject>Microscopy</subject><subject>Microscopy, Electron</subject><subject>Original</subject><subject>Paediatric Dermatology</subject><subject>Pandemics</subject><subject>Pediatrics</subject><subject>Pneumonia, Viral - complications</subject><subject>Pneumonia, Viral - pathology</subject><subject>Pneumonia, Viral - virology</subject><subject>Purpura</subject><subject>SARS-CoV-2</subject><subject>Severe acute respiratory syndrome coronavirus 2</subject><subject>Skin - blood supply</subject><subject>Skin - pathology</subject><subject>Skin - virology</subject><subject>Skin Diseases - pathology</subject><subject>Skin Diseases - virology</subject><subject>Thrombosis</subject><subject>Vasculitis</subject><subject>Vasculitis - pathology</subject><subject>Vasculitis - virology</subject><subject>Young adults</subject><issn>0007-0963</issn><issn>1365-2133</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2020</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp1kdtqFTEUhoModrv1wheQgDcKTpvDZA5eCHXXQ6VQsNrbkEkynWwyyTaHyr7zEXwBX84nMe2uRQVDyIK1Pv61Vn4AHmO0j8s5GNZqH_eUtHfAAtOGVQRTehcsEEJthfqG7oEHMa4RwhQxdB_sUcKactsF-HF2-PHs57fvK39eXgK1Uz5N2hphoXGjlsl4B6XIUUe4Oj0_PioY7qGcjB2sMC6-hJOJyW9Emrz1F0YK-wKaec7OXxfkpOerJBROwWxTEDGFLFMOJRdTVlvoRxj1pXZwI7QyIgUjS8vS8SG4Nwob9aObuASf3775tHpfnZy-O14dnlSyrmlbsa4hCkkmmBqZahsyYNIOtcCsH5pOlJ3boW80HaSSXU3HsZV9rRjumkHUqGZ0CV7tdDd5mLWS2pUxLd8EM4uw5V4Y_nfFmYlf-EveUkJJ-foleHYjEPyXrGPis4lSWyuc9jlyUmNGEcWkK-jTf9C1z8GV9QpVd4SQHqNCPd9RMvgYgx5vh8GIX5nOi-n82vTCPvlz-lvyt8sFONgBX43V2_8r8dcfjnaSvwB6U7v0</recordid><startdate>202010</startdate><enddate>202010</enddate><creator>Colmenero, I.</creator><creator>Santonja, C.</creator><creator>Alonso‐Riaño, M.</creator><creator>Noguera‐Morel, L.</creator><creator>Hernández‐Martín, A.</creator><creator>Andina, D.</creator><creator>Wiesner, T.</creator><creator>Rodríguez‐Peralto, J.L.</creator><creator>Requena, L.</creator><creator>Torrelo, A.</creator><general>Oxford University Press</general><general>John Wiley and Sons Inc</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7T5</scope><scope>H94</scope><scope>K9.</scope><scope>NAPCQ</scope><scope>7X8</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0001-5694-8536</orcidid><orcidid>https://orcid.org/0000-0002-5400-0693</orcidid><orcidid>https://orcid.org/0000-0001-5877-2992</orcidid><orcidid>https://orcid.org/0000-0002-1045-4810</orcidid><orcidid>https://orcid.org/0000-0002-5940-6916</orcidid><orcidid>https://orcid.org/0000-0001-6859-187X</orcidid><orcidid>https://orcid.org/0000-0001-7260-8718</orcidid></search><sort><creationdate>202010</creationdate><title>SARS‐CoV‐2 endothelial infection causes COVID‐19 chilblains: histopathological, immunohistochemical and ultrastructural study of seven paediatric cases</title><author>Colmenero, I. ; Santonja, C. ; Alonso‐Riaño, M. ; Noguera‐Morel, L. ; Hernández‐Martín, A. ; Andina, D. ; Wiesner, T. ; Rodríguez‐Peralto, J.L. ; Requena, L. ; Torrelo, A.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4437-5862d0c5a5df5d762b127b4a159b68a0507b96e3bcdc843ff7c94d5186ba40453</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2020</creationdate><topic>Betacoronavirus - isolation &amp; purification</topic><topic>Betacoronavirus - pathogenicity</topic><topic>Biopsy</topic><topic>Chilblains - pathology</topic><topic>Chilblains - virology</topic><topic>Child</topic><topic>Coronavirus Infections - complications</topic><topic>Coronavirus Infections - pathology</topic><topic>Coronavirus Infections - virology</topic><topic>Coronaviruses</topic><topic>COVID-19</topic><topic>Cytoplasm</topic><topic>Edema</topic><topic>Electron microscopy</topic><topic>Endothelial cells</topic><topic>Endothelial Cells - pathology</topic><topic>Endothelial Cells - ultrastructure</topic><topic>Endothelial Cells - virology</topic><topic>Endothelium</topic><topic>Endothelium, Vascular - pathology</topic><topic>Endothelium, Vascular - virology</topic><topic>Epithelial cells</topic><topic>Glands</topic><topic>Histopathology</topic><topic>Humans</topic><topic>Immunohistochemistry</topic><topic>Interferon</topic><topic>Ischemia</topic><topic>Microscopy</topic><topic>Microscopy, Electron</topic><topic>Original</topic><topic>Paediatric Dermatology</topic><topic>Pandemics</topic><topic>Pediatrics</topic><topic>Pneumonia, Viral - complications</topic><topic>Pneumonia, Viral - pathology</topic><topic>Pneumonia, Viral - virology</topic><topic>Purpura</topic><topic>SARS-CoV-2</topic><topic>Severe acute respiratory syndrome coronavirus 2</topic><topic>Skin - blood supply</topic><topic>Skin - pathology</topic><topic>Skin - virology</topic><topic>Skin Diseases - pathology</topic><topic>Skin Diseases - virology</topic><topic>Thrombosis</topic><topic>Vasculitis</topic><topic>Vasculitis - pathology</topic><topic>Vasculitis - virology</topic><topic>Young adults</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Colmenero, I.</creatorcontrib><creatorcontrib>Santonja, C.</creatorcontrib><creatorcontrib>Alonso‐Riaño, M.</creatorcontrib><creatorcontrib>Noguera‐Morel, L.</creatorcontrib><creatorcontrib>Hernández‐Martín, A.</creatorcontrib><creatorcontrib>Andina, D.</creatorcontrib><creatorcontrib>Wiesner, T.</creatorcontrib><creatorcontrib>Rodríguez‐Peralto, J.L.</creatorcontrib><creatorcontrib>Requena, L.</creatorcontrib><creatorcontrib>Torrelo, A.</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Immunology Abstracts</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>ProQuest Health &amp; Medical Complete (Alumni)</collection><collection>Nursing &amp; Allied Health Premium</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>British journal of dermatology (1951)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Colmenero, I.</au><au>Santonja, C.</au><au>Alonso‐Riaño, M.</au><au>Noguera‐Morel, L.</au><au>Hernández‐Martín, A.</au><au>Andina, D.</au><au>Wiesner, T.</au><au>Rodríguez‐Peralto, J.L.</au><au>Requena, L.</au><au>Torrelo, A.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>SARS‐CoV‐2 endothelial infection causes COVID‐19 chilblains: histopathological, immunohistochemical and ultrastructural study of seven paediatric cases</atitle><jtitle>British journal of dermatology (1951)</jtitle><addtitle>Br J Dermatol</addtitle><date>2020-10</date><risdate>2020</risdate><volume>183</volume><issue>4</issue><spage>729</spage><epage>737</epage><pages>729-737</pages><issn>0007-0963</issn><eissn>1365-2133</eissn><abstract>Summary Background Chilblains (‘COVID toes’) are being seen with increasing frequency in children and young adults during the COVID‐19 pandemic. Detailed histopathological descriptions of COVID‐19 chilblains have not been reported, and causality of SARS‐CoV‐2 has not yet been established. Objectives To describe the histopathological features of COVID‐19 chilblains and to explore the presence of SARS‐CoV‐2 in the tissue. Methods We examined skin biopsies from seven paediatric patients presenting with chilblains during the COVID‐19 pandemic. Immunohistochemistry for SARS‐CoV‐2 was performed in all cases and electron microscopy in one. Results Histopathology showed variable degrees of lymphocytic vasculitis ranging from endothelial swelling and endotheliitis to fibrinoid necrosis and thrombosis. Purpura, superficial and deep perivascular lymphocytic inflammation with perieccrine accentuation, oedema, and mild vacuolar interface damage were also seen. SARS‐CoV‐2 immunohistochemistry was positive in endothelial cells and epithelial cells of eccrine glands. Coronavirus particles were found in the cytoplasm of endothelial cells on electron microscopy. Conclusions Although the clinical and histopathological features were similar to other forms of chilblains, the presence of viral particles in the endothelium and the histological evidence of vascular damage support a causal relation of the lesions with SARS‐CoV‐2. Endothelial damage induced by the virus could be the key mechanism in the pathogenesis of COVID‐19 chilblains and perhaps also in a group of patients severely affected by COVID‐19 presenting with features of microangiopathic damage. What is already known about this topic? Despite the high number of cases of chilblains seen during the COVID‐19 pandemic, a definite causative role for SARS‐CoV‐2 has not yet been proven. Different pathogenetic hypotheses have been proposed, including coagulation anomalies, interferon release and external factors. What does this study add? The demonstration of SARS‐CoV‐2 in endothelial cells of skin biopsies by immunohistochemistry and electron microscopy confirms that these lesions are part of the spectrum of COVID‐19. Virus‐induced vascular damage and secondary ischaemia could explain the pathophysiology of COVID‐19 chilblains. Our findings support the hypothesis that widespread endothelial infection by SARS‐CoV‐2 could have a pathogenetic role in the severe forms of COVID‐19. Linked Comment: Wetter. Br J Dermatol 2020; 183:611. Linked Comment: Wetter. Br J Dermatol 2020; 183:611. 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source Oxford University Press Journals All Titles (1996-Current); MEDLINE; Wiley Online Library Journals Frontfile Complete
subjects Betacoronavirus - isolation & purification
Betacoronavirus - pathogenicity
Biopsy
Chilblains - pathology
Chilblains - virology
Child
Coronavirus Infections - complications
Coronavirus Infections - pathology
Coronavirus Infections - virology
Coronaviruses
COVID-19
Cytoplasm
Edema
Electron microscopy
Endothelial cells
Endothelial Cells - pathology
Endothelial Cells - ultrastructure
Endothelial Cells - virology
Endothelium
Endothelium, Vascular - pathology
Endothelium, Vascular - virology
Epithelial cells
Glands
Histopathology
Humans
Immunohistochemistry
Interferon
Ischemia
Microscopy
Microscopy, Electron
Original
Paediatric Dermatology
Pandemics
Pediatrics
Pneumonia, Viral - complications
Pneumonia, Viral - pathology
Pneumonia, Viral - virology
Purpura
SARS-CoV-2
Severe acute respiratory syndrome coronavirus 2
Skin - blood supply
Skin - pathology
Skin - virology
Skin Diseases - pathology
Skin Diseases - virology
Thrombosis
Vasculitis
Vasculitis - pathology
Vasculitis - virology
Young adults
title SARS‐CoV‐2 endothelial infection causes COVID‐19 chilblains: histopathological, immunohistochemical and ultrastructural study of seven paediatric cases
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