Diffuse alveolar damage and thrombotic microangiopathy are the main histopathological findings in lung tissue biopsy samples of COVID-19 patients
Since the outbreak of the novel coronavirus disease-2019 (COVID-19) in December 2019, limited studies have investigated the histopathologic findings of patients infected with severe acute respiratory syndrome coronavirus-2 (SARS-CoV-2). This study was conducted on 31 deceased patients who were hospi...
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creator | Sadegh Beigee, Farahnaz Pourabdollah Toutkaboni, Mihan Khalili, Neda Nadji, Seyed Alireza Dorudinia, Atosa Rezaei, Mitra Askari, Elham Farzanegan, Behrooz Marjani, Majid Rafiezadeh, Amir |
description | Since the outbreak of the novel coronavirus disease-2019 (COVID-19) in December 2019, limited studies have investigated the histopathologic findings of patients infected with severe acute respiratory syndrome coronavirus-2 (SARS-CoV-2).
This study was conducted on 31 deceased patients who were hospitalized for COVID-19 in a tertiary hospital in Tehran, Iran. A total of 52 postmortem tissue biopsy samples were obtained from the lungs and liver of decedents. Clinical characteristics, laboratory data, and microscopic features were evaluated. Reverse transcription polymerase chain reaction (RT-PCR) assay for SARS-CoV-2 was performed on specimens obtained from nasopharyngeal swabs and tissue biopsies.
The median age of deceased patients was 66 years (range, 30–87 years) and 25 decedents (81 %) were male. The average interval from symptom onset to death was 13 days (range, 6–34 days). On histopathologic examination of the lung specimens, diffuse alveolar damage and thrombotic microangiopathy were the most common findings (80 % and 60 %, respectively). Liver specimens mainly showed macrovesicular steatosis, portal lymphoplasmacytic inflammation and passive congestion. No definitive viral inclusions were observed in any of the specimens. In addition, 92 % of lung tissue samples tested positive for SARS-CoV-2 by RT-PCR.
Further studies are needed to investigate whether SARS-CoV-2 causes direct cytopathic changes in various organs of the human body. |
doi_str_mv | 10.1016/j.prp.2020.153228 |
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This study was conducted on 31 deceased patients who were hospitalized for COVID-19 in a tertiary hospital in Tehran, Iran. A total of 52 postmortem tissue biopsy samples were obtained from the lungs and liver of decedents. Clinical characteristics, laboratory data, and microscopic features were evaluated. Reverse transcription polymerase chain reaction (RT-PCR) assay for SARS-CoV-2 was performed on specimens obtained from nasopharyngeal swabs and tissue biopsies.
The median age of deceased patients was 66 years (range, 30–87 years) and 25 decedents (81 %) were male. The average interval from symptom onset to death was 13 days (range, 6–34 days). On histopathologic examination of the lung specimens, diffuse alveolar damage and thrombotic microangiopathy were the most common findings (80 % and 60 %, respectively). Liver specimens mainly showed macrovesicular steatosis, portal lymphoplasmacytic inflammation and passive congestion. No definitive viral inclusions were observed in any of the specimens. In addition, 92 % of lung tissue samples tested positive for SARS-CoV-2 by RT-PCR.
Further studies are needed to investigate whether SARS-CoV-2 causes direct cytopathic changes in various organs of the human body.</description><identifier>ISSN: 0344-0338</identifier><identifier>EISSN: 1618-0631</identifier><identifier>DOI: 10.1016/j.prp.2020.153228</identifier><identifier>PMID: 32979740</identifier><language>eng</language><publisher>Germany: Elsevier GmbH</publisher><subject>Adult ; Aged ; Aged, 80 and over ; Autopsy ; Betacoronavirus ; Biopsy ; Coronavirus disease-2019 ; Coronavirus Infections - pathology ; COVID-19 ; Diffuse alveolar damage ; Female ; Histology ; Humans ; Liver - pathology ; Lung - pathology ; Male ; Middle Aged ; Pandemics ; Pathology ; Pneumonia, Viral - pathology ; Pulmonary Alveoli - pathology ; SARS-CoV-2 ; Thrombotic Microangiopathies - pathology ; Thrombotic Microangiopathies - virology ; Thrombotic microangiopathy ; Tissue biopsy</subject><ispartof>Pathology, research and practice, 2020-10, Vol.216 (10), p.153228-153228, Article 153228</ispartof><rights>2020 Elsevier GmbH</rights><rights>Copyright © 2020 Elsevier GmbH. All rights reserved.</rights><rights>2020 Elsevier GmbH. All rights reserved. 2020 Elsevier GmbH</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c451t-2aadec54cf9323e05d042bde2cffcd6574daea744b9b5997cba55c60704a766b3</citedby><cites>FETCH-LOGICAL-c451t-2aadec54cf9323e05d042bde2cffcd6574daea744b9b5997cba55c60704a766b3</cites><orcidid>0000-0003-2654-9029 ; 0000-0001-8415-8996</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S0344033820320835$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>230,314,776,780,881,3537,27901,27902,65306</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/32979740$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Sadegh Beigee, Farahnaz</creatorcontrib><creatorcontrib>Pourabdollah Toutkaboni, Mihan</creatorcontrib><creatorcontrib>Khalili, Neda</creatorcontrib><creatorcontrib>Nadji, Seyed Alireza</creatorcontrib><creatorcontrib>Dorudinia, Atosa</creatorcontrib><creatorcontrib>Rezaei, Mitra</creatorcontrib><creatorcontrib>Askari, Elham</creatorcontrib><creatorcontrib>Farzanegan, Behrooz</creatorcontrib><creatorcontrib>Marjani, Majid</creatorcontrib><creatorcontrib>Rafiezadeh, Amir</creatorcontrib><title>Diffuse alveolar damage and thrombotic microangiopathy are the main histopathological findings in lung tissue biopsy samples of COVID-19 patients</title><title>Pathology, research and practice</title><addtitle>Pathol Res Pract</addtitle><description>Since the outbreak of the novel coronavirus disease-2019 (COVID-19) in December 2019, limited studies have investigated the histopathologic findings of patients infected with severe acute respiratory syndrome coronavirus-2 (SARS-CoV-2).
This study was conducted on 31 deceased patients who were hospitalized for COVID-19 in a tertiary hospital in Tehran, Iran. A total of 52 postmortem tissue biopsy samples were obtained from the lungs and liver of decedents. Clinical characteristics, laboratory data, and microscopic features were evaluated. Reverse transcription polymerase chain reaction (RT-PCR) assay for SARS-CoV-2 was performed on specimens obtained from nasopharyngeal swabs and tissue biopsies.
The median age of deceased patients was 66 years (range, 30–87 years) and 25 decedents (81 %) were male. The average interval from symptom onset to death was 13 days (range, 6–34 days). On histopathologic examination of the lung specimens, diffuse alveolar damage and thrombotic microangiopathy were the most common findings (80 % and 60 %, respectively). Liver specimens mainly showed macrovesicular steatosis, portal lymphoplasmacytic inflammation and passive congestion. No definitive viral inclusions were observed in any of the specimens. In addition, 92 % of lung tissue samples tested positive for SARS-CoV-2 by RT-PCR.
Further studies are needed to investigate whether SARS-CoV-2 causes direct cytopathic changes in various organs of the human body.</description><subject>Adult</subject><subject>Aged</subject><subject>Aged, 80 and over</subject><subject>Autopsy</subject><subject>Betacoronavirus</subject><subject>Biopsy</subject><subject>Coronavirus disease-2019</subject><subject>Coronavirus Infections - pathology</subject><subject>COVID-19</subject><subject>Diffuse alveolar damage</subject><subject>Female</subject><subject>Histology</subject><subject>Humans</subject><subject>Liver - pathology</subject><subject>Lung - pathology</subject><subject>Male</subject><subject>Middle Aged</subject><subject>Pandemics</subject><subject>Pathology</subject><subject>Pneumonia, Viral - pathology</subject><subject>Pulmonary Alveoli - pathology</subject><subject>SARS-CoV-2</subject><subject>Thrombotic Microangiopathies - pathology</subject><subject>Thrombotic Microangiopathies - virology</subject><subject>Thrombotic microangiopathy</subject><subject>Tissue biopsy</subject><issn>0344-0338</issn><issn>1618-0631</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2020</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9Uctu1DAUjRCITgsfwAZ5ySaDX4knQkJCUwqVKnUDbK0b-ybjkRMHOxlpPqN_jIcpFWxYWfeex7XOKYo3jK4ZZfX7_XqK05pTnudKcL55VqxYzTYlrQV7XqyokLKkQmwuisuU9pRSRSV7WVwI3qhGSboqHq5d1y0JCfgDBg-RWBigz_NoybyLYWjD7AwZnIkBxt6FCebdkUDEDCMZwI1k59L8ex986J0BTzo3Wjf2iWTUL2NPZpfSgqTN-nQkCYbJYyKhI9v7H7fXJWtI1jsc5_SqeNGBT_j68b0qvt98_rb9Wt7df7ndfrorjazYXHIAi6aSpmsEF0grSyVvLXLTdcbWlZIWEJSUbdNWTaNMC1Vl6lMCoOq6FVfFx7PvtLQDWpNvR_B6im6AeNQBnP4XGd1O9-Gg1UYoxng2ePdoEMPPBdOsB5cMeg8jhiVpLmVdK0WZzFR2puYQU4rYPZ1hVJ-q1Pu8mfSpSn2uMmve_v2_J8Wf7jLhw5mAOaWDw6iTyQkatC6imbUN7j_2vwAvFbPR</recordid><startdate>20201001</startdate><enddate>20201001</enddate><creator>Sadegh Beigee, Farahnaz</creator><creator>Pourabdollah Toutkaboni, Mihan</creator><creator>Khalili, Neda</creator><creator>Nadji, Seyed Alireza</creator><creator>Dorudinia, Atosa</creator><creator>Rezaei, Mitra</creator><creator>Askari, Elham</creator><creator>Farzanegan, Behrooz</creator><creator>Marjani, Majid</creator><creator>Rafiezadeh, Amir</creator><general>Elsevier GmbH</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>7X8</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0003-2654-9029</orcidid><orcidid>https://orcid.org/0000-0001-8415-8996</orcidid></search><sort><creationdate>20201001</creationdate><title>Diffuse alveolar damage and thrombotic microangiopathy are the main histopathological findings in lung tissue biopsy samples of COVID-19 patients</title><author>Sadegh Beigee, Farahnaz ; Pourabdollah Toutkaboni, Mihan ; Khalili, Neda ; Nadji, Seyed Alireza ; Dorudinia, Atosa ; Rezaei, Mitra ; Askari, Elham ; Farzanegan, Behrooz ; Marjani, Majid ; Rafiezadeh, Amir</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c451t-2aadec54cf9323e05d042bde2cffcd6574daea744b9b5997cba55c60704a766b3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2020</creationdate><topic>Adult</topic><topic>Aged</topic><topic>Aged, 80 and over</topic><topic>Autopsy</topic><topic>Betacoronavirus</topic><topic>Biopsy</topic><topic>Coronavirus disease-2019</topic><topic>Coronavirus Infections - pathology</topic><topic>COVID-19</topic><topic>Diffuse alveolar damage</topic><topic>Female</topic><topic>Histology</topic><topic>Humans</topic><topic>Liver - pathology</topic><topic>Lung - pathology</topic><topic>Male</topic><topic>Middle Aged</topic><topic>Pandemics</topic><topic>Pathology</topic><topic>Pneumonia, Viral - pathology</topic><topic>Pulmonary Alveoli - pathology</topic><topic>SARS-CoV-2</topic><topic>Thrombotic Microangiopathies - pathology</topic><topic>Thrombotic Microangiopathies - virology</topic><topic>Thrombotic microangiopathy</topic><topic>Tissue biopsy</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Sadegh Beigee, Farahnaz</creatorcontrib><creatorcontrib>Pourabdollah Toutkaboni, Mihan</creatorcontrib><creatorcontrib>Khalili, Neda</creatorcontrib><creatorcontrib>Nadji, Seyed Alireza</creatorcontrib><creatorcontrib>Dorudinia, Atosa</creatorcontrib><creatorcontrib>Rezaei, Mitra</creatorcontrib><creatorcontrib>Askari, Elham</creatorcontrib><creatorcontrib>Farzanegan, Behrooz</creatorcontrib><creatorcontrib>Marjani, Majid</creatorcontrib><creatorcontrib>Rafiezadeh, Amir</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Pathology, research and practice</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Sadegh Beigee, Farahnaz</au><au>Pourabdollah Toutkaboni, Mihan</au><au>Khalili, Neda</au><au>Nadji, Seyed Alireza</au><au>Dorudinia, Atosa</au><au>Rezaei, Mitra</au><au>Askari, Elham</au><au>Farzanegan, Behrooz</au><au>Marjani, Majid</au><au>Rafiezadeh, Amir</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Diffuse alveolar damage and thrombotic microangiopathy are the main histopathological findings in lung tissue biopsy samples of COVID-19 patients</atitle><jtitle>Pathology, research and practice</jtitle><addtitle>Pathol Res Pract</addtitle><date>2020-10-01</date><risdate>2020</risdate><volume>216</volume><issue>10</issue><spage>153228</spage><epage>153228</epage><pages>153228-153228</pages><artnum>153228</artnum><issn>0344-0338</issn><eissn>1618-0631</eissn><abstract>Since the outbreak of the novel coronavirus disease-2019 (COVID-19) in December 2019, limited studies have investigated the histopathologic findings of patients infected with severe acute respiratory syndrome coronavirus-2 (SARS-CoV-2).
This study was conducted on 31 deceased patients who were hospitalized for COVID-19 in a tertiary hospital in Tehran, Iran. A total of 52 postmortem tissue biopsy samples were obtained from the lungs and liver of decedents. Clinical characteristics, laboratory data, and microscopic features were evaluated. Reverse transcription polymerase chain reaction (RT-PCR) assay for SARS-CoV-2 was performed on specimens obtained from nasopharyngeal swabs and tissue biopsies.
The median age of deceased patients was 66 years (range, 30–87 years) and 25 decedents (81 %) were male. The average interval from symptom onset to death was 13 days (range, 6–34 days). On histopathologic examination of the lung specimens, diffuse alveolar damage and thrombotic microangiopathy were the most common findings (80 % and 60 %, respectively). Liver specimens mainly showed macrovesicular steatosis, portal lymphoplasmacytic inflammation and passive congestion. No definitive viral inclusions were observed in any of the specimens. In addition, 92 % of lung tissue samples tested positive for SARS-CoV-2 by RT-PCR.
Further studies are needed to investigate whether SARS-CoV-2 causes direct cytopathic changes in various organs of the human body.</abstract><cop>Germany</cop><pub>Elsevier GmbH</pub><pmid>32979740</pmid><doi>10.1016/j.prp.2020.153228</doi><tpages>1</tpages><orcidid>https://orcid.org/0000-0003-2654-9029</orcidid><orcidid>https://orcid.org/0000-0001-8415-8996</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Adult Aged Aged, 80 and over Autopsy Betacoronavirus Biopsy Coronavirus disease-2019 Coronavirus Infections - pathology COVID-19 Diffuse alveolar damage Female Histology Humans Liver - pathology Lung - pathology Male Middle Aged Pandemics Pathology Pneumonia, Viral - pathology Pulmonary Alveoli - pathology SARS-CoV-2 Thrombotic Microangiopathies - pathology Thrombotic Microangiopathies - virology Thrombotic microangiopathy Tissue biopsy |
title | Diffuse alveolar damage and thrombotic microangiopathy are the main histopathological findings in lung tissue biopsy samples of COVID-19 patients |
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