TY - JOUR
T1 - Clinico-pathological features in fatal COVID-19 infection
T2 - a preliminary experience of a tertiary care center in North India using postmortem minimally invasive tissue sampling
AU - Ray, Animesh
AU - Jain, Deepali
AU - Goel, Ayush
AU - Agarwal, Shubham
AU - Swaroop, Shekhar
AU - Das, Prasenjit
AU - Arava, Sudheer Kumar
AU - Mridha, Asit Ranjan
AU - Nambirajan, Aruna
AU - Singh, Geetika
AU - Arulselvi, S.
AU - Mathur, Purva
AU - Kumar, Sanchit
AU - Sahni, Shubham
AU - Nehra, Jagbir
AU - Nazneen,
AU - Bm, Mouna
AU - Rastogi, Neha
AU - Mahato, Sandeep
AU - Gupta, Chaavi
AU - Bharadhan, S.
AU - Dhital, Gaurav
AU - Goel, Pawan
AU - Pandey, Praful
AU - Kn, Santosh
AU - Chaudhary, Shitij
AU - Keri, Vishakh C.
AU - Chauhan, Vishal Singh
AU - Mahishi, Niranjan
AU - Shahi, Anand
AU - R, Ragu
AU - Gupta, Baidnath K.
AU - Aggarwal, Richa
AU - Soni, Kapil Dev
AU - Nischal, Neeraj
AU - Soneja, Manish
AU - Lalwani, Sanjeev
AU - Sarkar, Chitra
AU - Guleria, Randeep
AU - Wig, Naveet
AU - Trikha, Anjan
N1 - Publisher Copyright:
© 2021 Informa UK Limited, trading as Taylor & Francis Group.
PY - 2021
Y1 - 2021
N2 - Objectives: To study the histopathology of patients dying of COVID-19 using post-mortem minimally invasive sampling techniques. Methods: This was a single-center observational study conducted at JPNATC, AIIMS. Thirty-seven patients who died of COVID-19 were enrolled. Post-mortem percutaneous biopsies were taken from lung, heart, liver, kidney and stained with hematoxylin and eosin. Immunohistochemistry was performed using CD61 and CD163. SARS-CoV-2 virus was detected using IHC with primary antibodies. Results: The mean age was 48.7 years and 59.5% were males. Lung histopathology showed diffuse alveolar damage in 78% patients. Associated bronchopneumonia was seen in 37.5% and scattered microthrombi in 21% patients. Immunopositivity for SARS-CoV-2 was observed in Type II pneumocytes. Acute tubular injury with epithelial vacuolization was seen in 46% of renal biopsies. Seventy-one percent of liver biopsies showed Kupffer cell hyperplasia and 27.5% showed submassive hepatic necrosis. Conclusions: Predominant finding was diffuse alveolar damage with demonstration of SARS-CoV-2 protein in the acute phase. Microvascular thrombi were rarely identified in any organ. Substantial hepatocyte necrosis, Kupffer cell hypertrophy, microvesicular, and macrovesicular steatosis unrelated to microvascular thrombi suggested that liver might be a primary target of COVID-19.
AB - Objectives: To study the histopathology of patients dying of COVID-19 using post-mortem minimally invasive sampling techniques. Methods: This was a single-center observational study conducted at JPNATC, AIIMS. Thirty-seven patients who died of COVID-19 were enrolled. Post-mortem percutaneous biopsies were taken from lung, heart, liver, kidney and stained with hematoxylin and eosin. Immunohistochemistry was performed using CD61 and CD163. SARS-CoV-2 virus was detected using IHC with primary antibodies. Results: The mean age was 48.7 years and 59.5% were males. Lung histopathology showed diffuse alveolar damage in 78% patients. Associated bronchopneumonia was seen in 37.5% and scattered microthrombi in 21% patients. Immunopositivity for SARS-CoV-2 was observed in Type II pneumocytes. Acute tubular injury with epithelial vacuolization was seen in 46% of renal biopsies. Seventy-one percent of liver biopsies showed Kupffer cell hyperplasia and 27.5% showed submassive hepatic necrosis. Conclusions: Predominant finding was diffuse alveolar damage with demonstration of SARS-CoV-2 protein in the acute phase. Microvascular thrombi were rarely identified in any organ. Substantial hepatocyte necrosis, Kupffer cell hypertrophy, microvesicular, and macrovesicular steatosis unrelated to microvascular thrombi suggested that liver might be a primary target of COVID-19.
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U2 - 10.1080/17476348.2021.1951708
DO - 10.1080/17476348.2021.1951708
M3 - Article
C2 - 34227439
AN - SCOPUS:85111430831
SN - 1747-6348
VL - 15
SP - 1367
EP - 1375
JO - Expert Review of Respiratory Medicine
JF - Expert Review of Respiratory Medicine
IS - 10
ER -