Histologic and Immunohistochemical Evaluation of 65 Placentas From Women With Polymerase Chain Reaction–Proven Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2) Infection

Author:

Levitan Daniel12,London Viktoriya34,McLaren Rodney A.34,Mann Justin David5,Cheng Ke5,Silver Michael6,Balhotra Kimen Singh4,McCalla Sandra4,Loukeris Kristina12

Affiliation:

1. From the Department of Pathology & Laboratory Medicine (Levitan, Loukeris), at Maimonides Medical Center, Brooklyn, New York

2. The Department of Pathology, SUNY Downstate Medical Center, Brooklyn, New York (Levitan, Loukeris)

3. Division of Maternal Fetal Medicine (London, McLaren), at Maimonides Medical Center, Brooklyn, New York

4. Department of Obstetrics & Gynecology (London, McLaren, Balhotra, McCalla), at Maimonides Medical Center, Brooklyn, New York

5. HistoWiz Inc, Brooklyn, New York (Mann, Cheng)

6. Office of Research Administration (Silver), at Maimonides Medical Center, Brooklyn, New York

Abstract

Context.— Coronavirus disease 2019 (COVID-19) has been shown to have effects outside of the respiratory system. Placental pathology in the setting of maternal severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection remains a topic of great interest because earlier studies have shown mixed results. Objective.— To ascertain whether maternal SARS-CoV-2 infection is associated with any specific placental histopathology, and to evaluate the virus's propensity for direct placental involvement. Design.— Placentas from 65 women with polymerase chain reaction–proven SARS-CoV-2 infection underwent histologic evaluation using Amsterdam consensus group criteria and terminology. Another 85 placentas from women without SARS-CoV-2 constituted the negative control group. A total of 64 of the placentas from the SARS-CoV-2–positive group underwent immunohistochemical staining for SARS-CoV-2 nucleocapsid protein. Results.— Pathologic findings were divided into maternal vascular malperfusion, fetal vascular malperfusion, chronic inflammatory lesions, amniotic fluid infection sequence, increased perivillous fibrin, intervillous thrombi, increased subchorionic fibrin, meconium-laden macrophages (M-LMs) within fetal membranes, and chorangiosis. There was no statistically significant difference in prevalence of any specific placental histopathology between the SARS-CoV-2–positive and SARS-CoV-2–negative groups. There was no immunohistochemical evidence of SARS-CoV-2 virus in any of the 64 placentas that underwent staining for viral nucleocapsid protein. Conclusions.— Our study results and a literature review suggest that there is no characteristic histopathology in most placentas from women with SARS-CoV-2 infection. Likewise, direct placental involvement by SARS-CoV-2 is a rare event.

Publisher

Archives of Pathology and Laboratory Medicine

Subject

Medical Laboratory Technology,General Medicine,Pathology and Forensic Medicine

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