# Hepatic Decompensation Associated With COVID-19 in a Patient With Alcoholic Liver Cirrhosis: A Case Report

**Authors:** Martina Gengo

PMC · DOI: 10.7759/cureus.86615 · 2025-06-23

## TL;DR

A man with alcoholic liver cirrhosis experienced severe complications and died after contracting COVID-19, highlighting the risks for this vulnerable group.

## Contribution

This case report demonstrates that alcoholic liver cirrhosis significantly increases the risk of severe outcomes and mortality from COVID-19.

## Key findings

- A patient with alcoholic liver cirrhosis developed severe complications after contracting COVID-19.
- The patient's condition progressively worsened, leading to death one year after diagnosis.
- The case underscores the need for targeted care and long-term monitoring for cirrhotic patients with COVID-19.

## Abstract

Coronavirus disease 2019 (COVID-19) presents a spectrum of severity, ranging from asymptomatic infection to life-threatening respiratory failure. Patients with comorbidities, such as alcoholic liver cirrhosis, are at increased risk for adverse outcomes, as COVID-19 may precipitate hepatic decompensation. We report the case of a 60-year-old man with a history of alcoholic liver cirrhosis who was admitted with fever, cough, diarrhea, and fatigue. COVID-19 was confirmed via polymerase chain reaction (PCR) testing. He was diagnosed with bilateral pneumonia and had elevated liver enzymes. Treatment included azithromycin, doxycycline, enoxaparin, and dexamethasone. The patient showed clinical improvement following 10 days of therapy and was subsequently discharged. Two months later, he developed gastrointestinal bleeding due to ruptured esophageal varices. Over the following months, his condition worsened progressively, marked by severe malnutrition, recurrent ascites, and the development of hepatorenal syndrome. Despite ongoing care, he died one year after the initial COVID-19 diagnosis. This case highlights alcoholic liver cirrhosis as an independent risk factor for COVID-19-related complications and mortality, underscoring the need for targeted acute management and long-term follow-up in this vulnerable population, an essential consideration for future infectious disease outbreaks.

## Linked entities

- **Chemicals:** azithromycin (PubChem CID 447043), doxycycline (PubChem CID 54671203), dexamethasone (PubChem CID 5743)
- **Diseases:** alcoholic liver cirrhosis (MONDO:0006644), COVID-19 (MONDO:0100096), hepatorenal syndrome (MONDO:0001382)

## Full-text entities

- **Diseases:** Alcoholic Liver Cirrhosis (MESH:D008104), Hepatic Decompensation (MESH:D006333), cough (MESH:D003371), respiratory failure (MESH:D012131), diarrhea (MESH:D003967), malnutrition (MESH:D044342), esophageal varices (MESH:D004932), fatigue (MESH:D005221), infectious disease (MESH:D003141), gastrointestinal bleeding (MESH:D006471), COVID-19 (MESH:D000086382), ascites (MESH:D001201), hepatorenal syndrome (MESH:D006530), pneumonia (MESH:D011014), fever (MESH:D005334), infection (MESH:D007239)
- **Chemicals:** azithromycin (MESH:D017963), dexamethasone (MESH:D003907), enoxaparin (MESH:D017984), doxycycline (MESH:D004318)
- **Species:** Homo sapiens (human, species) [taxon 9606]

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Source: https://tomesphere.com/paper/PMC12286640