Paper
COVID-19 Presenting as Acute Hepatitis
Published Apr 15, 2020 · P. Wander, M. Epstein, D. Bernstein
The American Journal of Gastroenterology
108
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3
Influential Citations
Abstract
Coronavirus disease (COVID-19) is a novel enveloped RNA betacoronavirus that emerged from Wuhan, China, in December 2019 and rapidly has become a worldwide pandemic affecting hundreds of thousands of people and causing death in an estimated 0.5%–3% of infected cases (1). The most common clinical presentation is respiratory symptoms such as fever, shortness of breath, and cough associated with radiographical findings consistent with pneumonia (2). The prevalence of abnormal liver tests on the initial presentation of COVID-19 is still undetermined. Currently, there are no approved therapies for COVID-19 other than supportive care, enrollment in clinical trials, and the use of off-label therapies such as vitamin C and hydroxychloroquine without supportive, randomized clinical trials to support their efficacy. We report our first case of COVID-19 presenting as acute, nonicteric hepatitis. A 59-year-old woman presented to the emergency department with a chief concern of dark urine. On entering our facility, she was isolated and a surgical mask was placed on her face as per our protocol. She denied cough, sore throat, shortness of breath, diarrhea, nausea, vomiting, or abdominal pain. She lives alone and denied sick contacts. She had a medical history of well-controlled human immunodeficiency virus (CD4 499 and viral load undetectable), hypertension, hyperlipidemia, Graves disease, and a left facial paralysis secondary to previous actinomycosis infection. She denied recent intake of acetaminophen or any antibiotics. Her outpatient medications included clonidine, fish oil, levothyroxine, amlodipine, propranolol, hydrochlorothiazide, MVI, and Genvoya (elvitegravir, cobicistat, emtricitabine, and tenofovir alafenamide). Recent outpatient liver chemistries were normal. She was admitted because of the concern of rising liver tests in a patient with human immunodeficiency virus disease. On presentation, her temperature was 37.2 °C. There were no cutaneous manifestations, her lung examination was normal, and there was no jaundice, right upper quadrant tenderness, hepatomegaly, or splenomegaly. Laboratory results were as follows: white blood cell count 3.71 G/L, platelets 140 G/L, serum bilirubin 0.6 mg/dL (N: , 25), AST 1230 IU/L (N: , 50), ALT 697 IU/L (N: , 50), alkaline phosphatase 141 IU/L (N: , 125), serum albumin 3.1 g/dL (N:. 3.5), INR 1.08, and ferritin 6,606 ng/mL (N: ,150). An abdominal sonogram with Doppler revealed a normal liver with patent vasculature. The following serological tests were performed and all tested negative: hepatitis A, B, C, E, Cytomegalovirus, Epstein-Barr and respiratory viral panel. Blood cultures and screening for autoimmune markers were negative. On admission day 2, 18 hours after presentation to the emergency department, she developed a fever to 39 °C with SpO2 94% on room air. A chest x-ray showed bilateral interstitial opacities. Nasopharyngeal samples taken for the SARSCoV PCR test were positive, and the patient was placed on 3 L of oxygen. On admission day 4, she was started on a 5day course of hydroxychloroquine 200mg BID. She did well and was discharged to home on hospital day 8 with serum bilirubin 0.6 mg/dL, AST 114 IU/L, ALT 227 IU/L, alkaline phosphatase 259 IU/L, serum albumin 2.8 g/dL, and INR 1.13 (Figure 1). Her outpatient medications including her human immunodeficiency virus treatment were continued throughout her entire admission. COVID-19 infection typically presents with respiratory symptoms such as fever, sore throat, cough, and shortness of breath. In high-volume centers such as ours, liver test abnormalities are being noted following COVID-19 diagnosis. We report our first case of COVID-19 infection presenting as acute nonicteric hepatitis before the development of fever and respiratory symptoms. Our patient was on a stable outpatient medication regimen and had normal outpatient liver tests just before admission for COVID-19. Her initial presentation was not typical for COVID-19, and she was evaluated for acute hepatitis. This workup was negative, and 18 hours after admission, she developed respiratory symptoms and was subsequently diagnosed with COVID-19. She was treated for COVID-19 with hydroxychloroquine, and her symptoms improved, as did her liver chemistries. Because all other causes of acute nonicteric hepatitis were ruled out, it seems highly likely that her acute hepatitis was caused by COVID-19 infection. There is currently no standard of care for the treatment of COVID-19 infection. Current therapies include implementing infection control measures, symptomatic treatment, and supportive care including supplemental oxygen and mechanical ventilation when appropriate. There are currently no approved therapies to treat COVID-19 infection. Clinical trials are ongoing to evaluate antiviral therapies and immune-modulator therapies. The antimalarial and antiinflammatory medication, hydroxychloroquine, has been widely used to treat COVID-19 infection without any available data from randomized clinical trials to inform clinical guidance on the use, dosing, or duration of hydroxychloroquine for prophylaxis or the treatment of COVID-19 infection (3). Hydroxychloroquinehas been shown to have in vitro activity against SARS-CoV and SARS-CoV-2 (COVID-19) (4). A single, nonrandomized study of 36 patients in France suggested that hydroxychloroquine lowered coronavirus levels in the blood as compared to untreated controls and shortened recovery time (5). Six of the 20 patients who received hydroxychloroquine also received azithromycin, whereas none of the control received azithromycin. A randomized study from China reported
Case Report
Highly CitedCOVID-19 can present as acute, nonicteric hepatitis in patients with a history of human immunodeficiency virus disease.
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