Scarlatiniform eruption-a rare extrahepatic manifestation of acute hepatitis A infection
Chee Yik Chang
Corresponding author: Chee Yik Chang, Department of General Medicine, Sarawak General Hospital, Jalan Hospital, 93586 Kuching, Sarawak, Malaysia
Received: 21 May 2020 - Accepted: 27 May 2020 - Published: 28 May 2020
Domain: Infectious disease
Keywords: Scarlatiniform rash, hepatitis A, transaminitis
©Chee Yik Chang et al. PAMJ Clinical Medicine (ISSN: 2707-2797). This is an Open Access article distributed under the terms of the Creative Commons Attribution International 4.0 License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
Cite this article: Chee Yik Chang et al. Scarlatiniform eruption-a rare extrahepatic manifestation of acute hepatitis A infection. PAMJ Clinical Medicine. 2020;3:32. [doi: 10.11604/pamj-cm.2020.3.32.23665]
Available online at: https://www.clinical-medicine.panafrican-med-journal.com//content/article/3/32/full
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Scarlatiniform eruption-a rare extrahepatic manifestation of acute hepatitis A infection
Scarlatiniform eruption-a rare extrahepatic manifestation of acute hepatitis A infection
Chee Yik Chang1,&
1Department of General Medicine, Sarawak General Hospital, Jalan Hospital, 93586 Kuching, Sarawak, Malaysia
&Corresponding author
Chee Yik Chang, Department of General Medicine, Sarawak General Hospital, Jalan Hospital, 93586 Kuching, Sarawak, Malaysia
A 12-year-old girl presented with a one-week history of fever associated with jaundice, vomiting and skin rash on the fifth day of illness. She denied any abdominal pain, diarrhoea, history of recent shell-fish or traditional medication ingestion. On examination, she appeared jaundice, and there was sandpaper-like rash on the trunk and extremities (A). Laboratory investigations revealed severe transaminitis (AST 849 U/L, ALT of 1092 U/L) and predominantly direct hyperbilirubinaemia. Hepatitis A IgM was reactive whereas leptospirosis, hepatitis B and C serology were non-reactive. The antistreptolysin O titer and throat swab culture were negative. Ultrasound of the hepatobiliary system demonstrated normal liver parenchyma without sonographic evidence of biliary obstruction. She was admitted for intravenous fluid and symptomatic therapy. She remained well with improving transaminitis, and did not exhibit any signs of liver failure. She was discharged after 5 days of hospital stay. The rash disappeared and liver function test normalized during a followup review 2 weeks post-discharge. Many types of skin rashes can occur as a part of the serum sickness-like prodrome of acute viral hepatitis which is thought to be due to immune complex deposition. An evanescent rash was reported to be present in 14% of patients with acute hepatitis A. Cutaneous vasculitis associated with hepatitis A can appear as an erythematous maculopapular eruption affecting the buttocks and lower extremities. Scarlatiniform rash has not been reported previously in hepatitis A infection. Clinicians should be alert to this rare extrahepatic manifestation of hepatitis A infection when encountering patients with skin rash and severe transaminitis.
Figure 1: sandpaper-like rash over the back