Acute Alithiasic Cholecystitis and Human Herpes Virus Type-6 Infection: First Case

Author:

Gomes Maria Miguel1ORCID,Antunes Henedina234ORCID,Lobo Ana Luísa5,Branca Fernando6,Correia-Pinto Jorge347ORCID,Moreira-Pinto João347ORCID

Affiliation:

1. Department of Pediatrics, Hospital de Braga, Sete Fontes, São Victor, 4710-243 Braga, Portugal

2. Gastroenterology, Hepatology and Nutrition Unit, Department of Pediatrics, Hospital de Braga, Sete Fontes, São Victor, 4710-243 Braga, Portugal

3. Life and Health Sciences Research Institute (ICVS), School of Health Sciences, University of Minho, 4710-057 Braga, Portugal

4. ICVS/3B’s-PT Government Associate Laboratory, Braga/Guimarães, Portugal

5. Department of Pediatrics, Hospital de Alto Ave, 4835-044 Guimarães, Portugal

6. Department of Clinical Pathology, Hospital de Braga, Sete Fontes, São Victor, 4710-243 Braga, Portugal

7. Department of Pediatric Surgery, Hospital de Braga, Sete Fontes, São Victor, 4710-243 Braga, Portugal

Abstract

A three-year-old male child presented with erythematous maculopapular nonpruritic generalized rash, poor feeding, vomiting, and cramping generalized abdominal pain. He was previously healthy and there was no family history of immunologic or other diseases. On examination he was afebrile, hemodynamically stable, with painful palpation of the right upper quadrant and positive Murphy’s sign. Laboratory tests revealed elevated inflammatory markers, elevated aminotransferase activity, and features of cholestasis. Abdominal ultrasound showed gallbladder wall thickening of 8 mm with a positive sonographic Murphy’s sign, without gallstones or pericholecystic fluid. Acute Alithiasic Cholecystitis (AAC) was diagnosed. Tests for underlying infectious causes were negative except positive blood specimen for Human Herpes Virus Type-6 (HHV-6) by polymerase chain reaction. With supportive therapy the child became progressively less symptomatic with gradual improvement. The child was discharged on the sixth day, asymptomatic and with improved analytic values. Two months later he had IgM negative and IgG positive antibodies (1/160) for HHV-6, which confirmed the diagnosis of previous infection. In a six-month follow-up period he remains asymptomatic. To the best of our knowledge, this represents the first case of AAC associated with HHV-6 infection.

Publisher

Hindawi Limited

Subject

General Medicine

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