Acute Q Fever Hepatitis Mimicking Autoimmune Hepatitis

Abstract: A 44-year-old previously healthy man presented with 17 days of high-grade fevers, chills, night sweats, nausea, dark urine, and progressive jaundice after returning from a 2-week trip to Mexico during which he had eaten unpasteurized goat cheese daily and had contact with goats, horses, and dogs. Evaluation revealed mixed cholestatic and hepatocellular liver injury, splenomegaly, and significantly elevated inflammatory markers, with negative blood cultures and negative Brucella serologies. Strongly positive antinuclear, anti-smooth muscle, and antimitochondrial antibodies, together with a liver biopsy initially interpreted as autoimmune hepatitis, suggested an autoimmune process. Q fever serologies obtained during the diagnostic workup showed phase II IgM and IgG titers of 1:512, and pathology review demonstrated granulomatous hepatitis compatible with Q fever. Convalescent serology at 6 weeks confirmed phase I seroconversion. The patient was diagnosed with acute Q fever complicated by Q fever hepatitis and was treated with doxycycline-based therapy. Granulomatous hepatitis with prominent autoantibodies should prompt exposure history and phase-specific serologies before the findings are attributed to autoimmune disease.

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Publication Details

Journal
Private Practice Infectious Disease
Published
2026-11-05
DOI
https://doi.org/10.55636/ppid06040023
Primary Topic
Vector-borne infectious diseases
Type
article
Field-Weighted Citation Impact
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Acute Q Fever Hepatitis Mimicking Autoimmune Hepatitis

Martin Phillips
Private Practice Infectious Disease
Vector-borne infectious diseases
article

Acute Q Fever Hepatitis Mimicking Autoimmune Hepatitis

Martin Phillips
article en

Abstract

Abstract: A 44-year-old previously healthy man presented with 17 days of high-grade fevers, chills, night sweats, nausea, dark urine, and progressive jaundice after returning from a 2-week trip to Mexico during which he had eaten unpasteurized goat cheese daily and had contact with goats, horses, and dogs. Evaluation revealed mixed cholestatic and hepatocellular liver injury, splenomegaly, and significantly elevated inflammatory markers, with negative blood cultures and negative Brucella serologies. Strongly positive antinuclear, anti-smooth muscle, and antimitochondrial antibodies, together with a liver biopsy initially interpreted as autoimmune hepatitis, suggested an autoimmune process. Q fever serologies obtained during the diagnostic workup showed phase II IgM and IgG titers of 1:512, and pathology review demonstrated granulomatous hepatitis compatible with Q fever. Convalescent serology at 6 weeks confirmed phase I seroconversion. The patient was diagnosed with acute Q fever complicated by Q fever hepatitis and was treated with doxycycline-based therapy. Granulomatous hepatitis with prominent autoantibodies should prompt exposure history and phase-specific serologies before the findings are attributed to autoimmune disease.

Private Practice Infectious DiseaseVol. 6(4)
Infectious Disease Consultants (US)
Openalex Percentile: Top 12%
Vector-borne infectious diseases
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