Molecular diagnosis of autochthonous human anaplasmosis in Austria - an infectious diseases case report

Wolfgang Hoepler1, Mateusz Markowicz2, Anna-Margarita Schoetta2

  • 14th Medical Department with Infectious Diseases and Tropical Medicine, Sozialmedizinisches Zentrum Süd - Kaiser-Franz-Josef-Spital mit Gottfried von Preyer'schem Kinderspital, KFJ-Spital, Kundratstrasse 3, 1100, Vienna, Austria. w.hoepler@gmx.at.

Abstract

Insights

Human anaplasmosis, a tick-borne illness, is often missed. Molecular diagnostics like PCR offer a rapid and reliable method for identifying Anaplasma phagocytophilum infections.

Area of Science:

  • Infectious Diseases
  • Molecular Diagnostics
  • Tick-Borne Illnesses

Background:

  • Human anaplasmosis diagnosis is challenging and frequently overlooked.
  • This case report emphasizes the effectiveness of molecular diagnostic methods.

Observation:

  • A 74-year-old male presented with fever, chills, diplopia, and vertigo post-tick bites.
  • Lab results revealed anemia, thrombocytopenia, leukopenia, and elevated C-reactive protein.
  • Initial serology suggested Borrelia infection, but PCR confirmed Anaplasma phagocytophilum.

Findings:

  • Polymerase chain reaction (PCR) and sequencing successfully detected Anaplasma phagocytophilum in peripheral blood.
  • The patient recovered fully after treatment with ceftriaxone and doxycycline.

Implications:

  • Anaplasmosis should be considered in febrile patients with cytopenias and elevated CRP after tick exposure.
  • Molecular detection of Anaplasma phagocytophilum is crucial for timely and accurate diagnosis.

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