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Intra-abdominal actinomycosis with hepatic pseudotumor and xanthogranulomatous pyelonephritis in a 6-y-old boy

T P Lin1, L S Fu, H C Peng

  • 1Department of Pediatrics, Veterans General Hospital, Taichung, Taiwan.

Insights

A rare pediatric case of actinomycosis mimicked tumors, presenting as xanthogranulomatous pyelonephritis (XGP) and hepatic pseudotumor. Prompt diagnosis and antibiotic treatment led to complete recovery in a 6-year-old boy.

Area of Science:

  • Pediatric Infectious Diseases
  • Medical Microbiology
  • Abdominal Imaging

Background:

  • Actinomycosis is a rare bacterial infection often presenting with nonspecific symptoms.
  • Xanthogranulomatous pyelonephritis (XGP) is a rare chronic inflammatory condition of the kidney that can mimic malignancy.
  • Pediatric presentations of actinomycosis, especially mimicking abdominal tumors, are exceptionally uncommon.

Observation:

  • A 6-year-old boy presented with intermittent fever, abdominal pain, and weight loss.
  • Imaging studies (sonography and CT) revealed masses suggestive of hepatic pseudotumor and renal tumor.
  • Pathological examination confirmed actinomycosis and XGP.

Findings:

  • The patient was diagnosed with disseminated actinomycosis presenting as XGP, hepatic pseudotumor, and abdominal abscess.
  • Diagnosis was confirmed through histopathological analysis.
  • The child showed a complete clinical recovery following antibiotic therapy alone.

Implications:

  • This case highlights the importance of considering actinomycosis in the differential diagnosis of pediatric abdominal masses, even in the absence of typical risk factors.
  • Early and accurate diagnosis through pathology is crucial for effective management.
  • Antibiotic therapy alone can be sufficient for treating complex pediatric actinomycosis presentations.

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