Abdominal Actinomycosis misdiagnosed as liposarcoma

Eunice Vieira E Monteiro1, Joana Gaspar1, Claudia Paiva1

  • 1Centro Hospitalar Universitário do Porto, Serviço de Cirurgia Geral. Porto, Portugal.

Autopsy & Case Reports
|February 11, 2020
PubMed

Insights

Actinomycosis, a rare chronic infection, often mimics cancer, delaying diagnosis. This case highlights how a second biopsy confirmed actinomycosis, avoiding unnecessary surgery and enabling effective antibiotic treatment.

Area of Science:

  • Infectious Diseases
  • Oncology
  • Pathology

Background:

  • Actinomycosis is an uncommon, chronic bacterial infection presenting with nonspecific symptoms, often mimicking malignancies like liposarcoma.
  • Diagnosis is challenging due to low frequency and varied clinical presentations, including abdominal masses, fistulas, and constitutional symptoms.
  • The infection occurs when bacteria breach mucosal barriers and spread through fascial planes.

Observation:

  • A 72-year-old woman presented with an abdominal mass initially misdiagnosed as liposarcoma.
  • A subsequent biopsy of an abdominal wall skin lesion led to the correct diagnosis of actinomycosis.
  • Immunohistochemical positivity for MDM2 contributed to the initial misdiagnosis of liposarcoma.

Findings:

  • The patient received a long-term course of antibiotics for actinomycosis.
  • The patient experienced a favorable outcome with antibiotic therapy alone.
  • Surgical intervention was successfully avoided due to the timely and accurate diagnosis.

Implications:

  • Emphasizes the importance of considering actinomycosis in the differential diagnosis of abdominal masses, even when malignancy is suspected.
  • Highlights the critical role of biopsy in confirming the diagnosis and guiding appropriate treatment, potentially avoiding extensive surgery.
  • Suggests caution regarding overreliance on specific immunohistochemical markers when faced with atypical presentations.

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