Case report: retroperitoneal aspergilloma in a patient with rheumatoid arthritis presenting as malignant tumor

Risa Shinoki1, Teppei Takeshima1, Koichiro Horie2

  • 1Department of Urology, National Hospital Organization Sagamihara National Hospital, Sagamihara, Kanagawa, Japan.

BMC Urology
|August 2, 2018
PubMed
Abstract

Insights

Retroperitoneal aspergilloma is a rare fungal infection in immunocompromised patients. Surgical exploration is crucial for diagnosis, as pharmacological treatments show poor drug penetration in this location.

Area of Science:

  • Mycology
  • Immunocompromised Host
  • Surgical Pathology

Background:

  • Aspergillosis commonly affects immunocompromised individuals, typically presenting as invasive pulmonary disease with potential for systemic dissemination.
  • Retroperitoneal aspergilloma is an exceptionally rare clinical entity, with limited documented cases in medical literature.
  • This report details the second known case of retroperitoneal aspergilloma occurring in a patient with no prior surgical history.

Observation:

  • A 65-year-old male on long-term immunosuppressive therapy for rheumatoid arthritis presented with a retroperitoneal mass.
  • Computed tomography confirmed a retroperitoneal mass during treatment for pulmonary aspergilloma, raising suspicion for malignancy.
  • Surgical exploration was performed due to the inability to exclude malignancy, such as liposarcoma.

Findings:

  • Pathological examination of the retroperitoneal mass revealed Aspergillus hyphae and associated fat necrosis.
  • The diagnosis of retroperitoneal aspergilloma was established and the patient received appropriate treatment.
  • No recurrence of the retroperitoneal aspergilloma was observed post-treatment.

Implications:

  • The case highlights the diagnostic challenges in differentiating retroperitoneal aspergilloma from malignant retroperitoneal tumors.
  • Pharmacological treatments for retroperitoneal aspergilloma are limited by poor drug transit, rendering response ineffective for differential diagnosis.
  • Prompt surgical intervention and pathological confirmation are essential for managing this rare condition.

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