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[A case of malignant fibrous histiocytoma occurring in the retroperitoneum with giant pyonephrosis]

Insights

This case report details a rare retroperitoneal malignant fibrous histiocytoma (MFH) presenting with giant pyonephrosis. Despite aggressive treatment, the patient experienced rapid metastasis and recurrence, highlighting the aggressive nature of this rare tumor.

Area of Science:

  • Oncology
  • Pathology
  • Surgical Oncology

Background:

  • Malignant fibrous histiocytoma (MFH) is a rare soft tissue sarcoma.
  • Retroperitoneal MFH is exceptionally uncommon, posing diagnostic and therapeutic challenges.

Observation:

  • A 45-year-old male presented with a rapidly growing abdominal mass.
  • The mass was associated with a giant pyonephrosis (11,000 ml pus) of the left kidney.
  • The tumor invaded the kidney and colonic vasculature, necessitating en bloc resection.

Findings:

  • Pathological diagnosis confirmed retroperitoneal malignant fibrous histiocytoma.
  • Postoperative chemotherapy (PPM, CY-VA-DIC) and immunotherapy (OK-432) were administered.
  • The patient developed widespread metastases (liver, lungs, pleura, bones) and local recurrence within 5 months, succumbing on day 174.

Implications:

  • This case underscores the aggressive behavior and poor prognosis of retroperitoneal MFH.
  • The report contributes to the limited literature on retroperitoneal MFH, particularly in Japan.
  • Early diagnosis and multimodal treatment strategies are crucial for managing this rare malignancy.

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