CASE REPORTS: malignant fibrous histiocytoma of bone arising in chronic osteomyelitis

Michael Zlowodzki1, Bret Allen, Ken L Schreibman

  • 1Division of Orthopaedic Surgery, McMaster University, Hamilton, ON, Canada.

Insights

This case report highlights the critical role of pathology in diagnosing bone tumors, especially malignant fibrous histiocytoma, in patients with chronic osteomyelitis. Early diagnosis through frozen section or permanent section pathology is crucial for effective treatment.

Area of Science:

  • Orthopedic Surgery
  • Skeletal Pathology
  • Oncology

Background:

  • Chronic osteomyelitis poses diagnostic challenges, sometimes masking underlying neoplastic conditions.
  • Malignant fibrous histiocytoma (MFH) co-occurring with osteomyelitis is exceptionally rare, with few documented cases.
  • Accurate histopathological diagnosis is paramount for appropriate patient management.

Observation:

  • A 51-year-old male with a 15-year history of left distal femur chronic osteomyelitis presented with acute exacerbation.
  • Initial debridement lacked frozen section or permanent pathology analysis.
  • Radical resection of the distal femur revealed malignant fibrous histiocytoma of bone.

Findings:

  • Histologic examination confirmed malignant fibrous histiocytoma of bone.
  • Metastatic workup was negative.
  • Inguinal lymph node metastasis was identified following hip disarticulation and wide tumor resection.

Implications:

  • This case underscores the necessity of thorough histopathological evaluation, including frozen section and permanent section pathology, in chronic osteomyelitis cases.
  • Timely diagnosis and surgical intervention, including adjuvant chemotherapy, can improve outcomes for rare bone tumors like MFH.
  • Emphasizes the importance of considering neoplastic processes in non-healing or recurrent bone infections.

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