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Primary retroperitoneal liposarcoma: a rare case report.

Shu Wang1, Xu Han2, Shiyang Liu3

  • 1Department of Radiotherapy, The Second Hospital of Jilin University, Changchun Jilin, China.

The Journal of International Medical Research
|December 8, 2021
PubMed
Summary

Primary retroperitoneal liposarcoma (PRPLS) is a rare cancer. Complete surgical resection is the primary treatment, offering good outcomes and no relapse in this case.

Keywords:
Primary retroperitoneal liposarcomachemotherapycomputed tomographydiagnosishistopathologymalignantradiotherapysurgery

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Area of Science:

  • Oncology
  • Surgical Pathology

Background:

  • Primary retroperitoneal liposarcoma (PRPLS) is an exceptionally rare malignant tumor.
  • Early-stage PRPLS often presents with non-specific symptoms, delaying diagnosis.

Observation:

  • A 34-year-old female presented with acute abdominal pain, nausea, and vomiting.
  • Computed tomography (CT) revealed a large retroperitoneal mass (202 × 155 × 106 mm).
  • Initial differential diagnosis included lipoma or liposarcoma.

Findings:

  • Histopathology confirmed the mass as liposarcoma.
  • Complete surgical resection of the tumor was achieved without complications.
  • The patient experienced a successful recovery and remained relapse-free at 1-year follow-up.

Implications:

  • CT imaging is crucial for diagnosing PRPLS.
  • Surgical resection is the primary treatment modality for PRPLS.
  • Adjuvant therapies like radiotherapy and chemotherapy may enhance survival rates.