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Retroperitoneal Lipoblastoma With Cord Compression in an Adult Patient: A Case Report
Hosam A Alghanmi1, Ammar Bokhari1, Ahmed Zeeneldin1
1Department of Medical Oncology, Oncology Center, King Abdullah Medical City, Makkah, SAU.
Retroperitoneal lipoblastoma, a rare tumor, typically affects children. This case highlights a unique adult presentation with acute cord compression, emphasizing the need for awareness in diverse age groups.
Area of Science:
- Oncology
- Pathology
Background:
- Lipoblastoma is a rare benign tumor of adipocytes, predominantly affecting infants and children.
- It most commonly occurs in the extremities, head, and neck, with retroperitoneal involvement being exceptionally rare.
Observation:
- A 24-year-old male presented with acute spinal cord compression, an unusual initial symptom for retroperitoneal lipoblastoma.
- Diagnostic workup included biopsy, immunostaining (CD34 positive), and cytogenetics, which confirmed lipoblastoma and ruled out metastasis.
Findings:
- Histopathology confirmed retroperitoneal lipoblastoma in an adult patient.
- Immunostaining was positive for CD34 and negative for desmin, DDIT3, MDM2, and PLAG1.
- The patient underwent successful surgical resection with intraoperative radiation therapy, with no signs of recurrence or metastasis on follow-up CT scans.
Implications:
- This case underscores the potential for retroperitoneal lipoblastoma to occur in adults and present with atypical symptoms like acute cord compression.
- It highlights the importance of considering rare diagnoses in adult patients with seemingly common presentations.
- The successful management emphasizes a multidisciplinary approach involving surgery and radiation therapy for retroperitoneal lipoblastoma.
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