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[Giant pelvic lipoma mimicking a liposarcoma]
Bacha Dhouha1, Walha Maroua1, Baccouch Seifeddine2
1Université de Tunis El Manar, Faculté de Médecine de Tunis, Service d'Anatomie Pathologique, Hôpital Mongi Slim, Sidi Daoued, Tunis.
The Pan African Medical Journal
|July 18, 2019
Summary
Giant lipomas are rare tumors. This case highlights a large pelvic lipoma in the ischiorectal fossa, emphasizing the importance of accurate diagnosis and surgical resection for this uncommon condition.
Area of Science:
- Oncology
- Radiology
- Pathology
Background:
- Giant lipomas (GL) are rare, ubiquitous tumors, with pelvic lipomas being exceptionally uncommon, fewer than 10 cases reported.
- Differentiating pelvic lipomas from lipoma-like well-differentiated liposarcoma is a critical diagnostic challenge.
Observation:
- A 50-year-old female presented with a 3-month history of pelvic discomfort and a palpable mass in the left ischiorectal fossa.
- Abdominopelvic CT revealed a large (10x18 cm), homogeneous, hypodense, presacral lipomatous mass.
- MRI demonstrated a hyperintense lesion on T1 and T2-weighted images, extending to the second sacral vertebra.
Findings:
- Surgical resection via abdominoperineal approach was successfully performed without tumor capsule rupture.
- Anatomopathological examination confirmed the diagnosis of a giant pelvic lipoma.
Implications:
- This case contributes to the limited literature on giant presacral pelvic lipomas.
- Accurate radiological assessment and histopathological confirmation are crucial for managing these rare pelvic masses.
- Surgical intervention is the definitive treatment for symptomatic giant pelvic lipomas.
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