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[Mesenteric lymphangioma: report of a case]
C Pesce1, M L Cimaglia, P Donadio
1Divisione di Chirurgia Pediatrica, Ospedale Regionale di Vicenza, Italia.
La Pediatria Medica E Chirurgica : Medical and Surgical Pediatrics
|September 1, 1993
Summary
Mesenteric lymphangiomas, rare benign tumors from lymphatic malformations, require prompt surgical resection for excellent outcomes. Diagnosis is confirmed using imaging like ultrasound and CT scans.
Area of Science:
- Oncology
- Pediatric Surgery
- Vascular Malformations
Background:
- Lymphangiomas are benign congenital tumors originating from lymphatic malformations.
- They most frequently occur in the head and neck regions.
- Mesenteric lymphangiomas represent a rare clinical presentation.
Observation:
- This review focuses on a rare case of mesenteric lymphangioma.
- Clinical presentation, diagnostic methods, and treatment strategies are discussed.
- Intra-abdominal cystic lesions are effectively evaluated using ultrasound and computed tomography.
Findings:
- Diagnosis of mesenteric lymphangioma is confirmed via imaging modalities.
- Surgical resection of the affected intestine and mesentery is the primary treatment.
- Early diagnosis and intervention lead to favorable patient outcomes.
Implications:
- Highlights the importance of considering rare presentations of common conditions.
- Emphasizes the role of advanced imaging in diagnosing intra-abdominal masses.
- Supports surgical intervention as the definitive treatment for mesenteric lymphangiomas.