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A Giant Retroperitoneal Lymphangioma: A Case Report
Prabhu Hubli1, Muddasetty Rohith2, Basavaraju M Sachin2
1Professor, Department of Surgery, Vijayanagar Institute of Medical Sciences , Bellary, India .
Journal of Clinical and Diagnostic Research : JCDR
|September 16, 2016
Summary
A rare intra-abdominal lymphangioma in an adult, typically a childhood condition, presented diagnostic challenges. This case highlights a huge, asymptomatic retroperitoneal lymphangioma successfully treated with surgical excision.
Area of Science:
- Pediatric Surgery
- Surgical Oncology
- Gastrointestinal Surgery
Background:
- Lymphangiomas are congenital malformations of the lymphatic system, commonly affecting the head and neck in children.
- Intra-abdominal lymphangiomas are exceptionally rare, particularly in adults, often leading to diagnostic complexities.
- While frequently asymptomatic, lymphangiomas can manifest as acute abdominal conditions.
Observation:
- This report details an unusual case of a massive, asymptomatic retroperitoneal lymphangioma in an adult patient.
- The retroperitoneal location and large size of the tumor presented unique diagnostic and surgical considerations.
- The patient remained asymptomatic prior to diagnosis, underscoring the potential for silent progression.
Findings:
- Complete surgical excision of the retroperitoneal lymphangioma was successfully achieved.
- The postoperative period was uneventful, indicating a favorable outcome following surgical intervention.
- Histopathological confirmation of lymphangioma was established post-excision.
Implications:
- This case expands the understanding of adult intra-abdominal lymphangioma presentations and management.
- It emphasizes the importance of considering rare diagnoses in adult patients with abdominal masses.
- Successful surgical excision offers a curative option for symptomatic or incidentally discovered retroperitoneal lymphangiomas.
