Related Experiment Videos
Retroperitoneal cystic lymphangioma
G Nuzzo1, G Lemmo, M M Marrocco-Trischitta
1Department of Surgery, Chirurgia Geriatrica, Catholic University, School of Medicine, Policlinico A. Gemelli, Rome, Italy.
Journal of Surgical Oncology
|March 1, 1996
Summary
Retroperitoneal cystic lymphangioma (CL) is a rare lymphatic neoplasm. Surgical excision is the recommended treatment for this benign but potentially morbid retroperitoneal tumor.
Area of Science:
- Medicine
- Oncology
- Pathology
Background:
- Cystic lymphangioma (CL) is a rare, benign neoplasm originating from the lymphatic system.
- While commonly found in the neck and axilla, CL is infrequently observed in the retroperitoneum.
Observation:
- This report details two cases of retroperitoneal cystic lymphangioma.
- Retroperitoneal CL presents as cyst-like cavities containing serous, serosanguineous, or chylous fluid.
- The histogenesis of cystic lymphangioma remains uncertain.
Findings:
- Despite its benign nature, retroperitoneal CL can lead to significant morbidity.
- Large size and invasive characteristics are common features of retroperitoneal CL.
- Secondary infection is a frequent complication of retroperitoneal cystic lymphangioma.
Implications:
- Early diagnosis and surgical excision are crucial for managing retroperitoneal cystic lymphangioma.
- Understanding the clinical behavior of this rare tumor is essential for effective patient treatment.
- Further research into the histogenesis of CL may offer insights into its development and potential therapeutic targets.