Related Experiment Video
Updated: Jul 11, 2026
07:36
Isolation of Human Lymphatic Endothelial Cells by Multi-parameter Fluorescence-activated Cell Sorting
Published on: May 1, 2015
[Cystic lymphangioma. Our experience]
M Arzoz Fàbregas1, L L Ibarz Servio, J Areal Calama
1Servicio de Urologia, Hospital Universitari Germans Trias I Pujol, Badalona, Barcelona. 37031maf@comb.es
Actas Urologicas Espanolas
|October 25, 2006
Summary
Cystic lymphangioma, a congenital lymphatic malformation, can present as large masses in soft tissues. Early and complete surgical excision is crucial to prevent recurrence, especially in rare scrotal and retroperitoneal cases.
Area of Science:
- Medicine
- Pathology
- Surgery
Background:
- Cystic lymphangioma is a congenital lymphatic hamartoma.
- It typically presents as a soft tissue mass in childhood.
- Complete excision is necessary to prevent growth and recurrence.
Observation:
- Two cases are presented: one young male with scrotal and pelvic cystic lymphangioma, and one patient with retroperitoneal cystic lymphangioma.
- Scrotal cystic lymphangioma is rare and often misdiagnosed, leading to incomplete surgery.
- Retroperitoneal cystic lymphangioma is an uncommon entity, frequently diagnosed incidentally.
Findings:
- Cystic lymphangioma requires complete surgical excision due to its growth potential.
- Misdiagnosis of scrotal cystic lymphangioma can lead to suboptimal surgical outcomes and recurrence.
- Retroperitoneal cystic lymphangioma is a rare condition often found incidentally.
Implications:
- Highlights the importance of accurate diagnosis for scrotal cystic lymphangioma to ensure complete surgical resection.
- Underscores the rarity and diagnostic challenges of retroperitoneal cystic lymphangioma.
- Emphasizes the need for thorough surgical planning and execution for lymphatic hamartomas.
