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Updated: Jul 9, 2026

Isolation of Human Lymphatic Endothelial Cells by Multi-parameter Fluorescence-activated Cell Sorting

Isolation of Human Lymphatic Endothelial Cells by Multi-parameter Fluorescence-activated Cell Sorting

Published on: May 1, 2015

Lymphangioma scroti.

Jelica Vikicevic¹, Danica Milobratovic, Vojkan Vukadinovic

¹Institute for Dermatovenereology, University School of Medicine, KCS, Belgrade, Serbia and Montenegro.

Pediatric Dermatology

|November 27, 2007

Summary

This summary is machine-generated.

Scrotal lymphangiomas, rare congenital lymphatic malformations, can present as cystic scrotal masses in boys. Early diagnosis via ultrasonography is crucial for effective treatment and preventing recurrence.

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Last Updated: Jul 9, 2026

Isolation of Human Lymphatic Endothelial Cells by Multi-parameter Fluorescence-activated Cell Sorting

Isolation of Human Lymphatic Endothelial Cells by Multi-parameter Fluorescence-activated Cell Sorting

Published on: May 1, 2015

Area of Science:

Pediatric Surgery
Vascular Malformations
Lymphatic System Research

Background:

Lymphangiomas are rare congenital lymphatic system malformations.
Scrotal lymphangiomas are exceptionally uncommon, particularly in pediatric cases.
Understanding their presentation is key for accurate diagnosis.

Observation:

A 10-year-old boy presented with a multiloculated scrotal mass.
Associated symptoms included left thigh edema and left cryptorchidism.
Histopathology confirmed a scrotal lymphangioma cavernosum.

Findings:

Ultrasonography proved vital for preoperative diagnosis and lesion extent assessment.
The case highlights the importance of considering lymphangioma in scrotal masses.
Accurate diagnosis prevents misdiagnosis and inappropriate management.

Implications:

Early and accurate diagnosis of scrotal lymphangioma is essential in pediatric patients.
Ultrasonography is a key imaging modality for scrotal lymphatic malformations.
Timely intervention can prevent complications and recurrence of scrotal lymphangioma.