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Related Experiment Video

Updated: May 8, 2026

Isolation of Human Lymphatic Endothelial Cells by Multi-parameter Fluorescence-activated Cell Sorting
07:36

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

Published on: May 1, 2015

Cavernous lymphangioma: Two case reports.

Cynthia Sargunam1, Jayakar Thomas, P K Raneesha

  • 1Department of Dermatology, Sree Balaji Medical College and Hospital, Chromepet, Chennai, India.

Indian Dermatology Online Journal
|August 29, 2013
PubMed
Summary
This summary is machine-generated.

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Congenital lymphangiomas, malformations of the lymphatic system, can affect skin and subcutaneous tissues. This report details two rare cases of cavernous lymphangioma, highlighting their unusual presentation.

Area of Science:

  • Vascular Malformations
  • Pediatric Surgery
  • Dermatology

Background:

  • Lymphangiomas represent congenital malformations of the lymphatic system.
  • These benign tumors typically involve the skin and subcutaneous tissues.
  • Cavernous lymphangiomas are a less common subtype characterized by large, cystic lymphatic spaces.

Observation:

  • The report presents two distinct cases of cavernous lymphangioma.
  • Both cases involved extensive involvement of the skin and subcutaneous tissues.
  • The clinical presentation and diagnostic challenges of these rare lesions were noted.

Findings:

  • The two cases underscore the rarity of cavernous lymphangioma.
  • Detailed case descriptions provide insights into the anatomical extent and clinical behavior.
Keywords:
Cavernous lymphangiomacongenital malformationslymphatic malformation

Related Experiment Videos

Last Updated: May 8, 2026

Isolation of Human Lymphatic Endothelial Cells by Multi-parameter Fluorescence-activated Cell Sorting
07:36

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

Published on: May 1, 2015

  • Diagnostic imaging and histopathological findings confirmed the nature of the malformations.

    • Implications:

    • Increased awareness of rare lymphangioma subtypes is crucial for accurate diagnosis.
    • Understanding the presentation of cavernous lymphangioma aids in surgical planning.
    • Further research into the etiology and management of these rare lymphatic malformations is warranted.