Cystic hygroma: Case report

Sapna S Deshpande; Vishrabdha Pawar; AN Kurane; Anushree Modi

IP Archives of Cytology and Histopathology Research

Official Publication of Khyati Education and Research Foundation

IP Archives of Cytology and Histopathology Research

Print ISSN: 2581-5725

Online ISSN: 2456-9267

CODEN : IACHCL

IP Archives of Cytology and Histopathology Research (ACHR) open access, peer-reviewed quarterly journal publishing since 2016 and is published under the Khyati Education and Research Foundation (KERF), is registered as a non-profit society (under the society registration act, 1860), Government of India with the vision of various accredited vocational courses in healthcare, education, paramedical, yoga, publication, teaching and research activity, with the aim of faster and better dissemination of knowledge, we will be publishing the article more...

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Case Report

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129-131

Authors Details

Sapna S Deshpande*, Vishrabdha Pawar, AN Kurane, Anushree Modi

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Cystic hygroma: Case report

Case Report

Author Details : Sapna S Deshpande*, Vishrabdha Pawar, AN Kurane, Anushree Modi

Volume : 7, Issue : 2, Year : 2022

Article Page : 129-131

https://doi.org/10.18231/j.achr.2022.027

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Abstract

Cystic hygromas are the most common, cystic variety of lymphangioma, present at birth or period of infancy. Its common locations being cervico-facial regions and axilla. Respiratory distress, recurrent infections or cosmetic reasons are the main indications of the treatment. The ideal treatment is complete surgical excision; however, there is a gradual conversion towards sclerosant therapy.

Keywords: Cystic hygroma, Cystic spaces, Bleomycin, Complications

How to cite : Deshpande S S, Pawar V, Kurane A, Modi A, Cystic hygroma: Case report. IP Arch Cytol Histopathol Res 2022;7(2):129-131

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