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Phacomatosis cesioflammea with Klippel Trenaunay syndrome: A rare association

A 30-year-old Indian male presented with bilateral Nevus of Ota, extensive nevus flammeus over the trunk and left lower limb with soft tissue hypertrophy and varicosities affecting the left lower limb. He was otherwise in good general health. A diagnosis of Phacomatosis cesioflammea or Phacomatosis...

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Detalles Bibliográficos
Autores principales: Garg, Anubhav, Gupta, Lalit K., Khare, A. K., Kuldeep, C. M., Mittal, Asit, Mehta, Sharad
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3752481/
https://www.ncbi.nlm.nih.gov/pubmed/23984239
http://dx.doi.org/10.4103/2229-5178.115522
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author Garg, Anubhav
Gupta, Lalit K.
Khare, A. K.
Kuldeep, C. M.
Mittal, Asit
Mehta, Sharad
author_facet Garg, Anubhav
Gupta, Lalit K.
Khare, A. K.
Kuldeep, C. M.
Mittal, Asit
Mehta, Sharad
author_sort Garg, Anubhav
collection PubMed
description A 30-year-old Indian male presented with bilateral Nevus of Ota, extensive nevus flammeus over the trunk and left lower limb with soft tissue hypertrophy and varicosities affecting the left lower limb. He was otherwise in good general health. A diagnosis of Phacomatosis cesioflammea or Phacomatosis pigmentovasularis Type II with Klippel Trenaunay syndrome was made. The case is being reported on account of its rarity.
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spelling pubmed-37524812013-08-27 Phacomatosis cesioflammea with Klippel Trenaunay syndrome: A rare association Garg, Anubhav Gupta, Lalit K. Khare, A. K. Kuldeep, C. M. Mittal, Asit Mehta, Sharad Indian Dermatol Online J Case Report A 30-year-old Indian male presented with bilateral Nevus of Ota, extensive nevus flammeus over the trunk and left lower limb with soft tissue hypertrophy and varicosities affecting the left lower limb. He was otherwise in good general health. A diagnosis of Phacomatosis cesioflammea or Phacomatosis pigmentovasularis Type II with Klippel Trenaunay syndrome was made. The case is being reported on account of its rarity. Medknow Publications & Media Pvt Ltd 2013 /pmc/articles/PMC3752481/ /pubmed/23984239 http://dx.doi.org/10.4103/2229-5178.115522 Text en Copyright: © Indian Dermatology Online Journal http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open-access article distributed under the terms of the Creative Commons Attribution-Noncommercial-Share Alike 3.0 Unported, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Report
Garg, Anubhav
Gupta, Lalit K.
Khare, A. K.
Kuldeep, C. M.
Mittal, Asit
Mehta, Sharad
Phacomatosis cesioflammea with Klippel Trenaunay syndrome: A rare association
title Phacomatosis cesioflammea with Klippel Trenaunay syndrome: A rare association
title_full Phacomatosis cesioflammea with Klippel Trenaunay syndrome: A rare association
title_fullStr Phacomatosis cesioflammea with Klippel Trenaunay syndrome: A rare association
title_full_unstemmed Phacomatosis cesioflammea with Klippel Trenaunay syndrome: A rare association
title_short Phacomatosis cesioflammea with Klippel Trenaunay syndrome: A rare association
title_sort phacomatosis cesioflammea with klippel trenaunay syndrome: a rare association
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3752481/
https://www.ncbi.nlm.nih.gov/pubmed/23984239
http://dx.doi.org/10.4103/2229-5178.115522
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