“A case of vanishing bone disease complicated by chylothorax- diagnosis and treatment”

A 16-year old girl with Gorham-Stout disease is presented. She had progressive replacement of the bones of her left arm and shoulder girdle by fibroadipose tissue and numerous proliferated, non-neoplastic, lymphatic channels. The clinico-pathologic features of this condition are discussed, as are it...

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Autores principales: Suzuki, N, Cintra, FF, Cintra, ML, Maciel, MG, Amstalden, EMI, Teixeira, F, Kubba, F
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SAGE Publications 2022
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9237928/
https://www.ncbi.nlm.nih.gov/pubmed/35774987
http://dx.doi.org/10.1177/20542704221103912
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author Suzuki, N
Cintra, FF
Cintra, ML
Maciel, MG
Amstalden, EMI
Teixeira, F
Kubba, F
author_facet Suzuki, N
Cintra, FF
Cintra, ML
Maciel, MG
Amstalden, EMI
Teixeira, F
Kubba, F
author_sort Suzuki, N
collection PubMed
description A 16-year old girl with Gorham-Stout disease is presented. She had progressive replacement of the bones of her left arm and shoulder girdle by fibroadipose tissue and numerous proliferated, non-neoplastic, lymphatic channels. The clinico-pathologic features of this condition are discussed, as are its possible complications and available therapeutic modalities.
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spelling pubmed-92379282022-06-29 “A case of vanishing bone disease complicated by chylothorax- diagnosis and treatment” Suzuki, N Cintra, FF Cintra, ML Maciel, MG Amstalden, EMI Teixeira, F Kubba, F JRSM Open Case Report A 16-year old girl with Gorham-Stout disease is presented. She had progressive replacement of the bones of her left arm and shoulder girdle by fibroadipose tissue and numerous proliferated, non-neoplastic, lymphatic channels. The clinico-pathologic features of this condition are discussed, as are its possible complications and available therapeutic modalities. SAGE Publications 2022-06-23 /pmc/articles/PMC9237928/ /pubmed/35774987 http://dx.doi.org/10.1177/20542704221103912 Text en © 2022 The Author(s) https://creativecommons.org/licenses/by-nc/4.0/This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 License (https://creativecommons.org/licenses/by-nc/4.0/) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access page (https://us.sagepub.com/en-us/nam/open-access-at-sage).
spellingShingle Case Report
Suzuki, N
Cintra, FF
Cintra, ML
Maciel, MG
Amstalden, EMI
Teixeira, F
Kubba, F
“A case of vanishing bone disease complicated by chylothorax- diagnosis and treatment”
title “A case of vanishing bone disease complicated by chylothorax- diagnosis and treatment”
title_full “A case of vanishing bone disease complicated by chylothorax- diagnosis and treatment”
title_fullStr “A case of vanishing bone disease complicated by chylothorax- diagnosis and treatment”
title_full_unstemmed “A case of vanishing bone disease complicated by chylothorax- diagnosis and treatment”
title_short “A case of vanishing bone disease complicated by chylothorax- diagnosis and treatment”
title_sort “a case of vanishing bone disease complicated by chylothorax- diagnosis and treatment”
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9237928/
https://www.ncbi.nlm.nih.gov/pubmed/35774987
http://dx.doi.org/10.1177/20542704221103912
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