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A patient with macrodystrophia lipomatosa bilaterally affecting the entire upper extremity: reporting of a rare case and literature review

The patient, a 58-year-old Asian female, had the progressive, bilateral overgrowth of the entire upper extremity since her childhood and has undergone debulking surgery twice in her country. However, overgrowth progressed after surgery. The patient was diagnosed with Macrodystrophia lipomatosa (MDL)...

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Detalles Bibliográficos
Autores principales: Baba, Kyoko, Kashiwagi, Shinya, Nemoto, Mitsuru, Takeda, Akira, Fukumoto, Keizo, Uchinuma, Eiju
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Taylor & Francis 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8183515/
https://www.ncbi.nlm.nih.gov/pubmed/34124316
http://dx.doi.org/10.1080/23320885.2021.1872380
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author Baba, Kyoko
Kashiwagi, Shinya
Nemoto, Mitsuru
Takeda, Akira
Fukumoto, Keizo
Uchinuma, Eiju
author_facet Baba, Kyoko
Kashiwagi, Shinya
Nemoto, Mitsuru
Takeda, Akira
Fukumoto, Keizo
Uchinuma, Eiju
author_sort Baba, Kyoko
collection PubMed
description The patient, a 58-year-old Asian female, had the progressive, bilateral overgrowth of the entire upper extremity since her childhood and has undergone debulking surgery twice in her country. However, overgrowth progressed after surgery. The patient was diagnosed with Macrodystrophia lipomatosa (MDL) by physical and imaging findings in our departments.
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spelling pubmed-81835152021-06-11 A patient with macrodystrophia lipomatosa bilaterally affecting the entire upper extremity: reporting of a rare case and literature review Baba, Kyoko Kashiwagi, Shinya Nemoto, Mitsuru Takeda, Akira Fukumoto, Keizo Uchinuma, Eiju Case Reports Plast Surg Hand Surg Case Report The patient, a 58-year-old Asian female, had the progressive, bilateral overgrowth of the entire upper extremity since her childhood and has undergone debulking surgery twice in her country. However, overgrowth progressed after surgery. The patient was diagnosed with Macrodystrophia lipomatosa (MDL) by physical and imaging findings in our departments. Taylor & Francis 2021-06-04 /pmc/articles/PMC8183515/ /pubmed/34124316 http://dx.doi.org/10.1080/23320885.2021.1872380 Text en © 2021 The Author(s). Published by Informa UK Limited, trading as Taylor & Francis Group. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Report
Baba, Kyoko
Kashiwagi, Shinya
Nemoto, Mitsuru
Takeda, Akira
Fukumoto, Keizo
Uchinuma, Eiju
A patient with macrodystrophia lipomatosa bilaterally affecting the entire upper extremity: reporting of a rare case and literature review
title A patient with macrodystrophia lipomatosa bilaterally affecting the entire upper extremity: reporting of a rare case and literature review
title_full A patient with macrodystrophia lipomatosa bilaterally affecting the entire upper extremity: reporting of a rare case and literature review
title_fullStr A patient with macrodystrophia lipomatosa bilaterally affecting the entire upper extremity: reporting of a rare case and literature review
title_full_unstemmed A patient with macrodystrophia lipomatosa bilaterally affecting the entire upper extremity: reporting of a rare case and literature review
title_short A patient with macrodystrophia lipomatosa bilaterally affecting the entire upper extremity: reporting of a rare case and literature review
title_sort patient with macrodystrophia lipomatosa bilaterally affecting the entire upper extremity: reporting of a rare case and literature review
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8183515/
https://www.ncbi.nlm.nih.gov/pubmed/34124316
http://dx.doi.org/10.1080/23320885.2021.1872380
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