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Lymphedema Associated With Primary Amyloidosis: A Case Study

We reported on a 60-year-old man presenting lymphedema of both lower extremities and scrotum for 3 years with unknown cause. We took a computed tomography scan of the lower extremities as a follow-up. There were diffuse subcutaneous edema in both lower extremities and multiple enlarged lymph nodes a...

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Autores principales: Park, Gahee, Jeong, Hye Won, Lee, Junhee, Mun, Yeung-Chul, Sung, Sun Hee, Han, Soo Jeong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Korean Academy of Rehabilitation Medicine 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5698678/
https://www.ncbi.nlm.nih.gov/pubmed/29201830
http://dx.doi.org/10.5535/arm.2017.41.5.887
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author Park, Gahee
Jeong, Hye Won
Lee, Junhee
Mun, Yeung-Chul
Sung, Sun Hee
Han, Soo Jeong
author_facet Park, Gahee
Jeong, Hye Won
Lee, Junhee
Mun, Yeung-Chul
Sung, Sun Hee
Han, Soo Jeong
author_sort Park, Gahee
collection PubMed
description We reported on a 60-year-old man presenting lymphedema of both lower extremities and scrotum for 3 years with unknown cause. We took a computed tomography scan of the lower extremities as a follow-up. There were diffuse subcutaneous edema in both lower extremities and multiple enlarged lymph nodes along the para-aortic and bilateral inguinal areas. For further evaluation, biopsy of an enlarged inguinal lymph node was taken, yielding a diagnosis of primary amyloidosis. A treatment of chemotherapy for amyloidosis was recommended for him. To our knowledge, this is the first report of lymphedema presenting with primary amyloidosis in Asia. This case suggests that primary amyloidosis could be one of the differential diagnoses in patients with lymphedema in the lower extremities.
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spelling pubmed-56986782017-12-03 Lymphedema Associated With Primary Amyloidosis: A Case Study Park, Gahee Jeong, Hye Won Lee, Junhee Mun, Yeung-Chul Sung, Sun Hee Han, Soo Jeong Ann Rehabil Med Case Report We reported on a 60-year-old man presenting lymphedema of both lower extremities and scrotum for 3 years with unknown cause. We took a computed tomography scan of the lower extremities as a follow-up. There were diffuse subcutaneous edema in both lower extremities and multiple enlarged lymph nodes along the para-aortic and bilateral inguinal areas. For further evaluation, biopsy of an enlarged inguinal lymph node was taken, yielding a diagnosis of primary amyloidosis. A treatment of chemotherapy for amyloidosis was recommended for him. To our knowledge, this is the first report of lymphedema presenting with primary amyloidosis in Asia. This case suggests that primary amyloidosis could be one of the differential diagnoses in patients with lymphedema in the lower extremities. Korean Academy of Rehabilitation Medicine 2017-10 2017-10-31 /pmc/articles/PMC5698678/ /pubmed/29201830 http://dx.doi.org/10.5535/arm.2017.41.5.887 Text en Copyright © 2017 by Korean Academy of Rehabilitation Medicine http://creativecommons.org/licenses/by-nc/4.0 This is an open-access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0) which permits unrestricted noncommercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Report
Park, Gahee
Jeong, Hye Won
Lee, Junhee
Mun, Yeung-Chul
Sung, Sun Hee
Han, Soo Jeong
Lymphedema Associated With Primary Amyloidosis: A Case Study
title Lymphedema Associated With Primary Amyloidosis: A Case Study
title_full Lymphedema Associated With Primary Amyloidosis: A Case Study
title_fullStr Lymphedema Associated With Primary Amyloidosis: A Case Study
title_full_unstemmed Lymphedema Associated With Primary Amyloidosis: A Case Study
title_short Lymphedema Associated With Primary Amyloidosis: A Case Study
title_sort lymphedema associated with primary amyloidosis: a case study
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5698678/
https://www.ncbi.nlm.nih.gov/pubmed/29201830
http://dx.doi.org/10.5535/arm.2017.41.5.887
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