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Hyperechogenic renal parenchyma in potential live related kidney donors: Does it justify exclusion?
OBJECTIVES: To assess the predictive importance of ultrasonic grade 1 hyperechogenicity in potential live related kidney donors in the absence of urinary abnormalities and with perfect renal function. SUBJECTS AND METHODS: The study included 34 potential living related kidney donors with this abnorm...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2011
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4150590/ https://www.ncbi.nlm.nih.gov/pubmed/26579304 http://dx.doi.org/10.1016/j.aju.2011.10.013 |
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author | Fouda, Mohamed A. Shokeir, Ahmed A. Wafa, Ehab W. Refaie, Ayman F. El Diasty, Tarek Abdelrahim, Mona Sobh, Mohamed A. Ghoneim, Mohamed A. |
author_facet | Fouda, Mohamed A. Shokeir, Ahmed A. Wafa, Ehab W. Refaie, Ayman F. El Diasty, Tarek Abdelrahim, Mona Sobh, Mohamed A. Ghoneim, Mohamed A. |
author_sort | Fouda, Mohamed A. |
collection | PubMed |
description | OBJECTIVES: To assess the predictive importance of ultrasonic grade 1 hyperechogenicity in potential live related kidney donors in the absence of urinary abnormalities and with perfect renal function. SUBJECTS AND METHODS: The study included 34 potential living related kidney donors with this abnormality; their mean (SD, range) age was 32.7 (8.45, 23–48) years. Ten matched healthy donors with normal ultrasonographic appearance of the kidneys were studied as controls. All cases were thoroughly investigated, including measuring glomerular filtration rate by isotopic scintigraphy. The renal reserve was estimated by dopamine and amino-acid infusion in all subjects (study and control groups). A percutaneous renal biopsy was taken from 17 subjects in the abnormal echogenicity group and open renal biopsy was taken from eight of the control subjects. RESULTS: The renal reserve was comparable in both groups. Abnormal histopathological changes were found in seven subjects (41%) of the abnormal echogenicity group, i.e. partial glomerulosclerosis in one, mesangial thickening in two, interstitial fibrosis in one, focal tubular atrophy in one, immunoglobulin (Ig M) immune deposits in three and IgA in one. Only one subject in the control group showed mild mesangial thickening. CONCLUSION: Grade 1 echogenicity might be a sign of unrecognized kidney disease. Renal biopsy is mandatory when such related donors are the only available ones. Abnormal histopathology contraindicates donation. |
format | Online Article Text |
id | pubmed-4150590 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-41505902015-11-17 Hyperechogenic renal parenchyma in potential live related kidney donors: Does it justify exclusion? Fouda, Mohamed A. Shokeir, Ahmed A. Wafa, Ehab W. Refaie, Ayman F. El Diasty, Tarek Abdelrahim, Mona Sobh, Mohamed A. Ghoneim, Mohamed A. Arab J Urol Renal Transplantation Original article OBJECTIVES: To assess the predictive importance of ultrasonic grade 1 hyperechogenicity in potential live related kidney donors in the absence of urinary abnormalities and with perfect renal function. SUBJECTS AND METHODS: The study included 34 potential living related kidney donors with this abnormality; their mean (SD, range) age was 32.7 (8.45, 23–48) years. Ten matched healthy donors with normal ultrasonographic appearance of the kidneys were studied as controls. All cases were thoroughly investigated, including measuring glomerular filtration rate by isotopic scintigraphy. The renal reserve was estimated by dopamine and amino-acid infusion in all subjects (study and control groups). A percutaneous renal biopsy was taken from 17 subjects in the abnormal echogenicity group and open renal biopsy was taken from eight of the control subjects. RESULTS: The renal reserve was comparable in both groups. Abnormal histopathological changes were found in seven subjects (41%) of the abnormal echogenicity group, i.e. partial glomerulosclerosis in one, mesangial thickening in two, interstitial fibrosis in one, focal tubular atrophy in one, immunoglobulin (Ig M) immune deposits in three and IgA in one. Only one subject in the control group showed mild mesangial thickening. CONCLUSION: Grade 1 echogenicity might be a sign of unrecognized kidney disease. Renal biopsy is mandatory when such related donors are the only available ones. Abnormal histopathology contraindicates donation. Elsevier 2011-12 2011-12-01 /pmc/articles/PMC4150590/ /pubmed/26579304 http://dx.doi.org/10.1016/j.aju.2011.10.013 Text en © 2011 Arab Association of Urology. Production and hosting by Elsevier B.V. All rights reserved. http://creativecommons.org/licenses/by-nc-nd/3.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/3.0/). |
spellingShingle | Renal Transplantation Original article Fouda, Mohamed A. Shokeir, Ahmed A. Wafa, Ehab W. Refaie, Ayman F. El Diasty, Tarek Abdelrahim, Mona Sobh, Mohamed A. Ghoneim, Mohamed A. Hyperechogenic renal parenchyma in potential live related kidney donors: Does it justify exclusion? |
title | Hyperechogenic renal parenchyma in potential live related kidney donors: Does it justify exclusion? |
title_full | Hyperechogenic renal parenchyma in potential live related kidney donors: Does it justify exclusion? |
title_fullStr | Hyperechogenic renal parenchyma in potential live related kidney donors: Does it justify exclusion? |
title_full_unstemmed | Hyperechogenic renal parenchyma in potential live related kidney donors: Does it justify exclusion? |
title_short | Hyperechogenic renal parenchyma in potential live related kidney donors: Does it justify exclusion? |
title_sort | hyperechogenic renal parenchyma in potential live related kidney donors: does it justify exclusion? |
topic | Renal Transplantation Original article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4150590/ https://www.ncbi.nlm.nih.gov/pubmed/26579304 http://dx.doi.org/10.1016/j.aju.2011.10.013 |
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