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Sickle cell nephropathy with diffuse proliferative lupus nephritis: a case report

BACKGROUND: Sickle cell nephropathy (SCN) is an important cause of mortality in patients with sickle cell disease. SCA with systemic lupus erythematosus (SLE) is known in children and less common in adults, however diffuse proliferative lupus nephritis (DPLN) with SCN has rarely been reported in adu...

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Autores principales: Kanodia, Kamal V, Vanikar, Aruna V, Goplani, Kamal R, Gupta, Sonia B, Trivedi, Hargovind L
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2008
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2275218/
https://www.ncbi.nlm.nih.gov/pubmed/18307766
http://dx.doi.org/10.1186/1746-1596-3-9
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author Kanodia, Kamal V
Vanikar, Aruna V
Goplani, Kamal R
Gupta, Sonia B
Trivedi, Hargovind L
author_facet Kanodia, Kamal V
Vanikar, Aruna V
Goplani, Kamal R
Gupta, Sonia B
Trivedi, Hargovind L
author_sort Kanodia, Kamal V
collection PubMed
description BACKGROUND: Sickle cell nephropathy (SCN) is an important cause of mortality in patients with sickle cell disease. SCA with systemic lupus erythematosus (SLE) is known in children and less common in adults, however diffuse proliferative lupus nephritis (DPLN) with SCN has rarely been reported in adults. It requires early diagnosis and aggressive management. CASE PRESENTATION: We present here a 35 years old lady with sickle cell disease who presented with edema, dyspnoea on exertion, pyuria and had raised s. creatinine of 7 mg%. Her biopsy revealed SCN with DPLN. She is on maintenance hemodialysis after 2 months of diagnosis. CONCLUSION: DPLN with SCN is a rare entity with poor prognosis, which may be overlooked and needs aggressive management.
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spelling pubmed-22752182008-03-26 Sickle cell nephropathy with diffuse proliferative lupus nephritis: a case report Kanodia, Kamal V Vanikar, Aruna V Goplani, Kamal R Gupta, Sonia B Trivedi, Hargovind L Diagn Pathol Case Report BACKGROUND: Sickle cell nephropathy (SCN) is an important cause of mortality in patients with sickle cell disease. SCA with systemic lupus erythematosus (SLE) is known in children and less common in adults, however diffuse proliferative lupus nephritis (DPLN) with SCN has rarely been reported in adults. It requires early diagnosis and aggressive management. CASE PRESENTATION: We present here a 35 years old lady with sickle cell disease who presented with edema, dyspnoea on exertion, pyuria and had raised s. creatinine of 7 mg%. Her biopsy revealed SCN with DPLN. She is on maintenance hemodialysis after 2 months of diagnosis. CONCLUSION: DPLN with SCN is a rare entity with poor prognosis, which may be overlooked and needs aggressive management. BioMed Central 2008-02-28 /pmc/articles/PMC2275218/ /pubmed/18307766 http://dx.doi.org/10.1186/1746-1596-3-9 Text en Copyright © 2008 Kanodia et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( (http://creativecommons.org/licenses/by/2.0) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Report
Kanodia, Kamal V
Vanikar, Aruna V
Goplani, Kamal R
Gupta, Sonia B
Trivedi, Hargovind L
Sickle cell nephropathy with diffuse proliferative lupus nephritis: a case report
title Sickle cell nephropathy with diffuse proliferative lupus nephritis: a case report
title_full Sickle cell nephropathy with diffuse proliferative lupus nephritis: a case report
title_fullStr Sickle cell nephropathy with diffuse proliferative lupus nephritis: a case report
title_full_unstemmed Sickle cell nephropathy with diffuse proliferative lupus nephritis: a case report
title_short Sickle cell nephropathy with diffuse proliferative lupus nephritis: a case report
title_sort sickle cell nephropathy with diffuse proliferative lupus nephritis: a case report
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2275218/
https://www.ncbi.nlm.nih.gov/pubmed/18307766
http://dx.doi.org/10.1186/1746-1596-3-9
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