Amyloidosis in Behcet′s disease

Behcet′s disease (BD) is a multisystem vasculitis with protean manifestations. It is characterized by a heightened state of inflammation, although the factors that initiate and sustain this inflammation are not clear. We report some cases of BD-associated amyloidosis and have similar features. The p...

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Main Authors: I Ben Ghorbel, N Bel Feki, T Ben Salem, M Lamloum, M H Houman
Format: Article
Language:English
Published: Wolters Kluwer Medknow Publications 2015-01-01
Series:Saudi Journal of Kidney Diseases and Transplantation
Online Access:http://www.sjkdt.org/article.asp?issn=1319-2442;year=2015;volume=26;issue=1;spage=132;epage=134;aulast=Ghorbel
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author I Ben Ghorbel
N Bel Feki
T Ben Salem
M Lamloum
M H Houman
author_facet I Ben Ghorbel
N Bel Feki
T Ben Salem
M Lamloum
M H Houman
author_sort I Ben Ghorbel
collection DOAJ
description Behcet′s disease (BD) is a multisystem vasculitis with protean manifestations. It is characterized by a heightened state of inflammation, although the factors that initiate and sustain this inflammation are not clear. We report some cases of BD-associated amyloidosis and have similar features. The patients developed nephrotic syndrome due to secondary amyloidosis, which was refractory to the immunosuppressive agents. Two patients expired and the third was lost to follow-up during the course. The BD complicated with amyloidosis is associated with high mortality despite the current aggressive therapy.
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spelling doaj.art-af0b00f9c3d946e08f790978745c53602022-12-22T03:22:08ZengWolters Kluwer Medknow PublicationsSaudi Journal of Kidney Diseases and Transplantation1319-24422015-01-0126113213410.4103/1319-2442.148761Amyloidosis in Behcet′s diseaseI Ben GhorbelN Bel FekiT Ben SalemM LamloumM H HoumanBehcet′s disease (BD) is a multisystem vasculitis with protean manifestations. It is characterized by a heightened state of inflammation, although the factors that initiate and sustain this inflammation are not clear. We report some cases of BD-associated amyloidosis and have similar features. The patients developed nephrotic syndrome due to secondary amyloidosis, which was refractory to the immunosuppressive agents. Two patients expired and the third was lost to follow-up during the course. The BD complicated with amyloidosis is associated with high mortality despite the current aggressive therapy.http://www.sjkdt.org/article.asp?issn=1319-2442;year=2015;volume=26;issue=1;spage=132;epage=134;aulast=Ghorbel
spellingShingle I Ben Ghorbel
N Bel Feki
T Ben Salem
M Lamloum
M H Houman
Amyloidosis in Behcet′s disease
Saudi Journal of Kidney Diseases and Transplantation
title Amyloidosis in Behcet′s disease
title_full Amyloidosis in Behcet′s disease
title_fullStr Amyloidosis in Behcet′s disease
title_full_unstemmed Amyloidosis in Behcet′s disease
title_short Amyloidosis in Behcet′s disease
title_sort amyloidosis in behcet s disease
url http://www.sjkdt.org/article.asp?issn=1319-2442;year=2015;volume=26;issue=1;spage=132;epage=134;aulast=Ghorbel
work_keys_str_mv AT ibenghorbel amyloidosisinbehcetsdisease
AT nbelfeki amyloidosisinbehcetsdisease
AT tbensalem amyloidosisinbehcetsdisease
AT mlamloum amyloidosisinbehcetsdisease
AT mhhouman amyloidosisinbehcetsdisease