Title of article
Amyloidosis in Behcet s disease
Author/Authors
ghorbel, i.b. department of internal medicine,la rabta hospital, Tunisia , feki, n.b. department of internal medicine,la rabta hospital, Tunisia , salem, t.b. department of internal medicine,la rabta hospital, Tunisia , lamloum, m. department of internal medicine,la rabta hospital, Tunisia , houman, m.h. department of internal medicine,la rabta hospital, Tunisia
From page
132
To page
134
Abstract
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.
Journal title
Saudi Journal of Kidney Diseases and Transplantation
Journal title
Saudi Journal of Kidney Diseases and Transplantation
Record number
2521340
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