Behçet's disease and amyloidosis : Review of the literature
In this report, we present a patient with BD, amyloidosis and end-stage-renal-disease and discuss the literature on BD and amyloidosis. Forty-four patients with BD and amyloidosis are described in the literature. The type of amyloid fibrils were studied in 27 of this 44 patients and all were AA. The...
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Veröffentlicht in: | Scandinavian journal of rheumatology 1997, Vol.26 (6), p.477-479 |
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container_title | Scandinavian journal of rheumatology |
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creator | AKPOLAT, I AKPOLAT, T DANACI, M BARIS, Y. S KAYA, N KANDEMIR, B |
description | In this report, we present a patient with BD, amyloidosis and end-stage-renal-disease and discuss the literature on BD and amyloidosis. Forty-four patients with BD and amyloidosis are described in the literature. The type of amyloid fibrils were studied in 27 of this 44 patients and all were AA. The interval between the onset of first symptom of BD and the diagnosis of amyloidosis ranged from one to 27 years. This clinical observation and AA type amyloid fibrils in BD suggest that amyloidosis is secondary to inflammation. Behçet's disease should be considered in the differential diagnosis of AA amyloidosis. |
doi_str_mv | 10.3109/03009749709065723 |
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S ; KAYA, N ; KANDEMIR, B</creator><creatorcontrib>AKPOLAT, I ; AKPOLAT, T ; DANACI, M ; BARIS, Y. S ; KAYA, N ; KANDEMIR, B</creatorcontrib><description>In this report, we present a patient with BD, amyloidosis and end-stage-renal-disease and discuss the literature on BD and amyloidosis. Forty-four patients with BD and amyloidosis are described in the literature. The type of amyloid fibrils were studied in 27 of this 44 patients and all were AA. The interval between the onset of first symptom of BD and the diagnosis of amyloidosis ranged from one to 27 years. This clinical observation and AA type amyloid fibrils in BD suggest that amyloidosis is secondary to inflammation. Behçet's disease should be considered in the differential diagnosis of AA amyloidosis.</description><identifier>ISSN: 0300-9742</identifier><identifier>EISSN: 1502-7732</identifier><identifier>DOI: 10.3109/03009749709065723</identifier><identifier>PMID: 9433411</identifier><identifier>CODEN: SJRHAT</identifier><language>eng</language><publisher>Colchester: Taylor & Francis</publisher><subject>Adult ; Amyloidosis - complications ; Behcet Syndrome - complications ; Biological and medical sciences ; Humans ; Male ; Medical sciences ; Sarcoidosis. Granulomatous diseases of unproved etiology. Connective tissue diseases. Elastic tissue diseases. 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S</creatorcontrib><creatorcontrib>KAYA, N</creatorcontrib><creatorcontrib>KANDEMIR, B</creatorcontrib><title>Behçet's disease and amyloidosis : Review of the literature</title><title>Scandinavian journal of rheumatology</title><addtitle>Scand J Rheumatol</addtitle><description>In this report, we present a patient with BD, amyloidosis and end-stage-renal-disease and discuss the literature on BD and amyloidosis. Forty-four patients with BD and amyloidosis are described in the literature. The type of amyloid fibrils were studied in 27 of this 44 patients and all were AA. The interval between the onset of first symptom of BD and the diagnosis of amyloidosis ranged from one to 27 years. This clinical observation and AA type amyloid fibrils in BD suggest that amyloidosis is secondary to inflammation. Behçet's disease should be considered in the differential diagnosis of AA amyloidosis.</description><subject>Adult</subject><subject>Amyloidosis - complications</subject><subject>Behcet Syndrome - complications</subject><subject>Biological and medical sciences</subject><subject>Humans</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Sarcoidosis. Granulomatous diseases of unproved etiology. Connective tissue diseases. Elastic tissue diseases. 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Granulomatous diseases of unproved etiology. Connective tissue diseases. Elastic tissue diseases. Vasculitis</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>AKPOLAT, I</creatorcontrib><creatorcontrib>AKPOLAT, T</creatorcontrib><creatorcontrib>DANACI, M</creatorcontrib><creatorcontrib>BARIS, Y. S</creatorcontrib><creatorcontrib>KAYA, N</creatorcontrib><creatorcontrib>KANDEMIR, B</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>MEDLINE - Academic</collection><jtitle>Scandinavian journal of rheumatology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>AKPOLAT, I</au><au>AKPOLAT, T</au><au>DANACI, M</au><au>BARIS, Y. S</au><au>KAYA, N</au><au>KANDEMIR, B</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Behçet's disease and amyloidosis : Review of the literature</atitle><jtitle>Scandinavian journal of rheumatology</jtitle><addtitle>Scand J Rheumatol</addtitle><date>1997</date><risdate>1997</risdate><volume>26</volume><issue>6</issue><spage>477</spage><epage>479</epage><pages>477-479</pages><issn>0300-9742</issn><eissn>1502-7732</eissn><coden>SJRHAT</coden><abstract>In this report, we present a patient with BD, amyloidosis and end-stage-renal-disease and discuss the literature on BD and amyloidosis. Forty-four patients with BD and amyloidosis are described in the literature. The type of amyloid fibrils were studied in 27 of this 44 patients and all were AA. The interval between the onset of first symptom of BD and the diagnosis of amyloidosis ranged from one to 27 years. This clinical observation and AA type amyloid fibrils in BD suggest that amyloidosis is secondary to inflammation. Behçet's disease should be considered in the differential diagnosis of AA amyloidosis.</abstract><cop>Colchester</cop><pub>Taylor & Francis</pub><pmid>9433411</pmid><doi>10.3109/03009749709065723</doi><tpages>3</tpages></addata></record> |
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source | MEDLINE; Taylor & Francis Medical Library - CRKN; Taylor & Francis Journals Complete |
subjects | Adult Amyloidosis - complications Behcet Syndrome - complications Biological and medical sciences Humans Male Medical sciences Sarcoidosis. Granulomatous diseases of unproved etiology. Connective tissue diseases. Elastic tissue diseases. Vasculitis |
title | Behçet's disease and amyloidosis : Review of the literature |
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