Unusual Presentation of Recurrent Wegener's Granulomatosis
A 65-year-old woman presented with recurrent Wegener's granulomatosis following two years of immunosuppressive therapy and three years of complete remission. At her initial presentation, she had a characteristic x-ray picture showing multiple nodules with total resolution of these findings at t...
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| Veröffentlicht in: | Chest 1991-03, Vol.99 (3), p.781-784 |
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| container_title | Chest |
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| creator | Dugowson, Carin E. Aitken, Moira L. |
| description | A 65-year-old woman presented with recurrent Wegener's granulomatosis following two years of immunosuppressive therapy and three years of complete remission. At her initial presentation, she had a characteristic x-ray picture showing multiple nodules with total resolution of these findings at three months. Five years later, at the time of clinical relapse, her chest x-ray film showed bilateral diffuse infiltrative disease. This change in radiologic presentation upon relapse of Wegener's has not previously been reported. Other unusual features include diffuse infiltrates as the pulmonary presentation and the long interval between cessation of therapy and relapse. We review the radiologic manifestations of Wegener's granulomatosis. (Chest 1991; 99:781–84) |
| doi_str_mv | 10.1378/chest.99.3.781 |
| format | Article |
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At her initial presentation, she had a characteristic x-ray picture showing multiple nodules with total resolution of these findings at three months. Five years later, at the time of clinical relapse, her chest x-ray film showed bilateral diffuse infiltrative disease. This change in radiologic presentation upon relapse of Wegener's has not previously been reported. Other unusual features include diffuse infiltrates as the pulmonary presentation and the long interval between cessation of therapy and relapse. We review the radiologic manifestations of Wegener's granulomatosis. (Chest 1991; 99:781–84)</description><identifier>ISSN: 0012-3692</identifier><identifier>EISSN: 1931-3543</identifier><identifier>DOI: 10.1378/chest.99.3.781</identifier><identifier>PMID: 1995249</identifier><identifier>CODEN: CHETBF</identifier><language>eng</language><publisher>Northbrook, IL: Elsevier Inc</publisher><subject>Aged ; Biological and medical sciences ; Female ; Granulomatosis with Polyangiitis - diagnostic imaging ; Humans ; Lung - diagnostic imaging ; Medical sciences ; Radiography ; Recurrence ; Sarcoidosis. Granulomatous diseases of unproved etiology. Connective tissue diseases. Elastic tissue diseases. 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At her initial presentation, she had a characteristic x-ray picture showing multiple nodules with total resolution of these findings at three months. Five years later, at the time of clinical relapse, her chest x-ray film showed bilateral diffuse infiltrative disease. This change in radiologic presentation upon relapse of Wegener's has not previously been reported. Other unusual features include diffuse infiltrates as the pulmonary presentation and the long interval between cessation of therapy and relapse. We review the radiologic manifestations of Wegener's granulomatosis. (Chest 1991; 99:781–84)</description><subject>Aged</subject><subject>Biological and medical sciences</subject><subject>Female</subject><subject>Granulomatosis with Polyangiitis - diagnostic imaging</subject><subject>Humans</subject><subject>Lung - diagnostic imaging</subject><subject>Medical sciences</subject><subject>Radiography</subject><subject>Recurrence</subject><subject>Sarcoidosis. Granulomatous diseases of unproved etiology. Connective tissue diseases. Elastic tissue diseases. 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Vasculitis</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Dugowson, Carin E.</creatorcontrib><creatorcontrib>Aitken, Moira L.</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>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Chest</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Dugowson, Carin E.</au><au>Aitken, Moira L.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Unusual Presentation of Recurrent Wegener's Granulomatosis</atitle><jtitle>Chest</jtitle><addtitle>Chest</addtitle><date>1991-03-01</date><risdate>1991</risdate><volume>99</volume><issue>3</issue><spage>781</spage><epage>784</epage><pages>781-784</pages><issn>0012-3692</issn><eissn>1931-3543</eissn><coden>CHETBF</coden><abstract>A 65-year-old woman presented with recurrent Wegener's granulomatosis following two years of immunosuppressive therapy and three years of complete remission. At her initial presentation, she had a characteristic x-ray picture showing multiple nodules with total resolution of these findings at three months. Five years later, at the time of clinical relapse, her chest x-ray film showed bilateral diffuse infiltrative disease. This change in radiologic presentation upon relapse of Wegener's has not previously been reported. Other unusual features include diffuse infiltrates as the pulmonary presentation and the long interval between cessation of therapy and relapse. We review the radiologic manifestations of Wegener's granulomatosis. (Chest 1991; 99:781–84)</abstract><cop>Northbrook, IL</cop><pub>Elsevier Inc</pub><pmid>1995249</pmid><doi>10.1378/chest.99.3.781</doi><tpages>4</tpages></addata></record> |
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| ispartof | Chest, 1991-03, Vol.99 (3), p.781-784 |
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| language | eng |
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| source | MEDLINE; Alma/SFX Local Collection |
| subjects | Aged Biological and medical sciences Female Granulomatosis with Polyangiitis - diagnostic imaging Humans Lung - diagnostic imaging Medical sciences Radiography Recurrence Sarcoidosis. Granulomatous diseases of unproved etiology. Connective tissue diseases. Elastic tissue diseases. Vasculitis |
| title | Unusual Presentation of Recurrent Wegener's Granulomatosis |
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