Primary Multifocal Recurrent Urinary Bladder Amyloidosis: A Rare Case Report from Syria
Primary urinary bladder amyloidosis is a rare disorder of protein metabolism characterized by the extracellular deposition of fibrillin. To date, fewer than 200 cases have been reported in the literature. We herein present a case of 59-year-old female with primary multifocal recurrent urinary bladde...
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| Main Authors: | , , , , , , |
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| Format: | Article |
| Language: | English |
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Wiley
2021-01-01
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| Series: | Case Reports in Medicine |
| Online Access: | http://dx.doi.org/10.1155/2021/4476363 |
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| author | Leen Jamel Doya Lama Doya Khaled Al-Yousef Ali Adib Abedallah Al Shamali Basel Al Deeb Mohamad Kanan |
| author_facet | Leen Jamel Doya Lama Doya Khaled Al-Yousef Ali Adib Abedallah Al Shamali Basel Al Deeb Mohamad Kanan |
| author_sort | Leen Jamel Doya |
| collection | DOAJ |
| description | Primary urinary bladder amyloidosis is a rare disorder of protein metabolism characterized by the extracellular deposition of fibrillin. To date, fewer than 200 cases have been reported in the literature. We herein present a case of 59-year-old female with primary multifocal recurrent urinary bladder amyloidosis. The patient was treated with a new method (laser therapy) mentioned for the first time in the literature. After 18 months of treatment, the patient has no complaints. Our case illustrates a new procedure in the treatment of primary multifocal bladder amyloidosis. |
| format | Article |
| id | doaj-art-c35c5d755bf74538b2bef00ef6443523 |
| institution | Kabale University |
| issn | 1687-9627 1687-9635 |
| language | English |
| publishDate | 2021-01-01 |
| publisher | Wiley |
| record_format | Article |
| series | Case Reports in Medicine |
| spelling | doaj-art-c35c5d755bf74538b2bef00ef64435232025-02-03T07:24:00ZengWileyCase Reports in Medicine1687-96271687-96352021-01-01202110.1155/2021/44763634476363Primary Multifocal Recurrent Urinary Bladder Amyloidosis: A Rare Case Report from SyriaLeen Jamel Doya0Lama Doya1Khaled Al-Yousef2Ali Adib3Abedallah Al Shamali4Basel Al Deeb5Mohamad Kanan6Department of Pediatrics, Tishreen University Hospital, Lattakia, SyriaDepartment of Laboratory, Tishreen University Hospital, Faculty of Medicine, Lattakia, SyriaDepartment of Urology, Tishreen University Hospital, Lattakia, SyriaDepartment of Urology, Tishreen University Hospital, Lattakia, SyriaDepartment of Urology, Tishreen University Hospital, Lattakia, SyriaDepartment of Urology, Tishreen University Hospital, Lattakia, SyriaDepartment of Urology, Tishreen University Hospital, Lattakia, SyriaPrimary urinary bladder amyloidosis is a rare disorder of protein metabolism characterized by the extracellular deposition of fibrillin. To date, fewer than 200 cases have been reported in the literature. We herein present a case of 59-year-old female with primary multifocal recurrent urinary bladder amyloidosis. The patient was treated with a new method (laser therapy) mentioned for the first time in the literature. After 18 months of treatment, the patient has no complaints. Our case illustrates a new procedure in the treatment of primary multifocal bladder amyloidosis.http://dx.doi.org/10.1155/2021/4476363 |
| spellingShingle | Leen Jamel Doya Lama Doya Khaled Al-Yousef Ali Adib Abedallah Al Shamali Basel Al Deeb Mohamad Kanan Primary Multifocal Recurrent Urinary Bladder Amyloidosis: A Rare Case Report from Syria Case Reports in Medicine |
| title | Primary Multifocal Recurrent Urinary Bladder Amyloidosis: A Rare Case Report from Syria |
| title_full | Primary Multifocal Recurrent Urinary Bladder Amyloidosis: A Rare Case Report from Syria |
| title_fullStr | Primary Multifocal Recurrent Urinary Bladder Amyloidosis: A Rare Case Report from Syria |
| title_full_unstemmed | Primary Multifocal Recurrent Urinary Bladder Amyloidosis: A Rare Case Report from Syria |
| title_short | Primary Multifocal Recurrent Urinary Bladder Amyloidosis: A Rare Case Report from Syria |
| title_sort | primary multifocal recurrent urinary bladder amyloidosis a rare case report from syria |
| url | http://dx.doi.org/10.1155/2021/4476363 |
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