Musculoskeletal and cutaneous sarcoidosis: exuberant case report
Sarcoidosis is a multisystem granulomatous disease of unknown cause. The osteoarticular involvement in sarcoidosis is rare and is often associated with cutaneous and long-standing chronic multisystem disease. More common in black women, osseous sarcoidosis is difficult to diagnose, with an incidence...
Ausführliche Beschreibung
Autor*in: |
Natalie Haddad [verfasserIn] Jayme de Oliveira Filho [verfasserIn] Kassila da Rosa Nasser [verfasserIn] Ana Maria França Corbett [verfasserIn] Ana Carolina Franco Tebet [verfasserIn] Mariana Lacerda Junqueira Reis [verfasserIn] |
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Format: |
E-Artikel |
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Sprache: |
Englisch ; Portugiesisch |
Erschienen: |
2014 |
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Schlagwörter: |
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Übergeordnetes Werk: |
In: Anais Brasileiros de Dermatologia - Sociedade Brasileira de Dermatologia, 2004, 89(2014), 4, Seite 660-662 |
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Übergeordnetes Werk: |
volume:89 ; year:2014 ; number:4 ; pages:660-662 |
Links: |
Link aufrufen |
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DOI / URN: |
10.1590/abd1806-4841.20143053 |
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Katalog-ID: |
DOAJ012445444 |
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520 | |a Sarcoidosis is a multisystem granulomatous disease of unknown cause. The osteoarticular involvement in sarcoidosis is rare and is often associated with cutaneous and long-standing chronic multisystem disease. More common in black women, osseous sarcoidosis is difficult to diagnose, with an incidence of 3 to 13%. The most characteristic radiological clinical picture evidences rounded, well-defined cysts, with no periosteal reaction and without peripheral sclerosis. The small bones of hands and feet are the most frequently involved sites. This report aims to demonstrate a rare case of osteoarticular sarcoidosis with characteristic clinical presentation, and highlight the importance of detecting osteoarticular involvement in this pathology. | ||
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10.1590/abd1806-4841.20143053 doi (DE-627)DOAJ012445444 (DE-599)DOAJ97046bc44ad34f57a6fb89bb040cce15 DE-627 ger DE-627 rakwb eng por RL1-803 Natalie Haddad verfasserin aut Musculoskeletal and cutaneous sarcoidosis: exuberant case report 2014 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Sarcoidosis is a multisystem granulomatous disease of unknown cause. The osteoarticular involvement in sarcoidosis is rare and is often associated with cutaneous and long-standing chronic multisystem disease. More common in black women, osseous sarcoidosis is difficult to diagnose, with an incidence of 3 to 13%. The most characteristic radiological clinical picture evidences rounded, well-defined cysts, with no periosteal reaction and without peripheral sclerosis. The small bones of hands and feet are the most frequently involved sites. This report aims to demonstrate a rare case of osteoarticular sarcoidosis with characteristic clinical presentation, and highlight the importance of detecting osteoarticular involvement in this pathology. Bone resorption Granuloma Granulomatous disease, chronic Joint deformities, acquired Lumpy skin disease Sarcoidosis Skin abnormalities Skin diseases Skin and connective tissue diseases Dermatology Jayme de Oliveira Filho verfasserin aut Kassila da Rosa Nasser verfasserin aut Ana Maria França Corbett verfasserin aut Ana Carolina Franco Tebet verfasserin aut Mariana Lacerda Junqueira Reis verfasserin aut In Anais Brasileiros de Dermatologia Sociedade Brasileira de Dermatologia, 2004 89(2014), 4, Seite 660-662 (DE-627)387478906 (DE-600)2145422-X 03650596 nnns volume:89 year:2014 number:4 pages:660-662 https://doi.org/10.1590/abd1806-4841.20143053 kostenfrei https://doaj.org/article/97046bc44ad34f57a6fb89bb040cce15 kostenfrei http://www.scielo.br/scielo.php?script=sci_arttext&pid=S0365-05962014000400660&tlng=en kostenfrei http://www.scielo.br/pdf/abd/v89n4/0365-0596-abd-89-04-0660.pdf kostenfrei https://doaj.org/toc/0365-0596 Journal toc kostenfrei GBV_USEFLAG_A SYSFLAG_A GBV_DOAJ SSG-OLC-PHA GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_73 GBV_ILN_74 GBV_ILN_95 GBV_ILN_105 GBV_ILN_110 GBV_ILN_151 GBV_ILN_161 GBV_ILN_170 GBV_ILN_206 GBV_ILN_213 GBV_ILN_230 GBV_ILN_285 GBV_ILN_293 GBV_ILN_602 GBV_ILN_2014 GBV_ILN_4012 GBV_ILN_4037 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4249 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4338 GBV_ILN_4367 GBV_ILN_4700 AR 89 2014 4 660-662 |
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10.1590/abd1806-4841.20143053 doi (DE-627)DOAJ012445444 (DE-599)DOAJ97046bc44ad34f57a6fb89bb040cce15 DE-627 ger DE-627 rakwb eng por RL1-803 Natalie Haddad verfasserin aut Musculoskeletal and cutaneous sarcoidosis: exuberant case report 2014 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Sarcoidosis is a multisystem granulomatous disease of unknown cause. The osteoarticular involvement in sarcoidosis is rare and is often associated with cutaneous and long-standing chronic multisystem disease. More common in black women, osseous sarcoidosis is difficult to diagnose, with an incidence of 3 to 13%. The most characteristic radiological clinical picture evidences rounded, well-defined cysts, with no periosteal reaction and without peripheral sclerosis. The small bones of hands and feet are the most frequently involved sites. This report aims to demonstrate a rare case of osteoarticular sarcoidosis with characteristic clinical presentation, and highlight the importance of detecting osteoarticular involvement in this pathology. Bone resorption Granuloma Granulomatous disease, chronic Joint deformities, acquired Lumpy skin disease Sarcoidosis Skin abnormalities Skin diseases Skin and connective tissue diseases Dermatology Jayme de Oliveira Filho verfasserin aut Kassila da Rosa Nasser verfasserin aut Ana Maria França Corbett verfasserin aut Ana Carolina Franco Tebet verfasserin aut Mariana Lacerda Junqueira Reis verfasserin aut In Anais Brasileiros de Dermatologia Sociedade Brasileira de Dermatologia, 2004 89(2014), 4, Seite 660-662 (DE-627)387478906 (DE-600)2145422-X 03650596 nnns volume:89 year:2014 number:4 pages:660-662 https://doi.org/10.1590/abd1806-4841.20143053 kostenfrei https://doaj.org/article/97046bc44ad34f57a6fb89bb040cce15 kostenfrei http://www.scielo.br/scielo.php?script=sci_arttext&pid=S0365-05962014000400660&tlng=en kostenfrei http://www.scielo.br/pdf/abd/v89n4/0365-0596-abd-89-04-0660.pdf kostenfrei https://doaj.org/toc/0365-0596 Journal toc kostenfrei GBV_USEFLAG_A SYSFLAG_A GBV_DOAJ SSG-OLC-PHA GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_73 GBV_ILN_74 GBV_ILN_95 GBV_ILN_105 GBV_ILN_110 GBV_ILN_151 GBV_ILN_161 GBV_ILN_170 GBV_ILN_206 GBV_ILN_213 GBV_ILN_230 GBV_ILN_285 GBV_ILN_293 GBV_ILN_602 GBV_ILN_2014 GBV_ILN_4012 GBV_ILN_4037 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4249 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4338 GBV_ILN_4367 GBV_ILN_4700 AR 89 2014 4 660-662 |
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10.1590/abd1806-4841.20143053 doi (DE-627)DOAJ012445444 (DE-599)DOAJ97046bc44ad34f57a6fb89bb040cce15 DE-627 ger DE-627 rakwb eng por RL1-803 Natalie Haddad verfasserin aut Musculoskeletal and cutaneous sarcoidosis: exuberant case report 2014 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Sarcoidosis is a multisystem granulomatous disease of unknown cause. The osteoarticular involvement in sarcoidosis is rare and is often associated with cutaneous and long-standing chronic multisystem disease. More common in black women, osseous sarcoidosis is difficult to diagnose, with an incidence of 3 to 13%. The most characteristic radiological clinical picture evidences rounded, well-defined cysts, with no periosteal reaction and without peripheral sclerosis. The small bones of hands and feet are the most frequently involved sites. This report aims to demonstrate a rare case of osteoarticular sarcoidosis with characteristic clinical presentation, and highlight the importance of detecting osteoarticular involvement in this pathology. Bone resorption Granuloma Granulomatous disease, chronic Joint deformities, acquired Lumpy skin disease Sarcoidosis Skin abnormalities Skin diseases Skin and connective tissue diseases Dermatology Jayme de Oliveira Filho verfasserin aut Kassila da Rosa Nasser verfasserin aut Ana Maria França Corbett verfasserin aut Ana Carolina Franco Tebet verfasserin aut Mariana Lacerda Junqueira Reis verfasserin aut In Anais Brasileiros de Dermatologia Sociedade Brasileira de Dermatologia, 2004 89(2014), 4, Seite 660-662 (DE-627)387478906 (DE-600)2145422-X 03650596 nnns volume:89 year:2014 number:4 pages:660-662 https://doi.org/10.1590/abd1806-4841.20143053 kostenfrei https://doaj.org/article/97046bc44ad34f57a6fb89bb040cce15 kostenfrei http://www.scielo.br/scielo.php?script=sci_arttext&pid=S0365-05962014000400660&tlng=en kostenfrei http://www.scielo.br/pdf/abd/v89n4/0365-0596-abd-89-04-0660.pdf kostenfrei https://doaj.org/toc/0365-0596 Journal toc kostenfrei GBV_USEFLAG_A SYSFLAG_A GBV_DOAJ SSG-OLC-PHA GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_73 GBV_ILN_74 GBV_ILN_95 GBV_ILN_105 GBV_ILN_110 GBV_ILN_151 GBV_ILN_161 GBV_ILN_170 GBV_ILN_206 GBV_ILN_213 GBV_ILN_230 GBV_ILN_285 GBV_ILN_293 GBV_ILN_602 GBV_ILN_2014 GBV_ILN_4012 GBV_ILN_4037 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4249 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4338 GBV_ILN_4367 GBV_ILN_4700 AR 89 2014 4 660-662 |
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Sarcoidosis is a multisystem granulomatous disease of unknown cause. The osteoarticular involvement in sarcoidosis is rare and is often associated with cutaneous and long-standing chronic multisystem disease. More common in black women, osseous sarcoidosis is difficult to diagnose, with an incidence of 3 to 13%. The most characteristic radiological clinical picture evidences rounded, well-defined cysts, with no periosteal reaction and without peripheral sclerosis. The small bones of hands and feet are the most frequently involved sites. This report aims to demonstrate a rare case of osteoarticular sarcoidosis with characteristic clinical presentation, and highlight the importance of detecting osteoarticular involvement in this pathology. |
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Sarcoidosis is a multisystem granulomatous disease of unknown cause. The osteoarticular involvement in sarcoidosis is rare and is often associated with cutaneous and long-standing chronic multisystem disease. More common in black women, osseous sarcoidosis is difficult to diagnose, with an incidence of 3 to 13%. The most characteristic radiological clinical picture evidences rounded, well-defined cysts, with no periosteal reaction and without peripheral sclerosis. The small bones of hands and feet are the most frequently involved sites. This report aims to demonstrate a rare case of osteoarticular sarcoidosis with characteristic clinical presentation, and highlight the importance of detecting osteoarticular involvement in this pathology. |
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Sarcoidosis is a multisystem granulomatous disease of unknown cause. The osteoarticular involvement in sarcoidosis is rare and is often associated with cutaneous and long-standing chronic multisystem disease. More common in black women, osseous sarcoidosis is difficult to diagnose, with an incidence of 3 to 13%. The most characteristic radiological clinical picture evidences rounded, well-defined cysts, with no periosteal reaction and without peripheral sclerosis. The small bones of hands and feet are the most frequently involved sites. This report aims to demonstrate a rare case of osteoarticular sarcoidosis with characteristic clinical presentation, and highlight the importance of detecting osteoarticular involvement in this pathology. |
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