Garré's sclerosing osteomyelitis: case report
The aim of this study was to report on a rare case of Garré's sclerosing osteomyelitis. The patient was a 54-year-old woman with a history of treatment for lupus using corticoids for 20 years, and for osteoporosis using alendronate for five years. She presented edema and developed a limitation...
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2014-08-01
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doaj-f873ec0b68994f8a90b6d596ca95d62e2020-11-24T22:53:19ZengSociedade Brasileira de Ortopedia e TraumatologiaRevista Brasileira de Ortopedia1982-43782014-08-0149440140410.1016/j.rboe.2014.04.010S0102-36162014000400401Garré's sclerosing osteomyelitis: case reportFrederico Barra de MoraesTainá Melo Vieira MottaAlessandra Assis SeverinDeniel de Alencar FariaFernanda de Oliveira CésarSiderlei de Souza CarneiroThe aim of this study was to report on a rare case of Garré's sclerosing osteomyelitis. The patient was a 54-year-old woman with a history of treatment for lupus using corticoids for 20 years, and for osteoporosis using alendronate for five years. She presented edema and developed a limitation of left knee movement one year earlier, with mild effusion and pain on metaphyseal palpation, but without fever. She was in a good general state, without local secretion. Images of her knee showed trabecular osteolysis of the distal metaphysis of the femur and a periosteal reaction in both proximal tibias and both distal femurs, compatible with chronic osteomyelitis of low virulence and slow progression. Magnetic resonance imaging showed T2 hypersignal in the femur and tibia. Curettage was performed on the left distal femur, with release of secretion, but this was negative on culturing. A biopsy showed chronic infection and inflammation, fibrosis, xanthogranulomatous reaction and foci of suppuration. Antibiotic therapy was administered for six months. The etiology was not clarified: bacterial infection was suspected, but culturing was generally negative. The chronic process was maintained by low-virulence infection or even after treatment. The differential diagnoses were fibrous dysplasia, syphilis, pustulosis palmoplantaris, rectocolitis, Crohn's disease, SAPHO (synovitis, acne, pustulosis, hyperostosis and osteitis) and Paget's disease. The unifocal diseases were osteoid osteoma, Ewing's disease, osteosarcoma and eosinophilic granuloma.http://www.scielo.br/scielo.php?script=sci_arttext&pid=S0102-36162014000400401&lng=en&tlng=enOsteomielite/diagnósticoOsteomielite/cirurgiaOsteomielite/terapia |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Frederico Barra de Moraes Tainá Melo Vieira Motta Alessandra Assis Severin Deniel de Alencar Faria Fernanda de Oliveira César Siderlei de Souza Carneiro |
spellingShingle |
Frederico Barra de Moraes Tainá Melo Vieira Motta Alessandra Assis Severin Deniel de Alencar Faria Fernanda de Oliveira César Siderlei de Souza Carneiro Garré's sclerosing osteomyelitis: case report Revista Brasileira de Ortopedia Osteomielite/diagnóstico Osteomielite/cirurgia Osteomielite/terapia |
author_facet |
Frederico Barra de Moraes Tainá Melo Vieira Motta Alessandra Assis Severin Deniel de Alencar Faria Fernanda de Oliveira César Siderlei de Souza Carneiro |
author_sort |
Frederico Barra de Moraes |
title |
Garré's sclerosing osteomyelitis: case report |
title_short |
Garré's sclerosing osteomyelitis: case report |
title_full |
Garré's sclerosing osteomyelitis: case report |
title_fullStr |
Garré's sclerosing osteomyelitis: case report |
title_full_unstemmed |
Garré's sclerosing osteomyelitis: case report |
title_sort |
garré's sclerosing osteomyelitis: case report |
publisher |
Sociedade Brasileira de Ortopedia e Traumatologia |
series |
Revista Brasileira de Ortopedia |
issn |
1982-4378 |
publishDate |
2014-08-01 |
description |
The aim of this study was to report on a rare case of Garré's sclerosing osteomyelitis. The patient was a 54-year-old woman with a history of treatment for lupus using corticoids for 20 years, and for osteoporosis using alendronate for five years. She presented edema and developed a limitation of left knee movement one year earlier, with mild effusion and pain on metaphyseal palpation, but without fever. She was in a good general state, without local secretion. Images of her knee showed trabecular osteolysis of the distal metaphysis of the femur and a periosteal reaction in both proximal tibias and both distal femurs, compatible with chronic osteomyelitis of low virulence and slow progression. Magnetic resonance imaging showed T2 hypersignal in the femur and tibia. Curettage was performed on the left distal femur, with release of secretion, but this was negative on culturing. A biopsy showed chronic infection and inflammation, fibrosis, xanthogranulomatous reaction and foci of suppuration. Antibiotic therapy was administered for six months. The etiology was not clarified: bacterial infection was suspected, but culturing was generally negative. The chronic process was maintained by low-virulence infection or even after treatment. The differential diagnoses were fibrous dysplasia, syphilis, pustulosis palmoplantaris, rectocolitis, Crohn's disease, SAPHO (synovitis, acne, pustulosis, hyperostosis and osteitis) and Paget's disease. The unifocal diseases were osteoid osteoma, Ewing's disease, osteosarcoma and eosinophilic granuloma. |
topic |
Osteomielite/diagnóstico Osteomielite/cirurgia Osteomielite/terapia |
url |
http://www.scielo.br/scielo.php?script=sci_arttext&pid=S0102-36162014000400401&lng=en&tlng=en |
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