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Fortuitous Discovery of a Multifocal Enchondromatosis in a Case at the “Luxembourg” Hospital Center in Bamako
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作者 Mamoudou Camara Aboubacar Sidiki Keita +5 位作者 Mahamane Mariko Toumin Camara Issa Cisse Aly Traore Souleymane Sanogo Siaka Sidibe 《Open Journal of Radiology》 2022年第4期222-228,共7页
The aim of this study was to clarify the interest of standard radiography in the management of Ollier’s disease. Observation: Enchondromas are benign lesions that may present on imaging with nonspecific features in c... The aim of this study was to clarify the interest of standard radiography in the management of Ollier’s disease. Observation: Enchondromas are benign lesions that may present on imaging with nonspecific features in children, and they are relatively large lesions, with frequent endosteal erosion and rare matrix mineralization. We report a case of predominantly right-sided multifocal enchondromatosis in a 5-year-old girl with no known medical history, diagnosed fortuitously on standard radiography during a trauma assessment and confirmed by histology. No sign of pain was noted after a 6-month follow-up. But the radiographic control noted signs of diffuse osteoarthritic remodeling in the surgical areas and early fusion of the growth cartilages. Conclusion: Ollier’s disease is rare, you have to know how to think about it in the face of fortuitous discoveries, especially at an early age. Enchondromas are benign lesions that may present on imaging with nonspecific features in children. In all cases, standard radiography is essential in the diagnosis and follow-up of Ollier’s disease. 展开更多
关键词 enchondromatosis Fortuitous GIRL Standard Radiography
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Maffucci syndrome with unilateral limb: a case report and review of the literature 被引量:6
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作者 Hua Gao Baojun Wang +2 位作者 Xi Zhang Fengqi Liu Ying Lu 《Chinese Journal of Cancer Research》 SCIE CAS CSCD 2013年第2期254-258,共5页
Maffucci syndrome is a congenital, non-hereditary mesodermal dysplasia manifested by multiple enchondromas and hemangiomas. It is associated with diverse secondary musculoskeletal deformities, which is exceedingly rar... Maffucci syndrome is a congenital, non-hereditary mesodermal dysplasia manifested by multiple enchondromas and hemangiomas. It is associated with diverse secondary musculoskeletal deformities, which is exceedingly rare. We report a case of hemangiomas and enchondromas localized in the unilateral limb in a patient with Maffucci syndrome. Treatment consists of orthopedic and surgical intervention to minimize deformities and for cosmetic purpose. Careful surveillance for malignant degeneration of both skeletal and non-skeletal tumors, especially in the brain and abdomen, is essential. 展开更多
关键词 Maffucci syndrome enchondromatosis HEMANGIOMAS unilateteral limb
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Ovarian juvenile granulosa cell tumor associated with Maffucci’s syndrome: case report 被引量:3
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作者 袁键群 林小娜 +2 位作者 许敬尧 祝佳 郑伟良 《Chinese Medical Journal》 SCIE CAS CSCD 2004年第10期1592-1594,共3页
关键词 ovarian neoplasms granulosa cell tumors Maffucci’s syndrome enchondromatosis
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