Fibrous or desmoid tumors are grouped under the term fibromatosis; there are several groups; the pediatric aggressive form is rare, especially the pelvis and/or hip presentation. This causes a variable degree of destruction of the surrounding tissues. It is a diagnosis by exclusion and histopathologic testing; treatment is always surgical and conservative treatment is indicated only for special locations and/or patient conditions.
View Article and Find Full Text PDFIntroduction: Our institution implemented a minimally-invasive surgery program that included a thorough preoperative assessment and planning to provide the patient with an appropriate correction of the radiographic parameters as well as esthetic satisfaction, together with a shorter hospital stay and less analgesic use.
Material And Methods: Retrospective, comparative, longitudinal and observational clinical trial. The study period was from January 2002 to December 2007; 40 patients with hallux valgus underwent minimally invasive surgery, 12 of them underwent bilateral surgery, for a total of 52 feet with hallux valgus; 100% of them were females.
The defects of the spinal cord enclose diverse malformations that go from spina bifida to myelomeningocele but there is also a rare variant that is the intercalary bone. The incidence of this phenomenon may vary in 1 to 1,000 to 5,000. At our knowledge, there are no cases reported where it can be an association of intercalary bone and a bifid spine in different levels.
View Article and Find Full Text PDFOsteoarticular tuberculosis is a chronic inflammatory disease caused by Mycobacterium tuberculosis that affects joints. It reaches skeleton and joints by hematogenous spread. The clinical presentation includes localized pain associated with fever and weight loss.
View Article and Find Full Text PDFFibrous dysplasia affects principally bone, but it might comprise extraskeletal anomalies; bone is replaced by dysplastic fibrous tissue. It is classified accordingly to the number of affected bones, and its association to endocrine alterations in: monostotic, polyostotic and Albright's disease. A congenital etiology is suggested.
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