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1.
Arch Orthop Trauma Surg ; 124(5): 301-5, 2004 Jun.
Article in English | MEDLINE | ID: mdl-15014954

ABSTRACT

BACKGROUND: Simple curettage without bone grafting for enchondromas of the hand and its good clinical results have been reported. Yet, there have been no reports regarding simple curettage without bone grafting for enchondromas of the foot. The purpose of this study is to elucidate the clinical results of this method for enchondromas of the foot. METHODS: We studied eight patients (ten bones) with enchondromas of the foot treated with simple curettage without bone grafting. After making an oval or round fenestration, the enchondroma was curetted. The cortical window of the fenestration was excised in five bones, whereas it was replaced at the fenestration site in the other five bones. RESULTS: The affected toe was immobilized with a tape in two patients. All patients began to walk on the day of surgery or the next day without crutches. Sclerotic changes on the plain radiographs were seen 6.4 weeks (range: 4-10 weeks) postoperatively. The patients returned to their normal daily activity including occupation and sport in 8.6 weeks (range: 0-12 weeks) postoperatively. The radiographic appearance was almost normalized in 8.4 months on average (range: 3-14 months). Function was classified as excellent in all bones according to a modified Tordai classification. CONCLUSION: We conclude that simple curettage without bone grafting can be one of the standard surgical treatments for enchondromas of the foot.


Subject(s)
Bone Neoplasms/surgery , Chondroma/surgery , Curettage , Foot/surgery , Adult , Bone Neoplasms/diagnostic imaging , Chondroma/diagnostic imaging , Female , Foot/diagnostic imaging , Humans , Male , Middle Aged , Radiography , Treatment Outcome
2.
Skeletal Radiol ; 32(3): 156-60, 2003 Mar.
Article in English | MEDLINE | ID: mdl-12605281

ABSTRACT

The clinicoradiologic and pathologic aspects of an intracortical, diaphyseal chondromyxoid fibroma of the humerus are reported. Because of the location of the lesion, the possibility of chondromyxoid fibroma was not considered radiologically. The diagnosis was made only after histologic examination of tissue obtained via an open biopsy, which led to the appropriate treatment, surgical curettage.


Subject(s)
Bone Neoplasms/diagnostic imaging , Chondroblastoma/diagnostic imaging , Humerus , Adult , Bone Neoplasms/pathology , Chondroblastoma/pathology , Female , Humans , Humerus/pathology , Magnetic Resonance Imaging , Tomography, X-Ray Computed
3.
J Orthop Sci ; 7(2): 267-73, 2002.
Article in English | MEDLINE | ID: mdl-11956991

ABSTRACT

Leiomyosarcoma usually arises in the uterus, gastrointestinal tract, retroperitoneum, or soft tissue. Primary leiomyosarcoma of bone is rare. We encountered two patients with primary leiomyosarcoma of the femur; one was a 24-year-old woman and the other, a 41-year-old woman. Bone destruction observed on plain radiographs was minimal in both patients. Magnetic resonance imaging (MRI) showed low signal intensity on T1-weighted images and high signal intensity on T2-weighted images, with these areas being much larger than the findings to be expected from the plain radiographs. Histological examination revealed spindle-cell sarcoma, with an interlacing pattern, acidophilic cytoplasm and blunt-ended or "cigar-shaped" nuclei, in both patients. In both patients, immunohistochemical examination showed positive staining for vimentin, desmin, and alpha-smooth muscle actin. Extensive examination of the gastrointestinal tract and uterus revealed no primary lesion. Therefore, the leiomyosarcoma in the femur was considered to be primary rather than metastatic. Histological examination, including immunohistochemistry, and the exclusion of an extraskeletal primary lesion, is necessary in diagnosing primary leiomyosarcoma of bone.


Subject(s)
Femoral Neoplasms/diagnosis , Leiomyosarcoma/diagnosis , Adult , Combined Modality Therapy , Female , Femoral Neoplasms/pathology , Femoral Neoplasms/therapy , Humans , Immunohistochemistry , Leiomyosarcoma/pathology , Leiomyosarcoma/therapy , Magnetic Resonance Imaging
4.
J Orthop Sci ; 7(2): 274-80, 2002.
Article in English | MEDLINE | ID: mdl-11956992

ABSTRACT

We studied 12 patients (13 bones) with intraosseous lipoma to elucidate the clinical features of this disease. The patients ranged in age from 14 to 54 years. Eleven patients were men and 1 was a woman. The involved bones were the calcaneus in 6 patients (7 bones), humerus in 3, ischium in 2, and sacrum in 1. Three bones were in Milgram's stage I, 8 were in stage II, and 2 were in stage III. On plain radiographs, all bones showed a well-circumscribed radiolucent area. Nine bones showed calcification or ossification. Computed tomography or magnetic resonance imaging showed low density or high signal intensity, respectively, identical to the findings in normal adipose tissue. The tumor was curetted in 3 patients (3 bones), in whom local recurrence was not seen thereafter. In the remaining 9 patients (10 bones), we observed the natural course; in 1 of these patients, incisional biopsy was performed. During the follow-up period, only 1 patient showed slight enlargement of the lesion, while the findings in the others remained unchanged. Three patients had pain, which disappeared after the surgery or during the course of the observation. Partly because intraosseous lipoma tends to undergo spontaneous involution, and partly because diagnosis is easy from the radiological findings, surgery does not seem to be necessary in most patients.


Subject(s)
Bone Neoplasms/diagnosis , Lipoma/diagnosis , Adolescent , Adult , Bone Neoplasms/pathology , Female , Humans , Lipoma/pathology , Male , Middle Aged
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