1.Primary Osteosarcoma of the Breast: A case report.
Dong Chool KIM ; Yun Kyung LEE ; Ho Jong JEON ; Sung Chul LIM
Korean Journal of Pathology 2000;34(9):677-679
We report a case of primary osteosarcoma of the breast which is rare and exhibits poor prognosis. A 52 years-old-woman was admitted with rapidly growing right mammary mass. A huge lobulated dense mass with speckled calcifications, suggesting malignancy, was observed on mammography. She underwent a radical mastectomy. Grossly, the mass measured 16 14 6 cm and showed grayish white hard lobulated tissue with focal hemorrhage and necrosis. Light microscopically, the tumor was confirmed as an osteosarcoma devoid of any epithelial components. In postoperative whole body bone scan, there was no evidence of the other malignancy. To the best of our knowledge, the present case is the first report of primary osteosarcoma of the breast in Korea.
Breast*
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Hemorrhage
;
Korea
;
Mammography
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Mastectomy, Radical
;
Necrosis
;
Osteosarcoma*
;
Prognosis
2.Transoral Decompression and Anterior Fusion of Atlanto-axial Dislocation due to Os Odontoideum: Case Report.
Jong Chool LEE ; Shin Tae KIM ; Dong Kyu KIM ; Hwa Ryong RHEE
Journal of Korean Neurosurgical Society 1985;14(3):557-564
The Os odontoideum is a developmental anomaly of the axis in which the odontoid process is divided transversely. The Atlanto-axial dislocation due to Os odontoideum is presented. At first, we have performed the posterior atlanto-axial fusion with wire fixation. But the posterior fusion failed in realignment and did not adequately decompress the deformed cord by encroachment on its ventral surface. Next time, we have experienced further improvement following transoral decompression and anterior fusion.
Axis, Cervical Vertebra
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Decompression*
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Dislocations*
;
Odontoid Process
3.Two Cases of Granulosa Cell Tumor of the Ovary.
Hyo Won LEE ; Yoon Young JO ; Chool Hyun CHO ; Jin KIM ; Seok Dong YU ; Hyang Mi KIM ; In Duk CHOE ; Jong Bae PARK ; Haeng Ji KANG
Korean Journal of Obstetrics and Gynecology 2006;49(2):453-460
Granulosa cell tumors are relatively low-grade malignancies accounting for about 1 to 2% of all primary ovarian neoplasms and have an indolent growth pattern. There are two types of tumors, adult type granulosa cell tumor (AGCT) and juvenile type granulosa cell tumor (JGCT), and each tumor reveals different clinical or histopathological features. The clinical manifestations are mostly associated with estrogen produced by tumor, which are vaginal bleeding or menstrual irregularity in AGCT and precocious puberty in JGCT. Although most patients are diagnosed in early stage with favorable prognosis, some recur after several years. So, continuous follow up is required. Recently, we experienced two cases of adult type granulosa cell tumor and report with a brief review of literatures.
Adult
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Estrogens
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Female
;
Follow-Up Studies
;
Granulosa Cell Tumor*
;
Granulosa Cells*
;
Humans
;
Ovarian Neoplasms
;
Ovary*
;
Prognosis
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Puberty, Precocious
;
Uterine Hemorrhage