• 제목/요약/키워드: 관절종양

검색결과 573건 처리시간 0.023초

족부의 조갑하 외골종 (Subungual Exostosis of the Foot)

  • 안종철;신덕섭;손욱진;최준혁
    • 대한골관절종양학회지
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    • 제5권1호
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    • pp.56-62
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    • 1999
  • Purpose : This study was conducted to analyze the clinical materials and treatment results of 13 cases of subungual exostosis. Materials and Methods : Thirteen subungual exostoses of the foot treated from January 1991 to December 1997 were studied. We analyzed the clinical data and results of treatment to identify the clinical characteristics of this disease. We investigated the location, shape and relation of exostosis to phalanx with simple x-ray of the foot to identify the radiological characteristics. All the cases were sent to pathologic examination after resection to determine the pathological characteristics. Results : The results of physical examination on presentation were various. Most cases were located at the dorsomedial side of the distal phalanx and were involved in the toe nail. Eleven cases were located at great toes and one each at the 2nd and 3rd toe. Causes of exostosis were not clear, but 2 cases were related to trauma. For the type of exostosis, 7 cases were sessile and 6 were stalk type. On histologic examination, 9 cases showed a cartilaginous portion with overlying proliferating fibrous tissue and underlying bone formation. There was a gradual maturation of spindle cell proliferation from cartilage to cancellous bone. The cartilage was moderately cellular with some pleomorphism, but true anaplasia was not present. Conclusion : The clinical presentation and findings of simple x-rays were most helpful in diagnosing subungual exostosis. Complete excision of the mass achieved complete relief of symptoms and recovery without recurrence in all cases.

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종골의 골연골종에서 발생한 연골육종 - 1예 보고 - (c)

  • 한정수;박용구;정선택;권부경;노준하
    • 대한골관절종양학회지
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    • 제12권1호
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    • pp.52-56
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    • 2006
  • 골연골종에서 연골육종으로의 악성변화는 종종 보고 되고 있지만, 대개 다발성인 경우이며 단발성 골연골종에서 연골육종으로 변화하는 경우는 약 1~2% 정도로 드물게 보고 되고 있다. 또한, 연골육종이 수부나 족부에 발생하는 것은 드물며, 족부에 발생하는 경우 종골에 호발하는 것으로 되어있다. 그러나, 이러한 경우 대개 원발성으로서, 종골의 단발성 골연골종에서 연골육종으로의 악성변이는 매우 드물어 이에 대한 보고는 거의 없다. 저자들은 6년 전부터 서서히 자라는 무통성의 종골의 종괴를 주소로 내원한 38세 남자 환자에서 수술적 치료로 종괴를 제거하였으며 조직학적으로 골연골종에서 발생한 연골육종으로 판명되어 이를 문헌고찰과 함께 보고하고자 한다.

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경추에 발생한 거대 세포종 - 증례 보고 - (Giant Cell Tumor of the Cervical Spine - Case Report -)

  • 안기찬;정경칠;김윤준
    • 대한골관절종양학회지
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    • 제12권1호
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    • pp.57-62
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    • 2006
  • 척추의 거대 세포종은 진단이 어려운 경우가 많고, 고도의 악성도로 인해서 수술이 불가능한 경우가 많다. 척추의 거대 세포종은 높은 재발율과 함께 척수의 기계적 압박 가능성으로 인해 방사선 치료가 근간이었으나, 최근에는 근치적 절제술과 함께 기구를 이용한 전후방 고정술을 시행 하여 좋은 결과를 보고 하고있다. 본 정형외과학교실에서는 경부 동통을 유발하며 제3경추를 침범한 거대세포종에 대해서 근치적 절제술과 함께 후방 기기술을 통한 융합을 시행 하였으며, 추시 관찰상 우수한 치료 결과를 보였기에 문헌 고찰과 함께 보고하는 바이다.

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저 악성도 연골육종으로 악성 변화한 섬유성 이형성증으로 오진하여 치료방침의 오류가 발생한 연골 모세포형 골육종 - 증례 보고 - (Secondary Chondroblastic Osteosarcoma from Polyostotic Fibrous Dysplasia Initially Misdiagnosed as Low Grade Chondrosarcoma Provoking Fallacy in Treatment Strategy)

  • 이승준;고재수;원호현;전대근
    • 대한골관절종양학회지
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    • 제14권1호
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    • pp.62-67
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    • 2008
  • 섬유성 골 이형성증이 골육종, 연골육종, 섬유육종 등으로 악성 변환을 하는 것은 매우 드무나 잘 알려져 있다. 악성 변화가 흔히 일어나는 부위는 두경부, 근위 대퇴골, 상완골, 골반골, 경골, 및 견갑골 순이다. 41세 다발성 섬유성 이형성증 환자가 상완골의 동통을 주소로 내원하였다. 방사선 상 상완골 간부의 골 팽윤 및 파괴를 보였다. 생검 상 저악성도의 연골육종으로 진단하여 변연부 절제를 하였으나 7개월 만에 근위부에서 국소 재발 후 재 절제한 표본은 연골아세포형 골육종으로 진단하였다. 다발성 섬유성 이형성증에서 속발한 연골아세포형 골육종을 저악성도 연골육종으로 오진하여 치료방침에 오류가 있었던 1례를 문헌고찰과 함께 보고하는 바이다.

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견갑부에 발생한 기관지기원낭종 - 1예 보고 - (Bronchogenic Cyst of the Shoulder - A Case Report -)

  • 이동주;문경호;정재호;오인석
    • 대한골관절종양학회지
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    • 제15권2호
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    • pp.151-154
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    • 2009
  • 기관지기원낭종은 primitive foregut의 발생학적 이상에 의해 형성되는 드문 질환이며, 주로 폐실질과 종격동에 발생한다. 피부나 피하조직에서 발생한 기관지기원낭종은 흔하지 않으며, 이 중 견갑부에 발생한 것은 매우 드문 것으로 알려져 있다. 저자들은 20개월 된 남아의 좌측 견갑부에 발생한 기관지지원 낭종 1예를 보고하고자 한다. 환아는 피부과에서 절개 생검 및 소파술을 시행 받았고, 표피 낭종으로 진단되었다. 하지만 상흔 치유 도중 추가적인 낭성 종괴가 촉진되었다. MRI상 피하조직에 경계가 분명한 낭성 종괴가 관찰되었다. 절제된 낭종은 점액세포를 동반하는 pseudostratified ciliated columnar epithelium로 피복되어 있었으며, 기관지기원낭종으로 진단되었다.

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연부 조직 육종의 예후 인자 (Prognostic Factors of Soft Tissue Sarcomas - A Review of 94 Cases of Soft Tissue Sarcoma -)

  • 김재도;정철윤;손정환;홍영기;손영찬;박정호
    • 대한골관절종양학회지
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    • 제1권2호
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    • pp.210-219
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    • 1995
  • Many different factors which may affect the prognosis of the soft tissue sarcomas have been reported by many authors ; Generally, tumor size, histologic type, surgical margin, and multi modality therapy therapy as the prognostic factors were reported. The objectives of this retrospective study of soft tissue sarcomas are : 1) to define more clearly prognostic variables that have significant predictive value for disease-free and overall survival ; and 2) to evaluate tumor histologic grade based upon extent of tumor necrosis as a means of stratifying more aggressive soft tissue sarcomas(grade II & III) of the extremities. We treated 94 patients who had soft tissue sarcoma of the extremities and trunk from May 1984 to September 1994(average duration of follow-up was 5 years ranging from 2 months to 10 years) and evaluated the prognostic factors of the soft tissue sarcomas; age, sex, depth, size, location, histologic type and grade, stage, therapy modality, surgical margin, local recurrence and distant metastasis. The results were as follows. 1. The patients with poorer prognosis were over the age of fifty, whose mass was deeply located, size of the mass was over 10cm in diameter, grade III in histology, who had local recurrence, metastasis, and received only surgery. 2. Among these prognostic factors, the most significant prognostic factor was histologic grade base upon extent of tumor necrosis.

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횡문근육종의 치료 (Treatment of Rhabdomyosarcoma)

  • 이종석;전대근;김석준;이수용;박현수
    • 대한골관절종양학회지
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    • 제1권2호
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    • pp.200-204
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    • 1995
  • Twenty three rhabdomyosarcoma patients who were registered in Korea Cancer Center Hospital from Mar. 1985 to Apr. 1994 were analysed in the aspect of treatment and survival. Thirteen cases were male and 10 female. Average age was 29.5 years(range 1 to 66). Locations of the tumor were as follows: 13 in lower extremity, 6 in upper extremity and 4 in trunk. According to the UICC classification, stage II b was 1 case, stage III a 4, stage III b 10, stage IV a 3 and stage IV b 5. In histological categories, embryonal rhabdomyosarcoma was 7 cases, alveolar 7, pleomorphic 7 and undetermined 2. Average follow up period was 35.3 months(1 tk 7.5 years). Ten cases were continuous disease free, 3 no evidence of disease, 3 alive with disease and 7 died of disease at final follow up. Kaplan-Meier's actuarial 5-year survival rate was 60.3% and 5-year continuous disease free survival rate was 31.4%, Surgical margin was an important factor in local tumor control. Although there was no definite statistical significance, our results suggest chemotherapy and radiation therapy have meaningful roles in reducing local recurrence and improving survival.

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지방육종의 치료에서 술후 방사선 치료의 역할 (Role of Post-operative Irradiation in Treatment of Liposarcoma)

  • 강용구;박원종;송석환;김형민;이승구;우영균;김정만;문명상;인용
    • 대한골관절종양학회지
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    • 제1권2호
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    • pp.194-199
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    • 1995
  • To evaluate the role of post-operative irradiation in reducing local recurrence after surgical treatment of liposarcoma, 19 patients who were treated between July 1988 and June 1994 at Department of Orthopedic Surgery, Catholic University were studied retrospectively. The average follow up was 31 months. 1. There were 14 males and 5 females and an average age was 51 years old. 2. Thirteen cases were in extremities and buttock, 3 in neck, 2 in retroperitoneum and 1 in back. 3. Histologic types were 16 cases of myxoid type and 3 cases of well differentiated type. 4. Ten cases were achieved with wide margin and 9 with inadequate(intralesional or marginal) margin. 5. There were no local recurrence in 10 cases with wide margin, whereas 6(67%) local recurrences in 9 cases with inadequate margin. 6. Among 6 cases of local recurrence, 5 cases had been treated with post-operative irradiation. In conclusion, post-operative irradiation for inadequate margin(intralesional or marginal margin) was not sufficient to reducing local recurrence.

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골성 유잉 육종의 비 수술적 치료 (A Clinical Study of Ewing's Sarcoma)

  • 서승우;임홍철;문우남;김형석;최성태;김경수
    • 대한골관절종양학회지
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    • 제1권2호
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    • pp.164-170
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    • 1995
  • Eight patients with Ewing's sarcoma were treated between September 1983 and September 1992 at medical college, Department of Orthopaedic Surgery, Guro Hospital, Korea University. There were 5 males and 3 femails, with mean age of 28.2 years(ranging from 2-66 years). Three patients with soft tissue Ewing's tumor were excluded from the study. Of the eight patients, two patients presented with multiple metastasis, two cases occurred in the rib, and in the distal femur, mandible, scapular, 3rd, 4th thoracic spine in each patients. Chemotherapy alone was applied in 3 patients, radiotherapy alone in 1 patient, 2 patients were treated with chemotherapy and radiotherapy. Four patients died from the disease itself. Remissions were achieved in the other 4 patients. However, among them two patients relapsed 5 and 36 months later, I patient was not able to be followed, I patient died due to sepsis. The poor prognosis observed for patients with axial lesions should encourage other methods of managing these tumors.

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경골에 발생한 거대 골 섬 - 증례 보고 - (Giant Bone Island of the Tibia - A Case Report -)

  • 박호성;장규윤;이상용;김정렬
    • 대한골관절종양학회지
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    • 제10권1호
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    • pp.56-60
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    • 2004
  • 골 섬 (bone island)은 해면골 내에 성숙된 치밀골 병소가 존재하는 것이다. 골 섬은 특징적인 임상적 및 방사선학적 소견으로 진단될 수 있다. 병변은 무증상인 경우가 많으며 골반, 대퇴골, 그리고 다른 장골에서 호발한다. 방사선 검사상 병변은 해면골 내에 난원형, 원형, 또는 길게 늘어진 모양의 균질하고 진한 경화성 병변으로 관찰되며 "가시 방사" 또는 "위족"으로 알려진 방사상 뼈 줄무늬가 특징적인 소견이다. 대부분의 골 섬은 직경이 0.1 cm 부터 2.0 cm 로 크기가 작다. 직경이 2 cm 이상으로 정의된 거대 골 섬은 보고가 극히 드물다. 저자들은 31세 남자에서 발생한 10${\times}$1.7${\times}$1 cm 크기의 거대 골 섬 1예를 보고하고자 한다.

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