• Title/Summary/Keyword: 중족골 골종양

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Bizarre Parosteal Osteochondromatous Proliferation in the First Metatarsal Bone: A Case Report (제 1 중족골에 발생한 기괴 방골성 골연골성 증식증: 증례 보고)

  • Kim, Woo-Sung;Jung, Yu-Hun;Oh, Sang-Hun;Han, Eun-Mee
    • The Journal of the Korean bone and joint tumor society
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    • v.20 no.2
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    • pp.104-108
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    • 2014
  • Bizarre parosteal osteochondromatous proliferation (Nora's lesion) is a rare benign tumor and known to be primarily occur in the small tubular bone of the hands and feet. However, it is very unusual to be reported that it occurs in metatarsal bone in Korea. Thus, we report this tumor of metatarsal bone including the literature review because we have experienced this example.

Osteochondroma of the Os Calcaneum - A Case Report - (종골에서 발생한 골연골종 - 증례 보고 -)

  • Han, Chung-Soo;Park, Yong-Koo;Park, Jin-Sung;Park, Keun-Ho
    • The Journal of the Korean bone and joint tumor society
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    • v.14 no.2
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    • pp.152-156
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    • 2008
  • Osteochodromas are the most common benign osseous neoplasm, covered by a distinct hyaline cartilage cap, originating from the physis. They involve typically metaphyseal or metadiaphyseal region of a long bone, while they involve the foot rarely. In the foot, the osteochondromas mostly occur in short tubular bones such as metatarsal bones and phalanges. They are seldom found in calcaneus. We report a rare case of osteochondroma involving calcaneus.

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Chondroblastoma of the Base of Fifth Metatarsal Bone associated with Secondary Aneurysmal Bone Cystic Change - A Case Report - (제 5 중족골 기저부의 이차 동맥류성 골낭종변화를 동반한 연골모세포종 - 증례 보고 -)

  • Son, Hyun-Jin;Jang, Kyu-Yun;Lee, Dong-Geun;Lee, Sang-Yong;Kim, Jung-Ryul
    • The Journal of the Korean bone and joint tumor society
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    • v.10 no.1
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    • pp.45-49
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    • 2004
  • Chondroblastoma is a benign chondroid-forming tumor usually originating in the epiphysis. The base of metatarsal bone contains neither an epiphysis nor a secondary ossification center and so is the rare site of chondroblastoma. Here, we present a case of chondroblastoma of the base of fifth metatarsal bone in 34-year-old man. Histologically, the osteoclast-like giant cells were abundant enough to simulate a giant cell tumor. And the chondroid intercellular matrix was intermixed but scanty. However, the background mononuclear cells showed irregular and indented nuclei with longitudinal clefts and positive immunoreactivity for S-100 protein, as the evidence of chondroblasts.

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Enchondroma of the Calcaneus: A Case Report (종골에 발생한 내연골종: 증례 보고)

  • Min, Hak-Jin;Yoon, Ui-Seoung;Seo, Jae-Sung;Kim, Jin-Soo;Baek, Seung-Yub
    • The Journal of the Korean bone and joint tumor society
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    • v.16 no.2
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    • pp.87-90
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    • 2010
  • Enchondroma is a benign tumor mainly developed in the hand and uncommon in the foot. Even if it is in the foot, most are in the phalanges and distal metatarsals of the foot. Enchondroma in the calcaneus is very rare. A 44-year-old male suffered from left heel pain for several months, authors treated it with curettage and bone graft, it was histologically confirmed as an enchondroma in the calcaneus. The authors presented a rare case presentation of an enchondroma in the calcaneus with pain.

Chondromyxoid Fibroma of the First Metatarsal - A Case Recurred after Curettage and Bone Graft - (족부에 발생한 재발 연골 유점액 섬유종의 치료 - 1예 보고-)

  • Oh, In-Suk;Kim, Myung-Ku;Lee, Sang-Hyeong
    • The Journal of the Korean bone and joint tumor society
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    • v.9 no.1
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    • pp.110-114
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    • 2003
  • Chondromyxoid fibroma is a benign tumor in adolescents and young adults. The most common location of the tumor is the proximal one-third of the tibia. Chondromyxoid fibroma accounts for less then 1% of all bony neoplasms and foot is affected in about 20% of all cases. The authors have described a case of chondromyxoid fibroma of the first metatarsal which had been recurred 7 months after curettage and iliac bone graft. En bloc resection and reconstruction of the metatarsal with autogenous iliac bone graft were performed. The results were satisfactory and the patient was free of local recurrence at two years follow-up.

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Brown Tumors Due to Parathyroid Carcinoma; $^{99m}Tc-MIBI$ Scan Findings (Case Report) (부갑상선 암종에 의해 발생한 갈색 종양: $^{99m}Tc-MIBI$ 스캔 소견 (증례 보고))

  • Kim, Su-Zy;Yoon, Soek-Nam;Kim, Byung-Soek;Chung, Yoon-Soek;Park, Chan-Hee
    • The Korean Journal of Nuclear Medicine
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    • v.31 no.3
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    • pp.395-398
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    • 1997
  • Whole body $^{99m}Tc-MIBI$ scan in conjunction with parathyroid scan is an effective method in detecting parathyroid lesions in patients with bone pain and possible bone lesions such as brown tumors.

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The Clinical Outcome of Dedifferentiated Chondrosarcoma (역분화 연골육종의 임상 결과)

  • Kong, Chang-Bae;Lee, Seung Yong;Song, Won-Seok;Cho, Wan-Hyeong;Koh, Jae-Soo;Jeon, Dae-Geun
    • Journal of the Korean Orthopaedic Association
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    • v.54 no.2
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    • pp.164-171
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    • 2019
  • Purpose: A dedifferentiated chondrosarcoma is a rare lethal tumor characterized by a low grade chondrosarcoma juxtaposed with a high grade dedifferentiated sarcoma, such as osteosarcoma, fibrosarcoma. The aim of our study was to document the clinical manifestation and oncologic outcomes of a dedifferentiated chondrosarcoma. Materials and Methods: This study identified 11 patients who were diagnosed and treated for dedifferentiated chondrosarcoma between January 2007 and December 2016. The identified cohort was then reviewed regarding age, sex, symptom onset, tumor location, magnetic resonance imagings (MRIs), surgical margin, and pathologic diagnosis. The time to local recurrence and/or metastasis, follow-up duration, and the patients' final status were analyzed. Results: The patients were comprised of 7 males and 4 females with a mean age of 54 years (range, 33-80 years). The location of the tumor was in the femur in 6 cases, pelvis in 4 cases, and metatarsal in 1 case. The average tumor diameter was 12.7 cm (range, 6.0-26.1 cm). At the time of diagnosis, 2 patients showed pathologic fracture; 1 patient was Enecking stage IIA, 9 patients were stage IIB, and 1 patient was stage III. Eight patients were classified as a primary dedifferentiated chondrosarcoma and 3 patients were secondary. One of the primary lesions was misinterpreted initially as a low grade chondroid lesion by MRI and underwent curettage. Local recurrence occurred in 8 cases and distant metastasis occurred in 10 cases with a mean duration of 8 months (range, 2-23 months) and 7 months (range, 1-32 months), respectively. The three-year overall survival of patients with dedifferentiated chondrosarcoma was 18%, and 10 patients died due to disease progression. Conclusion: Dedifferentiated chondrosarcoma developed lung metastases in the early period of the clinical courses and the prognosis was dismal.