• Title/Summary/Keyword: Metastatic hand bone tumor

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Metastatic Clear Cell Sarcoma of the Kidney in a Child's Hand Bone - A Case Report - (소아의 수부골에 전이된 신장의 투명세포육종 -1례 보고-)

  • Shim, Jong-Sup;Kim, Jee-Hyoung;Suh, Yeon-Lim
    • The Journal of the Korean bone and joint tumor society
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    • v.4 no.2
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    • pp.94-98
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    • 1998
  • Clear cell sarcoma of the kidney (CCSK) is a rare malignant tumor of the renal origin in childhood, distinguished from Wilms tumor by its pathologic and clinical features. Bone metastasis is one of the characteristic clinical features. The common site of metastasis of the clear cell Sarcoma of the kidney is axial skeleton including skull, spines, ribs and femur. A cases of clear cell Sarcoma of the kidney presented to us, which solely metastasized to the hand bones without metastasizing to any other tissues including axial skeleton. We report this case with review of literatures.

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Metastatic Tumor in Hand (수부에 발생한 전이암)

  • Rhee, Seung-Koo;Chung, Do-Hyun;Kong, Chae-Gwan;Kim, Jeong-Ho
    • The Journal of the Korean bone and joint tumor society
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    • v.9 no.2
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    • pp.155-161
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    • 2003
  • Skeletal metastasis are common in terminal malignant tumor patients over 30% of incidence, but hand acrometastasis are very rare under 0.1% in terminal cancer patients. We have reported 5 cases of hand acrometastasis herewith the review of literatures. In the preterminal malignant tumor patients, sudden painful swelling on fingers and osteoporosis on X-rays are thought to be the earliest sign of hand metastasis.

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Malignant Tumor of the Hand (수부에 발생한 악성 종양)

  • Park, Hong-Jun;Shin, Kyoo-Ho;Bae, Im-Don;Hahn, Soo-Bong;Kang, Eung-Shick
    • The Journal of the Korean bone and joint tumor society
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    • v.5 no.4
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    • pp.201-207
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    • 1999
  • Malignant tumors of the hand are very rare. Between 1989 and 1998, 17 patients with malignant tumors of the hand were evaluated for clinical features, prevalence, treatment and results. The mean age was 45 years and median duration of follow-up was 38 months. A painless mass was the most common symptom and the most common lesion was the digit. Fifteen cases of soft tissue and 2 cases of bone tumor were diagnosed. On pathology, soft tissue tumors were comprised of 8 cases of malignant melanoma, 2 cases of angiosarcoma and 1 case each of malignant fibrous histiocytoma, malignant peripheral nerve sheath tumor, extraskeletal chondrosarcoma, and squamous cell carcinoma. Bone tumors were metastatic tumors and each originated from the rectal cancer or lung cancer. Lymph node involvements were noted in 4 cases of malignant melanoma and 1 case of squamous cell carcinoma. Six cases of metacarpo-phalangeal joint disarticulation and 4 cases of phalanx amputation were performed. Wide excision, ray amputation and below-elbow amputation were also performed. Three cases expired due to metastasis and progression of the original lesion. Among the surviving 14 cases, a malignant melanoma had metastasis on the axillary lymph node and 13 cases showed no local recurrence or metastasis during the follow-up.

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