毛细血管扩张性骨肉瘤——单中心经验

IF 0.6 Q4 ONCOLOGY South Asian Journal of Cancer Pub Date : 2023-07-28 DOI:10.1055/s-0043-1771386
G. Narayanan, Sugeeth M. Thambi, J. Kattoor, Bhaskar Subin Sugath, S. Nair
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引用次数: 0

摘要

摘要Geetha Narayanan毛细血管扩张型骨肉瘤是一种不常见的骨肉瘤亚型,占所有骨肉瘤病例的不到4%。其特征是具有独特的放射学、病理学特征和预后意义。在放射学和显微镜下,它模仿动脉瘤样骨囊肿。本研究的目的是研究毛细血管扩张型骨肉瘤患者的临床特点和治疗结果。在12年的时间里,13名患者在印度癌症三级中心的肿瘤内科被诊断为毛细血管扩张性骨肉瘤。所有患者年龄均在15岁以上。出现时的中位年龄为20岁,男性占主导地位,最常见的受累部位是股骨下端和肱骨上端。10名患者接受了包括异环磷酰胺、阿霉素、顺铂方案和保肢手术或截肢的新辅助和/或辅助化疗的治疗。目前,十分之八的患者在中位随访50个月时病情缓解,生存期从18个月到138个月不等。
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Telangiectatic Osteosarcoma—A Single-Center Experience
Abstract Geetha Narayanan Telangiectatic osteosarcoma is an uncommon subtype of osteosarcoma accounting for less than 4% of all cases of osteosarcoma. It is characterized by distinctive radiographic, pathologic features, and prognostic implications. Radiologically and microscopically, it mimics aneurysmal bone cyst. The objective of this study was to study the clinical profile and treatment outcome of patients with telangiectatic osteosarcoma. Thirteen patients were diagnosed with telangiectatic osteosarcoma in the department of medical oncology at a tertiary cancer center in India during a 12-year period. All patients were above 15 years of age. The median age at presentation was 20 years, males were predominant, and the commonest sites of involvement were lower end of femur and upper end of humerus. Ten patients underwent treatment that consisted of neoadjuvant and/or adjuvant chemotherapy with ifosfamide, doxorubicin, cisplatin regimen and limb sparing surgery or amputation. Currently, eight out of ten patients are alive in remission at a median follow-up of 50 months with survival ranging from 18 to 138 months.
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CiteScore
1.00
自引率
0.00%
发文量
80
审稿时长
35 weeks
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