一例49岁女性骨外骨肉瘤合并未确诊的佩吉特病。

IF 0.4 Q4 SURGERY
Journal of Surgical Case Reports Pub Date : 2025-01-09 eCollection Date: 2025-01-01 DOI:10.1093/jscr/rjae826
Milena Bogojevska Doksevska, Teodora Todorova, Danica Popovska, Vilijam Velkovski, Tamara Angelovska, Marta Foteva, Slavica Kostadinova Kunovska, Smiljana Bundovska Kocev, Katerina Rebok, Milan Samardziski
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引用次数: 0

摘要

骨骼外骨肉瘤(ESOS)是一种罕见的软组织实体,占所有软组织恶性肿瘤的⁓1%。一般认为其预后比骨性骨肉瘤更差,因此需要详细的调查和适当的治疗。发生在皮下组织的ESOSs比发生在深层组织的ESOSs更罕见,并且被认为有更好的结果。我们报告了一例49岁的患者,被诊断为皮下ESOS和骨Paget病,考虑到骨Paget病往往影响50岁以上的人群,这在患者的年龄中并不典型。这两个实体共存于一个病人和他们的所有特征使这个病例独特,据我们所知,这是第一例报告。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Conoccurence of extraskeletal osteosarcoma and undiagnosed Paget disease in a 49-year-old female.

Extraskeletal osteosarcoma (ESOS) represents a rare soft tissue entity, accounting for ⁓1% of all soft tissue malignancies. It is generally considered to have an even worse prognosis than bone osteosarcoma, therefore detailed investigations and proper treatment are required. ESOSs arising in the subcutaneous tissue are even rarer than the ones positioned in deep tissues, and they are considered to have far better outcomes. We present a case of a 49-year-old patient diagnosed with subcutaneous ESOS and Paget disease of the bone, which is not typical for the patient's age, considering that Paget disease of the bone tends to affect a population above 50 years. The coexistence of these two entities in a single patient and all their features make this case unique, and to the best of our knowledge, this is the first case reported.

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来源期刊
CiteScore
0.70
自引率
0.00%
发文量
559
审稿时长
11 weeks
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