巨细胞富骨肉瘤:3例病例报告,诊断困难,需要认真关注。

Mert Çiftdemir, Cihan Ünyilmaz, Fethi Emre Ustabaşioğlu, Ufuk Usta
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引用次数: 0

摘要

巨细胞富骨肉瘤(GCRO)是一种罕见的骨肉瘤变体,具有不寻常的放射学和组织病理学特征,使其诊断具有挑战性。GCRO最关键和最不寻常的特征是它具有纯粹的溶骨外观。因此,GCRO病例往往因误诊而延误诊断或错误治疗。这对这些患者的预后有负面影响。在本研究中,提出了3例年轻成人病例。第一个病例描述了一位年轻的女性患者,由于误诊为巨细胞骨肿瘤而进行了多次刮除,第二个病例描述了一位年轻的男性患者被误诊为动脉瘤性骨囊肿而延误诊断。最后的病例报告描述了一位年轻女性,她被早期诊断,及时治疗,预后良好。本报告中1例预后不良的病例采用截肢治疗,另1例存活并有多发转移灶。在这种情况下,误诊或延误诊断导致预后不良。为了做出诊断,有必要了解并怀疑这种罕见变异的放射学特征。当处理年轻成人纯干骺端溶骨性病变时,巨细胞富骨肉瘤应作为鉴别诊断选择之一。为了避免误诊或延误,有必要了解并怀疑这种罕见的变异。证据等级:IV级,治疗性研究。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Giant-cell rich osteosarcoma: A report of 3 cases depicting a diagnostic challenge requiring serious attention.

Giant cell-rich osteosarcoma (GCRO) is a rare variant of osteosarcoma with unusual radiological and histopathological features that make its diagnosis challenging. The most critical and unusual feature of GCRO is that it has a purely osteolytic appearance. Therefore, GCRO cases are frequently subject to delayed diagnosis or incorrect treatment owing to misdiagnosis. This negatively affects the prognosis of these patients. In this study, 3 young adult cases are presented. The first case describes a young female patient who underwent repeated curettages due to a misdiagnosis of a giant-cell bone tumor, and the second case describes a delay in diagnosis in a young male patient who was misdiagnosed with an aneurysmal bone cyst. The final case report describes a young woman who was diagnosed early, treated promptly, and had a good prognosis. One of the poor prognosis cases in this report was treated with amputation, and the other was alive with multiple metastases. Misdiagnosis or delayed diagnosis leads to a poor prognosis in such cases. To make a diagnosis, it is necessary to have knowledge and to be suspicious of the radiological features of this rare variant. Giant cell-rich osteosarcoma should be among the differential diagnosis options when dealing with pure metaphysiodiaphyseal osteolytic bone lesions in young adults. To avoid misdiagnosis or delay, it is necessary to have knowledge and to be suspicious of this rare variant. Level of Evidence: Level IV, Therapeutic study.

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