[继发于肋骨多骨纤维性发育不良的骨肉瘤]。

Q4 Medicine
Minoru Yamaki, Mai Nishina, Toshio Noriyuki, Syuji Yonehara
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引用次数: 0

摘要

纤维发育不良的肉瘤变极为罕见。本病例是一名 54 岁的男性,他有多处肋骨肿块、全身多处淋巴结肿大,计算机断层扫描(CT)显示有多处溶骨性病变。正电子发射断层扫描(PET)显示每个病灶都有异常强化。右锁骨上窝淋巴结针刺活检显示为肉样瘤病。考虑到肉样瘤病可能伴有恶性肿瘤,患者接受了肋骨肿瘤切除术和纵隔淋巴结活检,以确诊肋骨病变。病理结果显示,肋骨肿块为低级别中心性骨肉瘤,纵隔淋巴结为肉瘤病。病变分布符合继发于多发性纤维性骨发育不良的骨肉瘤。由于骨肉瘤级别较低,对患者进行了随访。术后三年,残留病灶没有增加。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
[Osteosarcoma Secondary to Polyostotoic Fibrous Dysplasia of the Ribs].

Sarcomatous transformation of fibrous dysplasia is extremely rare. We present the case of a 54-yearold man with multiple rib masses, multiple enlarged lymph nodes throughout the body, and multiple osteolytic lesions on computed tomography( CT). A positron emission tomography( PET) scan showed abnormal enhancement in each. A needle biopsy of the right supraclavicular fossa lymph node revealed sarcoidosis. Considering the possibility of malignancy associated with sarcoidosis, a rib tumor resection and mediastinal lymph node biopsy were performed to confirm the diagnosis of the rib lesion. The pathology results showed that the rib mass was a low-grade central osteosarcoma and the mediastinal lymph node was sarcoidosis. The distribution of the lesions was consistent with osteosarcoma secondary to multiple fibrous bone dysplasia. As the osteosarcoma was low grade, the patient was followed up. Three years after surgery, there was no increase in residual disease.

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