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Dedifferentiated chondrosarcoma mimicking a giant cell tumor. Is this low grade dedifferentiated chondrosarcoma?

机译:去分化软骨肉瘤模仿巨大的细胞瘤。这是低级去分化软骨肉瘤吗?

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We report a very rare case of a dedifferentiated chondrosarcoma mimicking a benign giant cell tumor. A 22-year-old male was admitted to our hospital with a history of mild left wrist pain after a skiing trauma. Radiology revealed an extensive meta-epiphyseal osteolytic lesion in the distal ulna, which appeared to be a giant cell tumor. Histological examination showed a biphasic tumor comprising chondroid and non-chondroid areas with a giant cell-rich lesion resembling a conventional giant cell tumor of the bone. Immunohistochemistry showed no expression of p16INK4a, VEGFR1, KDR (VEGFR2), VEGFR3, cKIT, MDM2 or CDK4. However, high expression of the tyrosine kinases PDGFRA and PDGFRB was observed. Molecular analysis showed no amplification of the cMYC gene and no activating mutations in the cKIT (exons 9 and 11) or PDGFRA (exon 18) genes.He has been on follow-up for ten months, with no evidence of local recurrence or metastatic disease. In summary, this report highlights a very rare case of a dedifferentiated chondrosarcoma in which the dedifferentiated component of the tumor bears histologic resemblance to a conventional giant cell tumor of bone. We suggest that this tumor might be categorized in the group of low-grade dedifferentiated chondrosarcomas.
机译:我们报告了一种罕见的模仿良性巨细胞瘤的软骨肉瘤的罕见病例。一名22岁的男性因滑雪创伤后因轻度左腕疼痛而入院。放射学发现尺骨远端广泛的上meta骨溶骨性病变,似乎是一个巨大的细胞瘤。组织学检查显示包括软骨样和非软骨样区域的双相性肿瘤,其具有富含细胞的巨大病变,类似于骨骼的常规巨大细胞肿瘤。免疫组织化学显示p16INK4a,VEGFR1,KDR(VEGFR2),VEGFR3,cKIT,MDM2或CDK4无表达。然而,观察到酪氨酸激酶PDGFRA和PDGFRB的高表达。分子分析显示cMYC基因没有扩增,cKIT(第9和11号外显子)或PDGFRA(第18外显子)基因中没有激活突变,他已经接受了十个月的随访,没有发现局部复发或转移性疾病的迹象。 。总而言之,本报告强调了软骨细胞肉瘤去分化的非常罕见的案例,其中肿瘤的去分化成分与常规的骨巨细胞瘤在组织学上相似。我们建议将这种肿瘤归类为低度去分化软骨肉瘤。

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