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Concurrent osteochondroma and osteoblastoma of the proximal humeral shaft.

机译:肱骨干近端并发骨软骨瘤和成骨细胞瘤。

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We present what we believe is the first reported case of synchronous osteochondroma and osteoblastoma, occurring in the proximal humerus of a young man. A 15-year-old boy presented with a painful left arm mass for 3 months. A firm mass was palpable in the proximal medial arm, and he had mild triceps weakness secondary to pain. Imaging showed an eccentric lesion involving the proximal one-third of the humerus, with central lysis, surrounding sclerosis and edema, endosteal scalloping, and cortical thinning and expansion. The humeral diaphysis contained a bony exostosis with corticomedullary continuity, consistent with an osteochondroma with a cartilage cap <5 mm thick. Within the proximal portion of the osteochondroma was a 2-cm, edematous, rim-enhancing cystic lesion, concerning for a secondary process such as malignant transformation. On open biopsy, the mass grossly appeared to be a sessile osteochondroma, and was removed with a rongeur. The cystic lesion was curetted out of the bone. Pathology confirmed that the raised lesion was an osteochondroma. The cystic lesion contained osteoblasts in a matrix of osteoid and immature bone, characteristic of an osteoblastoma. The multidisciplinary team agreed that this was an osteoblastoma within an exostosis. At follow-up, the patient's pain had fully resolved and radiographs showed good early healing. We wished to document the extraordinary, simultaneous existence of an osteochondroma and adjacent osteoblastoma in the proximal humerus of a young patient. Although similar in presentation, the tumors consist of cells of different origins, making the pathogenesis unclear.
机译:我们介绍了我们认为是首次报告的同步发生的骨软骨瘤和成骨细胞瘤病例,发生在一个年轻人的肱骨近端。一个15岁的男孩出现了三个月的左臂疼痛。在内侧近臂可触及硬块,他因疼痛继发轻度三头肌无力。影像学检查显示偏心病变累及肱骨近端三分之一,并伴有中枢溶解,周围硬化和水肿,骨内膜扇贝形,以及皮质变薄和扩张。肱骨干physi端具有骨皮质的连续性,具有皮质髓质的连续性,与软骨软骨<5 mm厚的骨软骨瘤一致。在骨软骨瘤的近端部分内有一个2厘米长的水肿,边缘增高的囊性病变,涉及恶性转化等继发过程。在开放活检中,肿块大体上似乎是无柄的骨软骨瘤,并用咬骨钳取出。囊状病变从骨头刮出。病理证实,病变为骨软骨瘤。囊性病变在成骨细胞和未成熟骨的基质中包含成骨细胞,这是成骨细胞瘤的特征。多学科团队一致认为,这是骨内增生的成骨细胞瘤。随访时,患者的疼痛已完全缓解,X光片显示早期愈合良好。我们希望记录年轻患者肱骨近端肱骨软骨瘤和相邻成骨细胞瘤的异常,同时存在。尽管表现相似,但肿瘤由不同来源的细胞组成,因此发病机理不清楚。

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