Biazzo Alessio, Armiraglio Elisabetta, Parafioriti Antonina, Confalonieri Norberto
Gaetano Pini-CTO, Milano.
.
Acta Biomed. 2018 Jun 7;89(2):269-273. doi: 10.23750/abm.v89i2.5278.
We reported the case of a 22 year-old boy who suffered a periosteal osteoblastoma of the distal fibula. The radiographic features of our case did not correlate with the majority of periosteal osteoblastomas of the long bones reported in the literature and were identical to a periosteal aneurysmal bone cyst. Periosteal osteoblastoma is a very rare tumor with a wide range of clinical and radiological features, showing in 15% of cases association with secondary aneurysmal bone cyst. Radiologist and orthopaedic surgeon should be aware of the atypical behavior of this rare entity in order to avoid mistakes with other more common tumors arising on the surface of the long bones.
我们报告了一例22岁男性患者,其患有腓骨远端骨膜下骨母细胞瘤。我们病例的影像学特征与文献中报道的大多数长骨骨膜下骨母细胞瘤不相关,而是与骨膜下动脉瘤样骨囊肿相同。骨膜下骨母细胞瘤是一种非常罕见的肿瘤,具有广泛的临床和放射学特征,15%的病例显示与继发性动脉瘤样骨囊肿有关。放射科医生和骨科医生应意识到这种罕见实体的非典型表现,以避免与长骨表面出现的其他更常见肿瘤混淆。