Sestan B, Miletic D, Jonjic N, Rakovac I, Ekl D, Djapic T, Stalekar H
Orthopaedic Clinical Hospital, Lovran, Croatia.
West Indian Med J. 2007 Dec;56(6):555-7.
Primary leiomyosarcoma of the bone is a rare malignancy. Clinical follow-up suggests that primary osseous leiomyosarcoma has an aggressive biologic behaviour with poor survival time. We report a case of primary leiomyosarcoma arising from the proximal metaphysis of the right tibia of a 55-year old woman with a long follow-up period, without recidivism. Primary leiomyosarcoma has to be considered as a differential diagnostic possibility in the case of bone tumours seen on routine initial plain radiographs as lytic lesions. If the tumour has been adequately excised at the time of diagnosis, as in the present case, with adjuvant therapy protocol, the long-term prognosis of such an aggressive tumour can be exceptionally good.
原发性骨平滑肌肉瘤是一种罕见的恶性肿瘤。临床随访表明,原发性骨平滑肌肉瘤具有侵袭性生物学行为,生存时间较短。我们报告一例55岁女性右胫骨近端干骺端发生的原发性平滑肌肉瘤病例,随访时间长,无复发。对于常规初次X线平片上表现为溶骨性病变的骨肿瘤病例,必须考虑原发性平滑肌肉瘤作为鉴别诊断的可能性。如果在诊断时肿瘤已被充分切除,如本病例,并采用辅助治疗方案,这种侵袭性肿瘤的长期预后可能会非常好。