Zhao Jingpin, Li Yuqing, Wu Wenjuan, Zhang Zekun, Ding Yang
Department of Radiology, Third Hospital of Hebei Medical University, Hebei Province Biomechanical Key Laboratory of Orthopedics, Shijiazhuang, Hebei 050051, P.R. China.
Oncol Lett. 2015 Jan;9(1):191-194. doi: 10.3892/ol.2014.2636. Epub 2014 Oct 24.
Solitary plasmacytomas (SPs) represent ≤5% of all plasma cell neoplasms and mostly occur in the spine, pelvis, ribs and pectoral girdle, while rarely occurring in the sternum. The tumors typically appear as osteolytic lesions. In rare cases, SPs can manifest as bony spicules on the surface of the bone. The present study reports the case of a 74 year-old female with an osteolytic tumor localized in the sternum. The tumor displayed extensive bony destruction, with a large quantity of thick straight spicules on the surface of the bone, resembling a sunray in appearance. The imaging, laboratory and pathological examinations of the patient met the diagnostic criteria of SP. The patient was initially treated with radiotherapy at a dose of 45 Gy. Six months later, chemotherapy consisting of vindesine, Adriamycin and dexamethasone was administered. Vindesine and Adriamycin were administered at a dose of 2 and 15 mg/day, respectively on days 1-4 in a 20-day cycle. Dexamethasone was administered at a dose of 20 mg/day on days 1-4, 9-12 and 17-20 in the 20-day cycle. In total, the patient underwent 6 cycles of chemotherapy, with a total duration of 7 months. The patient was followed-up for two years after beginning therapy. At present, the patient is well, without any evidence of progressive disease or multiple myeloma. To the best of our knowledge, this is the first case in the English literature of SP in the sternum, with an unusual sunray periosteal reaction on radiological imaging. The sites of bony spiculation in the lesions that have previously been described in the literature are the mandible, orbit, vertebral body and skull vault. To the best of our knowledge, the current study presents the first case of a SP of the sternum with a unusual spiculated periosteal reaction on radiological imaging to be reported in the English literature.
孤立性浆细胞瘤(SPs)占所有浆细胞肿瘤的比例≤5%,主要发生于脊柱、骨盆、肋骨和肩胛带,而极少发生于胸骨。肿瘤通常表现为溶骨性病变。在罕见情况下,SPs可表现为骨表面的骨针。本研究报告了1例74岁女性,其溶骨性肿瘤位于胸骨。肿瘤表现为广泛的骨质破坏,骨表面有大量粗大笔直的骨针,外观类似日光放射状。该患者的影像学、实验室及病理检查符合SP的诊断标准。患者最初接受了45 Gy的放射治疗。6个月后,给予长春地辛、阿霉素和地塞米松组成的化疗方案。长春地辛和阿霉素在20天周期的第1 - 4天分别以2 mg/天和15 mg/天的剂量给药。地塞米松在20天周期的第1 - 4天、第9 - 12天和第17 - 20天以20 mg/天的剂量给药。患者共接受了6个周期的化疗,总疗程7个月。开始治疗后对患者进行了两年的随访。目前,患者情况良好,无疾病进展或多发性骨髓瘤的任何证据。据我们所知,这是英文文献中首例胸骨SP病例,放射影像学上有不寻常的日光样骨膜反应。文献中先前描述的病变中骨针形成的部位有下颌骨、眼眶、椎体和颅顶。据我们所知,本研究是英文文献中首次报道的胸骨SP病例,放射影像学上有不寻常的骨针样骨膜反应。