Kulkarni Rahul S, Parikh Sonia K, Anand Asha S, Panchal Harsha P, Patel Apurva A, Trivedi Priti, Joshi Kshitij, Chirmade Pushpak
Department of Medical and Pediatric Oncology, Gujarat Cancer Research Institute, Ahmedabad, Gujarat, India.
Department of Pathology, Gujarat Cancer Research Institute, Ahmedabad, Gujarat, India.
J Pediatr Neurosci. 2017 Jan-Mar;12(1):67-71. doi: 10.4103/jpn.JPN_153_16.
Solitary plasmacytoma of the bone (SPB) is a rare plasma cell neoplasm representing only about 5% of plasma cell neoplasia. It usually presents as a lytic lesion mainly localized within the axial skeleton. SPB is exceedingly rare in young individuals, and only few cases have been reported so far in patients younger than 20 years of age. In view of rarity of disease, definitive treatment guidelines have not been established. We hereby report a case of SPB involving of lumbar vertebra (L5) in a 12-year-old boy. He was initially treated with antilymphoma therapy and curative radiotherapy considering as primary bone lymphoma. However, he had local recurrence with paraparesis after 9 months which was diagnosed as solitary bone plasmacytoma for which he was treated with decompressive laminectomy and chemotherapy (bortezomib, lenalidomide, and dexamethasone). The purpose of this article is to report a rare case of SPB in a pediatric patient and to review the available literature and treatment options. SPB should be considered in the differential diagnosis of osteolytic bone lesions even in young patients.
骨孤立性浆细胞瘤(SPB)是一种罕见的浆细胞肿瘤,仅占浆细胞肿瘤的约5%。它通常表现为主要局限于中轴骨骼的溶骨性病变。SPB在年轻人中极为罕见,迄今为止,年龄小于20岁的患者仅有少数病例报道。鉴于该疾病的罕见性,尚未确立明确的治疗指南。我们在此报告一例12岁男孩的腰椎(L5)SPB病例。他最初接受抗淋巴瘤治疗及根治性放疗,最初考虑为原发性骨淋巴瘤。然而,9个月后他出现局部复发并伴有双下肢轻瘫,被诊断为孤立性骨浆细胞瘤,为此接受了减压性椎板切除术及化疗(硼替佐米、来那度胺和地塞米松)。本文的目的是报告一例儿科患者的罕见SPB病例,并回顾现有文献及治疗选择。即使在年轻患者中,骨溶骨性病变的鉴别诊断也应考虑到SPB。