Giant plasmocytoma of frontal cranium as a rare first manifestation of multiple myeloma – case report

Z. Nowaczyk, P. Kawalec, W. Andrusewicz, L. Sagan
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Abstract

Abstract Introduction: Plasmocytomas are lesions that are rarely encountered in neurosurgical practice. Whereas multiple myeloma (MM) occures primarly in bone marrow, solitary plasmocytomas present exclusively extramedullary or as a solitary bone plasmocytoma. Although typical first manifestation of MM are osseus lesions, there are only few case reports in medical world literature of first MM presentation as a single cranial tumor of the skull vault. Clinical presentation: A 63-year-old male with a 4-month history of painless scalp swelling was sent to our department after an unsuccessful attempt to remove the tumor. The patient was neurologically intact and his general condition was good. Bifrontal craniectomy was performed in order to obtain a total resection of the lesion. The tumor was histologically diagnosed as plasmocytoma. Postoperative bone marrow biopsy demonstrated myeloma cells. The subsequent combined therapy had been successful and the patient is in a good condition almost 3 years after the procedure. Conclusion: As an uncommon type of solid tumors, plasmocytomas may mimic other neoplasms, which can lead to delay of diagnosis and proper treatment. Satisfying effects of treatment might occur only with proper diagnostic schema, which should be employed despite the rarity of plasmocytomas in daily clinical practice.
额颅骨巨大浆细胞瘤是多发性骨髓瘤的罕见首发表现之一例报告
摘要简介:浆细胞瘤是神经外科手术中罕见的病变。多发性骨髓瘤(MM)主要发生在骨髓中,孤立性浆细胞瘤仅表现为髓外或孤立性骨浆细胞瘤。虽然多发性骨髓瘤的典型首发表现是骨关节病变,但在医学界文献中,只有少数病例报告首次多发性MM表现为颅骨拱顶的单个颅骨肿瘤。临床表现:一名63岁男性,有4个月无痛性头皮肿胀病史,在尝试切除肿瘤失败后被送往我科。患者神经系统完整,总体情况良好。为了获得病变的全切除,进行了双侧颅骨切除术。肿瘤经组织学诊断为浆细胞瘤。术后骨髓活检显示骨髓瘤细胞。随后的联合治疗取得了成功,患者在手术后近3年处于良好状态。结论:浆细胞瘤是一种不常见的实体瘤,可能与其他肿瘤相似,导致诊断和治疗的延误。只有在正确的诊断模式下,才能达到满意的治疗效果,尽管在日常临床实践中浆细胞瘤很少见,但仍应采用正确的诊断方案。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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