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颅骨孤立性浆细胞瘤:成功治疗长期存在的大病灶并进行长期随访

Solitary plasmacytoma of the calvarium: A successful management of a long-standing large lesion with a long-term follow-up.

作者信息

Alghamdi Abdulaziz M, Alsinani Taghreed A, Samkari Alaa

机构信息

College of Medicine, King Saud Bin Abdulaziz University for Health Sciences, Jeddah, Saudi Arabia.

King Abdullah International Medical Research Center, Jeddah, Saudi Arabia.

出版信息

Surg Neurol Int. 2024 Jan 26;15:27. doi: 10.25259/SNI_817_2023. eCollection 2024.

Abstract

BACKGROUND

Solitary plasmacytoma of the calvarium (SPC), without evidence of multiple myeloma (MM), is extremely rare. We report a case of a long-standing large SPC that was treated successfully by surgical excision and adjuvant radiotherapy with a long follow-up period.

CASE DESCRIPTION

A 58-year-old male patient presented with a 5-year history of painless skull swelling. On the physical examination, the mass was 6 × 6 cm in size, oval, not tender, and firm in consistency with normal skin color. A brain computed tomography scan showed a destructive skull lesion. A brain magnetic reasoning imaging (MRI) showed a large expansile lytic mass lesion arising from the skull vault in the frontal-parietal region with multiple internal septa. The patient underwent a craniectomy and excision of the lesion, followed by cranioplasty using methyl methacrylate. The final diagnosis was consistent with plasmacytoma based on the histopathological features. One month follow-up brain MRI showed no evidence of residual tumor. The skeletal survey and bone marrow biopsy did not reveal any evidence of MM. The patient was referred to medical oncology for further treatment and received radiation therapy. During nine years of clinical and radiological follow-up, there was no evidence of any metastasis or recurrence.

CONCLUSION

SPC is a rare disease with high rates of misdiagnosis. Careful evaluations are crucial to exclude systemic involvement. Surgical resection followed by radiotherapy may be adequate for the disease control. Close follow-up with regular lifelong examinations is important to avoid a generalized incurable disease.

摘要

背景

颅骨孤立性浆细胞瘤(SPC),无多发性骨髓瘤(MM)证据,极为罕见。我们报告一例长期存在的大型SPC病例,经手术切除和辅助放疗成功治疗,随访期长。

病例描述

一名58岁男性患者,有无痛性颅骨肿胀5年病史。体格检查时,肿块大小为6×6cm,椭圆形,无压痛,质地硬,皮肤颜色正常。脑部计算机断层扫描显示颅骨有破坏性病变。脑部磁共振成像(MRI)显示额顶叶区域颅骨穹窿部有一个巨大的膨胀性溶骨性肿块病变,内有多个间隔。患者接受了颅骨切除术和病变切除,随后使用甲基丙烯酸甲酯进行颅骨成形术。根据组织病理学特征,最终诊断与浆细胞瘤一致。术后1个月的脑部MRI显示无残留肿瘤迹象。骨骼检查和骨髓活检未发现MM的任何证据。患者转诊至肿瘤内科接受进一步治疗并接受了放射治疗。在9年的临床和影像学随访中,未发现任何转移或复发迹象。

结论

SPC是一种误诊率高的罕见疾病。仔细评估对于排除全身受累至关重要。手术切除后放疗可能足以控制疾病。定期进行终身密切随访对于避免疾病发展为全身性不治之症很重要。

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