Suppr超能文献

[髓外浆细胞瘤]

[Extramedullary plasmocytomas].

作者信息

Ben Salah H, Hdiji S, Makni S, Ghorbel A M, Boudawara T, Elloumi M, Daoud J

机构信息

Service de radiothérapie carcinologique, CHU Habib-Bourguiba, Sfax, Tunisie.

出版信息

Cancer Radiother. 2012 Jul-Aug;16(4):282-7. doi: 10.1016/j.canrad.2012.03.008. Epub 2012 Jun 20.

Abstract

PURPOSE

To study the localization, treatment and prognosis of extramedullary plasmocytoma through a series of eight patients and a literature review.

PATIENTS AND METHODS

Eight patients with extramedullary plasmocytoma were treated in the university's hospital of Sfax in Tunisia. The average age was 57.3 years. Female represented 75% of patients. The diagnosis of plasmocytoma was based on anatomo-pathology and immunohistochemistry of a biopsy or resected tumour. Extramedullary location was confirmed if biological and radiological exams and medullary biopsy were normal. The therapeutic decision was made after multidisciplinary meetings regarding tumour location and anterior treatment.

RESULTS

Solitary extramedullary plasmocytoma was located in nasal cavity, cervical node, testis, ovary, bladder and the tongue. One patient was treated for three simultaneous locations of extramedullary plamocytoma (node, bowel, pleura) without evidence of myeloma. Radiotherapy was proposed in six cases but refused in one case (plasmocytoma of the bladder is currently receiving radiotherapy). Treatment consisted in chemotherapy in two cases. Evaluation after treatment revealed complete remission in 86% of the cases. Nodal recurrence was noted in two cases. These two patients were lost to follow up. The five other patients were in complete remission after a mean follow up of 5.7 years. No local recurrence or myeloma was noted.

CONCLUSION

Extramedullary plasmocytoma is a rare affection. It can occur in any region of the body. Head and neck is most frequent localization. The treatment is irradiation or surgery in some localization. Progression to myeloma is the most important factor that influences the prognosis of the disease.

摘要

目的

通过对8例患者的系列研究及文献回顾,探讨髓外浆细胞瘤的定位、治疗及预后。

患者与方法

8例髓外浆细胞瘤患者在突尼斯斯法克斯大学医院接受治疗。平均年龄为57.3岁。女性占患者的75%。浆细胞瘤的诊断基于活检或切除肿瘤的解剖病理学及免疫组化检查。若生物学和放射学检查及骨髓活检正常,则可确认髓外定位。在多学科会议上根据肿瘤位置及前期治疗情况做出治疗决策。

结果

孤立性髓外浆细胞瘤位于鼻腔、颈部淋巴结、睾丸、卵巢、膀胱及舌部。1例患者同时有3个髓外浆细胞瘤部位(淋巴结、肠、胸膜)接受治疗,未发现骨髓瘤证据。6例患者建议接受放疗,但1例拒绝(膀胱浆细胞瘤目前正在接受放疗)。2例患者接受化疗。治疗后评估显示86%的病例完全缓解。2例出现淋巴结复发。这2例患者失访。其他5例患者平均随访5.7年后完全缓解。未发现局部复发或骨髓瘤。

结论

髓外浆细胞瘤是一种罕见疾病。可发生于身体的任何部位。头颈部是最常见的发病部位。治疗方法为某些部位进行放疗或手术。进展为骨髓瘤是影响该疾病预后的最重要因素。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验