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Extramedullary plasmocytomas [Plasmocytomes extraosseux]

机译:髓外浆细胞瘤[Plasmocytomes extraosseux]

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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.
机译:目的:通过一系列8例患者并文献复习,研究髓外浆细胞瘤的定位,治疗和预后。患者和方法:八名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和免疫组织化学。如果生物学和放射学检查以及髓样活检正常,则确认髓外位置。在有关肿瘤位置和前处理的多学科会议后做出了治疗决定。结果:孤立性髓外浆细胞瘤位于鼻腔,颈淋巴结,睾丸,卵巢,膀胱和舌头。一名患者同时接受了三个髓外浆细胞瘤(淋巴结,肠,胸膜)的治疗,而没有骨髓瘤的证据。建议放疗6例,但拒绝1例(膀胱浆细胞瘤目前正在接受放疗)。治疗包括化疗2例。治疗后的评估显示86%的病例完全缓解。在两个病例中发现结节复发。这两名患者失去随访。在平均随访5.7年后,其他5例患者完全缓解。没有发现局部复发或骨髓瘤。结论:髓外浆细胞瘤是一种罕见的疾病。它可以发生在身体的任何部位。头和脖子是最常见的定位。治疗是局部照射或手术。进展为骨髓瘤是影响疾病预后的最重要因素。

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