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脊髓黑色素性施万细胞瘤:一种预后不良的肿瘤。

Spinal melanotic schwannoma: a tumour with poor prognosis.

作者信息

Vallat-Decouvelaere A V, Wassef M, Lot G, Catala M, Moussalam M, Caruel N, Mikol J

机构信息

Department of Pathology, Lariboisière Hospital, Paris, France.

出版信息

Histopathology. 1999 Dec;35(6):558-66. doi: 10.1046/j.1365-2559.1999.00786.x.

Abstract

AIM

To clarify the prognosis of melanotic schwannoma. This is a rare tumour which is generally considered as a benign lesion, reported in many cases with a short follow-up only.

METHODS AND RESULTS

Five cases of spinal melanotic schwannoma were retrospectively studied. The tumours were examined using standard histological, immunohistochemical and ultrastructural methods. No features of malignancy (high mitotic count, atypia or necrosis) were found in the primary tumours. The follow-up period ranged from 3 to 7 years. Malignant clinical behaviour was clear-cut in four cases: three patients died from metastases to various sites and one presented several discrete spinal tumours of the same type seven years after the first operation. Only one patient presented no recurrence and was free of disease 6 years after initial diagnosis. The review of 57 cases of the literature (including our cases), showed that 15% of the cases had recurrences and 26.3% were complicated by metastasis. Only 53% of the cases followed for more than 5 years, were free of disease vs. 67.5% of the cases with shorter follow-up. Twenty additional cases had no follow-up.

CONCLUSION

Appropriate long-term follow-up is required for all melanotic schwannomas, as it may recur or metastasize after more than 5 years, even in the absence of overt malignant histological features.

摘要

目的

明确黑色素性神经鞘瘤的预后。这是一种罕见肿瘤,通常被视为良性病变,许多病例报告的随访时间较短。

方法与结果

对5例脊柱黑色素性神经鞘瘤进行回顾性研究。采用标准组织学、免疫组织化学和超微结构方法对肿瘤进行检查。在原发性肿瘤中未发现恶性特征(高有丝分裂计数、异型性或坏死)。随访时间为3至7年。4例患者出现明确的恶性临床行为:3例患者死于多处转移,1例在首次手术后7年出现多个同一类型的散在脊柱肿瘤。只有1例患者未复发,在初始诊断6年后无疾病。对57例文献病例(包括我们的病例)进行回顾,发现15%的病例复发,26.3%的病例出现转移。随访超过5年的病例中只有53%无疾病,而随访时间较短的病例中这一比例为67.5%。另外20例病例无随访。

结论

所有黑色素性神经鞘瘤均需要进行适当的长期随访,因为即使没有明显的恶性组织学特征,其也可能在5年后复发或转移。

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