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一名儿童在先前治疗过的髓母细胞瘤部位发生了毛细胞型星形细胞瘤。

Pilocytic astrocytoma developing at the site of a previously treated medulloblastoma in a child.

作者信息

Koksal Yavuz, Toy Hatice, Unal Ekrem, Baysal Tamer, Esen Hasan, Paksoy Yahya, Ustun M Erkan

机构信息

Department of Pediatrics, Meram Faculty of Medicine, Selcuk University, Meram, Konya 42080, Turkey.

出版信息

Childs Nerv Syst. 2008 Mar;24(3):289-92. doi: 10.1007/s00381-007-0444-0. Epub 2007 Jul 27.

Abstract

BACKGROUND

After the achieved high cure rates, the survivors of medulloblastoma have come to face other complications associated with treatment regimes. One of these complications is secondary malignant neoplasm (SMN), which is rare but generally fatal.

CASE HISTORY

We report a case of an 8-year-old girl in whom a pilocytic astrocytoma developed at the site of previously excised medulloblastoma 26 months earlier. The patient had then received postoperative radiotherapy and chemotherapy for the treatment of medulloblastoma. Twenty-five months after the cessation of treatment, she had no complaint and physical examination was unremarkable, but a mass in the operation region was detected. Surgical excision of the secondary pilocytic astrocytoma was performed with a good clinical recovery without any evidence of residue or recurrence at 9-month follow-up.

CONCLUSION

Clinicians must be vigilant for the risk of expected SMNs. Rigorous and prolonged follow-up of patients with central nervous system (CNS) tumors is warrant.

摘要

背景

在髓母细胞瘤实现高治愈率之后,其幸存者开始面临与治疗方案相关的其他并发症。这些并发症之一是继发性恶性肿瘤(SMN),它很罕见但通常致命。

病例史

我们报告一例8岁女孩的病例,其在26个月前髓母细胞瘤切除部位发生了毛细胞型星形细胞瘤。该患者当时接受了髓母细胞瘤的术后放疗和化疗。治疗停止25个月后,她没有不适主诉,体格检查无异常,但在手术区域发现了一个肿块。对继发性毛细胞型星形细胞瘤进行了手术切除,临床恢复良好,9个月随访时没有残留或复发的迹象。

结论

临床医生必须警惕预期的继发性恶性肿瘤风险。对中枢神经系统(CNS)肿瘤患者进行严格且长期的随访是必要的。

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