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Pleomorphic Xanthoastrocytoma: Clinicopathological spectrum of an intriguing neoplasm

机译:多形性黄体星形细胞瘤:有趣的肿瘤的临床病理频谱。

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Background & Objective: Pleomorphic xanthoastrocytoma (PXA) is a rare primary WHO Grade II astrocytic tumor comprising of < 1% of all astrocytomas. It is generally benign and slow growing however disease progression and malignant transformation with anaplastic features have been infrequently reported. Our objective was to assess clinicopathological characteristics of this rare tumor at our center. Methods: A retrospective study was conducted at Aga Khan University Hospital from January 1992 till January 2016. Data was entered on a proforma including patient demographics, clinical features, tumor location, histological features and follow-up, where available. Results: Forty Seven cases of PXA were retrieved during the study period. The mean age was 23.8 years (SD=15.1) and median age was 19 years. The most frequent symptom was head ache (n=31). Male were more frequently affected (n=26). The commonest location was temporal lobe. On microscopic examination, tumors were pleomorphic without mitoses or necrosis, however two cases showed increased mitotic activity, and one case revealed associated gliosarcoma. Follow-up of only 29 cases was available for a period ranging between 2 and 184 months (85 months +/- 56 months). Outcome was good in 27 patients with the last follow up showing no radiographic or clinical evidence of tumor recurrence. Conclusions: PXA is an infrequent tumor in our population also, with less than 50 cases identified in two decades study period. Due to its rarity and its bizarre histomorphology, it should be diagnosed correctly, as it has got better prognosis than other astrocytic tumors. doi: https://doi.org/10.12669/pjms.342.14663 How to cite this:Abid M, Haroon S, Memon AH, Ahmad Z, Hasan SH. Pleomorphic Xanthoastrocytoma: Clinicopathological spectrum of an intriguing neoplasm. Pak J Med Sci. 2018;34(2):277-281. doi: https://doi.org/10.12669/pjms.342.14663 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
机译:背景与目的:多形性黄体星形细胞瘤(PXA)是一种罕见的原发性WHO II级星形细胞肿瘤,占所有星形细胞瘤的<1%。它通常是良性的且生长缓慢,但是很少报道疾病的进展和具有变性特征的恶性转化。我们的目标是在我们中心评估这种罕见肿瘤的临床病理特征。方法:从1992年1月至2016年1月在阿迦汗大学医院进行了一项回顾性研究。输入的数据包括患者的人口统计学资料,临床特征,肿瘤位置,组织学特征和随访情况。结果:在研究期间共检索到47例PXA病例。平均年龄为23.8岁(SD = 15.1),中位年龄为19岁。最常见的症状是头痛(n = 31)。男性受影响更为频繁(n = 26)。最常见的位置是颞叶。在显微镜下检查,肿瘤为多形性,无有丝分裂或坏死,但是有2例显示有丝分裂活性增加,有1例显示有相关的眼胶质瘤。仅29例的随访时间为2到184个月(85个月+/- 56个月)。 27例患者的结果良好,最后一次随访未显示放射学或肿瘤复发的临床证据。结论:PXA在我们的人群中也是很少见的肿瘤,在二十年的研究期内,发现不到50例。由于它的稀有性和奇异的组织形态,应正确诊断,因为它比其他星形细胞肿瘤的预后更好。 doi:https://doi.org/10.12669/pjms.342.14663如何引用:Abid M,Haroon S,Memon AH,Ahmad Z和Hasan SH。多形性黄体星形细胞瘤:有趣的肿瘤的临床病理学频谱。朴J医学。 2018; 34(2):277-281。 doi:https://doi.org/10.12669/pjms.342.14663这是根据知识共享署名许可(http://creativecommons.org/licenses/by/3.0)的条款分发的开放访问文章,该文章允许不受限制在适当引用原始作品的前提下,可以在任何媒介中使用,分发和复制。

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