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巴基斯坦卡拉奇南部软组织肉瘤的流行病学研究(1995 - 1997年)

Epidemiology of soft tissue sarcomas in Karachi South, Pakistan (1995-7).

作者信息

Bhurgri Yasmin, Bhurgri Hadi, Pervez Shahid, Kayani Naila, Usman Ahmed, Bashir Imtiaz, Bhurgri Asif, Hasan Sheema H, Zaidi S M H

机构信息

Karachi Cancer Registry, Aga Khan University Hospital, Karachi, Pakistan.

出版信息

Asian Pac J Cancer Prev. 2008 Oct-Dec;9(4):709-14.

Abstract

INTRODUCTION

The present study was conducted with the objective of examining epidemiological characteristics of soft tissue sarcomas (STSs) in Karachi.

PATIENTS AND METHODS

Epidemiological data of 96 (63 male and 33 female) incident STS cases registered at Karachi Cancer Registry (KCR) for Karachi South (KS), from 1st January 1995 to 31st December 1997, were reviewed.

RESULTS

The age standardized rate (ASR) world per 100,000 were 3.3 (2.9%) and 2.1 (1.6%) in males and females, respectively, with mean ages of of 41.4 years (95% CI 35.77-46.97) and 40.2 years (95% CI 31.27-49.03). The age-specific curves showed a gradual increase in risk from the first until the eighth decade in both genders, with the highest peak at 75+ in females and 70-74 years in males. In males, 8 (12.7%) STS cases were diagnosed in the pediatric age group (0-14), 12 (19.1%) in adolescents and young adults (15-24 years), 19 (30.1%) in adults 25-49 years of age and 24 (38.1%) in the 50 years+ age group. In females the respective frequencies were 11%, 26%, 30% and 33%. The most common histological tumor was rhabdomyosarcoma, though the occurrence of the histological subtypes was age-dependent. Rhabdomyosarcomas and Ewing's sarcomas were more frequent in children and adolescents whereas fibrosarcomas, leiomyosarcomas, liposarcomas, malignant fibrous histiocytomas (MFHs) and schwannomas were encountered in the elderly.

CONCLUSION

Karachi falls into a high risk region for STS, observed in a relatively younger population, with a male predominance, high frequency of rhabdomyosarcoma and advanced stage at diagnosis. Information on grading and staging remain incomplete for most cases, which negatively affect disease management and survival.

摘要

引言

本研究旨在调查卡拉奇软组织肉瘤(STS)的流行病学特征。

患者与方法

回顾了1995年1月1日至1997年12月31日在卡拉奇癌症登记处(KCR)登记的96例(63例男性和33例女性)卡拉奇南部(KS)新发STS病例的流行病学数据。

结果

男性和女性的年龄标准化发病率(ASR)分别为每10万人3.3(2.9%)和2.1(1.6%),平均年龄分别为41.4岁(95%可信区间35.77 - 46.97)和40.2岁(95%可信区间31.27 - 49.03)。年龄特异性曲线显示,两性从第一个十年到第八个十年风险逐渐增加,女性在75岁及以上年龄段达到最高峰,男性在70 - 74岁年龄段达到最高峰。在男性中,8例(12.7%)STS病例在儿童年龄组(0 - 14岁)被诊断,12例(19.1%)在青少年和青年成人(15 - 24岁),19例(30.1%)在25 - 49岁的成年人,24例(38.1%)在50岁及以上年龄组。在女性中,相应的频率分别为11%、26%、30%和33%。最常见的组织学肿瘤是横纹肌肉瘤,不过组织学亚型的发生与年龄有关。横纹肌肉瘤和尤因肉瘤在儿童和青少年中更常见,而纤维肉瘤、平滑肌肉瘤、脂肪肉瘤、恶性纤维组织细胞瘤(MFH)和神经鞘瘤在老年人中更为常见。

结论

卡拉奇属于STS的高风险地区,在相对年轻的人群中观察到,男性占主导,横纹肌肉瘤发生率高且诊断时处于晚期。大多数病例的分级和分期信息仍然不完整,这对疾病管理和生存产生负面影响。

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