Epidemiological data in polycythaemia vera: a study of 842 cases.

Hematology and cell therapy Pub Date : 1998-08-01
Y Najean, J D Rain, C Billotey
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Abstract

An epidemiological study of 842 polycythaemic patients (entered between 1980 and 1997 in the French investigational prospective protocols) is presented. The global incidence is approximately 0.8-1.5/100,000/year in the reference area (Ile-de-France and surrounding areas). It increases linearly with age until 80, which suggests that several mutational somatic events are necessary. There was a slight male excess (sex-ratio 1.2, after correction for the percentage of male and female French people still living at risk). We did observe a slight excess of PV in the population of Jewish ancestry. A surprising excess of former blood donors (20.7% of the PV cases, compared to 8% estimated in the reference population) was observed. Only a few cases of familial myeloproliferative diseases and occurence of leukemia in the family of our patients have been observed; even if slight, this excess is statistically significant. In contrast, no excess of carcinomas was observed either in the family or in the patients' antecedents. We did not find any excess of radiation exposure in our cases. When analysing the previous occupation of our patients a possible excess of physicians and of patients previously working in occupations using solvents and glues was found, but this finding needs confirmation.

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真性红细胞增多症的流行病学资料:842例的研究。
对842例红细胞增多症患者(1980年至1997年在法国前瞻性研究方案中进入)进行了流行病学研究。参考区(法兰西岛及周边地区)的全球发病率约为0.8-1.5/100,000/年。它随着年龄的增长而线性增长,直到80岁,这表明一些体细胞突变事件是必要的。男性略多于男性(性别比为1.2,在校正了法国男性和女性仍然生活在危险中的比例后)。我们确实观察到,在犹太血统的人群中,PV有轻微的过量。观察到惊人的前献血者过量(PV病例的20.7%,而参考人群的估计为8%)。本组患者中仅有少数家族性骨髓增生性疾病和白血病的发生;即使是轻微的,这种过剩在统计上也是显著的。相比之下,无论是在家族中还是在患者的祖先中,都没有观察到过多的癌症。在我们的病例中没有发现任何过量的辐射暴露。在分析患者以前的职业时,发现可能有过多的医生和患者以前从事使用溶剂和胶水的职业,但这一发现需要证实。
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