Neurofibromatosis in Gothenburg, Sweden. I. Background, study design and epidemiology.

Neurofibromatosis Pub Date : 1989-01-01
B Samuelsson, S Samuelsson
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Abstract

In this study, a clinical evaluation was carried out for all patients who were at or beyond 20 years of age and known to the health services as cases of neurofibromatosis (NF) and who were resident in Gothenburg, Sweden, as of January 1, 1978. The approach of the study was clinical, with emphasis on the general somatic, psychiatric and genetic aspects of NF. The patients included in the study were ascertained by scrutiny of all available archives of medical records in the area, and by requests to every doctor in the city of Gothenburg to report any possible case of NF known to him or her. This search identified 74 patients with NF living in Gothenburg on the census day. All but 3 of these patients had definite von Recklinghausen NF (NF-1). This represents a prevalence of 1 case of NF in 4,600 adults, which must be considered a minimum frequency estimate. The 74 patients included 35 women with a mean age of 46 (+/- 17) years and 39 men with a mean age of 43 (+/- 14) years. The prevalence of NF was highest in the age range of 40-50 years, while it was significantly reduced in the ages above this range, most probably owing to an excess mortality. Sixty-nine of the original seventy-four patients were personally interviewed and examined, including the 3 without definite NF-1. The patients were classified according to the degree of severity of NF into three categories: mild, moderate and severe. The number of patients in each groups was, respectively, 18, 43 and 13. A detailed description of each patient's pigmentary abnormalities and neurofibromas (number, appearance and localization) was recorded. Findings of osseous dysplastic changes (12-16%), endocrine changes (pheochromocytoma, 3%), malignant disease (sarcoma, 4%), epilepsy (3%) and other somatic diseases were also recorded. Mild mental retardation was present in 45% of the patients. The mental retardation did not appear progressive, and severe retardation was not found. Mental illness occurred in 23 (33%) patients, defined as mild in 8, moderate in 7 and severe in 8. No uniform psychiatric syndrome was found. Depressive syndrome, anxiety state with vegetative dysfunction and organic brain syndrome were most frequently observed. Hostile feelings and autonomic disturbances were the most common symptoms, each found in 50% of all patients. The frequency of abnormal neurological findings, presumably indicating manifestations of NF-1 in the central nervous system, was significantly increased among the patients with mental illness.(ABSTRACT TRUNCATED AT 400 WORDS)

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瑞典哥德堡的神经纤维瘤病。1 .背景、研究设计和流行病学。
在这项研究中,对1978年1月1日居住在瑞典哥德堡的所有年龄在20岁或以上、被卫生服务部门称为神经纤维瘤病(NF)的患者进行了临床评估。该研究的方法是临床的,重点是NF的一般躯体、精神和遗传方面。通过仔细检查该地区所有现有的医疗记录档案,并要求哥德堡市的每位医生报告他或她所知道的任何可能的NF病例,确定了研究中包括的患者。这项研究在人口普查当天确定了74名居住在哥德堡的NF患者。除3例外,其余均有明确的冯氏NF (NF-1)。这表明在4600名成年人中有1例NF病例,这必须被视为最低频率估计值。74例患者中女性35例,平均年龄46(+/- 17)岁,男性39例,平均年龄43(+/- 14)岁。NF患病率在40-50岁年龄段最高,而在此年龄段以上显著降低,很可能是由于死亡率过高。在最初的74名患者中,有69人接受了个人访谈和检查,包括3名没有明确NF-1的患者。根据NF的严重程度将患者分为轻度、中度和重度3类。各组患者数分别为18例、43例、13例。详细记录每位患者的色素异常和神经纤维瘤(数量、外观和定位)。骨骼发育不良(12-16%)、内分泌变化(嗜铬细胞瘤,3%)、恶性疾病(肉瘤,4%)、癫痫(3%)和其他躯体疾病的发现也有记录。45%的患者存在轻度智力障碍。智力发育迟滞未出现进行性进展,未见严重智力迟滞。23例(33%)患者出现精神疾病,其中8例为轻度,7例为中度,8例为重度。没有发现统一的精神症状。抑郁综合征、焦虑状态伴植物功能障碍和器质性脑综合征最为常见。敌对情绪和自主神经紊乱是最常见的症状,在所有患者中各占50%。神经系统异常发现的频率,可能表明中枢神经系统NF-1的表现,在精神疾病患者中显著增加。(摘要删节为400字)
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