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瑞典哥德堡的神经纤维瘤病。I. 背景、研究设计与流行病学

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

作者信息

Samuelsson B, Samuelsson S

机构信息

Psychiatric Department III, University of Gothenburg, Lillhagen's Hospital, Sweden.

出版信息

Neurofibromatosis. 1989;2(1):6-22.

PMID:2517025
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)

摘要

在本研究中,对所有年龄在20岁及以上、被卫生服务机构认定为神经纤维瘤病(NF)病例且截至1978年1月1日居住在瑞典哥德堡的患者进行了临床评估。该研究采用临床方法,重点关注NF的一般躯体、精神和遗传方面。通过详细查阅该地区所有可用的医疗记录档案,并要求哥德堡市的每位医生报告其所知的任何可能的NF病例,确定了纳入研究的患者。通过这种搜索,在普查日发现有74名NF患者居住在哥德堡。除3名患者外,所有这些患者均患有明确的冯雷克林霍增氏神经纤维瘤病(NF - 1)。这意味着每4600名成年人中就有1例NF病例,这必须被视为最低频率估计值。这74名患者包括35名女性,平均年龄为46(±17)岁,以及39名男性,平均年龄为43(±14)岁。NF的患病率在40 - 50岁年龄组最高,而在该年龄范围以上则显著降低,很可能是由于死亡率过高。最初的74名患者中有69名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三类:轻度、中度和重度。每组患者人数分别为18、43和13。记录了每位患者色素沉着异常和神经纤维瘤的详细情况(数量、外观和位置)。还记录了骨发育异常变化(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。45%的患者存在轻度智力障碍。智力障碍并非进行性的,也未发现严重智力障碍。23名(33%)患者出现精神疾病,其中8名定义为轻度,7名中度,8名重度。未发现统一的精神综合征。最常观察到的是抑郁综合征、伴有植物神经功能障碍的焦虑状态和器质性脑综合征。敌意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%。在患有精神疾病的患者中,推测表明中枢神经系统中NF - 1表现的异常神经学发现的频率显著增加。(摘要截取自400字)

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