Mukoyama M, Hizawa K, Kagawa N, Takahashi K
Department of Clinical Research, Chubu National Hospital.
Rinsho Shinkeigaku. 1993 Nov;33(11):1154-6.
The case cards for autopsied patients with Fukuyama type congenital muscular dystrophy (FCMD) which included clinical data and pathological findings were filled in 10 national hospitals and 2 other institutes in Japan. The cards of 24 patients who died between 1978 and 1991 were collected and analysed for this study. The ages at death ranged from 2 to 27 years with a mean of 14.29 +/- 6.18 years and represented a nearly unimodal distribution. The age at death in the 12 patients who died before 1983 ranged from 2 to 21 years and averaged 11.58 +/- 5.11 years, whereas the 12 patients who died after 1984 ranged from 3 to 27 years of age and averaged 17.00 +/- 6.44 years. The latter group lived significantly longer than the former (p < 0.05). Pulmonary infection was a more frequent cause of demise in the group of patients who died before 1983 than in those who died after 1984 (83.3% vs 25.0%). On the other hand, cardiac failure was a more common cause of death in the latter group (8.3% vs 50.0%). These data on the life spans and cause of death of FCMD were similar to those studied of Duchenne muscular dystrophy by Mukoyama et al (1984, 1986, 1987).(ABSTRACT TRUNCATED AT 250 WORDS)
日本10家国立医院及其他2家机构填写了福山型先天性肌营养不良症(FCMD)尸检患者的病例卡,其中包含临床数据和病理结果。本研究收集并分析了1978年至1991年间死亡的24例患者的病例卡。死亡年龄在2岁至27岁之间,平均为14.29±6.18岁,呈近似单峰分布。1983年前死亡的12例患者死亡年龄在2岁至21岁之间,平均为11.58±5.11岁,而1984年后死亡的12例患者年龄在3岁至27岁之间,平均为17.00±6.44岁。后一组患者的存活时间明显长于前一组(p<0.05)。1983年前死亡的患者组中,肺部感染导致死亡的情况比1984年后死亡的患者组更常见(83.3%对25.0%)。另一方面,心力衰竭在后一组中是更常见的死亡原因(8.3%对50.0%)。这些关于FCMD患者寿命和死亡原因的数据与Mukoyama等人(1984年、1986年、1987年)对杜氏肌营养不良症的研究结果相似。(摘要截断于250字)