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我们从1992年10月~1996年5月间,在儿科矮身材专科门诊中,曾收治随访了64例垂体性侏儒患者,临床疗效较好,报告如下.1 临床资料1.1 一般资料 64例中,男性56例,女性8例,男女之比7:1.年龄5岁~20岁.平均年龄为12.1岁.起病年龄1~3岁16例,4~10岁47例,14岁1例.病程2~13年,平均8.4年.治疗前身高增长率均值为2.0cm/年.40例(62.5%)有难产史.骨龄较实际年龄落后3~14岁,平均6.4岁.64例患者头颅蝶鞍区X线摄片;蝶鞍区小12例(18.7%)、蝶鞍区有钙化点3例(4.7%),蝶鞍区内有占位病变1例(1.5%).2例做头部冠状位增强CT片:垂体发育小1例,无异常1例.
We from October 1992 to May 1996, in pediatric short stature specialist outpatient, had treated 64 cases of pituitary dwarf patients were followed up, the clinical efficacy is better, the report is as follows.1 Clinical data 1.1 General information 64 cases, 56 males and 8 females, the ratio of men to women 7: 1. The age of 5 to 20. The average age was 12.1 years old, onset age of 1 to 3 years old in 16 cases, 4 to 10 years old in 47 cases, 14 years old in 1 case. Duration of 2 to 13 years, an average of 8.4 years. The mean height growth rate before treatment was 2.0cm / year .40 (62.5%) had a history of dystocia. Bone age than the actual age of 3 to 14 years old, an average of 6.4 years .64 patients with head Sellar area X-ray; 12 cases (18.7%) in the sellar region, 3 cases (4.7%) in the sellar region, and 1 case (1.5%) in the sellar region. Coronal CT enhancement: a small pituitary development, no abnormalities in 1 case.