Ahmed Ijaz, Nasreen Sarwat, Bhatti Rabnawaz
Department of Dermatology, Ziauddin University, Karachi.
J Coll Physicians Surg Pak. 2007 Oct;17(10):587-90. doi: 10.2007/JCPSP.587590.
To determine the clinical presentations of alopecia areata in children as well as the frequency of associated disorders.
Cross-sectional study.
Department of Dermatology, Ziauddin University Hospital, KDLB Campus, Karachi during the calendar years 2005 and 2006.
Children of either gender suffering from alopecia areata, upto 15 years of age, who fulfilled the selection criteria were included in the study. Only freshly registered cases were studied. Severity of the disease was graded as mild, moderate and severe disease, and other clinical patterns including alopecia totalis, alopecia universalis and ophiasis. Hematological and biochemical profile was evaluated. Chi-square test was applied for statistical analysis in order to determine p-value using the percentages of variables.
One hundred and fourteen patients comprising 54 males (47%) and 60 females (53%), aged 4 upto 15 years, the mean age being 9.1 years, were enrolled. Family history of alopecia areata was positive in 11 patients (10%). Fifty nine patients (51%) were of age 6-10 years, 39 patients (35%), aged 11-15 years, and 16 (14%) were of age below 5 years. Mild alopecia areata (41%, p < 0.05) was the most common presentation followed by moderate disease (31%, p < 0.05), severe alopecia (17%, p < 0.05), alopecia totalis (7%, p < 0.05), alopecia universalis (2.7%, p=0.05) and ophiasis (1.7%, p=0.05). Nail changes were found in 40 patients (35%, p < 0.05). Definite evidence of atopy was obtained in 23 patients (20%, p< 0.05). The autoimmune disorders associated with alopecia areata included: hypothyroidism (4.3%), vitiligo (3.5%), psoriasis (1.8%), systemic lupus erythematosus (SLE 0.9%), hypoparathyroidism (0.9%) and diabetes mellitus (0.9%).
The spectrum of childhood alopecia areata ranges from mild, moderate and severe alopecia, ultimately to alopecia totalis, alopecia universalis and ophiasis. Nail changes as well as atopy and autoimmune disorders are the associated disorders.
确定儿童斑秃的临床表现以及相关疾病的发生率。
横断面研究。
2005年和2006年期间,在卡拉奇KDLB校区的齐亚丁大学医院皮肤科。
纳入符合入选标准的15岁及以下斑秃患儿,无论性别。仅研究新登记的病例。疾病严重程度分为轻度、中度和重度,其他临床类型包括全秃、普秃和匐行性脱发。评估血液学和生化指标。应用卡方检验进行统计分析,以确定变量百分比的p值。
共纳入114例患者,其中男性54例(47%),女性60例(53%),年龄4至15岁,平均年龄9.1岁。11例患者(10%)有斑秃家族史。59例患者(51%)年龄在6至10岁,39例患者(35%)年龄在11至15岁,16例(14%)年龄在5岁以下。轻度斑秃(41%,p<0.05)最为常见,其次是中度疾病(31%,p<0.05)、重度斑秃(17%,p<0.05)、全秃(7%,p<0.05)、普秃(2.7%,p = 0.05)和匐行性脱发(1.7%,p = 0.05)。40例患者(35%,p<0.05)出现指甲改变。23例患者(20%,p<0.05)有明确的特应性证据。与斑秃相关的自身免疫性疾病包括:甲状腺功能减退(4.3%)、白癜风(3.5%)、银屑病(1.8%)、系统性红斑狼疮(SLE 0.9%)、甲状旁腺功能减退(0.9%)和糖尿病(0.9%)。
儿童斑秃的范围从轻度、中度和重度脱发,最终发展为全秃、普秃和匐行性脱发。指甲改变以及特应性和自身免疫性疾病是相关疾病。