Atta Irum, Laghari Taj Muhammad, Khan Yasir Naqi, Lone Saira Waqar, Ibrahim Mohsina, Raza Jamal
Department of Pediatric Medicine, Unit II, National Institute of Child Health, Karachi.
J Coll Physicians Surg Pak. 2015 Feb;25(2):124-8.
To determine the etiology of precocious puberty in children and to compare the clinical and laboratory parameters of central and peripheral precocious puberty.
Cross-sectional study.
Endocrine Clinic at National Institute of Child Health, Karachi, from January 2009 to December 2011.
Children presenting with precocious puberty were included. The age of onset of puberty was documented. Clinical evaluation, Tanner staging, height, height SDS, weight, weight SDS, body mass index, bone age, pelvic USG, plasma estradiol level and GnRH stimulation were done. Ultrasound of adrenal glands, serum level of 17 hydroxyprogesterone, ACTH, Renin, aldosterone and testosterone were performed in children with peripheral precocious puberty. MRI of adrenal glands and gonads was done in patients with suspected tumor of that organ and MRI of brain was done in patients with central precocious puberty. Skeletal survey was done in patients with Mc Cune-Albright syndrome.
CAH (81.8%) indentified as a main cause in peripheral percocious puberty and idiopathic (67.74%) in central precocious puberty. Eighty five patients were registered during this period. The conditions causing precocious puberty were central precocious puberty (36.47%), peripheral precocious puberty (38.82%), premature pubarche (10.58%) and premature thelarche (14.11%). There was a difference in the age of onset of puberty in case of central precocious puberty (mean=3, 2-6 years) versus peripheral precocious puberty (mean=5.25; 3.62 - 7.0 years). Children with central precocious puberty showed higher height SDS, weight SDS, FSH, LH than those with peripheral precocious puberty.
Etiology in majority of cases with peripheral precocious puberty was congenital adrenal hyperplasia and idiopathic in central precocious puberty. Central precocious puberty children showed higher height SDS, weight SDS, FSH, LH than peripheral precocious puberty.
确定儿童性早熟的病因,并比较中枢性和外周性性早熟的临床及实验室参数。
横断面研究。
2009年1月至2011年12月,卡拉奇国家儿童健康研究所内分泌门诊。
纳入出现性早熟的儿童。记录青春期开始年龄。进行临床评估、坦纳分期、身高、身高标准差分值(SDS)、体重、体重SDS、体重指数、骨龄、盆腔超声检查、血浆雌二醇水平及促性腺激素释放激素(GnRH)刺激试验。对外周性早熟儿童进行肾上腺超声检查、血清17羟孕酮、促肾上腺皮质激素(ACTH)、肾素、醛固酮及睾酮水平检测。对怀疑该器官有肿瘤的患者进行肾上腺和性腺磁共振成像(MRI)检查,对中枢性早熟患者进行脑部MRI检查。对McCune-Albright综合征患者进行骨骼检查。
先天性肾上腺皮质增生症(CAH)(81.8%)被确定为外周性性早熟的主要原因,特发性(67.74%)为中枢性性早熟的主要原因。在此期间登记了85例患者。导致性早熟的情况有中枢性性早熟(36.47%)、外周性性早熟(38.82%)、青春期早现(10.58%)和乳房早发育(14.11%)。中枢性性早熟(平均=3岁,范围2 - 6岁)与外周性性早熟(平均=5.25岁;范围3.62 - 7.0岁)的青春期开始年龄存在差异。中枢性性早熟儿童的身高SDS、体重SDS、卵泡刺激素(FSH)、黄体生成素(LH)高于外周性性早熟儿童。
大多数外周性性早熟病例的病因是先天性肾上腺皮质增生症,中枢性性早熟的病因是特发性。中枢性性早熟儿童的身高SDS、体重SDS、FSH、LH高于外周性性早熟儿童。