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به نام خدا. Delayed puberty. Mehdi salek MD. Delayed puberty. Initial physical changes of puberty are not present by age 13 years in girls 14 years in boys. Delayed puberty. lack of appropriate progression of puberty more than 4.5-5 years
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Delayed puberty Mehdi salek MD
Delayed puberty Initial physical changes of puberty are not present by age • 13 years in girls • 14 years in boys
Delayed puberty lack of appropriate progression of puberty more than 4.5-5 years • A boy who has’nt completed secondary sexual development within 4.5 years • A girl who does’nt menstruate within 5 years
Classification of Delayed Puberty Gonadotropin deficiency • CNS tumors • Functional HH • Infiltrative • Trauma • Isolated Gonadotropin • Genetic forms • CDP Hypergonadotropic Hypogonadism
Classification of Delayed Puberty • Non-pathologic • pathologic
Classification of Delayed Puberty • Transient • Permanent
Evaluation History • Infertility • Anosmia → HH • Cryptorchidism → HH • Small penis in neonate → HH • low Gn in neonatal period → HH
Evaluation • Family pattern attainment of menarche • Family history of delay pubertal • Constitutional delay often have a positive family • Birth trauma • Familial marriage
Evaluation • Chemotherapy • Glucocorticoid therapy • Surgery • History of intense exercise • Exposures to irradiation
Growth chart • Growth pattern Late onset growth failure CNS mass lesion Organic disease Occasionally MRI IS necessary
Growth chart • Normal growth velocity for BA →CDGP Normal growth pattern without growth spurt • With anosmia Kallmann syndrom • Without anosmia ↓isolated gonadotropin
Physical Examination • Neurologic examination • Gynecomastia • midline facial malformations • Size of glandular breast tissue ,areolarsize • Testing of sense of smell • Galactorrhea • Turner stigma • Retractile testes
Physical Examinatin • Height especially HT velocity at least 6 -12 months • upper to lower segment ratio • ↑↑U/L → CDG • ↓↓U/L → Hypogonadism
Physical Examinatin • Signs of puberty • Testicular location ,size, and consistency Prepubertal: • Normal size testis <2.0 cc or longer<1.5 cm Early puberty: • Normal size testis >3.0 cc or longer >2.5 cm pubertal-aged • A testis ≤1.0cm particularly if unusually firm or soft suggestive of a hypogonadal state.
initialApproach • Skeletal age • Gonadotropin status
initialApproach BA = 11-13 years Gonadotropin measurement HighPrimary gonadal failure Girl Turner Boy Klinefelter
initialApproach Mild Elevated→ GnRH Test Exaggerated response Primary gonadal failure
initialApproach Low or lower limit of normal level • Constitutional Delay • Chronic disease • permanent Gonadotropin
initialApproach • Low gonadotropin levels and pubertal delay may result from a physiologic delay or a permanent defect
General Approach Diagnosis of HH versus CDP is more difficult because of Overlap in physical and laboratory finding
General Approach Hypogona Hypogo • FSH and LH are low • They haven't a pulsatile LH with↑ bone age
General Approach Overlap between HH and an immature hypothalamus if BA<10–11 years for girls BA<12–13 for boys
General Approach In older adolescent • Minimal response to GnRH Test suggests Gonadotropin Deficiency • Pubertal rise in the child with delayed puberty suggests CDP
General Approach • Patients with HH have normal height in early or mid adolescent • Patients with CDP have a normal growth rate for BA but are short for CA.
Laboratory assessment • CBC • Electrolytes • LFT • ESR • Prolactin • Cortisol • IGF-1 • TSH, Free T4 • Sex steroids ,DHEAS • FSH, LH • MIH,INSL3,PSA
Laboratory assessment • Karyotype • Bone age • Brain imaging for HH or hyperprolactinemia • pelvic ultrasound • urinary pH,SG • urea nitrogen, creatinine
Management • Girls • low dose estrogen therapy started at 13 years or bone age >11 years • Continue 3- to 4-month in CDP
Management • 0.3mg of conjugated estrogens every other day • 5ug of ethinyl estradiol daily • 0.025 mg transdermal estrogen twice weekly
Management If permanent HH Estrogen can be increased every 6 to 12 months in order to reach full replacement doses after two to three years of therapy
Management During 2-3 years • Daily doses of 0.6 - 1.25mg of conjugated estrogen or 10 -20ug ethinylestradiol are accepted as full replacement doses • Cyclical progesterone 5 to 10mg of daily for 12 days can be added every month to induce monthly menstrual bleeding
Management • Boys • The initial dosage should be low to avoid priapism and rapid pubertal development • Dose should be adjusted based on • intellectual maturation, and psychological needs • Response, age, social
Treatment If skeletal age is immature • Risk of accelerating BA, short adult height If it is started at pubertal bone age 12-13 • No detrimental effect on adult height • leads to somatic and genital growth
Treatment In boys of age 14 Testosterone Dose • 50 to 100mg IM every four weeks • Three to six months Oxandrolone 2.5mg/day
Management After a few months Treatment should be stopped for Differentiation temporary from permanent Then Testosterone level to determine for endogenous androgen production.
Management • Testosterone <50 ng/dl • Give another course After a few months Treatment should be stopped for Differentiation temporary from permanent • Given 1-2 course
Management • If testosterone remain low→Gona • Continue treatment with androgen • Dosages gradually increase to full replacement after three to four years • 100 mg/wk, 200 mg/ two wk or 300mg three week intervals
Management • The skin gel preparation 50, 75, or 100 mg Absorption over a 24-hours • Recommended sites are the shoulders, upper arms and abdomen
Management • Testosterone >50 ng/dl →CDP • Treatment should be stop • To assess progression of puberty Hypothalamic-pituitary-testicular function can be assumed if • Testosterone > 275 ng/dl • Testicular examination is normal
Management Bone age • 12 to 13 years in girls • 13 or 14 years in boys • patients with CDP usually continue pubertal development • patients with gonadotropin deficiency do not progress and may regress.
Management when fertility is desired • Biosynthetic LH and FSH administration is utilized • Episodic administration of LHRH • Portable pumps to administer LHRH in episodic fashion over prolonged periods
Case History • 15yr old boy • Shortest in his class • No problem at school • Always a small boy • No chronic disease • Father didn’t grow till he entered college
Case physical • No dysmorphic features • CVS, Resp, Abd Exam normal • Normal development • Ht= 135cm • Wt= 30kg • U/l = near one • Testicular volume =2.5ml
Case physical • Testicular length = 1.5cm • Penis = 4cm • Normal Testicular consistency • No gynecomastia • Arm span – height span= 2cm • GV =5cm/yr • PH=1
Hormonal and biochemical studies • Normal BUN /ESR • Normal T4 &TSH • Low IGF1& IGFBP3 for age • Normal IGF1& IGFBP3 for BA • Decreased FSH& LH
Hormonal and biochemical studies • Testosterone= 0/15ng / ml • Celiac test= ok • Cortisol levels = ok • LHRH shows not yet in puberty • Normal prolactin