Puberty
Dr Haider Al Shamma’aObjectives
Know the definition of puberty The student should be able to understand and describe the physiology of the pre-puberty and puberty The student able to detect the normal sequence of puberty The student should be able to detect the somatic changes associated with puberty The student can diagnose abnormal puberty ( history , examination )Objectives continue…. Able to request the suitable investigations to diagnose the cause and type of abnormal puberty Can describe the outline of treatment for precocious puberty
Puberty :- is the sequence of events in the transformation of a child into young adult with the development of secondary sexual characteristics and reproductive capability
During this process there are Physical Endocrine Psychological changes a Increased sex steroid hormone
Age of onset 10 – 16 yearsOnset depend on:-Genetic factorsGeographic locationNutritional statusPsychological factors
Endocrinological changes of puberty
The physiology of pre-pubertal period Fetal period Neonatal period Childhood period Late pre-pubertal period Pubertal onsetFetal period
By 20 wks. FSH & LH start to increaseSome ovarian follicular developmentsE2 → -ve feedback →↓FSH & ↓LHMost estrogens from placental origin
New born period
↓↓ estrogen and progesterone (from placental origin) → FSH ↑ & LH ↑At 3 months FSH & LH near adult level but estrogen remain lowFSH & LH gradually reduced reaching lowest level at 4 years of ageChildhood period (4-10 years)
Low estrogenLow FSH & LHSuppression of FSH & LH due to 2 mechanismsIntrinsic central inhibition of hypothalamic GnRH release ( main mechanism)Very sensitive –ve feedback inhibitionLate prepubertal period ( 6-9 years)
Gradual ↑ androgen from zona reticularis of the adrenals ( ↑ DHEA , ↑DHEAS & androstendione ) → pubic and axillary hair growth ( pubarche & adrenarche )Pubertal onset (11 years)
↓sensitivity of the –ve feedback ( ie higher estrogen needed to suppress the pituitary secretion of FSH & LH )Loss of the intrinsic CNS inhibition of GnRH from the hypothalamusAt first nocturnal GnRH secretion then Adult type pulsetile pattern ( every 90-120 min )Pubertal onset (11 years)
↑ovarian follicular developments↑ steroid production ( E2)Development of secondary sexual characteristics By mid – late puberty maturation of the +ve feedback mechanism of E2 on LH release and ovulatory cycle established at 14 -16 yearsSomatic changes
Breast buding ( thelarche) Axillary & pubic hair ( adrenarche ,pubarche) Accelerated linear growth (growth spurt) First menstrual cycle (menarche) Adult shape breast and pubic hairs * Somatic changes takes about 4.5 years average , ( range 1.5 - 6 years )Precocious puberty
Precocious puberty :- the development of any sign of secondary sexual maturation at an age earlier than 2.5 standard deviations below the expected age of puberty 8 years Incidence 1/ 10000 Male / female ratio 1/5 75% of all cases are constitutional idiopathic Typically taller than their peers as children but short as adult due to premature closure of epiphysesClassification of female precocious puberty
Heterosexual precocious puberty (male type puberty) a. virilizing neoplasm (tumors secreting androgens ) ovarian adrenal b. congenital adrenal hyperplasia c. exogenous androgen exposure2. Isosexual precocious puberty:- (female type maturity) A. complete I . true precocious puberty i) idiopathic (constitutional) 90% ii) brain disease 10% II. Pseudo precocious puberty i) ovarian tumor secret estrogen ii) adrenal tumor iii) hypothyroidism in girls* (delayed bone age) iv) exogenous v) McCune –Albright syndrome vi) Peutz-Jegher syndrome (associated with ov.tumor) B. incomplete I . Premature thelarche (breast bud only) II. Premature pubarche ( pubic hair only ) 50% CNS disease III . Premature adrenarche ( axillary hair only )
True precocious puberty
McCune-Albright syndromePolyostotic fibrous dysplasiaMcCune-Albright syndrome
True precocious pubertyThere is activation of the hypothalamus pituitary ovarian axis (like normal adults) Normal sequence of events ( 1st breast bud ,2nd axillary & pubic hair, 3rd accelerated growth, menarche )
Diagnosis of precocious puberty
History:-Similar family historySequence of sexual maturationSpeed of sexual maturationExposure to drug or hormonesCNS (meningitis, encephalitis, abscess, TB, tumor, neurofibromatosis trauma, seizures, headache, blurring of vision, numbness, muscle weakness,… etc.)Physical examination
InvestigationsSkull X ray Serial bone age estimations X ray hands&elbow CT, MRI head sella turcica & hypothalamous U/S , MRI abdomen & pelvis FSH, LH, hCG DEHAS, androsteindione, testosterone, E2, P4 Prolactin Thyroid functon tests GnRH stimulation test EEG Visual field
Treatment of precocious puberty
75% constitutional true precocious puberty The most important problem of untreated girls is short stature (< 150 cm )* due to early closure of epiphysis of long bonesTreatment
GnRH analogues (triptorrilin , decapeptyl )It is similar to GnRH but it is of long action attach to pituitary GnRH receptors permanently and cause stimulation of FSH & LH at first week and then cause down regulation of pituitary receptors ie. Decrease the number of functioning receptors → suppression of the pituitary gland → suppression of ovarian activities.Triptorrilin injection every 28 daysTill reach the determined height by 13-14 years then stop GnRH analogues and the hypothalamo - piuitary – ovarian axis resume normal activities
Treatment of other types of precocious puberty
GnRH analogues are ineffective in cases of pseudo-precocious puberty CNS diseases have unfavorable outcomesTreatment of other types of precocious puberty
Ovarian, adrenal, brain tumors treated surgically Exogenous hormones by remove source McCune-Albright syndrome by antiestrogen (aromatase inhibitor Lotrizole + orthopedic care Hypothyroidism by thyroxine
Precocious thelarche no treatment usually transientPremature pubarche more common in boys 50% CNS disease ………exclude CNS disease …..no treatment Premature adrenarche……exclude adrenal disease …………..no treatment