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Puberty Disorders. Dr. Sarar Mohamed MBBS, FRCPCH(UK), MRCP (UK), MRCPCH(UK), DCH(Ire), CCST(Ire), CPT(Ire), MD Consultant Pediatric Endocrinologist & Metabolic Physician Assistant Professor of Pediatrics King Saud University. Definition of puberty. What is puberty?
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Puberty Disorders Dr. Sarar Mohamed MBBS, FRCPCH(UK), MRCP (UK), MRCPCH(UK), DCH(Ire), CCST(Ire), CPT(Ire), MD Consultant Pediatric Endocrinologist & Metabolic Physician Assistant Professor of Pediatrics King Saud University
Definition of puberty • What is puberty? • It is the transitional period of development during which an individual mature from childhood to physical, psychosocial, sexual & reproductive maturity.
PUBERTY Gonadal maturation with acquisition of secondary sexual characteristics and associated growth spurt FERTILITY AND FINAL HEIGHT
Endocrine Regulation • Negative feedback: • Inhibits GnRH from hypothalamus. • Inhibits anterior pituitary response to GnRH. • Inhibin secretion inhibits anterior pituitary release of FSH. • Female: • Estrogen and progesterone. • Male: • Testosterone. Insert fig. 20.9
Onset of puberty • The age of onset of puberty • Females 8-13 • Males 9-14 • Average age of onset: • GIRLS 10 to 11 years (range 8 to 13 years) • BOYS 11 to 12 years (range 9 to 14 years) • 1st sign of puberty in females is breast development, and testicular enlargement in males. Axiliary and pubic hair follows along with other 2ndary sexual characteristics. • The maximum growth velocity occurs at 12 years. • The age of menarche has decreased over the last 3-4 decades due to improved nutrition, general health & life style. • Menarche marks the attainment of reproductive maturity.
Duration of puberty • The time from onset to completion of puberty • Average 4.2 years • Range 1.5-6 years
Factors That Affect Puberty • Genetics • Race/Ethnicity (blacks before white) • Previous nutrition ,malnourished they go to puberty later. • Subcutaneous fat (overweight reach puberty faster) • Obesity • Increased leptin and estrogen production • Insulin stimulation of ovaries & uterus • Birth weight
Initial signs of puberty • GIRLS – Breast Development • BOYS – Testicular Enlargement • Volume > 3.0 cm³ • Length > 2.5 cm
Growth in puberty • Female enter growth spurt before males because females (around 10 years) enter puberty before males (around 12 years). Insert fig. 20.10
Evaluation of disorder of puberty • CLINICAL ASSESSMENT • History • Behavioural changes • Pubertal staging • Skin examination • Height measurement / Growth velocity • Bone age assessment • Hormone study if needed
Assessment of Puberty • History • Parents • onset of puberty • Menarche • Male Age of first shaving regularly • Parental heights (mid-parental height) • prenatal and perinatal (exposure to exogenous sex steroids in intrauterine period; birth weight; perinatal asphyxia) • Concomitant illnesses, postnatal exposure to sex steroids • Time of first sign of puberty • Thelarche (galactorrhea) development of breast, testicles • Adrenarche/pubarche (body odor, axillary & pubic hair, acne) development of pubic and axillary hair. • Menarche menstruation • Gonadarche
Premature thelarche is different the precocious puberty. Premature thelarche is when there is breast or testicular enlargement before the age of 8 or 9 years in females and males respectively. • In premature thelarche the X-ray images and hormonal levels are normal with no other signs of puberty.
History • Important to include: • Past medical history (history of brain tumor, radiation, chemotherapy, known genetic disorder, chronic disease affecting growth) • Eating habits • Any evidence of disordered eating • Activity level • Is exercise excessive or is this an athlete with a high level of training • Growth history • Previous growth chart can be extremely helpful
History • Review of Systems • CNS: visual changes/visual field abnormalities, headaches, anosmia • Cardiac: congenital anomaly • Respiratory: asthma • Renal: • GI: diarrhea, blood in stools
Physical Examination • Examination of Growth • Height • Weight • Pubertal Assessment (Tanner staging) • Axillary hair • Pubic hair & staging • Breast development & staging • Genital development & staging • skin, hair, thyroid • Neurological assessment
Staging of pubertal development in girls (Tanner) B 1-5, Pu 1-5, A 1-5. (B2 – first sign of female puberty)
Staging of pubertal development in bpys (Tanner) G1-5, Pu 1-5, A 1-5, testicular volum > 4 ml – first sign of male puberty
Its used to measure the testicular size and development. Prader orchidometer along with tanner staging is used to asses puberty in males.
Diagnostic evaluation • Laboratory • gonadotropins (FSH, LH) basal and peak after LHRH stimulation (prepubertal LH/FSH<1) • estradiol • testosteron (basal value and value after LH stimulation) • adrenal androgens (17-OHP, A-dion,...) and ACTH • bone age by hand X-ray. • Pelvic US (ovarian and uterine size) • CT or MRI of adrenals, Brain to exclude tumors. • Vaginoscopy • Genetic – karyotype, DNA analysis
Bone age 2 yrs 6 m. 10 yrs 12 yrs
Summary:Variants of puberty • Premature thelarché • Only premature breast development, with normal hormones. • exclude the start of precocious puberty! • Premature adrenarché • Only premature axillary and pubic hair, with normal hormones. • exclude simple virilising form of CAH! • Premature menarché • exclude vaginal bleeding due to trauma of vagine or rare ovarian cyst! • Bone age is not accelerated! • FSH and LH levels after LH-RH are normal • Gonadal and adrenal steroid levels are normal • Pelvic and adrenal ultrasonography is normal • Reassurance & f/u
Landmark Case of Precocious Puberty • 5 year old Lina Medina of Peru • Menses onset age 8 months • Breast development age 4 • Advanced bone maturation age 5 • Was evaluated for abdominal tumor due to increasing abdominal size at age 5 • On 5/14/1939 gave birth to a 2.9 kg baby boy
Definition of Precocious Puberty • ONSET OF PUBERTY BEFORE • Females 8 years • Males 9 years • Lawson Wilkins Pediatric Endocrine Society recommended 7 for white girls/ 6 for black • Prevalence • is estimated to be between one in 5,000 to 10,000 children annually in the United States. • They can conceive.
Classification • Central (true), gonadotropin-dependent • Early stimulation of hypothalamic-pituitary-gonadal axis. • Idiopathic. • Peripheral resistance, GnRH independent (precocious pseudopuberty) • The source of sex steroid may be endogenous or exogenous, gonadal or extragonadal, independent of gonadotropins stimulation. • Look for ovarian tumor.
True precocious puberty(central, GnRH dependent) • Idiopatic, constitutional sporadic or familial (common) • CNS abnormalities • Congenital (hydrocephalus, arachnoid cysts, ...) • Acquired pathology (posttraumatic, infections, radiation,.. • Tumors (LH secreting pituitary microadenoma, glioma – may be associated with neurofibromatosis, hamartoma,.. • Reversible forms - space occuping or pressure-associated lesion (abscess, hydrocephalus,...) • Adopted children or children emigrating from developping countries • Improved nutrition, environmental stability and psychosocial support
True precocious puberty(central, gonadotropin-dependent) • Bone age is accelerated • FSH and LH elevation after LH-RH is diagnostic test • (LH/FSH > 2) • LH LH/FSH ratio < 1 Prepubertal • LH LH/FSH ratio > 1 Pubertal • MRI of CNS is necessary to exclude the neoplasia
Treatment of true precocious puberty • Purpose of treatment • To prevent psychosocial distress • To improve final height outcome because growth will stop at that age, resulting in short stature. • Treat the underlying cause • GnRH analogue • Lupron depot ped, leuprolide acetate • Desensitizes the pituitary • Blocks LH and FSH secretion • Prevents continued sexual development for the duration of the treatment • Growth may almost stop while on therapy • ± addition of growth hormone remains controversy
Precocious pseudopuberty in girls(gonadotropin-independent) • McCune - Albright syndrome • Ovarian cysts • Isolated follicular cysts with E2 production. Self-limiting with spontaneousregression • Ovarian tumors • Acceleration of bone age • FSH and LH are low after LH-RH stimulation • Estrogens are elevated
Precocious pseudopuberty in boys(gonadotropin-independent) • Congenital adrenal hyperplasia (CAH) • Undiagnosed or inadequately treated simple virilising form of CAH caused by 21-hydoxylase deficiency. • Neonatal screening. • Testotoxicosis • Activating mutation of LH receptor. AD inheredited. • Tumors • Gonadal (testosterone-secreting Leydig cell tumor) • Adrenal (adenoma, carcinoma) • Exogenous androgens (anabolic steroids – iatrogene, doping) • McCune Albright Syndrome • Acceleration of bone age • FSH and LH are low after LH-RH stimulation • Testicular or adrenal steroids are elevated
Precoccious puberty-treatment • Gonadotropin-dependent PP • Idiopathic • GnRH (LH-RH) analog to block LH-RH receptor of pituitary gland • Organic – tumor or cysts • Surgery • Gonadotropin independent (pseudopuberty) • Treat underline cause • Testicular, ovarian or adrenal tumors –surgery • CAH – substitution of corticosteroids
Delayed puberty - definition • Initial physical changes of puberty are not present • by age 13 years in girls • (or primary amenorhoe at 15.5-16y) • by age 14 years in boys
Types of delayed puberty • Gonadotropin dependent • Hypogonadotropic hypogonadism • Low LH/FSH • Central, chronic disease • Gonadotropin independent • Hypergonadotropic hypogonadism • High LH/FSH • Peripheral cause (gonads)
GnRH or gonadotropin dependent • Idiopathic • sporadic or familial (associated with constitutional growth delay) • Chronic diseases with bone age delay and growth retardation due to different pathophysical mechanismes (malnutrition, anemia, acidosis, hypoxia,...anorexia nervosa, cystic fibrosis, chronic renal insuficiency,..) • Psychosocial deprivation
GnRH or gonadotropin dependent • Hypogonadotropic hypogonadism • Gonadotropin deficiency • LH only (fertile eunuch syndrome) • FSH and LH • Congenital (genetic, syndromes) - Kallman syndrome –mutation of KAL gene, mutation of DAX1 gene, Prader-Willi syndrome ,... • Acquired - cranial irradiation, hemosiderosis, granulomtous disease • Associated with others pituitary hormones deficiencies • Congenital – empty sella syndrome, genetic-transcription factors, disruption of pituitary stalk (breech delivery),... • Acquired – tumors, inflamation, irradiation, trauma....
Kallman Syndrome • A syndrome of isolated gonadotropin deficiency • 1/10,000 males, 1/50,000 females • KAL-1 gene • Present with ANOSMIA or HYPOSMIA • Can also be associated with harelip, cleft palate, and congenital deafness
Syndromes Associated with Pubertal Delay • Prader-Willi syndrome • Laurence Moon syndrome • Septo-optic dysplasia • Bardet-Biedl syndrome
Gonadotropin independent(hypergonadotrophic) Boys • Congenital • Anorchia • Chromosomal abnormalities (Klinefelter syndrome, Noonan syndrome…) • Disorders in androgen synthesis or action • Acquired • Autoimunne inflamation (APS) • Radio or chemotherapy • Traumatic • Surgery
Klinefelter’s Syndrome • 45 XXY most common (2/3) • Tall in childhood, with euchanoid body habitus • More female type fat distribution • puberty is delayed • Small testicles & gynecomastia • 90-100% are infertile
Klinefelter's syndrome (Williams Textbook of Endocrinology, 10th ed, 2003)
Previous photos • A 19-year-old phenotypic male with chromatin-positive seminiferous tubule dysgenesis (Klinefelter's syndrome). • The karyotype was 47,XXY, gonadotropin levels were elevated, and testosterone levels were low normal. • Note normal virilization with long legs and gynecomastia (B, C). The testes were small and firm and measured 1.8 × 0.9 cm. • Testicular biopsy revealed a severe degree of hyalinization of the seminiferous tubules and clumping of Leydig cells. • D, A 48-year-old male with 47,XXY Klinefelter's syndrome with severe leg varicosities.
Gonadotropin independent(hypergonadotrophic hypogonadism) Girls • Congenital • Billateral ovarian torsion • Chromosomal abnormalities (Turner syndrome, pure gonadal dysgenesis, Noonan syndrome…) • Acquired • Autoimunne inflamation (APS) • Radio or chemotherapy • Traumatic • Surgery
Turner syndrome • Karyotype 45,X (60%), (45,X/46,XX, structural abnormalities of X chromosome) • Incidence 1/2000 • Short stature (final height 142-147 cm) • web neck • Gonadal dysgenesis - streak gonad • Autoimmune: Hashimoto’s thyroditis, Addison’s • Mild insulin resistance • Essential hypertension • hearing loss /No mental defect • Impairment of cognitive function: mathematical ability↓ • Visual–motor coordination, spatial-temporal processing↓ • Y chromosome predisposed to gonadoblastoma H. Turner, 1938
Investigation of Delayed Puberty • Investigations depend on clinical presentation, but may include • Bone age • Hormone levels (IGF-1, FSH, LH, estradiol, testosterone, DHEAS, prolactin, TSH) • Karyotype • Hormone stimulation tests • GnRH stimulation test • GH stimulation test • Imaging • MRI brain if gonadotropins low & no obvious cause of hypogonadotropic hypogonadism • US or MRI pelvis
Treatment of delayed Puberty • Treat underline cause • Time of therapy initiation may vary and individualized • Testosterone supplementation • Estrogen for girls