Sex
Precocious Puberty
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Precocious Puberty
, Premature Sexual Development
See Also
Precocious Puberty Causes
Benign Premature Adrenarche
Benign Premature Thelarche
Sexual Development
Male Tanner Stage
Female Tanner Stage
Epidemiology
Girls: Benign central cause in 50 to 90%
Boys: Pathologic peripheral cause in 50%
Definitions
Precocious Puberty
Female Precocious Puberty
Secondary sexual characteristics before age 8 years in girls
Breast
gland development
Abnormal if before age 7-8 years
Most will have onset after age 8 years, but occurs age 7-8 years in 20% of black, 5-10% of white girls
Early
Breast
gland development (at age 7-8 years) also occurs with
Obesity
Menarche
before age 10 years
Pubic
Hair
(modified 1999)
White: Before age 7 years
Black: Before age 6 years
Referral recommended if 2 signs at age <8 years
References
Kaplowitz (1999) Pediatrics 104:936-41 [PubMed]
Midyett (2003) Pediatrics 111:47-51 [PubMed]
Male Precocious Puberty
Testes
> 2.5 cm (>3 ml vol) before age 9 years
Pubic hair before age 9 years
History
Timing of secondary sexual characteristics
Body odor
Breast
Development or
Testicular Development
Pubic and axillary hair
Acne
Exposures
Exogenous sex steroids
Head Trauma
Radiation Therapy
or exposure
Other history
Family History
of Precocious Puberty
Brain malignancy
Meningoencephalitis
Cranial radiation
Cranial surgery
Head Trauma
Symptoms
Hypothyroidism
or
Hyperthyroidism
symptoms
Abdominal Pain
(malignancy)
Vaginal Bleeding
Genital
Trauma
or sexual abuse
McCune-Albright Syndrome
Neurologic Symptoms
Headache
Seizure
Vision
change
Exam
Constitutional
Plot height, weight and
Body Mass Index
on growth curves
Calculate
Growth Velocity
Calculate
Midparental Height
Compare
Midparental Height
with projected height from growth curve
Abnormal if difference >10 cm
Findings
Body mass increased (associated with Precocious Puberty)
Pubertal growth spurt (greater than the 5 cm basal rate)
Short Stature
(
Thyroid
disease)
Head and Neck
Thyromegaly
Genitourinary
Sexual maturity staging (Tanner Stage)
Asymmetric
Testes
(gonadal mass)
Clitoromegaly (
Hyperandrogenism
)
Vagina
Dull pink instead of red due to
Estrogen
exposure
Neurologic
Focal neurologic deficits (intracranial lesion)
Skin
Hirsutism
Hyperandrogenism
(androgen-
Secretin
g tumor,
Congenital Adrenal Hyperplasia
)
Cafe Au Lait
spots
McCune-Albright Syndrome
Neurofibromatosis
Findings
Red Flags suggesting pathologic cause
Premature
Puberty
in very young children
Contrasexual development
Feminization in boys
Virilization
in girls
Peripheral cause (often asynchronous development)
Penis
enlarges without scrotal enlargement
Extensive pubic
Hair Growth
Menarche
without
Breast
bud development in girls
Precocious Puberty in boys (50% pathologic)
Visual Field Deficit
suggests pituitary mass
Causes
See
Precocious Puberty Causes
Labs (See Evaluation below)
Labs may not needed for early
Puberty
in age >6 years (esp. without red flags and consistent with normal variation)
First-line early morning labs
Follicle Stimulating Hormone
(FSH)
Luteinizing Hormone
(LH)
Estradiol
Level (in girls)
Total Testosterone
Level (in boys)
Thyroid Stimulating Hormone
(TSH)
Other testing if indicated
Serum
Human Chorionic Gonadotropin
(HCG)
Screen for gonadotropin
Secretin
g tumor in males
Consider
GnRH Stimulation Test
Hyperandrogenism
or
Virilization
signs or symptoms (see additional evaluation for Step 2c below)
Total Testosterone
17-Hydroxyprogesterone
Serum Dehydroepiandrosterone
(
Serum DHEA
)
Imaging (See Evaluation below)
See additional evaluation for Step 2c below
Left hand
Bone Age Film
Head MRI
contrast enhanced (including sella turcica)
Screen for pituitary or other
CNS Lesion
Indications
Focal neurologic deficits,
Headache
,
Seizure
,
Vision
change or
Polyuria
, polydipsia
Central Precocious Puberty (female age <6 years, male age <9 years)
Abdominal Imaging (MRI or
Ultrasound
)
Indicated in elevated
Estradiol
levels
Indicated in
Hyperandrogenism
or
Virilization
Indicated in elevated
Serum DHEA
, 17-Hydroxyprogesterone or
Total Testosterone
in girls
Testicular Ultrasound
Indicated in asymmetric
Testes
Evaluation
Step 1 - Initial Evaluation
Clinical history and physical
Exogenous Sex
Hormone
sources
Androgens and
Anabolic Steroid
s in boys
Oral Contraceptive
use in girls
Estrogen
or placental containing hair products
Common use in African American girls
Associated with
Breast
or pubic hair development
Evaluate
Pubertal Milestone
s (See
Tanner Staging
)
Evaluate growth chart
Obtain Left
Wrist XRay
for
Bone Age
Evaluation
Step 2a - Unremarkable Evaluation in Step 1 (Constitutional or Idiopathic Precocious Puberty)
Findings
Early, but normal
Puberty
Girls:
Breast
s enlarge early
Boys:
Testicle
s enlarge early
Bone Age
is GREATER than
Chronological Age
(key distinction from step 2b below)
Early growth spurt and initially taller than peers
Early epiphyseal closure and short in adulthood
Diagnosis
Constitutional or Idiopathic Precocious Puberty
Further evaluation
Observation
Consider further diagnostic testing (see above)
All labs at pubertal levels
All imaging studies normal
Management
Counseling and reassurance
Consider
GnRH
analog to suppress FSH and LH
Leuprolide
(
Lupron
) long acting injectable
Nafarelin (
Synarel
) short acting intranasal
Evaluation
Step 2b - Normal Variation in Step 1 (Benign Variations of Early
Puberty
)
Findings
Early, but normal
Puberty
Bone Age
consistent with
Chronological Age
Diagnosis: Common Benign Variations of Early
Puberty
Girls
Fatty
Breast
tissue (
Lipoma
stia)
Benign Premature Thelarche
Glandular
Breast
tissue
Indications to refer to pediatric endocrinology (based on serial exams every 3-6 months)
Progressive
Breast
development
See general referral indications below
Benign premature
Menarche
Prepubertal
Vaginal Bleeding
Evaluate for secondary causes
Hypothyroidism
McCune-Albright Syndrome
Genital
Trauma
Vaginal foreign body
Pelvic mass
Vaginal or Pelvic infection
Consider pediatric endocrinology referral for
Menorrhagia
, continuous or recurrent bleeding
Benign Premature Adrenarche
Pubic and axillary hair, body odor or acne
Distinguish from
Congenital Adrenal Hyperplasia
,
Cortisol
excess, adrenal tumor (see step 2c)
Indications for pediatric endocrinology
Pathologic adrenal causes suspected (esp. age <6 years)
Virilization
See general referral indications below
Boys
Benign Gynecomastia of Adolescence
Familial Gynecomastia
Consider evaluation for alternative causes of persistent
Gynecomastia
for >18-24 months
Testicular Cancer
Adrenal Adenoma
Performance enhancing drugs
Hypogonadism
(e.g.
Klinefelter Syndrome
)
Infants
Isolated Pubic
Hair
in Infancy
Evaluate for exgenous exposure to
Hormone
s (
Testosterone
gel,
Estrogen Cream
s)
Evaluate for endocrine disruptors (e.g.
Pesticide
s, BPA, phthalates, flame retardants)
Evaluate for red flag findings (e.g. other signs of
Puberty
)
Isolated pubic hair of infancy typically resolves by age 6-24 months
Minipuberty of infancy
Transient activation of hypothalamic-pituitary axis after birth
Onset day of life 1 week with peak at 2-3 months of age
Resolves by age 6 months in males and 2-4 years in females
Transient elevation of sex
Hormone
s (
Estradiol
,
Testosterone
)
Acne
Males with mild, self-limited
Penile Growth
Females with small
Breast
development, uterine enlargement or
Vaginal Bleeding
Evaluation
Benign and resolves without treatment
Evaluate for other associated abnormalities suggesting endocrinopathy
Consider labs (FSH, LH and sex
Hormone
s)
Further evaluation
Observation over 3-6 months
Gene
ral pediatric endocrinology referral indications (in addition to specific indications above)
Associated other signs of pubertal development
Increased
Growth Velocity
Advanced
Bone Age
Consider further laboratory testing and pediatric endocrinology referral for progressive symptoms
See diagnostics above and Step 2c below
Management
Counseling and reassurance
Evaluation
Step 2c - Abnormal Evaluation in Step 1
Findings
Abnormal
Pubertal Milestone
sequence
Bone Age
variable
May be consistent with
Chronological Age
Differential Diagnosis (pathologic cause suspected)
See
Precocious Puberty Causes
Central Precocious Puberty due to idiopathic or
CNS Lesion
(pubertal LH and gonad size)
Features
Despite Precocious Puberty, otherwise normal development
More common in girls than boys (by 10 fold)
Typically idiopathic in girls, but more likely to be pathologic in boys (e.g.
Head Trauma
,
Brain Tumor
)
Consider
Gonadotropin Releasing Hormone
(
GnRH
) therapy (e.g.
Lupron
)
Early initiation before epiphyseal closure preserves height potential
Brain MRI
indications
Boys with Precocious Puberty (age <9 years)
Girls under age 6 years old
Neurologic findings (
Headache
,
Seizure
,
Vision
changes)
Peripheral Precocious Puberty (prepubertal LH and gonad size)
Congenital Adrenal Hyperplasia
,
Cortisol
excess, adrenal tumor
Consider
Corticotropin Stimulation Test
, adrenal imaging,
Cushing Syndrome
Endocrinology referral
Exogenous sex steroid exposure
Hypothyroidism
Ovarian tumor
Elevated
Estradiol
level and low LH level seen with
Estrogen
-
Secretin
g tumors
Testicular Tumor
McCune-Albright Syndrome
Neurofibromatosis
Further evaluation
Further laboratory testing (see above)
Additional lab testing (esp.
Virilization
, hyperandrogenic effects in girls)
Total Testosterone
17-Hydroxyprogesterone
Serum Dehydroepiandrosterone
(
Serum DHEA
)
Additional imaging (suspect peripheral cause)
Pelvic
Ultrasound
of Ovaries
Consider MRI
Abdomen
and
Pelvis
(including adrenal MRI)
Management
Assess for exogenous sex steroid exposure
Treat based on underlying cause
References
Blondell (1999) Am Fam Physician 60:209-24 [PubMed]
Brown (2025) Am Fam Physician 112(5): 513-21 [PubMed]
Fahmy (2000) Br J Radiol 73(869):560-7 [PubMed]
Foster (1992) Obstet Gynecol Clin North Am 19:59-70 [PubMed]
Klein (2017) Am Fam Physician 96(9): 590-99 [PubMed]
Styne (1997) Pediatr Clin North Am 44(2):505-29 [PubMed]
Tiwary (1998) Clin Pediatr 37(12):733-9 [PubMed]
Walvoord (1999) Pediatrics 104(4):1010-4 [PubMed]
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