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%
Definition
Precocious Puberty
Girls
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]
Boys
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
Symptoms
Hypothyroidism
or
Hyperthyroidism
symptoms
Abdominal Pain
(malignancy)
Vaginal Bleeding
Genital
Trauma
or sexual abuse
McCune-Albright Syndrome
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)
Follicle Stimulating Hormone
(FSH)
Luteinizing Hormone
(LH)
Estradiol
Level (in girls)
Testosterone Level
(in boys)
Thyroid Stimulating Hormone
(TSH)
Serum
Human Chorionic Gonadotropin
(HCG)
Screen for gonadotropin
Secretin
g tumor
Consider
GnRH Stimulation Test
See additional evaluation for Step 2c below
17-Hydroxyprogesterone
Serum Dehydroepiandrosterone
(
Serum DHEA
)
Imaging (See Evaluation below)
Left wrist radiograph for
Bone Age
Consider
Head MRI
Screen for pituitary or other
CNS Lesion
See additional evaluation for Step 2c below
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
Findings
Early, but normal
Puberty
Girls:
Breast
s enlarge early
Boys:
Testicle
s enlarge early
Bone Age
exceeds
Chronological age
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
Findings
Early, but normal
Puberty
Bone Age
consistent with
Chronological age
Diagnosis:
Benign Premature Adrenarche
Girls
Benign Premature Thelarche
Glandular
Breast
tissue
Benign premature
Menarche
Prepubertal
Vaginal Bleeding
Benign Premature Adrenarche
Pubic and axillary hair, body odor or acne
Distinguish from
Congenital Adrenal Hyperplasia
,
Cortisol
excess, adrenal tumor (see step 2c)
Fatty
Breast
tissue (
Lipoma
stia)
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
)
Further evaluation
Observation over 3-6 months
Consider further laboratory testing for progressive symptoms (see diagnostics above and to 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
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)
17-Hydroxyprogesterone
Serum Dehydroepiandrosterone
(
Serum DHEA
)
Additional imaging (suspect peripheral cause)
Pelvic
Ultrasound
of Ovaries
Consider Adrenal MRI
Management
Assess for exogenous sex steroid exposure
Treat based on underlying cause
References
Blondell (1999) Am Fam Physician 60:209-24 [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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