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Dr / mazen al-harbi
Dept of Clinincal
Biochemistry
College of Medicine,
jeddah
Male hypogonadism
Definition
 A decrease in either of the two major functions
of the testes:
 sperm production
 testosterone production
Male Hypogonadism
 Primary hypogonadism
 Testes
 Serum Testosterone↓, FSH & LH ↑
 Secondary hypogodism
 Pituitary gland or Hypothalamus
 Serum Testosterone↓, FSH & LH ↔ , ↓
Male hypogonadism: Onset
 Prepubertal onset: Eunuchoidism
 Lack of adult male hair distribution
 Sparse axillary, pubic hair
 Lack of temporal hair recession
 High-pitched voice
 Infantile genitalia
 Small penis, testes and scrotum
 ↑ fat deposition in pectoral, hip, thigh and
lower abdomen
 Eunuchoidal proportion
 Arm span > Height > 5 cm
 Upper/ lower segment ratio < 1
Primary hypogonadism:
Cause
 Prepubertal onset
 Klinefelter's syndrome
 Other chromosomal abnormalities
 Mutation in the FSH and LH receptor genes
 Cryptorchidism
 Disorders of androgen biosynthesis
 Myotonic dystrophy
 Congenital anorchia
 Varicocele
Klinefelter's syndrome
 Most common congenital abnormality causing
primary hypogonadism
 Male who has an extra X chromosome
 Genotype
 47,XXY (most common)
 48,XXXY
 46,XY/46,XXY mosaicism
 46,XX
Klinefelter's syndrome
 Postpubertal onset
 Loss of libido
 Impotence
 Infertility
Male hypogonadism: Onset
 Postpubertal onset
 Infections — Mumps orchitis
 Radiation
 Drugs
 Trauma
 Bilateral orchiectomy
 Autoimmune damage
 Chronic systemic diseases
 Cirrhosis
 Chronic renal failure
 HIV
Primary hypogonadism:
Cause
Drugs: 1° hypogonadism
 ↓ Leydig cell production of testosterone
 Corticosteroids, ethanol, ketoconazole
 ↓ Androgen receptor blockers
 Spironolactone, flutamide, cimetidine
Secondary hypogonadism:
Cause
 Prepubertal onset
 hypogonadotropic hypogonadism e.g. Kallmann's
syndrome
 Postpubertal onset
 Sella or suprasellar tumor
 Infection: meningitis
 Trauma
 Critical illness: surgery, MI, head trauma
 Chronic systemic illness : cirrhosis, CKD, HIV
 Drugs
Secondary hypogonadism:
Cause
 Serum testosterone : 8.00 AM
 Free testosterone: Equilibrium dialysis
 Bioavailable testosterone
 Total testosterone
 Serum SHBG
 Serum FSH,LH
 Semen analysis
 Others
 Peripheral leukocyte karyotype
 Other pituitary hormones
 Serum prolactin
 Iron saturation
 MRI brain
Investigation
Hx + PE
Morning Total T Normal T
Low T (< 300 ng/dL)
Exclude reversible illness, drugs, nutritional deficiency
Repeat T ( use free or bio T, if suspect altered SHBG )
LH + FSH
Confirmed low T
Low T, Low or normal FSH + LH
Secondary hypogonadism
Low T, High FSH + LH
Primary hypogonadism
Normal T, FSH + LH
Follow up

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Male hypogonadism

  • 1. Dr / mazen al-harbi Dept of Clinincal Biochemistry College of Medicine, jeddah Male hypogonadism
  • 2. Definition  A decrease in either of the two major functions of the testes:  sperm production  testosterone production
  • 3. Male Hypogonadism  Primary hypogonadism  Testes  Serum Testosterone↓, FSH & LH ↑  Secondary hypogodism  Pituitary gland or Hypothalamus  Serum Testosterone↓, FSH & LH ↔ , ↓
  • 4. Male hypogonadism: Onset  Prepubertal onset: Eunuchoidism  Lack of adult male hair distribution  Sparse axillary, pubic hair  Lack of temporal hair recession  High-pitched voice  Infantile genitalia  Small penis, testes and scrotum  ↑ fat deposition in pectoral, hip, thigh and lower abdomen  Eunuchoidal proportion  Arm span > Height > 5 cm  Upper/ lower segment ratio < 1
  • 5. Primary hypogonadism: Cause  Prepubertal onset  Klinefelter's syndrome  Other chromosomal abnormalities  Mutation in the FSH and LH receptor genes  Cryptorchidism  Disorders of androgen biosynthesis  Myotonic dystrophy  Congenital anorchia  Varicocele
  • 6. Klinefelter's syndrome  Most common congenital abnormality causing primary hypogonadism  Male who has an extra X chromosome  Genotype  47,XXY (most common)  48,XXXY  46,XY/46,XXY mosaicism  46,XX
  • 8.  Postpubertal onset  Loss of libido  Impotence  Infertility Male hypogonadism: Onset
  • 9.  Postpubertal onset  Infections — Mumps orchitis  Radiation  Drugs  Trauma  Bilateral orchiectomy  Autoimmune damage  Chronic systemic diseases  Cirrhosis  Chronic renal failure  HIV Primary hypogonadism: Cause
  • 10. Drugs: 1° hypogonadism  ↓ Leydig cell production of testosterone  Corticosteroids, ethanol, ketoconazole  ↓ Androgen receptor blockers  Spironolactone, flutamide, cimetidine
  • 11. Secondary hypogonadism: Cause  Prepubertal onset  hypogonadotropic hypogonadism e.g. Kallmann's syndrome
  • 12.  Postpubertal onset  Sella or suprasellar tumor  Infection: meningitis  Trauma  Critical illness: surgery, MI, head trauma  Chronic systemic illness : cirrhosis, CKD, HIV  Drugs Secondary hypogonadism: Cause
  • 13.  Serum testosterone : 8.00 AM  Free testosterone: Equilibrium dialysis  Bioavailable testosterone  Total testosterone  Serum SHBG  Serum FSH,LH  Semen analysis  Others  Peripheral leukocyte karyotype  Other pituitary hormones  Serum prolactin  Iron saturation  MRI brain Investigation
  • 14. Hx + PE Morning Total T Normal T Low T (< 300 ng/dL) Exclude reversible illness, drugs, nutritional deficiency Repeat T ( use free or bio T, if suspect altered SHBG ) LH + FSH Confirmed low T Low T, Low or normal FSH + LH Secondary hypogonadism Low T, High FSH + LH Primary hypogonadism Normal T, FSH + LH Follow up