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♀♀ PATHOPHYSIOLOGYPATHOPHYSIOLOGY
Kashmeera N.A.
II Sem MSc.Zoology
Roll no: 37
Christ college
FEMALE PRECOCIOUS PUBERTY
Precocious pseudopuberty True precocious puberty
Early devpt of 2° sexual
characteristics without
gametogenesis
Caused by abnormal
exposure of immature ♀♀ to
estrogen
Due to early secretion of
gonadotropin from pituitary
Due to hypothalamic
damage
– lesions of ventral
hypothalamus near
infundibulum.
-this lesions interrupt neural
pathways that produce
inhibition of GnRH
Delayed puberty
• Primary amenorrhea – menstrual bleeding never
occured
• Turner’s syndrome [45 XO] – gonadal
dysgenesis
• Testicular feminization/androgen resistance –
• Patients are genetic ♂♂ [46 XY]
• Lack testosterone receptors – insensitivity to androgen –
wolffian structures primordial
• MIS present – mullerian structures absent
• External genitalia ♀,but vagina ends blindly because there is no
♀ internal genitalia
Hypogonadotropic hypogonadism
• Caused by defect in GnRH or LH/FSH
secretion.
• LH & FSH levels are low.
• Gonad is hypofunctional due to decreased
stimulation.
DEFECTS IN OVULATORY
FUNCTION
Ovulatory defects can be classified into three
groups based on the World Health Organization
(WHO) definition.
1. Group I: hypogonadotropic hypogonadism:
• These patients have low LH & FSH levels.
• This category includes women with
hypothalamic amenorrhea (HA), stress-related
amenorrhea etc
2. Group II: eugonadotropic hypogonadism:
 Patients are eugonadotropic ,
normoestrogenic, but anovulatory .
• They exhibit normal FSH and estradiol
levels.
• This category includes women with
polycystic ovary syndrome (PCOS)
3. Group III: hypergonadotropic
hypogonadism:
Caused by defective gonads,resulting in
hypogonadism and high gonadotropin
level (as hypothalamus & pituitary fn
normally)
These patients tend to be amenorrheic
and hypoestrogenic,
category includes all variants of premature
ovarian failure(POF)
Hypothalamic amenorrhea (HA)
• Functional abnormality in GnRH secretion -LH & FSH levels
are low.
• Result in low gonadotropin level & secondary
amenorrhea.
• Common in young women with increased psychological
stress.
• lesions of the hypothalamus or pituitary
gland can lead to hypothalamic
amenorrhea
• Hypothalamic tumors can lead to HA
Polycystic Ovary Syndrome
Polycystic Ovary Syndrome
• It is a disorder of chronic anovulation
leading to increased estrogen production
& infertility.
In ovaries, androgens are produced through
de novo synthesis from cholesterol.
They can be aromatized to estrogens
• Excessive androgen levels may also
directly inhibit follicle development at the
ovarian level,
• Which may result in the accumulation of
multiple small cysts
• within the ovarian cortex, the so-called
polycystic ovary
FEMALE PSEUDOHERMAPHRODITISM
A pseudohermaphrodite is an individual with
genetic constitution and gonads of one sex and
genitalia of the other.
After 13th
week, genitalia are fully formed,but
exposure to androgens cause hypertrophy of the
clitoris
Congenital adrenal virilism
By androgens administered to mother.
Chiari –Frommel syndrome
• Persistence of lactation(galactorrhea) &
amenorrhea in women who donot nurse
after delivery.
• Associated with some genital atrophy
• Due to persistent prolactin secretion
without secretion of FSH & LH necessary
to produce maturation of new follicles &
ovulation.
• Non pregnant ♀ - pituitary tumour -CFS
HORMONES & CANCERHORMONES & CANCER
• About 35% of carcinomas of the breast in
women of childbearing age are estrogen-
dependent.
• Their continued growth depends upon the
presence of estrogen in the circulation.
• Women with estrogen dependent tumours
often have a remission when their ovaries
are removed.
• There is also some evidence that growth
hormone & prolactin stimulate the growth
of breast carcinomas.
Pathophysiology   kashmeera

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Pathophysiology kashmeera

  • 1. ♀♀ PATHOPHYSIOLOGYPATHOPHYSIOLOGY Kashmeera N.A. II Sem MSc.Zoology Roll no: 37 Christ college
  • 2. FEMALE PRECOCIOUS PUBERTY Precocious pseudopuberty True precocious puberty Early devpt of 2° sexual characteristics without gametogenesis Caused by abnormal exposure of immature ♀♀ to estrogen Due to early secretion of gonadotropin from pituitary Due to hypothalamic damage – lesions of ventral hypothalamus near infundibulum. -this lesions interrupt neural pathways that produce inhibition of GnRH
  • 3. Delayed puberty • Primary amenorrhea – menstrual bleeding never occured • Turner’s syndrome [45 XO] – gonadal dysgenesis • Testicular feminization/androgen resistance – • Patients are genetic ♂♂ [46 XY] • Lack testosterone receptors – insensitivity to androgen – wolffian structures primordial • MIS present – mullerian structures absent • External genitalia ♀,but vagina ends blindly because there is no ♀ internal genitalia
  • 4. Hypogonadotropic hypogonadism • Caused by defect in GnRH or LH/FSH secretion. • LH & FSH levels are low. • Gonad is hypofunctional due to decreased stimulation.
  • 5. DEFECTS IN OVULATORY FUNCTION Ovulatory defects can be classified into three groups based on the World Health Organization (WHO) definition. 1. Group I: hypogonadotropic hypogonadism: • These patients have low LH & FSH levels. • This category includes women with hypothalamic amenorrhea (HA), stress-related amenorrhea etc
  • 6. 2. Group II: eugonadotropic hypogonadism:  Patients are eugonadotropic , normoestrogenic, but anovulatory . • They exhibit normal FSH and estradiol levels. • This category includes women with polycystic ovary syndrome (PCOS)
  • 7. 3. Group III: hypergonadotropic hypogonadism: Caused by defective gonads,resulting in hypogonadism and high gonadotropin level (as hypothalamus & pituitary fn normally) These patients tend to be amenorrheic and hypoestrogenic, category includes all variants of premature ovarian failure(POF)
  • 8. Hypothalamic amenorrhea (HA) • Functional abnormality in GnRH secretion -LH & FSH levels are low. • Result in low gonadotropin level & secondary amenorrhea. • Common in young women with increased psychological stress.
  • 9. • lesions of the hypothalamus or pituitary gland can lead to hypothalamic amenorrhea • Hypothalamic tumors can lead to HA
  • 11. Polycystic Ovary Syndrome • It is a disorder of chronic anovulation leading to increased estrogen production & infertility. In ovaries, androgens are produced through de novo synthesis from cholesterol. They can be aromatized to estrogens
  • 12. • Excessive androgen levels may also directly inhibit follicle development at the ovarian level, • Which may result in the accumulation of multiple small cysts • within the ovarian cortex, the so-called polycystic ovary
  • 13. FEMALE PSEUDOHERMAPHRODITISM A pseudohermaphrodite is an individual with genetic constitution and gonads of one sex and genitalia of the other. After 13th week, genitalia are fully formed,but exposure to androgens cause hypertrophy of the clitoris Congenital adrenal virilism By androgens administered to mother.
  • 14. Chiari –Frommel syndrome • Persistence of lactation(galactorrhea) & amenorrhea in women who donot nurse after delivery. • Associated with some genital atrophy • Due to persistent prolactin secretion without secretion of FSH & LH necessary to produce maturation of new follicles & ovulation. • Non pregnant ♀ - pituitary tumour -CFS
  • 15. HORMONES & CANCERHORMONES & CANCER • About 35% of carcinomas of the breast in women of childbearing age are estrogen- dependent. • Their continued growth depends upon the presence of estrogen in the circulation.
  • 16. • Women with estrogen dependent tumours often have a remission when their ovaries are removed. • There is also some evidence that growth hormone & prolactin stimulate the growth of breast carcinomas.