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ASSESSMENT OF A CASE OF AMENORRHEA

ASSESSMENT OF A CASE OF AMENORRHEA. Prof. Ashis Kumar Mukhopadhyay Professor, G & O Medical Superintendent-cum-Vice Principal CSS College of Obstetrics & Gynaecology, Kolkata National Chairperson, Medical Education Committee of FOGSI. AMENORRHEA.

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ASSESSMENT OF A CASE OF AMENORRHEA

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  1. ASSESSMENT OF A CASE OF AMENORRHEA

  2. Prof. Ashis Kumar Mukhopadhyay Professor, G & O Medical Superintendent-cum-Vice Principal CSS College of Obstetrics & Gynaecology, Kolkata National Chairperson, Medical Education Committee of FOGSI

  3. AMENORRHEA • Amenorrhea is the absence or abnormal cessation of the menses. A patient is diagnosed with primary amenorrhea if she has not reached menarche by age 14 without the appearance of secondary sex characterististics and by the age 16 with secondary sex characteristics. • She meets the criteria for secondary amenorrhea if established menses have ceased for longer than 6 months or at least 3 of the previous cycle intervals.

  4. Types Physiological Pathological Primary --Before puberty Secondary pregnancy Lactation Menopause Real (True) Concealed (Cryptomenorrhoea) Primary Secondary Acquired Congenital

  5. Five basic factors for normal menstruation • Normal female chromosome 46 XX • Co-ordination of H-P-O axis • Responsive Endometrium • Patent outflow tract • Ancillary glands like Thyroid and Adrenal

  6. Causes Disorders of H-P-O axis HypogonadotropicHypogonadism Constitutional delayed puberty Kallman’s syndrome CNS tomours like craniopharyngioma Isolated FSH deficiency HypergonadotropicHypogonadism Primary Ovarian Failure 17-alpha Hydroxylase deficiency Gonadaldysgenesis

  7. Causes Abnormal chromosomal pattern • Turner’s syndrome (45XO) • Mosaicism 45 X/ 46 XX • Pure Gonadal dysgenesis (46 XX or 46 XY) • Androgen Insensitivity Syndrome • Partial deletion of X chromosome:- Deletion of long arm (Xq-)  Streak Gonads but no somatic abnormalities Deletion of short arm (Xp-) Somatic features like Turner’s

  8. Causes Developmental defect of Genital tract • Imperforate Hymen • Transverse Vaginal Septum • Atresia of upper 1/3rd. Of vagina • Complete absence of vagina • Absent Uterus Dysfunction of Thyroid and Adrenal Cortex • Adrenogenital syndrome • Cretinism

  9. Causes Metabolic disorders Juvenile DM Systemic illness Malnutrition Anaemia Wt. Loss Tuberculosis Unresponsive Endometrium Congenital Synaechiae (rare)

  10. Etiology of Amenorrhea Primary • Gonadal failure (43%)  • Congenital absence of uterus and vagina (15%)  • Constitutional delay (14%) Secondary • Chronic anovulation (39%) •  Hypothyroidism / hyperprolactinemia(20%)  • Weight loss/anorexia(16%)

  11. THE ASSESSMENT

  12. Primary amenorrhea breasts have developed vagina yes no no Pubic hair the (MPA) challenge yes no - + • congenital uterovaginal agenesis imperforate hymen complete transverse vaginal septum complete androgen insensitivity syndrome (CAIS) FSH Level Estrogenized high low Chromosome Analysis abnormal ovaries abnormal hormonal stimulation of normal ovaries

  13. Secondary Amenorrhea

  14. Incidence 1% of women of reproductive age.

  15. The most common cause of secondary amenorrhea in reproductive age women ispregnancyand this should always be excluded by physical exam and laboratory testing for the pregnancy hormone - HCG.

  16. History A good history can reveal the etiologic diagnosis in up to 85% of cases of amenorrhea.

  17. History Galactorrhoea Hot flashes, breast atrophy and decreased libido Certain medications A large amount of weight loss or gain Anorexia nervosa Cushing's disease  and hypothyroidism Sheehan's syndrome. Asherman's syndrome Amenorrhoea following cervical conization Following discontinuation of oral contraception Psychological dysfunction or emotional stress Family history of apparent genetic anomalies

  18. Physical examination • Height, Weight and nutrition • Growth and development • Signs of androgen excess • Endocrinal stigma • The breast exam may reveal galactorrhoea • Estrogen deficiency may be suggested on pelvic exam by a smooth vagina that lacks the normal rugae (wrinkles) and a dry endocervix with no mucous. • Size of pelvic organs.

  19. What we will do next?

  20. If the history and physical exam are suggestive of a certain etiology : • for the sake of efficiency and cost-effectiveness, the workup can sometimes be more directed. ( in 85% of cases .)

  21. Some patients will not demonstrate any obvious etiology for their amenorrhea on history and physical exam. These patients can be worked up in a logical manner using a stepwise approach.

  22. The first tests to perform after pregnancy is ruled out are : • a progesterone withdrawal test • TSH (thyroid stimulating hormone) • prolactin level.

  23. -VE Preg.test TSH ,PROLACTIN’, Prog.challenge test without withdrawal bleeding withdrawal bleeding compromised outflow tract. hypoestrogenic +ve.est,progest.challenge test anovulation -ve.est, progest. challenge test 2wk FSH>30-40 FSH norm. Normal FSH Repeat+serum ,est.level repeat HSG OR hysteroscopyasherman hypothalamic-pituitary failure PROF

  24. -VE Preg.test TSH ,PROLACTIN’, Prog.challenge test without withdrawal bleeding withdrawal bleeding compromised outflow tract. hypoestrogenic +ve.est,progest.challenge test anovulation -ve.est,progest .challenge test 2wk FSH>30-40 FSH norm. Normal FSH Repeat+serum ,est.level repeat HSG OR hysteroscopyasherman hypothalamic-pituitary failure PROF

  25. Ovarian failure (premature menopause) chromosomal anomalies autoimmune disease If the woman is under 30, a karyotype should be performed to rule out any mosaicism involving a Y chromosome. it is prudent to screen for thyroid, parathyroid, and adrenal dysfunction Laboratory evidence of autoimmune phenomenon is much more prevalent than clinically significant disease If a Y chromosome is found the gonads should be surgically excised.

  26. Autoimmune Related Dysfunction • The most common association is with thyroid disease, but the parathyroids and adrenals can also be affected. • Several studies have shown laboratory evidence of immune problems in about 15-40% of women with premature ovarian failure. • In general, ovarian biopsy is not indicated in patients with premature ovarian failure since no clinically useful information will be obtained.

  27. Hypothalamic-pituitary failure • Patients who do not bleed after the progestin challenge but do after estrogen/progestin and have normal or low FSH and LH levels

  28. Hypothalamic-pituitary failure • Some medications (e.g. phenothiazines) as well as extremes of weight loss, stress or exercise can cause this type of secondary amenorrhea. • A pituitary or hypothalamic tumor would be a rare finding in these patients who were all screened with prolactin levels at the beginning of the diagnostic evaluation. • However, if there is no cause apparent from the history, it would be prudent to obtain a baseline CT (or MRI) evaluation of the sellar region to rule out a space occupying lesion.

  29. Hypothalamic-pituitary failure • Patients with normal prolactin levels and normal imaging studies have hypothalamic amenorrhea of uncertain etiology. • If the amenorrhea and lack of withdrawal bleeding persists, prolactin levels should be measured annually since a small microadenoma could be present that is escaping laboratory and radiographic detection.

  30. Hypothalamic-pituitary failure • In this condition, as well as in the other hypothalamic amenorrhea situations, the patients can be significantly hypo estrogenic (a low estrogen situation similar to menopause). If the state is persistent, hormone replacement therapy should be considered for protection against osteoporosis. One approach is to get an estradiol level and if it is less than 30 pg/ml, counsel the patient that hormonal replacement therapy is indicated

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