First principle: localise the lesion on one axis
Nearly every reproductive complaint is a disturbance of a single control loop:
Whatever the presentation — amenorrhoea, infertility, hirsutism, abnormal bleeding — the discipline is the same: decide which level is failing. A single test does most of the localising, because the pituitary reports on the ovary for you.
The move that localises: read the gonadotropins
When estrogen is low, FSH tells you where the problem is:
| FSH / LH | Interpretation | The lesion is… |
|---|---|---|
| High | hypergonadotropic hypogonadism | the ovary (it can't respond) |
| Low / inappropriately normal | hypogonadotropic hypogonadism | hypothalamus / pituitary |
The ovary failing means the pituitary shouts louder (FSH up). A silent brain means the pituitary never shouts (FSH down). This one idea recurs in menopause, amenorrhoea and infertility.
Reasoning workflow
- Anchor in time & safety: could she be pregnant? Is anything an emergency (ectopic, torsion, sepsis)? 🚩
- Localise the level using history + FSH/estradiol ± prolactin/TSH.
- Ask about structure only when the endocrine picture doesn't explain it (outflow obstruction, Müllerian anomaly, Asherman).
- Treat the level, framed by the patient's goal (symptom relief vs fertility vs cancer risk).
Pitfalls
- Reaching for imaging or karyotype before the two free questions — pregnant? and where on the axis?
- Treating a number instead of a patient (an ultrasound finding is not a syndrome).
Pearls
- 🎯 FSH is the localiser. High = ovarian; low = central. Commit this before anything else.
- 🩺 In any woman of reproductive age with pelvic pain or amenorrhoea, the first test is a pregnancy test — reflex, not optional.
Next → Before the axis can run, the body must become female — reasoning from SRY to phenotype (Concept 2).