This skill guides clinicians to confirm that anatomic or organic causes of amenorrhea have been ruled out before labeling the condition as functional hypothalamic amenorrhea. Triggers include statements such as “We need to exclude organic causes first” or “Before calling it FHA, let’s get an MRI and prolactin level.”
Scanned 9/9/2026
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---
name: endo-fha-diagnosis-exclude-organic
description: This skill guides clinicians to confirm that anatomic or organic causes of amenorrhea have been ruled out before labeling the condition as functional hypothalamic amenorrhea. Triggers include statements such as “We need to exclude organic causes first” or “Before calling it FHA, let’s get an MRI and prolactin level.”
---
# Exclude organic pathology before diagnosing FHA
## STEP 1 — Gather Information
Obtain a detailed personal history focusing on diet, eating disorders, exercise intensity, attitudes, weight fluctuations, sleep, stressors, mood, menstrual pattern, fractures, and substance abuse; review family history of eating or reproductive disorders. Perform a physical exam including gynecological evaluation. Rule out pregnancy with serum or urine hCG. Order baseline labs: CBC, electrolytes, glucose, bicarbonate, BUN, creatinine, liver panel, ESR/CRP, TSH, free T4, prolactin, LH, FSH, estradiol, AMH; add total testosterone and DHEA‑S if hyperandrogenism is suspected. Consider pelvic ultrasound or MRI if outflow tract abnormality or pituitary lesion is clinically suspected.
## STEP 2 — Rule In / Rule Out
If any laboratory or imaging result suggests an anatomic/organic etiology (e.g., prolactin >25 ng/mL, abnormal TSH with corresponding free T4 abnormality, MRI showing pituitary mass or outflow tract anomaly, or evidence of Müllerian tract defect on ultrasound), then pursue further evaluation/treatment for that organic cause; otherwise, proceed to step 3.
## STEP 3 — Classify or Stratify
When pregnancy is excluded, amenorrhea persists for ≥3 months or cycle intervals >45 days, and no organic pathology is identified, classify the condition as functional hypothalamic amenorrhea (FHA).
## STEP 4 — Decide
If FHA is confirmed, initiate FHA‑directed management (nutritional rehabilitation, psychological support such as CBT, bone density assessment, and address energy balance); if an organic cause is found, treat the underlying pathology according to standard guidelines.
## Clinical Guardrails / Mimics / Pitfalls
Do not diagnose FHA without first excluding pregnancy; avoid misinterpreting mild prolactin elevations (consider macroprolactin) as diagnostic of prolactinoma; ensure pituitary MRI includes dedicated cuts and contrast; evaluate outflow tract especially in primary amenorrhea; be aware that medications (antipsychotics, opioids, continuous contraceptives) can mimic FHA; do not overlook thyroid dysfunction or adrenal disease; in primary amenorrhea, always assess for Müllerian anomalies before labeling as FHA.
## Clinical Guardrails / Mimics / Pitfalls
Do not diagnose FHA without first excluding pregnancy; avoid misinterpreting mild prolactin elevations (consider macroprolactin) as diagnostic of prolactinoma; ensure pituitary MRI includes dedicated cuts and contrast; evaluate outflow tract especially in primary amenorrhea; be aware that medications (antipsychotics, opioids, continuous contraceptives) can mimic FHA; do not overlook thyroid dysfunction or adrenal disease; in primary amenorrhea, always assess for Müllerian anomalies before labeling as FHA.
## Concrete Clinical Example
A 22‑year‑old woman reports 4 months of amenorrhea, BMI 17, runs 40 mi/week, denies disordered eating. Pregnancy test negative. Prolactin 12 ng/mL, TSH 2.1 µIU/mL, LH 3 IU/L, FSH 4 IU/L, estradiol 18 pg/mL, AMH 2 ng/mL. Pelvic ultrasound shows normal uterus, no outflow obstruction; pituitary MRI with contrast is normal. No galactorrhea, headaches, or visual changes. After excluding organic causes, FHA is diagnosed and she is started on nutritional rehabilitation and weekly CBT.
**Source:** Functional Hypothalamic Amenorrhea: An Endocrine Society Clinical Practice Guideline, Endocrine Society, 2017, doi:10.1210/jc.2017-00131
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