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🧠 Pituitary Adenomas in PLAB 2: Master Hormonal Disorders, Mass Effects, and Emergencies

Updated: Jun 28

🧠 What Is a Pituitary Adenoma?

A pituitary adenoma is a benign tumour of the anterior pituitary gland. Though benign, it can cause significant systemic effects due to:

  • Pituitary adenomas can cause either hormonal excess or hormonal deficiency, depending on the type, size, and location of the tumor

  • Pressure effects on adjacent structures (non-functioning adenomas)


🧪 Hormones Secreted by the Anterior Pituitary

Hormone

Full Name

Target Organ(s)

Main Function(s)

ACTH

Adrenocorticotropic hormone

Adrenal cortex

Stimulates cortisol production (mainly from the zona fasciculata)

TSH

Thyroid-stimulating hormone

Thyroid gland

Stimulates T3 and T4 synthesis and secretion

LH

Luteinising hormone

Gonads (ovaries/testes)

Triggers ovulation and corpus luteum formation in females


 Stimulates testosterone production in males

FSH

Follicle-stimulating hormone

Gonads (ovaries/testes)

Stimulates follicle development in ovaries


 Stimulates spermatogenesis  in testes

GH

Growth hormone (somatotropin)

Liver, bones, muscles

Stimulates growth, cell reproduction, and IGF-1 secretion from the liver

Prolactin

Mammary glands

Stimulates milk production

🧪 Hormones Released by the Posterior Pituitary

Hormone

Produced By

Main Functions

ADH (Vasopressin)

Hypothalamus (supraoptic nucleus)

- Increases water reabsorption in the kidneys (collecting ducts)


 - Helps maintain blood pressure by conserving water

Oxytocin

Hypothalamus (paraventricular nucleus)

- Stimulates uterine contractions during labour


 - Promotes milk ejection ("let-down reflex") in lactating women


🚨 Clinical Presentations (GP Setting)

Symptom Group

Presentation

Hormonal excess Hormonal overproduction (functioning adenomas)

- Galactorrhoea, amenorrhoea, infertility (↑ Prolactin)


 - Acromegaly signs (↑ GH)


 - Cushingoid features (↑ ACTH)

Mass effects

- Headache


 - Visual field defect (classically bitemporal hemianopia)

Hypopituitarism

- Fatigue, cold intolerance, weight gain (↓ TSH)


 - Amenorrhoea, loss of libido (↓ LH/FSH)


 - Secondary adrenal insufficiency

🔍 OSCE Tip: Look for progressive symptoms, visual changes, or multiple hormone disturbances to suspect pituitary involvement.

Prolactin-secreting adenoma (Prolactinoma)

  • Galactorrhoea (nipple discharge)

  • Amenorrhoea or oligomenorrhoea in females

  • Infertility

  • Loss of libido (both genders)

  • Erectile dysfunction in males

Growth Hormone-secreting adenoma (Acromegaly)

  • Increase in shoe or ring size

  • Coarse facial features

  • Jaw protrusion (prognathism)

  • Excessive sweating (hyperhidrosis)

  • Joint pain (arthralgia)

  • Headaches

  • Carpal tunnel syndrome symptoms (tingling, numbness in hands)

ACTH-secreting adenoma (Cushing’s Disease)

  • Weight gain (especially central obesity)

  • Facial rounding (“moon face”)

  • Thin skin, easy bruising

  • Purple striae (especially abdomen)

  • Proximal muscle weakness

  • New onset hypertension or diabetes

  • Mood changes (depression, irritability)

TSH-secreting adenoma (very rare)

  • Symptoms of hyperthyroidism:

    • Palpitations

    • Heat intolerance

    • Tremors

    • Weight loss despite normal/increased appetite

Non-functioning adenoma (mass effect symptoms)

  • Headache

  • Visual changes (especially bitemporal hemianopia)

  • Hypopituitarism symptoms:

    • Fatigue, weakness

    • Cold intolerance

    • Loss of body hair

    • Amenorrhoea, infertility

    • Hypotension (if adrenal insufficiency)

General Red Flags for Pituitary Apoplexy

  • Sudden severe headache

  • Visual loss or diplopia

  • Ophthalmoplegia (e.g. ptosis, inability to move eye)

  • Altered consciousness


Systematic Questioning Framework

When ruling out functional symptoms in PLAB 2:

✅ Ask about menstrual history, libido, and galactorrhoea

✅ Ask about changes in appearance, hands, feet, and facial features

✅ Ask about weight changes and features of cortisol excess

✅ Ask about thyroid symptoms

✅ Always screen for headaches and visual symptoms


🏥 Examination Findings

Systemic Clues

What to Look for

Eyes (visual fields)

Bitemporal hemianopia on confrontation test (compression of optic chiasm)

Face & Hands

Coarse facial features, prognathism, large hands (Acromegaly)

Skin

Thin skin, striae, hirsutism (Cushing’s)

Breast

Galactorrhoea


🧪 Investigations (Initial Workup in GP)

Test

Purpose

Serum Prolactin

For prolactin-secreting tumours

IGF-1

For growth hormone excess (acromegaly)

Overnight dexamethasone suppression test

Screening for Cushing’s disease

TSH, Free T4

Check for secondary hypothyroidism

LH, FSH, Oestradiol/Testosterone

Assess gonadal function

9 AM Cortisol

Assess for adrenal insufficiency

📌 PLAB 2 Station Alert: If the patient is acutely unwell with fatigue and hypotension, consider secondary adrenal insufficiency and give hydrocortisone before awaiting cortisol results.

🔎 Red Flags Needing Urgent Referral

  • Visual field defect or sudden vision loss

  • Features of raised intracranial pressure

  • Pituitary apoplexy (sudden headache, visual loss, ophthalmoplegia, hypotension)

  • Suspicion of functioning macroadenoma


🧑‍⚕️ Specialist Investigations (Endocrinology & Neurosurgery)

Investigation

Why It's Done

MRI Pituitary

Confirm diagnosis, measure tumour size

Formal Visual Field Testing

Quantify and document extent of chiasmal involvement

Dynamic hormonal testing (e.g. OGTT for GH, CRH test)

Confirm diagnosis of hormone excess

ACTH levels

Differentiate between Cushing’s disease and other causes


💊 Management Summary

In General Practice:

Task

Details

Identify & suspect

Based on symptoms and basic labs

Safety netting

Headaches + visual symptoms = red flag

Refer to endocrinology/neuro

As per local 2-week wait or urgent referral

Initiate treatment (if trained)

E.g., dopamine agonists in known prolactinoma (with specialist input)

In Specialist Setting:

Adenoma Type

Management

Prolactinoma

Dopamine agonists (e.g. Cabergoline) first-line

GH-secreting

Surgery + somatostatin analogues (e.g. Octreotide)

ACTH-secreting

Transsphenoidal surgery + medical therapy if needed

Non-functioning

Surgery if mass effect; otherwise monitor

Large macroadenomas

Surgical debulking; monitor hormonal recovery

🧠 Complications to Know

  • Hypopituitarism post-treatment

  • Permanent visual loss if not addressed early

  • Recurrence of tumour after surgery

  • Pituitary apoplexy (emergency) is a sudden and life-threatening condition caused by hemorrhage or infarction (loss of blood supply) within the pituitary gland, usually in a pituitary adenoma (often undiagnosed).


🪜 Differential Diagnoses

Condition

How to Differentiate

Hypothyroidism

Normal prolactin, diffuse symptoms, no mass effect

PCOS

Raised LH:FSH, no visual symptoms

Depression

Non-specific symptoms, normal pituitary hormones

Cushing’s syndrome (non-pituitary)

Dexamethasone suppression test not suppressed, no pituitary mass

Craniopharyngioma

More common in children, calcifications on imaging

👨‍⚕️ PLAB 2 Communication Tip

  • Be empathetic and avoid jargon (e.g., say “a growth near a gland in your brain” instead of “pituitary adenoma”)

  • Always address fertility concerns, vision symptoms, and hormonal imbalances

  • Offer safety-net advice: “If you get a sudden severe headache, vomiting or changes in vision, go to A&E immediately.”


📌 Take-Home for PLAB 2

✅ Think pituitary if symptoms suggest hormonal imbalance + visual symptoms + fatigue

✅ Initial bloods can be done in GP; refer early if suspicion is high

✅ Know urgent features: visual loss, apoplexy, headache with vomiting

✅ Management depends on hormone excess and mass effect

✅ Effective communication and referral are key in PLAB 2 scenarios


📚 References:

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