Endocrine Imaging Flashcards

(38 cards)

1
Q

What is the most common type of functional pituitary adenoma?

A

Prolactinoma

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2
Q

What imaging modality is preferred for pituitary pathology?

A

MRI

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3
Q

What are the contents of the dural venous sinus through which the ICA passes?

A

CNIII, CNIV, CNVI, CNV1, CNV2 (superior to inferior), ICA with sympathetic plexus

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4
Q

What is the anatomical mechanism underlying bitemporal hemianopia in pituitary adenoma?

A

Compression of the optic chiasm by an enlarged pituitary gland

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5
Q

Which multiple endocrine neoplasia (MEN) syndrome do pituitary tumours occur in?

A

MEN1- parathyroid tumours, Pancreatic Neuroendocrine Tumors (pNET),
pituitary tumours

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6
Q

Describe the pathology demonstrated in the MRI study.

A

Enlarged pituitary gland.

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7
Q

Why is the sphenoid sinus important in transsphenoidal hypophysectomy?

A

Because it provides a direct surgical corridor to the pituitary gland, allowing access without opening the skull or retracting brain tissue.

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8
Q

Q: What are the typical imaging features of a multinodular goitre?

A

Enlarged thyroid with multiple nodules of varying size and echogenicity.

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9
Q

What is the difference between toxic and non-toxic multinodular goitre?

A

Toxic: TSH-independent hormone production; Non-toxic: euthyroid.

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10
Q

What is the relation of the carotid sheath to the thyroid?

A

Carotid sheath lies posteriolateral to the lobes of the thyroid

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11
Q

What are the contents of the carotid sheath?

A

Common carotid artery (A), internal
jugular vein (B), vagus nerve (C)

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12
Q

Which follow-up imaging study would characterise the functional status of the nodule?

A

Thyroid scintigraphy

Tc99m pertechnetate is administered IV, images captured with scintillation camera.

Pertechnetate behaves similarly to iodine.

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13
Q

What are the expected TSH and T3/T4 levels in patients with Graves disease, multinodular goitre, or autonomous nodule?

A

Low TSH, High T3/T4

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14
Q

What are key ultrasound features that raise suspicion for thyroid malignancy?

A

Microcalcifications, irregular margins, hypoechogenicity, loss of pseudocapsule.

The findings pre biopsy are highly suspicious for thyroid
malignancy. If the pseudocapsule disappears and you lose the
interface between the lesion and the normal parenchyma, be
careful. The presence of microcalcifications is a second
indication for FNA. This is a confirmed papillary carcinoma of
the thyroid.

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15
Q

What are the major types of primary thyroid cancers?

A

Papillary, follicular, medullary, anaplastic

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16
Q

Why are microcalcifications concerning on thyroid ultrasound?

A

They are associated with papillary thyroid carcinoma.

17
Q

Which thyroid malignancy subtype is the most common?

A

Papillary thyroid carcinoma.

18
Q

What are the risk factors for thyroid malignancy?

A

Head and neck irradiation, family history, age <30 or >60, male, >2 cm nodule

19
Q

How does the functional status of a thyroid nodule affect management?

A

Functioning (hot) nodules are often benign; non-functioning (cold) nodules may need biopsy.

20
Q

What is a tumour of the chromaffin cells in the adrenal medulla called?

A

Phaeochromocytoma

21
Q

What is the function of chromaffin cells?

A

Release catecholamines (epinephrine/norepinephrine) from adrenal medulla.

22
Q

What imaging modalities are relevant for adrenal pathology?

A

MRI, MIBG scan

MIBG - Metaiodobenzylguanidine

23
Q

How does MIBG uptake help differentiate adrenal masses?

A

It confirms catecholamine-producing tumors like pheochromocytoma.

MIBG (Metaiodobenzylguanidine) is a radiolabeled molecule similar to norepinephrine. It is taken up by chromaffin cells in the adrenal medulla, which are the cells involved in phaeochromocytoma.

When injected intravenously, MIBG is absorbed by these cells. Because phaeochromocytomas actively take up norepinephrine, they accumulate the MIBG tracer. A gamma camera then detects this uptake on a scan, highlighting the tumor.

Key Point:
Phaeochromocytomas appear as areas of increased uptake on the MIBG scan, helping localize and confirm the diagnosis, even if the tumor is extra-adrenal or metastatic.

25
Adrenal vein sampling is used to investigate autonomous hormone production. Describe the catheter path from femoral vein to left adrenal vein.
Left femoral vein → Left external iliac vein → Left common iliac vein → IVC → Left renal vein → Left adrenal vein
26
MIBG scans may be positive in which other conditions?
Neuroblastoma, carcinoid, paraganglioma, medullary thyroid carcinoma, ganglioneuroma
27
What is the prevalence of adrenal incidentalomas?
3–7% in adults.
28
What proportion of adrenal incidentalomas are benign and non-functioning?
80%.
29
What was the indication for the abdominal CT showing an adrenal incidentaloma?
Status post left nephrectomy (renal cell carcinoma) ## Footnote Surgical clips visible.
30
What are relevant imaging studies for pNET?
Endoscopic ultrasound, CT, Nuclear medicine
31
Describe the relationship between the superior mesenteric vessels and the pancreas.
The superior mesenteric vessels run posterior to the neck of the pancreas
32
Where do pNETs commonly metastasize?
Liver
33
34
What is the clinical importance of the splenic vein's proximity to the pancreas?
Risk of splenic vein thrombosis in pancreatitis.
35
What is Sheehan Syndrome?
Pituitary apoplexy following postpartum hemorrhage leading to anterior pituitary necrosis
36
What are the early MRI signs of Sheehan Syndrome?
Enlarged pituitary with ring enhancement
37
What are the late MRI signs of Sheehan Syndrome?
Empty sella turcica of normal size
38
# Clinical Case Conundrum: A 35 year old Italian women presented to the emergency department eight days following delivery complaining of asthenia, abdominal pain and lower limb cramps. This was preceded by persistent headache. In addition, the patient reported lack of milk secretion after childbirth. Obstetric History: Uncomplicated pregnancy Spontaneous vaginal delivery at 39.5 weeks gestation Male infant weighing 3200 g Postpartum haemorrhage of 500 mL due to uterine atony Mother and infant discharged 48 hours post-delivery Haematological Findings: Normocytic, normochromic anaemia Haemoglobin: 8.8 g/dL (low) RBC count: 3.06 × 10⁶/μL (normal range: 4.2–5.4 × 10⁶/μL) Haematocrit: 24.9% (normal range: 37–48%) Platelet count: 516 × 10⁹/L (elevated; normal range: 150–450 × 10⁹/L) Electrolytes: Sodium (Na⁺): 108 mEq/L (low) Chloride (Cl⁻): 83 mEq/L (low) Endocrine Findings: Hypothalamic-pituitary axis suppression: ACTH: <5.00 pg/mL (normal: 0–46 pg/mL) Cortisol (baseline): <1 μg/100 mL (normal: 10–20 μg/100 mL) Cortisol after Synacthen stimulation: 2.5 μg/100 mL (inadequate response) Thyroid axis: TSH: 0.282 μU/mL (low; normal: 0.400–4.000 μU/mL) Gonadotropins and sex hormones: FSH: <0.10 mIU/mL (normal: 0.4–11 mIU/mL) LH: <0.10 mIU/mL (normal: 0.08–7.3 mIU/mL) Oestradiol: <10 pg/mL (normal: 40–100 pg/mL) Prolactin: Basal: 3.57 ng/mL (normal: 3.50–30.00 ng/mL) Poor response to TRH stimulation Growth hormone (GH): 0.05 ng/mL (low; normal: 0.1–10 ng/mL) Antidiuretic hormone (ADH): 2.9 pg/mL (normal: 0.0–6.7 pg/mL)
Diagnosis:** Sheehan Syndrome** Obstetric History Postpartum hemorrhage (500 mL) from uterine atony Recent delivery (39.5 weeks gestation) Haematological/Electrolyte Findings Severe anaemia Hyponatremia: Na⁺ = 108 mEq/L Hypochloremia: Cl⁻ = 83 mEq/L (suggests adrenal insufficiency and/or hypothyroidism) Pituitary Hormone Deficiencies ACTH: <5.00 pg/mL (↓) Cortisol (basal): <1 μg/100 mL (↓) Poor cortisol response to Synacthen (2.5 μg/100 mL) → Secondary adrenal insufficiency TSH: 0.282 μU/mL (↓) Free T4 likely low (not provided), indicating central hypothyroidism FSH & LH: <0.10 mIU/mL (↓↓) Oestradiol: <10 pg/mL (↓↓) → Hypogonadotropic hypogonadism Prolactin: 3.57 ng/mL (borderline low) with blunted TRH stimulation → Impaired lactotroph function GH: 0.05 ng/mL (↓) → Growth hormone deficiency Summary of Pituitary Dysfunction Consistent with Sheehan’s Syndrome **Multiple anterior pituitary hormone deficiencies (panhypopituitarism) Postpartum hemorrhage, a classic precipitating event No evidence of posterior pituitary involvement (normal ADH)**