Adrenal Cortical Tumors1 Flashcards

1
Q

What ia a key surgical anatomic fact about adrenal glands?

A

The adrenal vein is inferomedial to the gland on the left side and drains into the left renal vein, and it is superiomedial on the right side and drains directly into the inferior vena cava posterolaterally.

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2
Q

What are the layers of the adrenal gland and what they produce?

A

About 80% of the adrenal gland consists of the adrenal cortex, which is subdivided into the zona glomerulosa, which produces aldosterone, the zona fasciculata, which makes glucocorticoids, and the zona reticularis, which produces sex hormones.

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3
Q

Which are usually the patients referred for an adrenalectomy?

A
  1. functional tumor causing a clinical syndrome due to hormonal excess, which includes aldosteronoma, Cushing syndrome, and virilizing/feminizing tumors
  2. adrenocortical cancer
  3. adrenal metastasis
  4. incidentaloma
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4
Q

On whom should you suspect primary hyperaldoteronism?

A

Should be suspected in any patient with hypertension and hypokalemia, persistent hypertension refractory to medical treatment, or hypertension and an adrenal mass.ᅠ

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5
Q

How is primary aldosteronism diagnosed?

A

Diagnosed by an elevated plasma aldosterone concentration (PAC >15 ng/dL) with a suppressed plasma renin activity (PRA 14 g/day) during IV saline infusion confirm the diagnosis.

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6
Q

How is secondary hypoaldosteronism diagnosed?

A

Increased plasma renin activity and a PAC/PRA less than 30 may indicate secondary hyperaldosteronism, which is treated medically.

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7
Q

What test is diagnostic of a unilateral functioning adenoma?

A

An adrenal vein aldosterone/cortisol ratio on one side that is five times higher than the contralateral side is diagnostic of unilateral functioning adenoma.

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8
Q

What preoperative preparation is needed for a patient with aldosteronoma?

A

Hypertension and hypokalemia should be managed preoperatively with a 3 to 5 week course of spironolactone (100 to 400 mg daily) and/or oral potassium. Preoperative normalization of blood pressure with spironolactone is a good predictor of a successful outcome after adrenalectomy.

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9
Q

What is one of the first laboratory signs of Cushing syndrome?

A

Loss of diurnal variation in cortisol levels is one of the first signs of Cushing syndrome.ᅠ

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10
Q

What is the most sensitive and specific test for diagnosing Cushing syndrome?

A

Elevated 24-hour urinary free cortisolᅠ

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11
Q

What is the most common cause of Cushing syndrome?

A

Exogenous steroid use

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12
Q

What is the most common cause of endogenous excess cortisol production?

A

Pituitary tumor or hyperplasia (Cushing disease, 60% to 70%); ectopic ACTH (10% to 20%); or an adrenal adenoma or adrenocortical carcinoma (10% to 20%).

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13
Q

What tumors can produced ACTH?

A

Bronchial carcinoids, small cell lung cancer, pancreatic islet cell cancers, and thymomas

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14
Q

Are stress glucocorticoids needed perioperatively for patients undergoing surgery for Cushing syndrome?

A

They should receive stress glucocorticoids perioperatively, usually 100 mg IV hydrocortisone preoperatively followed by 100 mg every 6 hours postoperatively. These doses are gradually transitioned to oral steroids, which are tapered once the ACTH-stimulation test normalizes, and the contralateral gland is no longer suppressed. Patients undergoing bilateral adrenalectomy will require lifelong replacement therapy.

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15
Q

How can you control cortisol excess preoperatively?

A

Cytochrome P-450 inhibitors such as ketoconazole (600 to 1200 mg daily).ᅠ

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16
Q

What % of virilizing and feminizing tumors are malignant?

A

80%

17
Q

What physical exam findings are characteristic of a virilizing tumor?

A

Women with hirsutism, alopecia, irregular menses, and other virilizing signs may have a hypersecreting adrenal tumor or a functioning ovarian tumor.ᅠ

18
Q

What lab values are concerning for virilizing tumors?

A

Elevated serum testosterone, dehydroepiandrostenedione (DHEA-S), and 24-hour urinary 7-hydroxysteroids and 17-ketosteroids establish the diagnosis of a virilizing tumor.

19
Q

What physical exam findings are characteristic of a feminizing tumor?

A

Men with gynecomastia, gonadal atrophy, impotence, or loss of libido may have an estrogen-secreting adrenal tumor, which may be adrenocortical carcinoma, or a testicular tumor.ᅠ

20
Q

What lab values are concerning for feminizing tumors?

A

Elevated serum estrogen levels with suppressed gonadotropins, follicle stimulating hormone (FSH), and luteinizing hormones suggest a feminizing tumor.ᅠ

21
Q

What percentage of all adrenal masses accounts for sdrenocortical carcinoma?

A

1%

22
Q

What are the most frequent sites of metastasis for adrenocortical carcinoma?

A

Lung and Liver

23
Q

Which is more helpful between MRI and CT to plan an excision of adrenocortical carcinoma?

A

Although CT and MRI are equally effective, MRI may be more useful than CT in determining extension of tumor into the renal vein and inferior vena cava (IVC). Invasion into the IVC and/or the presence of thrombus are considered regional involvement and are not contraindications to resection.

24
Q

What are two most important prognostic factors of adrenocortical carcinoma?

A

completeness of resection and stage of disease

25
Q

What is the TNM staging for adrenocortical carcinoma?

A
TNM
T1: 5 cm, no invasion
T3: Any size, locally invading (but not adjacent organs)
T4: Any size, locally invading adjacent organs
N0: No regional positive nodes
N1: Positive regional nodes
M0: No distant metastatic disease
M1: Distant metastasis present
Stage
I: T1N0M0
II: T2N0M0
III: T1N1M0, T2N1M0, T3N0M0
IV: T3N1M0, T4N1M0, TXNXM1
26
Q

What marker has been associated with poor clinical outcome in adrecortical carcinoma?

A

Ki67 expression

27
Q

What is the single most important drug for adjuvant ACC treatment?

A

Mitotane is the single most important drug for adjuvant ACC treatment for patients with residual, recurrent, or metastatic ACC. Some centers use mitotane after complete R0 resection if the tumor is large (>8 cm), or if it appears aggressive (Ki67 >10%). Prolonged mitotane treatment is limited by gastrointestinal and neurologic toxicity. Since mitotane can induce adrenal insufficiency, patients may need glucocorticoid and mineralocorticoid supplementation during treatment. Up to 80% of mitotane-treated patients with functioning tumors will show significant decreases in hormone production.

28
Q

Does radiotherapy has any role in ACC?

A

Radiotherapy is recommended in patients with incomplete resection or, in some centers, with advanced local disease (stage III) or aggressive tumors (Ki67 >20%).

29
Q

Which are the most common tumor to metastasize to the adrenal glands?

A

Lung carcinoma (especially small cell), renal cell carcinoma, melanoma, gastric adenocarcinoma, hepatocellular carcinoma, esophageal adenocarcinoma, and breast adenocarcinoma.

30
Q

What findings on CT or MRI are characteristics of adrenal metastases?

A

Irregular borders, hemorrhage, tumor necrosis, and a region of interest (ROI) greater than 20 HU on unenhanced CT.

31
Q

What can be used to confirm the diagnosis of adrenal metastases?

A

Fine needle aspiration may be required to confirm the diagnosis, but only after pheochromocytoma has been ruled out to avoid potentially life-threatening hypertensive crisis.