Endocrine Neoplasms Flashcards

1
Q

What percentage of all cancers in 2020 were endocrine cancers?

A

3.1%

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2
Q

What is the most common type of endocrine cancer?

A

Thyroid cancer

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3
Q

What is the estimated incidence of new cases of thyroid carcinoma in the US for 2020?

A

52,890

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4
Q

What is the median age of diagnosis for thyroid cancer?

A

45-50 years

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5
Q

What is the 5-year relative survival rate for thyroid cancer?

A

98%

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6
Q

What is the primary diagnostic tool for thyroid cancer?

A

Fine-needle aspiration

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7
Q

Fill in the blank: The majority of thyroid nodules are ______.

A

benign

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8
Q

What are the two main types of differentiated thyroid cancer?

A
  • Papillary carcinoma
  • Follicular carcinoma
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9
Q

What is the classification of thyroid cancer according to the Bethesda system?

A
  • Nondiagnostic
  • Benign
  • Atypia of undetermined significance
  • Follicular neoplasm
  • Suspicious for malignancy
  • Malignant
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10
Q

What is a key risk factor for thyroid cancer related to family history?

A

First degree relative with thyroid cancer

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11
Q

What is the role of calcitonin in medullary thyroid cancer?

A

It is a tumor marker for MTC.

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12
Q

What are the three types of Multiple Endocrine Neoplasia (MEN) syndromes?

A
  • MEN1
  • MEN2A
  • MEN2B
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13
Q

Which MEN syndrome is characterized by medullary thyroid cancer, pheochromocytoma, and parathyroid tumors?

A

MEN2A

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14
Q

What is the most common type of pituitary tumor in MEN1?

A

Prolactinoma

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15
Q

What percentage of medullary thyroid cancer cases are familial?

A

25%

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16
Q

What is the most important treatment variable influencing prognosis in thyroid cancer?

A

Adequate surgery

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17
Q

True or False: Most patients with thyroid cancer have significant symptoms.

A

False

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18
Q

What is the typical age range for the peak incidence of adrenal carcinoma?

A

Less than 5 years and between 40 and 50 years

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19
Q

What is the typical survival rate for patients with adrenal carcinoma?

A

3-4 years

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20
Q

What is the most common symptom of nonfunctioning adrenal tumors?

A

Abdominal mass

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21
Q

Fill in the blank: Hypercortisolism, or ______ syndrome, is present in 50%-70% of hormone-secreting adrenal carcinoma.

A

Cushing

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22
Q

What is the mutation associated with MEN1?

A

MEN1 gene at 11q13

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23
Q

What is the primary treatment for children with thyroid cancer?

A

Thyroidectomy

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24
Q

What is the role of TSH in the initial evaluation of a thyroid nodule?

A

To determine if a radioactive iodine scan is needed

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25
What is the most common type of tumor found in MEN1 affecting the pancreas?
Gastrinoma
26
What is the inheritance pattern of MEN syndromes?
Autosomal dominant
27
What is the prevalence of adrenal carcinoma in childhood cancers?
1.3%
28
What percentage of patients with functioning tumors may present symptoms of nonfunctioning tumors plus those due to excess hormone?
40%–60% ## Footnote This percentage indicates the complexity of diagnosing adrenal tumors due to overlapping symptoms.
29
What is hypercortisolism also known as?
Cushing syndrome ## Footnote Hypercortisolism is a condition characterized by excess cortisol, which can lead to various health issues.
30
In adrenal carcinoma, what percentage of cases might present with androgen excess in female patients?
20%–30% ## Footnote This condition can lead to symptoms of virilization in affected females.
31
What nodular characteristic is suggestive of adrenal carcinoma?
Large tumors >4–6 cm or increasing tumor growth over a 6-month period ## Footnote These growth patterns indicate a higher likelihood of malignancy.
32
What is the most common hormone produced by adrenal tumors?
Cortisol ## Footnote Approximately 50% of adrenal tumors produce hormones, with cortisol being the most prevalent.
33
What is the primary treatment for adrenal cancer?
Surgery ## Footnote Surgical intervention is the primary method for managing adrenal carcinoma.
34
What are the Weiss criteria used for?
Histologically distinguish adrenocortical cancer from adrenocortical adenoma ## Footnote These criteria help in the accurate diagnosis of adrenal tumors.
35
According to Weiss, how many findings are needed to diagnose adrenocortical carcinoma?
Three or more ## Footnote Specific findings include high nuclear grade, necrosis, and vascular invasion among others.
36
What is carcinoid syndrome most commonly associated with?
Small bowel NETs ## Footnote Carcinoid syndrome symptoms can include diarrhea, flushing, and bronchospasm.
37
What are the four D symptoms associated with glucagonoma?
Dermatosis, Diabetes, Deep Vein Thrombosis, and Depression ## Footnote These symptoms reflect the systemic effects of glucagon excess.
38
What is the prognosis for well-differentiated neuroendocrine tumors (NETs)?
Much better prognosis, with an overall five-year survival of approximately 67 percent ## Footnote This contrasts with poorly differentiated neuroendocrine carcinomas, which have a worse prognosis.
39
What is the primary risk factor for thyroid cancer?
Age, being female, and exposure to radiation ## Footnote These factors significantly increase the likelihood of developing thyroid cancer.
40
What is the common presentation of insulinoma?
Hypoglycemia that is insulin mediated ## Footnote This condition leads to episodes of low blood sugar due to excess insulin production.
41
What is a characteristic rash associated with glucagonoma?
Necrolytic Migratory Erythema ## Footnote This rash is a distinguishing feature of glucagonoma.
42
True or False: Biopsy is indicated if adrenal cancer is suspected.
False ## Footnote A biopsy is not recommended due to the risk of spreading the cancer.
43
What is the main treatment for gastrinomas?
Surgery if possible or anti-acid medications ## Footnote Gastrinomas are often associated with severe reflux and peptic ulcer disease.
44
What percentage of NCD deaths globally occurs in low- and middle-income countries?
More than three quarters ## Footnote This statistic highlights the disparity in health outcomes related to NCDs.
45
What are the main types of noncommunicable diseases (NCDs)?
* Cardiovascular diseases * Cancers * Chronic respiratory diseases * Diabetes ## Footnote These diseases account for a significant portion of global mortality.
46
What is the role of detection, screening, and treatment in managing NCDs?
Key components of the response to NCDs ## Footnote These strategies are essential for improving outcomes in affected populations.
47
T or F: most pts. w/ thyroid cancer will have abnormal thyroid functioning
false most have normal thyroid function tests
48
Iodine scans should be ordered if what is low?
TSH
49
T or F: hyperfunctioning nodules are rarely malignant
true
50
what sonographic features raise red-flags for a potential thyroid malignancy
hypoechoic thyroid irregular border microcalcifications
51
what is the biomarker used to detect reoccurrence of thyroid cancer
thryoglobulin
52
what gene is involved in 25% cases of medullary thyroid cancer?
RET proto-oncogene AKA: MEN syndromes
53
T or F: calcitonin concentration correlates to extent of disease as well as stage
true
54
what gene/protein is defective for MEN Type 1
MEN1: menin (tumor suppressor gene)
55
tumors of what endocrine structures are assoc. w/ MEN Type I?
pituitary parathyroid pancreas
56
w/ neoplasm is most commonly assoc. w/ MEN type I affecting the parathyroid?
hyperplasia or adenoma
57
MEN Type I malignant tumors are limited to what endocrine structure
pancreas
58
list the assoc. symptoms of MEN Type 1 hyperparathyroidism.
hypercalcemia kidney stones PUD hypopituitarism
59
what is MEN Type 2B characterized by
Medullary thyroid cancer pheochromocytoma
60
compare and contrast the differences b/t MEN 2A & 2B.
2b: not assoc. w/ hyperparathyroidism 2b: assoc. w/ ganglioneuromas & marfanoid habitus
61
why are biopsies a CI for adrenal carcinomas?
can spread the cancer also, cannot distinguish b/t benign and malignant tumors
62
what pharmaceutical agents are indicated for treatment of adrenal carcinoma
etoposide doxorubicin cisplatin mitotane
63
List the symptoms of carcinoid syndrome?
diarrhea facial flushing bronchospasm
64
T or F: most pts. w/ carcinoid syndrome have hepatic metastases
true
65
what bioactive substances are generally elevated in carcinoid syndrome
serotonin histamine prostaglandins tachykinins
66
chronic levels of bioactive substances produced from carcinoid tumors can lead to what long-term complications
valvular heart disease leading to right-sided heart failure mesenteric fibrosis
67
what foods can stimulate the flushing presentations for carcinoid syndrome
rich in amines: chocolate, avocados, nuts, alcohol
68
gastrinomas are most common in what region of the GI tract
duodenum
69
what are the symptoms of gastrinoma (AKA ZE syndrome)
severe reflux PUD
70
list the 4D symptoms of glucagonoma.
dermatosis diabetes DVT depression
71
Necrolytic migratory erythema is a characteristic rash of what neoplasm?
glucagonoma
72
list the symptoms of somatostatinoma
typically presents w/ diabetes cholelithiasis steatorrhea hypochlorhydria
73
what are the assoc. symptoms of Vipoma?
watery diarrhea hypokalemia hypochlorhydria