Endo Flashcards

1
Q

Adrenal anatomy

A

The adrenal glands are paired retroperitoneal glands that sit on each kidney.
The right gland is triangular in shape, and the left gland tends to be more crescent shaped. If
the kidney is congenitally absent the glands will be more flat, straight, discoid, or “pancake ”
in appearance. Each gland gets arterial blood from three arteries (superior from the inferior
phrenic, middle from the aorta, and inferior from the renal artery). The venous drainage is via
just one main vein (on the right into the IVC, on the left into the left renal vein).

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2
Q

adrenal cortex layers

A

Zona glomerulosa
zona fasciculata
zona reticularis

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3
Q

Adrenal 4 zones

A
Zona Glomerulosa: Makes Aldosterone
- prolonged stimulation here leads to hypertrophy.
Zona Fasciculata: Makes Cortisol
Zona Reticularis — Makes Androgens
Medulla - Makes Catecholamines
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4
Q

Adrenal Ultrasound Cases - Gamesmanship

overview

A

If you get shown an adrenal case on ultrasound, then you are almost certainly dealing with a
peds case. What that means is that your choices are narrowed down to: (a) normal,
(b) neuroblastoma, (c) hemorrhage, and (d) hyperplasia.

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5
Q

Adrenal Ultrasound Cases - Gamesmanship

normal

A

In babies, the cortex is hypoechoic, and the medulla is hyperechoic. This gives
the adrenal a triple stripe appearance (dark cortex, bright medulla, dark cortex).

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6
Q

normal adrenal us quick

A

Hypoechoic Cortex, Hyperechoic Medulla, Hypoechoic Cortex

- like an Oreo, with a cream filling.

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7
Q

Neuroblastoma (adrenal)

A

I talk about this a ton in the peds chapter. To rehash the
important parts, they form in the adrenal medulla
(usually), and typically look like an enlarged gland with
a hyperechoic component. Having said that they can
have cystic components and look like hemorrhage. For
the purpose o f multiple choice I ’d go with hyperechoic.

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8
Q

Adrenal hemorrhage

overview

A

This occurs most commonly in the setting of
trauma or stress (neonates). What this typically
looks like on ultrasound is an enlarged gland with
an anechoic component. With time, the clot
changes and it can be more and more echogenic.
So basically, it can look like anything but for the
purpose o f multiple choice I’d go with anechoic.

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9
Q

Adrenal hemorrhage

stress

A

It’s classically seen after a breech birth, but can also be seen with fetal
distress, and congenital syphilis. Imaging features change based on the timing of
hemorrhage. Calcification is often the end result (that could be shown on CT or
MR). It should be avascular. This can occur bilaterally, but favors the right side
(75%).
o Classic Next Step: Serial ultrasounds (or MRI) can differentiate it from a
cystic neuroblastoma. The hemorrhage will get smaller (cancer will not).
o So which is it? Serial ultrasound or MRI? - If forced to pick you want serial
ultrasounds. It’s cheaper and doesn’t require sedation.

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10
Q

Adrenal hemorrhage

trauma

A

This is going to be an adult (in the setting o f trauma). Most likely it will be shown on CT. It’s more common on the right.

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11
Q

Waterhouse-Friderichsen Syndrome

A

Hemorrhage o f the adrenal in the

setting of fulminant meningitis (from Neisseria Meningitidis).

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12
Q

Adrenal hyperplasia

overview

A

What this typically looks like on ultrasound is a “big
adrenal” that “looks like a brain.” So what does “b ig ”
mean ? Most sources will say longer than 20mm, and a
limb that is thicker than 4 mm (although this is debated -
and will likely not be asked). For the purpose o f multiple
choice I would say that if they stick calibers on it. then it is
too big. So what does “looks like a brain ” mean ? That
means the surface is wrinkled, like it has gyri and sulci.

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13
Q

Adrenal hyperplasia

21-Hydroxylase Deficiency:

A

Congenital adrenal hypertrophy is caused by 21-
hydroxylase deficiency in > 90% o f cases. It will manifest clinically as either genital
ambiguity (girls) or some salt losing pathology (boys). The salt losing can actually be
life threatening. The look on imaging is adrenal limb width greater than 4mm. In some
cases you lose the central hyperechoic stripe (the whole thing looks like cortex).

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14
Q

Adrenal hyperplasia

Too much cortisol

A

from overproduction o f ACTH - which results in bilateral
adrenal gland hyperplasia. If someone wanted to be a real asshole they could get into the
weeds with vocabulary. For example, the “Disease” vs “Syndrome” THIS vs THAT:

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15
Q

I say “Genital ambiguity”, you say

A

21-Hydroxylase Deficiency

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16
Q

Cushing Disease:

A

This is an overproduction o f ACTH by a pituitary adenoma,

resulting in too much cortisol. This is actually the most common cause o f excess cortisol (75%).

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17
Q

Cushing Syndrome

A

The “syndrome” is basically a variety o f causes resulting
in common symptoms. So you can have overproduction o f ACTH by an ACTH
secreting tumor (classic step 1 example is the small cell lung tumor), or
overproduction o f ACTH via an adrenal adenoma (these cases will not have
hyperplasia), or you can have straight up primary adrenal hyperplasia. You could even
get the “syndrome” by taking chronic high dose steroids. Any way you end up with a
fat moon face and big gross lines all over you belly counts as “syndrome.”

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18
Q

Adrenal rapid review

normal

A
" Triple Stripe
■ Hypoechoic Cortex,
“ Hyperechoic Medulla,
' Hypoechoic Cortex
■ Smooth Surface
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19
Q

Adrenal rapid review

hyperplasia

A

’ Big (longer than 20mm)
■ Looks like a brain (wrinkled surface)
‘ Can sometimes lose the central bright layer
- “Genital ambiguity”, = 21-OH Deficiency

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20
Q

Adrenal rapid review

hemorrhage

A

■ Big with an anechoic (or echogenic) component
■ Gets smaller over time
- Seen with “stress” or trauma

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21
Q

Adrenal rapid review

neuroblastoma

A

” Big with an echogenic (or anechoic) component

- Does NOT gets smaller over time

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22
Q

Adrenal Adenoma

overview

A

These things are easily the most common tumor in the adrenal gland. Up to 8% o f people
have them. Proving it is an adenoma is an annoying (testable) problem.

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23
Q

Adrenal Adenoma

non con

A

less than 10 HU

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24
Q

Adrenal Adenoma

absolute washout

A

Enhanced CT - Delayed CT/
Enhanced CT - Unenhanced CT
x 100

Greater than 60% = Adenoma

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25
Q

Adrenal Adenoma

relative washout

A

Enhanced CT - Delayed CT /
Enhanced CT x 100

Greater than 40% = Adenoma

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26
Q

Adrenal ademo

hypervascular mets

A
Hypervascular mets (usually renal, less likely HCC) can mimic adenoma washout.
Portal venous HU values > 120 should make you think about a met.
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27
Q

adrenal pheo

A

Along those lines Pheochromocytomas can also exhibit washout. The trick is the same,
if you are getting HU measurements > 120 on arterial or portal venous phase you can
NOT call the thing an adenoma.

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28
Q

adreanl adenoma mri

A

Look for drop out on in and out o f phase T l.

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29
Q

Real Life = Mass in Adrenal =

A

adenoma

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30
Q

Multiple Choice = Mass in the Adrenal =

A

possible stuffery

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31
Q

Although most adenomas are not functional,

A

Cushings (too much cortisol) and Conn’s (too

much aldosterone) can present as functional adenoma.

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32
Q

adrenal adenoma tips

A

• Adenoma are usually homogeneous. If they are showing you hemorrhage (in the absence of
trauma), calcifications, or necrosis you should start thinking about other things.
• Adenomas are usually small (less than 3 cm). The bigger the mass, the more likely it is to be a cancer. Hom> b ig ? Most people will say more than 4 cm = 70% chance cancer, and
more than 6 cm = 85% chance cancer. The exceptions are bulk fat (myelolipomas) or
biochemical catecholamines in the question stem (pheo) - those can be big.
• Bilateral Small = Probably adenoma
• Bilateral Large = Pheo or Met (Lung cancer)
• Portal Venous Phase HU > 120 — Probably a met (RCC, HCC) or pheo.

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33
Q

“Collision Tumors”

A

Two different tumors that smash together to look like one mass.
Usually one o f them is an adenoma. Remember adenoma should be homogenous and small.
If you see heterogenous morphology consider that you could have two tumors. FDG PET
and MRI can both usually tell if the tumor is actually a collision of two different tumors -
those would be the appropriate next steps.

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34
Q

Conn’s Syndrome

A

Syndrome o f excessive aldosterone production. This is most
commonly caused by a benign adenoma (70%). Cortical-carcinoma can also do it, but that
is much more rare and usually accompanied by hypercortisolism.

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35
Q

Pheochromocyioma

overview

A

Uncommon in real life (common on multiple choice tests). They are usually large at presentation
(larger than 3 cm). The look is variable (heterogenous, homogenous, cystic areas, calcifications,
sometimes even fat). Having said that, the most classic look is a heterogeneous mass with AVID
ENHANCEMENT. On MRI they are T2 bright. Both MIBG and Octreotide could be used (but
MIBG is better since Octreotide also uptakes in the kidney).

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36
Q

Pheochromocyioma

gamesmanship 1

A
The hyper
enhancement washout trick. They
could show you what looks like an
adenoma study (multiple phases to
calculate washout) - but with
mega enhancement (HU > 120).
Remember, I don't care what the
fuck washout out numbers you get
- if they show you HU
measurements > 120 on arterial or
portal venous phase you can NOT
call the thing an adenoma.
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37
Q

Pheochromocyioma

gamesmanship 2

A

This thing isn’t
always in the adrenals. They can
be extra adrenal (organ of
Zuckerkandl - usually at the IMA).

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38
Q

Pheochromocyioma

rule of 10s

A

10% are extra adrenal (organ o f Zuckerkandl - usually at the IMA), 10% are bilateral, 10% are in children, 10% are hereditary, 10% are NOT active (no HTN).

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39
Q

Pheochromocyioma

syndromes

A

Associated syndromes: First think Von Hippel Lindau, then think MEN Ha and lib. Other things less likely to be tested include NF-1, Sturge Weber, and TS.

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40
Q

Pheochromocyioma

carney triad

A
  • Extra-Adrenal Pheo, GIST, and Pulmonary Chondroma (hamartoma).
  • Don ’/ confuse this with the Carney Complex (Cardiac Myxoma, and Skin Pigmentation).
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41
Q

Pheochromocyioma

Men 2

A

Both subtypes o f MEN 2 are associated with Pheochromocytomas (50% o f patients).

In the case o f MEN 2 they usually occur multiple and bilateral.

MEN 2 + Adrenal Mass = Pheo

42
Q

Adrenal myelolipoma

A

Benign tumor that contains bulk fat. About 1/4 have calcifications. If they are big (> 4 cm) they can bleed, and present
with a retroperitoneal hemorrhage. Another piece of trivia is the
association with endocrine disorders (Cushings, Congenital
Adrenal Hyperplasia, Conns).
Don’t get it twisted, these tumors arc NOT functional, they just
happen to have associated disorders about 5-10% of the time.

43
Q

adrenal cyst

A

You can get cysts in your adrenal. They are often
unilateral, and can be any size. The really big ones can bleed
They have a thin wall, and do NOT enhance.

44
Q

adrenal mets

A

Think breast, lung, and melanoma. They have no
specific imaging findings and look like lipid poor adenomas.
If the dude has a known primary (especially lung, breast, or
melanoma), and it’s not an adenoma then it’s probably a met.

45
Q

adreanl cortical carcinoma

A

These are large (4 cm -10 cm), may be functional (Cushings), and calcify in about 20% of cases.

They are bad news and often met everywhere (direct invasion often first).

As a pearl, an adrenal carcinoma is not likely to be less than 5 cm and often has central necrosis.

46
Q

Myelolipoma quick

A

bulk fat

hyperechoic on us

47
Q

adrenal calcifications

A

This is often the result o f prior trauma or infection (TB). Certain tumors (cortical carcinoma,
neuroblastoma) can have calcifications. Melanoma mets are known to calcify.

48
Q

wolman disease

A

This is a total Aunt Minnie (and massive
zebra / unicorn). Bilateral enlarged calcified adrenals. It’s a fat
metabolism error thing that kills (“booka” - Ali G) before the first year of life.

49
Q

MEN 1

A
Parathyroid Hyperplasia (90%), Pituitary Adenoma, Pancreatic Tumor
(Gastrinoma most commonly)
50
Q

MEN 2

A

Medullary Thyroid Cancer (100%), Parathyroid hyperplasia,

Pheochromocytoma (33%)

51
Q

MEN 2b

A

Medullary Thyroid Cancer (80%), Pheochromocytoma (50%), Mucosal
Neuroma, Marfanoid Body Habitus

52
Q

MEN I (3 Ps)

A
  • Pituitary, Parathyroid, Pancreas
53
Q

MEN lla (1M,2 Ps)

A

Medullary Th yro id Ca,

Phe ochrom ocytoma , Parathyroid

54
Q

MEN lib (2Ms, 1P)

A
  • Medullary Thyroid Ca, Marfanoid Habitus /mucosa l neuroma,

Phe o chrom oc y tom a

55
Q

Carcinoid Syndrome

A

Flushing, diarrhea, pain, right heart failure from serotonin manufactured by the carcinoid
tumor. The syndrome does not occur until the lesion mets to the liver (normally the liver
metabolizes the serotonin). The typical primary location for the carcinoid tumor is the GI
tract (70%). The most common primary location is the distal ileum (older literature says
appendix). The actual syndrome only occurs in 10% o f cases - and is actually very rare (in
real life - not on tests).

56
Q

GI carcinoids are associated with

A

oterh GI tumors (GI adenocarcinoma)

57
Q

urine test for carcinoid

A

5-HIAA (5-hydroxyindoleacetic acid)

58
Q

Carcinod nukes test of choid

A

11’In-Octreotide (Octreoscan)

59
Q

systemic serotonin

A

degrades the heart valves (right sided), and classically causes
tricuspid regurgitation

60
Q

VHL

A

Hemangioblastoma is the most common tumor (seen in the retina, cerebellum, spinal cord)

Endolymph Sac Tumor is common (10%)

Bilateral clear cell RCC (-risk -70%)

Papillary Cystadeoma of the epididymis (-55%)

Pheochromocytoma (risk -10%). Less likely to be associated with catecholamine
production.

Pancreatic Cysts (-75%) and serous cystadeomas

61
Q

PGL Syndrome (Paraganglioma & Pheochromocytoma)

A

Multiple head and neck paragangliomas (risk - 70%)

Pheochromocytoma risk is variable depending on the subtype

62
Q

Tuberous Sclerosis (Bourneville Disease)

A

Clinical Triad (Facial Angiofibroma, Seizures, Retard Brain)

Cortical Tubers, Subependymal Nodules,

Subependymal Giant Cell Astrocytoma (SEGA) - found at the caudothalamic groove adjacent to the foramen of monro

cardiac rhabdomyoma

pulmonary cysts (LAM)

63
Q

MEN 1 overview

A

Parathyroid
Pituitary
Pancreas

Less commonly carcinoids of the bronchus, and bowel

Primary Hyperparathyroidism is the most common (risk - 100%), related to adenomas

Prolactinoma is the most common pituitary tumor

Gastrinoma is the most common pancreas / duodenal tumor — jejunal ulcers and gastric fold thickening (Zollinger Ellison)

64
Q

MEN 2 A overview

A

Medullary Thyroid Cancer

Pheochromocytoma (-50%) and often bilateral

Primary Hyperparathyroidism

Thyroid cancers occur at younger ages and are multicentric

Elevated levels of calcitonin cause flushing and diarrhea similar to carcinoid syndrome

65
Q

MEN 2 B overview

A

Medullary Thyroid Cancer

Pheochromocytoma

Marfanoid Appearance
Mucosal Neuromas
Intestinal Ganglioneuromas
These patients fart alot
(seriously)

Thyroid cancers occur at younger ages and are multicentric

Elevated levels of calcitonin cause flushing and diarrhea similar to carcinoid syndrome

66
Q

Familial Medullary

Thyroid (FMTC)

A

Can be
considered a
subtype of MEN 2

67
Q

Thyroid anatomy

A

The thyroid gland is a butterfly shaped gland, with two lobes connected by an
isthmus. The thyroid descends from the foramen cecum at the anterior midline base of the
tongue along the thyroglossal duct. The posterior nodular extension of the thyroid (Zuckerkandl
tubercle) helps give a location of the recurrent laryngeal nerve (which is medial to it).

68
Q

Thyroid nodules

A

Usually evaluated with ultrasound. Nodules are super super common and
almost never cancer. This doesn’t stop Radiologists from imaging them, and sticking needles
into them. Ultrasound guided FNA of colloid nodules is a major cash cow for many body
divisions, that on very rare occasions will actually find a cancer. Qualities that make them more
suspicious include: more solid (cystic more benign), calcifications (especially
microcaicifications). Microcalcifications are supposed to be the buzzword for papillary
thyroid cancer. “Comet Tail” artifact is seen in Colloid Nodules. “Cold Nodules” on 1-123
scans are still usually benign but have cancer about 15% of the time, so they actually deserve
workup.

69
Q

Thyroid colloid nodules

A

These are super super common. Suspicious features include
microcaicifications, increased vascularity, solid size (larger than 1.5 cm), and being cold on a
nuclear uptake exam. As above, Comet tail artifact is the buzzword.

70
Q

Ultrasound Characteristics of Thyroid Nodules

calcification

A

Increased Risk
• Micro x3
• Macro x2

Microcaicifications have the highest accuracy, specificity, and positive predictive value for detecting malignancy

Microcaicifications = the “hallmark” o f papillary CA

Macrocalcification = most common calcification in medullary CA

Macrocalcifications in a single nodule = higher risk

Macrocalcifications in a multi-nodule goiter = lower risk

71
Q

Ultrasound Characteristics of Thyroid Nodules

margins and shape

A

Complete hypoechoic halo is highly suggestive o f benign disease

irregular, spiculated, & microlobulated margins suggest malignancy

72
Q

Ultrasound Characteristics of Thyroid Nodules

vascularity

A

Peripheral pattern o f flow is suggestive o f benign disease

Central pattern o f flow is suggestive o f malignancy

Solid hypervascular nodules are more likely to be malignant

73
Q

Ultrasound Characteristics of Thyroid Nodules

echotexture

A

Solid composition has the highest sensitivity for malignancy (although not specific - many benign nodules are also solid.)

Pure cystic, or spongiform with more than 50% specific are likely benign.

Change over time from solid to cystic suggests benign disease

Most hyperechoic or isoechoic nodules are benign.

Solid Hypoechoic = feature of malignancy

74
Q

Ultrasound Characteristics of Thyroid Nodules

size and multiplicity

A

Nodule size is NOT predictive o f malignancy.

Suspicious features should be the primary consideration when targeting for biopsy (not size)

Multiple nodules = decreased cancer rate per nodule — but the overall rate o f having cancer in one nodule is fairly constant.

75
Q

Thyroid Adenoma

A

These look just like solid colloid nodules on ultrasound. They can
be hyper functioning (hot on uptake scan). Usually if you have a hyper-functioning nodule
(toxic adenoma), your background thyroid will be colder than normal (which makes sense).

76
Q

Goiter

A

Thyroid that is too big. In North America it’s gonna be a multi-nodular goiter or
Graves. In Africa it’s low iodine. You can get compressive symptoms if it mashes the
esophagus or trachea. These are often asymmetric - with one lobe bigger than the other.

77
Q

Subacute Thyroiditis I De Quervains Thyroiditis

A

The classic clinical
scenario is a female with a painful gland after an upper respiratory infection. There is a
similar subtype that happens in pregnant women, although this is typically painless. You get
hyperthyroidism (from spilling the hormone) and then later hypothyroidism. As you get over
your cold, the gland recovers to normal function. Radiotracer uptake will be decreased during
the acute phase.

78
Q

Acute Suppurative Thyroiditis

A

This is an actual bacterial infection of the thyroid.
It is possible to develop a thyroid abscess in this situation. A unique scenario (highly
testable) is that in kids this infection may start in a 4th branchial cleft anomaly (usually
on the left), travel via a pyriform fistula and then infect the thyroid. Honestly, that is
probably too much for the exam - but could show up on a certification exam under neuro.

79
Q

Reidels Thyroiditis

A

This is one of those IgG4 associated diseases (others include
orbital pseudotumor, retroperitoneal fibrosis, sclerosing cholangitis). You see it in women in
their 40s-70s. The thyroid is replaced by fibrous tissue and diffusely enlarges causing
compression o f adjacent structures (dysphagia, stridor, vocal cord palsy). On US there will
be decreased vascularity. On an uptake scan you are going to have decreased values. A
sneak trick would be to show you a MR (it’s gonna be dark on all sequences - like a fibroma).

80
Q

Thyroglossal Duct Cyst (TGDC

overview

A

The most common congenital neck cyst in Pediatrics.
This can occur anywhere between the foramen
cecum (the base o f the tongue) and the thyroid
gland (or below). It looks like a thin walled cyst.

81
Q

Thyroglossal Duct Cyst (TGDC

why care

A
  • They can get infected
  • They can have ectopic thyroid tissue
  • Rarely, that ectopic tissue can get
    papillary thyroid cancer (if you see an
    enhancing nodule)
82
Q

Thyroglossal Duct Cyst (TGDC

location

A

These are the general numbers to think about:
Suprahyoid = 25%
At the Hyoid = 30%
Infrahyoid = 45%
So, where is the most common location?
Well, it depends on how they ask. If all things are equal the answer is Infrahyoid (which seems
counterintuitive based on the embryology but is non the less true).
BUT - if “at or above the hyoid” is a choice - then that is actually the right answer
(25+30 > 45). As always, read every choice carefully.

83
Q

Ectopic and Lingual Thyroid

A

Similar to a thyroglossal duct cyst, this can be found
anywhere from the base of the tongue through the central neck. The most common location
(90%) is the tongue base (“Lingual Thyroid”). It will look hyperdense because o f its
iodine content (just like a normally located thyroid gland). If you find this, make sure you
check for a normal thyroid (sometimes this is the only thyroid the dude has). As a point of
trivia, the rate o f malignant transformation is rare (3%).

84
Q

Graves

A

Autoimmune disease that causes hyperthyroidism (most common cause). It’s
primarily from an antibody directed at the TSH receptor. The actual TSH level will be low.
The gland will be enlarged and “inferno hot” on Doppler.

85
Q

graves orbitopahty

A

Spares the tendon insertions, doesn’t hurt (unlike pseudotumor).
Also has increased intra-orbital fat.

86
Q

graves nuclear medicine

A

Increased uptake o f 1-123 %RAIU usually 50-80%. Visualization of
pyramidal lobe is accentuated.

87
Q

Hashimotos

overview

A

The most common cause of goitrous hypothyroidism (in the US). It is
an autoimmune disease that causes hyper then hypo thyroidism (as the gland bums out later).
It’s usually hypo - when it’s seen. It has an increased risk of primary thyroid lymphoma.

88
Q

Hashimotos

step one triia

A

associated with autoantibodies to thyroid peroxidase (TPO) and antithyroglobulin.

89
Q

Hashimotos

on ultrasound

A

(a) Heterogeneous “giraffe skin” appearance,
(b) White Knights - uniform hyperechoic nodules -
which are actually regenerative nodules.

90
Q

Level 6 Nodes - “Delphian Nodes”

A

• These are the nodes around the thyroid in the front of the neck.
- You can commonly see them enlarged with Hashimotos.
■ However, for the purpose of multiple choice tests, a sick looking level 6 node - or
“Delphian Node” is a laryngeal cancer met.

91
Q

Papillary thyroid cancer

A

The Most Common Subtype. “Papillary is Popular ”

Microcalcifications is the buzzword and key finding (seen in the cancer and nodes).

Mets via the lymphatics.

Has an overall excellent prognosis, and responds well to 1-131.

92
Q

follicular thyroid cancer

A

The second most common subtype.

Mets hematogenously to bones, lung, liver, etc.. Survival is still ok, (less good than papillary). Does respond to 1-131.

93
Q

medullary thyroid cancer

A

Uncommon

Association with MEN II syndrome. Calcitonin production is a buzzword.

Tendency towards local invasion, lymph nodes, and hematogenous spread. Does NOT respond to 1-131.

94
Q

anaplastic thyroid cancer

A

Uncommon

Seen in Elderly. Seen in people who have had radiation treatment.

Rapid growth, with primary lymphatic
spread. Does NOT respond to 1-131.

95
Q

hurthle cell (varian of follicular)

A

Uncommon

Seen more in Elderly.

Does not take up 1-131 as well as normal follicular. FDG-PET is the way to go for surveillance.

96
Q

Thyroid mets

A

The buzzword is going to be microcalcifications in a node (with papillary).
The nodes are typically hyperechoic compared to regular nodes, hyperenhancing on CT, and
T1 bright on MR. Remember that thyroid cancer is hypervascular, and it can bleed like stink
when it mets to the brain. If there are mets to the lungs, the classic pattern is “miliary.” The
additional pearl with regard to lung mets is that they can be occult on cross sectional imaging,
and only seen on whole body scintigraphy. For the purpose of multiple choice tests pulmonary
fibrosis is a risk o f treating with 1-131 i f you have diffuse lung mets.

97
Q

parathyroid anatomy

A

There are normally 4 parathyroid glands located posterior to the thyroid. The
step 1 trivia is that the superior 2 are from the 4th branchial pouch, and the inferior 2 are
from the 3rd branchial pouch. The inferior two are more likely to be in an ectopic location.

98
Q

Parathyroid Adenoma

A

This is by far the most common cause of
hyperparathyroidism (90%). On ultrasound these things look like hypoechoic beans
posterior to the thyroid. A 4D-CT can be used to demonstrate early wash-in and delayed
wash-out. Nuclear medicine can use two techniques (1) the single-tracer, dual-phase
Sestamibi, or (2) the dual tracer Sestamibi +1-123 (or Pertechnetate). These are discussed
in detail in the nukes section.

99
Q

Parathyroid Adenoma quick imaging

A

4D CT shows early enhancement, and delayed washout

100
Q

Parathyroid Carcinoma

A

This is pretty uncommon, and only makes up about 1% of
the causes o f hyperparathyroidism. It looks exactly like an adenoma on imaging. The only
way you can tell on imaging is if they show you cervical adenopathy or invasion o f adjacent
structures.

101
Q

High Yield Parathyroid Trivia

A

Q: What are the causes o f hyperparathyroidism?
A: Hyperfunctioning Adenoma (85-90%),
Multi-Gland Hyperplasia (8 -10%), Cancer (1 -3%).
Q: What factors does sestamibi parathyroid imaging depend on ?
A: Mitochondrial density and blood flow