MCQ Flashcards

(72 cards)

1
Q

Cholestasis of pregnancy

A

.

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2
Q

Breast MRI enhancment patterns

A

Rapid early enhancement with washout suspicious for malignancy
If intermediate early enhancement, may be type 1 (persistant, most benign but could still be malignant) type 3 (plateau - suspicious), or type 3 (washout - highly suspicious)

Peripheral enhancement first is suspicious for malignancy
Central more benign

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3
Q

Benign breast ultrasound features

A
Marked hyperechogenicity
Thin echogenic pseudocapsule
Wider than tall / parallel
Circumscribed
Ellipsoid
Gentle lobulations
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4
Q

Malignant breast ultrasound features

A
Spiculate - most specific
Taller than wide
Angular or microlobulated
Shadowing
Markedly hypoechoic
Calcs
Poorly defined margin
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5
Q

Linguine sign

A

Hypoinense lines on MR

Intracapsular silicone implant rupture

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6
Q

Tomosynthesis radiation dose

A

Single DBT images has dose similar to single FFDM image

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7
Q

Atypical ductal hyperplasia on biopsy

A

Spectrum of change from normal, to flat epithelial atypia, to atypical ductal hyperplasia, to DCIS
If core biopsy shows ADH, treat with open biopsy - 18% are upstaged to DCIS or invasive carcinoma

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8
Q

Cleopatra view

A

AKA axillary view

A supplementary exaggerated CC to see the axillary tail, performed if a lesion is only seen in the axilla on MLO

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9
Q

Failed pregnancy

A
CRL >/= 7mm with no heartbeat
MSD >/= 25mm with no embryo
Absence of embryo with heartbeat:
2 weeks after GS without yolk sac
11 days after GS with yolk sac
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10
Q

Cervical carcinoma

A

High T2 signal compared with background low signal Cervix
T2 to assess parametrial invasion to see if surgical candidate - if T2 hypointense cervical ring intact, parametrial infasion unlikely.
CT is primarily for assessing adenopathy (although MR can do similar?)
Most are squamous - HPV 16 and 18
Several adenocarcinoma types- clear cell, endometrioid, mucinous, serous
Also neuroendocrine (small) and adenosquamous) - small cell have a poor outcome
Adenos generally though to give higher rates of mets - thoracic and adrenal

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11
Q

Ovarian cycle

A
Proliferative - becomes trilaminar
Secretory - uniformly hyperechogenic
Imaging best performed in early proliferative
Proliferative = follicular
Secretory = luteal
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12
Q

Twin demise

A

Flatenned remnant known as fetus papyraceus
Surviving co-twin at risk of growth restriction, encephalomalacia and microcephaly
Twin embolisation syndrome a rare complication - multi-organ ischaemia, usually antecedent twin-twin transfusion syndrome

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13
Q

Fitz-Hugh-Curtis syndrome

A

Perihepatitis from peritoneal spread of infection in PID

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14
Q

Molar pregnancy

A

Complete, 90% diploid 46XX (less commonly XY) - single sperm or less likely two sperm
Partial, triploid 69XXY, normally from two separate sperm, one X and one Y (other triploid combos possible)
Complete - multiple intrauterine cystic space - bunch of grapes or snow storm
Partial - large cystic placenta and growth retarded fetus

Increased incidence in Asia

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15
Q

Physiological gut herniation of fetus

A

Should not be seen after 12 weeks

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16
Q

Ultrasound screening

A

Unacceptably high rates of biopsy of benign lesions

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17
Q

How many Ca does screening miss

A

1 in 8 pre-menopausal, 1 in 10 post

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18
Q

Clinical exam breast sensitivity

A

Detects 50% of cancers, including 5% of cancers not visible on mammography. May modestly improve early detection

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19
Q

Mammogram timing

A

Early follicular phase, as breasts are less dense

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20
Q

Fibroadenoma, epi

A

Commonest breast lesion in <40

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21
Q

Stellate

A

93% are malignant.

Most invasive breast cancers are stellate (2:1 stellate:circular)

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22
Q

Radial scar

A

Must have no skin thickening or retraction
Long spicules with intervening lucencies, different on different projections
AKA complex sclerosing lesion
Removed as can have associated carcinoma which is not distinguished on core biopsy
Black star - lucent centre (different from carcinoma)

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23
Q

Single reader v double reader v CAD

A

Routine use of CAD significantly increases recall rates. No significant effect on positive predictive value for biopsy – can increase detection rate by 4.7%, sensitivity by 4%.
CADET II study showed cancer detection rates attained with single reading with CAD were equivalent to those attained with double reading.
Performed equally well at recalling patients with cancer in whom the predominant radiologic feature was either a mass or a microcalcification.
Double reading showed superior performance for parenchymal deformities and in women with denser background pattern – i.e. CAD poor at detecting architectural distortion.
Single reader with CAD was better than double reading for asymmetric densities, but the number of these is small and accounted for only 35 of cancers.

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24
Q

Digital mammography

A

40% more sensitive with no change in recall rate

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25
MRI indications
``` Lump with normal mammogram and USS Young with BRCA (annual from 30) Dense breast and LCIS Staging multicentric multifocal disease Positive node with negative uss and mammo Post surgical review of lumpectomy ```
26
Maternal AFP
Elevated in 80% of cases with open spina bifida Normal in most fetuses with closed spina bifida Also elevated in omphalocele, multiple fetuses And liver tumours and germ cell tumours (esp. yolk sac tumour) Elevated in placental chorioangioma (the most common placental tumour) Reduced in Trisomies and Turners
27
Spina bifida
Associated with trisomy 18, 13 Limb anomalies - DDH, talipes, rockerbottom feet Neurenteric cysts Lemon skull, banana cerebellum/Chiari
28
Pregnancy screening
1st trimester: Nuchal translucency, PAPP-A, HCG 1:300 or less is increased risk - offer diagnostic testing <3mm is normal nuchal translucency 11.3-13.6 weeks, manigified, neutral neck, midline, fluid behind neck (CRL 45-84mm) 2nd trimester: AFP, HCG, oestriol and inhibin A In Downs, HCG up and PAPP-A down. AFP would also be down. Inhibin A higher, oestriol lower
29
Ovarian tumour markers
CA125 AFP - teratomas and yolk sac tumours (esp) bHCG - small number of dysgerminomas (AFP positive in mothers with fetuses with neural cord defects)
30
Endodermal sinus tumour
Is a synonym for yolk sac tumour
31
Ovarian cystadenoma
Serous unilocular Serous more commonly bilateral (15% v 5%) (65% of malignant serous bilateral, 15% benign - 60% are benign, 25% malignant) Serous more common Mucinous multiloculated thin septations, and more commonly calcify (mural), and tend to be larger. 80% of mucinous are benign Serous have papillary projections, psammoma bodies Serous associated with BRCA1 Serous 60% benign, 25% malignant, rest boderline Mucinous 80% benign 10% malignant, rest boderline Mucinous associated with KRAS mutation
32
CMV
Necrotising inflammation 90% asymptomatic (in utero infection) Prominent cytomegalic cells with intranuclear and intracytoplasmic inclusions Tendendy to localise in ependymal and subependymal regions of brain.
33
Duodenal atresia
30% have Downs | Present in 3-5% of Downs
34
Meckel Gruber syndrome
Triad Renal cystic dysplasia Occipital encephalocele / holoprosencephaly Post axial polydactyl (post axial is ulnar side) AR AKA pseudotrisomy 13
35
Cleft palate
``` Approximately 1:1000 Amniocentesis as high rate of chromosomal abnormality 1-4 classification 1 lip 2 palate 3 bilateral lip 4 lip and palate 50% 4, 25% 1 and 25% 2 ```
36
Hydrops
``` Immune - rhesus Non-immune - heart failure, infection, Parvovirus is the most common infection to cause hydrops TORCH Aneuploidy Turners - lymphatic failure ``` Any cause of failure - shunts from tumours, vascular malformations, Fetal anaemia - beta thalassamia not til 6-9 months. Homozygous alpha may be commonest cause of fetal hydrops in some parts of world Errors of metabolism CPAM could cause caval compression
37
CPAM
Can cause caval compression and hydrops (33-80%), (although another source said 10%, and false when asked if most cases have an effusion) polyhydramnios from oesophageal compression (25-75%)
38
Single umbilical artery
``` IUGR Velamentous cord Trisomy (if other abnormalities) Renal agenesis same side Sirenomelia / mermaid syndrome ```
39
Ovarian sex-cord stromal
Granulosa (5% bilateral - most common oestrogenic tumour of ovary, 50% post-menopause, 45% pre) Thecoma The above two produce oestrogen, cause precocious puberty or endometrial hyperplasia / carcinoma Sertoli-Leydig - rare, virilisation (testosterone) Fibroma - most common one to cause Meigs (90% of M if fibroma. 40% of F causes Meigs)
40
Physiologic bowel herniation
Should not be seen after 12-13 weeks
41
Polycystic ovary syndrome
``` Clinical and biochemical diagnosis Peripheral cysts - 12 or more follicles in each ovary (Rotterdam - new study says 25) "String of pearls" 2-9mm Volume of ovary > 10mL ``` ``` 2 out of 3 of Oligomenorrhoea Clinical and biochemical hyperandrogenism Polycystic ovaries on ultrasound AND Exclusion of other causes ``` Can cause endometrial hyperplasia / cancer / polyps 20% of reproductive age women
42
Ovarian hyperstimulation syndrome
Bilateral ovaries > 5mL Numerous large follicular cysts, with increased blood flow Echogenic stromal tissue Ascites and effusions
43
Ectopic pregnancy
2% of all pregnancies
44
Clinodactyly
Angulation at interphalangeal joint, typically 5th finger Associated with aneuploidy - Down (60%), 18, Klinefelter, Turner (In Downs often also have hypoplasia of middle phalanx of 5th)
45
Uterine malformations, outcomes
Bicornuate similar to general population | Didelphus and septate have increased miscarriage rates- 30% and 60%
46
Twin peak sign / lambda sign
Sign of dichorionicity - placental tissue on separating membrane
47
Tuberculous salpingitis
Thickwalled, cystic masses | Painful, afebrile
48
Molar pregnancy
Complete mole haploid - 2 sperm empty egg or duplicated single sperm Partial mole - two sperm in an egg with chromosomes - triploid Bilateral theca lutein cysts from high HCG - upto 50%, more common in complete Invasiv mole 5-10% Choriocarcinoma 1-5%
49
Echogenic bowel
``` Soft marker of T21 CF Intra-amniotic haemorrhage with swallowed blood products CMV IUGR Fetal hypoxia Hydrops ```
50
Placental praevia
Low lying <2cm Marginal covers part of cervix but not os Partial - partially covers os Complete
51
Omphalocele
Associated with trisomies - 18 most common, also 13 and 21. And Turners, Klinefelters Beckwith Weidemann Bladder exstrophy and cloacal exstrophy Raised maternal AFP (along with neural cord defects more commonly, and tumours)
52
Toxoplasmosis
Calc in thalamus, basal ganglia, choroid plexus. If just periventricular think CMV or TS Microcephaly and mental retardation Or macrocephaly from aqueduct stenosis Head size may return to normal
53
Fetal heart rate
100bpm 5-6 weeks | 140-160 at 8 weeks
54
Monozygotic twins
MCDA 60%, DCDA 30%, MCMA 10%
55
Number of yolk sacs
Is equal to the number of amnions
56
Fused placentas, twins
Dichorionic can fuse, giving appearance of monochorionicitiy
57
DCDA twins
2/3 dizygotic, 1/3 monozygotic
58
FIGO cervical cancer staging
.
59
Cervical MR appearance
T1 uniform intermediate High T2 mucosa Low T2 fibrous inner zone Intermediate T2 outerzone continuous with myometrium
60
Fetal enteric duplication cyst
80% cystic, 20% tubular - more likely to communicate with GI tract Located in the mesentery 30% will have associated abnormalities - GI for hindgut and spine for foregut
61
Urinary tract
In the fetus, ureteric dilatation more significant than renal pelvis dilatation, which may be normal
62
Fetal pleural effusion
``` Most commonly chylo Associated with Aneuploidy Hydrops (and pulmonary masses e.g CPAM, sequestration, cardiac disease) May get secondary polyhydramnios ``` 10% resolve spontaneously May require thoracocentesis or thoracoamniotic shunting if large or recurrent Karyotyping advised -6% abnormal
63
Normal placenta
>2cm thick | Thinned in diabetes, HTN. Puts fetus at risk of growth restriction
64
Abruption
Clinical diagnosis. Ultrasound may be negative. Marginal most common Separation of chorionic plate and placenta (pre-placental collection) Raised placental edge in 50%
65
Pseudoomphalocele
Deformation of abdomen from transducer pressure, and oblique scan angle. More common in oligohydramnios Also physiological gut herniation at early gestation
66
Twins
``` 80% Didi, monodi 30%, mm 1% 5x risk of preterm delivery MCMA 54% perinatal mortality Didi 10% md 20% ```
67
TTTS
10-20% of monochorionic pregnancies | More common if diamniotic
68
Maternal diabetes
Associated with: Heart - VSD, truncus transposition Lung - RDS, TTN GI - situs, meconium plug CNS - lots - neural tube, holoprosencephaly, caudal regression, sirenomelia Renal - agenesis, hydronephrosis, ureteric duplication Skeletal - polydactyly, syndactyly Other - poly, macrosomia, IUGR, single UA
69
Fetal intracranial calc
Toxoplasmosis and CMV - toxo random, CMV periventricular Tumours Sturge Weber and TS
70
Mega cisterna magna
>10mm antenatally | Trisomy 18, CMV, infarction
71
2,59,uterine cancer staging (endometrial), ovarian, others?
.
72
Chorioangioma
.