a. Multiple small peripheral perfusion defects
b. Multiple large perfusion defects
c. Matched defects
d. Decreased ventilation with normal perfusion
e. Complete loss of unilateral perfusion.
b. Multiple large perfusion defects
b. Splenosis
d. Intercostal catheter immediately
a. PAPVR
*AJL - the answer above does not reflect the most recent fleicshner guidelines (2017).
Solitary solid node
<6mm - low risk (nothing), high risk (optional F/U at 12 months)
6-8mm - low risk and high risk (6-12/12 and 18-24/12 (optional low risk))
>8mm - 3/12 CT, PET or biopsy.
c. Agenesis of the corpus callosum
a. Hyperdense mass in the cerebellar vermis
b. Hyperdense mass in the cerebellar hemisphere
c. Hypodense mass in the cerebellar vermis
d. Hypodense mass in the cerebellar hemisphere
e. Hypodense mass with an enhancing nodule in the cerebellar hemisphere.
e. Hypodense mass with an enhancing nodule in the cerebellar hemisphere.
*AJL - Favours ependymoma
Difficult to distinguish between ependymoma, astrocytoma and TM on these details.
Astrocytoma spans an average of 4-7 segments (RP) and likely homogeneous signal abnormality.
Ependymoma is more likely in an adult and can have extensive oedema accounting for the long segment change but may be more heterogeneous signal abnormality.
TM is usually acute change.
I think given it’s progressive rather than acute and in an adult perhaps ependymoma is more likely (also favoured by a neuroradiologist).
I think the important thing is that we’ve all learnt something?
Previous answer…
a. Transverse myelitis
Acute transverse myelitis (ATM) is an inflammatory condition affecting both halves of the spinal cord and associated with rapidly progressive motor, sensory, and autonomic dysfunction.It is mostly imaged with MRI, which generally shows a long segment (3-4 segments or more) of T2 increased signal occupying greater than two-thirds of the cross-sectional area of the cord, with variable pattern of enhancement and no diffusion restriction.
Cause:acute infection (most commonly viral)post-infection (ADEM )post-vaccination autoimmune (SLE, MS)systemic malignancy
Treatment and prognosis
Treatment of secondary ATM depends on the underlying cause. No treatment currently exists for idiopathic cases.One-third of patients recover with little or no sequelae, one-third are left with a moderate degree of permanent disability, and one-third are left with severe disabilities 3.
DDX:
- MS
- NMO
- ADEM
- infarct
*LW:
Favouring radicular cyst
AJL agree. Ameloblastoma is usually more expansile and erodes roots.
**LJS - unsure. Mets have been chosen for this stem previously. Radicular cyst typically well circumscribed and centered on tooth. Age of pt would be useful for ?mets
Previous answer
Ameloblastoma?
d. Lefort 2
b. Dermoid
**LJS - Cyst containing proteinaceous fluid would be T1 high and T2 high
Haemorrhagic cyst with high T1 signal could have variable T2 depending on age of blood. Radiopedia says low T2 in haemorrhagic cyst –> hence favored answer is Haemorrhagic cyst
b. Proteinaceous cyst
Haemorrhagic cyst would be high T1 and T2
Differential for a low T2 renal lesion
d. VIPoma
*LW:
Neuroenteric systs usually intra dural extramedullary in location, ventrally located, usually thoracic.
Associated with vertebral anomalies (Klippel feil, hemi vertebrae, spina bifida)
Variable signal intensity on T1 and T2.
Arachnoid cyst, can be intra or extra dural, and can be associated with spina bifida, although vertebral anomalies generally uncommmon, following CSF signal intensity on T1 and T2.
so…..
I think incomplete recall, and question stem was aiming towards neuroenteric cyst, given vertebral anomalies component, and axial location may have been incompletely recalled.
c. Neurenteric cyst
For this question the answer can only be 3a or 3c stage -> so answer is C (3a)
Can’t be 3b (T4NoMo)
Stage:
Primary tumor (T)TX: primary tumor cannot be assessed T0: no evidence of primary tumor Tis: carcinoma in situ (Bowen disease, high-grade squamous intraepithelial lesion [HSIL], anal intraepithelial neoplasia II-III (AIN II-III)
T1: tumor 2 cm or less in greatest dimension
T2: tumor >2 cm but <5 cm in greatest dimension
T3: tumor >5 cm in greatest dimension
T4: tumor of any size invades adjacent organ(s), e.g. vagina, urethra, bladder (note that direct invasion of the rectal wall, perirectal skin, subcutaneous tissue, or the sphincter muscle(s) is not classified as T4)
Regional lymph nodes (N)
Nx: regional lymph nodes cannot be assessed
N0: no regional lymph node metastasis
N1: metastasis in regional lymph nodes
N1a: metastases in inguinal, mesorectal, and/or internal iliac lymph nodes
N1b: metastases in external iliac lymph nodes
N1c: metastases in external iliac and in inguinal, mesorectal, and/or internal iliac lymph nodes
Distant metastasis (M)
Mx: distant metastasis cannot be assessed
M0: no distant metastasis
M1: distant metastasisInvolvement of para-aortic or more distant lymph nodes is considered as M1.
c. Haematoma
d. Osteitis condensans ilii
Triangular, bilateral, normal joint space. Lower iliac bones only.
Sacroiliac joint- upper 1/3 fibrocartilaginous- lower 2/3 synovial
d. Adventitial bursitis. Only option that can be subcutaneous
ADventitial bursitis- occurs are area of friction- formed from coalescing fluid pockets which becomes well cirucmscribed with time. - superficial
dorsal triquetrum fracture - less common then scaphoid
b. Modic type II changes
a. Hyperinflation of the lung
a. Tetralogy of Fallot
b. Transposition of the great arteries
c. Tricuspid atresia
d. Ventricular septal defect
e. Consolidation
b. Transposition of the great arteries
*LW:
Complete tracheal rings are a rare, isolated tracheal or tracheobronchial anomaly resulting from abnormal cartilage growth, forming a complete ring and often causing airway stenosis.
Associated with:
- aberrant left pulmonary artery (pulmonary artery sling) in 35-50%
- >75% have associated oesophageal, cardiac, skeletal, and/or genitourinary anomalies
- congenital heart disease in 25%
- trisomy 21
Pulmonary aplasia: has ipsilateral absence of pulmonary artery, with contralateral hyper inflation. No mention about complete tracheal rings.
c. Pulmonary agenesis because of the absent PA? Not sure though.
e. Polycystic ovaries
*LW:
TOA could be also be included within this…
Stem same multilocular cystic mass (i.e. singular, PCOS usually bilateral), however obesity associated with PCOS.
Although there is stated ectopic risk with PCOS (but not in radiopedia or STATDx), ectopic more associated with PID - TOA….
So hopefully incomplete recall, as another discriminator between the two options of TOA and PCOS would be helpful…..but I would favour TOA
**LJS - agree with LW