Spontaneous bilateral internal carotid artery occlusion



Case: A 48 years old female patient, previously healthy, presented with right hemiparesis which improved rapidly over two days with some residual weakness. She was found to have left perforator infarct on CT, and a doppler study showed absence of bilateral ICA flow.

CT

Fig1: CECT (actually source image of CTA) showing left gangliocapsular infarct

 

CT Angiogram was done which confirmed bilateral ICA occlusion.

KAVITA_YADAV_48YRS_F.CT.CT_ANGIO.451.1.2011.03.30.10.40.50.78125.19589448KAVITA_YADAV_48YRS_F.CT.CT_ANGIO.27495.10320.2011.03.30.10.40.12.687500.19587230

Fig 2: CTA; 3D color SSD images; AP and oblique views; both internal carotids are completely occluded – right one from origin while on the left side a small stump is seen, right vertebral artery is dominat, left vertebral artery is hypoplastic, entire brain in almost dependent upon a solitary vessel –right vertebral, patent circle of Willis saving the patient from any major catastrophe with supratentorial parenchyma being supplied via posterior and anterior communicating arteries.

Discussion:

Spontaneous ICA dissection is an uncommon but increasingly recognized entity, with the increased awareness among physicians and the advent of modern imaging technologies, especially USG (and doppler) which is fast, ubiquitous and cheap.

Cervicocephalic dissections may occur spontaneously or secondary trauma which may be major but many patients have only minor trauma, something like playing cricket, yogasana, hiccups etc, while many housewives don't exactly recollect even trivial injuries. In some patients, they are associated with an underlying arteriopathy like

  • Fibromuscular dysplasia, vessel tortuosity , Marfan syndrome , Ehlers-Danlos syndrome, Alpha-1-antitrypsin deficiency, Cystic medial necrosis, Type 1 collagen point mutation, Other connective tissue disorders
  • In many, no cause of spontaneous dissection is found.
  • systemic infections, hypertension,  elevated homocysteine, alcohol, OCP have also been associated..

The cervical internal carotid artery is affected in 75% of patients (usually approximately 2 cm distal to the bifurcation) and the extracranial vertebral artery in 15%. The remaining cases usually involve the intracranial internal carotid artery, intracranial vertebral artery, middle cerebral artery, or basilar artery. Anterior cerebral arteries have been traditionally considered resistant, however modern imaging esp. DSA has found dissections in them too.

15% of cases are bilateral, and one half of these occur in patients with underlying fibromuscular dysplasia.

Age/Sex: Females> males, young- middle aged; cervicocephalic dissections are responsible for 1-2.5% of ischemic strokes in the general population and for 5-20% of strokes in individuals younger than 45 years.

Clinical features: commonest-focal unilateral headache; common- focal cerebral ischemic symptoms, oculosympathetic paresis, bruits, light-headedness, and neck pain; less common- syncope, amaurosis fugax, scalp tenderness, swelling in the neck, and dysgeusia

*Cephalic pain is frequent and often inaugural in carotid dissection; its recognition is important for early diagnosis and treatment, many also have painful Horner’s syndorme.

Cerebral ischemia occurs in at least 75% of reported cases (TIAs in 30%, infarcts in 45-50%).

Imaging: fat sat axial T1WI on MR very well show the dissected artery with hematoma and thrombus

Puppy sign in bilateral ICA dissection

 J Neurol Neurosurg Psychiatry2007;78:1055 doi:10.1136/jnnp.2007.115857

puppy sign

However, sometimes MRI, MRA and Doppler will miss the dissections, and DSA is still the best for diagnosing as well as planning treatment.

Further reading:

  1. Mokri Bahram et al. Spontaneous dissection of the cervical internal carotid artery. Annals of Neurology. http://dx.doi.org/10.1002/ana.410190204
  2. image
  3. Lucas C, Moulin T, Deplanque D, Tatu L, Chavot D. Stroke patterns of internal carotid artery dissection in 40 patients. Stroke 1998;29: 2646-8. [PubMed]
  4. Bradley Scott Townend, Laura Traves, Denis Crimmins, Bilateral spontaneous carotid artery dissection, Journal of Clinical Neuroscience, Volume 12, Issue 5, June 2005, Pages 592-594, ISSN 0967-5868, DOI: 10.1016/j.jocn.2004.08.020. (http://www.sciencedirect.com/science/article/B6WHP-4G1PKN8-8/2/c30c4ff302aaca48e64cc69e26ee967e)


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READ THE IMAGING CORRECTLY 2: MISSED ANEURYSM



A middle aged patient had history of neck and occipital pain and presented to the neurologist who ordered an MRI cervical spine and brain. The report came as degenerative spine (Fig 1) and normal brain (Fig 2). the neurologist ordered physiotherapy and medications.

Patient had again transient LOC a month later.

An MRI brain was ordered which again was reported normal and patient was exhaustively investigated for various conditions, all of which were within normal limits.

A month and half later patient came to casualty with unconscious for 4 hours. An NCCT head was done which was reported as SAH.

A DSA was done which showed left ophthalmic ICA aneurysm which was promptly coiled.

Patient was declared dead two days later.

Now lets review the images again:

ARTI_KUMAR_F_51Y.MR.C-SPINE_GENERAL.11.7.2011.03.28.16.33.11.125000.17633533

Fig 1: MR cervical spine, sagittal section, T1WI, showing the degenerative changes

ARTI_KUMAR_F_51Y.MR.C-SPINE_GENERAL.4.7.2011.03.28.16.34.00.703125.17619172

Fig 2: Axial FLAIR image done on first visit, reported normal, shows the aneurysm very well

ARTI_KUMAR_F_51Y.MR.HEAD_GENERAL.2.8.2011.03.28.16.36.25.578125.17640767ARTI_KUMAR_F_51Y.MR.HEAD_GENERAL.3.8.2011.03.28.16.36.09.125000.17640900ARTI_KUMAR_F_51Y.MR.HEAD_GENERAL.7.11.2011.03.28.16.35.40.515625.17644334ARTI_KUMAR_F_51Y.MR.HEAD_GENERAL.8.12.2011.03.28.16.35.24.312500.17644554

Fig3: MR brain done on 2nd visit very well shows the aneurysm on all planes and in all sequences

AARTI_KUMAR_51Y_F.CT.NCCT_HEAD.2.9.2011.03.28.16.31.21.390625.17561738

Fig 4: NCCT head, at admission on 3rd visit, shows subtle supratentorial brain parenchymal swelling and the ‘reversal sign’ suggestive of diffuse hypoxia with a ‘brain dead’ state probably already setting inARTI KUMAARTI KUMAR 4

Fig 5: DSA images, pre and post –coiling, showing ophthalmic ICA aneurysm.

 

The images tell the entire story and also the sorry state of present medicine: both the radiologist and the neurologist had missed the lesion(s) repeatedly


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ruptured SCALP AVM with large recurrent hematoma in A CHILD



A 3 years old child’s parents noticed a small swelling on the head at 2 months of age. the swelling increased gradually in size for a year then spontaneously decreased over a year. Following trivial fall, the swelling increased dramatically 3 days prior to presentation. He was otherwise normal.

On examination, the swelling was firm, smooth and pulsatile. No change related to posture or crying was seen.

A CTA was done.

SANSKAR SCALP AVM_1.CT.10.1.2011.04.15.10.22.53.515625.22632588SANSKAR SCALP AVM_1.CT.10.2.2011.04.15.10.22.53.515625.22632602SANSKAR SCALP AVM_1.CT.10.3.2011.04.15.10.22.53.515625.22632616SANSKAR SCALP AVM_1.CT.10.4.2011.04.15.10.22.53.515625.22632630SANSKAR SCALP AVM_1.CT.10.5.2011.04.15.10.22.53.515625.22632644SANSKAR SCALP AVM_1.CT.10.6.2011.04.15.10.22.53.515625.22632658SANSKAR SCALP AVM_1.CT.10.7.2011.04.15.10.22.53.515625.22632672SANSKAR SCALP AVM_1.CT.10.8.2011.04.15.10.22.53.515625.22632686SANSKAR SCALP AVM_1.CT.10.9.2011.04.15.10.22.53.515625.22632700SANSKAR SCALP AVM_1.CT.10.10.2011.04.15.10.22.53.515625.22632714SANSKAR SCALP AVM_1.CT.10.11.2011.04.15.10.22.53.515625.22632728SANSKAR SCALP AVM_1.CT.10.12.2011.04.15.10.22.53.515625.22632742SANSKAR SCALP AVM_1.CT.10.13.2011.04.15.10.22.53.515625.22632756SANSKAR SCALP AVM_1.CT.10.14.2011.04.15.10.22.53.515625.22632770

CTA, SSD and MIP images showing the right parietal swelling (hematoma) with a small AVM posteriorly, fed by branches of right superficial temporal artery. the feeders are elevated by the swelling. Also seen are a couple of phleboliths.

The AVM per-se was not filling a lot with contrast, probably partially thrombosed.

The baby was given antiinflammatory drugs and called for AVM excision after the hematoma resolved subsequently.


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internal carotid artery perforation by microguidewire during acomm aneurysm coiling



43 years old male patient had a ruptured Acomm artery aneurysm and came for coiling after 1.5 months.

the first coil was successfully placed, however there was stretching of the second coil hence it was removed along with the microcatheter.

Subsequently a fresh catheter was intriduced over a microwire. During the manipulation, contrast leakage was noted from the supraclinoid ICA

MD.RASEL AKHTER MD.RASEL AKHTER A

 

LICA injection AP and Lat views showing  contrast extravasation from terminal ICA. Note that the micocatheter has been pulled down now

Fortunately, the extravasation stopped spontaneously and rather quickly.MD.RASEL AKHTERAMD.RASEL AKHTER SAIDUR

LICA injection after 3 minute of perforation, AP and Lat views, showing normal arteries with no e/o leakage anymore

Further coiling was abandoned. Intracranial blood circulation was normal and patient was hemodynamically stable.

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DynaCT at end of procedure showing diffuse SAH. Dense contrast is seen in ambient cistern

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NCCT head done next morning, patient still intubated, showing diffuse SAH, IVH, e/o residual contrast and significant hydrocephalus

MOHAMMAD_RASEL_43_M.CT.NCCT_BRAIN.2.7.2011.03.25.15.18.48.859375.17550552MOHAMMAD_RASEL_43_M.CT.NCCT_BRAIN.2.9.2011.03.25.15.19.02.312500.17553508

NCCT head, post EVD, which was done immediately after seeing the preceding scan; patient was hemodynamically stable throughout

On day 3, patient was extubated and had bilateral lower limb paresis (2/5) as well as left upper limb paresis (4/5). He was irritable with intermittent comprehension and response. Gradually, over a period of 6-7 days, his neurology improved, however he still had significant left lower limb weakness nad the irritability persisted.

MOHAMMAD_RASEL_43_M.CT.NCCT_BRAIN.3.85.2011.03.25.15.19.46.250000.18606024

NCCT on day 7 showing near complete resolution of hemorrhage, hydrocephalus still persists

MOHD_RASEL_AKHTER_SAIDUR_M_43Y.MR.HEAD_GENERAL.11.8.2011.03.25.15.21.49.390625.18924832MOHD_RASEL_AKHTER_SAIDUR_M_43Y.MR.HEAD_GENERAL.11.11.2011.03.25.15.21.37.375000.18924925MOHD_RASEL_AKHTER_SAIDUR_M_43Y.MR.HEAD_GENERAL.11.16.2011.03.25.15.22.05.937500.18926844

MRI on day 7, done as no focal lesion was seen on the preceding CT, shows hydrocephalus, left temporal region hematoma and underlying parenchymal signal change, but no other focal lesions.

EVD drainage was done for two days, during which time , he improved significantly.

After a total of 2 weeks, he was discharged in a stable condition, with only mild residual weakness in left ankle and slight behavioral change but otherwise with good mental score.


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complicated carotid plaque with acute thrombus shows complete resolution of thrombus and plaque stabilisation with medical management



This middle aged patient was admitted with history of sudden onset weakness of the left hand about 8-10 days ago. There was past history of transient numbness of left upper limb lasting for 1-2mins about one month ago. MRI brain revealed multiple acute right fronto-parietal infarcts the arranged as a ‘string of pearls’.

1

DWI images on day of stroke showing multiple acute infarcts in right frontal and parietal region involving both the cortex as well as the subcortical white matter and centrum semiovale

 

MRA revealed ~ 70% stenosis of proximal RICA.

2

CE-MRA MIP image showing signal loss and stenosis at right carotid bulb (hand-marked arrow); remaining neck vessels are normal

Carotid DSA was planned with the aim for revascularization.

Right common carotid artery injection revealed a plaque with filling defect in the RICA just beyond the bifurcation with a meniscus sign (suggestive of fresh intraluminal thrombus), causing a 70% stenosis.

4

RCCA injection lateral view showing the thrombus and stenosis of the carotid bulb

As there was a fresh intraluminal thrombus, revascularization was deferred in view of a high risk of distal embolization. The patient was kept on medications  (heparin for a week, clopidogrel, aspirin, atorvastatin)for a period of 2 weeks.

She had gradual and continuous improvement in power and came for DSA after a month.

DSA this time showed resolution of the thrombus and now only a mild smooth stenosis remained.

3

Follow up DSA after a month showing mild stenosis with no evidence of thrombus

She has been doing well till now and had near complete recovery of power with no further ischemic neurological events


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Read the NCCT correctly



A patient presented to the medicine casualty with left hemiparesisof 5 hours duration. His NCCT head was sought correctly and immediately, the images are underneath, what do they show??
Well the casualty resident took his time and came to the conclusion that this was normal, and surprisingly informed the clinical neurology resident instead of the interventional guys. By the time the interventionist 'intervened' it was 8 hours and an MRI also had got done, which 'showed' that there were acute infarcts on right side (see ADC images below)

So where was the problem????
1. the patient lost an opportunity to have a possible treatment----endovascular thrombolysis; he had come in the window period for the same!!!
2. Our emergencies are just not geared up for neurological emergencies...stroke...
3. Residents are not exposed to nor adequately trained in emergency radiology
4. radiology residents are not available most of the time when needed most....I am saying this even though I tack...I am one
5.people are unaware of stroke and its treatment...unlike myocardial infarction ...heart attack...which even villagers know about
6. Clinical neurologists are not keen to go beyond intravenous thrombolysis, neither are they keen to improve mass awareness----probably they will have to do lot of emergency night work....ha ha....
7. etc etc etc etc...
have a look at the marked region in the original CT...clear evidence of acute infarct...missed entirely by casualty and clinical neurology resident!!!!

What they did however was get a CT after 3 days which showed the expected results...

What treatment can we offer now!!!
PHYSIOTHERAPY..
AND...a lot of investigations.....Homocystiene, B12, Lipids, MRI, MRA, Doppler...so on, so forth


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Inguinal canal and retroperitoneal hematoma during femoral puncture



Hemorrhage during femoral puncture prior to angiography is a rare complication and if unnoticed can lead to fatal retroperitoneal hematoma.
In this case we were able to identify the hemorhage only because the guidewire was not passing up straight and there was a very deceptive free back flow of blood from the sheath. However the arterial lumen was patent and the internal bleeding stopped soon after after removing the sheath and manual compression for 5 min.
Figure showing right inguinal canal and retroperitoneal hematoma. large arrow in fig A shows the constriction at the site of inguinal ligament. Small arrow indicates the femoral sheath. Double small arrow in Fig B shows the femoral catheter passed up the left femoral artery, dotted arrow in Fig B indicates free antegrade flow in right femoral artery. Note that the contrast pool has decreased in Fig B.


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