Carotid Artery Dissection in Older Adults
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Spontaneous extracranial internal carotid artery dissection (ICAD) causes a broad spectrum of symptoms, ranging from minor headache to permanent ischemia of the brain or retina. Although ICAD is one of the most common causes of ischemic stroke in young and middle-aged adults, it can occur in older adults and pose a diagnostic challenge due to its local signs and symptoms such as headache, neck pain, Horner syndrome, tinnitus, and cranial nerve palsy, which mimic other conditions. This article provides a comprehensive overview of the possible causes, clinical features, diagnostic modalities, and treatments, as well as differential diagnoses of ICAD.
Case Vignette
A 62-year-old male was admitted to the hospital with a 3-week history of severe, persistent right-sided headache and blurred vision. He was initially diagnosed with sinusitis and treated with three courses of antibiotics without much improvement. There was moderate relief of his headache with the addition of 5 days of daily prednisone 60 mg for presumptive sinusitis; however, it quickly recurred after discontinuation of the drug. On admission, the patient reported dull right-sided headache associated with nausea and vomiting, right-sided scalp tingling, visual loss, and right temporal pain. He also complained of neck pain with extreme flexion. He denied jaw claudication, myalgia, muscle weakness, arthralgia, or morning stiffness. The remainder of the review of systems was negative. His past medical history was significant for allergic rhinitis, hypothyroidism, hyperlipidemia, essential tremor, posttraumatic stress disorder, and testicular cancer treated with orchiectomy and radiation therapy. The patient reported that he fell on ice 2 months prior to admission and sustained ecchyomosis of his right cheek. At presentation, his medications included prednisone, indomethacin, levothyroxine, simvastatin, fluoxetine, primidone, trimethoprim/sulfamethoxazole, and mometasone nasal spray.
On physical examination, the patient’s vital signs were normal except for a temperature of 100.94 degrees F (38.3 degrees C), and he appeared in mild distress due to pain. There was marked tenderness over the angle of the right jaw, temporal region, maxillary sinus, and sternocleidomastoid muscle. There was no erythema, swelling, or beading of the temporal arteries, and no carotid bruits were heard. He had full range of motion of the temporomandibular joints. A fundoscopic examination of dilated pupils showed no evidence of hemorrhage, cotton-wool spots, or disc ischemia. No peripheral synovitis was noted. The neurologic examination was significant for right ocular ptosis and miosis, with the rest of the cranial nerves intact.
Admission laboratory values were significant for platelets of 102 x103/µL. Westergren erythrocyte sedimentation rate (ESR) was 25 mm/h (0-20 mm/h) and C-reactive protein was 9.77 mg/dL (< 0.744 mg/dL). Computed tomography of the head was unremarkable except for bilateral moderate mucosal thickening with opacification of the ethmoid and maxillary sinuses.
The patient was restarted on high-dose prednisone 80 mg daily because of the concern that giant cell arteritis (GCA) could be a potential cause of his headaches and blurred vision. He had significant improvement in his symptoms the following day, and the next day underwent right temporal artery biopsy, which showed mild arteriosclerosis but no evidence of GCA. Magnetic resonance imaging and angiography (MRI/MRA) of the brain/neck was obtained, which showed dissection of the right internal carotid artery (ICA) with subacute thrombus extending from the right extracranial ICA bulb to the skull base with involvement of the proximal ICA petrous segment. The axial T1-weight MRI revealed a crescent sign, an elliptical bright signal within the arterial wall from blood (Figure).
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