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Unusual Case of Cerebral Venous Thrombosis in Patient with Crohn's Disease
Inha Kim1, Kyung-Hyun Min1, Minju Yeo1
1Neurology, Chungbuk National University Hospital, Cheongju, Korea.
Insights
Cerebral venous thrombosis (CVT) can occur in Crohn's disease (CD) patients, even without active disease. This case suggests CVT risk may be linked to Crohn's disease itself, not just its flare-ups.
Area of Science:
- Neurology
- Gastroenterology
- Hematology
Background:
- Crohn's disease (CD) is associated with an increased risk of hypercoagulable states, potentially leading to complications like cerebral venous thrombosis (CVT).
- While CVT is considered a rare complication of CD, its development is often linked to active disease states.
Observation:
- A 17-year-old male with a history of CD, managed with mesalazine and azathioprine, presented with acute neurological deficits including right-sided weakness and hypesthesia.
- Brain MRI revealed acute infarction and cortical subarachnoid hemorrhage. Magnetic resonance venography identified a filling defect in the superior sagittal sinus, indicative of CVT.
- The patient exhibited no symptoms of active CD flare-up, such as bloody stools, abdominal pain, or weight loss.
Findings:
- This case demonstrates CVT occurring in a patient with Crohn's disease during a period of clinical remission.
- The findings suggest that the underlying Crohn's disease pathology, independent of active inflammation, may contribute to the hypercoagulable state leading to CVT.
Implications:
- The risk of CVT in Crohn's disease patients may persist even in the absence of active disease.
- This highlights the importance of considering CVT in CD patients presenting with neurological symptoms, regardless of their current disease activity status.
- Further research is warranted to elucidate the specific mechanisms linking Crohn's disease to CVT outside of active disease phases.
Abstract:
The development of cerebral venous thrombosis (CVT) as a secondary complication of Crohn's disease (CD) seems to be rare, but it is generally accepted that the disease activity of CD contributes to the establishment of a hypercoagulable state. Here, we describe a case of CVT that developed outside the active phase of CD. A 17-year-old male visited the emergency room because of a sudden onset of right-sided weakness and right-sided hypesthesia. He had been diagnosed with CD 1 year before and was on a maintenance regimen of mesalazine and azathioprine. He did not exhibit any symptoms indicating a CD flare-up (bloody stools, abdominal pain, complications, or weight loss). A brain MRI scan revealed an acute infarction of the left frontal cortex and a cortical subarachnoid hemorrhage. Additionally, a magnetic resonance venography revealed a segmental filling defect in the superior sagittal sinus and also the non-visualizability of some bilateral cortical veins. The characteristics of the present case suggest that the risk of CVT is most likely related to CD per se rather than disease activity associated with CD.
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