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Nishimoto-Takeuchi-Kudo disease: case report.
Journal of Neurology, Neurosurgery, and Psychiatry
|October 1, 1970
Summary
A rare cerebrovascular disorder caused an extensive network of blood vessels in a child. This condition, similar to moyamoya disease, affects large intracranial arteries.
Area of Science:
- Neurology
- Vascular Medicine
- Pediatric Neurology
Background:
- Obliterating disorders of large intracranial arteries are rare and can lead to significant neurological deficits.
- The development of collateral circulation, such as a rete mirabile, is a compensatory mechanism in response to arterial occlusion.
- Moyamoya disease, a specific type of progressive cerebrovascular disease, is characterized by stenosis or occlusion of the internal carotid arteries and the development of a collateral network.
Purpose of the Study:
- To report a unique case of an obliterating disorder of the large intracranial arteries in a pediatric patient.
- To describe the formation of an extensive collateral network of the rete mirabile type.
- To compare this case with previously described conditions such as abnormal cerebrovascular networks, occlusion of the circle of Willis, and moyamoya disease.
Main Methods:
- Case report of a 7-year-old boy.
- Clinical presentation and diagnostic imaging findings were analyzed.
- Pathological characteristics of the cerebrovascular network were described.
Main Results:
- The patient presented with an obliterating disorder affecting large intracranial arteries.
- An extensive collateral network, described as a rete mirabile, was observed.
- The findings were analogous to descriptions of abnormal cerebrovascular networks and moyamoya disease.
Conclusions:
- This case highlights a rare presentation of intracranial arterial disease in a child.
- The formation of a rete mirabile-type collateral network is a significant finding in response to arterial occlusion.
- Further research is needed to understand the etiology and optimal management of such conditions.