Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Case Reports
. 2020 Jul 15:2020:7689450.
doi: 10.1155/2020/7689450. eCollection 2020.

Postpartum-Onset Moyamoya Disease: A Rare Cause of Stroke in Unexpected

Affiliations
Case Reports

Postpartum-Onset Moyamoya Disease: A Rare Cause of Stroke in Unexpected

Muhammet Ozer et al. Case Rep Neurol Med. .

Abstract

Moyamoya disease (MMD) is a chronic cerebrovascular occlusive disease that is characterized by progressive bilateral stenosis of the terminal portion of the internal carotid artery and its main branches. Cerebrovascular events are the primary presenting symptoms and are related both to stenosis and occlusion of the ICAs and their main branches. Detection of bilateral stenosis by cerebral angiography is considered the gold standard, but computed tomography angiography (CTA) is also an acceptable method of diagnosis. In the current literature, there are no precise data on the incidence of moyamoya disease in Europe and the United States. Also, the pathogenesis of MMD remains obscure, and genetic factors and inflammation are the two most representative mechanisms. Here, we report the case of MMD in a 29-year-old African American female who presented with an ischemic stroke for the second time that manifested after pregnancy. This case is important to increase awareness of the probability of this rare disease in Western countries as well as to call attention to pregnancy's accelerating effects of MMD. Careful, long-term neurologic and radiologic follow-up is essential in adult patients with MMD to prevent additional stroke events and improve outcomes.

PubMed Disclaimer

Conflict of interest statement

The authors declare that there are no conflicts of interest.

Figures

Figure 1
Figure 1
Axial MRI brain imaging: (a)—(d) images from the first episode of stroke, with regions of restricted diffusion indicative of acute ischemia (arrows), primarily noted in the right cerebral hemisphere; (e)—(h) images from the second episode, with progressive bilateral ischemic changes (arrows).
Figure 2
Figure 2
Digital subtraction angiography images: (a) left internal cerebral artery (ICA) with focal distal ICA and proximal M1 arteriopathy (arrows) with prominent lateral lenticulostriate branches, indicating early collateralization of flow (arrowheads); (b) right internal cerebral artery (ICA) with focal distal ICA, proximal MCA (M1), and proximal ACA (A1) arteriopathy (arrows) with prominent lateral lenticulostriate branches, indicating early collateralization of flow (arrowheads).

References

    1. Takeuchi K. Hypoplasia of bilateral internal carotid arteries. Brain Nerve. 1957;9:37–43.
    1. Miao W., Zhao P.-L., Zhang Y.-S., et al. Epidemiological and clinical features of moyamoya disease in Nanjing, China. Clinical Neurology and Neurosurgery. 2010;112(3):199–203. doi: 10.1016/j.clineuro.2009.11.009. - DOI - PubMed
    1. Uchino K., Johnston S. C., Becker K. J., Tirschwell D. L. Moyamoya disease in Washington state and California. Neurology. 2005;65(6):956–958. doi: 10.1212/01.wnl.0000176066.33797.82. - DOI - PubMed
    1. Kleinloog R., Regli L., Rinkel G. J. E., Klijn C. J. M. Regional differences in incidence and patient characteristics of moyamoya disease: a systematic review. Journal of Neurology, Neurosurgery & Psychiatry. 2012;83(5):531–536. doi: 10.1136/jnnp-2011-301387. - DOI - PubMed
    1. Ma J. C., Burlingame J. M. Moyamoya disease in pregnancy: a case series and review of management options. Hawaii Medical Journal. 2011;70(8):161–163. - PMC - PubMed

Publication types

LinkOut - more resources