Literature DB >> 32731220

Cerebral Cavernous Malformations, Developmental Venous Anomaly, and Its Coexistence: A Review.

Pretty Sara Idiculla1, Dhineshreddy Gurala2, Jobin Philipose2, Kartikeya Rajdev3, Prateek Patibandla4.   

Abstract

BACKGROUND: Cerebral cavernous malformations (CCMs) are intracranial vascular malformations that can exist as a single lesion or mixed vascular lesions. The most common mixed form is the coexistence of CCM with an associated developmental venous anomaly (DVA). In this paper, we aim to give a comprehensive review of CCM, DVA, and their coexistence as mixed lesions. A PubMed search using the keywords "Cerebral cavernous malformations, Developmental venous anomaly, Mixed Cerebral cavernous malformations with Developmental venous anomaly" was done. All studies in the English language in the past 10 years were analyzed descriptively for this review.
SUMMARY: The search yielded 1,249 results for "Cerebral cavernous malformations," 271 results for "Developmental venous anomaly," and 5 results for "Mixed Cerebral cavernous malformations with Developmental venous anomaly." DVA is the most common intracranial vascular malformation, followed by CCM. CCM can have a wide array of clinical presentations like hemorrhage, seizures, or focal neurological deficits or can also be an incidental finding on brain imaging. DVAs are benign lesions by nature; however, venous infarction can occur in a few patients due to acute thrombosis. Mixed CCM with DVA has a higher risk of hemorrhage. CCMs are angiographically occult lesion, and cerebral digital subtraction angiography is the gold standard for the diagnosis of DVA. Mixed lesions, on the other hand, are best diagnosed with magnetic resonance imaging, which has also been effective in detecting specific abnormalities. Asymptomatic lesions are treated through a conservative approach, while clinically symptomatic lesions need surgical management.
CONCLUSION: Individual CCM or DVA lesions have a benign course; however, when they coexist in the same individual, the hemorrhagic risk is increased, which prompts for rapid diagnosis and treatment.
© 2020 S. Karger AG, Basel.

Entities:  

Keywords:  Cerebral cavernous malformations; Developmental venous abnormality; Mixed cerebral vascular malformations

Year:  2020        PMID: 32731220     DOI: 10.1159/000508748

Source DB:  PubMed          Journal:  Eur Neurol        ISSN: 0014-3022            Impact factor:   1.710


  2 in total

1.  Intracerebral Hemorrhage Caused by Thrombosis of a Developmental Venous Anomaly with an Unusual Structure: A Case Report.

Authors:  Sunhyang Lee; Dae Yoon Kim; Mi Kyung Kim; Hyun Jin Kim
Journal:  Taehan Yongsang Uihakhoe Chi       Date:  2021-09-27

2.  Multiple spinal intramedullary cavernous angiomas with bleeding episode mimicking an intramedullary tumor.

Authors:  Sri Andreani Utomo; Abdul Hafid Bajamal; Yuyun Yueniwati; Muhammad Arifin Parenrengi; Dyah Fauziah
Journal:  J Radiol Case Rep       Date:  2022-03-01
  2 in total

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