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Published on: September 4, 2017
Cavernous malformations in pregnancy
Shuichi Yamada1, Hiroyuki Nakase, Ichiro Nakagawa
1Department of Neurosurgery, Nara Medical University, Kashihara, Nara, Japan. syamada@naramed-u.ac.jp
Insights
Cerebral cavernous malformations pose a risk of hemorrhage in pregnant women, especially with prior bleeding history. Management involves conservative follow-up or surgery, with multidisciplinary collaboration crucial for pregnant patients.
Area of Science:
- Neurology
- Obstetrics
- Genetics
Background:
- Cerebral cavernous malformations (CCMs) are rare but significant causes of cerebral hemorrhage in pregnant and puerperal women.
- Pregnancy hormones and vascular growth factors can increase CCM bleeding risk and size.
- Genetic factors and a history of bleeding or familial CCMs elevate hemorrhage risk.
Observation:
- CCMs are more prone to bleeding or enlargement during pregnancy.
- Conservative management with MRI monitoring is typical for asymptomatic or mildly symptomatic cases.
- Surgical intervention is recommended for severe or progressive CCM symptoms.
Findings:
- Surgery is also considered for mild CCM symptoms if risk factors for bleeding are present.
- Multidisciplinary collaboration involving anesthesiology and obstetrics is vital for surgical planning in pregnant women.
- Perioperative management must address pregnancy-specific complications like weight gain and airway management challenges.
Implications:
- This strategy optimizes treatment for pregnant women with cerebral cavernous malformations.
- It highlights the importance of considering hormonal influences and genetic predispositions.
- Emphasizes the need for specialized, collaborative surgical planning to ensure maternal and fetal safety.
Abstract:
Cavernous malformation is a relatively rare disease, but is important in the etiology of cerebral hemorrhage in pregnant and puerperal women. The risk of bleeding is particularly high in patients with a previous history of bleeding, patients with a family history of cavernous malformations, and patients with the causative cerebral cavernous malformation gene. Cavernous malformations are more likely to bleed or to increase in size during pregnancy, under the influence of female hormones and vascular growth factors such as vascular endothelial growth factor. We report our strategy for the treatment of cavernous malformations in pregnant women, with reference to the relevant literature. Asymptomatic patients and those with mild symptoms are usually followed up conservatively by magnetic resonance imaging, without active treatment, but surgical treatment is indicated in patients with severe or progressive symptoms; surgery should also be considered in patients with mild symptoms having risk factors for bleeding. If surgical treatment is selected, the operation plan needs to be devised in collaboration with the specialties of anesthesiology and obstetrics and gynecology, rather than by the brain surgeon alone, in view of the possibility of occurrence of complications specific to pregnant women, such as complications related to weight gain and difficulty in securing the airway, which develop during the perioperative period.
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