Genotype-Guided Medical Treatment of an Arteriovenous Malformation in a Child.
case_report · Level V
Where this comes from
- Record sourced from PubMed, PMID 30566190.
- Also identified by DOI 10.1001/jamadermatol.2018.4653 and PMC identifier 7186908.
- No licence information is recorded for this record.
- Because redistribution is not established, this page shows the abstract only. Follow the links below for the full text.
Abstract
Genetic testing results can provide guidance in developing personalized treatment plans for patients with vascular anomalies. To explore the efficacy of tramitinib in the treatment of an extracranial arteriovenous malformation with a somatic <i>MAP2K1</i> mutation. Case report of a child with an arteriovenousu malformation that was successfully treated with trametinib after identification of a specific somatic mutation within the malformation. Outpatient Vascular Anomalies Clinic, Stanford University, Stanford, CA. An 11-year-old girl with an arteriovenous malformation on the back who had failed treatment with systemic sirolimus. Paired exome sequencing using tumor and saliva DNA was performed and identified a somatic mutation within the <i>MAP2K1</i> gene. The patient was then transitioned to trametinib at a starting dose of 0.5 mg once daily then increased to 0.5 mg twice daily after one month. Tramitinib was effective in reducing the size of and blood flow to the arteriovenous malformation. After one month on tramitinib, the patient and parents noticed the malformation reduced in size and became lighter in color. After six months of treatment, quantitative analyses were performed using magnetic resonance imaging and showed significant interval decrease in the volume of the malformation and the caliber of the vasculature compared to prior examinations. To date, she has tolerated the treatment well with development of a mild acneiform eruption responding well to over the counter adapalene and benzoyl peroxide. Management of arteriovenous malformations is very challenging due to almost inevitable disease progression and high recurrence rates after surgical resection. The discovery of a somatic mutation associated with this arteriovenous malformation provided guidance for targeted therapy. Trametinib may be a promising targeted therapeutic option for sporadic extracranial arteriovenous malformations harboring <i>MAP2K1</i> mutations.
Medical subject headings
- Arteriovenous Malformations
- Microtubule-Associated Proteins
- Molecular Targeted Therapy
- Pyridones
- Pyrimidinones