Pilsicainide Administration Unmasks a Phenotype of Brugada Syndrome in a Patient with Overlap Syndrome due to the E1784K SCN5A Mutation
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- Hasebe Hideyuki
- Division of Arrhythmology, Shizuoka Saiseikai General Hospital, Japan Cardiovascular Division, Faculty of Medicine, University of Tsukuba, Japan
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- Yokoya Tomoyo
- Division of Arrhythmology, Shizuoka Saiseikai General Hospital, Japan
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- Murakoshi Nobuyuki
- Cardiovascular Division, Faculty of Medicine, University of Tsukuba, Japan
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- Kurebayashi Nobutake
- Division of Cardiology, Chutoen General Medical Center, Japan
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Description
<p>Mutations in the cardiac sodium channel SCN5A can cause phenotypic overlap syndrome of long QT syndrome and Brugada syndrome. However, Brugada-type ST elevations in patients with overlap syndrome are often concealed, which creates a diagnostic challenge. A 38-year-old man was admitted due to ventricular fibrillation (VF). The 12-lead electrocardiogram showed a prolonged QT interval and saddleback-type ST elevation. Pilsicainide administration induced coved-type ST elevation and VF triggered by a single premature ventricular contraction. A genetic analysis showed an SCN5A c.5350G>A p.E1784K mutation. The present case suggests the importance of a drug administration test being performed in the clinical management of overlap syndrome. </p>
Journal
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- Internal Medicine
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Internal Medicine 59 (1), 83-87, 2020-01-01
The Japanese Society of Internal Medicine
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Details 詳細情報について
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- CRID
- 1390846609790740608
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- NII Article ID
- 130007779214
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- NII Book ID
- AA10827774
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- ISSN
- 13497235
- 09182918
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- HANDLE
- 2241/00161439
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- PubMed
- 31484910
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- Text Lang
- en
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- Data Source
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- JaLC
- IRDB
- Crossref
- PubMed
- CiNii Articles
- OpenAIRE
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- Abstract License Flag
- Disallowed