2016
DOI: 10.1097/mjt.0000000000000107
|View full text |Cite
|
Sign up to set email alerts
|

Sudden Cardiac Arrest in a Patient With Apical Hypertrophic Cardiomyopathy

Abstract: Apical hypertrophic cardiomyopathy (HCM) is a phenotypic variant of nonobstructive HCM, in which hypertrophy of the myocardium predominantly involves the left ventricular apex. It is common in Japanese and other Asian populations but is rare in the United States. Apical HCM has a relatively benign prognosis in terms of cardiovascular mortality; however, morbid events such as ventricular aneurysms, apical thrombi, diastolic dysfunction, atrial fibrillation, and myocardial infarction are not uncommon. We report … Show more

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
1

Citation Types

0
1
0

Year Published

2016
2016
2020
2020

Publication Types

Select...
5

Relationship

0
5

Authors

Journals

citations
Cited by 7 publications
(1 citation statement)
references
References 37 publications
0
1
0
Order By: Relevance
“…Although most patients with RV wall hypertrophy have significant LV involvement, isolated severe cases such as in our patient are rare [3][4][5]. Compared with severe LV wall hypertrophy, severe RV wall hypertrophy is characterized by progressive clinical deterioration and increased cardiovascular-related death at an early stage [6].…”
Section: Commentmentioning
confidence: 96%
“…Although most patients with RV wall hypertrophy have significant LV involvement, isolated severe cases such as in our patient are rare [3][4][5]. Compared with severe LV wall hypertrophy, severe RV wall hypertrophy is characterized by progressive clinical deterioration and increased cardiovascular-related death at an early stage [6].…”
Section: Commentmentioning
confidence: 96%