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Tricuspid valve hemangioma associated with hypoplastic left heart syndrome presenting as sudden infant death syndrome
Author(s) -
Brijnandan Gupta,
Shouriyo Ghosh,
Maikal Kujur,
Khushbu Khetan,
Tarun Kumar
Publication year - 2016
Publication title -
turkish journal of pathology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.305
H-Index - 14
eISSN - 1309-5730
pISSN - 1018-5615
DOI - 10.5146/tjpath.2015.01362
Subject(s) - medicine , hypoplastic left heart syndrome , autopsy , tricuspid valve , ventricle , cardiology , hemangioma , tricuspid atresia , incidence (geometry) , population , heart disease , surgery , physics , environmental health , optics
Primary cardiac tumors are rare in children with a low incidence varying from 0.0017 to 0.28% in autopsy studies. Approximately 90% of the reported primary cardiac tumors in the pediatric population are benign and the most common subtype is rhabdomyomas accounting for approximately 60%, while hemangiomas are rare primary tumors with a 5% incidence. Hypoplastic left heart syndrome is abnormal development of the left-sided cardiac structures, leading to obstruction of blood flow from the left ventricle out-flow tract. Here we report a case of tricuspid hemangioma in association with hypoplastic left heart syndrome, a rare association not previously reported in the literature.

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