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A Case of Infantile Cardiac Rhabdomyoma Complicated by Tuberous Sclerosis
We experienced a case with fetal cardiac tumor, which was diagnosed by prenatal ultrasonographic examination, and the diagnosis was confirmed after birth. A pregnancy woman of the 26th week of gestation was referred to our hospital for close examinations of fetal cardiac tumor. Ultrasonographic exam...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elmer Press
2010
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5358235/ https://www.ncbi.nlm.nih.gov/pubmed/28352373 http://dx.doi.org/10.4021/cr104e |
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author | Serikawa, Takehiro Takahashi, Yasuhiro Kikuchi, Akira Takakuwa, Koichi Usuda, Tohei Hasegawa, Satoshi Tanaka, Kenichi |
author_facet | Serikawa, Takehiro Takahashi, Yasuhiro Kikuchi, Akira Takakuwa, Koichi Usuda, Tohei Hasegawa, Satoshi Tanaka, Kenichi |
author_sort | Serikawa, Takehiro |
collection | PubMed |
description | We experienced a case with fetal cardiac tumor, which was diagnosed by prenatal ultrasonographic examination, and the diagnosis was confirmed after birth. A pregnancy woman of the 26th week of gestation was referred to our hospital for close examinations of fetal cardiac tumor. Ultrasonographic examinations revealed single homogeneous tumor with the diameter of 14 mm intracardiac space. The tumor was considered to emerge from the ventricular septum and to be occupied in left ventricle. Other cardiac abnormalities were not detected. The fetus was diagnosed to be complicated with the intracardiac tumor, and with the possible rhabdomyoma of heart. The serial ultrasonographic examinations revealed that the fetal cardiac function was normal. The size of the tumor gradually increased, although the fetal cardiac function revealed within normal range. The patient delivered a female infant weighing 2716g with the Apgar score of 9 and 10 at one and 5 minutes after delivery. The infant was confirmed to have cardiac tumors after examination by pediatric cardiologist, and the cardiac function of the infant was diagnosed as normal condition. The computed tomography of the head revealed the intracranial multiple calcification lesions, which indicated the symptoms of tuberous sclerosis. |
format | Online Article Text |
id | pubmed-5358235 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2010 |
publisher | Elmer Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-53582352017-03-28 A Case of Infantile Cardiac Rhabdomyoma Complicated by Tuberous Sclerosis Serikawa, Takehiro Takahashi, Yasuhiro Kikuchi, Akira Takakuwa, Koichi Usuda, Tohei Hasegawa, Satoshi Tanaka, Kenichi Cardiol Res Case Report We experienced a case with fetal cardiac tumor, which was diagnosed by prenatal ultrasonographic examination, and the diagnosis was confirmed after birth. A pregnancy woman of the 26th week of gestation was referred to our hospital for close examinations of fetal cardiac tumor. Ultrasonographic examinations revealed single homogeneous tumor with the diameter of 14 mm intracardiac space. The tumor was considered to emerge from the ventricular septum and to be occupied in left ventricle. Other cardiac abnormalities were not detected. The fetus was diagnosed to be complicated with the intracardiac tumor, and with the possible rhabdomyoma of heart. The serial ultrasonographic examinations revealed that the fetal cardiac function was normal. The size of the tumor gradually increased, although the fetal cardiac function revealed within normal range. The patient delivered a female infant weighing 2716g with the Apgar score of 9 and 10 at one and 5 minutes after delivery. The infant was confirmed to have cardiac tumors after examination by pediatric cardiologist, and the cardiac function of the infant was diagnosed as normal condition. The computed tomography of the head revealed the intracranial multiple calcification lesions, which indicated the symptoms of tuberous sclerosis. Elmer Press 2010-12 2010-11-20 /pmc/articles/PMC5358235/ /pubmed/28352373 http://dx.doi.org/10.4021/cr104e Text en Copyright 2010, Serikawa et al. http://creativecommons.org/licenses/by/2.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Case Report Serikawa, Takehiro Takahashi, Yasuhiro Kikuchi, Akira Takakuwa, Koichi Usuda, Tohei Hasegawa, Satoshi Tanaka, Kenichi A Case of Infantile Cardiac Rhabdomyoma Complicated by Tuberous Sclerosis |
title | A Case of Infantile Cardiac Rhabdomyoma Complicated by Tuberous Sclerosis |
title_full | A Case of Infantile Cardiac Rhabdomyoma Complicated by Tuberous Sclerosis |
title_fullStr | A Case of Infantile Cardiac Rhabdomyoma Complicated by Tuberous Sclerosis |
title_full_unstemmed | A Case of Infantile Cardiac Rhabdomyoma Complicated by Tuberous Sclerosis |
title_short | A Case of Infantile Cardiac Rhabdomyoma Complicated by Tuberous Sclerosis |
title_sort | case of infantile cardiac rhabdomyoma complicated by tuberous sclerosis |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5358235/ https://www.ncbi.nlm.nih.gov/pubmed/28352373 http://dx.doi.org/10.4021/cr104e |
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