Cargando…
Primary Multiple Cardiac Myxomas in a Patient without the Carney Complex
Cardiac tumors are rare, and multiple myxomas are even rarer. The latter phenomenon is mostly associated with the Carney complex, a dominantly inherited disease characterized by multiple primary cardiac myxomas, endocrinopathy, and spotty pigmentation of the skin. We report the rare case of a patien...
Autores principales: | , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Korean Society of Echocardiography
2016
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4828420/ https://www.ncbi.nlm.nih.gov/pubmed/27081449 http://dx.doi.org/10.4250/jcu.2016.24.1.71 |
_version_ | 1782426569386491904 |
---|---|
author | Kataoka, Shohei Otsuka, Masato Goto, Masayuki Kahata, Mitsuru Kumagai, Asako Inoue, Koji Koganei, Hiroshi Enta, Kenji Ishii, Yasuhiro |
author_facet | Kataoka, Shohei Otsuka, Masato Goto, Masayuki Kahata, Mitsuru Kumagai, Asako Inoue, Koji Koganei, Hiroshi Enta, Kenji Ishii, Yasuhiro |
author_sort | Kataoka, Shohei |
collection | PubMed |
description | Cardiac tumors are rare, and multiple myxomas are even rarer. The latter phenomenon is mostly associated with the Carney complex, a dominantly inherited disease characterized by multiple primary cardiac myxomas, endocrinopathy, and spotty pigmentation of the skin. We report the rare case of a patient who did not have the Carney complex but had multiple primary cardiac tumors. A 78-year-old woman with a past history of breast cancer was referred to our hospital for further examination of multiple cardiac tumors. Echocardiography showed 4 tumors in the left atrium and left ventricle. We could not diagnose them preoperatively and decided to resect them surgically because they were mobile and could have caused embolism and obstruction. The postoperative pathological findings of all 4 tumors were myxomas, although the patient did not meet the diagnostic criteria of the Carney complex. Therefore, a rare case of multiple primary cardiac myxomas was diagnosed. |
format | Online Article Text |
id | pubmed-4828420 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Korean Society of Echocardiography |
record_format | MEDLINE/PubMed |
spelling | pubmed-48284202016-04-14 Primary Multiple Cardiac Myxomas in a Patient without the Carney Complex Kataoka, Shohei Otsuka, Masato Goto, Masayuki Kahata, Mitsuru Kumagai, Asako Inoue, Koji Koganei, Hiroshi Enta, Kenji Ishii, Yasuhiro J Cardiovasc Ultrasound Case Report Cardiac tumors are rare, and multiple myxomas are even rarer. The latter phenomenon is mostly associated with the Carney complex, a dominantly inherited disease characterized by multiple primary cardiac myxomas, endocrinopathy, and spotty pigmentation of the skin. We report the rare case of a patient who did not have the Carney complex but had multiple primary cardiac tumors. A 78-year-old woman with a past history of breast cancer was referred to our hospital for further examination of multiple cardiac tumors. Echocardiography showed 4 tumors in the left atrium and left ventricle. We could not diagnose them preoperatively and decided to resect them surgically because they were mobile and could have caused embolism and obstruction. The postoperative pathological findings of all 4 tumors were myxomas, although the patient did not meet the diagnostic criteria of the Carney complex. Therefore, a rare case of multiple primary cardiac myxomas was diagnosed. Korean Society of Echocardiography 2016-03 2016-03-24 /pmc/articles/PMC4828420/ /pubmed/27081449 http://dx.doi.org/10.4250/jcu.2016.24.1.71 Text en Copyright © 2016 Korean Society of Echocardiography http://creativecommons.org/licenses/by-nc/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Case Report Kataoka, Shohei Otsuka, Masato Goto, Masayuki Kahata, Mitsuru Kumagai, Asako Inoue, Koji Koganei, Hiroshi Enta, Kenji Ishii, Yasuhiro Primary Multiple Cardiac Myxomas in a Patient without the Carney Complex |
title | Primary Multiple Cardiac Myxomas in a Patient without the Carney Complex |
title_full | Primary Multiple Cardiac Myxomas in a Patient without the Carney Complex |
title_fullStr | Primary Multiple Cardiac Myxomas in a Patient without the Carney Complex |
title_full_unstemmed | Primary Multiple Cardiac Myxomas in a Patient without the Carney Complex |
title_short | Primary Multiple Cardiac Myxomas in a Patient without the Carney Complex |
title_sort | primary multiple cardiac myxomas in a patient without the carney complex |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4828420/ https://www.ncbi.nlm.nih.gov/pubmed/27081449 http://dx.doi.org/10.4250/jcu.2016.24.1.71 |
work_keys_str_mv | AT kataokashohei primarymultiplecardiacmyxomasinapatientwithoutthecarneycomplex AT otsukamasato primarymultiplecardiacmyxomasinapatientwithoutthecarneycomplex AT gotomasayuki primarymultiplecardiacmyxomasinapatientwithoutthecarneycomplex AT kahatamitsuru primarymultiplecardiacmyxomasinapatientwithoutthecarneycomplex AT kumagaiasako primarymultiplecardiacmyxomasinapatientwithoutthecarneycomplex AT inouekoji primarymultiplecardiacmyxomasinapatientwithoutthecarneycomplex AT koganeihiroshi primarymultiplecardiacmyxomasinapatientwithoutthecarneycomplex AT entakenji primarymultiplecardiacmyxomasinapatientwithoutthecarneycomplex AT ishiiyasuhiro primarymultiplecardiacmyxomasinapatientwithoutthecarneycomplex |