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Calcified amorphous tumor of the heart with mitral annular calcification: a case report

BACKGROUND: Calcified amorphous tumor of the heart is a rare, non-neoplastic cardiac mass characterized by nodular calcium in the background of amorphous degenerating fibrinous material. Clinical diagnosis of calcified amorphous tumor can be difficult, and current single imaging techniques do not sp...

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Autores principales: Nakamaru, Ryo, Oe, Hiroki, Iwakura, Katsuomi, Masai, Takafumi, Fujii, Kenshi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5516357/
https://www.ncbi.nlm.nih.gov/pubmed/28720119
http://dx.doi.org/10.1186/s13256-017-1337-9
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author Nakamaru, Ryo
Oe, Hiroki
Iwakura, Katsuomi
Masai, Takafumi
Fujii, Kenshi
author_facet Nakamaru, Ryo
Oe, Hiroki
Iwakura, Katsuomi
Masai, Takafumi
Fujii, Kenshi
author_sort Nakamaru, Ryo
collection PubMed
description BACKGROUND: Calcified amorphous tumor of the heart is a rare, non-neoplastic cardiac mass characterized by nodular calcium in the background of amorphous degenerating fibrinous material. Clinical diagnosis of calcified amorphous tumor can be difficult, and current single imaging techniques do not specifically differentiate calcified amorphous tumor from other cardiac tumors such as calcified atrial myxoma, calcified thrombi, or vegetation. Complete surgical resection is the treatment of choice for both symptom improvement and prevention of embolization, as well as for pathological diagnosis. CASE PRESENTATION: A 70-year-old Asian man with end-stage renal disease complained of chest discomfort during exercise. He had no history of thromboembolism or endocarditis. A transthoracic echocardiogram revealed mitral annular calcification as well as a highly mobile mass (8 × 6 mm) attached to the ventricular side of the posterior mitral valve leaflet. As the mass was highly mobile, suggesting a high risk of embolization, he underwent surgical resection. A histopathological examination revealed multiple nodular amorphous calcifications, along with fibrous connective tissue. There were no identifiable myxoma or malignancy cells. Consequently, the diagnosis of calcified amorphous tumor was confirmed. CONCLUSIONS: In the present case, a calcified amorphous tumor arose from mitral annular calcification. A characteristic of mitral annular calcification-related calcified amorphous tumor is its highly mobile nature, with a high risk of stroke or other systemic embolism. Therefore, surgical therapy should be considered for treatment of calcified amorphous tumors.
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spelling pubmed-55163572017-07-20 Calcified amorphous tumor of the heart with mitral annular calcification: a case report Nakamaru, Ryo Oe, Hiroki Iwakura, Katsuomi Masai, Takafumi Fujii, Kenshi J Med Case Rep Case Report BACKGROUND: Calcified amorphous tumor of the heart is a rare, non-neoplastic cardiac mass characterized by nodular calcium in the background of amorphous degenerating fibrinous material. Clinical diagnosis of calcified amorphous tumor can be difficult, and current single imaging techniques do not specifically differentiate calcified amorphous tumor from other cardiac tumors such as calcified atrial myxoma, calcified thrombi, or vegetation. Complete surgical resection is the treatment of choice for both symptom improvement and prevention of embolization, as well as for pathological diagnosis. CASE PRESENTATION: A 70-year-old Asian man with end-stage renal disease complained of chest discomfort during exercise. He had no history of thromboembolism or endocarditis. A transthoracic echocardiogram revealed mitral annular calcification as well as a highly mobile mass (8 × 6 mm) attached to the ventricular side of the posterior mitral valve leaflet. As the mass was highly mobile, suggesting a high risk of embolization, he underwent surgical resection. A histopathological examination revealed multiple nodular amorphous calcifications, along with fibrous connective tissue. There were no identifiable myxoma or malignancy cells. Consequently, the diagnosis of calcified amorphous tumor was confirmed. CONCLUSIONS: In the present case, a calcified amorphous tumor arose from mitral annular calcification. A characteristic of mitral annular calcification-related calcified amorphous tumor is its highly mobile nature, with a high risk of stroke or other systemic embolism. Therefore, surgical therapy should be considered for treatment of calcified amorphous tumors. BioMed Central 2017-07-18 /pmc/articles/PMC5516357/ /pubmed/28720119 http://dx.doi.org/10.1186/s13256-017-1337-9 Text en © The Author(s). 2017 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Case Report
Nakamaru, Ryo
Oe, Hiroki
Iwakura, Katsuomi
Masai, Takafumi
Fujii, Kenshi
Calcified amorphous tumor of the heart with mitral annular calcification: a case report
title Calcified amorphous tumor of the heart with mitral annular calcification: a case report
title_full Calcified amorphous tumor of the heart with mitral annular calcification: a case report
title_fullStr Calcified amorphous tumor of the heart with mitral annular calcification: a case report
title_full_unstemmed Calcified amorphous tumor of the heart with mitral annular calcification: a case report
title_short Calcified amorphous tumor of the heart with mitral annular calcification: a case report
title_sort calcified amorphous tumor of the heart with mitral annular calcification: a case report
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5516357/
https://www.ncbi.nlm.nih.gov/pubmed/28720119
http://dx.doi.org/10.1186/s13256-017-1337-9
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