Skip to main content
Top
Published in: Journal of Medical Case Reports 1/2014

Open Access 01-12-2014 | Case report

Recurrent right ventricular cardiac myxoma in a patient with Carney complex: a case report

Authors: Muhammad Rizwan Sardar, Ankush Lahoti, Amanulla Khaji, Wajeeha Saeed, Khawar Maqsood, Harry G Zegel, Jeanine E Romanelli, Frank C McGeehin III

Published in: Journal of Medical Case Reports | Issue 1/2014

Login to get access

Abstract

Introduction

Carney complex is a multiple neoplasia syndrome involving cardiac, endocrine, neural and cutaneous tumors with a variety of pigmented skin lesions. It has an autosomal dominant mode of inheritance. Approximately 7% of cardiac myxomas are related to the Carney complex. Myxomas that occur as part of the Carney complex affect both sexes with equal frequency. Cardiac myxomas with Carney complex are reported mostly in the left side of the heart and are less common on the right side. As per our review, this is the first reported case of Carney complex with right ventricle cardiac myxoma.

Case presentation

We present a rare case of recurrent cardiac myxoma in a patient later diagnosed to have Carney complex. A 46-year-old Caucasian man with a history of thyroid hyperplasia came to out-patient cardiology department with new onset atrial fibrillation. A transthoracic echocardiogram revealed a right ventricular mass attached to his interventricular septum, which was later seen on a transesophageal echocardiogram and cardiac magnetic resonance imaging. He underwent resection of the ventricular mass which on pathology revealed myxoma. He later developed skin lesions, pituitary adenoma and Sertoli cell tumor suggesting Carney complex. Two years later he developed a new mass within his right atrium which was later resected.

Conclusions

Carney complex is a rare autosomal dominant disease with variable penetrance. Since it involves multiple organs, patients diagnosed with Carney complex should undergo serial endocrine workup, neural assessments, echocardiograms and testicular ultrasounds. Of the total number of cases of Carney complex, 65% are linked to PRKAR1A gene mutation. It is important for clinicians to be cognizant of a link between cardiac myxoma and Carney complex. The use of multi-imaging modalities allows better delineation of the mass before planned resection. Carney complex-related cardiac myxoma comprises 7% of all cardiac myxomas. Right ventricular cardiac myxomas are rare. This case report is the first to describe right ventricular myxoma with Carney complex.
Appendix
Available only for authorised users
Literature
1.
go back to reference Stratakis CA, Horvath A: Carney Complex [Updated 2012 Sep 20]. GeneReviews™ [Internet]. Edited by: Pagon RA, Adam MP, Bird TD. 2003, Seattle: University of Washington, 1993-2014. Stratakis CA, Horvath A: Carney Complex [Updated 2012 Sep 20]. GeneReviews™ [Internet]. Edited by: Pagon RA, Adam MP, Bird TD. 2003, Seattle: University of Washington, 1993-2014.
2.
go back to reference Stratakis CA, Kirschner LS, Carney JA: Clinical and molecular features of the Carney complex: diagnostic criteria and recommendations for patient evaluation. J Clin Endocrinol Metab. 2001, 86 (9): 4041-4046. 10.1210/jcem.86.9.7903.CrossRefPubMed Stratakis CA, Kirschner LS, Carney JA: Clinical and molecular features of the Carney complex: diagnostic criteria and recommendations for patient evaluation. J Clin Endocrinol Metab. 2001, 86 (9): 4041-4046. 10.1210/jcem.86.9.7903.CrossRefPubMed
3.
go back to reference Pinede L, Duhaut P, Loire R: Clinical presentation of left atrial cardiac myxoma. A series of 112 consecutive cases. Medicine (Baltimore). 2001, 3: 159-172.CrossRef Pinede L, Duhaut P, Loire R: Clinical presentation of left atrial cardiac myxoma. A series of 112 consecutive cases. Medicine (Baltimore). 2001, 3: 159-172.CrossRef
4.
go back to reference Peachell JL, Mullen JC, Bentley MJ, Taylor DA: Biatrial myxoma: a rare cardiac tumor. Ann Thorac Surg. 1998, 6: 1768-1769.CrossRef Peachell JL, Mullen JC, Bentley MJ, Taylor DA: Biatrial myxoma: a rare cardiac tumor. Ann Thorac Surg. 1998, 6: 1768-1769.CrossRef
5.
go back to reference Chen M, Wang JH, Chao SF, Hsu YH, Wu DC, Lai CP: Cardiac myxoma originating from the anterior mitral leaflet. Jpn Heart J. 2003, 44: 429-434. 10.1536/jhj.44.429.CrossRefPubMed Chen M, Wang JH, Chao SF, Hsu YH, Wu DC, Lai CP: Cardiac myxoma originating from the anterior mitral leaflet. Jpn Heart J. 2003, 44: 429-434. 10.1536/jhj.44.429.CrossRefPubMed
6.
go back to reference Grebenc ML, Rosado-de-Christenson ML, Green CE, Burke AP, Galvin JR: Cardiac myxoma: Imaging features in 83 patients. Radio Graphics. 2002, 22 (3): 673-689. Grebenc ML, Rosado-de-Christenson ML, Green CE, Burke AP, Galvin JR: Cardiac myxoma: Imaging features in 83 patients. Radio Graphics. 2002, 22 (3): 673-689.
7.
go back to reference Sa MI, Abreu A, Cabral S, Reis AH, Torres S, de Oliveira F, Oliveira R, Branco L, Galrinho A, Abreu A, Abreu J, Fiarresga A, Mamede A, Ramos R, Leal A, Pinto E, Fragata J, Ferreira R: Myxoma in the right ventricular outflow tract. Rev Port Cardiol. 2007, 26 (4): 377-381.PubMed Sa MI, Abreu A, Cabral S, Reis AH, Torres S, de Oliveira F, Oliveira R, Branco L, Galrinho A, Abreu A, Abreu J, Fiarresga A, Mamede A, Ramos R, Leal A, Pinto E, Fragata J, Ferreira R: Myxoma in the right ventricular outflow tract. Rev Port Cardiol. 2007, 26 (4): 377-381.PubMed
8.
go back to reference Carney JA, Gordon H, Carpenter PC, Shenoy BV, Go VL: The complex of myxomas, spotty pigmentation, and endocrine overactivity. Medicine (Baltimore). 1985, 64: 270-283.CrossRef Carney JA, Gordon H, Carpenter PC, Shenoy BV, Go VL: The complex of myxomas, spotty pigmentation, and endocrine overactivity. Medicine (Baltimore). 1985, 64: 270-283.CrossRef
9.
go back to reference Kirschner LS, Sandrini F, Monbo J, Lin JP, Carney JA, Stratakis CA: Genetic heterogeneity and spectrum of mutations of the PRKAR1A gene in patients with the Carney complex. Hum Mol Genet. 2000, 9: 3037-3046. 10.1093/hmg/9.20.3037.CrossRefPubMed Kirschner LS, Sandrini F, Monbo J, Lin JP, Carney JA, Stratakis CA: Genetic heterogeneity and spectrum of mutations of the PRKAR1A gene in patients with the Carney complex. Hum Mol Genet. 2000, 9: 3037-3046. 10.1093/hmg/9.20.3037.CrossRefPubMed
10.
go back to reference Groussin L, Kirschner L, Vincent-Dejean C, Perlemoine K, Jullian E, Delemer B, Zacharieva S, Pignatelli D, Carney JA, Luton JP, Bertagna X, Stratakis CA, Bertherat J: Molecular analysis of the cyclic AMP-dependent protein kinase A (PKA) regulatory subunit 1A (PRKAR1A) gene in patients with Carney complex and primary pigmented nodular adrenocortical disease (PPNAD) reveals novel mutations and clues for pathophysiology: augmented PKA signaling is associated with adrenal tumorigenesis in PPNAD. Am J Hum Genet. 2002, 71: 1433-1442. 10.1086/344579.CrossRefPubMedPubMedCentral Groussin L, Kirschner L, Vincent-Dejean C, Perlemoine K, Jullian E, Delemer B, Zacharieva S, Pignatelli D, Carney JA, Luton JP, Bertagna X, Stratakis CA, Bertherat J: Molecular analysis of the cyclic AMP-dependent protein kinase A (PKA) regulatory subunit 1A (PRKAR1A) gene in patients with Carney complex and primary pigmented nodular adrenocortical disease (PPNAD) reveals novel mutations and clues for pathophysiology: augmented PKA signaling is associated with adrenal tumorigenesis in PPNAD. Am J Hum Genet. 2002, 71: 1433-1442. 10.1086/344579.CrossRefPubMedPubMedCentral
11.
go back to reference Carney JA, Young WF: Primary pigmented nodular adrenocortical disease and its associated conditions. Endocrinologist. 1992, 2: 6-10.1097/00019616-199201000-00003.CrossRef Carney JA, Young WF: Primary pigmented nodular adrenocortical disease and its associated conditions. Endocrinologist. 1992, 2: 6-10.1097/00019616-199201000-00003.CrossRef
12.
go back to reference MacGowan SW, Sidhu P, Aherne T, Luke D, Wood AE, Neligan MC: Atrial myxoma: National incidence, diagnosis and surgical management. Ir J Med Sci. 1993, 162: 223-226. 10.1007/BF02945200.CrossRefPubMed MacGowan SW, Sidhu P, Aherne T, Luke D, Wood AE, Neligan MC: Atrial myxoma: National incidence, diagnosis and surgical management. Ir J Med Sci. 1993, 162: 223-226. 10.1007/BF02945200.CrossRefPubMed
13.
go back to reference Carney JA: Carney complex: the complex of myxoma, spotty, pigmentation, endocrine overactivity and schwannomas. Semin Dermotal AM J Cardiol. 1989, 63: 1006-1008. 10.1016/0002-9149(89)90162-8.CrossRef Carney JA: Carney complex: the complex of myxoma, spotty, pigmentation, endocrine overactivity and schwannomas. Semin Dermotal AM J Cardiol. 1989, 63: 1006-1008. 10.1016/0002-9149(89)90162-8.CrossRef
14.
go back to reference Kacerovská D, Michal M, Síma R, Grossmann P, Kazakov DV: Carney complex. Cesk Patol. 2011, 47 (4): 192-197.PubMed Kacerovská D, Michal M, Síma R, Grossmann P, Kazakov DV: Carney complex. Cesk Patol. 2011, 47 (4): 192-197.PubMed
15.
go back to reference Obeid AI, Marvasti M, Parker F, Rosenberg J: Comparison of transthoracic and transesophageal echocardiography in diagnosis of left atrial myxoma. Am J Cardiol. 1989, 63: 1006-1008. 10.1016/0002-9149(89)90162-8.CrossRefPubMed Obeid AI, Marvasti M, Parker F, Rosenberg J: Comparison of transthoracic and transesophageal echocardiography in diagnosis of left atrial myxoma. Am J Cardiol. 1989, 63: 1006-1008. 10.1016/0002-9149(89)90162-8.CrossRefPubMed
16.
go back to reference Wr C: Cardiac neoplasms: Current diagnosis, pathology and therapy. J Card Surg. 1988, 3: 119-154. 10.1111/j.1540-8191.1988.tb00232.x.CrossRef Wr C: Cardiac neoplasms: Current diagnosis, pathology and therapy. J Card Surg. 1988, 3: 119-154. 10.1111/j.1540-8191.1988.tb00232.x.CrossRef
17.
go back to reference Jérôme B: Carney Complex. Orphanet J Rare Dis. 2006, 1: 21-10.1186/1750-1172-1-21.CrossRef Jérôme B: Carney Complex. Orphanet J Rare Dis. 2006, 1: 21-10.1186/1750-1172-1-21.CrossRef
Metadata
Title
Recurrent right ventricular cardiac myxoma in a patient with Carney complex: a case report
Authors
Muhammad Rizwan Sardar
Ankush Lahoti
Amanulla Khaji
Wajeeha Saeed
Khawar Maqsood
Harry G Zegel
Jeanine E Romanelli
Frank C McGeehin III
Publication date
01-12-2014
Publisher
BioMed Central
Published in
Journal of Medical Case Reports / Issue 1/2014
Electronic ISSN: 1752-1947
DOI
https://doi.org/10.1186/1752-1947-8-134

Other articles of this Issue 1/2014

Journal of Medical Case Reports 1/2014 Go to the issue