- Case report
- Open Access
Case studies of two related Chinese patients with Carney complex presenting with extensive cardiac myxomas and PRKAR1A gene mutation of c.491_492delTG
© Guo et al.; licensee BioMed Central. 2015
- Received: 22 July 2014
- Accepted: 17 January 2015
- Published: 27 February 2015
Carney complex is an autosomal dominant disease that is clinically characterized by cardiac myxomas, spotty skin pigmentation, and endocrine overactivity. Carney complex is most commonly caused by mutations in the PRKAR1A gene on chromosome 17q22-24. Currently, there are at least 117 pathogenic mutations in PRKAR1A that have been identified. Herein, we report on two cases of Carney complex in related Chinese patients with a c.491_492delTG mutation that presented with multiple and extensive cardiac myxomas and skin pigmentation.
- Carney complex
Carney complex was initially described by J. Aiden Carney in 1985. It is an autosomal dominant disorder characterized by myxomas, spotty pigmentation, and endocrine overactivity. The initial diagnosis of Carney complex is based on clinical criteria and can be confirmed using genetic testing. The genetic tests have a mutation detection rate of approximately 60% in patients with Carney complex. There are 12 clinical criteria that are the major diagnostic indicators of Carney complex. In addition, there are two supplemental diagnostic criteria that pertain to genetic testing and family history [1,2].
The genetic disease Carney complex includes two distinct syndromes: LAMB syndrome (lentigines, atrial myxomas, mucocutaneous myxomas, and blue nevi) and NAME syndrome (nevi, atrial myxoma, myxoid neurofibroma, and ephelides). These are autosomal dominant conditions that comprise myxomas in the heart and skin, skin hyperpigmentation (lentiginosis), and endocrine-related overactivity or tumors . Carney complex is most commonly caused by mutations in the PRKAR1A gene on chromosome 17q22-24 . It is less commonly caused by a variety of genetic changes on chromosome 2p16. Currently, 117 different PRKAR1A mutations have been identified [4-7]. Herein, we identify two Chinese Carney complex patients that are siblings with a 491_492delTG PRKAR1A gene mutation. The patients presented with multiple and extensive cardiac myxomas and skin pigmentation.
Case report 1
Further evaluation of the two patients
Case 1 (14-year-old male)
Case 2 (22-year-old male)
MRI pituitary examination
No sign of pituitary microadenoma was found in sellar MRI scanning
A low signal shadow with unclear boundary was found at the lower left medial side of the pituitary
CT adrenal gland examination
No obvious lesion in the bilateral adrenal glands was identified
No obvious lesion in the bilateral adrenal glands was identified
Examination of Cushing symptoms
Cortisol: 457.9 nmol/L (8 o’clock), 327.2 nmol/L (16 o’clock), 197.3 nmol/L (0 o’clock), corresponding adrenocorticotrophic hormone (ACTH) (8/16/0 o’clock): 18.57 pg/ml; 8.85 pg/ml; <1.0 pg/ml; 24-h urinary free cortisol (UFC): 309.4 nmol/24 h
Cortisol: 353.4 nmol/L(8 o’clock), 218.6 nmol/L (16 o’clock), 70.8 nmol/L (0 o’clock), adrenocorticotrophic hormone (ACTH) (8/16/0 o’clock): 41.80 pg/ml; 31.53 pg/ml; 22.73 pg/ml; 24-h urinary free cortisol (UFC): 308.4 nmol/24 h
During the operation, the aortic cross-clamp time was 110 min and the cardiopulmonary bypass time was 146 min. The patient was in need of assisted mechanical ventilation for 15.55 h. Patient 1 remained in the intensive care unit for 20.80 h and had a postoperative stay of 10 days.
The patient’s recovery was uneventful. A postoperative echocardiograph indicated that no myxomas remained in any of the cardiac chambers. Follow-ups were performed at 3, 6, and 33 months after surgery. In each follow-up, echocardiography indicated no myxomas. The patient was evaluated as being in New York Heart Association functional class I.
Novel PRKAR1A oligonucleotide sequences for mutation detection
Case report 2
The patient reported on above has a 22-year-old brother who was also diagnosed with multiple cardiac myxomas in February 2011 and who had undergone surgical treatment in another hospital, the Central Hospital of Handan, Hebei province. Upon physical examination, patient 2 also had spotty skin pigmentation on his face (Figure 3B). Primary symptoms were palpitations and shortness of breath after activity over the previous 2 years that had become aggravated over 15 days by sudden syncope.
Ultrasound examination results showed a mural mass with medium echo (5.7 × 3.4 cm) in the left atrium, and the base of the mass was at the lower interatrial septum near the origin of the anterior mitral valve leaflet; a mural mass with medium echo (7.5 × 5.1 cm) was found in the left ventricle, and the base of the mass was wide and located at the lower ventricular anterior wall; a mural mass with medium echo (3.4 × 2.5 cm) was found in the right atrium, and the base of the mass was relatively wide and located at the trabecular of the right ventricular anterior wall; and a mural mass with medium echo (2.2 × 1.4 cm) was found at the right ventricular outflow tract, and the base was at the anterior wall. The results of further evaluations are presented in Table 1.
Patient 2 underwent surgery on 24 February 2011. Two myxomas were removed from the right ventricle through the tricuspid valve; a 20 × 25 × 30 mm3 myxoma from the inlet area and a 30 × 30 × 30 mm3 myxoma from the outlet area. In the left atrium, one myxoma measuring 30 × 35 × 40 mm3 was attached to the fossa ovalis and removed through an interatrial septum incision. In the left ventricle, a 25 × 30 × 30 mm3 myxoma was attached to the apical area and removed through an interatrial septum incision and the mitral valve. The cardiopulmonary bypass time was 105 min, and the aortic cross-clamp time was 68 min.
Follow-up on patient 2 was initially performed 3 months after surgery. Echocardiography revealed a 10 × 15 × 20 mm3 myxoma remaining in the left ventricle (Figure 1C). At 46-month follow-up, the size of the myxoma in his left ventricle was considered to be stable, and the estimated size this time was 9 × 15 × 21 mm3.
Beijing Ginkgo Wheat Biotechnology Co., Ltd, Beijing, 100084, China, provided genomic sequencing of the patient’s DNA in the PRKAR1A gene. The results indicated that he shared the same c.491_492delTG mutation, as his sibling patient 1 (Figure 5B).
Diagnostic criteria for Carney complex
Skin pigmentation disorders
1. Spotty skin pigmentation with a typical distribution (lips, conjunctiva and inner or outer canthi, vaginal, and penile mucosa)
2. Blue nevus, epithelioid blue nevus (multiple)
1. Myxoma (cutaneous and mucosal)
2. Cardiac myxoma
3. Breast myxomatosis or fat-suppressed magnetic resonance imaging findings suggestive of this diagnosis
1. PPNAD or paradoxical positive response of urinary glucocorticosteroids to dexamethasone administration during Liddle’s test
2. Acromegaly due to GH-producing adenoma
3. LCCSCT or characteristic calcification on testicular ultrasonography
4. Thyroid carcinoma or multiple, hypoechoic nodules on thyroid ultrasonography, in a young patient
5. Psammomatous melanotic schwannoma
6. Breast ductal adenoma (multiple)
1. Affected first-degree relative
2. Inactivating mutation of the PRKAR1A gene
The case studies presented here suggest to us these important points: Myxoma in patients with Carney complex always has an early onset, but we should be careful if the patient with multiple myxoma is under 40 years old. The following assessments should be undertaken: skin exam, ask for family history, or PRKAR1A gene test if necessary. The recurrence of myxoma is quite common after surgery. But in case 2, the recurrence occurred early, within 3 months after surgery, and the size of myxoma did not grow with a quite long follow-up, while case 1 did not have any recurrence. This may suggest that the most important period is within 3 months of surgery.
In general, cardiac myxomas occur sporadically as an isolated left atrial mass attached to the fossa ovalis. They generally occur between the third and sixth decades of life, and most do not recur after surgical resection. However, Carney complex cardiac myxomas occur in families and usually at considerably younger ages than non-familial myxomas. Single myxoma associated with Carney complex can occur, but most often there are more than one and they occur in any cardiac chamber. Following surgical resection, Carney complex myxomas frequently recur both at the initial resection site and at distant sites . Both patients had multiple cardiac myxomas. Patient 2 had a recurring myxoma in the left ventricle 3 months after the operation. Unlike most myxomas, in these cases, the myxomas were attached directly to cardiac muscle and did not have pedicels.
Carney complex is most commonly due to mutations in the PRKAR1A gene on chromosome 17q22-q24. This gene may function as a tumor-suppressor gene encoding the regulatory subunit type 1-alpha (R1) of protein kinase A. Recently, mutations in the PRKAR1A gene were estimated to occur in more than 60% of Carney complex patients . Approximately 20% of the families affected with Carney complex have 2p16 mutations. To date, there are at least 117 pathogenic variants in PRKAR1A that have been identified [4-7]. In this study, we identified a PRKAR1A mutation, c.491_492delTG, in both patients.
The study protocol was approved by the Ethics Committees of Fuwai Hospital, Beijing, and all of the parents provided written informed consent.
We thank Zhao Li for helping us carry out the molecular genetic studies and participate in the sequence alignment and also thank Zhou Zhou for the English writing assistance.
- Horvath A, Bertherat J, Groussin L, Guillaud-Bataille M, Tsang K, Cazabat L, et al. Mutations and polymorphisms in the gene encoding regulatory subunit type 1-alpha of protein kinase A (PRKAR1A): an update. Hum Mutat. 2010;31:369–79.View ArticlePubMed CentralPubMedGoogle Scholar
- 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;86:4041–6.View ArticlePubMedGoogle Scholar
- Sandrini F, Stratakis C. Clinical and molecular genetics of Carney complex. Mol Genet Metab. 2003;78:83–92.View ArticlePubMedGoogle Scholar
- Rothenbuhler A, Stratakis CA. Clinical and molecular genetics of Carney complex. Best Pract Res Clin Endocrinol Metab. 2010;24:389–99.View ArticlePubMedGoogle Scholar
- Bertherat J. Carney complex (CNC). Orphanet J Rare Dis. 2006;1:21.View ArticlePubMed CentralPubMedGoogle Scholar
- Vezzosi D, Vignaux O, Dupin N, Bertherat J. Carney complex: clinical and genetic 2010 update. Ann Endocrinol (Paris). 2010;71:486–93.View ArticlePubMedGoogle Scholar
- Halaszlaki C, Takacs I, Butz H, Patocs A, Lakatos P. Novel genetic mutation in the background of Carney complex. Pathol Oncol Res. 2012;18:149–52.View ArticlePubMedGoogle Scholar
This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. 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.