|Reversible pulmonary hypertension in adolescent with left atrial myxoma.|
|Jump to Full Text|
|PMID: 22259669 Owner: NLM Status: PubMed-not-MEDLINE|
|We report a patient of left atrial huge myxoma presenting with severe pulmonary hypertension in adolescents. A patient was a 14-year-old boy presented with sudden onset dyspnea. Transthoracic echocardiographic study revealed the presence of a nodular, 4.34 × 8.11 cm sized, mobile, hyperechoic mass in the left atrium and severe pulmonary hypertension with tricuspid insufficiency. After surgical therapy, tricuspid regurgitation and pulmonary hypertension was decreased and the patient was stabilized and had an uneventful clinical course.|
|Byong-Kyu Kim; Jung-Nam Cho; Hye-Jin Park; Seung-Pyo Hong; Ja-Yung Son; Jin-Bae Lee; Jae-Keun Ryu; Ji-Yong Choi; Sung-Guk Chang; Kee-Sik Kim|
Related Documents :
|19463639 - Two cases of pulmonary homograft replacement for isolated pulmonary valve endocarditis.
22258419 - Pulmonary hypertension in chronic hypersensitivity pneumonitis.
808399 - Diphtheroid endocarditis after aortic valve replacement.
7073909 - Homograft replacement of aortic root with reimplantation of coronary arteries. results ...
18365579 - Reoperative right ventricular outflow tract conduit reconstruction: risk analyses at fo...
12928649 - Use of bovine jugular vein to reconstruct the right ventricular outflow tract: early re...
10763509 - Intra-operative measurement of cortical arterial flow volumes in posterior circulation ...
637969 - Isolated acquired pulmonary valve regurgitation. report of long-term follow-up.
9817499 - Results of biocor stentless valve replacement for infective endocarditis of the native ...
|Type: Journal Article Date: 2011-12-27|
|Title: Journal of cardiovascular ultrasound Volume: 19 ISSN: 2005-9655 ISO Abbreviation: J Cardiovasc Ultrasound Publication Date: 2011 Dec|
|Created Date: 2012-01-19 Completed Date: 2012-10-02 Revised Date: 2013-05-29|
Medline Journal Info:
|Nlm Unique ID: 101477138 Medline TA: J Cardiovasc Ultrasound Country: Korea (South)|
|Languages: eng Pagination: 221-3 Citation Subset: -|
|Division of Cardiology, Daegu Catholic University Medical Center, Daegu, Korea.|
|APA/MLA Format Download EndNote Download BibTex|
Journal ID (nlm-ta): J Cardiovasc Ultrasound
Journal ID (publisher-id): JCU
Publisher: Korean Society of Echocardiography
Copyright © 2011 Korean Society of Echocardiography
Received Day: 21 Month: 8 Year: 2011
Revision Received Day: 04 Month: 10 Year: 2011
Accepted Day: 30 Month: 11 Year: 2011
Print publication date: Month: 12 Year: 2011
Electronic publication date: Day: 27 Month: 12 Year: 2011
Volume: 19 Issue: 4
First Page: 221 Last Page: 223
PubMed Id: 22259669
|Reversible Pulmonary Hypertension in Adolescent with Left Atrial Myxoma|
|Byong-Kyu Kim, MD1|
|Jung-Nam Cho, MD2|
|Hye-Jin Park, MD3|
|Seung-Pyo Hong, MD1|
|Ja-Yung Son, MD1|
|Jin-Bae Lee, MD1|
|Jae-Keun Ryu, MD1|
|Ji-Yong Choi, MD1|
|Sung-Guk Chang, MD1|
|Kee-Sik Kim, MD, PhD1|
1Division of Cardiology, Daegu Catholic University Medical Center, Daegu, Korea.
2Department of Internal Medicine, Daegu Catholic University Medical Center, Daegu, Korea.
3Department of Pediatrics, Daegu Catholic University Medical Center, Daegu, Korea.
Address for Correspondence: Kee-Sik Kim, Division of Cardiology, Daegu Catholic University Medical Center, 3056-6 Daemyeong 4-dong, Nam-gu, Daegu 705-718, Korea. Tel: +82-53-650-3010, Fax: +82-53-621-3166, firstname.lastname@example.org
Cardiac myxoma make a few symptoms. But rarely severe complications like systemic embolism, heart failure, pulmonary hypertension were shown. The signs and symptoms produced by tumors are related to the size and location of the tumors. When situated in the left side of the heart, they may cause symptoms of left atrial outflow obstruction such as pulmonary hypertension. We report one case of severe complications of myxoma in adolescents with severe pulmonary hypertension that were recovered by surgical removal.
A 14-year-old boy was admitted to our hospital due to sudden onset dyspnea. The patient had no past medical history and family history of lung disease and cardiac disease. Two weeks before admission, he suffered from non-productive cough. At the time, physical findings included a regular heart rate of 98 beats/minutes, a blood pressure of 120/80 mm Hg, respiratory rate of 28/minutes represented tachypnea, a body temperature of 36.4℃, resting oxygen saturation of 96%. He had a palpable four finger sized hepatomegaly, pre-tibial pitting edema. Thoracic auscultation revealed mid-diastolic murmur (Grade II) and inspiratory crackle was audible in both lower lung fields. An electrocardiogram revealed a normal sinus rhythm with right axis deviation, right atrial enlargement. A chest X-ray showed mild cardiomegaly and mild pulmonary congestion (Fig. 1). On laboratory findings, Aspartate Aminotransferase/Alanine Aminotransferase 136/106 IU/L, total bilirubin 1.0 mg/dL, pro-brain nitrouretic peptide 6,291 pg/mL. Transthoracic echocardiography to find cause of murmur showed a nodular, mobile, hyperechoic, 4.34 × 8.11 cm sized left atrial mass (Fig. 2) with moderate tricuspid regurgitation suggestive of pulmonary hypertension (maximal pressure gradient = 81.61 mm Hg, pulmonary artery systolic pressure = 101 mm Hg) (Fig. 4), and markedly enlarged right atrium and right ventricle. Left ventricular ejection fraction and regional wall motion were normal. We performed excisional biopsy for mass evaluation. The mass were grossly composed of several friable hemorrhagic nodular mass, measuring 6 × 5 × 4.5 cm in size (Fig. 6). On microscopic view, the mass were composed of setellate myxoma cells, inflammatory cells, much basophilic substance and slit like vessels that were compatible with myxoma.
After 3 days of mass removal, the follow-up echocardiography showed no visible mass lesion (Fig. 3) with mild tricuspid regurgitation suggestive of decreased pulmonary arterial pressure (pressure gradient = 39.37 mm Hg, pulmonary artery systolic pressure = 54 mm Hg) (Fig. 5).
The postoperative course was uneventful and the patient remained well during the 3 years follow-up period.
Myxomas most commonly occur between the third and the sixth decade of life.
Sixty-five percent of cardiac myxomas occur in women and are rare in children.1) Early diagnosis is difficult because the symptoms of atrial myxoma are frequently nonspecific.1), 2) Large myxomas may remain asymptomatic if tumour growth is very slow. The heart auscultation can be quite similar to that of mitral valve disease, and may be associated with a tumoral sound. The most useful examination in the diagnosis is the echocardiogram that is highly sensitive and can diagnose up to 100% of the cases. Although histopathologically benign, cardiac myxomas can cause chronic systemic inflamation, embolism or intracardiac obstructions, leading to increased morbidity.3)
The symptoms of left-sided heart failure were usual in patients with left atrial myxomas, such as dyspnea on exertion, may progress to orthopnea, paroxysmal nocturnal dyspnea or pulmonary edema because of obstruction at the mitral valve orifice.4), 5)
Dyspnea on exertion was the most prominent symptom in our patient. Pulmonary edema was also present but obstruction at the mitral valve orifice was not present. Most etiologies of pulmonary hypertension were chronic obstructive lung disease, pulmonary thromboembolism, mitral stenosis. Especially, reversible pulmonary hypertension was usually case of mitral stenosis, pulmonary thromboembolism. But pulmonary hypertension that revealed primary cardiac myxoma was rare.
Nakano et al.6) described positive correlation between the size of tumor and pulmonary artery pressure. The New York Heart Association function class and mean pulmonary artery pressure were decreased after tumor resection.
In our case, severe pulmonary hypertension was caused by large left side myxoma. After surgical removal, severe pulmonary hypertension and symptom were decreased.
|1.||Kuon E,Kreplin M,Weiss W,Dahm JB. The challenge presented by right atrial myxomaHerzYear: 20042970270915580325|
|2.||Reynen K. Cardiac myxomasN Engl J MedYear: 1995333161016177477198|
|3.||Pucci A,Gagliardotto P,Zanini C,Pansini S,di Summa M,Mollo F. Histopathologic and clinical characterization of cardiac myxoma: review of 53 cases from a single institutionAm Heart JYear: 200014013413810874274|
|4.||Vasquez A,Sethi G,Maximov M,Marcus FI. Atrial myxomas in the elderly: a case report and review of the literatureAm J Geriatr CardiolYear: 200413394414724400|
|5.||Goswami KC,Shrivastava S,Bahl VK,Saxena A,Manchanda SC,Wasir HS. Cardiac myxomas: clinical and echocardiographic profileInt J CardiolYear: 1998632512599578352|
|6.||Nakano T,Mayumi H,Hisahara M,Yasui H,Tokunaga K. The relationship between functional class, pulmonary artery pressure and size in left atrial myxomaCardiovasc SurgYear: 199643203238782928|
Keywords: Cardiac tumour, Pulmonary hypertension, Left atrial myxoma.
Previous Document: Right coronary cusp prolapse resembling subpulmonic stenosis in an old adult patient with ventricula...
Next Document: Importance of clinical and echocardiographic hemodynamic assessment in chronic pulmonary embolism.