Home Print this page Email this page Small font sizeDefault font sizeIncrease font size
Users Online: 1967

 

Home About us Editorial board Search Ahead of print Current issue Archives Submit article Instructions Subscribe Advertise Contacts Login 
     

  Table of Contents  
CASE REPORT
Year : 2012  |  Volume : 53  |  Issue : 2  |  Page : 102-104  

Right atrial myxoma as a possible cause of hemorrhagic stroke and sudden death


1 Department of Morbid Anatomy and Histopathology, Ladoke Akintola University of Technology, Ogbomoso, Oyo State, Nigeria
2 Morbid Anatomy and Forensic Medicine, Obafemi Awolowo University Teaching Hospitals Complex, Ile Ife, Osun State, Nigeria

Date of Web Publication17-Nov-2012

Correspondence Address:
Donatus Sabageh
Department of Morbid Anatomy and Histopathology, Ladoke Akintola University of Technology, Ogbomoso, Oyo State
Nigeria
Login to access the Email id

Source of Support: None, Conflict of Interest: None


DOI: 10.4103/0300-1652.103551

Rights and Permissions
   Abstract 

Right atrial myxomas are rare primary tumors of the heart. They may remain asymptomatic or eventually cause constitutional signs and symptoms. Less frequently, obstruction of the tricuspid valve occurs, resulting in exertional dyspnea, syncope, or sudden death. Neurological manifestation as initial presentation of atrial myxomas is rarely, if ever, associated with right atrial myxomas and may be secondary to cerebral infarction, cerebral hemorrhage and, more rarely subarachnoid hemorrhage. We review the case of a previously unknown, middle-aged Nigerian man who presented to hospital with severe headache and sudden loss of consciousness. A clinical diagnosis of hypertensive hemorrhagic cerebrovascular accident was made. The patient died suddenly a few hours after presentation. Post-mortem examination revealed a small intracerebral hemorrhage in the left superior temporal lobe as well as a large right atrial myxoma, a ventricular septal defect in the muscular septum, and right ventricular hypertrophy. The liver showed fatty change while the kidneys showed evidence of benign nephrosclerosis. Right atrial myxomas may, therefore, be remotely considered as a cause of intracranial hemorrhage, especially in the presence of predisposing cardiac anomalies such as a ventricular septal defect. Similarly, being a known cause of right heart failure, sudden death, and other constitutional derangements, it may contribute significantly to disease outcome. Hence, it should be given due consideration in the differential diagnosis of cerebrovascular accidents.

Keywords: Cause and contributor, disease outcome, left hemorrhagic stroke, right atrial myxoma, sudden death


How to cite this article:
Sabageh D, Odujoko OO, Komolafe AO. Right atrial myxoma as a possible cause of hemorrhagic stroke and sudden death. Niger Med J 2012;53:102-4

How to cite this URL:
Sabageh D, Odujoko OO, Komolafe AO. Right atrial myxoma as a possible cause of hemorrhagic stroke and sudden death. Niger Med J [serial online] 2012 [cited 2019 Aug 21];53:102-4. Available from: http://www.nigeriamedj.com/text.asp?2012/53/2/102/103551


   Introduction Top


Primary tumors of the heart are rare, with an incidence between 0.0017% and 0.19% in unselected patients at autopsy. [1] Nonetheless, cardiac myxomas are the most common primary tumors of the heart, accounting for 40%-50% of primary cardiac tumors. [2] About 90% of myxomas, however, occur in the atria with a left-to-right ratio of approximately 4:1, making right atrial myxoma a very rare tumor. [3]

Myxomas are most frequently encountered between the third and sixth decades of life, more commonly in women. [4] Most cases are sporadic while approximately 10% are familial and show an autosomal dominant mode of transmission. [1] Approximately 90% of these tumors are solitary and pedunculated.

Right atrial myxomas may remain asymptomatic or eventually cause constitutional signs and symptoms due to the production of interleukin-6. [5] Pulmonary embolism of tumor fragments or thrombus from the tumor surface may also occur. [5] Less frequently, obstruction of the tricuspid valve occurs, resulting in exertional dyspnea, syncope or sudden death. [5] Signs and symptoms, however, depend greatly on tumor size, position and mobility.

Neurological manifestations in patients with atrial myxoma are reported in 25%-45% of cases and may be secondary to cerebral infarction, cerebral hemorrhage and, more rarely, subarachnoid hemorrhage. [6] Neurological manifestation as initial presentation of atrial myxoma is found in approximately 36% of cases. [7] Neurological manifestations are, however, almost the exclusive preserve of left atrial myxomas and are rarely, if ever, associated with right atrial myxomas.

We present the case of a middle-aged Nigerian man who died 6 h after presenting with severe headache and sudden loss of consciousness. Autopsy revealed a large right atrial myxoma, a ventricular septal defect, and a small area of hemorrhage in the left temporal lobe of the brain.


   Case Report Top


Case summary

A 50-year-old man presented for the first time at the accident and emergency department of our hospital with an hour's history of headache and subsequent loss of consciousness. Examination revealed a middle-aged man who was unconscious with a Glasgow coma score of 7/15. His blood pressure was 190/130 mmHg and his pulse rate was 86 beats per min. The first and second heart sounds were normal and no murmurs were heard on auscultation. The patient was tachypneic and had a respiratory rate of 40 cycles/ min. Fine crepitations were heard in both lung fields. The intra-abdominal organs were not palpably enlarged.

An assessment of cerebrovascular disease was made. He was subsequently admitted into the accident and emergency unit and appropriate treatment instituted. He, however, died about 6 h after presentation.

Autopsy findings

At autopsy, the patient's heart weighed about 600 g. The left ventricular free wall thickness was 1.5 cm. The right ventricle was flabby and hypertrophic with a right ventricular free wall thickness of 1.1 cm. The tricuspid valve ring circumference measured 12.6 cm while the pulmonary valve ring measured 7.2 cm. An interventricular septal defect measuring 4.5Χ1.5 cm was seen in the posterior portion of the muscular septum.

Within the right atrium, there was a globular, multinodular mass filling the entire right atrial cavity and attached to its posterolateral wall by a short stalk. The mass measured 9.2Χ7.5.0Χ4.0 cm [Figure 1]. The external surface of the mass was smooth and grayish-white in color while the cut surfaces revealed grayish-white tissue with a gelatinous consistency. A large thrombus measuring 2Χ2Χ2 cm was seen firmly adherent to the tip of the mass. The coronary and pulmonary arteries were all normal.
Figure 1: The large myxoma can be seen almost completely filling the right atrial cavity. The left ventricular cavity is visible through the posteriorly situated muscular interventricular septal defect. Note the gelatinous consistency of the tumor on the cut surface

Click here to view


The brain weighed 1400 g. There was a localized, well-circumscribed intraparenchymal hemorrhage within the superior left temporal lobe. The hemorrhagic area measured 1.2Χ 1.0Χ0.8 cm. There was no evidence of brain herniation or injury to the brain stem.

The liver was mildly enlarged and showed fatty change while the kidneys showed macro- and micro-scopic evidence of benign nephrosclerosis.

Microscopically, sections from the globular mass showed typical round to polygonal myxoma cells with abundant cytoplasm dispersed in a markedly loose amorphous myxoid extracellular matrix [Figure 2]. Focal areas of calcification and hemorrhage were seen within the mass.
Figure 2: Histopathology of atrial myxoma. Round to polygonal tumor cells with abundant cytoplasm can be seen in the loose myxoid extracellular background (H and E ×400)

Click here to view



   Discussion Top


From its large size, it may be assumed that the tumor was of long standing duration. Many patients with atrial myxoma experience a significant delay in diagnosis that can be attributed to the absence of symptoms, to misleading cardiac symptoms, or to the presence of extracardiac symptoms that fail to suggest the proper etiology. [1] A recent study showed that the mean duration from the onset of neurologic symptoms to correct diagnosis was 36 months, and only 5.7% of patients with atrial myxoma had the proper diagnosis suggested clinically. [8] It is, therefore, not surprising that this tumor was only discovered at autopsy in this patient.

When myxomas become more bulky, constitutional signs become more prominent, reflecting the tumor's obstructive presence. The most common symptom is dyspnea, which occurs in approximately 80% of patients with atrial myxoma. Nonspecific constitutional symptoms are reported in 10%-45% of patients. Not surprisingly, constitutional symptoms are reported most often in patients with left atrial myxoma, which occurs five times as often as its right atrial counterpart. Our patient serves as a reminder that such symptoms can also predominate with pathology on the right side of the heart. Right atrial myxomas may present with dyspnea, syncope, distension of neck veins, and other symptoms, which are related to tricuspid stenosis or frank interference with blood flow through the right heart. Our patient presented with both tachypnea and loss of consciousness. We suspect that these clinical symptoms and signs are the result of the obstruction to blood flow through the right heart by the tumor owing to its large size. This is further supported by the presence of hepatic steatosis in this patient. This obstruction may have significantly contributed to disease outcome in this patient as syncope and sudden death from complete obstruction of the tricuspid valve orifice are known to be the commonest causes of death in patients with right atrial myxomas. [9],[10] A temporal lobe bleed of the size seen in this patient cannot solely account for the sudden loss of consciousness and death within 6 h of presentation especially in the absence of any detectable abnormality in the brain stem.

Myxomas may also lead to multiple emboli in the cerebral circulation, depending on their location or other associated abnormalities, causing cerebral infarcts and hemorrhages. Formation of intracranial aneurysms, a less common phenomenon, may also be an associated event. Several possible mechanisms of aneurysm formation have been proposed. [11] Indeed, some histopathologic studies have detected myxoma cells in the wall of aneurysms and others the interruption of the internal elastic lamina of cerebral arteries by invading tumor cells. [10] Even though severe hypertension is a major cause of intracerebral hemorrhage in our environment, it is also possible that the hemorrhage in this patient could have resulted from an aneurysmal rupture following tumor migration from the right atrium through the ventricular septal defect into the systemic circulation - a form of paradoxical embolism. This association is extremely rare as extensive literature search did not yield any positive results. Interestingly, some authors have suggested that the hypertension found in patients with atrial myxoma may just be a stress response to the cerebral embolism as a result of the elaboration of pro-inflammatory cytokines and other mediators of paraneoplastic syndromes. [12] Thus, the atrial myxoma in this patient may ultimately be linked to the intracerebral hemorrhage.

The diagnosis of atrial myxomas can be established by echocardiography, gated radionuclide blood-pool scan, or cardiac catheterization. Occasionally, the diagnosis is made by histologic examination of an embolus removed at operation.

Surgical excision is important for preventing obstruction of the tricuspid orifice, eliminating tumor emboli, maintaining systolic function, and restoring biventricular diastolic function. [13] This gives excellent short- and long-term results especially with non-familial myxomas. [14] Right atrial myxomas are rare and intracranial hemorrhage (in the context of a ventricular septal defect), syncope, and dyspnea are possible, though uncommon, initial clinical presentations. They should be considered in the differential diagnosis of cerebrovascular accidents.

 
   References Top

1.Novendstern SL, Silliman SL, Booth RP. Cerebrovascular complications of atrial myxoma. Hosp Physician 2001;8:39-42.  Back to cited text no. 1
    
2.McCoskey EH, Metha JB, Krishnan K, Roy TM. Right atrial myxoma with extracardia manifestations. Chest 2000;118:547-9.  Back to cited text no. 2
    
3.Markel ML, Waller BF, Armstrong WF. Cardiac myxoma: A review. Medicine (Baltimore) 1987;66:114-25.  Back to cited text no. 3
[PUBMED]    
4.Browne WT, Wijdicks EF, Parisi JE, Viggiano RW. Fulminant brain necrosis from atrial myxoma showers. Stroke 1993;24:1090-2.  Back to cited text no. 4
[PUBMED]    
5.Azevedo O, Almeida J, Nolasco T, Medeiros R, Casanova J, Bartosch C, et al. Massive right atrial myxoma presenting as syncope and exertional dyspnoea: Case report. Cardiovasc Ultrasound 2010;8:23-5.  Back to cited text no. 5
[PUBMED]    
6.Azevedo de Almeida L, Heub JC, Silva MA, Bazan R, Estrozi B, Raffin CN. Cerebral ischaemia as initial neurologic manifestation of atrial myxoma: Case report. ArqNeuropsiquiatr 2006;64:660-3.  Back to cited text no. 6
    
7.Knepper LE, Biller J, Adams HP, Bruno A. Neurologic manifestations of atrial myxoma: A 12-year experience and review. Stroke 1998;19:1435-40.  Back to cited text no. 7
    
8.Herbst M, Wattjes MP, Urbach H, Inhetvin-Hutter C, Becker D, Klockgether T, et al. Cerebral embolism from left atrial myxoma leading to cerebral and retinal aneurysms: A case report. AJNR Am J Neuroradiol 2005;26:666-9.  Back to cited text no. 8
    
9.Modi K, Venkatesh P, Agnani S, Rowland T, Reddy P. Sudden death in a patient with left atrial myxoma: Report of two cases and review of literature. BJMP 2010;3:311-8.  Back to cited text no. 9
    
10.Ojji DB, AjidukuSS, Omonua OO, Abdulkareem LL, Parsonage W. A probable right atrial myxoma prolapsing through the tricuspid valve into the right ventricle: A case report. J Med Case Reports 2009;3:9328.  Back to cited text no. 10
    
11.Baikoussis NG, Siminelakis, Kotsanti A, Achenbach K, Argyropoulou M, Goudevenos J. Multiple cerebral mycotic aneurysms due to left atrial myxoma: Are there any pitfalls for the cardiac surgeon? Hellenic J Cardiol 2011;52:466-8.  Back to cited text no. 11
    
12.Anvari MS, Boroumand MA, Karimi A, Abbasi K, Ahmadi H, MArzban M, et al. Histopathologic and clinical characterization of atrial myxoma: A review of 19 cases. Lab Med 2009;40:596-9.  Back to cited text no. 12
    
13.Shimizu M, Okuri H, Yokoyama H, Kawada H, Takizawa T, Kikawada R. A case of right atrial myxoma- effect of a large myxoma in the right atrium studied by M-mode and Doppler echocardiography. JpnCirc J 1995;59:579-86.  Back to cited text no. 13
    
14.Bhan A, Mehrotra P, Choudhary SK, Sharma R, Prabhakar D, Airan B, et al. Surgical experience with intracardiacmyxomas: Long-term follow-up. Ann ThoracSurg 1998;66:810-3.  Back to cited text no. 14
    


    Figures

  [Figure 1], [Figure 2]


This article has been cited by
1 Right Atrial Myxoma and Chronic Transudative Ascites: A Rare and Challenging Clinical Presentation
Mohammadbagher Sharifkazemi,Gholamreza Rezaian,Firouzeh Abtahi
CASE. 2018;
[Pubmed] | [DOI]
2 Iatrogenic retained foreign body in the right atrium. Lessons to Learn
Charles H. Choi,Maqsood M. Elahi,Subbareddy Konda
International Journal of Surgery Case Reports. 2013; 4(11): 985
[Pubmed] | [DOI]



 

Top
  
 
  Search
 
    Similar in PUBMED
   Search Pubmed for
   Search in Google Scholar for
 Related articles
    Access Statistics
    Email Alert *
    Add to My List *
* Registration required (free)  

 
  In this article
    Abstract
   Introduction
   Case Report
   Discussion
    References
    Article Figures

 Article Access Statistics
    Viewed1955    
    Printed87    
    Emailed1    
    PDF Downloaded160    
    Comments [Add]    
    Cited by others 2    

Recommend this journal