Case Report | Open Access
Syuichi Tetsuka, Kunihiko Ikeguchi, "Prevention of Cerebral Embolism Progression by Emergency Surgery of the Left Atrial Myxoma", Case Reports in Medicine, vol. 2015, Article ID 151802, 4 pages, 2015. https://doi.org/10.1155/2015/151802
Prevention of Cerebral Embolism Progression by Emergency Surgery of the Left Atrial Myxoma
A 21-year-old woman developed left hemiparesis during work and was hospitalized. Her National Institutes of Health Stroke Scale score was 4. Hyperintense areas in the left basal ganglia, corona radiata, and cortex of the temporal lobe were found by brain diffusion-weighted magnetic resonance imaging, indicating acute cerebral infarction. Echocardiography showed a giant mass of diameter 7 × 4 cm in the left atrium. Therefore, she was diagnosed with cerebral embolism due to a left atrial myxoma. Currently, thrombolytic therapy may continue to be effective because the embolic source may be composed of tumor tissue itself. In case of atrial myxoma, we considered that the use of tPA as emergency treatment in all patients with infarction by atrial myxoma may be questioned. Thus, cardiac tumor extraction was performed the next day after hospitalization without thrombolytic therapy. The excised myxoma measured 7 × 6 × 4 cm. The patient recovered and her neurological symptoms also improved. Furthermore, her National Institutes of Health Stroke Scale score improved to 0. Thirteen days after admission, the patient was discharged from our hospital. Cardiac myxoma is often associated with a high risk of embolic episodes, which emphasizes the need for prompt surgical excision as soon as the diagnosis is confirmed.
Cardiac myxoma has an incidence of 0.002% among the general population and is the most common heart tumor that represents 50% of all cardiac tumors. About 75% of cardiac myxomas are located in the left atrium . At least 25% of patients with left atrial myxoma present with ischemic neurological events secondary to embolism [2, 3]. The embolic source may be composed of tumor tissue itself, blood clots, or both [4, 5].
Currently, studies reporting that thrombolytic therapy with recombinant tissue plasminogen activator (tPA) in patients with sudden cerebral infarction associated with myxoma is highly effective are increasing [6–11]. However, because the embolic source may be composed of tumor tissue itself in case of atrial myxoma, we considered that the use of tPA as emergency treatment in all patients with infarction due to atrial myxoma may be questioned. In addition, the guidelines [12–14] do not discuss stroke with myxoma, and there are a few reports that emphasize the need for the prompt surgical excision of myxoma without thrombolytic therapy as soon as the diagnosis is confirmed [15, 16]. Here we present a case of a 21-year-old female with left atrial myxoma who developed an acute cerebral arterial infarction. She underwent immediate removal of the myxoma after stroke with no major enlargement of the infarct or hemorrhagic transformation without thrombolytic therapy.
2. Case Report
A 21-year-old female presented with a migraine. For about 3 years, she at times experienced being likely to faint upon standing and dimmed vision. However, she did not show neurological dysfunction; therefore, cerebral infarction was not suspected. When she was working in standing position for a long time in the middle of the night, she started experiencing dimmed vision, labile vertigo, and hindrance in the ability to stand at her workplace. Such episodes were associated with a following numbness and weakness in the lower extremities on the left half of her body. The estimated time from the onset of symptoms to hospital presentation was about 6 h. This consequently caused the delay between neurologic symptoms onset and diagnostic of stroke in the patient. She was hospitalized in Jichi Medical University Hospital (Shimotuke, Japan) on the morning of the same day. Upon examination, her level of consciousness was alert, and she had a body weight of 47 kg, height of 160 cm, body mass index of 18, blood pressure of 84/64 mmHg, and pulse rate of 84 beats/min. A “gallop” sound was heard along with her heart sound, but her pulmonary sound was normal, and there was no pedal edema. Neurological examination revealed muscle weakness of the left upper and lower limbs (manual muscle testing; MMT 4: holds test position against slight to moderate pressure), a decrease of superficial sensation and dysesthesia of the left half of the body, and ataxia of the left upper limb. The National Institutes of Health Stroke Scale (NIHSS) score was 4. Increasing scores indicate a more severe stroke and have been shown to correlate with the size of the infarction on both CT and MRI evaluation. Many guidelines and protocols warn that administering tPA in patients with a high NIHSS score (>22) is associated with increased risk of hemorrhagic conversion. Laboratory findings showed no abnormalities except for a slight increase in C-reactive protein (1.61 mg/dL). Her electrocardiogram showed a normal sinus rhythm. Multiple hyperintense areas in the left basal ganglia, corona radiata, and cortex of the temporal lobe were found by brain diffusion-weighted magnetic resonance imaging (MRI), indicating acute cerebral infarction (Figure 1(a)). Therefore, we diagnosed the patient with cerebral embolisms. MR angiography did not reveal cervical angiostenosis (Figure 1(b)) or intracranial aneurysm (Figure 1(c)). Transthoracic 2D-echocardiography revealed a giant left atrial tumor of the diameter cm attached to the atrial septum causing mitral valve prolapse that moved during diastole and occluded the mitral orifice (Figure 2).
Therefore, we diagnosed the patient with cerebral embolisms due to left atrial myxoma. The reason to not select tPA as the emergency treatment was that the estimated time from the onset of symptoms to hospital presentation was too long for patients with cerebral embolism to treat by tPA. To prevent recurrence, she underwent the resection of the myxoma with cardiopulmonary bypass and the reconstruction of the atrial septum using a bovine pericardial patch 1 day after her stroke. Gross examination showed a cm brown, gray, and whitish myxoid mass (Figure 3). Pathology confirmed atrial myxoma. The patient uneventfully recovered from cardiac surgery, and her postoperative general and neurological symptoms improved. Thirteen days after admission, her NIHSS score improved to 0 and she was discharged from our hospital.
Myxoma is a benign tumor of the heart most commonly occurring in the left atrium and is attached by a pedicle to the fossa ovalis in the atrial septum. Clinical symptoms include the classic triad of embolic, obstructive, and constitutional signs such as cerebral infarction, syncope, dyspnea, fever, weight loss, and arthralgia. In this study, the patient showed a past history of obstruction; cerebral infarction was a secondary presentation and C-reactive protein level was mildly elevated. Myxoma can generally be easily diagnosed by transthoracic echocardiography. In cases like the present where there is no risk factor for cerebrovascular disorders or atrial fibrillation, it is important to consider the possibility of myxoma as a cause of cerebral embolism despite its rarity. If time constraints and available facilities permit, transthoracic echocardiography should be performed. In spite of the benign histological character of these tumors, they can lead to unfavorable consequences. These tumors could aggravate preexisting complications or lead to sudden death due to their fragmentability or valve obstruction [17, 18].
Ischemic cerebral infarction is one of the most common as well as serious presentations of cardiac myxoma [2, 3]. However, there are no clear guidelines for immediate medical management following stroke due to atrial myxoma. The treatment of acute ischemic strokes caused by embolic atrial myxoma is controversial, largely because the embolus could be composed of the tumor itself or thrombus, adhered thrombotic material, or a combination of both . It is reasonable to argue that the best possible course of action is thrombolytic therapy, depending on the composition of the emboli. Studies have reported that patients with sudden cerebral infarction associated with myxoma in whom thrombolytic therapy was highly effective and pathologic findings suggest thrombotic embolism are increasing [6–11]. But it is difficult to draw a firm conclusion from the paucity of existing data, which consists of single-case reports employing a variety of methods and the administration of different thrombolytic drugs.
On the other hand, the patient had a good outcome by emergency surgery of the left atrial myxoma without thrombolytic therapy. Such reports are rare because systemic anticoagulation required for cardiopulmonary bypass may become an issue in patients who have suffered a recent stroke, and there is a risk of hemorrhagic transformation associated with cardiopulmonary bypass in patients with a recent stroke. A large embolic stroke may become hemorrhagic and result in brain damage, particularly during the first week after stroke . There are no clear guidelines in the literature indicating a safe interval from the onset of a stroke to the time of surgery; therefore, we believe the timing of surgery is still controversial and needs to be clarified. Because of the immediate diagnosis of stroke, the presence of myxomatous intracranial aneurysm and the increased risk of recurrent ischemic stroke with delayed surgery. However, the patient was taken for emergency cardiac surgery within 24 h of the stroke without such obstruction. This case suggests that, in cases without a large embolic stroke or high NIHSS score, the emergency surgery of the left atrial myxoma often gives patients with cardiogenic embolism a good outcome. Because patients with atrial myxomas are at risk of sudden death due to tumor embolism or occlusion of valve orifices, prompt surgical excision after diagnosis is mandatory. Surgery is generally curative and is associated with a perioperative mortality rate of less than 5%. Cardiac surgery with cerebral infarction has the abovementioned risk; however, there is no effective alternative to prevent cerebral embolism progression . However, further epidemiological analyses in larger case studies are required before confirming its clinical utility as a treatment.
Thrombolytic therapy may be an exciting alternative to surgery. Cardiac myxoma has a high tendency to produce disabling neurological complications due to the risk of embolic episodes, which emphasize the need for its prompt surgical excision as soon as the diagnosis is confirmed. Moreover, in cases with a small embolism stroke and low NIHSS score, at present, we consider the emergency surgery of the left atrial myxoma to be an effective therapy for the prevention of cerebral embolism progression.
Conflict of Interests
The authors declare that there is no conflict of interests regarding the publication of this paper.
The authors thank the Department of Cardiovascular Surgery at Jichi Medical University for helping with the collection of patient data.
- K. Reynen, “Cardiac myxomas,” The New England Journal of Medicine, vol. 333, no. 19, pp. 1610–1617, 1995.
- V. H. Lee, H. M. Connolly, and R. D. Brown Jr., “Central nervous system manifestations of cardiac myxoma,” Archives of Neurology, vol. 64, no. 8, pp. 1115–1120, 2007.
- L. E. Knepper, J. Biller, H. P. Adams Jr., and A. Bruno, “Neurologic manifestations of atrial myxoma. A 12-year experience and review,” Stroke, vol. 19, no. 11, pp. 1435–1440, 1988.
- L. E. Wold and J. T. Lie, “Cardiac myxomas. A clinicopathologic profile,” American Journal of Pathology, vol. 101, no. 1, pp. 219–240, 1980.
- A. P. Burke and R. Virmani, “Cardiac myxoma. A clinicopathologic study,” The American Journal of Clinical Pathology, vol. 100, no. 6, pp. 671–680, 1993.
- M. Acampa, F. Guideri, R. Tassi et al., “Thrombolytic treatment of cardiac myxoma-induced ischemic stroke: a review,” Current Drug Safety, vol. 9, no. 2, pp. 83–88, 2014.
- J. Y. Chong, P. Vraniak, M. Etienne, D. Sherman, and M. S. V. Elkind, “Intravenous thrombolytic treatment of acute ischemic stroke associated with left atrial myxoma: a case report,” Journal of Stroke and Cerebrovascular Diseases, vol. 14, no. 1, pp. 39–41, 2005.
- C. D. Nagy, M. Levy, T. J. Mulhearn IV et al., “Safe and effective intravenous thrombolysis for acute ischemic stroke caused by left atrial myxoma,” Journal of Stroke and Cerebrovascular Diseases, vol. 18, no. 5, pp. 398–402, 2009.
- C.-T. Ong and R.-Y. Chang, “Intravenous thrombolysis of occlusion in the middle cerebral and retinal arteries from presumed ventricular myxoma,” Stroke Research and Treatment, vol. 2011, Article ID 735057, 3 pages, 2011.
- H. Nishimura, T. Nakajima, T. Ukita et al., “A case of acute cerebral infarction associated with left atrial myxoma treated by intravenous tissue plasminogen activator,” Nosotchu, vol. 32, no. 2, pp. 156–162, 2010.
- G. B. Kulkarni, R. Yadav, V. Mustare, and S. Modi, “Intravenous thrombolysis in a patient with left atrial myxoma with acute ischemic stroke,” Annals of Indian Academy of Neurology, vol. 17, no. 4, pp. 455–458, 2014.
- Y. Shinohara, A. Ogawa, N. Suzuki, Y. Katayama, and A. Kimura, Japanese Guidelines for Management of Stroke 2009, Kyowakikaku, Tokyo, Japan, 2009 (Japanese).
- H. P. Adams Jr., G. del Zoppo, M. J. Alberts et al., “Guidelines for the early management of adults with ischemic stroke: a guideline from the American Heart Association/American Stroke Association Stroke Council, Clinical Cardiology Council, Cardiovascular Radiology and Intervention Counsil, and the Atherosclerotic Peripheral Vascular Disease and Quality of Care Outcomes in Research Interdiscriplinary Working Groups: the American Academy of Neurology affirms the value of this guideline as an educational tool for neurologists,” Stroke, vol. 38, no. 6, pp. 1655–1711, 2007.
- T. S. Olsen, P. Langhorne, H. C. Diener et al., “European stroke initiative recommendations for stroke management-update 2003,” Cerebrovascular Diseases, vol. 16, no. 4, pp. 311–337, 2003.
- Y. Al-Said, H. Al-Rached, S. Baeesa, K. Kurdi, I. Zabani, and A. Hassan, “Emergency excision of cardiac myxoma and endovascular coiling of intracranial aneurysm after cerebral infarction,” Case Reports in Neurological Medicine, vol. 2013, Article ID 839270, 5 pages, 2013.
- S. Baek, S. Park, N. J. Lee, Y. Kang, and K. H. Cho, “Effective mechanical thrombectomy in a patient with hyperacute ischemic stroke associated with cardiac myxoma,” Journal of Stroke and Cerebrovascular Diseases, vol. 23, no. 9, pp. e417–e419, 2014.
- J. Robert, M. Brack, S. Hottinger, A. Kadner, and H.-R. Baur, “A rare case of left ventricular cardiac myxoma with obstruction of the left ventricular outflow tract and atypical involvement of the mitral valve,” European Journal of Echocardiography, vol. 10, no. 4, pp. 593–595, 2009.
- E. Natale, G. Minardi, G. Casali, G. Pulignano, and F. Musumeci, “Left ventricular myxoma originating from the interventricular septum and obstructing the left ventricular outflow tract,” European Journal of Echocardiography, vol. 9, no. 1, pp. 84–85, 2008.
- D. Toni, M. Fiorelli, S. Bastianello et al., “Hemorrhagic transformation of brain infarct: predictability in the first 5 hours from stroke onset and influence on clinical outcome,” Neurology, vol. 46, no. 2, pp. 341–345, 1996.
- F. M. Rosenberg, A. Chan, S. V. Lichtenstein, and B. M. McManus, “Cardiac neoplasms,” Current Treatment Options in Cardiovascular Medicine, vol. 1, no. 3, pp. 243–252, 1999.
Copyright © 2015 Syuichi Tetsuka and Kunihiko Ikeguchi. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.