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CARDIOVASCULAR JOURNAL OF AFRICA • Volume 28, No 5, September/October 2017

AFRICA

e1

Case Report

Atrial myxoma: a rare cause of hemiplegia in children

Uchenna Onubogu, Boma West, Boma Orupabo-Oyan

Abstract

Background:

Atrial myxoma is an uncommon cause of hemi-

plegia in children. However hemiplegia is the commonest

manifestation of atrial myxoma in the paediatric age group.

Case report:

An 11-year-old girl presented with left hemi-

plegia and palpitations. Three months later she had a deep-

vein thrombosis of the right common iliac vein. MRI of

the brain showed a subacute right thalamic infarct, and an

ECG showed left atrial and left ventricular hypertrophy.

Transthoracic echocardiography revealed a left atrial myxoma

impinging on the mitral valve. A diagnosis of left atrial

myxoma with multiple thromboembolic events was made. She

was placed on anticoagulants until she died while awaiting

surgical tumour resection.

Conclusion:

Echocardiography should be done early in chil-

dren presenting with ischaemic thromboembolic diseases in

order to reduce morbidity and mortality rates resulting from

cardiac pathology.

Keywords:

atrial myxoma, hemiplegia, thromboembolic, cardiac,

children

Submitted 17/5/16, accepted 30/10/16

Published online 9/12/16

Cardiovasc J Afr

2016;

27

: e1–e3

www.cvja.co.za

DOI: 10.5830/CVJA-2016-093

Cardiac myxoma is a rare cause of cerebrovascular disease

(CVD), especially in children. The common cause of CVD in

African children is sickle cell disease.

1

Other common causes are

cyanotic congenital heart diseases, arrhythmias, coagulopathies

and systemic infection (meningitis, sepsis).

1,2

The term myxoma is the Latin translation of a Greek word

‘muxa’, which literally means mucus. A cardiac myxoma is a

benign tumour of the heart arising from primitive mesenchyme.

Cardiac myxoma is the most common primary tumour of

the heart in adults but is very infrequent in the paediatric

population.

3

Among primary cardiac tumours in children, the

rhabdomyomas are the commonest.

4

Cardiac myxomas can be seen in any of the cardiac chambers

but rarely on the heart valves. The atria are more affected

than the ventricles, therefore cardiac myxomas are said to be

predominantly intra-atrial. About 90% of cardiac myxomas are

located in the atria with a left-to-right ratio of about 4:1.

5

Our

patient had a left atrial cardiac myxoma. The size of a cardiac

myxoma can range from small (unnoticeable) to as large as 8 cm

in length.

Case report

An 11-year-old girl was referred to the cardiology clinic

on account of left hemiplegia of one month duration. The

hemiplegia was of sudden onset and was associated with

headache, dizziness and vomiting at onset. She had also been

having intermittent episodes of palpitations and had just

been discharged from hospital two weeks earlier after being

managed for an intracranial space-occupying lesion, with raised

intracranial pressure, left hemiplegia and multiple cranial nerve

palsy. She had a positive history of sudden death in her family

(an uncle and her grandmother).

On examination, she had a hemiplegic gait, a left CN V1,

VII palsy and decreased power, tone and reflexes in the left

upper and lower limb. A regular pulse and wide blood pressure

difference was noted in both right and left upper limbs (right

120/50 mmHg, left 60 mmHg/unrecordable).

Previous tests had been done when she was admitted. MRI

of the brain showed subacute right thalamic infarct, and her

blood lipid profile and random blood glucose results were

normal. Her genotype was AA, mantoux was negative, chest

radiograph was normal, and PT/PTTK was also normal.

A diagnosis of peripheral artery disease was entertained and

magnetic resonance angiography of both carotid arteries was

done, which was normal. The ECG showed sinus rhythm with

evidence suggestive of left atrial and left ventricular hypertrophy.

An echocardiography could not be done immediately but was

requested.

She was subsequently placed on aspirin, encephabol and

regular physiotherapy while angiography was being awaited.

She defaulted from follow up and was seen in hospital three

months later when she collapsed at school after complaining

of heaviness of the right side of the body and inability to walk.

Her history revealed that she had stopped her aspirin two days

earlier.

On examination, she was conscious, and the blood pressure

in both upper limbs was equal and normal (110/70 mmHg). Her

pulse was a good volume but irregularly irregular, both legs were

cold to the touch, and the dorsalis pedis was barely palpable. A

diagnosis of deep-vein thrombosis was entertained.

Braithwaite Memorial Specialist Hospital, Portharcourt,

Rivers, Nigeria

Uchenna Onubogu, MB BS, FWACP,

utchayonubogu@yahoo.co.uk

Boma West, MB BS, FWACP

Boma Orupabo-Oyan, MB BS, FWACP