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Papillary Fibroelastoma: A significant lesion in cardiac medicine
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Dear Sir/Madam
Madam, Primary cardiac tumours are rare, with papillary fibroelastoma being the third most common tumour following atrial myxoma and lipoma. It is considered a benign neoplasm with an incidence of less than 0.1%, emanating from the valvular endocardium [1]. However, it is regarded as an asymptomatic tumour and is diagnosed incidentally via routine echocardiography or during autopsy. Despite being a silent tumour, it still holds the risk of severe future complications, which are associated with systemic emboli, stroke, myocardial infarction, and sudden death. Hence, early diagnosis is the principal step that allows prioritising the management options suggesting close monitoring or surgery [2].
Due to the rarity of this disease, there is still insufficient data that could provide us with the associated etiological risk factors. It arises from the valvular endocardium in most cases with each valve of the heart having a varying percentage of involvement. The aortic valve accounts for 29% of cases, the mitral valve for 25%, the tricuspid valve for 17%, and the pulmonary valve for 13% [3]. Predominantly patients suffering from papillary fibroelastoma have no clinical features but it does have a few manifestations such as syncope, angina, and shortness of breath. The fragility of this tumour implies a probable risk of embolization which could ultimately result in transient ischemic attacks and myocardial infarction. Additionally, some cases of congestive heart failure, thromboembolism, ventricular fibrillation, and sudden death have been reported. Embolization usually occurs due to the abrupt formation of thrombus frequently on the tumour nidus resulting from platelet aggregation. A highly mobile pedunculated mass attached to a valve or endocardium is a typical incidental finding of papillary fibroelastoma through an echocardiogram [4]. However, new techniques including 3-D echocardiography, magnetic resonance imaging, and multi-slice spiral computed tomography have also been reported to be beneficial for the diagnosis. The tumour almost always appears as a solo lesion yet can also emerge in multiple forms. Treatment strategies comprises of early anticoagulation therapy, and surgical correction implying tumour resection and replacement of an entire diseased valve [5].
Papillary fibroelastoma is an infrequent diagnosis and prior detection is an appropriate tool to prevent its life-threatening complications. Implementation of proper screening methods for high-risk patients and the elderly is necessary. More research should be conducted on this rare tumour for favourable outcomes. Moreover, the latest and less invasive treatment modalities should be introduced for better disease control.
Pakistan Medical Association
Title: Papillary Fibroelastoma: A significant lesion in cardiac medicine
Description:
Dear Sir/Madam
Madam, Primary cardiac tumours are rare, with papillary fibroelastoma being the third most common tumour following atrial myxoma and lipoma.
It is considered a benign neoplasm with an incidence of less than 0.
1%, emanating from the valvular endocardium [1].
However, it is regarded as an asymptomatic tumour and is diagnosed incidentally via routine echocardiography or during autopsy.
Despite being a silent tumour, it still holds the risk of severe future complications, which are associated with systemic emboli, stroke, myocardial infarction, and sudden death.
Hence, early diagnosis is the principal step that allows prioritising the management options suggesting close monitoring or surgery [2].
Due to the rarity of this disease, there is still insufficient data that could provide us with the associated etiological risk factors.
It arises from the valvular endocardium in most cases with each valve of the heart having a varying percentage of involvement.
The aortic valve accounts for 29% of cases, the mitral valve for 25%, the tricuspid valve for 17%, and the pulmonary valve for 13% [3].
Predominantly patients suffering from papillary fibroelastoma have no clinical features but it does have a few manifestations such as syncope, angina, and shortness of breath.
The fragility of this tumour implies a probable risk of embolization which could ultimately result in transient ischemic attacks and myocardial infarction.
Additionally, some cases of congestive heart failure, thromboembolism, ventricular fibrillation, and sudden death have been reported.
Embolization usually occurs due to the abrupt formation of thrombus frequently on the tumour nidus resulting from platelet aggregation.
A highly mobile pedunculated mass attached to a valve or endocardium is a typical incidental finding of papillary fibroelastoma through an echocardiogram [4].
However, new techniques including 3-D echocardiography, magnetic resonance imaging, and multi-slice spiral computed tomography have also been reported to be beneficial for the diagnosis.
The tumour almost always appears as a solo lesion yet can also emerge in multiple forms.
Treatment strategies comprises of early anticoagulation therapy, and surgical correction implying tumour resection and replacement of an entire diseased valve [5].
Papillary fibroelastoma is an infrequent diagnosis and prior detection is an appropriate tool to prevent its life-threatening complications.
Implementation of proper screening methods for high-risk patients and the elderly is necessary.
More research should be conducted on this rare tumour for favourable outcomes.
Moreover, the latest and less invasive treatment modalities should be introduced for better disease control.
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