scholarly journals Calcified Amorphous Tumor of Left Ventricle: A Rare Cardiac Tumor

Cureus ◽  
2021 ◽  
Author(s):  
Rupesh Kumar ◽  
Vikram Halder ◽  
Soumitra Ghosh ◽  
Basant Kumar ◽  
Subhrashis Guha Neogi ◽  
...  
1986 ◽  
Vol 27 (2) ◽  
pp. 273-277 ◽  
Author(s):  
Tohru IZUMI ◽  
Akira MATSUOKA ◽  
Koichi NAGAI ◽  
Takashi TSUDA ◽  
Yutaka ARAI ◽  
...  
Keyword(s):  

2021 ◽  
Author(s):  
Tom Langenaeken ◽  
Alaaddin Yilmaz ◽  
Aydin Basoglu

Abstract Background: Left ventricle (LV) lipoma is a very rare, benign cardiac tumor. Due to its rarity, LV lipoma is often misdiagnosed. Aspecific symptoms such as murmurs, arrhythmias, memory loss and palpitation may occur due to the mass effect. Case presentation: We report a case report of a 42 year old woman who was found to have left ventricle mass after check-up for arrhytmia. By a fully endoscopic approach, the mass was successfully resected from the left ventricle without the need for sternotomy. Conclusion: Total endoscopic removal of left ventricle lipoma’s can be done safely and has several advantages to conventional sternotomy. Larger studies are needed to confirm this hypothesis.


2020 ◽  
Vol 17 (2) ◽  
pp. 148-151
Author(s):  
Elena I. Naumenko ◽  
Valeria G. Anufrieva ◽  
Irina A. Grishutkina

Background. The most common cardiac tumor in children is rhabdomyoma. Its frequency is 58.3% in the early neonatal period. Rhabdomyoma is associate with tuberous sclerosis pretty often (50-86% of all cases) and it be its diagnostic marker.Clinical case description. This article presents case study of the newborn from the mother with burdened obstetric and gynecological anamnesis, type 1 diabetes, nicotine addiction. Multiple mass lesions were revealed in the child’s heart on the 31 st week of gestation. On examination: systolic murmur over the heart region, fibrous nodules on the skin all over the body up to 1-5 mm in diameter, indurated on palpation. Diagnosed echocardiographically: multiple attached, round masses were revealed in the cavity of left ventricle of 7.9×4.1 mm in size, in outflow track of left ventricle (near the aortic root) — 9.3×4.8 mm, in the cavity of right ventricle — 4.3×3.2 mm, in the cavity of right auricle — 5.1×5.0 mm. Pathologic activity of cardiac conduction system was presented only by single supra-ventricular and ventricular extrasystoles due to the results of 24-hour monitoring.Conclusion. Children with cardiac rhabdomyoma diagnosed in prenatal period are threatened by tuberous sclerosis, thus, complex dynamic observation and molecular genetic testing is needed.


2021 ◽  
Vol 16 (1) ◽  
Author(s):  
Tom Langenaeken ◽  
Aydin Basoglu ◽  
Abdullah Kaya ◽  
Alaaddin Yilmaz

Abstract Background Left ventricle (LV) lipoma is a very rare, benign cardiac tumor. Due to its rarity, LV lipoma is often misdiagnosed. Aspecific symptoms such as murmurs, arrhythmias, memory loss and palpitation may occur due to the mass effect. Case presentation We report a case report of a 42 year old woman who was found to have left ventricle mass after check-up for arrhytmia. By a fully endoscopic approach, the mass was successfully resected from the left ventricle without the need for sternotomy. Conclusion Total endoscopic removal of left ventricle lipoma’s can be done safely and has several advantages to conventional sternotomy. Larger studies are needed to confirm this hypothesis.


2015 ◽  
Vol 01 (01) ◽  
pp. e35-e37 ◽  
Author(s):  
Reinhard Besser ◽  
Mohammed Al-Azani ◽  
Christian Frank ◽  
Manfred Bohrer ◽  
Falk-Udo Sack ◽  
...  

2019 ◽  
Vol 9 (1) ◽  
Author(s):  
Mercedes Olaya-C ◽  
Jorge Andres Franco ◽  
Oscar Alberto Messa

AbstractBackgroundCongenital tumors, including mesenchymal rhabdomyoma, are highly infrequent. The combination of a congenital tumor and rhabdomyoma is rarer yet, even more so when primary origin is in the heart.Case presentationWe present a case of fetal hydrops fetalis, wherein the post-mortem exam revealed a cardiac tumor more than twice the size of the heart itself; histological study confirmed primary rhabdomyoma involving the left ventricle.ConclusionIt is essential to keep in mind that fetal tumors should always be differentiated from malformations; in fetuses tissue immaturity must be taken into account for categorization; despite benign labeling, they can be lethal.


1999 ◽  
Vol 1 ◽  
pp. S101-S101
Author(s):  
O FOKINA ◽  
N TVERDOKHLEBOV ◽  
V SANDRIKOV ◽  
L KOUZNETZOVA

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