Year : 2017  |  Volume : 10  |  Issue : 2  |  Page : 218--219

Massive biventricular rhabdomyoma in a neonate


Manish Pandey1, Rimlee Dutta2, Shyam S Kothari1,  
1 Department of Cardiology, AIIMS, New Delhi, India
2 Department of Pathology, AIIMS, New Delhi, India

Correspondence Address:
Shyam S Kothari
Department of Cardiology AIIMS, New Delhi
India

Abstract

Rhabdomyoma is a well characterised entity in a neonate. Herein, we report a massive biventricular rhabdomyoma in a neonate presenting with cyanosis and congestive heart failure which was confirmed on autopsy. The report is for documentation of an unusually large tumour.



How to cite this article:
Pandey M, Dutta R, Kothari SS. Massive biventricular rhabdomyoma in a neonate.Ann Pediatr Card 2017;10:218-219


How to cite this URL:
Pandey M, Dutta R, Kothari SS. Massive biventricular rhabdomyoma in a neonate. Ann Pediatr Card [serial online] 2017 [cited 2021 May 16 ];10:218-219
Available from: https://www.annalspc.com/text.asp?2017/10/2/218/205153


Full Text



Rhabdomyoma as the most common benign cardiac tumor presenting in infancy is a well-characterized entity, and its association with tuberous sclerosis is also well known.[1] Most patients with small tumors are asymptomatic, but some patients may present with arrhythmias, obstruction, and rarely embolism.[2] Spontaneous partial or complete regression of rhabdomyomas during growth is the rule.[1],[3] We recently encountered a 20-day-old neonate in congestive heart failure with cyanosis resulting from massive multiple biventricular rhabdomyoma [Figure 1]a and [Figure 1]b and [Supplementary Video 1]a and [Supplementary Video 1]b and wish to document the same in view of its size. The neonate also had macules over the chest suggestive of tuberous sclerosis, but further evaluation could not be performed. He was planned for debulking surgery but had ventricular fibrillation from which he could not be revived. An autopsy confirmed the diagnosis [Figure 2]a,[Figure 2]b,[Figure 2]c. More recently, salutary effects of everolimus (mammalian target of rapamycin) in regression of rhabdomyomas have been reported and possibly could have been utilized in this neonate.[4],[5]{Figure 1}{Figure 2}

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Financial support and sponsorship

Nil.

Conflicts of interest

There are no conflicts of interest.

References

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