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Pseudopancreatic Cyst in a Patient with Hypertrophic Cardiomyopathy


Affiliations
1 M.G.M Medical College & M.Y Hospital, Indore, India
 

Hypertrophic cardiomyopathy (HCM) is a rare genetic disorder characterised by massive myocardial hypertrophy leading to left ventricular outflow tract obstruction. Clinical presentation ranges from absence of symptoms to sudden death. A 17 yr old male patient, known case of hypertrophic cardiomyopathy was posted for excision of pseudopancreatic cyst. Anaesthetic management of these patients poses considerable challenges. Factors like tachycardia, hypovolemia, vasodilatation and increased cardiac contractility lead to exacerbation of the obstruction.

Keywords

Anaesthesia, Hypertrophic Cardiomyopathy, Pseudo-Pancreatic Cyst.
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  • Pseudopancreatic Cyst in a Patient with Hypertrophic Cardiomyopathy

Abstract Views: 267  |  PDF Views: 104

Authors

Shaily Gokharu
M.G.M Medical College & M.Y Hospital, Indore, India
Rashmi Pal
M.G.M Medical College & M.Y Hospital, Indore, India
Gaurav Acharya
M.G.M Medical College & M.Y Hospital, Indore, India
K. K. Arora
M.G.M Medical College & M.Y Hospital, Indore, India

Abstract


Hypertrophic cardiomyopathy (HCM) is a rare genetic disorder characterised by massive myocardial hypertrophy leading to left ventricular outflow tract obstruction. Clinical presentation ranges from absence of symptoms to sudden death. A 17 yr old male patient, known case of hypertrophic cardiomyopathy was posted for excision of pseudopancreatic cyst. Anaesthetic management of these patients poses considerable challenges. Factors like tachycardia, hypovolemia, vasodilatation and increased cardiac contractility lead to exacerbation of the obstruction.

Keywords


Anaesthesia, Hypertrophic Cardiomyopathy, Pseudo-Pancreatic Cyst.

References