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{{WBRQuestion
{{WBRQuestion
|QuestionAuthor=Gonzalo Romero
|QuestionAuthor=Gonzalo Romero (Reviewed by Rim Halaby and Yazan Daaboul)
|ExamType=USMLE Step 1
|ExamType=USMLE Step 1
|MainCategory=Pathology
|MainCategory=Pathology
|SubCategory=Cardiology
|SubCategory=Cardiology
|MainCategory=Pathology
|Prompt=A 21-year-old male college student suddenly loses consciousness and falls while playing football. The player is unresponsive to verbal or physical stimuli, and has an undetectable pulse. Despite CPR and resuscitation efforts, the patient diesAccording to his family and friends, the patient has always been healthy and has been playing soccer since high school. Further history reveals that two of the patient's relatives also died the same way. Autopsy is obtained in order to determine the cause of death. Which of the following cardiac changes is most likely present in this patient?
|SubCategory=Cardiology
|Explanation=This young athlete presents with [[sudden cardiac death]] during intense exercise due to [[ventricular arrhythmias]], a typical clinical presentation of [[hypertrophic obstructive cardiomyopathy]] (HOCM). HOCM is a genetic disorder caused by a missense mutation that encodes sarcomere proteins of the heart. It is relatively common, occurring in approximately 1 of every 500 adults.
|MainCategory=Pathology
 
|SubCategory=Cardiology
*Macroscopically, the heart demonstrates [[hypertrophy]] more prominent in the ventricular septum, obstructing the outflow from the [[left ventricle]]. Additional complications of the observed hypertrophy include mitral regurgitation due to systolic anterior motion (SAM) of the mitral valve, systolic and diastolic dysfunction, myocardial ischemia, and fatal ventricular arrhythmias.
|MainCategory=Pathology
 
|MainCategory=Pathology
*Histologically, there are hypertrophied [[cardiomyocytes]] in disarray that alter the conduction system and subsequently predispose to [[arrhythmias]].
|SubCategory=Cardiology
 
|MainCategory=Pathology
HOCM should be suspected based on physical exam findings and abnormal findings on echocardiogram or even ECG. On physical exam, a systolic ejection murmur is typically heard at the left sternal border. The intensity of the murmur characteristically increases as preload decreases. Decreasing preload may be performed by changing the patient's position from a seated or squatting position to a standing position. Ultrasound is the diagnostic test of choice, demonstrating asymmetric myocardial hypertrophy with septal thickness greater than the thickness of the free wall.
|SubCategory=Cardiology
 
|MainCategory=Pathology
The mainstay of HOCM therapy includes symptomatic relief and prevention of occurrence of arrhythmias, which may be the cause of death in these patients. Although the risk of death is less than 1% per year, young athletes with HOCM are specifically at risk of developing ventricular arrhythmias and death.
|SubCategory=Cardiology
|MainCategory=Pathology
|SubCategory=Cardiology
|MainCategory=Pathology
|MainCategory=Pathology
|SubCategory=Cardiology
|Prompt=A 21-year-old healthy male college student is concerned about a final he has to take next week.  The grade on this exam could compromise his scholarship if he does not pass. He has been playing football since high school and plays in the College Football team. The next week they are going to have the school Football finale, which will decide if the local college qualifies to go to State competition. He has decent grades in school and has many friends. The following week he takes his exam. The following day the game starts with a lot of cheering and energy from the audience and players, because this is a decisive game. He is excited and tries to perform his best on the field. While jogging after catching the ball, he falls onto the groundAt first he appeared to have hurt his knee while running.  The game is stopped.  The coach and teammates find him unresponsive and try their best to help him. After several minutes laying on the ground, the EMS arrive to the scene and find him without vitals. They start CPR immediately and take him to the nearest Hospital where they run the ACLS protocol without any success. An autopsy is scheduled due to the uncertainty of his cause of death. Which of the following Macroscopic or Microscopic changes is most specific for the most likely diagnosis?
|Explanation=This young athlete presents with a sudden death during intense exercise due to ventricular arrhythmias, a typical clinical presentation of [[Hypertrophic cardiomyopathy]], hypertrophic obstructive cardiomyopathy (HOCM), also known as asymmetrical septal hypertrophy or idiopathic hypertrophic subaortic stenosis (IHSS). Commonly causes sudden death in young athletes. It can be autosomal dominant or idiopathic.
'''Macroscopically''' the heart shows hypertrophy more prominent in the ventricular septum, obstructing the outflow from the left ventricle. The ventricular cavity acquires a banana shaped appearance. [[File:2369.jpg|center|200px]]
'''Histologically''' there are hypertrophied cardio-myocytes in disarray which alters the conduction system leading to arrhythmias. [[File:438.jpg|center|200px]]


<br>
Other members of the family should also be included in the management plan. Immediate family members should be requested to perform periodic ultrasound because hypertrophy may become evident as late as 60 - 70 years of age.
<font color="MediumBlue"><font size="4">'''Educational Objective:''' </font></font>
Hypertrophic Obstructive Cardiomyopathy (HOCM) is a common cause of sudden death in young athletes during intense exercise
|AnswerA=Symmetric left ventricular hypertrophy
|AnswerA=Symmetric left ventricular hypertrophy
|AnswerAExp=<font color="red">'''Incorrect.'''</font> Symmetric left ventricular hypertrophy is characteristically present in patients with increased afterload, such as [[Aortic stenosis|aortic stenosis]] or [[Hypertension|hypertension]], which leads to increased synthesis of actin and myosin which are arranged in a "organized fashion".  Ultimately the patient develops diastolic dysfunction due to the inability of the heart to fill in with blood during diastole.
|AnswerAExp=Symmetric left ventricular hypertrophy is characteristically present in patients with increased [[afterload]], such as [[aortic stenosis]] or [[hypertension]]. This leads to the increased synthesis of [[actin]] and [[myosin]], which are normally arranged in a "organized fashion".  Ultimately, these patients develop diastolic dysfunction due to the inability of the heart to fill in with blood during [[diastole]].
|AnswerB=White appearance of the endocardium
|AnswerB=White appearance of the endocardium
|AnswerBExp=<font color="red">'''Incorrect.'''</font> This can be present in [[Endocardial fibroelastosis]], a rare restrictive [[cardiomyopathy]] present in young children less than 2 years old. It is due to an excessive fibrosis of the endocardium that causes diastolic dysfunction.
|AnswerBExp=A white appearance of the [[endocardium]] can be present in [[endocardial fibroelastosis]], a rare restrictive [[cardiomyopathy]] present in young children less than 2 years of age. It is caused by excessive [[fibrosis]] of the [[endocardium]] that causes diastolic dysfunction.
|AnswerC=Cardiomyocytes hypertrophy in an organized fashion
|AnswerC=Cardiomyocyte hypertrophy in an organized fashion
|AnswerCExp=<font color="red">'''Incorrect.'''</font> This corresponds with the hypertrophy seen in patients with increased afterload, such as [[Aortic stenosis|aortic stenosis]] or [[Hypertension|hypertension]].
|AnswerCExp=Cardiomyocyte [[hypertrophy]] in an organized fashion is found among patients with increased [[afterload]] such as [[aortic stenosis]] or [[hypertension]].
|AnswerD=Prominent ventricular septum hypertrophy compared to the ventricular wall
|AnswerD=Prominent ventricular septum hypertrophy
|AnswerDExp=<font color="Green">'''Correct.'''</font>
|AnswerDExp=Prominent ventricular septum [[hypertrophy]] is a characteristic finding of [[hypertrophic cardiomyopathy]].
|AnswerE=Fibrotic thickening of endocardium and valves of the right side of the heart
|AnswerE=Fibrotic thickening of the endocardium and the valves of the right side of the heart
|AnswerEExp=<font color="red">'''Incorrect.'''</font> This is the macroscopic description of an endocardium affected by a [[Carcinoid syndrome|carcinoid syndrome]] due to chronic serotonin exposure, which causes fibrosis of the tricuspid valve and pulmonary valve. It is present when the carcinoid tumor metastasize to the liver. The patient clinically presents with diarrhea, wheezing, telangiectasias, flushing of the skin and cramping.
|AnswerEExp=[[Fibrosis|Fibrotic thickening]] of the [[endocardium]] and the valves of the right side of the heart is the macroscopic description of an endocardium affected by a [[carcinoid syndrome|carcinoid syndrome]] due to chronic [[serotonin]] exposure, which causes fibrosis of the tricuspid and pulmonary valves. [[Carcinoid syndrome]] occurs when the [[carcinoid tumor]] metastasizes to the liver, thereby bypassing the first-pass metabolism of the liver. These patients present with [[diarrhea]], [[wheezing]], [[telangiectasias]], and [[flushing]] of the skin.
|EducationalObjectives=Hypertrophic obstructive cardiomyopathy (HOCM) is a common cause of sudden death in young athletes during intense exercise. It is characterized by the presence of cardiac hypertrophy more prominent in the ventricular septum and presence of hypertrophied [[cardiomyocytes]] in disarray.
|References=Nishimura, RA; Holmes, DR. Hypertrophic obstructive cardiomyopathy. N Engl J Med. 2004;350:1320-1327.
First Aid 2014 page 290
|RightAnswer=D
|RightAnswer=D
|WBRKeyword=Cardiology, Pathology, Hypertrophic cardiomyopathy, HOCM, HCM, Ischemia, Sudden death, Cardiomyopathy,
|Approved=Yes
|Approved=Yes
}}
}}
{{WBRImage}}
{{WBRImage}}

Latest revision as of 23:08, 27 October 2020

 
Author PageAuthor::Gonzalo Romero (Reviewed by Rim Halaby and Yazan Daaboul)
Exam Type ExamType::USMLE Step 1
Main Category MainCategory::Pathology
Sub Category SubCategory::Cardiology
Prompt [[Prompt::A 21-year-old male college student suddenly loses consciousness and falls while playing football. The player is unresponsive to verbal or physical stimuli, and has an undetectable pulse. Despite CPR and resuscitation efforts, the patient dies. According to his family and friends, the patient has always been healthy and has been playing soccer since high school. Further history reveals that two of the patient's relatives also died the same way. Autopsy is obtained in order to determine the cause of death. Which of the following cardiac changes is most likely present in this patient?]]
Answer A AnswerA::Symmetric left ventricular hypertrophy
Answer A Explanation [[AnswerAExp::Symmetric left ventricular hypertrophy is characteristically present in patients with increased afterload, such as aortic stenosis or hypertension. This leads to the increased synthesis of actin and myosin, which are normally arranged in a "organized fashion". Ultimately, these patients develop diastolic dysfunction due to the inability of the heart to fill in with blood during diastole.]]
Answer B AnswerB::White appearance of the endocardium
Answer B Explanation [[AnswerBExp::A white appearance of the endocardium can be present in endocardial fibroelastosis, a rare restrictive cardiomyopathy present in young children less than 2 years of age. It is caused by excessive fibrosis of the endocardium that causes diastolic dysfunction.]]
Answer C AnswerC::Cardiomyocyte hypertrophy in an organized fashion
Answer C Explanation [[AnswerCExp::Cardiomyocyte hypertrophy in an organized fashion is found among patients with increased afterload such as aortic stenosis or hypertension.]]
Answer D AnswerD::Prominent ventricular septum hypertrophy
Answer D Explanation [[AnswerDExp::Prominent ventricular septum hypertrophy is a characteristic finding of hypertrophic cardiomyopathy.]]
Answer E AnswerE::Fibrotic thickening of the endocardium and the valves of the right side of the heart
Answer E Explanation [[AnswerEExp::Fibrotic thickening of the endocardium and the valves of the right side of the heart is the macroscopic description of an endocardium affected by a carcinoid syndrome due to chronic serotonin exposure, which causes fibrosis of the tricuspid and pulmonary valves. Carcinoid syndrome occurs when the carcinoid tumor metastasizes to the liver, thereby bypassing the first-pass metabolism of the liver. These patients present with diarrhea, wheezing, telangiectasias, and flushing of the skin.]]
Right Answer RightAnswer::D
Explanation [[Explanation::This young athlete presents with sudden cardiac death during intense exercise due to ventricular arrhythmias, a typical clinical presentation of hypertrophic obstructive cardiomyopathy (HOCM). HOCM is a genetic disorder caused by a missense mutation that encodes sarcomere proteins of the heart. It is relatively common, occurring in approximately 1 of every 500 adults.
  • Macroscopically, the heart demonstrates hypertrophy more prominent in the ventricular septum, obstructing the outflow from the left ventricle. Additional complications of the observed hypertrophy include mitral regurgitation due to systolic anterior motion (SAM) of the mitral valve, systolic and diastolic dysfunction, myocardial ischemia, and fatal ventricular arrhythmias.
  • Histologically, there are hypertrophied cardiomyocytes in disarray that alter the conduction system and subsequently predispose to arrhythmias.

HOCM should be suspected based on physical exam findings and abnormal findings on echocardiogram or even ECG. On physical exam, a systolic ejection murmur is typically heard at the left sternal border. The intensity of the murmur characteristically increases as preload decreases. Decreasing preload may be performed by changing the patient's position from a seated or squatting position to a standing position. Ultrasound is the diagnostic test of choice, demonstrating asymmetric myocardial hypertrophy with septal thickness greater than the thickness of the free wall.

The mainstay of HOCM therapy includes symptomatic relief and prevention of occurrence of arrhythmias, which may be the cause of death in these patients. Although the risk of death is less than 1% per year, young athletes with HOCM are specifically at risk of developing ventricular arrhythmias and death.

Other members of the family should also be included in the management plan. Immediate family members should be requested to perform periodic ultrasound because hypertrophy may become evident as late as 60 - 70 years of age.
Educational Objective: Hypertrophic obstructive cardiomyopathy (HOCM) is a common cause of sudden death in young athletes during intense exercise. It is characterized by the presence of cardiac hypertrophy more prominent in the ventricular septum and presence of hypertrophied cardiomyocytes in disarray.
References: Nishimura, RA; Holmes, DR. Hypertrophic obstructive cardiomyopathy. N Engl J Med. 2004;350:1320-1327. First Aid 2014 page 290]]

Approved Approved::Yes
Keyword WBRKeyword::Cardiology, WBRKeyword::Pathology, WBRKeyword::Hypertrophic cardiomyopathy, WBRKeyword::HOCM, WBRKeyword::HCM, WBRKeyword::Ischemia, WBRKeyword::Sudden death, WBRKeyword::Cardiomyopathy
Linked Question Linked::
Order in Linked Questions LinkedOrder::


Image [[WBRImage::|]] Caption WBRImageCaption::no-display Position [[WBRImagePlace::|]]