Presentation on theme: "Rheumatic Valvular Heart Disease Acute Rheumatic fever (RF) & Chronic rheumatic heart disease (RHD) Doç. Dr. Işın DOĞAN EKİCİ Department of Pathology."— Presentation transcript:
1Rheumatic Valvular Heart Disease Acute Rheumatic fever (RF) & Chronic rheumatic heart disease (RHD) Doç. Dr. Işın DOĞAN EKİCİ Department of Pathology
2IntroductionRheumatic fever (RF) is a systemic, immune mediated multisystem inflammatory disease that occurs few weeks after an episode triggered by Group A b-hemolytic streptococcal throat infection,rarely with streptococcal infection of other sites.Rheumatic Heart Disease is the cardiac manifestations of RF and is associated with inflamation of the valves, myocardium and/or pericardiumAround 3-5% of untreated streptococcal pharyngitis turns into rheumatic fever.Most patients are kids 5-15 years old.The disease is endemic in the poor nations.
3A painful migratory arthritis (approx. 80%). The earliest and most common featureLarge joints such as knees, ankles, elbows, or shoulders typically are affected.Sydenham choreawas a common late-onset clinical manifestation in the past but rarely is observed now.Carditis(with progressive congestive heart failure, a new murmur, or pericarditis) may be the presenting sign of unrecognized past episodes and is the most lethal manifestation.
4Jones Criteria of Diagnosis of RF Major CriteriaMigratory polyarthritis of the large joints,PancarditisSubcutaneous nodulesErythema marginatum of the skinSydenham Chorea –a neurologic disorder with involuntary purposeless, rapid movements.Minor CriteriaFeverArthralgiaHigh acute phase reactants (CRP, SAA, SAP, Complements, Coagulation Proteins)High ESRprolonged PR interval on ECGFor Diagnosis: Two Major or one major and two minor criteria following Group-A streptococcus pharyngitis.
5Sydenham ChoreaPatients present with difficulty writing, involuntary grimacing, purposeless (choreiform) movements of the arms and legs, speech impairment, generalized weakness, and emotional lability.Physical findings include hyperextended joints, hypotonia, diminished deep tendon reflexes, tongue fasciculations ("bag of worms"), and a "milk sign" or relapsing grip demonstrated by alternate increases and decreases in tension when the patient grips the examiner's hand.
6Outcome of the DiseaseThe acute attack may induce (licks) arthritis and sometimes myocarditis (bites).The most important consequence of Rheumatic fever is Chronic rheumatic heart diseaseChronic rheumatic heart disease (RHD) is characterized principally by deforming fibrotic valvular disease (particularly mitral stenosis), which produces permanent dysfunction and severe, sometimes fatal, cardiac failure decades later.
7Endocarditis is manifested as valve insufficiency. Acute rheumatic heart disease often produces a pancarditis characterized by endocarditis, myocarditis, and pericarditis.Endocarditis is manifested as valve insufficiency.The mitral valve is most commonly and severely affected (65-70% of patients), and the aortic valve is second in frequency (25%).The tricuspid valve is deformed in only 10% of patients and almost always is associated with mitral and aortic lesions.The pulmonary valve is rarely affected.Severe valve insufficiency during the acute phase may result in congestive heart failure and even death (1% of patients).
8Pathogenesis and key morphologic changes of acute rheumatic heart disease. Acute rheumatic fever causes changes in the endocardium, myocardium, and pericardium.Chronic rheumatic heart disease is almost always caused by deformity of the heart valves, particularly the mitral and aortic valves.
9Etiology and Pathogenesis RF is a post-infectious, immunologic disease that results either from(1) heightened immunologic reactivity to streptococcal antigens that evoke antibodies cross reactive with human tissue antigens (the M-protein of the streptococcus, and at least one other antigen now being characterized, are attacked by antibodies which then cross-react with the heart anti-myosin antibody, brain, skin, and joints), or(2) some form of autoimmune reaction incited by a streptococcal infection.
10Initial attacks of RF follow some weeks (1 to 5 weeks) after streptococcal infection. Elevated serum titers of antibodies to streptolysin O (ASO) and hyaluronidase (both elaborated by the streptococcal organism) are almost always present.The tissue lesions of RF and RHD are sterile and do not result from direct bacterial invasion.Recurrent acute RF is preceded by a streptococcal infection.
11Potential antigenic targets (1) heart valve glycoproteins that cross-react with the hyaluronate capsule of the streptococcus, itself identical to human hyaluronate;(2) myocardial and smooth muscle sarcolemma that are cross-reactive with streptococcal membrane antigens; and(3) cardiac myosin (that shares antigenic determinants with streptococcal M protein, the chief virulence factor of group A streptococci).
12JointsThe likelihood of acute arthritis increases with age at the time of the attack, appearing in about 90% of adults and less commonly in children.The large joints, such as the knees, are most often affected.The changes are transitory and resolve without sequelae.
13Skin lesionsSubcutaneous nodules or Erythema marginatum (present in 10 to 60% of cases, more often in children):Subcutaneous nodulesessentially giant Aschoff bodies, are most oftenlocated overlying the extensor tendons of the extremities at thewrists,elbows,ankles,and knees.
14Erythema marginatumbegins as flat to slightly elevated, slightly reddened maculopapules with reddened and elevated erythematous marginsprogressively enlargeit tends to have a “bathing-suit” distributionmay also occur over the thighs, lower extremities, and face.
16Morphology of Acute RF The cardiac pathology is a pancarditis. The characteristic lesion in the myocardium (especially near the vessels) is the Aschoff body (Aschoff nodule).Aschoff body is a a mass of fibrinoid surrounded byT lymphocytes,macrophages,few plasma cells, andplump “activated” histiocytes called Anitschkow cells (caterpillar cells), bloated, pale-purple-staining macrophages with a curious caterpillar-shaped mass of heterochromatin running the length of the nucleus (in cross-section, this is an owl eye instead).Some of the larger altered histiocytes are multinucleated to form Aschoff giant cells.
17Acute and chronic rheumatic heart disease. A.Aschoff body in a patient with acute rheumatic carditis;B, Acute rheumatic mitral valvulitis superimposed on chronic rheumatic heart disease. Small vegetations (verrucae) are visible along the line of closure of the mitral valve leafletC-D, Mitral stenosis with diffuse fibrous thickening and distortion of the valve leaflets, commissural fusion (arrows), and thickening and shortening of the chordae tendineae.D, Opened valve.E, Surgically removed specimen of rheumatic aortic stenosis, demonstrating thickening and distortion of the cusps with commissural fusion
20During acute RF, Aschoff bodies may be found in any of the three layers of the heart–pericardium, myocardium, or endocardium–hence a pancarditis.In the pericardium, they are located in the subserosal fat and fibrous tissue and are accompanied by a fibrinous or serofibrinous pericardial exudate, described as a “bread-and-butter” pericarditis, which generally resolves without sequelae.The myocardial involvement takes the form of scattered Aschoff bodies within the interstitial connective tissue, often perivascular. Adjacent myocytes may be damaged.
22Endocardium and the left-sided valves: the endocarditis manifests as verrucae, small (1-2 mm), sterile masses of fibrin and platelets along the lines of closure of the valve leaflets.The verrucae are prone to organize, causing deformity of the heart.If the cusps stick together, stenosis results.If scar contraction shortens and bends the valve leaflets, insufficiency (regurgitation) results.The aortic and mitral valves are usually affected; the tricuspid sometimes, the pulmonic rarely.
25Chronic rheumatic heart disease (RHD) Chronic manifestations due to residual and progressive valve deformity occur in 9-39% of adults with previous rheumatic heart disease.Fusion of the valve apparatus resulting in stenosis or a combination of stenosis and insufficiency develops 2-10 years after an episode of acute rheumatic fever, and recurrent episodes may cause progressive damage to the valves.Fusion occurs at the level of the valve commissures, cusps, chordal attachments, or any combination of these.
26Rheumatic heart disease is responsible for 99% of mitral valve stenosis in adults. Associated atrial fibrillation or left atrial thrombus formation from chronic mitral valve involvement and atrial enlargement may be observed.
28Subendocardial lesions: perhaps exacerbated by regurgitant jets, may induce irregular thickenings called MacCallum’s plaques (usually in the left atrium),One hallmark of old rheumatic mitral valve disease is thickening of the chordae tendineae.
29Valves in Chronic Rheumatic Heart Disease Valve leaflet thickening.Shortening, thickening and fusion of tendinous cordsFish mouth Mitral stenosis
30The cardinal anatomic changes of the mitral valve are: Chronic rheumatic heart disease (RHD) is characterized principally by deforming fibrotic valvular disease (particularly mitral stenosis), which producespermanent dysfunction andsevere, sometimes fatal, cardiac failure.The cardinal anatomic changes of the mitral valve are:leaflet thickening,commissural fusion and shortening,thickening and fusion of the chordae tendineae.
31If the cusps stick together, stenosis results. If scar contraction shortens and bends the valve leaflets, insufficiency (regurgitation) results.Fibrous bridging across the valvular commissures and calcification create “fish mouth” or “buttonhole” stenoses.
34PrognosisDespite damaged valves, the heart may remain compensated for the duration of a long life, but usually over the span of decades, decompensation and eventual full-blown cardiac failure develop.This course can now be altered by surgical repair or replacement of damaged valves.
35Complications of ARF 1. Myocarditis induces arrhythmias (particularly atrial fibrillation) 2. Thromboembolism (fibrillation potentiates atrial thrombi that constitute potential sources of emboli) 3. Myocarditis may lead to cardiac dilation and resultant functional mitral insufficiency 4. Cardiac failure (the major cause of death during acute RF). Complications of Chronic RHD 1. Aortic and mitral stenosis/insufficiency 2. Infective endocarditis (superimposed on chronically deformed valves) 3. Decompensation ( full-blown cardiac failure develop in Chronic RHD).