<?xml version="1.0" encoding="UTF-8"?><!DOCTYPE article  PUBLIC "-//NLM//DTD Journal Publishing DTD v3.0 20080202//EN" "http://dtd.nlm.nih.gov/publishing/3.0/journalpublishing3.dtd"><article xmlns:mml="http://www.w3.org/1998/Math/MathML" xmlns:xlink="http://www.w3.org/1999/xlink" dtd-version="3.0" xml:lang="en" article-type="research article"><front><journal-meta><journal-id journal-id-type="publisher-id">CRCM</journal-id><journal-title-group><journal-title>Case Reports in Clinical Medicine</journal-title></journal-title-group><issn pub-type="epub">2325-7075</issn><publisher><publisher-name>Scientific Research Publishing</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="doi">10.4236/crcm.2018.73017</article-id><article-id pub-id-type="publisher-id">CRCM-82895</article-id><article-categories><subj-group subj-group-type="heading"><subject>Articles</subject></subj-group><subj-group subj-group-type="Discipline-v2"><subject>Medicine&amp;Healthcare</subject></subj-group></article-categories><title-group><article-title>
 
 
  Isolated Right-Sided Infective Endocarditis—An Infected Right Ventricular Myxoma Masquerading as “Tricuspid Vegetation”—A Case Report
 
</article-title></title-group><contrib-group><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Ramachandran</surname><given-names>Muthiah</given-names></name><xref ref-type="aff" rid="aff1"><sub>1</sub></xref><xref ref-type="corresp" rid="cor1"><sup>*</sup></xref></contrib></contrib-group><aff id="aff1"><label>1</label><addr-line>Thoothukudi Medical College Hospital, Thoothukudi, India</addr-line></aff><author-notes><corresp id="cor1">* E-mail:<email>cardioramachandran@yahoo.co.uk</email></corresp></author-notes><pub-date pub-type="epub"><day>06</day><month>03</month><year>2018</year></pub-date><volume>07</volume><issue>03</issue><fpage>182</fpage><lpage>209</lpage><history><date date-type="received"><day>30,</day>	<month>January</month>	<year>2018</year></date><date date-type="rev-recd"><day>5,</day>	<month>March</month>	<year>2018</year>	</date><date date-type="accepted"><day>8,</day>	<month>March</month>	<year>2018</year></date></history><permissions><copyright-statement>&#169; Copyright  2014 by authors and Scientific Research Publishing Inc. </copyright-statement><copyright-year>2014</copyright-year><license><license-p>This work is licensed under the Creative Commons Attribution International License (CC BY). http://creativecommons.org/licenses/by/4.0/</license-p></license></permissions><abstract><p>
 
 
  Aim: To report a case of right ventricular myxoma prolapsing through the tricuspid valve with an attachment of vegetation in a 3-year-old male child. 
  Introduction: Right-sided endocarditis commonly involves the tricuspid valve. Low pressure and low oxygen saturation in the right sided cardiac chambers protect the tricuspid and pulmonary valves from being subjected to excessive strained and damage occurs from injected particulate matter, contaminated venous lines and drug solutions causing endocarditis. RV (right ventricular) myxoma harboured the infection due to trauma as a result of friction movement across the tricuspid valve. 
  Case Report: A 3-year-old male child having the spikes of fever for 2 weeks, presented with tumor “plop” and 3/6 systolic murmur in lower left sternal border and echocardiography revealed a tumor-mimicking vegetation visible as a mass lesion across the tricuspid valve, which is attached to the interventricular septum by a pedicle suggesting a RV myxoma. The vegetation was found to be attached with the tumor and it disappeared with antibiotics and aspirin therapy and the child was advised surgical removal of the tumor. 
  Conclusion: A diagnosis of infective endocarditis can be made in tricuspid valve dysfunction with a floating mass and fever. The cardiac myxoma with an attached vegetation is masquerading as vegetation mass on transthoracic echocardiography in this child.
 
</p></abstract><kwd-group><kwd>RV Myxoma</kwd><kwd> Vegetation</kwd><kwd> Tricuspid Regurgitation</kwd><kwd> Aspirin Therapy</kwd><kwd> AngioVac</kwd></kwd-group></article-meta></front><body><sec id="s1"><title>1. Introduction</title><p>Infective endocarditis (IE) is a microbial infection of the endocardial (endothelial) surface of the heart. It accounts for about 0.75 admissions per 1000 per year in large community hospitals [<xref ref-type="bibr" rid="scirp.82895-ref1">1</xref>] and a population based incidence of 4 - 10 per 100,000 per year, with a slightly higher rate in men [<xref ref-type="bibr" rid="scirp.82895-ref2">2</xref>] [<xref ref-type="bibr" rid="scirp.82895-ref3">3</xref>] . Children with underlying cardiovascular disease may develop endocarditis at any age. It is most frequent on the left side of the heart [<xref ref-type="bibr" rid="scirp.82895-ref4">4</xref>] . Right-sided infective endocarditis is relatively rare and occurring in 5% - 10% of cases [<xref ref-type="bibr" rid="scirp.82895-ref5">5</xref>] . It involves the tricuspid valve in 90%, pulmonary valve in &lt;10% of cases [<xref ref-type="bibr" rid="scirp.82895-ref6">6</xref>] and predominantly occurs in intravenous drug users. The majority of cases of neonatal infective endocarditis are right-sided and occur on structurally normal hearts [<xref ref-type="bibr" rid="scirp.82895-ref7">7</xref>] , probably due to increased use of prosthetic intravascular devices and indwelling venous catheters [<xref ref-type="bibr" rid="scirp.82895-ref8">8</xref>] .</p><p>Tricuspid valve infective endocarditis accounts for 2.5% - 3.1% of IE cases [<xref ref-type="bibr" rid="scirp.82895-ref9">9</xref>] . The right-sided infective endocarditis involving the right ventricular myxoma, prolapsing through tricuspid valve is uncommon and so this case had been reported.</p></sec><sec id="s2"><title>2. Case Report</title><p>A 3-year-old male child with 2 weeks fever was referred for echocardiographic evaluation. His pulse rate was 112 bpm with a temperature elevation up to 101˚F. Blood chemistry revealed leukocytosis with an elevation of total count up to 42,700 cells/cubic mm of blood (normal―6000 to 18,000 cells/cubic mm of blood), Polymorphs―80% (normal―50% to 70%), Lymphocytes―17% (normal―20% to 40%), Eosinpphils―3% (normal―2% to 6%), Platelets―2.27 lakhs/cubic mm of blood (normal―1.5 to 4.5 lakhs/cubic mm of blood). The child was mildly anemic normochromic, normocytic red blood cell indices (Hb―7.7 gm% (normal-13 to 16 gm/dl). ESR (erythrocyte sedimentation rate) was elevated―48 mm/hour (normal―0 to 20 mm/hr). Serum rheumatoid factor (RA factor) was negative (which may be detected in 50% of cases). Blood widal, Dengue antibody test, smear for malarial parasites and blood cultures were negative. Urinalysis revealed no microscopic hematuria. He had no other features of infective endocarditis such as Osler’s nodes, Janeway lesions, Roth spots, splinter hemorrhages which are relatively rare in children and no spotty skin pigmentation, a characteristic feature of myxoma in Carney complex. Abdominal examination revealed no splenomegaly (which occurs only in 10% to 15% of cases). ECG and X-ray chest PA (postero-anterior) were normal as shown in <xref ref-type="fig" rid="fig1">Figure 1</xref> and <xref ref-type="fig" rid="fig2">Figure 2</xref>. Physical examination revealed a grade 3/6 systolic murmur which increases with inspiration (Carvallo’s sign) and an early diastolic tumor “plop” due to abrupt diastolic seating of a mass in the right atrioventricular orifice [<xref ref-type="bibr" rid="scirp.82895-ref10">10</xref>] in the lower left sternal border on auscultation. 2 D echocardiography revealed a large, mobile homogeneous mass in the tricuspid orifice, visible as a “tumor-mimicking vegetation” as shown in Figures 3-9 .</p><p>An irregular homogeneous hypodense mass suggesting a vegetation was attached to the mass, which is globular shape and a heterogeneous or mottled appearance throughout, with echolucent areas representing hemorrhage or necrosis suggesting a myxoma [<xref ref-type="bibr" rid="scirp.82895-ref12">12</xref>] as shown in Figures 10-12 .</p><p>The mass was attached to the interventricular septum by a pedicle (stalk), protruding through the tricuspid valve and appear as “cluster of grapes” [<xref ref-type="bibr" rid="scirp.82895-ref13">13</xref>] as shown in <xref ref-type="fig" rid="fig1">Figure 1</xref>3 and <xref ref-type="fig" rid="fig1">Figure 1</xref>4, suggesting a RV (right ventricular) myxoma.</p><p>The mass produces a traumatic regurgitation across the tricuspid valve due to friction movement as shown in Figures 15-17.</p><p>The child was treated with a course of intravenous ceftriaxone (250 mg twice daily) combined with gentamycin (20 mg twice daily) along with oral aspirin therapy (75 mg daily) for a period of 10 days, the tricuspid regurgitation decreases as in <xref ref-type="fig" rid="fig1">Figure 1</xref>8 and the vegetation was found to be disappeared as shown</p><p>in <xref ref-type="fig" rid="fig1">Figure 1</xref>9. The child was symptom free and advised periodic echocardiographic evaluation with a continuation of medications up to 4 weeks period and</p><p>early surgical removal of the tumor. On follow-up, the child died due to a syncopal episode before the surgical intervention.</p></sec><sec id="s3"><title>3. Discussion</title><sec id="s3_1"><title>3.1. Review of Literature</title><p>Lewis and Grant were the first to describe the infective endocarditis [<xref ref-type="bibr" rid="scirp.82895-ref14">14</xref>] . Gould,</p><p>et al. [<xref ref-type="bibr" rid="scirp.82895-ref15">15</xref>] found that bacteria most frequently responsible for endocarditis (e.g., viridans streptococci) displayed a propensity for adherence to human valves. There are only few reports of large tricuspid valve vegetations in the literature.</p><p>Song, et al. [<xref ref-type="bibr" rid="scirp.82895-ref16">16</xref>] reported a vegetation on tricuspid valve in a 33-year old male, presented with right-sided heart failure and Furui, et al. [<xref ref-type="bibr" rid="scirp.82895-ref17">17</xref>] reported a 1.5 cm</p><p>vegetation on tricuspid valve in a 71-year-old male who developed ventricular septal perforation caused by right-sided infective endocarditis.</p></sec><sec id="s3_2"><title>3.2. Etiopathogenesis</title><p>The endothelial lining of the heart and its valve is normally resistant to infection with bacteria and fungi. When there is a pressure gradient with resultant turbulence of blood flow, which against either the mural endocardium or vascular endothelium results in tissue damage due to high velocity jet (“jet lesions”). Endocarditis begins as endothelial damage, followed by focal adherence of platelets and fibrin. The initial sterile platelet-fibrin nidus, first recognized by Angrist [<xref ref-type="bibr" rid="scirp.82895-ref18">18</xref>] and called as ‘nonbacterial thrombus’, then becomes infected by microorganisms circulating in the blood stream. Platelet-fibrin nidus involves a complex interactions of the components of microbial cell wall such as dextran in the cell wall of gram positive organisms and valvular endothelium [<xref ref-type="bibr" rid="scirp.82895-ref19">19</xref>] , intrinsic binding affinity to fibronectin [<xref ref-type="bibr" rid="scirp.82895-ref20">20</xref>] and glucosyl transferases which may act as “modulins” to express various cytokines (interleukin-6) or adhesions that in turn further recruit leukocytes into the vegetation [<xref ref-type="bibr" rid="scirp.82895-ref21">21</xref>] . The other factors which mediate adherence include fibrinogen, laminin, type 4 collagen which are the components found in the damaged endothelium or platelet-fibrin aggregate. Following colonization of platelet-fibrin aggregate [<xref ref-type="bibr" rid="scirp.82895-ref22">22</xref>] , microbial growth results in the secondary accumulation of platelets and fibrin to form a vegetation. It consists of bacteria encashed in a meshwork of platelets and fibrin, serves as a barrier to host defences and it is not vascularized.</p><p>The propensity for vegetation to form at specific sites may also relate to a decrease in lateral pressure downstream from the regurgitant flow, which causes a decrease in the perfusion of intimal lining at these sites [<xref ref-type="bibr" rid="scirp.82895-ref23">23</xref>] . Tricuspid vegetations are large due to the low pressure in right heart chambers, allowing them to grow and may be in excess of 2 cm [<xref ref-type="bibr" rid="scirp.82895-ref24">24</xref>] . Vegetation often prevent proper valvular leaflet or cusp coaptation, thereby causing valvular incompetence resulting in congestive heart failure [<xref ref-type="bibr" rid="scirp.82895-ref25">25</xref>] or leaflet perforation secondary to vegetation growth [<xref ref-type="bibr" rid="scirp.82895-ref26">26</xref>] with recruitment of matrix metalloproteinases (MMPs) and eventually destroy the collagen. Pneumonia or septic pulmonary embolism resulting from dislodgement of vegetative material is common. Recurrent pulmonary events, anemia and microscopic hematuria, the so called “tricuspid syndrome” is a feature of right-sided tricuspid valve endocarditis [<xref ref-type="bibr" rid="scirp.82895-ref27">27</xref>] .</p><p>Tricuspid valve endocarditis may occur in community-acquired or hospital-acquired infection and the organisms responsible for both are shown in <xref ref-type="table" rid="table1">Table 1</xref>.</p><p>Cardiac myxomas are seen initially with protean manifestations that mimic many disease processes. About 5% of myxomas are found in the ventricles, usually solitary and attached to the interventricular serptum by a pedicle [<xref ref-type="bibr" rid="scirp.82895-ref28">28</xref>] . Small myxomas are silent and manifest if they become infected or embolize. The systemic manifestations consists of fever, weight loss, malaise, with leukocytosis, thrombocytopenia, elevated ESR (erythrocyte sedimentation rate), increase in gamma globulins, polycythemia and Raynaud’s phenomenon [<xref ref-type="bibr" rid="scirp.82895-ref29">29</xref>] may occur in 90% of myxomas.</p></sec><sec id="s3_3"><title>3.3. Echocardiographic Features</title><p>The most common and direct evidence of infective endocarditis is the vegetation and it must be at least 3 to 6 mm in size to be reliably seen. Transthoracic echocardiography (TTE) can, at best, detect vegetation to a minimum size of 2 mm and it is usually the more sensitive technique, with sensitivities in children up to 80% [<xref ref-type="bibr" rid="scirp.82895-ref30">30</xref>] . The characteristic echo appearance of a vegetation is of an echogenic mass, irregular in shape, attached to the “upstream” side of a valve leaflet, i.e., atrial side of atrioventricular valves, most commonly at the coaptation line and prolapsed through the tricuspid valve as shown in <xref ref-type="fig" rid="fig3">Figure 3</xref> and <xref ref-type="fig" rid="fig4">Figure 4</xref>. The</p><table-wrap id="table1" ><label><xref ref-type="table" rid="table1">Table 1</xref></label><caption><title> Showing the organisms responsible for infective endocarditis. MRSA―methicillin resistant staphylococcus aureus</title></caption><table><tbody><thead><tr><th align="center" valign="middle" >Organism</th><th align="center" valign="middle" >Community acquired endocarditis (IV drug users)</th><th align="center" valign="middle" >Hospital acquired endocarditis (intravascular devices)</th></tr></thead><tr><td align="center" valign="middle" >Staphylococcus aureus α-hemolytic streptococci (viridans) Enterococcus Culture negative Fungi Staphylococcus epidermidis (coagulase negative) Others (Escherichia coli, Klebsiella, Corynebacterium)</td><td align="center" valign="middle" >30% - 50% (MRSA-minority) 10% - 35% 5% - 10% 5% - 30% &lt;5% &lt;5% &lt;5%</td><td align="center" valign="middle" >60% - 80% (MRSA-majority) &lt;5% 5% 5% 10% &lt;5% 5% - 10%</td></tr></tbody></table></table-wrap><p>vegetation vary in size, sometimes reaching 2 - 3 cm in diameter and can be so big that they are mistaken for a cardiac tumor as shown in Figures 5-9 .</p><p>The gold standard for diagnosis of infective endocarditis is the modified Duke criteria [<xref ref-type="bibr" rid="scirp.82895-ref31">31</xref>] and it emphasized the essential relationship between clinical and echocardiographic findings. Duke’s criteria have been predominantly applied for left-sided endocarditis and have not been studied specifically in tricuspid valve endocarditis [<xref ref-type="bibr" rid="scirp.82895-ref32">32</xref>] and it may be difficult to determine [<xref ref-type="bibr" rid="scirp.82895-ref33">33</xref>] in its diagnosis.</p><p>Echocardiography remains the most safe and simple noninvasive method to diagnose the presence of an intracavitary myxoma [<xref ref-type="bibr" rid="scirp.82895-ref34">34</xref>] . Myxomas are typically nonhomogeneos in texture with lucent centers or areas of calcification. They may be smooth surfaced but are more often irregularly shaped with filamentous fronds or have the appearance of “cluster of grapes” as shown in <xref ref-type="fig" rid="fig1">Figure 1</xref>3 and <xref ref-type="fig" rid="fig1">Figure 1</xref>4. They are either sessile or pedunculated with a distinct stalk (pedicle), variably friable and originates from subendocardial nests of primitive mesenchymal cells. The tumor arising from the ventricular cavity was attached by a stalk to the interventricular septum as shown in Figures 10-14.</p><p>Vegetation can occur on any surface [<xref ref-type="bibr" rid="scirp.82895-ref35">35</xref>] . Endocarditis usually begins as a mechanical traumatic event during the protrusion of myxoma through the tricuspid valve and the vegetations are attached to its surface as shown in Figures 10-12. The tumor mass is seen to oscillate into the right atrium through the tricuspid valve and producing regurgitation as shown in <xref ref-type="fig" rid="fig1">Figure 1</xref>5 and <xref ref-type="fig" rid="fig1">Figure 1</xref>6 and the oscillations visible as “tiger-stripe” appearance in the Spectral Doppler imaging as shown in <xref ref-type="fig" rid="fig1">Figure 1</xref>7.</p></sec><sec id="s3_4"><title>3.4. Management</title><sec id="s3_4_1"><title>3.4.1. Medical Therapy</title><p>Fever, multiple pulmonary emboli and sustained bacteremia by staphylococcus aureus are the signs of clinical alert for right-sided endocarditis [<xref ref-type="bibr" rid="scirp.82895-ref36">36</xref>] . After the diagnosis of tricuspid valve endocarditis, medical treatment with antibiotics is indicated and should be continued for 4 to 6 weeks until the signs of infection disappear. Prolonged therapy is necessary since very high densities of bacteria approaching 10<sup>9</sup> to 10<sup>10</sup> organisms per gram of tissue, become metabolically dormant and are difficult to eradicate since the organisms are relatively protected within the vegetation from phagocytic and other host defence mechanisms. Bactericidal antibiotics or antibiotic combination rather than bacteriostatic agents with high serum concentration may reach the central area of avascular vegetation by passive diffusion [<xref ref-type="bibr" rid="scirp.82895-ref37">37</xref>] . In small children, intravenous antibiotics with the use of heparin lock devices are preferred and home intravenous therapy is generally not recommended.</p><p>Uncomplicated tricuspid valve endocarditis is successfully treated medically in 80% of cases. Given the low likelihood of adherence to 4 - 6 week therapy, shorter courses of therapy with a combination of β-lactam with or without an aminoglycoside (for 2 weeks) have become an accepted standard in methicillin-sensitive staphylococcus aureus native valve endocarditis. Experience with 2 weeks regimen in children is limited, but it appears promising [<xref ref-type="bibr" rid="scirp.82895-ref38">38</xref>] . Short course therapy should not be used for patients infected with a relatively penicillin-resistant organism, nutritionally deficient streptococcus and a presence of vegetation visible by echocardiography.</p><p>Unless the clinical or epidemiologic clues suggest an etiological diagnosis, the recommended treatment for culture-negative native valve endocarditis is ampicillin plus gentamycin. Ceftriaxone can be used in this regimen instead of ampicillin. Isolated native non-rheumatic fungal tricuspid valve endocarditis with a large and more friable vegetation is the most severe form of endocarditis. Aspergillus species (mostly Aspergillus fumigatus) are the second most common fungi isolated from cardiac vegetation (25%), whilst Candida accounts for 53% and Histoplasma for 6% of cases of fungal endocarditis. Amphotericin B has been the ‘gold standard’ treatment for Aspergillus endocarditis, despite its known poor penetration into vegetation [<xref ref-type="bibr" rid="scirp.82895-ref39">39</xref>] . The role of new echinocandins such as caspofungin has been recently approved and a combination of voriconazole with caspofungin is an alternative approach with promising results in refractory Aspergillus infection [<xref ref-type="bibr" rid="scirp.82895-ref40">40</xref>] .</p></sec><sec id="s3_4_2"><title>3.4.2. Aspirin Therapy</title><p>Bacteria-platelet interaction appears to be important in both the induction of a vegetation and its enlargement after colonization. Acetylsalicylic acid (aspirin) was shown to have an effect on both platelets and organisms in a rabbit model of staphylococcus aureus endocarditis. Animals treated with aspirin had reduction in the weight of valvular vegetation, its growth, density of bacteria and a decrease in embolic events compared to controls [<xref ref-type="bibr" rid="scirp.82895-ref41">41</xref>] .</p></sec><sec id="s3_4_3"><title>3.4.3. Surgical Therapy</title><p>Although tricuspid valve endocarditis is successfully treated medically in about 75% of patients, conservative treatment is not always effective, and surgical treatment is required in approximately the remaining 25% [<xref ref-type="bibr" rid="scirp.82895-ref42">42</xref>] [<xref ref-type="bibr" rid="scirp.82895-ref43">43</xref>] . The indications of surgery in right-sided infective endocarditis are not well defined, but it should be considered in the following circumstances as shown in <xref ref-type="table" rid="table2">Table 2</xref> [<xref ref-type="bibr" rid="scirp.82895-ref44">44</xref>] .</p><p>Timing of surgery in right-sided infective endocarditis is less clear. The optimum timing for the surgery was also stated previously [<xref ref-type="bibr" rid="scirp.82895-ref45">45</xref>] . The ESC (European Society of Cardiology) guidelines classified surgical indications in infective endocarditis as emergent (within 24 hours), urgent (within a few days), and</p><table-wrap id="table2" ><label><xref ref-type="table" rid="table2">Table 2</xref></label><caption><title> Indications of surgery in right-sided infective endocarditis</title></caption><table><tbody><thead><tr><th align="center" valign="middle" >Indications of surgery in right-sided infective endocarditis</th></tr></thead><tr><td align="center" valign="middle" >TV (tricuspid valve) vegetation &gt; 20 mm and recurrent septic pulmonary embolism with or without concomitant right heart failure IE (infective endocarditis) caused by microorganisms that are difficult to eradicate (e.g. fungi) or bacteremia for at least 7 days (e.g. Staphylococcus aureus, Pseudomonas aeruginosa) despite adequate antimicrobial therapy Right heart failure secondary to severe tricuspid regurgitation with poor response to diuretic therapy.</td></tr></tbody></table></table-wrap><p>elective (after 1 to 2 weeks of antibiotic therapy). The AHA/ACC guidelines define early surgery as occurring during the initial hospitalization and before completion of a full therapeutic course of antibiotics. Early surgery of tricuspid valve infective endocarditis is considered if there is infected indwelling catheters or pacing leads and a dehiscence of prosthetic valve due to perivalvular infection (unstable prostheses) [<xref ref-type="bibr" rid="scirp.82895-ref46">46</xref>] . Vegetation size is a questionable indication for surgery and a study by Lutas, et al. [<xref ref-type="bibr" rid="scirp.82895-ref47">47</xref>] showed that the size of vegetation is not an indication for surgery by itself. According to the current guidelines, patients with large vegetation (&gt;15 mm) should be operated [<xref ref-type="bibr" rid="scirp.82895-ref48">48</xref>] [<xref ref-type="bibr" rid="scirp.82895-ref49">49</xref>] on urgently (within days) and those with fungal infection that are resistant to medical treatment should be operated during the hospitalization period.</p><p>Tricuspid valve infective endocarditis can be especially perilous because the proliferation of growth called vegetation, may cause the valve to regurgitate. After the infection causes structural damage to the valve, antibiotics alone cannot cure and require surgery to stem the “snowball effect” the leaking valve as in <xref ref-type="fig" rid="fig1">Figure 1</xref>8 [<xref ref-type="bibr" rid="scirp.82895-ref50">50</xref>] . The principles of surgery include radical debridement of vegetation/infected tissue and valve repair using a variety of techniques [<xref ref-type="bibr" rid="scirp.82895-ref51">51</xref>] [<xref ref-type="bibr" rid="scirp.82895-ref52">52</xref>] such as autologous pericardial patch augmentation of the destroyed leaflets, implantation of an annuloplasty ring and expanded polytetrafluoroethylene neochord whenever possible. If the damage is too severe, the valve should be excised and replaced with a bovine pericardial valve, a bioprothesis preferably since there is a high risk of thrombosis due to low velocity of blood flow in right-sided chambers. The complete excision of the tricuspid valve was first described by Arbulu, et al. [<xref ref-type="bibr" rid="scirp.82895-ref53">53</xref>] and valvectomy accounts for 7.2% of operations performed for tricuspid valve endocarditis in North America [<xref ref-type="bibr" rid="scirp.82895-ref54">54</xref>] . TV (tricuspid valve) excision should be limited to extreme cases only when the pulmonary artery pressure and vascular resistance are not elevated, and subsequent valve replacement should be considered once the infection is resolved. Fungal endocarditis remains a ‘stand-alone’ indication for surgical replacement of an infected valve. Tricuspid valve replacement resulted heart block in 16% of cases and epicardial lead placement should be considered since the placement of permanent endocardial leads across a bioprosthesis may cause regurgitation and reduces the prosthesis durability due to leaflet fibrosis and retraction.</p><p>Prompt surgical removal of the intracardiac tumor is mandatory as systemic emboli or valvular obstruction can occur unexpectedly. The first surgical excision of a myxoma was performed in 1954 [<xref ref-type="bibr" rid="scirp.82895-ref55">55</xref>] . The myxoma is removed en bloc with its attachment to the interventricular septum [<xref ref-type="bibr" rid="scirp.82895-ref56">56</xref>] and every effort should be made to avoid fragmentation and embolization. Laser photocoagulation of a 1-cm area around the stalk attachment site has also been suggested as a way of eradicating pretumorous cells [<xref ref-type="bibr" rid="scirp.82895-ref57">57</xref>] .</p></sec><sec id="s3_4_4"><title>3.4.4. Interventional Therapy</title><p>Surgical management of acute infective endocarditis is a major challenge. AngioVac [<xref ref-type="bibr" rid="scirp.82895-ref58">58</xref>] , a suction thrombectomy device approved for removal of undesirable intravascular material, such as clots, tumors, or any foreign material in the vascular system. It can be an option in the management of right-sided infective endocarditis in critically ill patients with high surgical risk. Debulking the infection site and achieving lower bacterial load can increase antibiotic efficacy. Percutaneous vegetation removal has been used as a bridge to surgery in acute tricuspid valve endocarditis [<xref ref-type="bibr" rid="scirp.82895-ref59">59</xref>] [<xref ref-type="bibr" rid="scirp.82895-ref60">60</xref>] .</p></sec></sec><sec id="s3_5"><title>3.5. Outcome</title><p>The long-term prognosis of patients with negative blood culture infective endocarditis has been found to be similar to that of patients with positive blood culture infective endocarditis across all age groups [<xref ref-type="bibr" rid="scirp.82895-ref61">61</xref>] . Tricuspid valve infective endocarditis has a benign prognosis and an in-hospital mortality of &lt;10%, long-term mortality of &lt;15% and the reported operative mortality ranges from 9 to 15% for isolated tricuspid valve endocarditis [<xref ref-type="bibr" rid="scirp.82895-ref62">62</xref>] . The presence of vegetation or vegetation size could be a predictor of outcome for a subgroup of patients who are at risk for the development of complications [<xref ref-type="bibr" rid="scirp.82895-ref63">63</xref>] [<xref ref-type="bibr" rid="scirp.82895-ref64">64</xref>] . In-hospital mortality was higher in those with vegetations larger than 10 mm and mortality rate increases even with smaller vegetations [<xref ref-type="bibr" rid="scirp.82895-ref65">65</xref>] . In some studies, the relationship between vegetation size and the likelihood of mortality as assessed as &gt;15 mm [<xref ref-type="bibr" rid="scirp.82895-ref66">66</xref>] and, &gt;20 mm and fungal etiology [<xref ref-type="bibr" rid="scirp.82895-ref67">67</xref>] are the predictors of increase in mortality rate. Right heart failure is also a predictor of poor outcome in right-sided endocarditis [<xref ref-type="bibr" rid="scirp.82895-ref68">68</xref>] [<xref ref-type="bibr" rid="scirp.82895-ref69">69</xref>] .</p><p>Numerous reports documented complete cure of myxoma with follow-up period of 10 to 15 years [<xref ref-type="bibr" rid="scirp.82895-ref70">70</xref>] [<xref ref-type="bibr" rid="scirp.82895-ref71">71</xref>] and the surgical results are excellent with resolution of associated symptoms [<xref ref-type="bibr" rid="scirp.82895-ref72">72</xref>] . In about 1 to 5% of cases, a recurrence or secondary cardiac myxoma has been reported after resection of the initial tumor [<xref ref-type="bibr" rid="scirp.82895-ref73">73</xref>] [<xref ref-type="bibr" rid="scirp.82895-ref74">74</xref>] .</p></sec><sec id="s3_6"><title>3.6. Case Analysis</title><p>A 3-year-old febrile male child despite antibiotic treatment for 2 weeks with an auscultatory findings of a right-sided regurgitant lesion as evidenced by grade 3/6 systolic murmur and a mass lesion as evidenced by tumor “plop” in lower left sternal border, suggesting a right-sided infective endocarditis of acute onset clinically. The non-drug users are generally present with symptoms of &gt;2 weeks duration [<xref ref-type="bibr" rid="scirp.82895-ref75">75</xref>] and if tricuspid valve is involved, heart murmurs are found with variable frequency in 35% to 72% of cases [<xref ref-type="bibr" rid="scirp.82895-ref76">76</xref>] . The source of infection is from in-situ intravenous canulas and the blood cultures were negative due to prior antibiotic therapy. Elevated total leukocyte count up to 42,700 cells/cubic mm of blood was due to leukemoid reaction as the result of infection. The mass lesion can be confused as valvular vegetation by echocardiography as shown in Figures 5-9. The vegetation is adherent to the mass , which is attached to the interventricular septum by a pedicle suggesting the RV (right ventricular) myxoma as in Figures 10-14 and it is masquerading as tricuspid valve vegetation in Figures 5-9. The infective process and trauma due to mass lesion results in significant valve damage and producing moderate to severe tricuspid regurgitation as shown in Figures 15-17.</p><p>Right-sided endocarditis, often allows time for medical treatment to take effect because the regurgitant lesion is well tolerated. Hence, it is recommended to treat medically with antibiotics initially before sending the patient for surgery. With effective treatment, regurgitant lesion decreased as in <xref ref-type="fig" rid="fig1">Figure 1</xref>8, the vegetation gradually shrink and disappeared as shown in <xref ref-type="fig" rid="fig1">Figure 1</xref>9 even though disappearance of a vegetation should raise a suspicion that the vegetation has broken free and embolized elsewhere, but there was no signs of septic pulmonary emboli since the X-ray chest PA view revealed normal as in <xref ref-type="fig" rid="fig2">Figure 2</xref>. Because there is a high risk of relapse after short-term antibiotic therapy, prolonged therapy is recommended for a minimum period of 4 weeks [<xref ref-type="bibr" rid="scirp.82895-ref77">77</xref>] with an advise of surgical removal of tumor in this child.</p></sec><sec id="s3_7"><title>3.7. Screening of Population</title><p>Calcification is present approximately in 10% to 20% of cardiac myxomas and right atrial myxomas appear to calcify more readily than left atrial myxoma [<xref ref-type="bibr" rid="scirp.82895-ref78">78</xref>] as shown in <xref ref-type="fig" rid="fig2">Figure 2</xref>0 and it is associated with rheumatic AV valve (mitral and tricuspid) regurgitation as in <xref ref-type="fig" rid="fig2">Figure 2</xref>1 in a 28-year-old female. A left atrial myxoma, attached to fossa ovalis, is associated with rheumatic AV valve stenosis (mitral and tricuspid) and tricuspid regurgitation as shown in Figures 22-25 (Note: Thrombus typically produces a “layered appearance” and is generally situated in the posterior portion of the atrium).</p><p>A vegetation on pulmonary valve in a 1-year-old febrile male with different shapes are shown in Figures 26-29.</p></sec></sec><sec id="s4"><title>4. Conclusion</title><p>Right-sided endocarditis is generally considered to have a better prognosis and the initial approach to the treatment is conservative with antibiotics according to</p><p>ESC (European Society of Cardiology) guidelines. The medical treatment yielded very good results in this case as the disappearance of vegetation mass as shown in <xref ref-type="fig" rid="fig1">Figure 1</xref>9. Even though optimum management of tricuspid valve infective</p><p>endocarditis has not yet been defined, it is a serious and potentially lethal condition in an infant or child [<xref ref-type="bibr" rid="scirp.82895-ref79">79</xref>] and so early surgical intervention to remove the</p><p>large obstructive vegetation is indicated. The surgical treatment can be performed with low risk and good early, mid and long-term results [<xref ref-type="bibr" rid="scirp.82895-ref80">80</xref>] .</p></sec><sec id="s5"><title>Cite this paper</title><p>Muthiah, R. 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