CITATION: Waggie, Z., Van der Merwe, P.-L. & Kalis, N. N. 1999. Kawasaki disease masquerading as anomalous origin of left coronary artery from the pulmonary artery. South African Medical Journal, Supplement 3 June.The original publication is available at http://www.samj.org.zaAlthough myocardial ischaemia/infarction is rare in childhood, it is a well-described complication of both Kawasaki disease (KD) and anomalous origin of the left coronary artery from the pulmonary artery (AOLCA). We describe a case of Kawasaki disease appearing as an AOLCA in a 2-year-old boy with myocardial infarction.Publisher’s versio

Kalis, N. N.

Van der Merwe, P.-L.

Waggie, Z.

Stellenbosch University SUNScholar Repository

• • • • • • CARDIOVASCULAR JOURNAL OF SOUTH AFRICA (SAMJ Supplement 3 June 1999) C157 Case Report Kawasaki disease masquerading as anomalous origin of left coronary artery from the pulmonary artery Z. WAGGlE, P.-L. VAN DER MERWE, N. N. KALIS Summary Although myocardial ischaemia/infarction is rare in childhood, it is a wen-described complication of both Kawasaki disease (KD) and anomalous origin of the left coronary artery from the pulmonary artery (AOLCA). We describe a case of Kawasaki disease appearing as an AOLCA in a 2-year-old boy with myocardial infarction. S Afr Med J 1999; 89: Cardiovascular suppl3, CI57·CI60. Acute myocardial infarction (MI) in children is well described, albeit rare in practice.3•9 Both Kawasaki disease (KD) and anomalous origin of the left coronary artery from the pulmonary artery (AOLCA) can result in MI. The clini-cal features of KD complicated by coronary thrombosis and myocardial ischaemia/infarction and those of AOLCA are similar. Case report A 2-year-old boy Of mixed racial origin was admitted to hospital with a I-day history of cough, shortness of breath, Department of Paediatrics and Child Health, University of Stellenbosch and Tygerberg Hospital, Tygerberg, W. Cape Z. WAGGlE, M.B. Ch.B. P.-L. VAN DER MERWE, M.B. Ch.B., M.Med. (Paed.), F.C.P. (SA), M.D. . N .. N. KALIS, M.B. Ch.B., M.Med. (Paed.), F.C.P. (SA) vomiting and loss of appetite. There was no previous history of fever, rash, red eyes, or mucosal lesions. The only medi-cal history of note was that he had been on tuberculosis pro-phylaxis (under 2 years of age: rifampicin, isoniazid, pyrazi-namide) for the past 6 months due to an adult contact. No documentation of active tuberculosis was ever demon-strated. Clinical examination showed an acutely ill-looking, mis-erable boy. He had a temperature of 38°C (this was the only recorded fever during his entire hospital admission). Heart rate was 168/min, blood pressure 95/45 mmHg and respira-tory rate 72/min. He was pale and had good peripheral per-fusion. There was no lymphadenopathy, oedema, conjuncti-val congestion, skin rash or desquamation. The growth parameters were all on the,25th percentile. Cardiovascular examination revealed a jugular venous pressure (JVP) of 4 cm, the apex beat was in the 5th intercostal space lateral to the midclavicular line, and heart sounds were normal, with a gallop rhythm and a systolic murmur at the apex radiating to the axilla. There was intercostal recession with wheezing and crepitations heard in both lung fields. The liver was pal-pable 6 cm below the costal margin in the right midclavicu-lar line. The chest radiograph showed an enlarged heart with a cardiothoracic ratio of 0.58, with evidence of pulmonary oedema. ECG showed possible evidence of a MI (Fig. I). Echocardiography revealed left atrial and ventricular dilata-tion, a shortening fraction of 29% with an ejection fraction of 55%. The right coronary artery was not dilated and showed a normal colour Doppler flow pattern, but the origin of the left coronary artery was uncertain. Reproduced by Sabinet Gateway under licence granted by the Publisher (dated 2010)C158 CARDIOVASCULAR JOURNAL OF SOUTH AFRICA (SAMJ Supplement 3 June 1999) rlJ.,-~'~~,J i.,j l, h .1-.. I '" " .~ T I - 11'...--' ~-<~ ----' .~~~)\)\}I~ Fig. 1. Twelve-lead ECG. Leads 51, SIl, aVL and V3-V6 show picture of hyperacute Infarction (non-Q wave), while changes In leads V1 and V2 may be Indicative of a posterlor Infarction. The white cell count was 14.6 x 109/1 (with a nonnal dif-ferential count for age), the haemoglobin concentration 9.6 g/dl. and the platelet count 421 x I (J>I\. The clotting profile, including antithrombin m and protein C levels, were nor-mal. The erythrocyte sedimentation rate was 18 mmJIst h Fig. 2. First aortogram. Normal right coronary artery and the C-reacti ve protein was repeatedly negative. (RCA), with absence of left coronary artery. Antistreptolysin 0 hire and complement levels were normal. Collagen and metabolic screens were negative. Serial car-diac iso-enzymes are shown in Table L Day I 2 10 IB 23 30 37 42 59 74 85 173 TABLE I. SERIAL CARDIAC ENZYMES CK (UII) 73 47 94 !O3 107 84 6B 101 6B 78 105 MBfroclion AIT" (%) (UII) 128 96 54 242 57 20.9 52 57 51 51 44 41 ALT fUll) 64 29 19 21 20 WH (UlI) 509 388 285 358 353 305 334 334 229 333 CK = crealinine kinase; AST = aspartate transaminase; AL T = alan; ne rransaminase; LDH = lacLale dehydrogenase; MB " muscle brain. Blood, urine. and stool cultures were negative for bacte-ria and viruses and blood antibody tests were negative for any recent viral infection. A presumptive diagnosis of AOLCA from the pulmonary artery was made and radio-isotope scan (pyrophosphate and resting MIBI scanning) was requested as work-up to angio-graphy. This could not exclude an area of infarction in the antero-apical region. Aonic angiography showed only the right coronary artery arising from the aorta, but no fistulas or retrograde flow to the left coronary artery could be demonstrated (Fig. 2). Repeat angiography 3 weeks later showed no left coro-nary artery arising from the pulmonary artery, but both coronary arteries arising normally from the aorta and no evi-dence of aneurysmal dilatation (Fig. 3). Fig. 3. Repeat aortogram. Normal Origin and distribution of left and right coronary arteries (LCA and RCA). Clinical course Antifailure therapy in the fonn of digoxin and furosentide was commenced. The heart failure resolved speedily, but the ECG changes of infarction remained. The boy had intra-Venous gammaglobulin (lVIG) (2 gfkg) 7 days after admis-sion and aspirin anticoagulation was commenced. He cur~ rently remains asymptomatic on the antiplatelet and antifailure therapy. The ECG has normalised. but a repeat echocardiogram at 5 months after presentation shows a clear 5 mm aneurysmal dilatation of the proximal left coronary artery with no stenotic flow pattern (Fig. 4). Reproduced by Sabinet Gateway under licence granted by the Publisher (dated 2010)CARDIOVASCULAR JOURNAL OF SOUTH AFRICA (SAMJ Supplement 3 June 1999) C159 Fig. 4. Short-axis view of aorta (AO) and coronary arter-Ies showing 5 mm aneurysm at origin of left coronary artery (LCA) with normal size right coronary artery (RCA). Discussion Vasculitis syndromes are characterised by inflammation of the blood vessels. The clinical p1cture depends on the size and distriblllion of the vessels affected. When the coronary arteries are involved. coronary arteril is results. It may there-fore be a manifestation of several multisystem diseases.~ The necrotising va<;culitides may be divided into polyaneri-tis (including infantile polyarteritis nodosa (PAN) and Kawasaki disease), allergic vasculitis, giant cell arteritis, and vasculitis associated with collagen diseases. Each has clinical features that allows classification into subgroups. but the vasculitis present in one patient may have features of more than one subgroup, making exact classifIcation diffi-cult and at times somewhat arbitrary. KD or acute febrile mucocutaneous lymph node syn-drome was first described by Dr Tomisaku Kawasaki in 1967.' It has a worldwide distribution, with 20% of untreated cases developing coronary artery lesions.'"' The coronary arteritis can lead to aneurysm formation, myocar-dial thrombosis with infarction, and dysrhythmias: The aeti-ology and pathogenesis of this disease still remains an enigma. Pathologically) KD is an acute systemic inflammatory disease with systemic vasculitis' mainly affecting children under 5 years of age: There are as yet no diagnostic tests, the diagnosis being based on the presence of 5 out of 6 prin-cipal symptoms.7 Atypical or subclinical cases occur, which do not meet the diagnostic criteria. as coronary aneurysms have been found on echocardiography or at autopsy.' The incidence of this form of disease has been reported to be as high as 18.5% in patients with acquired coronary artery dis-ease." These cases have been shown to have a mild clinical course by Japanese researchers, with their American coun-terparts showing severe residual coronary artery lesions.' The association of KD and coronary aneurysms was fi~t described between 1974 and 1975. Coronary aneurysms are neither exclusive nor pathognomonic of KD, as they have also been described with atherosclerosis. congenital arterio-venous fistulas, PAN, trauma and infection.l Although exceptional, coronary aneurysms have also been described with Takayasu's arteritis in association with the aortitis.'o A giant thrombus of a coronary artery affected by aneri-tis will have the same clinical presentation a~ an AOLCA, namely clinical features of heart failure. systolic murmur, cardiomegaly on radiography, and ECG changes indicative of myocardial ischaemia/infarction. What confounded (he diagnosis in our patient was the absence of the principal fea-tures governing the diagnosis of KD; we therefore assume it to be a subclinical or atypical presentation. The second angiogram showing both coronary arteries arising from the aorta can only mean that a giant thrombus was occluding the left coronary artery completely. with ECG and angiographic features suggestive of AOLCA. A case of a giant coronary thromb us ina coronary a rtery co m p I icat i ng K D was described previously by Kadar el al.· In our patient the diagnosis of infantile PAN was consid-ered, but this distinction is now only of academic value. Landing and Larson' compared the clinical and pathological (both gross and microscopic) features of both the vascular lesions and their patterns of distribution, and they concluded that there was no evidence for a separation of infantile PAN from fatal cases of KD. Fatal cases of KD were first described as having the autopsy findings of infantile PAN.IO The clinical presentation of our patient, namely conges-tive hean failure, a systolic murmur, cardiomegaly and pul-monary oedema on chest radiography, and ECG changes of MI. is classically that of AOLCA.ul Although rare, with an incidence of 0.025 - 0.05% ,'1 the first paediatric case was described by Kossof in 1911." Aortic angiography is stili the described diagnostic lest for this enliey. 1.11 In our case the angiographic findings were misleading. although we should have looked for the presence of a left-to-right shunt initially, as this has important prognostic implications." The flow of blood from the AOLCA to the pulmonary artery is a prerequisite for surgery, if ligation is considered, in order to prevent fatal consequences. Although the clinical presentation of our patient was ryp-ically that of AOLCA, the clinical course, later demonstra-tion of both coronary arteries arising from the aorta and coronary aneurysm formation, is in favour of KD with a subclinical or atypical presentation. Conclusion We present a case of a 2-year-oJd boy presenting in cardiac failure with an ischaemic pattern on ECG, and showing only one coronary artery (the right) arising from the aona on ini-tial aortic angiography. the latter being the gold standard for diagnosing AOLCA. The ischaemic pattern on ECG remained for many months and follow-up echocardiogram showed an aneurysm on the left coronary artery. We there-fore assume his primary disease to be KD, presenting atypi-cally or subclinically. Careful evaluation of aortic angio-graphy and pulmonary artery injection is necessary to confirm the diagnosis of AOLCA. Reproduced by Sabinet Gateway under licence granted by the Publisher (dated 2010)C160 CARDIOVASCULAR JOURNAL OF SOUTH AFRICA (SAMJ Supplement 3 June 1999) References I. Askenazi J, Nadas AS. Anomalous left coronary artery originating from the pUlmonary artery. Report on 15 cases. Circulation 1975; 51: 976-987. 2. Bowyer S, Mason WH, McCurdy DK, Takahashi M. Polyarteritis nodasa (PAN) with coronary aneurysms: the Kawasaki-PAN contro-versy revisited.] Rheumatol1994; 21: 1585. 3. Ce1ermajer DS, Sholler GF, Howman-Giles R, Celermajer JM. Myocardial infarction in childhood: clinical analysis of 17 cases and medium term follow up of survivors. Br Heart] 1991; 65: 332-336. 4. Curtis N. Kawasaki disease: early recognition is vital to prevent cardiac complications. BM] 1997; 315: 322-323. 5. Fink CW. Polyarteritis and other diseases with necrotizing vasculitis in childhood. Arthritis Rheum 1977; 20: Suppl2, 378-384. 6. Kadar K, Piskothy A, Bendig L. Giant coronary thrombus as a compli-cation of Kawasaki disease. Orv-HetiI1993; 134: 2431-2433, 7. Kawasaki T. General review and problems in Kawasaki disease. ]pn Heart] 1995; 36: 1-12. 8. Landing BH, Larson EJ. Are infantile periarteritis nodosa with coronary artery involvement and fatal mucocutaneous lymph node syndrome the same? Comparison of 20 patients from North America with patients from Hawaii and Japan. Pediatrics 1977; 59: 651-662. 9. Pick RA, Glover MU, Viewed VW. Myocardial infarction in a young woman with isolated coronary arteritis. Chest 1982; 82: 378-380. 10. Rose AG, Sinclair-Smith CC. Takayasu's arteritis: A study of 16 autopsy cases. Arch Pathol Lab Med 1980; 104: 231-237. II. Rowley AH, Gonzalez-Crussi F, Gidding SS, Duffy CE, Shulman ST. Incomplete Kawasaki disease with coronary artery involvement. ] Pediatr 1987; 110: 409-413. 12. Wesselhoeft H, Fawcett JS. Johnson AL. Anomalous origin of left coronary artery from the pulmonary trunk: Its clinical spectrum, pathology, and pathophysiology, based on a review of 140 cases with seven further cases. Circulation 1968; 38: 403-425. • • • • • • Reproduced by Sabinet Gateway under licence granted by the Publisher (dated 2010)

Kawasaki disease masquerading as anomalous origin of left coronary artery from the pulmonary artery

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Kawasaki disease masquerading as anomalous origin of left coronary artery from the pulmonary artery

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