- Case report
- Open Access
Difficult diagnosis of atypical kawasaki disease in an infant younger than six months: a case report
Italian Journal of Pediatricsvolume 43, Article number: 30 (2017)
Kawasaki disease (KD) is an acute inflammatory vasculitis of unknown origin.
We report the case of a 5-month-old child with an atypical form of KD, characterized by undulating symptoms, who developed an aneurysm of the right coronary artery and an ectasia of the left anterior descending coronary artery.
This case report underlines the difficulties in recognizing incomplete forms of the illness in young infants, who are at higher risk of cardiac complications.
Kawasaki disease (KD) is an acute inflammatory vasculitis of small- and medium-sized arteries that can cause coronary artery weakening, aneurysm development and myocardial infarction. The disease usually occurs in infants and young children . Although one or multiple infectious triggers are most likely, the precise etiology is still unknown. Due to the absence of a specific diagnostic test or pathognomonic clinical feature, currently, the diagnosis of KD is still made on clinical criteria . Atypical or incomplete forms of KD are common (15–20% of all patients) especially in children younger than 6 months  or older than 5 years, with a higher incidence of coronary artery abnormalities [4, 5], long term consequences  and resistance to therapy . Therefore, a high index of suspicion is needed for any infant or child with protracted fever of unknown origin, in order to avoid a missed diagnosis. Here we report the case of a 5-month-old child with an atypical form of KD, characterized by undulating symptoms, who developed an aneurysm of the right coronary artery and an ectasia of the left anterior descending coronary artery.
A full term delivered, previously healthy, 5-month-old boy presented at our Emergency Room Department with fever for a total of 4 days, diarrhea, cough and irritability. He was being treated with oral amoxicillin + clavulanic acid prescribed by the pediatrician for a left medium otitis diagnosed two days before. Fleeting hives was reported.
On physical examination, he presented good general condition, body temperature was 37.5 °C, no signs of dehydration (capillary refill time <2 s) and a reduction in air penetration in the lower lobes on chest auscultation. Normal physical examination of heart and abdomen. Blood tests showed a very high value of C-Reactive Protein (C-RP: 49.32 mg/dL); hemoglobin (Hb) was 8.8 g/dL, white blood cell (WBC) count was 11,080/mm3 with 79.3% neutrophils, and platelet (PLT) count was 429,000/mm3. Transaminases were normal, while gamma glutamyl transferase (GGT) was high (126 UI/L). Chest radiograph showed peribronchial cuffing and we started an additional therapy with oral clarithromycin at a dose of 15 mg/kg. Resin blood culture and serology for Epstein Barr Virus, Mycoplasma pneumoniae, Chlamydia pneumoniae, type 1 and 2 Herpes simplex virus, Parvovirus B19, Coxsackie viruses and Toxoplasma Gondii ruled out infective origin of symptoms. All serological tests were negative except for IgG anti-Cytomegalovirus. Abdominal ultrasonography showed a focal bowel wall thickening, mild edema around the gallbladder, mild hepatosplenomegaly and a lymphadenomegaly near the hepatic hilum.
After 3 days from admission, the infant continued to have fever and presented erythema involving the palms and the soles. Suspecting a KD for the presence of fever (>7 days), changes in extremities, history of rash and high C-RP levels, we requested a transthoracic echocardiography, which only showed a mild mitral valve regurgitation but no abnormalities of the coronary arteries.
On the fifth day of hospitalization the infant presented a subsidence of the fever and blood tests showed a reduction of C-RP (6.2 mg/dL), GGT (85 UI/mL) and Hb (7.3 g/dL), together with an increase in the WBC count (17,180/mm3) and platelet (594,000/mm3).
In order to rule out an early onset of inflammatory bowel disease, we performed fecal calprotectin and fecal occult blood, both tested negative, and a second abdominal ultrasonography, which showed an improvement of the picture (reduced bowel thickening and no edema around the gallbladder). Moreover, the infant had always fed willingly and his diarrhea had gradually resolved.
However, on the sixth day of hospitalization reappearance of the fever was registered (38.0 °C) and blood tests were performed on the eighth day showing an additional worsening of the anemia (Hb 7.2 g/dL), thrombocytosis (platelets 751,000/mm3), high WBCs (17,920/mm3) and an increase of C-RP (15.7 mg/dL). Serum iron, transferrin, lipid profile were within normal limits. We performed a second echocardiography, which revealed a fusiform aneurysm of the right coronary artery measuring 5.4 mm in diameter and an ectasia of the left anterior descending coronary artery, whose maximum diameter was 3.7 mm with a z-score +9.72 based on international standards  (Fig. 1). According to the American Heart Association (AHA) criteria the diagnosis of KD was made . He received intravenous immunoglobulin (IVIG: one bolus of 2 g/kg) and high-dose oral acetylsalicylic acid (ASA) (100 mg/kg/day). However, after two days of persistent fever, a second bolus of IVIG was administered.
On the eleventh day of hospitalization, a severe anemia occurred: red blood cells (RBC) 2,660,000/mm3, Hb 5.9 mg/dl, Ht 19.8%, MCV 78 fL, RDW 15.2%. Bone marrow examination showed mild eosinophilia (5%), and a RBC transfusion was necessary. We reduced ASA dose to 5 mg/kg/day to achieve an anti-aggregant effect for the presence of a severe thrombocytosis (PLT 1,147,000/mm3).
Forty-eight hours after the second dose of IVIG, due to persisting fever, we started intravenous methylprednisolone at a dose of 30 mg/kg/day for three subsequent days, with initial benefit. However, after three days from the last administration of corticosteroid therapy we recorded a reappearance of the fever (38.0 °C) together, with a further dilatation of the left anterior descending coronary artery and we started oral prednisolone at a dose of 2 mg/kg/day for 30 days. Fever disappeared after 48 h.
The patient was discharged after 26 days of hospitalization, afebrile, with oral ASA. He is being regularly monitored to check the size of the coronary arteries. The last echocardiography performed 18 months after the KD onset showed a mild reduction of the aneurysm of the right coronary artery (3.6 mm) and of the ectasia of the left anterior descending coronary artery (2.5 mm, z-score +2.46). He is still on therapy with oral ASA.
KD is an autoimmune vasculitis of unknown etiology that occurs predominantly in infants and young children, with an age distribution ranging from 3 months to 10 years .
The classic diagnosis of KD is based on clinical evidence of prolonged fever (≥5 days) associated to the presence of at least four out of five principal clinical features (change in extremities, polymorphous exanthema, bilateral bulbar conjunctival injection without exudate, changes in lips and oral cavity, cervical lymphadenopathy) . Typically, all of the clinical features are not present at a single point in time, as was the case with our young patient, in which the exanthema was present within the first two days of the onset of the fever.
Coronary artery aneurysms or ectasia develop in 15 to 25% of untreated children with the disease and may lead to myocardial infarction, sudden death, or ischemic heart disease .
In our case KD diagnosis was extremely difficult because the child presented an atypical manifestation of the disease. Albeit KD was considered one of the possible diagnosis we have been initially misled by the first echocardiography that showed no coronary artery alterations together with the disappearance of the fever for 36 h. We didn’t start the IVIG immediately because the patient presented only two out of five typical clinical features besides prolonged fever. According to the AHA guidelines (2) in this case, KD diagnosis can be made only if coronary abnormalities are present.
Our patient, after an initial defervescence, developed coronary artery aneurysm (currently still present), which was evident at the second echocardiography performed after 10 days from the onset of the fever, and showed an IVIG resistant disease.
This case report underlines the usefulness of guidelines in preventing overdiagnosis of KD, but also the difficulties in recognizing incomplete forms of the illness when following them, especially in very young infants, of less than six month of age, who are at higher risk of cardiac complications. Moreover, our case emphasizes the usefulness of ancillary laboratory findings (high C-RP, GGT and WBC, thrombocytosis, anemia) for suspected KD and, as reported in literature, high C-RP end GGT levels at presentation are significant predictors for IVIG resistant disease [7, 8].
In conclusion, our case report suggests that KD should always considered in the diagnostic flow-chart of protracted fever of unknown origin, especially in very young children. Moreover, due to the fact that in children with incomplete KD, early echocardiography could be negative for specific signs of coronary disease, it is mandatory to perform frequently repeated exams during the hospitalization, in order to detect the most feared complication of the disease.
American heart association
Gamma glutamyl transferase
White blood cell
Zhu H, Yu SF, Bai YX, Liang YY, Su XW, Pan JY. Kawasaki disease in children: Epidemiology, clinical symptoms and diagnostics of 231 cases in 10 years. Exp Ther Med. 2015;10:357.
Newburger JW, Takahashi M, Gerber MA, Gewitz MH, Tani LY, Burns JC, et al. Diagnosis, treatment, and long-term management of Kawasaki disease: a statement for health professionals from the Committee on Rheumatic Fever, Endocarditis and Kawasaki Disease, Council on Cardiovascular Disease in the Young, American Heart Association. Circulation. 2004;110:2747.
Singh S, Agarwal S, Bhattad S, Gupta A, Suri D, Rawat A, et al. Kawasaki disease in infants below 6 months: a clinical conundrum? Int J Rheum Dis. 2016;19:924–8.
Genizi J, Miron D, Spiegel R, Fink D, Horowitz Y. Kawasaki disease in very young infants: high prevalence of atypical presentation and coronary arteritis. Clin Pediatr (Phila). 2003;42:263.
McCrindle BW, Li JS, Minich LL, Colan SD, Atz AM, Takahashi M, Pediatric Heart Network Investigators, et al. Coronary artery involvement in children with Kawasaki disease: risk factors from analysis of serial normalized measurements. Circulation. 2007;116:174.
Kato H, Sugimura T, Akagi T, Sato N, Hashino K, Maeno Y, et al. Long-term consequences of Kawasaki disease. A 10- to 21-year follow-up study of 594 patients. Circulation. 1996;94:1379.
Tremoulet AH, Best BM, Song S, Wang S, Corinaldesi E, Eichenfield JR, et al. Resistance to intravenous immunoglobulin in children with Kawasaki disease. J Pediatr. 2008;153:117.
Eladawy M, Dominguez SR, Anderson MS, Glodé MP. Abnormal liver panel in acute kawasaki disease. Pediatr Infect Dis J. 2011;30:141–4.
None to declare.
Availability of data and materials
LP and NR wrote the manuscript as first draft. PV, CM and FM revised the work critically for important content, AF, GC, AN acquired the data. FS, LLR, PP handled clinical managment. All authors read and approved the final manuscript.
The authors declare that they have no competing interests.
Consent for publication
The patient’s parents had given their consent for the Case Reports to be published.
Ethics approval and consent to participate
The paper has been approved by local Committee.