A 9-year-old girl with Kawasaki disease and pulmonary nodules
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CLINICAL IMAGE
A 9-year-old girl with Kawasaki disease and pulmonary nodules Yousuke Higuchi 1
&
Motoharu Ochi 1 & Junya Shimizu 1 & Mahoko Furujo 1
Received: 11 May 2020 / Revised: 1 June 2020 / Accepted: 2 June 2020 # International League of Associations for Rheumatology (ILAR) 2020
Presentation A 9-year-old girl was referred for low-grade fever, posterior cervical pain, maculopapular rash, erythema of pharyngeal mucosa, and bilateral conjunctival injection on 28 January 2020. The remaining examination was unremarkable, including auscultation, meningeal irritation signs, cervical lymphadenopathy, and extremity changes. She and her family had no travel history. Laboratory data showed slightly elevated white blood cell (WBC) count 9.7 × 109/L and C-reactive protein (CRP) levels 3.3 mg/ L. She scheduled a follow-up visit for 3 days’ time but returned later that evening complaining of chest pain. A chest radiograph showed no apparent findings, and she went home. The next day, she revisited our hospital due to a high-grade fever, neck pain, and cough. Rapid antigen tests for group A streptococcus, adenovirus, and influenza A/B were negative. Repeated blood tests showed elevated WBC count 13.4 × 10 9 /L and CRP levels 82.0 mg/L; therefore, she was admitted for further examination. Contrast-enhanced computed tomography (CT) on the second hospital day revealed no abnormalities in the neck region, but pulmonary nodules, pleural and pericardial effusion, and gallbladder hydrops were identified (Fig. 1a). Serum antibodies against Epstein-Bar virus, cytomegalovirus, and parvovirus B19 showed uninfected pattern. Blood culture and cryptococcal half quantity test
* Yousuke Higuchi [email protected] 1
Department of Pediatrics, National Hospital Organization Okayama Medical Center, 1711-1, Tamasu, Kita-ku, Okayama, Okayama 701-1192, Japan
were negative. Therefore, she was diagnosed with an incomplete Kawasaki disease (KD). We administrated intravenous immunoglobulin single-dose 2 g/kg and aspirin 50 mg/kg/day and her symptoms and laboratory results rapidly improved. Her pericardial effusion gradually decreased, with no coronary artery abnormalities detected. On the thirteenth hospital day, follow-up CT resolved the findings (Fig. 1b), and serum mycoplasma pneumoniae particle agglutination antibody titer was not elevated.
Discussion Pulmonary nodules are described as sub-symptom in the American Heart Association scientific statement on KD, as well as pericarditis and gallbladder hydrops [1]. There have only been seven reported cases of infants affected by pulmonary nodules associated with KD, all of which also presented with coronary artery involvement [2–5]. Histological study of the nodules showed inflammatorycell infiltration as is seen in coronary artery aneurysms in patients with KD [2]. Rapid involution of pulmonary nodules via standard KD treatment may reflect the inflammatory nature of the lesions. We believe that the involvement of severe acute respiratory syndrome coronavirus 2 was quite low because she was
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