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An Unusual Presentation of Kawasaki Disease: Gallbladder Hydrops and Acute Cholestatic Hepatitis.

1. Case

A 7-year-old boy presented due to ongoing fever and abdominal pain for 5 days. He had vomiting once and watery stool twice on the same day. On physical examination, he had fever of 39[degrees], restlessness, bilateral nonpurulent conjuctival hyperemia, redness of the lip and tongue, polymorphic rash in the face and trunk, and obvious abdominal tenderness in the right upper quadrant (Figure 1).

In laboratory examination, hemoglobin was 13 g/dl, leukocytewas 15700/[mm.sup.3], thrombocyte was 9300/[mm.sup.3], CRP was 171mg/dl (0-5mg/dl), erytrocyte sedimentation rate was 75 mm/h, aspartate aminotransferase was 109 U/L (15-50 U/L), alanine aminotransferase was 202 U/L (10-50 U/L), total bilirubin was 3.49mg/dl (0.3-1.35 mg/dl), direct biluribine was 3.42mg/dl (0.05-0.5 mg/dl) and sodium was 126meq/l (130-150 meq/L). Adenovirus was negative in nasal swab and stool. Stool microscopy was normal. Serology tests were negative for hepatitis A, B, and C. Abdominal ultrasonography showed acute cholangitis/cholecystitis, thickening of the gallbladder wall, hydrops, and intrahepatic bile duct stasis.

Echocardiography (ECHO) showed minimal pericardial effusion, and mild mitral and tricuspid regurgitation in the left ventricle. Troponin I value (HST) was found to be 22.3 ng/L (normal value < 0.2).

The patient was considered to have incomplete Kawasaki disease, and he was given a single dose of immunuglobulin (IVIG) with a 12-hour intravenous infusion of 2 g/kg and acethylsalicylic acid (ASA) of 50 mg/kg/day divided into 4 doses.

Cultures were taken, and treatment with ceftriaxone 80 mg/kg for enteric fever and cholecystitis was initiated. The next day, antibiotic was stopped because of negative results of microbial cultures. Forty-eight hours after the patient's fever returned to normal, aspirin was reduced to only one dose of 3-5 mg/kg.

The patient's platelet count increased to 676,000/[mm.sup.3] in the second week. Coronary artery involvement was not observed in the first echocardiography. Troponin I level also fell below 1.5 ng/L. In the third week, sedimentation and CRP values returned to normal and ASA treatment was terminated.

2. Discussion

In addition to fever as a classical symptom of Kawasaki disease, our patient had nonpurulent conjunctivitis, redness of lip and tongue, and polymorph rash, with no coronary artery involvement at the ECHO. Febrile cholestatic hepatitis with gallblader hydrops was thought to be the symptoms for atypical Kawasaki disease. Diarrhea, vomiting, abdominal pain, hepatic dysfunction, and bile duct hydrops had been reported at different rates among nonspecific symptoms even though they are not the part of the diagnostic criteria [1].

In a case-control study, approximately 30% of the 280 patients had moderate transaminase elevation and occasionally obstructive jaundice since gallblader hydrops was observed [2]. In a cohort study from Italy with 219 kawasaki disease cases, incomplete Kawasaki presentation was seen in 9 of 10 children with severe abdominal discomfort, and it was shown that the gastrointestinal system symptoms were not recognized early in Kawasaki disease [3]. However, acute cholestasis and gallblader hydrops were also reported as atypical baseline findings [4].

In another study, Kawasaki disease was detected in 6% of the patients with fever and abdominal pain [5].

In a Kawasaki disease series with 35 cases, reported from Turkey, acute cholestasis was not reported as a baseline finding [6]. However, in another study of 23 patients, hydrops of gallblader was reported in 1 case and transaminase elevation in 7 cases [7]. Kaman et al. also reported 2 cases of atypical kawasaki disease with acute febrile jaundice [8].

Vasculitis-associated inflammation and obstruction in the liver and gallbladder are thought to be the cause of increased transaminase levels and cholestasis. It is also known that the sodium level below 135meq/l increases the risk for coronary artery disease, and the risk is higher in atypical cases than in classical cases. In addition to the atypical clinical presentation of our patient, hyponatremia and high transaminases increased the risk for complication developed that is why IVIG treatment was started on the sixth day of fever, and no complication was observed.

With this case report, we would like to remind that gallblader hydrops and cholestasis can be nonclassical early findings of Kawasaki disease, and if considered, early IVIG treatment can rapidly improve the clinical findings and prevent complications.

Conflicts of Interest

The authors declare that they have no conflicts of interest. References

[1] A. L. Baker, M. Lu, L. L. Minich et al., "Associated symptoms in the ten days before diagnosis of Kawasaki disease," Journal of Pediatrics, vol. 154, no. 4, pp. 592.e2-595.e2, 2009.

[2] J. C. Burns, W. H. Mason, M. P. Glode et al., "Clinical and epidemiologic characteristics of patients referred for evaluation of possible Kawasaki disease," Journal of Pediatrics, vol. 118, no. 5, pp. 680-686, 1991.

[3] F. Zulian, F. Falcini, L. Zancan et al., "Acute surgical abdomen as presenting manifestation of Kawasaki disease," Journal of Pediatrics, vol. 142, no. 6, pp. 731-735, 2003.

[4] P. Valentini, E. Ausili, A. Schiavino et al., "Acute cholestasis: atypical onset of Kawasaki disease," Digestive and Liver Disease, vol. 40, no. 7, pp. 582-584, 2008.

[5] M. Eladawy, S. R. Dominguez, M. S. Anderson, and M. P. Glode, "Kawasaki disease and the pediatric gastroenterologist: a diagnostic challenge," Journal of Pediatric Gastroenterology and Nutrition, vol. 56, no. 3, pp. 297-299, 2013.

[6] B. Aldemir-Kocabac, A. Karbuz, C. Karadeniz et al., "Another face of Kawasaki disease," Turkish Journal of Pediatrics, vol. 56, no. 4, pp. 392-398, 2014.

[7] H. Ozdemir, E. Ciftci, A. Tapisiz et al., "Clinical and epidemiological characteristics of children with Kawasaki disease in Turkey," Journal of Tropical Pediatrics, vol. 56, no. 4, pp. 260-262, 2010.

[8] A. Kaman, T. Aydin-Teke, Z. G. Gayretli-Aydin et al., "Two cases of Kawasaki disease presented with acute febrile jaundice," Turkish Journal of Pediatrics, vol. 59, no. 1, pp. 84-86, 2017.

B. O. Kilic, S Baysun, T. C. Goksen, I. Akinbingol, and Z. Arslan

Departments of Pediatrics, Faculty of Medicine, TOBB University of Economics and Technology, Ankara, Turkey

Correspondence should be addressed to B. O. Kilic;

Received 24 March 2018; Accepted 12 April 2018; Published 3 July 2018

Academic Editor: William B. Silverman

Caption: Figure 1: Nonpurulent conjunctivitis, malar rash, and mucosal changes on the lip and on the tongue.
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Title Annotation:Case Report
Author:Kilic, B.O.; Baysun, S.; Goksen, T.C.; Akinbingol, I.; Arslan, Z.
Publication:Case Reports in Medicine
Date:Jan 1, 2018
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