Back to Search
Start Over
Bilateral facial nerve palsy complicating Kawasaki disease: A case report and literature review.
- Source :
-
Medicine [Medicine (Baltimore)] 2024 Aug 16; Vol. 103 (33), pp. e39389. - Publication Year :
- 2024
-
Abstract
- Rationale: Kawasaki disease (KD) manifests as an acute, self-limited vasculitis disease that constitutes the primary cause of acquired heart disease in children under 5 years of age. Facial nerve palsy (FNP) is a rare complication associated with coronary artery lesions (CALs) in patients with KD. Patients with KD and FNP usually present atypically, leading to a delayed diagnosis and treatment of KD.<br />Patient Concerns: A 4-month-old boy with fever, left FNP and bilateral conjunctival injection with spontaneous resolution, was admitted to the hospital, received a short course of intravenous dexamethasone, and experienced rapid FNP recovery on the first admission. The patient experienced a resurgence of fever, bilateral conjunctival injection, and right FNP, which led to readmission. Physical examination revealed redness at the site of Bacillus Calmette-Guérin inoculation, reddening of lips, and desquamation of the distal extremities. Echocardiography revealed right-sided CALs.<br />Diagnoses: The patient initially missed KD on the first admission, and was later diagnosed with complete KD with FNP on the second admission.<br />Interventions and Outcomes: After a short course of intravenous dexamethasone, the left FNP resolved quickly. However, right FNP recurred after corticosteroids withdrawal. Meanwhile, more typical symptoms were observed, and KD was diagnosed. Treatment ensued with intravenous immunoglobulin (IVIG), aspirin, and dexamethasone. The patient achieved rapid remission, without recurrence. Echocardiography continued to show normal findings during 1-year follow-up after discharge.<br />Lessons: The clinical symptoms of FNP complicating KD in children are atypical and can easily lead to delayed diagnosis and treatment. FNP in patients with KD may serve as a risk factor for CALs, which are more challenging to resolve than the FNP itself. Adding corticosteroids to IVIG may be recommended to reduce IVIG resistance, decrease the risk of developing CALs, and alleviate CALs.<br />Competing Interests: The authors have no funding and conflicts of interest to disclose.<br /> (Copyright © 2024 the Author(s). Published by Wolters Kluwer Health, Inc.)
- Subjects :
- Humans
Male
Infant
Dexamethasone therapeutic use
Dexamethasone administration & dosage
Glucocorticoids therapeutic use
Glucocorticoids administration & dosage
Immunoglobulins, Intravenous therapeutic use
Immunoglobulins, Intravenous administration & dosage
Mucocutaneous Lymph Node Syndrome complications
Mucocutaneous Lymph Node Syndrome diagnosis
Facial Paralysis etiology
Subjects
Details
- Language :
- English
- ISSN :
- 1536-5964
- Volume :
- 103
- Issue :
- 33
- Database :
- MEDLINE
- Journal :
- Medicine
- Publication Type :
- Academic Journal
- Accession number :
- 39151496
- Full Text :
- https://doi.org/10.1097/MD.0000000000039389