Background: Kimura’s disease (KD), also known as Eosinophilic Granuloma, is a benign, rare and chronic inflammatory disorder of unknown etiology and it affects subcutaneous tissues, lymph nodes, and salivary glands. Unusual presentations of KD might cause diagnostic difficulty or be misdiagnosed as malignancy if clinical suspicion is insufficiently high. Here, we aimed to explore the clinical characteristics, diagnosis and the therapeutic effect of children’s KD in China, in order to improve pediatricians’ knowledge of children’s KD. Methods: The Clinical data of 18 cases of KD diagnosed at Shenzhen Children's Hospital from January 2015 to January 2022 were analyzed retrospectively through case record review. Results: Of 18 cases, 17 were male and one is female. The masses appear as focal, painless, and immovable with an unclear boundary. The most common predilection is head-neck region (n=8, 44.4%). 12 patients showed cutaneous pruritus, 3 patients with nephrotic syndrome and 2 with simple hematuria. 16 patients showed peripheral blood eosinophilia. 12 of 13 patients presented with increased serum Immunoglobulin E (IgE) level. The prominent pathological characteristic is marked lymphoid hyperplasia accompanied by various degrees of vascular hyperplasia and eosinophil infiltration. Among the 18 patients followed for more than 6 months, 9 experienced recurrence of disease after treatment (surgical resection alone: 6/12; oral corticosteroids combined with immunosuppressants: 3/3; surgical resection followed by oral corticosteroids combined with immunosuppressants: 0/3). Through comparison with the clinical features of adult kimura disease, it showed that there was no significant difference between children and adults. Conclusion: KD is characterized by subcutaneous masses but it is also a systemic disease. The diagnosis should be confirmed by pathology. Surgical resection, radiotherapy, hormone or chemotherapy has definite therapeutic effects, but the rate of recurrence in children is high. Given the high rate of recurrence and reported association with lymphoma, patients require careful long-term follow-up.

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