소아에서 스테로이드 반응성 신증후군의 관해기에 발병한 Kimura 병의 1례
A Case of Kimura's Disease Occurring During Remission of Steroid-responsive Nephrotic Syndrome
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참고문헌
초록
저자들은 스테로이드 반응성 재발성 신증후군의 과거력이 있는 환아에서 관해기에 발병한 Kimura 병을 종괴의 전절제 후 스테로이드 및 cyclosporin 투여로 치료한 증례를 경험하고 이를 보고하는 바이다.
Abstract
Kimura's disease is a rare chronic inflammatory disease of unknown etiology which appears primarily in young Asian males as non-tender subcutaneous swellings in the head and neck region. Histologic characteristics are the presence of lymphoid follicles, vascular proliferation and infiltration of eosinophils. Peripheral eosinophilia and elevated serum IgE are frequently combined. Systemic steroid therapy with surgical excision is the mainstay of treatment, though recurrence after surgery or discontinued steroid treatment is common. It has been known that about 16% of the cases are associated with renal diseases, particularly nephrotic syndrome. We present an 8-year-old boy with a past history of steroid-responsive, infrequently relapsing nephrotic syndrome who developed right buccal swelling and peripheral eosinophilia during the remission state. He has been managed with surgical resection, steroid and cyclosporine due to multiple recurrences.
참고문헌 (25)
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