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患有联合免疫缺陷的儿童的皮肤肉芽肿

Cutaneous granulomas in children with combined immunodeficiency.

作者信息

Siegfried E C, Prose N S, Friedman N J, Paller A S

机构信息

Department of Dermatology, University of Iowa School of Medicine, Iowa City.

出版信息

J Am Acad Dermatol. 1991 Nov;25(5 Pt 1):761-6. doi: 10.1016/s0190-9622(08)80965-6.

Abstract

Noninfectious cutaneous granulomas, particularly in an acral distribution, may be an early sign of mixed cellular and humoral immunodeficiency. Special stains of skin biopsy sections and cultures for bacteria, acid-fast bacilli, and fungi are important in eliminating the possibility of underlying pathogens. In three children with combined immunodeficiency and cutaneous granulomas, the administration of moderate- to high-dose systemic corticosteroids was the most effective therapy. However, careful consideration should be given before administering systemic corticosteroids to an immunocompromised patient.

摘要

非感染性皮肤肉芽肿,尤其是发生于肢体末端的,可能是细胞免疫和体液免疫混合缺陷的早期迹象。对皮肤活检切片进行特殊染色以及对细菌、抗酸杆菌和真菌进行培养,对于排除潜在病原体的可能性很重要。在三名患有联合免疫缺陷和皮肤肉芽肿的儿童中,给予中至大剂量全身性皮质类固醇是最有效的治疗方法。然而,在给免疫功能低下的患者使用全身性皮质类固醇之前应谨慎考虑。

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