The Gianotti-Crosti Syndrome

Author:

Rubenstein Denise1,Esterly Nancy B.1,Fretzin David1

Affiliation:

1. Division of Dermatology, Department of Medicine, Pritzker School of Medicine, University of Chicago, and the Divisions of Dermatology, Departments of Pediatrics and Medicine, Michael Reese Hospital and Medical Center, Chicago

Abstract

The Gianotti-Crosti syndrome is an infrequently recognized disorder with distinctive characteristics. The eruption, which lasts for two to eight weeks, consists of large, flat-topped, nonpruritic papules on the face, buttocks, and limbs. Its onset may be preceded by fever and upper respiratory tract symptoms. Associated findings include generalized lymphadenopathy, anicteric hepatitis, and HBs antigenemia. Two children with the syndrome are described to bring this entity to the attention of pediatricians.

Publisher

American Academy of Pediatrics (AAP)

Subject

Pediatrics, Perinatology, and Child Health

Cited by 27 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献

1. Gianotti-Crosti Syndrome: A Benign Dermatosis;Cureus;2023-06-12

2. Gianotti–Crosti Syndrome;Harper's Textbook of Pediatric Dermatology;2019-11-20

3. Febrile Illness with Skin Rashes;Infection & Chemotherapy;2015

4. The epidemiology, etiology and Chuh and Zawar’s diagnostic criteria of Gianotti–Crosti syndrome;Expert Review of Dermatology;2013-02

5. Gianotti-Crosti Syndrome;Harper's Textbook of Pediatric Dermatology;2011-05-24

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