Literature DB >> 25274975

Visual diagnosis: 12-month-old boy with persistent rash and lymphadenopathy.

William Sears1, Bethany Hodge1, Brooke Jones1, Matthew Thompson2, Navjyot Vidwan1.   

Abstract

Gianotti-Crosti syndrome (GCS) is a self-limiting, papular or papulovesicular, symmetric, acral exanthem that typically presents subsequent to viral infection, bacterial infection, or immunization in a child 1 to 4 years old. The rash can persist for 2 to 10 weeks. Recent infection with Epstein-Barr virus is the most common serologic finding in patients who have developed GCS. The diagnosis is often made after the child has been unsuccessfully treated for a more common cause of an acral rash (eg, scabies). There are no pathognomonic laboratory or histopathologic findings. GCS, therefore, is still a clinical diagnosis of exclusion. The rash is self-limited, and treatment is usually not necessary. However, topical corticosteroids are anecdotally reported to reduce duration of rash. Oral antihistamines can be used to treat pruritus. Parents should be assured that resolution is almost always complete, scarring seldom occurs, and recurrence is rare.

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Year:  2014        PMID: 25274975     DOI: 10.1542/pir.35-10-452

Source DB:  PubMed          Journal:  Pediatr Rev        ISSN: 0191-9601


  2 in total

Review 1.  Gianotti-Crosti syndrome (papular acrodermatitis of childhood) in the era of a viral recrudescence and vaccine opposition.

Authors:  Alexander K C Leung; Consolato Maria Sergi; Joseph M Lam; Kin Fon Leong
Journal:  World J Pediatr       Date:  2019-05-27       Impact factor: 9.186

2.  The Serum Immunoglobulin E Level: Is There a Relationship With the Clinical Course of the Gianotti-Crosti Syndrome?

Authors:  Andrea Bassi; Fausto Pedaci; Teresa Oranges; Chiara Azzari; Luisa Galli; Silvia Ricci; Cesare Filippeschi; Elisabetta Venturini
Journal:  Front Pediatr       Date:  2021-02-25       Impact factor: 3.418

  2 in total

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