Gianotti–Crosti syndrome

Gianotti–Crosti syndrome (/dʒəˈnɒti ˈkrɒsti/), also known as infantile papular acrodermatitis,[1] papular acrodermatitis of childhood,[1] and papulovesicular acrolocated syndrome,[2]: 389  is a reaction of the skin to a viral infection.[3] Hepatitis B virus[4] and Epstein–Barr virus are the most frequently reported pathogens. Other viruses implicated are hepatitis A virus, hepatitis C virus, cytomegalovirus,[5] coxsackievirus, adenovirus, enterovirus, rotavirus, rubella virus, HIV, and parainfluenza virus.[6]

Gianotti–Crosti syndrome
SpecialtyDermatology 

It is named for Ferdinando Gianotti and Agostino Crosti.[7][8]

Presentation

Gianotti–Crosti syndrome mainly affects infants and young children. Children as young as 1.5 months and up to 12 years of age are reported to be affected.[9] It is generally recognized as a papular or papulovesicular skin rash occurring mainly on the face and distal aspects of the four limbs. Purpura is generally not seen but may develop upon tourniquet test. However, extensive purpura without any hemorrhagic disorder has been reported.[9] The presence of less florid lesions on the trunk does not exclude the diagnosis. Lymphadenopathy and hepatomegaly are sometimes noted. Raised AST and ALT levels with no rise in conjugated and unconjugated bilirubin levels are sometimes detectable, although the absence of such does not exclude the diagnosis. Spontaneous disappearance of the rash usually occurs after 15 to 60 days.

Diagnosis

The diagnosis of Gianotti–Crosti syndrome is clinical. A validated diagnostic criterion[10][11][12] is as follows:

A patient is diagnosed as having Gianotti–Crosti syndrome if:

  1. On at least one occasion or clinical encounter, he/she exhibits all the positive clinical features,
  2. On all occasions or clinical encounters related to the rash, he/she does not exhibit any of the negative clinical features,
  3. None of the differential diagnoses is considered to be more likely than Gianotti–Crosti syndrome on clinical judgment, and
  4. If lesional biopsy is performed, the histopathological findings are consistent with Gianotti–Crosti syndrome.

The positive clinical features are:

  • Monomorphous, flat-topped, pink-brown papules or papulovesicles 1-10mm in diameter.
  • At least three of the following four sites involved – (1) cheeks, (2) buttocks, (3) extensor surfaces of forearms, and (4) extensor surfaces of legs.
  • Being symmetrical, and
  • Lasting for at least ten days.

The negative clinical features are:

  • Extensive truncal lesions, and
  • Scaly lesions.

Differential diagnosis

The differential diagnoses are: acrodermatitis enteropathica, erythema infectiosum, erythema multiforme, hand-foot-and-mouth disease, Henoch–Schönlein purpura, Kawasaki disease, lichen planus, papular urticaria, papular purpuric gloves and socks syndrome, and scabies.

Treatment

Gianotti-Crosti disease is a harmless and self-limiting condition, so no treatment may be required.[13] Treatment is mainly focused on controlling itching, symptomatic relief and to avoid any further complications. For symptomatic relief from itching, oral antihistamines or any soothing lotions like calamine lotion or zinc oxide may be used. If there are any associated conditions like streptococcal infections, antibiotics may be required.[10][11][12][13]

See also

References
  1. Rapini, Ronald P.; Bolognia, Jean L.; Jorizzo, Joseph L. (2007). Dermatology: 2-Volume Set. St. Louis: Mosby. p. 1228. ISBN 978-1-4160-2999-1.
  2. James, William D.; Berger, Timothy G.; et al. (2006). Andrews' Diseases of the Skin: clinical Dermatology. Saunders Elsevier. ISBN 0-7216-2921-0.
  3. "Gianotti-crosti syndrome, papulovesicular acrodermatitis. DermNet NZ".
  4. Michitaka K, Horiike N, Chen Y, et al. (August 2004). "Gianotti-Crosti syndrome caused by acute hepatitis B virus genotype D infection". Internal Medicine (Tokyo, Japan). 43 (8): 696–9. doi:10.2169/internalmedicine.43.696. PMID 15468968.
  5. Haki M, Tsuchida M, Kotsuji M, et al. (October 1997). "Gianotti-Crosti syndrome associated with cytomegalovirus antigenemia after bone marrow transplantation". Bone Marrow Transplantation. 20 (8): 691–3. doi:10.1038/sj.bmt.1700945. PMID 9383234.
  6. Chandrasekaran M, Mukherjee S (September 2007). "Gianotti Crosti syndrome". Indian Pediatrics. 44 (9): 695. PMID 17921560.
  7. synd/4051 at Who Named It?
  8. CROSTI A, GIANOTTI F (November 1957). "[Eruptive dermatosis of probable viral origin situated on the acra.]". Dermatologica (in French). 115 (5): 671–7. doi:10.1159/000256031. PMID 13500859.
  9. Sarma, N; Sarkar UK (Jan–Mar 2013). "Hemorrhagic Gianotti-Crosti Syndrome in a One and Half Month old Infant: An Extremely Unusual Presentation". Indian J Dermatol. 58 (1): 65–67. doi:10.4103/0019-5154.105313. PMC 3555378. PMID 23372217.
  10. Chuh, AA (September 2001). "Diagnostic criteria for Gianotti-Crosti syndrome: a prospective case-control study for validity assessment". Cutis; Cutaneous Medicine for the Practitioner. 68 (3): 207–13. PMID 11579787.
  11. Chuh, Antonio; Lee, Albert; Zawar, Vijay (1 September 2004). "The Diagnostic Criteria of Gianotti-Crosti Syndrome: Are They Applicable to Children in India?". Pediatric Dermatology. 21 (5): 542–547. doi:10.1111/j.0736-8046.2004.21503.x. PMID 15461758. S2CID 22924542.
  12. Chuh, Antonio; Zawar, Vijay; Law, Michelle; Sciallis, Gabriel (2 January 2012). "Gianotti-Crosti syndrome, pityriasis rosea, asymmetrical periflexural exanthem, unilateral mediothoracic exanthem, eruptive pseudoangiomatosis and papular-purpuric gloves and socks syndrome: a brief review and arguments for diagnostic criteria". Infectious Disease Reports. 4 (1): 12. doi:10.4081/idr.2012.e12. PMC 3892651. PMID 24470919.
  13. "Gianotti-crosti syndrome. Dermatalk".
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