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Asia Pac Allergy. 2012 July; 2(3): 223–226.
Published online 2012 July 25. doi:  10.5415/apallergy.2012.2.3.223
PMCID: PMC3406302

Gianotti-Crosti syndrome: case report of a pruritic acral exanthema in a child

Abstract

Gianotti-Crosti syndrome (GCS) is a sporadic dermatosis affecting mainly children. It is characterized by multiple, confluent, monomorphic and pruritic pink to red-brown papules or papulovesicles, distributed symmetrically on the face, extensor surfaces of the extremities and buttocks, commonly sparing the trunk, palms and soles. This can be preceded by a viral infection, and may be accompanied by fever, hepatosplenomegaly, or lymphadenopathy. Personal and family history of atopy appears to be a risk factor in the subsequent development of GCS, thus frequently diagnosed as atopic dermatitis. We report a case of a 4-year-old boy from our institution with generalized, pruritic, papulovesicular rashes on the face and extremities for one month. He was diagnosed to have atopic dermatitis and treated as such, before presentation to our institution. As the signs and symptoms in GCS are similar to atopic dermatitis, we suggest that this diagnosis be considered when presented with a similar case.

Keywords: Gianotti-Crosti syndrome, Acrodermatitis, Atopic dermatitis, Allergy, Infantile papular eruption

INTRODUCTION

Gianotti-Crosti syndrome (GCS) is a self-limiting exanthem of acute onset with a characteristic acral distribution, usually occurring in young children. The term GCS now comprises both papular acrodermatitis of childhood and papulovesicular acrolocated syndrome, once thought to be distinct clinical entities but now proven to be clinically and histologically indistinguishable [1]. Classically associated with hepatitis B virus, GCS is now seen more commonly with Epstein-Barr virus (EBV) [2]. We report a case of GCS suspected as and treated for allergic eczema in a four-year-old male patient who presented at our institution with symmetrical erythematous papulovesicular eruptions on the face, and both upper and lower extremities.

CASE REPORT

A four-year-old Indonesian boy presented with a generalized papulovesicular rash on his face, and both upper and lower extremities that had persisted for one month. The eruption first started on his lower limbs, and spread to his upper limbs and face. It was pruritic, the vesicles discharged serous fluid, and it was not associated with fever or preceding illness. His parents reported a previous similar episode one year ago where the eruptions left large areas of hyperpigmentation up to 4 cm in diameter, and resolved in two weeks. He was previously worked up in Indonesia for allergic dermatitis, with moderate levels of specific IgE antibodies to cow's milk protein and egg white (RAST test score of 2 for both allergens). Response to the medications prescribed then was minimal. He has a positive family history of allergic rhinitis secondary to house dust mite allergy.

Examination revealed an otherwise healthy, active child. Multiple pink to red-brown papules and vesicles, coalescing into plaques with secondary excoriations were noted on his face, extensor surfaces of upper and lower extremities and buttocks (Figs. 1--3).3). Individual lesions measured 2 to 5 mm in diameter and some were flat-topped. Some ruptured vesicles were weepy and crusted suggestive of secondary bacterial infection. Other than a few redbrown papules on the back, the patient's trunk was spared. There were also no lesions on the patient's palms and soles. The rash appeared to affect the exposed areas of the body more severely. No hepatosplenomegaly or lymphadenopathy was detected.

Fig. 1
Partially-resolving erythematous papules on forehead and cheeks. Child appears non-toxic.
Fig. 3
Symmetrical distribution of characteristic red-brown, partly flat-topped papules on extensor surface of lower limbs that are partially-resolving.

The patient was treated symptomatically with Atarax (hydroxyzine), chlorhexidine lotion and moisturizing lotion, and advised to go swimming in chlorinated water to help lower the risk of secondary bacterial infections.

DISCUSSION

GCS is a sporadic dermatosis that commonly affects children three months to 15 years of age, with more than 90% younger than four years. However, it has been reported in adults where exclusively women are affected, suggesting that hormonal factors play a role [2].

It is characterized by the acute onset of multiple monomorphous, pink to red-brown papules or papulovesicles that may become confluent. The papules are distributed symmetrically on the face, extensor surfaces of the extremities, and buttocks. The rash may be pruritic and is typically nonhyperkeratotic; spares the trunk, palms of the hands, and soles of the feet. The eruptions can persist longer than 6 weeks in more than 50% of patients and complete resolution typically takes more than 2 months. The cutaneous manifestations can be preceded by an upper respiratory tract infection or diarrhea. The rash may be accompanied by a low-grade fever, hepatosplenomegaly, or cervical, inguinal or axillary lymphadenopathy. Koebner's phenomenon may also be present [2-4].

Although the exact underlying pathophysiologic mechanisms remain unclear, GCS is considered a cutaneous response to various immunologic triggers, with viral infections being the key factor. The most likely process is a local type IV hypersensitivity reaction to the offending antigen [2]. However, immunohistochemistry and electron microscopy findings are nonspecific and fail to demonstrate the presence of viral particles or antigens in skin lesions, thus suggesting that lesion development does not involve a direct local interaction between viral antigens and immune cells in the skin [5]. The syndrome was first described by Gianotti in association with hepatitis B virus. But other viruses such as EBV, cytomegalovirus, coxsackievirus, hepatitis A virus, parainfluenza virus, respiratory syncytial virus, rotavirus, mumps, parvovirus and molluscum contagiosum have been reported to be associated with this distinctive exanthema, EBV being the most common etiologic factor worldwide [2]. Studies have also shown that recent immunization and rarely, bacterial infections such as Bartonella henselae, Mycoplasma pneumoniae, and group A streptococci may trigger GCS [2, 6, 7]. In addition, a study has shown a higher prevalence of atopic dermatitis, family history of atopy and elevated IgE (total and specific) in GCS cases than controls [8], thus indicating that atopy is significantly associated with GCS.

GCS is diagnosed clinically by the presence of a characteristic rash and its distribution, with differential diagnoses including erythema multiforme, lichen planus, papular urticaria, scabies and atopic dermatitis [2, 3]. Being primarily a clinical diagnosis, no investigations were performed in this patient to determine the causative agent since he was well with no localizing signs of infection. Also, the diagnosis of GCS requires clinical suspicion, lest it be mistaken for one of its differential diagnoses such as atopic dermatitis as in this case. This is because the lesions in atypical, early or resolving cases can resemble that of atopic dermatitis. The presence of specific IgE on RAST testing and positive family history of atopy in this patient is consistent with findings of Ricci et el. [8] and could make distinguishing between atopic dermatitis difficult.

As GCS is generally benign and self-limiting condition, no definitive treatment is required. However, oral antihistamines and topical anti-pruritics can be prescribed as needed for pruritis. The effectiveness of topical steroids has not been established in a controlled setting [2]. Anti-virals such ribavirin have been reported to induce dramatic symptomatic remission in prolonged and disabling cases, but further studies are also required to confirm its efficacy in GCS [9]. Patients' parents should be reassured that the rash usually resolves without scarring within 10 to 60 days. Recurrences are rare.

Fig. 2
Symmetrical distribution of monomorphous papulovesicles on extensor surface of right and left forearms.

References

1. Caputo R, Gelmetti C, Ermacora E, Gianni E, Silvestri A. Gianotti-Crosti syndrome: a retrospective analysis of 308 cases. J Am Acad Dermatol. 1992;26:207–210. [PubMed]
2. Brandt O, Abeck D, Gianotti R, Burgdorf W. Gianotti-Crosti syndrome. J Am Acad Dermatol. 2006;54:136–145. [PubMed]
3. Xia Y, Davies BE, Gunning S. Pruritic acral rash in a child. Gianotti-Crosti syndrome. Am Fam Physician. 2008;78:103–105. [PubMed]
4. Chandrasekaran M, Mukherjee S. Gianotti Crosti syndrome. Indian Pediatr. 2007;44:695. [PubMed]
5. Smith KJ, Skelton H. Histopathologic features seen in Gianotti-Crosti syndrome secondary to Epstein-Barr virus. J Am Acad Dermatol. 2000;43:1076–1079. [PubMed]
6. Draelos ZK, Hansen RC, James WD. Gianotti-Crosti syndrome associated with infec tions other than hepatitis B. JAMA. 1986;256:2386–2388. [PubMed]
7. Taïeb A, Plantin P, Du Pasquier P, Guillet G, Maleville J. Gianotti-Crosti syndrome: a study of 26 cases. Br J Dermatol. 1986;115:49–59. [PubMed]
8. Ricci G, Patrizi A, Neri I, Specchia F, Tosti G, Masi M. Gianotti-Crosti syndrome and allergic background. Acta Derm Venereol. 2003;83:202–205. [PubMed]
9. Zawar V, Chuh A. Efficacy of ribavirin in a case of long lasting and disabling Gianotti-Crosti syndrome. J Dermatol Case Rep. 2008;2:63–66. [PMC free article] [PubMed]

Articles from Asia Pacific Allergy are provided here courtesy of Asia Pacific Association of Allergy, Asthma and Clinical Immunology