Molluscum contagiosum
Last Updated: 2026-07-16
Author(s): Navarini A.
Reviewer(s): -
ICD11: -
Molluscum warts; Mollusca contagiosa
Common, self-limited viral infection of the epidermis caused by the molluscum contagiosum virus (MCV) from the Poxviridae family. It primarily affects preschool- and school-aged children; clustered, extensive, or persistent courses are seen in atopic dermatitis and in immunosuppression.
MCV infections occur worldwide, with higher prevalence in warm, humid climates and in community settings. Peak incidence is in childhood, approximately between 2 and 10 years of age. In adults, lesions are more often localized to the genital area or occur in the context of immunosuppression. Atopic dermatitis is considered a major risk factor for extensive disease.
MCV is divided into four genotypes:
MCV type 1 (most common type, especially in children)
MCV type 2 (more common in adults and immunosuppressed patients)
MCV types 3 and 4 (rare)
MCV infects exclusively epidermal keratinocytes and induces lobular epidermal hyperplasia with characteristic intracytoplasmic inclusion bodies. The virus evades the innate and adaptive immune response through various immune evasion mechanisms, which explains its often prolonged persistence.
Transmission:
Direct skin contact with infected lesions
Autoinoculation through scratching, rubbing, or shaving
Contaminated objects (fomites: towels, washcloths, sports equipment)
Sexual transmission in adults with genital lesions
Predisposing factors:
Incubation period usually several weeks to months (approximately 2–7 weeks, occasionally longer)
Atopic skin promotes dissemination and perilesional eczematization
Immunosuppression (HIV, transplantation, biologics) promotes extensive and atypical courses
Typically, 1–5 mm skin-colored, whitish, or pink, smooth, shiny, dome-shaped papules with a characteristic central dell (umbilication) are present. They are often multiple, grouped, or arranged linearly due to autoinoculation.
Key features:
Monomorphic, broad-based papules with a waxy surface
Centrally expressible, whitish, crumbly, infectious content
Usually asymptomatic; occasional pruritus
Clinical practice:
Perilesional eczema (molluscum dermatitis) is common, especially in atopic patients
Inflammatory erythema and swelling of individual lesions may be part of the spontaneous immune reaction and regression — not automatically a sign of bacterial superinfection
In immunosuppression: lesions may be larger (>5 mm, so-called “giant molluscum”), more numerous, and atypically configured
The diagnosis is usually clinical and does not require further ancillary testing.
Typical clinical criteria:
Monomorphic, centrally umbilicated, dome-shaped papules
Smooth, waxy surface
Grouping or linear arrangement due to autoinoculation
Expressible whitish content
Dermoscopy (helpful in diagnostic uncertainty):
Central white-yellowish amorphous structures (“white core”)
Peripheral vascular loops or crown vessels
Biopsy/histology: Indicated only in cases of diagnostic uncertainty, atypical course, or suspicion of a differential diagnosis.
Pitfalls — further evaluation in:
Solitary lesion in adults (DD: basal cell carcinoma, keratoacanthoma)
Very large, ulcerated, or treatment-resistant lesions
Extensive involvement without known immunosuppression
Genital lesions with atypical appearance (DD: condylomata acuminata)
Suspected opportunistic infection in immunosuppressed patients (DD: cryptococcosis)
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Common warts
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Milia
- Syringom
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Sebaceous gland hyperplasia
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Dermal nevus
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Keratosis follicularis
- Seborrhoeic keratosis
- Basal cell carcinoma (incl. subtypes)
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Keratoacanthoma
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Epidermal cyst
- Condylomata acuminata
- Dermatofibroma, histiocytoma, DF
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Cryptococcosis
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Histoplasmosis
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Histiocytoma
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Cryptococcosis in immunosuppression
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Other disseminated opportunistic infections in immunosuppression
Preferred sites in children:
Face, neck
Axillae, flexures
Trunk, extremities
More common in adults:
Lower abdomen, inner thighs, genital region (sexually transmitted)
Extensive distribution in immunosuppression
Palms and soles are typically not affected.
Slowly increasing, small umbilicated papules over weeks to months
Contact with affected children or household members
Spread of new lesions after scratching, shaving, or friction
Known atopic dermatitis
In adults with genital lesions: possible sexual transmission
In very numerous, large, atypical, or treatment-resistant lesions: indication of possible immunosuppression (ask about HIV status and immunosuppressive medication)
Lobular epidermal hyperplasia with an endophytic growth pattern. Characteristic findings are large intracytoplasmic inclusion bodies in keratinocytes — the so-called Henderson-Patterson bodies (also molluscum bodies). These arise through accumulation of viral particles and displace the nucleus to the periphery. An inflammatory dermal reaction with lymphocytic infiltrate may occur in the surrounding tissue, especially during spontaneous regression or superinfection.
Autoinoculation with increase in lesion number
Molluscum dermatitis (perilesional eczema), especially in atopic patients
Secondary bacterial superinfection
Postinflammatory hypo- or hyperpigmentation
Scarring, especially after manipulation or aggressive destructive therapy
Psychosocial burden due to cosmetic impairment
In immunosuppression: extensive, persistent, or atypical course with therapeutic challenges
Avoid scratching and squeezing the lesions
Use personal towels, washcloths, and razors; do not share them
Treat concomitant eczema consistently to reduce autoinoculation
Cover manipulated or inflamed lesions whenever possible
In genital lesions, address sexual transmission and recommend condoms
A general exclusion from school, daycare, or swimming pools is usually not necessary and is not evidence-based
In immunocompetent children, molluscum lesions usually heal spontaneously, but often only after months; courses lasting 12–18 months or longer are possible. Complete spontaneous remission is the rule. In pronounced atopic dermatitis and in immunosuppression, persistent, disseminated, or recurrent courses are more likely. Scars arise mainly from manipulation or aggressive therapy, not from the infection itself.
Principle
The treatment decision depends on age, number and location of lesions, degree of distress, eczematization, transmission risk in the environment, and immune status. In immunocompetent children with few asymptomatic lesions, a watchful waiting approach is often appropriate. Patients should be informed about the self-limited nature of the condition, but also about the potentially long time to resolution.
Mechanical and destructive procedures (first-line options)
Curettage: Effective with immediate results; often painful in children — local anesthesia with lidocaine/prilocaine cream (EMLA cream) is recommended
Cryotherapy: Effective; painful, with risk of blistering, hypopigmentation, and scarring, especially in darker skin types
Cantharidin (available in some countries): Topical application by the physician; effective, well tolerated in children, but not approved everywhere
Topical options (alternatives)
Potassium hydroxide (KOH) 5–10%: Topical self-application possible; note irritant potential, application instructions required
Tretinoin cream: Possible alternative, especially in widespread involvement; irritant potential
Imiquimod 5%: Not recommended as routine treatment; Cochrane analysis shows no consistent benefit over placebo in uncomplicated disease; may be considered in selected cases
Intralesional immunotherapy (escalation)
Intralesional injection of antigens (e.g., Candida antigen, MMR vaccine): Increasingly described, especially for multiple or treatment-resistant lesions; evidence is still limited, but promising
Special situations
Genital lesions in adults: Inform sexual partners; curettage or cryotherapy preferred; consider STI screening
Immunosuppressed patients: Extensive courses may require optimization of the underlying disease/immunosuppression; systemic antiviral therapy (e.g., cidofovir) has been described in individual cases of severe immunodeficiency, but without robust controlled evidence
Molluscum dermatitis: First use topical corticosteroids to treat the eczema; destructive treatment of the molluscum lesions only after eczema control
Pitfalls
Avoid aggressive therapy in toddlers with few lesions — the risk of scarring often outweighs the benefit
Do not use imiquimod as standard therapy
Do not mistake the inflammatory regression phase for superinfection and avoid unnecessary antibiotics
Campos LR, Carpi GC, da Silva ABN, Mendes BX, Lopes FCPS. Molluscum Contagiosum Treatments in Children: A Systematic Review with Network Meta-Analysis. Paediatr Drugs. 2026. PMID: 42360610. PubMed: https://pubmed.ncbi.nlm.nih.gov/42360610/
Santacroce L, Magrone T. Molluscum Contagiosum Virus: Biology and Immune Response. Adv Exp Med Biol. 2024;1451:151-170. PMID: 38801577. PubMed: https://pubmed.ncbi.nlm.nih.gov/38801577/
Caussade MC, Downey C, Krämer D. [Skin reactions related to molluscum contagiosum infection]. Andes Pediatr. 2024;95(2):136-142. PMID: 38801360. PubMed: https://pubmed.ncbi.nlm.nih.gov/38801360/
Oganesyan A, Sivesind TE, Dellavalle R. From the Cochrane Library: Interventions for Cutaneous Molluscum Contagiosum. JMIR Dermatol. 2023;6:e41514. PMID: 37632925. PubMed: https://pubmed.ncbi.nlm.nih.gov/37632925/
Wells A, Saikaly SK, Schoch JJ. Intralesional immunotherapy for molluscum contagiosum: A review. Dermatol Ther. 2020;33(6):e14386. PMID: 33044025. PubMed: https://pubmed.ncbi.nlm.nih.gov/33044025/
Sil A, Bhanja DB, Chandra A, Biswas SK. BOTE sign in molluscum contagiosum. BMJ Case Rep. 2020;13(9). PMID: 32938659. PubMed: https://pubmed.ncbi.nlm.nih.gov/32938659/
Elmas ÖF, Kilitçi A. Subungual Molluscum Contagiosum: A Rare Presentation. Skin Appendage Disord. 2020;6(1):55-57. PMID: 32021865. PubMed: https://pubmed.ncbi.nlm.nih.gov/32021865/
Meza-Romero R, Navarrete-Dechent C, Downey C. Molluscum contagiosum: an update and review of new perspectives in etiology, diagnosis, and treatment. Clin Cosmet Investig Dermatol. 2019;12:373-381. PMID: 31239742. PubMed: https://pubmed.ncbi.nlm.nih.gov/31239742/
Ferrari B, Lösch AI, Larralde M. Comment on "Molluscum contagiosum: Review and update on management". Pediatr Dermatol. 2018;35(2):280-281. PMID: 29575072. PubMed: https://pubmed.ncbi.nlm.nih.gov/29575072/
Lacarrubba F, Verzì AE, Ardigò M, Micali G. Handheld reflectance confocal microscopy for the diagnosis of molluscum contagiosum: Histopathology and dermoscopy correlation. Australas J Dermatol. 2017;58(3):e123-e125. PMID: 27282954. PubMed: https://pubmed.ncbi.nlm.nih.gov/27282954/
Olsen JR, Gallacher J, Piguet V, Francis NA. Epidemiology of molluscum contagiosum in children: a systematic review. Fam Pract. 2014;31(2):130-6. PMID: 24297468. PubMed: https://pubmed.ncbi.nlm.nih.gov/24297468/
Nguyen HP, Franz E, Stiegel KR, Hsu S, Tyring SK. Treatment of molluscum contagiosum in adult, pediatric, and immunodeficient populations. J Cutan Med Surg. 2014;18(5):299-306. PMID: 25186990. PubMed: https://pubmed.ncbi.nlm.nih.gov/25186990/
Ianhez M, Cestari Sda C, Enokihara MY, Seize MB. Dermoscopic patterns of molluscum contagiosum: a study of 211 lesions confirmed by histopathology. An Bras Dermatol. 2011;86(1):74-9. PMID: 21437525. PubMed: https://pubmed.ncbi.nlm.nih.gov/21437525/
Dohil MA, Lin P, Lee J, Lucky AW, Paller AS, Eichenfield LF. The epidemiology of molluscum contagiosum in children. J Am Acad Dermatol. 2006;54(1):47-54. PMID: 16384754. PubMed: https://pubmed.ncbi.nlm.nih.gov/16384754/
Braue A, Ross G, Varigos G, Kelly H. Epidemiology and impact of childhood molluscum contagiosum: a case series and critical review of the literature. Pediatr Dermatol. 2005;22(4):287-94. PMID: 16060861. PubMed: https://pubmed.ncbi.nlm.nih.gov/16060861/
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