Abstract
Pityriasis versicolor, a common skin fungal infection, is typically observed on trunk and limb skin. Here, we highlight an unusual presentation: scalp involvement, often overlooked due to its asymptomatic, mildly scaly patches. We report four pediatric cases, emphasizing the potential underestimation of this scalp variant. This case series underscores the importance of considering this diagnosis in patients with unexplained scalp hypopigmentation, especially in males with short hair who may readily notice these subtle changes. The report contributes to the understanding of this variant's clinical presentation and emphasizes the need for awareness among clinicians to ensure accurate diagnosis and appropriate management.
Keywords: pityriasis versicolor, tinea versicolor, scalp, Malassezia, children
Introduction
Pityriasis versicolor, also known as tinea versicolor, is a prevalent superficial cutaneous fungal infection caused by dimorphic lipophilic and lipid-dependent yeasts in the genus Malassezia (formerly known as Pityrosporum), notably Malassezia globosa, Malassezia furfur and Malassezia sympodialis (1). This condition occurs globally, with significantly high prevalence rates observed in hot and humid climates, reaching up to 50% in some tropical countries (2). In contrast, countries like Sweden report much lower prevalence rates, as low as 0.5% (3). Pityriasis versicolor primarily affects adolescents and young adults, possibly due to increased sebum production within these age groups (4). It is less common in children, but the causative species appear to be the same in children and adults (5). Clinically, it is characterized by mildly scaly hypopigmented or hyperpigmented macules/patches, typically found on areas of the skin rich in sebum production such as the trunk (especially the upper part), neck, shoulders, and upper arms (1). However, it can also occur in unusual regions of the body, including the face, scalp, arms, legs, intertriginous sites, genitalia, areolae, and palms and soles (6). In this case series, we present instances of scalp pityriasis versicolor in pediatric patients, highlighting a rare distribution of this common disease.
Case description
This case series explores four distinct cases of pediatric pityriasis versicolor, ranging from infants to teenagers. All patients exhibited gradually emerging, asymptomatic hypopigmented lesions on the scalp. Notably, the lesions in the older children were coincidentally identified during routine haircuts. Significantly, none of these patients reported any history of animal contact and maintained overall good health.
Upon examination, all patients exhibited distinctive, well-defined, round-to-oval, hypopigmented macules and patches on the scalp (Figures 1A–D). No involvement of other body sites was observed in any of the patients. Direct microscopic examination of these lesions revealed the presence of characteristic thick-walled yeasts and short angular hyphae, reminiscent of the classic “spaghetti and meatballs” appearance (Figures 1E–H). Based on these findings, all patients were diagnosed with pityriasis versicolor.
Treatment strategies are outlined in Table 1. Patient 1 and 2 were treated with topical terbinafine hydrochloride cream twice daily for 6 and 8 weeks respectively, while Patient 3 and 4 received topical ketoconazole shampoo twice weekly for 8 and 12 weeks respectively. Remarkably, no adverse reactions were observed during the course of topical antifungal therapy for any patient. At the 3-month follow-up, no recurrence was reported, indicating the efficacy and safety of the prescribed topical antifungal treatments for pediatric pityriasis versicolor.
Table 1.
Patient no. | Age | Sex | Treatment | Time of therapy (weeks) | Adverse reaction | Follow up |
---|---|---|---|---|---|---|
1 | 8 m | Male | Terbinafine cream | 6 | None | No recurrence |
2 | 7 m | Male | Terbinafine cream | 8 | None | No recurrence |
3 | 14 y | Male | Ketoconazole shampoo | 8 | None | No recurrence |
4 | 8 y | Male | Ketoconazole shampoo | 12 | None | No recurrence |
m, month; y, year.
Discussion
Malassezia species, unique fungi residing on the skin of humans and non-human mammals, are notably absent from environmental sources. With the exception of Malassezia pachydermatitis, these fungi specifically inhabit sebum-rich areas of the skin, relying on various fatty acids for growth. Consequently, culturing Malassezia species requires the addition of specific compounds like Tween, oleic acid, and bile salts to the medium (4, 7).
Within the Malassezia genus, 18 species are identified, ten of which are associated with human skin, while the remaining eight inhabit non-human animal skin (8). The most recent human-derived discovery was Malassezia yamatoensis in 2004, isolated from a patient with seborrheic dermatitis (9). Although typically commensal, Malassezia species can induce conditions like pityriasis versicolor, seborrheic dermatitis, Malassezia folliculitis, and atopic dermatitis (4). M. restricta and M. globosa dominate healthy and diseased skin, but their ratios vary: M. restricta surpasses M. globosa in seborrheic dermatitis, whereas M. globosa dominates in pityriasis versicolor (10).
Pityriasis versicolor shows a slightly higher prevalence in men, likely attributed to increased sebaceous activity among males (1). Interestingly, there are limited documented cases of scalp pityriasis versicolor, predominantly involving male patients, as observed in our report (11–15). This prevalence among males could be linked to the common practice of shorter haircuts in men, increasing the likelihood of detecting scalp pityriasis versicolor. Notably, our older patients noticed the condition during haircuts, underscoring the importance of this factor.
The location of pityriasis versicolor lesions varies based on the individual's age, with the face and neck being more prevalent sites in children (11). While scalp involvement is rare in both children and adults, seborrheic dermatitis, another Malassezia-associated skin condition, commonly affects the scalp (16). A likely explanation for this underreporting lies in the distinctive characteristics of the two conditions. Seborrheic dermatitis typically manifests as itching and scaling, accompanied by well-defined erythematous patches. These symptoms readily draw patients' attention. In contrast, scalp pityriasis versicolor presents as mildly scaly hypopigmented or hyperpigmented macules/patches, often escaping notice. Consequently, the inconspicuous nature of this condition might contribute to its underdiagnosis.
Pityriasis versicolor lesions display a spectrum of colors, ranging from nearly white to reddish-brown or fawn. Notably, hypopigmentation, especially discernible on dark skin, has been identified as an independent variant (17). While children are less commonly affected by this condition than adults, it is intriguing that 72% of pediatric cases present in the hypopigmented form (18), a consistency found in our study where all pediatric scalp pityriasis versicolor cases demonstrated this hypopigmented variant. The precise mechanism behind this hypopigmentation remains elusive; however, recent literature posits a hypothesis. It suggests that Malassezia spp. could produce malassezin, a substance capable of stimulating melanocyte apoptosis, and azelaic acid, which has the potential to inhibit tyrosinase activity, thus contributing to the observed hypopigmentation (19).
Diagnosing pityriasis versicolor typically relies on clinical observations, rooted in the condition's distinct features. However, the diverse manifestations of tinea versicolor can perplex inexperienced clinicians. Using a Wood lamp, lesions may exhibit fluorescence in shades of gold-yellow, yellowish-green, or coppery-orange, although not all lesions fluoresce (1). Microscopic examination reveals short, stubby hyphae mingled with spore clusters, creating the characteristic “spaghetti and meatballs” appearance (20). Culturing or molecular analysis of Malassezia species from skin scrapings lacks diagnostic value and isn't part of pityriasis versicolor's diagnostic protocol (20). Although dermoscopy aids in confirming scaling, it doesn't pinpoint specific diagnostic markers (21).
When dealing with pityriasis versicolor, initial treatment typically involves topical antifungals, with systemic antifungals reserved for severe or persistent cases. Effective topical treatments include creams, lotions, and shampoos, applied once or twice daily for varying durations, often swiftly alleviating clinical symptoms. Non-specific treatments, such as selenium sulphide (available in lotions, creams, or shampoos), zinc pyrithione, propylene glycol, and Whitfield's ointment, have demonstrated efficacy against the condition (22, 23). Recent studies have primarily focused on ketoconazole and terbinafine among topical antifungals (23). However, patient adherence might be influenced by the need for frequent applications or mild skin irritation. The efficacy of oral agents like ketoconazole, itraconazole, and fluconazole is well-established (1). Notably, oral terbinafine, effective for various superficial fungal infections, does not effectively treat pityriasis versicolor (24). This limitation arises because oral terbinafine is not excreted through sweat, preventing the attainment of fungicidal levels in the stratum corneum (24). In our case series, older children opted for topical ketoconazole shampoo, mainly due to the discomfort associated with applying cream on the scalp.
In conclusion, we have documented four cases of pityriasis versicolor on the scalp, representing an uncommon manifestation of this common diseases. Due to the scalp's concealment by hair and the asymptomatic nature of pityriasis versicolor, characterized by hypopigmented or hyperpigmented macules/patches, it often goes unnoticed by patients. We posit that scalp pityriasis versicolor might be significantly underestimated.
Funding Statement
The author(s) declare financial support was received for the research, authorship, and/or publication of this article.
This research was supported by the the National Key R&D Program of China (2022YFC2504800).
Data availability statement
The original contributions presented in the study are included in the article/Supplementary Material, further inquiries can be directed to the corresponding author.
Ethics statement
Written informed consent was obtained from the individual(s), and minor(s)' legal guardian/next of kin, for the publication of any potentially identifiable images or data included in this article.
Author contributions
YZ: Conceptualization, Methodology, Writing – original draft. JC: Data curation, Writing – review & editing. LM: Funding acquisition, Writing – review & editing. YX: Funding acquisition, Methodology, Supervision, Writing – review & editing.
Conflict of interest
The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.
Publisher's note
All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article, or claim that may be made by its manufacturer, is not guaranteed or endorsed by the publisher.
References
- 1.Leung AK, Barankin B, Lam JM, Leong KF, Hon KL. Tinea versicolor: an updated review. Drugs Contex. (2022) 11:2022–9–2. 10.7573/dic.2022-9-2 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 2.Gupta AK, Bluhm R, Summerbell R. Pityriasis versicolor. J Eur Acad Dermatol Venereol. (2002) 16(1):19–33. 10.1046/j.1468-3083.2002.00378.x [DOI] [PubMed] [Google Scholar]
- 3.Hellgren L, Vincent J. The incidence of tinea versicolor in central Sweden. J Med Microbiol. (1983) 16(4):501–2. 10.1099/00222615-16-4-501 [DOI] [PubMed] [Google Scholar]
- 4.Harada K, Saito M, Sugita T, Tsuboi R. Malassezia species and their associated skin diseases. J Dermatol. (2015) 42(3):250–7. 10.1111/1346-8138.12700 [DOI] [PubMed] [Google Scholar]
- 5.Ben Salah S, Makni F, Marrakchi S, Sellami H, Cheikhrouhou F, Bouassida S, et al. Identification of Malassezia species from Tunisian patients with pityriasis versicolor and normal subjects. Mycoses. (2005) 48(4):242–5. 10.1111/j.1439-0507.2005.01091.x [DOI] [PubMed] [Google Scholar]
- 6.Varada S, Dabade T, Loo DS. Uncommon presentations of tinea versicolor. Dermatol Pract Concept. (2014) 4(3):93–6. 10.5826/dpc.0403a21 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 7.Suzuki K, Inoue M, Takayama K, Nagahama T, Cho O, Kurakado S, et al. Development of artificial-sebum-containing leeming and notman agar medium to enhance the growth of Malassezia. Mycopathologia. (2022) 187(4):393–6. 10.1007/s11046-022-00634-9 [DOI] [PubMed] [Google Scholar]
- 8.Takashima M, Sugita T. Taxonomy of pathogenic yeasts Candida, Cryptococcus, Malassezia, and Trichosporon. Med Mycol J. (2022) 63(4):119–32. 10.3314/mmj.22.004 [DOI] [PubMed] [Google Scholar]
- 9.Sugita T, Tajima M, Takashima M, Amaya M, Saito M, Tsuboi R, et al. A new yeast, Malassezia yamatoensis, isolated from a patient with seborrheic dermatitis, and its distribution in patients and healthy subjects. Microbiol Immunol. (2004) 48(8):579–83. 10.1111/j.1348-0421.2004.tb03554.x [DOI] [PubMed] [Google Scholar]
- 10.Sugita T, Zhang E, Tanaka T, Nishikawa A, Tajima M, Tsuboi R. Recent advances in research on Malassezia microbiota in humans. Med Mycol J. (2013) 54(1):39–44. 10.3314/mmj.54.39 [DOI] [PubMed] [Google Scholar]
- 11.Wang L, Xing H. Pityriasis versicolor on the scalp: an unusual distribution of a common disease. Pediatr Investig. (2023) 7(3):216–7. 10.1002/ped4.12387 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 12.Silverio AD, Zeccara C, Serra F, Ubezio S, Mosca M. Pityriasis versicolor in a newborn. Mycoses. (1995) 38(5–6):227–8. 10.1111/j.1439-0507.1995.tb00055.x [DOI] [PubMed] [Google Scholar]
- 13.Naseri M, Namazi MR. Isolated scalp involvement with pityriasis versicolor alba (pityrias versicolor albus capitis) in a patient from a dry, temperate region. Dermatol Online J. (2003) 9(3):17. [PubMed] [Google Scholar]
- 14.Rice JS. Tinea versicolor confined to the hairy scalp. Arch Dermatol. (1963) 87:643. 10.1001/archderm.1963.01590170101018 [DOI] [PubMed] [Google Scholar]
- 15.Goncalves AP. Unusual locations of pityriasis versicolor with particular reference to scalp lesions. Dermatol Trop Ecol Geogr. (1963) 15:211–6. [PubMed] [Google Scholar]
- 16.Leroy AK, Cortez de Almeida RF, Obadia DL, Frattini S, Melo DF. Scalp seborrheic dermatitis: what we know so far. Skin Appendage Disord. (2023) 9(3):160–4. 10.1159/000529854 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 17.Thoma W, Krämer HJ, Mayser P. Pityriasis versicolor alba. J Eur Acad Dermatol Venereol. (2005) 19(2):147–52. 10.1111/j.1468-3083.2004.01085.x [DOI] [PubMed] [Google Scholar]
- 18.Bouassida S, Boudaya S, Ghorbel R, Meziou TJ, Marrekchi S, Turki H, et al. Pityriasis versicolor in children: a retrospective study of 164 cases. Ann Dermatol Venereol. (1998) 125(9):581–4. [PubMed] [Google Scholar]
- 19.Kurniadi I, Wijaya WH, Timotius KH. Malassezia virulence factors and their role in dermatological disorders. Acta Dermatovenerol Alp Pannonica Adriat. (2022) 31(2):65–70. [PubMed] [Google Scholar]
- 20.Saunte DML, Gaitanis G, Hay RJ. Malassezia-associated skin diseases, the use of diagnostics and treatment. Front Cell Infect Microbiol. (2020) 10:112. 10.3389/fcimb.2020.00112 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 21.Mathur M, Acharya P, Karki A, Kc N, Shah J. Dermoscopic pattern of pityriasis versicolor. Clin Cosmet Investig Dermatol. (2019) 12:303–9. 10.2147/CCID.S195166 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 22.Gupta AK, Batra R, Bluhm R, Faergemann J. Pityriasis versicolor. Dermatol Clin. (2003) 21(3):413–29. 10.1016/s0733-8635(03)00039-1 [DOI] [PubMed] [Google Scholar]
- 23.Gupta AK, Lyons DCA. Pityriasis versicolor: an update on pharmacological treatment options. Expert Opin Pharmacother. (2014) 15(12):1707–13. 10.1517/14656566.2014.931373 [DOI] [PubMed] [Google Scholar]
- 24.Gupta AK, Foley KA. Antifungal treatment for pityriasis versicolor. J Fungi. (2015) 1(1):13–29. 10.3390/jof1010013 [DOI] [PMC free article] [PubMed] [Google Scholar]
Associated Data
This section collects any data citations, data availability statements, or supplementary materials included in this article.
Data Availability Statement
The original contributions presented in the study are included in the article/Supplementary Material, further inquiries can be directed to the corresponding author.