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Pityriasis lichenoides: assessment of 41 pediatric patients

Abstract

Objectives

This study aims to evaluate the characteristics and treatment response of patients with pityriasis lichenoides seen in the last 43 years in a pediatric dermatology service.

Methods

This was a retrospective, analytical, longitudinal study of patients under 15 years of age. The medical records were reviewed and data were presented as frequencies, means and variances. Student's t-test, Mann-Whitney test, Fisher's exact test, Pearson/Yates chi-square test and multivariate logistic regression model were used, with p < 0.05 considered.

Results

41 patients were included, 32 (78.0%) with pityriasis lichenoides chronica (PLC), five (12.2%) with pityriasis lichenoides et varioliformis acuta (PLEVA) and four (9.8%) with clinical PLC without biopsy. The age range of school children and adolescents was 19 (46.3%) and 13 (31.7%) respectively and 27 (65.8%) were male. Two peaks of the highest frequency were observed between 2004 and 2006 (10 patients - 24.4%) and another between 2019 and 2021 (6 patients - 14.7%). There was remission in 71.9% (n = 23), with 56.6% (n = 17) of those who used antibiotic therapy and 80% (n = 4) of those who had phototherapy. The chance of remission was 13 times greater in patients with disease onset after 5 years of age.

Conclusions

The clinical form most commonly found was PLC mainly in school children and adolescents. The frequency peaks coincided with infectious outbreaks. The remission rate was satisfactory with antibiotic therapy, but higher with phototherapy. Remission was greater in patients with disease onset after 5 years of age.

Keywords
Child; Clinical diagnosis; Pityriasis lichenoides; Treatment

Introduction

Pityriasis lichenoides (PL) is an inflammatory dermatitis that mainly affects children and young adults.11 Khachemoune A., Byumin M.L. Pityriasis lichenoides: pathophysiology, classification and treatment. Am J Clin Dermatol. 2007;8:29-36.,22 Lupu J., Chosidow O., Wolkenstein P., Bergqvist C., Ortonne N., Ingen-Housz-Oro S. Pityriasis lichenoides: a clinical and pathological case series of 49 patients with emphasis on follow-up. Clin Exp Dermatol. 2021;46:1561-6. Its prevalence, incidence, and risk factors are yet to be defined.33 Chen Y., Zhao M., Xiang X., Wang Z., Xu Z., Ma L. Oral erythromycin in pityriasis lichenoides chronica and pityriasis lichenoides et varioliformis acuta. Dermatol Ther. 2020;33:e13311.

Several hypotheses have been raised about its pathophysiology. It is considered to be a lymphoproliferative disease, possibly triggered by antigenic stimuli, mainly viruses and drugs,44 Bellinato F., Maurelli M., Gisondi P., Girolomoni G. A systematic review of treatments for pityriasis lichenoides. J Eur Acad Dermatol Venereol. 2019;33:2039-49.,55 Durusu G., Gurel G., Tokyol C. [A case of pityriasis lichenoides chronica in a patient with COVID-19 infection]. Actas Dermosifiliogr. 2022;113:S18-9. representing the benign spectrum of cutaneous lymphoproliferative disorders.66 Borra T., Custrin A., Saggini A., Fink-Puches R., Cota C., Vermi W., et al. Pityriasis lichenoides, atypical pityriasis lichenoides, and related conditions - a study of 66 cases. Am J Surg Pathol. 2018;00:1-12.

Few epidemiological studies are available and the number of pediatric patients included is even smaller.77 Zang J.B., Coates S.J., Huang J., Vonderheld E.C., Cohen B.A. Pityriasis lichenoides: long-term follow-up study. Pediatr Dermatol. 2018; 35:213-9.

8 Ersoy-Evans S., Greco M.F., Mancini A.J., Subasi N., Paller As. Pityriasis lichenoides in childhood: a retrospective review of 124 patients. J Am Acad Dermatol. 2007;56:205-10.
-99 Romaní J., Puig L., Fernández-Figueras M.T., Moragas J.M. Pityriasis lichenoides in children: clinicopathologic review of 22 patients. Pediatr Dermatol. 1998;15:1-6.

Clinical forms include pityriasis lichenoides et varioliformis acuta (PLEVA), febrile ulceronecrotic Mucha-Habermann disease (a subtype of PLEVA associated with fever), and pityriasis lichenoides chronica (PLC). More than one type can coexist in the same patient.22 Lupu J., Chosidow O., Wolkenstein P., Bergqvist C., Ortonne N., Ingen-Housz-Oro S. Pityriasis lichenoides: a clinical and pathological case series of 49 patients with emphasis on follow-up. Clin Exp Dermatol. 2021;46:1561-6. The acute form tends to be self-limiting and is characterized by generalized papules, which progress to necrosis, and a varioliform scar may remain.1010 Jung F., Sibbald C., Bohdanowicz M., Ingram J.R., Piguet V. Systematic review of the efficacies and adverse effects of treatments for pityriasis lichenoides. Br J Dermatol. 2020;183:1026-32. The chronic form is the most common, with periods of remission and recurrence over several months or years. It is characterized by erythematous to brownish papules and plaques, with peeling from the periphery to the center of the lesion (Mica-like scale),11 Khachemoune A., Byumin M.L. Pityriasis lichenoides: pathophysiology, classification and treatment. Am J Clin Dermatol. 2007;8:29-36. and evolving into hypochromic patches without scarring.1111 Markus J.R., Carvalho V.O., Lima M.N., Abagge K.T., Nascimento A., Werner B. The relevance of recognizing clinical and morphologic features of pityriasis lichenoides: clinicopathological study of 29 cases. Dermatol Pract Concept. 2013;3:7-10. The distribution of lesions is usually central, preferentially affecting the trunk and proximal extremities.77 Zang J.B., Coates S.J., Huang J., Vonderheld E.C., Cohen B.A. Pityriasis lichenoides: long-term follow-up study. Pediatr Dermatol. 2018; 35:213-9.

The literature regarding treatment in children is scarce but oral antibiotics (such as erythromycin and tetracycline), phototherapy, topical corticosteroids, and immunosuppressants have been reported as options.44 Bellinato F., Maurelli M., Gisondi P., Girolomoni G. A systematic review of treatments for pityriasis lichenoides. J Eur Acad Dermatol Venereol. 2019;33:2039-49.,77 Zang J.B., Coates S.J., Huang J., Vonderheld E.C., Cohen B.A. Pityriasis lichenoides: long-term follow-up study. Pediatr Dermatol. 2018; 35:213-9.

The objectives of this study were to evaluate the clinical characteristics, time for diagnosis, triggering factors and response to treatment of patients with PL seen over the last 43 years in a tertiary service in Southern Brazil.

Methods

Study design and population

A retrospective cross-sectional study was conducted in the pediatric dermatology department of a university hospital in Southern Brazil from 1980 to 2023.

For data analysis, four decades were compared: 1980-1989, 1990-1999, 2000-2009 and 2010-2019, as were the four seasons.

Variables

Medical records of patients under 15 years of age diagnosed with PL were reviewed using a protocol prepared for the study to assess sex, age at symptom onset, age at diagnosis, time to diagnosis, season of the year at symptom onset, triggering factors, duration of the disease, characteristics and distribution of lesions, associated symptoms, histopathological findings, treatment used, treatment time, and response to treatment. The photographs of the included patients were reviewed.

Statistical analyses

The variables collected were analyzed using descriptive statistics with frequency distribution for categorical data and median and interquartile range for asymmetric continuous data.

The Pearson/Yates chi-squared test was used to compare categorical variables. The multivariate logistic regression model, considering remission for more than six months or the permanence of skin lesions as the dependent variable, was used to identify the most predictive variables and their respective odds ratio (OR).

The sample confers 95% testing power considering the type II error of 5%, type error of 5% and estimated prevalence of 3%. Statistical significance was deemed present in p-values less than 0.05. The data were analyzed with the Statistica® program (StatSoft Power Solutions, Inc., Palo Alto, California, USA).

Ethics statements

The study was approved by the institution's Research Ethics Committee, under No. 69842723.1.0000.0096. All patients sign the consent form.

Results

Population description

Of the 43 years of the study time, the authors evaluated 41 patients with PL: 37 (90%) confirmed by biopsy, of which 32 (78.0%) had PLC and five (12.2%) PLEVA. Four (9.8%) patients without biopsy, but with a clinical presentation compatible with PLC. On average, each patient had four images of lesions, which allowed us to confirm the description in the medical records.

Table 1 presents the patients’ characteristics.

Table 1
Characteristics of patients, frequency of skin lesions in all patients and frequency of skin lesions according to age group.

Prevalence over the decades and seasons

Figure 1A shows the prevalence distribution of PL over the 43-year study period, with two peaks of higher frequency, one from 2004 to 2006 (10 patients - 24.4%) and another from 2019 to 2021 (6 patients - 14.7%).

Figure 1
Frequency distribution of pityriasis lichenoides. (A) Distribution from 1980 to 2023. (B) Distribution according to the seasons of the year. (C) Probability of remission of pityriasis lichenoides according to the age at disease onset.

The authors found no significant difference in terms of disease onset according to the seasons of the year (p = 0.26; Figure 1B).

Disease characteristics

Papules were the predominant lesion, found in 38 (92.7%) patients, followed by peeling, in 30 (73.2%) patients, hypopigmentation, also seen in 30 (73.2%) patients, and annular lesions, in 25 (61.0%) patients. A total of 22 (53.6%) and 17 (41.5%) of patients had erythema and crusts, respectively. Hyperpigmentation, necrosis, and erythematous plaques were less frequent. The types of lesions did not vary according to age group, but hyperpigmentation was more frequent in preschool children (p = 0.07; Table 1).

The lesions were diffuse in 19 (46.3%) cases, central in 18 (43.9%), and peripheral in four (9.7%).

In total, 18 (43.9%) patients had associated symptoms. Pruritus was the most common symptom.

Triggering factors were present in 11 (26.8%) cases, including fever (three cases), COVID-19 infection (two cases), and sun exposure, HIV, parotitis, tonsillitis, cold weather, and COVID-19 vaccination (one case each).

Treatment features

Among the treatments used, with a median duration of 14.5 months (IQR = 5.5-48), 30 (73.2%) patients underwent antibiotic therapy, six (14.6%) corticotherapy, five (12.2%) phototherapy, and three (7.3%) topical hydration. The antibiotics administered were erythromycin in 14 (46.3%) patients and tetracycline in 11 (36.6%), and in 5 (17.1%) cases used both erythromycin and tetracycline at different times. The median number of consultations was four (IQR = 2-7), with a minimum of one and a maximum of 27.

The antibiotics used for treatment were erythromycin and tetracycline. The choice of antibiotic depended on the age of the patient (tetracycline was not used in children under eight years of age) and the availability of the medication. Of the 30 (73,1%) patients treated with antibiotic therapy, 17 (56.6%) had remission.

Treatment with narrowband ultraviolet B (NB-UVB) phototherapy, which was implemented at the service in 2019, was indicated according to the patient's availability to attend the sessions and in the absence of contraindications. Of the five patients treated with NB-UVB, four (80%) progressed to complete remission by the end of the study. Figure 2 shows the treatments used and the patient's progress.

Figure 2
Progress of the patients evaluated according to the treatment used.

Follow-up characteristics

Of the 41 patients, nine (21,9%) did not return for follow-up. Among the remaining 32, 23 (71.9%) showed resolution of the disease and nine (28.1%) remained symptomatic at the last evaluation.

The absence of lesions for more than six months at the last evaluation was observed more frequently among school children (12 patients - 54.5%) and adolescents (9 patients - 40.9%) (p < 0.001).

In the multivariate logistic regression model, considering remission for more than six months or permanence of skin lesions as the dependent variable, only the time of disease onset showed a significant association, with 13 times greater chances of remission with disease onset after five years of age (p = 0.01) (OR = 13.33; 95% CI = 2.11-84.13) (Table 2).

Table 2
Strength of association between the variables studied and remission of pityriasis lichenoides.

The univariate logistic regression model also showed that the later the disease onset, the higher the estimated probability of remission (Figure 1C).

Discussion

Although some clinical findings are characteristic of PL, its diagnosis is challenging and therefore sometimes delayed. In this study, the mean time from symptom onset to diagnosis was five months, with a maximum of 10 years. A previous series from The Johns Hopkins Hospital in the United States demonstrated a mean time from symptom onset to diagnosis of one year, varying up to a maximum of three years, a mean age at onset of 8 years old as in the present study with a slight male predominance also in concordance with these findings.77 Zang J.B., Coates S.J., Huang J., Vonderheld E.C., Cohen B.A. Pityriasis lichenoides: long-term follow-up study. Pediatr Dermatol. 2018; 35:213-9.

The most frequent clinical form of the disease was PLC (78%), corroborating Khachemoune in a review on the topic11 Khachemoune A., Byumin M.L. Pityriasis lichenoides: pathophysiology, classification and treatment. Am J Clin Dermatol. 2007;8:29-36. and Zang and Romaní in epidemiological studies.77 Zang J.B., Coates S.J., Huang J., Vonderheld E.C., Cohen B.A. Pityriasis lichenoides: long-term follow-up study. Pediatr Dermatol. 2018; 35:213-9.,99 Romaní J., Puig L., Fernández-Figueras M.T., Moragas J.M. Pityriasis lichenoides in children: clinicopathologic review of 22 patients. Pediatr Dermatol. 1998;15:1-6. The clinical presentation of PLC includes papules, desquamation, hypopigmentation, and annular lesions,11 Khachemoune A., Byumin M.L. Pityriasis lichenoides: pathophysiology, classification and treatment. Am J Clin Dermatol. 2007;8:29-36.,22 Lupu J., Chosidow O., Wolkenstein P., Bergqvist C., Ortonne N., Ingen-Housz-Oro S. Pityriasis lichenoides: a clinical and pathological case series of 49 patients with emphasis on follow-up. Clin Exp Dermatol. 2021;46:1561-6.,77 Zang J.B., Coates S.J., Huang J., Vonderheld E.C., Cohen B.A. Pityriasis lichenoides: long-term follow-up study. Pediatr Dermatol. 2018; 35:213-9. which were also the most frequent skin lesions in this study.

The lesions were mainly diffusely distributed in 19 (46.3%) patients, similar to the study by Romaní in Spain, which retrospectively evaluated 22 pediatric patients with PL and found that 64.2% had diffusely distributed lesions.99 Romaní J., Puig L., Fernández-Figueras M.T., Moragas J.M. Pityriasis lichenoides in children: clinicopathologic review of 22 patients. Pediatr Dermatol. 1998;15:1-6.

Regarding associated symptoms, Ersoy-Evans, in a retrospective analysis of 124 pediatric patients, observed that 85.7% were symptomatic and 62% of the symptoms were pruritus.1010 Jung F., Sibbald C., Bohdanowicz M., Ingram J.R., Piguet V. Systematic review of the efficacies and adverse effects of treatments for pityriasis lichenoides. Br J Dermatol. 2020;183:1026-32. In this study, most patients 25 (56.1%) were asymptomatic, but when present, the most prevalent symptom was also pruritus.

Triggering factors, such as fever, tonsillitis, parotitis, COVID-19 infection, and COVID-19 vaccination, were correlated with infectious diseases. Ersoy-Evans et al. identified infectious agents preceding disease onset in 30% of cases.88 Ersoy-Evans S., Greco M.F., Mancini A.J., Subasi N., Paller As. Pityriasis lichenoides in childhood: a retrospective review of 124 patients. J Am Acad Dermatol. 2007;56:205-10. In the study by Durusu et al., the onset of PL in a 42-year-old patient was 10 days after COVID-19 infection.55 Durusu G., Gurel G., Tokyol C. [A case of pityriasis lichenoides chronica in a patient with COVID-19 infection]. Actas Dermosifiliogr. 2022;113:S18-9. This supports the etiological hypothesis of lymphoproliferative disorders possibly triggered by antigenic stimuli, such as viruses or other infectious agents.55 Durusu G., Gurel G., Tokyol C. [A case of pityriasis lichenoides chronica in a patient with COVID-19 infection]. Actas Dermosifiliogr. 2022;113:S18-9. Another important finding of this study that corroborates this hypothesis was the peak incidence from 2004 to 2006, corresponding to a peak of viral meningitis that occurred in Southern Brazil in this period,1212 Ministério da Saúde (BR). Secretaria de Vigilância em Saúde. Vigilância em Saúde no Brasil 2003|2019: da criação da Secretaria de Vigilância em Saúde aos dias atuais. Bol Epidemiol.2019 set;50:51-52. [Cited 2024 Mar 12]. Available from: http://www.saude.gov.br/boletins-epidemiologicos.
http://www.saude.gov.br/boletins-epidemi...
and from 2019 to 2021, coinciding with the COVID-19 pandemic and its period of greatest contagion.1313 Ministério da Saúde (BR). Secretaria de Vigilância em Saúde. Guia de vigilância epidemiológica: emergência de saúde pública de importância nacional pela doença pelo covid-19. 2022;4:1-136. [Cited 2024 Mar 12]. Available from:https://www.gov.br/saude/pt-br/coronavirus/publicacoes-tecnicas/guias-e-planos/guia-de-vigilancia-epidemiologica-covid-19.
https://www.gov.br/saude/pt-br/coronavir...

Both Ersoy-Evans and Zang observed a seasonal characteristic of PL, with worsening in fall and winter. Although this study found a slightly higher prevalence in fall (11 patients - 26.8%) and winter (12 patients - 29.3%), this difference was not statistically significant and thus the authors could not affirm the existence of a seasonality for the disease.

The remission rate in this study was 71.9% (n = 23). When considering each treatment in isolation, 56.6% (n = 17) of patients treated with antibiotic therapy and 80% (n = 4) of patients treated with NB-UVB phototherapy had remission. These data are similar to the findings of Jung et al. in a systematic review of the treatment of PL with 27 articles, in which remission with antibiotic therapy ranged from 53 to 66% and with NB-UVB phototherapy was 75%.

Remission was greater the later the disease onset, up to 13 times greater when PL started after five years of age. Bellinato showed this in a systematic review of PL treatments, including 37 articles, in which pediatric patients had worse response rates to the proposed treatments compared with adults.44 Bellinato F., Maurelli M., Gisondi P., Girolomoni G. A systematic review of treatments for pityriasis lichenoides. J Eur Acad Dermatol Venereol. 2019;33:2039-49.

One of the main limitations of this study is its retrospective design and the lack of follow-up for nine of the 41 patients, besides the 4 patients without skin biopsy to confirm the diagnosis. Longer follow-up of patients treated with phototherapy is also necessary in order to assess whether the rate of remission is maintained.

In conclusion, PL is a rare disease, which makes its diagnosis challenging and late. Infectious agents should be considered important triggers of the disease. Remission was greater in patients with disease onset after five years of age and, although the response to antibiotic therapy was satisfactory, the response to phototherapy was superior.

Abbreviations

  • PL  Pityriasis lichenoides
  • PLEVA  Pityriasis lichenoides et varioliformis acuta
  • PLC  Pityriasis lichenoides chronica
  • OR  Odds ratio
  • HIV  Human Immunodeficiency Virus
  • NB-UVB  Narrowband ultraviolet B
  • USA  United States of America
  • Funding sources
    No funding was received to assist in the preparation of this manuscript.

References

  • 1
    Khachemoune A., Byumin M.L. Pityriasis lichenoides: pathophysiology, classification and treatment. Am J Clin Dermatol. 2007;8:29-36.
  • 2
    Lupu J., Chosidow O., Wolkenstein P., Bergqvist C., Ortonne N., Ingen-Housz-Oro S. Pityriasis lichenoides: a clinical and pathological case series of 49 patients with emphasis on follow-up. Clin Exp Dermatol. 2021;46:1561-6.
  • 3
    Chen Y., Zhao M., Xiang X., Wang Z., Xu Z., Ma L. Oral erythromycin in pityriasis lichenoides chronica and pityriasis lichenoides et varioliformis acuta. Dermatol Ther. 2020;33:e13311.
  • 4
    Bellinato F., Maurelli M., Gisondi P., Girolomoni G. A systematic review of treatments for pityriasis lichenoides. J Eur Acad Dermatol Venereol. 2019;33:2039-49.
  • 5
    Durusu G., Gurel G., Tokyol C. [A case of pityriasis lichenoides chronica in a patient with COVID-19 infection]. Actas Dermosifiliogr. 2022;113:S18-9.
  • 6
    Borra T., Custrin A., Saggini A., Fink-Puches R., Cota C., Vermi W., et al. Pityriasis lichenoides, atypical pityriasis lichenoides, and related conditions - a study of 66 cases. Am J Surg Pathol. 2018;00:1-12.
  • 7
    Zang J.B., Coates S.J., Huang J., Vonderheld E.C., Cohen B.A. Pityriasis lichenoides: long-term follow-up study. Pediatr Dermatol. 2018; 35:213-9.
  • 8
    Ersoy-Evans S., Greco M.F., Mancini A.J., Subasi N., Paller As. Pityriasis lichenoides in childhood: a retrospective review of 124 patients. J Am Acad Dermatol. 2007;56:205-10.
  • 9
    Romaní J., Puig L., Fernández-Figueras M.T., Moragas J.M. Pityriasis lichenoides in children: clinicopathologic review of 22 patients. Pediatr Dermatol. 1998;15:1-6.
  • 10
    Jung F., Sibbald C., Bohdanowicz M., Ingram J.R., Piguet V. Systematic review of the efficacies and adverse effects of treatments for pityriasis lichenoides. Br J Dermatol. 2020;183:1026-32.
  • 11
    Markus J.R., Carvalho V.O., Lima M.N., Abagge K.T., Nascimento A., Werner B. The relevance of recognizing clinical and morphologic features of pityriasis lichenoides: clinicopathological study of 29 cases. Dermatol Pract Concept. 2013;3:7-10.
  • 12
    Ministério da Saúde (BR). Secretaria de Vigilância em Saúde. Vigilância em Saúde no Brasil 2003|2019: da criação da Secretaria de Vigilância em Saúde aos dias atuais. Bol Epidemiol.2019 set;50:51-52. [Cited 2024 Mar 12]. Available from: http://www.saude.gov.br/boletins-epidemiologicos
    » http://www.saude.gov.br/boletins-epidemiologicos
  • 13
    Ministério da Saúde (BR). Secretaria de Vigilância em Saúde. Guia de vigilância epidemiológica: emergência de saúde pública de importância nacional pela doença pelo covid-19. 2022;4:1-136. [Cited 2024 Mar 12]. Available from:https://www.gov.br/saude/pt-br/coronavirus/publicacoes-tecnicas/guias-e-planos/guia-de-vigilancia-epidemiologica-covid-19
    » https://www.gov.br/saude/pt-br/coronavirus/publicacoes-tecnicas/guias-e-planos/guia-de-vigilancia-epidemiologica-covid-19

Publication Dates

  • Publication in this collection
    23 Sept 2024
  • Date of issue
    2024

History

  • Received
    25 Nov 2023
  • Accepted
    28 Mar 2024
  • Published
    24 Apr 2024
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