Alexandra Savage, Vera Y Miao, Gayle Fischer, Matthew Merriman, Kylie-Ann Mallitt, Rebecca B Saunderson
{"title":"Long-Term Outcomes of Prepubertal-Onset Vulvar Lichen Sclerosus.","authors":"Alexandra Savage, Vera Y Miao, Gayle Fischer, Matthew Merriman, Kylie-Ann Mallitt, Rebecca B Saunderson","doi":"10.1111/pde.70056","DOIUrl":"https://doi.org/10.1111/pde.70056","url":null,"abstract":"<p><strong>Background: </strong>Vulvar lichen sclerosus (VLS) is a chronic inflammatory dermatosis affecting the vulvar and perianal skin. VLS has a bimodal age of onset, in pre-pubertal and post-menopausal age groups. Long-term outcomes of pre-pubertal VLS are unclear. This study aimed to establish the long-term disease activity, factors that influence disease progression, and the physical and psychological complications of pediatric VLS persisting into adulthood.</p><p><strong>Methods: </strong>A cohort study was conducted in women diagnosed with VLS pre-menarche. A retrospective chart review of 135 case records was completed. The remaining data collection occurred prospectively through (i) study questionnaires, including quality of life as assessed by the Vulvar Quality of Life Index (VQLI), and (ii) dermatologist assessments.</p><p><strong>Results: </strong>Of 135 patients screened, 68 were included. The mean age of diagnosis was 7.5 years, and the mean duration of follow-up was 12.8 years. 62% of cases achieved remission. Of patients who were adherent to treatment, 92.3% achieved remission, compared to 56.6% of patients who were non- or partially adherent. Adherence declined from menarche into early adolescence. Patients who were adherent had 60% fewer structural abnormalities. In addition, VQLI scores indicated significantly better quality of life with adherence (mean = 1.6/45) compared to partially or non-adherence (mean = 5.2/45).</p><p><strong>Conclusions: </strong>This study informs clinicians of the long-term prognosis of VLS diagnosed pre-pubertally: 62% of patients achieved remission, and the rates of remission were higher in those who adhered to treatment. Structural changes and scarring were reduced in those who adhered to treatment.</p>","PeriodicalId":19819,"journal":{"name":"Pediatric Dermatology","volume":" ","pages":""},"PeriodicalIF":1.2,"publicationDate":"2025-10-13","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145286701","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Rahwa Hailemichael, Sydney A Martin, Austin Hwang, Julia M Riley, Kelsey S Flood, Ziyou Ren
{"title":"Comorbidities of Pediatric Patients With Hidradenitis Suppurativa in the Emergency Department Setting: A Cross-Sectional Study.","authors":"Rahwa Hailemichael, Sydney A Martin, Austin Hwang, Julia M Riley, Kelsey S Flood, Ziyou Ren","doi":"10.1111/pde.70054","DOIUrl":"https://doi.org/10.1111/pde.70054","url":null,"abstract":"<p><p>Hidradenitis suppurativa (HS) often leads to painful episodes requiring emergency department (ED) care, yet little is known about the comorbidities associated with these visits in pediatric patients. This study examined the Nationwide Emergency Department Sample (NEDS) from 2006 to 2019, identifying HS diagnoses via ICD-9 and ICD-10 codes to evaluate associated comorbidities. Pediatric HS ED visits were linked with 17 comorbidities, including systemic lupus erythematosus, as well as various psychosocial, endocrine, and dermatologic conditions. These findings highlight the need for expanded comorbidity screening in pediatric HS care.</p>","PeriodicalId":19819,"journal":{"name":"Pediatric Dermatology","volume":" ","pages":""},"PeriodicalIF":1.2,"publicationDate":"2025-10-13","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145286711","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Mia A Mologousis, Racquel A Bitar, Anna L Pinto, Joanne M Rispoli, Marilyn G Liang
{"title":"Early Magnetic Resonance Imaging as a Screen for Sturge-Weber Syndrome-Related Seizures in Infants With Upper-Facial Capillary Malformations.","authors":"Mia A Mologousis, Racquel A Bitar, Anna L Pinto, Joanne M Rispoli, Marilyn G Liang","doi":"10.1111/pde.70032","DOIUrl":"https://doi.org/10.1111/pde.70032","url":null,"abstract":"<p><strong>Background: </strong>Upper-facial capillary malformation (CM) may be concerning for Sturge-Weber syndrome (SWS). Use of screening magnetic resonance imaging (MRI) for neuroradiographic findings of SWS is controversial. MRI within a few months of life may allow for prompt reassurance, preventive treatments, and avoidance of contrast and sedation. However, false-negative MRI before 1 year of age has been reported. We examined the ability of early MRI to predict seizure development in infants with upper-facial CM.</p><p><strong>Methods: </strong>Infants with forehead or temple CM presenting to the Sturge-Weber Clinic at Boston Children's Hospital from 2012 to 2022 were identified. The records were reviewed for clinical features and for findings from MRI performed before 1 year of age (MRI 1) and repeated around or after 2 years of age (MRI 2). Patients with seizures before MRI 1 or with a diagnosis of nevus simplex were excluded.</p><p><strong>Results: </strong>Thirty-three patients with forehead or temple CM without seizures before MRI 1 were identified. MRI 1 was abnormal in 20/33 and normal in 13/33. Fourteen of 20 patients with abnormal MRI 1 developed seizures. Of the 13 patients with normal MRI 1, 11 underwent MRI 2. In patients with MRI 2, 3/11 developed SWS-related abnormalities, but none (0/11) developed seizures. The remaining 2 patients with normal MRI 1 also did not develop seizures. Mean follow-up age was 6.1 years (0.83-15 years).</p><p><strong>Conclusion: </strong>Early, high-quality non-contrast 3 T MRI may screen for seizure development in infants with upper-facial CM.</p>","PeriodicalId":19819,"journal":{"name":"Pediatric Dermatology","volume":" ","pages":""},"PeriodicalIF":1.2,"publicationDate":"2025-10-13","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145286644","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
{"title":"Examining the Impacts of Social Drivers of Health and Adverse Childhood Experiences in Children With Dermatological Disease: Part I: An Update and Review for Pediatric Dermatologists.","authors":"Toyosi Oluwole, Jeanette Zambito, Sarah J Coates","doi":"10.1111/pde.70050","DOIUrl":"https://doi.org/10.1111/pde.70050","url":null,"abstract":"<p><p>Social drivers of health (SDH) are defined as the conditions in which people are born, live, learn, work, play, and age. These non-medical factors affect a wide range of health-related behaviors and outcomes and can be predictive of the development of chronic medical conditions. Moreover, having one or more negative SDH can influence the availability and feasibility of treatment options, as well as response to treatment. While research has increasingly shown that addressing SDH is critical to achieving optimal health outcomes for all patients across multiple fields of medicine, the field of dermatology is trailing behind other specialties in identifying and addressing SDH. Children face special barriers to care due to their relative inability to advocate for themselves and their increased likelihood of experiencing poverty, food insecurity, and housing insecurity in the United States. Many children also experience adverse childhood experiences (ACEs), and these traumatic stressors are associated with the development of chronic health conditions and diminished life expectancy. Numerous studies have demonstrated the effects of SDH and ACEs on the prevalence of and outcomes for common pediatric skin conditions, including atopic dermatitis, psoriasis, hidradenitis suppurativa, and acne vulgaris. Pediatric dermatologists should learn how to identify and screen for social risk in the clinical environment and know how to address these effectively in their practice to improve the health of all children.</p>","PeriodicalId":19819,"journal":{"name":"Pediatric Dermatology","volume":" ","pages":""},"PeriodicalIF":1.2,"publicationDate":"2025-10-13","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145286655","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Maria Fernanda Alvarez-Alatriste, Andrea Gallardo-Villamil, Cristian M Salgado-Flores, Carrie C Coughlin, Liza Siegel, Leah Lalor, Kelly M Cordoro, Christine Wong, María Teresa García-Romero
{"title":"Agminated, Eruptive Nevi in Patients With a History of Langerhans Cell Histiocytosis.","authors":"Maria Fernanda Alvarez-Alatriste, Andrea Gallardo-Villamil, Cristian M Salgado-Flores, Carrie C Coughlin, Liza Siegel, Leah Lalor, Kelly M Cordoro, Christine Wong, María Teresa García-Romero","doi":"10.1111/pde.70040","DOIUrl":"https://doi.org/10.1111/pde.70040","url":null,"abstract":"<p><p>This multicenter, descriptive, retrospective study conducted at four centers aimed to describe the clinical, histological, and/or genetic characteristics and clinical course of pediatric patients with a history of Langerhans cell histiocytosis (LCH) who later developed eruptive melanocytic nevi from 2003 to 2023. Of seven patients diagnosed with LCH (average age of 18 months, range 0-96), five patients showed multisystem involvement affecting low-risk organs, while two presented with single-system disease localized to the skin. Agminated eruptive melanocytic nevi developed at an average of 48 months (SD ± 27.37) after initial LCH diagnosis, predominating on the trunk, groin, and upper extremities (in three patients at sites of previous LCH lesions). Agminated eruptive melanocytic nevi may appear in patients with LCH; further research is required to achieve a more comprehensive understanding.</p>","PeriodicalId":19819,"journal":{"name":"Pediatric Dermatology","volume":" ","pages":""},"PeriodicalIF":1.2,"publicationDate":"2025-10-09","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145258805","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
{"title":"Quality of Life in Pediatric Hidradenitis Suppurativa: A Cross-Sectional Study.","authors":"Charles B Lau, Eric Xia, Lisa Y Shen","doi":"10.1111/pde.70042","DOIUrl":"https://doi.org/10.1111/pde.70042","url":null,"abstract":"<p><p>Hidradenitis Suppurativa (HS) in children and adolescents is underrecognized and understudied, despite its significant impact during a critical period of identity formation and psychosocial development. We conducted a cross-sectional survey of 18 pediatric HS patients at a safety-net hospital, assessing quality of life (QoL) burden using three instruments: (1) the Patient Health Questionnaire-2 (PHQ-2) for depression screening, (2) the Children's Dermatology Life Quality Index (CDLQI), and (3) a pediatric-adapted version of the Hidradenitis Suppurativa Quality of Life Score (HiSQOL-Adolescent). While QoL impairment generally correlated with disease severity, some patients with early-stage disease (Hurley Stage I) screened positive for depression and reported the highest QoL burden, highlighting that clinical severity may not fully capture the lived experience of patients. These findings support the need for psychosocial screening and holistic care in pediatric HS.</p>","PeriodicalId":19819,"journal":{"name":"Pediatric Dermatology","volume":" ","pages":""},"PeriodicalIF":1.2,"publicationDate":"2025-10-09","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145258798","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Adaora Ewulu, Theresa Chikodi Ohaya, Natasha Mesinkovska, Maria Gnarra Buethe
{"title":"Connecting Families to Care: Nonprofit Wig Resources for Children.","authors":"Adaora Ewulu, Theresa Chikodi Ohaya, Natasha Mesinkovska, Maria Gnarra Buethe","doi":"10.1111/pde.70075","DOIUrl":"https://doi.org/10.1111/pde.70075","url":null,"abstract":"<p><p>Children with hair loss experience significant psychosocial impacts, yet access to wigs, also known as cranial prostheses, remains limited by high costs, inconsistent insurance coverage, and lack of family knowledge about available resources. We identified eight nonprofit organizations providing free or low-cost wigs to children in the United States. We developed a standardized questionnaire to properly assess cranial prosthetic services among those organizations. Providers caring for children with hair loss will be able to use this updated resource list and incorporate wig information into patient alopecia education to help families navigate these vital but fragmented services.</p>","PeriodicalId":19819,"journal":{"name":"Pediatric Dermatology","volume":" ","pages":""},"PeriodicalIF":1.2,"publicationDate":"2025-10-09","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145258882","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
{"title":"Teaching Pediatric Dermatology to Primary Care Residents: Valued in Principle, Undervalued in Practice.","authors":"Maria Gnarra Buethe, Jennifer Schoch","doi":"10.1111/pde.70058","DOIUrl":"https://doi.org/10.1111/pde.70058","url":null,"abstract":"","PeriodicalId":19819,"journal":{"name":"Pediatric Dermatology","volume":" ","pages":""},"PeriodicalIF":1.2,"publicationDate":"2025-10-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145252379","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Sarah Lee, Valerie M Carlberg, Patricia Todd, Birgitta A R Schmidt, Anna Cristina Garza-Mayers, Tina Ho
{"title":"Continuous Subcutaneous Insulin Infusion (CSII)-Associated Granulomatous Suppurative Reaction in Four Children With Type 1 Diabetes.","authors":"Sarah Lee, Valerie M Carlberg, Patricia Todd, Birgitta A R Schmidt, Anna Cristina Garza-Mayers, Tina Ho","doi":"10.1111/pde.70030","DOIUrl":"https://doi.org/10.1111/pde.70030","url":null,"abstract":"<p><p>With the increasing use of continuous glucose monitors and continuous subcutaneous insulin infusion (CSII) devices in pediatric patients with type 1 diabetes (T1DM), dermatologic complications are being reported more frequently. We describe four children with T1DM who developed persistent erythematous nodules with suppurative granulomatous inflammation at prior CSII injection sites. Treatment responses varied: one child improved after transitioning to subcutaneous insulin injections, another with oral dapsone, a third after switching CSII devices and limiting placement to the abdomen, and a fourth with topical corticosteroids and antibiotic ointment. This rare complication appears unrelated to specific device models or insulin types, highlighting the need for further studies to identify risk factors and guide optimal management.</p>","PeriodicalId":19819,"journal":{"name":"Pediatric Dermatology","volume":" ","pages":""},"PeriodicalIF":1.2,"publicationDate":"2025-10-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145252368","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Francesco Zulian, Luca Spiezia, Antonio Amabile, Francesca Tirelli, Alessandra Meneghel
{"title":"Successful Treatment of Severe Purpura Fulminans With Anakinra.","authors":"Francesco Zulian, Luca Spiezia, Antonio Amabile, Francesca Tirelli, Alessandra Meneghel","doi":"10.1111/pde.70034","DOIUrl":"https://doi.org/10.1111/pde.70034","url":null,"abstract":"<p><p>Purpura fulminans (PF) is a rare, often fatal pediatric condition characterized by intravascular thrombosis and hemorrhagic infarction of the skin. A timely diagnosis and treatment are paramount to prevent the involvement of internal organs, causing disseminated intravascular coagulation and gangrene of the extremities. The management of PF requires a comprehensive approach, including the treatment of the underlying infection, anticoagulation, and anti-inflammatory therapy. Herein we present the case of a child with severe PF successfully treated with anakinra, an anti-IL1-receptor monoclonal antibody.</p>","PeriodicalId":19819,"journal":{"name":"Pediatric Dermatology","volume":" ","pages":""},"PeriodicalIF":1.2,"publicationDate":"2025-10-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145252361","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}