Ery A Ko, Maria E Cappetta, Milena Rangel, Maria Echeverria, Marina Abed, Cecilia Navarro Tuculet, Luis D Mazzuoccolo
Introduction: Frontal fibrosing alopecia (FFA) has been associated with hair cosmetic habits, yet causality and frequency-dependent effects remain uncertain. This study aimed to evaluate the association between hair care habits and FFA.
Methods: An analytical case-control study was conducted including 115 FFA patients and 112 matched controls, evaluated at the Hospital Italiano de Buenos Aires between 2015 and 2024. Participants reported current hair washing frequency, cosmetic hair practices, leave-in-product use, and sunscreen use; FFA cases also reported habits 5 years before symptom onset. Logistic regression models were performed.
Results: Decreasing hair washing frequency was associated with progressively higher odds of FFA (adjusted OR 18.7 for washing ≤1 time/week compared with daily washing). In dichotomized models, daily washing remained protective (adjusted OR 0.31; p = 0.012). Cosmetic hair procedures ≥2/year and leave-in product use ≥1/week significantly increased risk (adjusted OR 2.39 and 4.98, respectively). Sunscreen use showed no association with FFA in any model.
Conclusion: Frequent cosmetic procedures and leave-in product use were associated with higher odds of FFA, whereas daily washing was protective. These findings underscore the potential contribution of cumulative exposure to cosmetic substances in FFA pathogenesis and highlight modifiable behavioral factors warranting further study.
额部纤维化性脱发(FFA)与头发美容习惯有关,但因果关系和频率依赖性影响仍不确定。本研究旨在评估护发习惯与游离脂肪酸之间的关系。方法:对2015年至2024年在布宜诺斯艾利斯意大利医院进行的115例FFA患者和112例匹配对照进行分析性病例-对照研究。参与者报告了目前的洗头频率、美容美发习惯、免洗产品使用情况和防晒霜使用情况;FFA病例还报告了症状出现前5年的习惯。采用Logistic回归模型。结果:洗头频率的减少与FFA的发生率逐渐升高相关(与每日洗头相比,每周洗头≤1次的调整OR为18.7)。在二分类模型中,每日洗涤仍然具有保护作用(调整OR 0.31; p = 0.012)。美容美发≥2次/年和留发产品≥1次/周显著增加风险(调整后OR分别为2.39和4.98)。在任何模型中,防晒霜的使用都与FFA没有关联。结论:频繁的美容程序和使用免洗产品与FFA的几率较高有关,而日常洗涤则具有保护作用。这些发现强调了累积暴露于化妆品物质在FFA发病机制中的潜在作用,并强调了值得进一步研究的可改变的行为因素。
{"title":"Hair Care Habits and Frontal Fibrosing Alopecia: A Case-Control Study.","authors":"Ery A Ko, Maria E Cappetta, Milena Rangel, Maria Echeverria, Marina Abed, Cecilia Navarro Tuculet, Luis D Mazzuoccolo","doi":"10.1159/000549427","DOIUrl":"10.1159/000549427","url":null,"abstract":"<p><strong>Introduction: </strong>Frontal fibrosing alopecia (FFA) has been associated with hair cosmetic habits, yet causality and frequency-dependent effects remain uncertain. This study aimed to evaluate the association between hair care habits and FFA.</p><p><strong>Methods: </strong>An analytical case-control study was conducted including 115 FFA patients and 112 matched controls, evaluated at the Hospital Italiano de Buenos Aires between 2015 and 2024. Participants reported current hair washing frequency, cosmetic hair practices, leave-in-product use, and sunscreen use; FFA cases also reported habits 5 years before symptom onset. Logistic regression models were performed.</p><p><strong>Results: </strong>Decreasing hair washing frequency was associated with progressively higher odds of FFA (adjusted OR 18.7 for washing ≤1 time/week compared with daily washing). In dichotomized models, daily washing remained protective (adjusted OR 0.31; <i>p</i> = 0.012). Cosmetic hair procedures ≥2/year and leave-in product use ≥1/week significantly increased risk (adjusted OR 2.39 and 4.98, respectively). Sunscreen use showed no association with FFA in any model.</p><p><strong>Conclusion: </strong>Frequent cosmetic procedures and leave-in product use were associated with higher odds of FFA, whereas daily washing was protective. These findings underscore the potential contribution of cumulative exposure to cosmetic substances in FFA pathogenesis and highlight modifiable behavioral factors warranting further study.</p>","PeriodicalId":21844,"journal":{"name":"Skin Appendage Disorders","volume":" ","pages":""},"PeriodicalIF":1.3,"publicationDate":"2025-11-06","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12707933/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145775764","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Katherine Benandi, Diego A Ramos-Briceño, Francisco J La Bella-Villanueva, Alyssa Hansen, Ayezel Munoz Gonzalez
Introduction: Prior studies suggest that androgenetic alopecia (AGA) may increase cardiovascular and metabolic disease risk, but findings have been inconsistent due to methodological limitations, reliance on self-reported data, and small sample sizes. This study aimed to evaluate the association between AGA and cardiometabolic outcomes using large-scale clinical data.
Methods: We conducted a retrospective cohort study using the TriNetX US Collaborative Network to evaluate cardiometabolic outcomes, including abdominal obesity, dyslipidemia, hypertension, and diabetes mellitus, in 30,282 propensity-matched male patients (aged 18-45 years) diagnosed with AGA compared to 30,282 controls from general screening encounters. Outcomes were analyzed up to 5 years post-diagnosis using risk ratios (RRs), risk differences, and Kaplan-Meier survival analysis.
Results: Patients with AGA demonstrated significantly lower risks of abdominal obesity (RR: 0.53; 95% confidence interval [CI]: 0.45-0.61), dyslipidemia (RR: 0.63; 95% CI: 0.60-0.67), hypertension (RR: 0.59; 95% CI: 0.54-0.65), and diabetes mellitus (RR: 0.43; 95% CI: 0.36-0.51) compared to controls. Kaplan-Meier analysis confirmed a reduced hazard for diabetes mellitus (hazard ratio: 0.44; 95% CI: 0.37-0.52).
Conclusion: AGA diagnosis was not associated with increased cardiometabolic risk. The observed risk reduction may reflect healthcare-seeking behaviors rather than a biological relationship.
{"title":"Androgenetic Alopecia Is Not Associated with Increased Incidence of Cardiovascular Disease Risk Factors: A Retrospective Cohort Study.","authors":"Katherine Benandi, Diego A Ramos-Briceño, Francisco J La Bella-Villanueva, Alyssa Hansen, Ayezel Munoz Gonzalez","doi":"10.1159/000549420","DOIUrl":"10.1159/000549420","url":null,"abstract":"<p><strong>Introduction: </strong>Prior studies suggest that androgenetic alopecia (AGA) may increase cardiovascular and metabolic disease risk, but findings have been inconsistent due to methodological limitations, reliance on self-reported data, and small sample sizes. This study aimed to evaluate the association between AGA and cardiometabolic outcomes using large-scale clinical data.</p><p><strong>Methods: </strong>We conducted a retrospective cohort study using the TriNetX US Collaborative Network to evaluate cardiometabolic outcomes, including abdominal obesity, dyslipidemia, hypertension, and diabetes mellitus, in 30,282 propensity-matched male patients (aged 18-45 years) diagnosed with AGA compared to 30,282 controls from general screening encounters. Outcomes were analyzed up to 5 years post-diagnosis using risk ratios (RRs), risk differences, and Kaplan-Meier survival analysis.</p><p><strong>Results: </strong>Patients with AGA demonstrated significantly lower risks of abdominal obesity (RR: 0.53; 95% confidence interval [CI]: 0.45-0.61), dyslipidemia (RR: 0.63; 95% CI: 0.60-0.67), hypertension (RR: 0.59; 95% CI: 0.54-0.65), and diabetes mellitus (RR: 0.43; 95% CI: 0.36-0.51) compared to controls. Kaplan-Meier analysis confirmed a reduced hazard for diabetes mellitus (hazard ratio: 0.44; 95% CI: 0.37-0.52).</p><p><strong>Conclusion: </strong>AGA diagnosis was not associated with increased cardiometabolic risk. The observed risk reduction may reflect healthcare-seeking behaviors rather than a biological relationship.</p>","PeriodicalId":21844,"journal":{"name":"Skin Appendage Disorders","volume":" ","pages":""},"PeriodicalIF":1.3,"publicationDate":"2025-11-04","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12707934/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145775817","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Introduction: Pincer nail deformity (PND) involves excessive transverse nail plate over-curvature which pinches up distal nail bed and causes pain. Conventional surgical options are invasive with high complication risks. We treated pincer nails with a simplified, reproducible technique.
Methods: Records of PND patients treated over 7 years with a simplified technique were retrospectively analyzed. After confirming the absence of any distal bony abnormality, lateral 1/5th-1/6th of the nail plate was avulsed on both sides, with chemical matricectomy of the lateral matrix horn. Thereafter, the distal one-third nail plate was avulsed to relieve traction on the pinched nail bed, not typically included in earlier techniques. This dual approach targeted both the causative (broad matrix) and resultant (distal traction) components of PND.
Results: Records of 11 patients (15 great toenails) with symptomatic PND, without distal osteophytes, treated with this technique were analyzed. A mean follow-up of 28.6 ± 30.95 months with complete symptomatic relief and maintained nail flattening was seen. Patient-rated cosmetic outcomes were good (13), fair (3), or poor (1). Complications recorded were secondary infection (1), severe dystrophy (1), mild dystrophy (2), and malalignment (2).
Conclusion: This simplified surgical technique for PND is easy to learn and perform, and offers long-term effectiveness with minimal complications for PND without distal osteophytes.
{"title":"Surgical Management of Pincer Nail Deformity: A Simplified Technique.","authors":"Nikhil Mehta, Chander Grover","doi":"10.1159/000549343","DOIUrl":"10.1159/000549343","url":null,"abstract":"<p><strong>Introduction: </strong>Pincer nail deformity (PND) involves excessive transverse nail plate over-curvature which pinches up distal nail bed and causes pain. Conventional surgical options are invasive with high complication risks. We treated pincer nails with a simplified, reproducible technique.</p><p><strong>Methods: </strong>Records of PND patients treated over 7 years with a simplified technique were retrospectively analyzed. After confirming the absence of any distal bony abnormality, lateral 1/5th-1/6th of the nail plate was avulsed on both sides, with chemical matricectomy of the lateral matrix horn. Thereafter, the distal one-third nail plate was avulsed to relieve traction on the pinched nail bed, not typically included in earlier techniques. This dual approach targeted both the causative (broad matrix) and resultant (distal traction) components of PND.</p><p><strong>Results: </strong>Records of 11 patients (15 great toenails) with symptomatic PND, without distal osteophytes, treated with this technique were analyzed. A mean follow-up of 28.6 ± 30.95 months with complete symptomatic relief and maintained nail flattening was seen. Patient-rated cosmetic outcomes were good (13), fair (3), or poor (1). Complications recorded were secondary infection (1), severe dystrophy (1), mild dystrophy (2), and malalignment (2).</p><p><strong>Conclusion: </strong>This simplified surgical technique for PND is easy to learn and perform, and offers long-term effectiveness with minimal complications for PND without distal osteophytes.</p>","PeriodicalId":21844,"journal":{"name":"Skin Appendage Disorders","volume":" ","pages":""},"PeriodicalIF":1.3,"publicationDate":"2025-10-31","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12707960/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145775850","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Introduction: Psoriasis is a chronic, immune-mediated skin disease that affects approximately 125 million people worldwide. Psoriatic arthritis (PsA), a complex chronic inflammatory arthritis, is classified as part of the spondyloarthritis spectrum, along with primary ankylosing spondylitis, reactive arthritis, arthritis associated with inflammatory bowel disease, and undifferentiated spondyloarthritis.
Case presentation: We report 2 cases of patients with arthropathy who were referred by a rheumatologist. Thorough physical examination of the skin and nails revealed no psoriatic changes. However, despite the absence of scalp-related complaints, a diagnosis of psoriasis was established based on trichoscopic findings.
Conclusion: Cases in which patients with PsA have even mild cutaneous psoriatic lesions are common, making the diagnosis easier. The 2 cases described above highlight the role of trichoscopy and emphasize the importance of collaboration between dermatologists and rheumatologists. When rheumatologists investigate possible causes of arthritis and consider PsA as a differential diagnosis, referring the patient to a dermatologist is important. On the other hand, in cases of scalp psoriasis, if arthropathy is present, the patient should consult a rheumatologist to determine whether joint involvement is caused by another rheumatologic condition. In clinical practice, scalp psoriasis is frequently observed as an independent condition, and its presence does not exclude the possibility of other coexisting pathologies.
{"title":"How Scalp Trichoscopy Aids in the Diagnosis of Psoriasis in the Setting of Psoriatic Arthritis: Case Report.","authors":"Nino Khutsishvili, Mamuka Lortkipanidze, Irma Buchukuri, Giorgi Tkeshelashvili, Nino Lortkipanidze","doi":"10.1159/000549170","DOIUrl":"10.1159/000549170","url":null,"abstract":"<p><strong>Introduction: </strong>Psoriasis is a chronic, immune-mediated skin disease that affects approximately 125 million people worldwide. Psoriatic arthritis (PsA), a complex chronic inflammatory arthritis, is classified as part of the spondyloarthritis spectrum, along with primary ankylosing spondylitis, reactive arthritis, arthritis associated with inflammatory bowel disease, and undifferentiated spondyloarthritis.</p><p><strong>Case presentation: </strong>We report 2 cases of patients with arthropathy who were referred by a rheumatologist. Thorough physical examination of the skin and nails revealed no psoriatic changes. However, despite the absence of scalp-related complaints, a diagnosis of psoriasis was established based on trichoscopic findings.</p><p><strong>Conclusion: </strong>Cases in which patients with PsA have even mild cutaneous psoriatic lesions are common, making the diagnosis easier. The 2 cases described above highlight the role of trichoscopy and emphasize the importance of collaboration between dermatologists and rheumatologists. When rheumatologists investigate possible causes of arthritis and consider PsA as a differential diagnosis, referring the patient to a dermatologist is important. On the other hand, in cases of scalp psoriasis, if arthropathy is present, the patient should consult a rheumatologist to determine whether joint involvement is caused by another rheumatologic condition. In clinical practice, scalp psoriasis is frequently observed as an independent condition, and its presence does not exclude the possibility of other coexisting pathologies.</p>","PeriodicalId":21844,"journal":{"name":"Skin Appendage Disorders","volume":" ","pages":""},"PeriodicalIF":1.3,"publicationDate":"2025-10-23","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12707961/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145775832","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Laiza Bertolucci Ferrero, Guilherme Camargo Julio Valinoto, Gustavo Carvalho, John Verrinder Veasey
Introduction: Onychomycosis is the most common nail disorder in dermatology. Treatment can be challenging due to factors related to the pathogen and the patient's health status. Therapeutic options include topical and oral antifungals; while oral agents offer higher cure rates, they also present drawbacks such as prolonged treatment duration and potential adverse effects, with liver toxicity being the most frequently reported. Previous reviews highlight a scarcity of studies addressing the actual frequency of liver enzyme alterations during therapy.
Methods: This retrospective study analyzed medical records from 313 patients treated at the Dermatology Clinic of a tertiary hospital. Changes in hepatic transaminases (aspartate aminotransferase, aspartate aminotransferase/TGO, and alanine aminotransferase, alanine aminotransferase/TGP) were evaluated in patients with a confirmed diagnosis of onychomycosis undergoing treatment with systemic antifungals.
Results: Among 229 patients, 22 (9.6%) exhibited elevated hepatic transaminase levels. Oral antifungals demonstrated an overall favorable safety profile, with a low rate of transaminase elevation and no cases of hepatotoxicity. Patients with multiple comorbidities and concomitant medication use were more likely to present laboratory abnormalities, suggesting a possible cumulative effect on hepatic metabolism.
Conclusion: In a real-world tertiary hospital setting, where most patients carried multiple comorbidities and were on continuous medications, oral antifungals for onychomycosis demonstrated a reassuring hepatic safety profile. The low incidence of enzyme alterations, all reversible after drug withdrawal, supports the continued use of systemic therapy in appropriately selected patients, reinforcing that comorbidities alone should not preclude oral antifungal treatment when clinically indicated.
{"title":"Hepatic Transaminases Evaluation in Patients with Onychomycosis Treated with Oral Antifungals: A Retrospective Study with 229 Patients.","authors":"Laiza Bertolucci Ferrero, Guilherme Camargo Julio Valinoto, Gustavo Carvalho, John Verrinder Veasey","doi":"10.1159/000548989","DOIUrl":"10.1159/000548989","url":null,"abstract":"<p><strong>Introduction: </strong>Onychomycosis is the most common nail disorder in dermatology. Treatment can be challenging due to factors related to the pathogen and the patient's health status. Therapeutic options include topical and oral antifungals; while oral agents offer higher cure rates, they also present drawbacks such as prolonged treatment duration and potential adverse effects, with liver toxicity being the most frequently reported. Previous reviews highlight a scarcity of studies addressing the actual frequency of liver enzyme alterations during therapy.</p><p><strong>Methods: </strong>This retrospective study analyzed medical records from 313 patients treated at the Dermatology Clinic of a tertiary hospital. Changes in hepatic transaminases (aspartate aminotransferase, aspartate aminotransferase/TGO, and alanine aminotransferase, alanine aminotransferase/TGP) were evaluated in patients with a confirmed diagnosis of onychomycosis undergoing treatment with systemic antifungals.</p><p><strong>Results: </strong>Among 229 patients, 22 (9.6%) exhibited elevated hepatic transaminase levels. Oral antifungals demonstrated an overall favorable safety profile, with a low rate of transaminase elevation and no cases of hepatotoxicity. Patients with multiple comorbidities and concomitant medication use were more likely to present laboratory abnormalities, suggesting a possible cumulative effect on hepatic metabolism.</p><p><strong>Conclusion: </strong>In a real-world tertiary hospital setting, where most patients carried multiple comorbidities and were on continuous medications, oral antifungals for onychomycosis demonstrated a reassuring hepatic safety profile. The low incidence of enzyme alterations, all reversible after drug withdrawal, supports the continued use of systemic therapy in appropriately selected patients, reinforcing that comorbidities alone should not preclude oral antifungal treatment when clinically indicated.</p>","PeriodicalId":21844,"journal":{"name":"Skin Appendage Disorders","volume":" ","pages":""},"PeriodicalIF":1.3,"publicationDate":"2025-10-21","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12707920/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145775766","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Claudia Montoya, Juan Camilo Marchán Cárdenas, Jairo Fuentes-Carrascal, Esperanza Meléndez, Beatriz Orozco-Sebá, Oscar Niebles
Introduction: Follicular mucinosis (FM) is characterized by mucin deposition within hair follicles and sebaceous glands, sometimes causing irreversible alopecia. In adults, it is often secondary to cutaneous T-cell lymphoma (CTCL), particularly the folliculotropic mycosis fungoides (FMF) variant. Extensive scalp involvement is rare and may mimic inflammatory or infectious disorders, delaying diagnosis.
Case presentation: A 64-year-old woman presented with progressive diffuse alopecia, suppurative scalp nodules, comedones, leonine facies, and multiple erythematous plaques. Initial biopsies elsewhere suggested tuberculoid leprosy, and multidrug therapy produced no improvement. Trichoscopy showed nonspecific signs suggestive of dissecting cellulitis, but histopathology revealed mucinous follicular destruction and a perifollicular lymphocytic infiltrate with immunophenotypic features of CTCL. Large-cell transformation was present in 10% of the infiltrate. Staging confirmed advanced FMF with secondary FM. Treatment with brentuximab vedotin achieved partial hair regrowth and skin improvement.
Conclusion: This case describes an unusual presentation of FMF, in which diffuse alopecia with suppurative nodules was the first manifestation of secondary FM. Brentuximab vedotin may have a therapeutic role in mucinous alopecia in this context.
{"title":"Extensive Alopecia Mucinosa and Response to Brentuximab Vedotin: A Case Report.","authors":"Claudia Montoya, Juan Camilo Marchán Cárdenas, Jairo Fuentes-Carrascal, Esperanza Meléndez, Beatriz Orozco-Sebá, Oscar Niebles","doi":"10.1159/000548941","DOIUrl":"10.1159/000548941","url":null,"abstract":"<p><strong>Introduction: </strong>Follicular mucinosis (FM) is characterized by mucin deposition within hair follicles and sebaceous glands, sometimes causing irreversible alopecia. In adults, it is often secondary to cutaneous T-cell lymphoma (CTCL), particularly the folliculotropic mycosis fungoides (FMF) variant. Extensive scalp involvement is rare and may mimic inflammatory or infectious disorders, delaying diagnosis.</p><p><strong>Case presentation: </strong>A 64-year-old woman presented with progressive diffuse alopecia, suppurative scalp nodules, comedones, leonine facies, and multiple erythematous plaques. Initial biopsies elsewhere suggested tuberculoid leprosy, and multidrug therapy produced no improvement. Trichoscopy showed nonspecific signs suggestive of dissecting cellulitis, but histopathology revealed mucinous follicular destruction and a perifollicular lymphocytic infiltrate with immunophenotypic features of CTCL. Large-cell transformation was present in 10% of the infiltrate. Staging confirmed advanced FMF with secondary FM. Treatment with brentuximab vedotin achieved partial hair regrowth and skin improvement.</p><p><strong>Conclusion: </strong>This case describes an unusual presentation of FMF, in which diffuse alopecia with suppurative nodules was the first manifestation of secondary FM. Brentuximab vedotin may have a therapeutic role in mucinous alopecia in this context.</p>","PeriodicalId":21844,"journal":{"name":"Skin Appendage Disorders","volume":" ","pages":""},"PeriodicalIF":1.3,"publicationDate":"2025-10-14","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12707941/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145775834","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Introduction: Dyskeratosis congenita (DC) is a rare inherited telomere biology disorder characterized by mucocutaneous and systemic manifestations. There are limited descriptions of hair involvement.
Case presentation: We present the case of a 19-year-old male from a consanguineous family, diagnosed with DC, who exhibited classical dermatological and hematological features, as well as distinctive trichoscopic findings, including scattered irregular black dots, pigtail hairs, S-shaped and zigzag hairs, and microscopic evidence of cuticular abnormalities, including ruffled surfaces, flat fractures, and trichoptilosis.
Conclusion: This case highlights the under-recognized spectrum of hair pathology in DC, supporting the role of telomere dysfunction in impairing hair follicle homeostasis and structural integrity.
{"title":"Case Report of Hair Abnormalities in Dyskeratosis Congenita: A Trichoscopic and Microscopic Analysis.","authors":"Mariem Tabka, Asmahane Souissi, Feriel Amri, Malek Mrad, Mourad Mokni","doi":"10.1159/000548845","DOIUrl":"10.1159/000548845","url":null,"abstract":"<p><strong>Introduction: </strong>Dyskeratosis congenita (DC) is a rare inherited telomere biology disorder characterized by mucocutaneous and systemic manifestations. There are limited descriptions of hair involvement.</p><p><strong>Case presentation: </strong>We present the case of a 19-year-old male from a consanguineous family, diagnosed with DC, who exhibited classical dermatological and hematological features, as well as distinctive trichoscopic findings, including scattered irregular black dots, pigtail hairs, S-shaped and zigzag hairs, and microscopic evidence of cuticular abnormalities, including ruffled surfaces, flat fractures, and trichoptilosis.</p><p><strong>Conclusion: </strong>This case highlights the under-recognized spectrum of hair pathology in DC, supporting the role of telomere dysfunction in impairing hair follicle homeostasis and structural integrity.</p>","PeriodicalId":21844,"journal":{"name":"Skin Appendage Disorders","volume":" ","pages":""},"PeriodicalIF":1.3,"publicationDate":"2025-10-13","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12707919/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145775847","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-10-01Epub Date: 2025-02-12DOI: 10.1159/000544184
Wenjianbin Zhou, Shenghao Xu
{"title":"Insights and Recommendations from a Case-Control Study of Trichotillomania.","authors":"Wenjianbin Zhou, Shenghao Xu","doi":"10.1159/000544184","DOIUrl":"10.1159/000544184","url":null,"abstract":"","PeriodicalId":21844,"journal":{"name":"Skin Appendage Disorders","volume":"11 5","pages":"472-474"},"PeriodicalIF":1.3,"publicationDate":"2025-10-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12500293/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145245220","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-10-01Epub Date: 2025-02-05DOI: 10.1159/000544026
Amnuay Kleebayoon, Viroj Wiwanitkit
{"title":"Hurley Staging Training for Hidradenitis Suppurativa Patients: Comment.","authors":"Amnuay Kleebayoon, Viroj Wiwanitkit","doi":"10.1159/000544026","DOIUrl":"10.1159/000544026","url":null,"abstract":"","PeriodicalId":21844,"journal":{"name":"Skin Appendage Disorders","volume":"11 5","pages":"398"},"PeriodicalIF":1.3,"publicationDate":"2025-10-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12500292/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145245227","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-10-01Epub Date: 2025-02-14DOI: 10.1159/000544023
Olivia M Burke, Brianna Sa, David Alvarez Cespedes, Antonella Tosti
Background: Glucagon-like peptide-1 receptor agonists (GLP-1RAs) are an innovative class of medications primarily used to manage type 2 diabetes and obesity. These agents not only improve glycemic control but also promote significant weight loss and reduce cardiovascular risk.
Summary: GLP-1RAs are associated with various dermatologic effects, including injection-site reactions and immune-mediated responses such as hypersensitivity, urticaria, and bullous pemphigoid. "Ozempic face," a term describing facial fat loss, has gained media attention due to its cosmetic implications. Additionally, hair loss, particularly in the form of telogen effluvium, has been observed, potentially linked to rapid weight loss from GLP-1RA use. Emerging evidence also highlights the therapeutic potential of GLP-1RAs in enhancing wound healing and treating inflammatory skin conditions like psoriasis.
Key messages: With the increasing use of GLP-1RAs for weight management, clinicians should remain alert to dermatologic side effects and consider appropriate dermatologic consultations when needed. Further research is essential to optimize the safe and effective use of GLP-1RAs, ensuring therapeutic benefits are maximized while minimizing adverse dermatologic outcomes.
{"title":"Dermatologic Implications of Glucagon-Like Peptide-1 Receptor Agonist Medications.","authors":"Olivia M Burke, Brianna Sa, David Alvarez Cespedes, Antonella Tosti","doi":"10.1159/000544023","DOIUrl":"10.1159/000544023","url":null,"abstract":"<p><strong>Background: </strong>Glucagon-like peptide-1 receptor agonists (GLP-1RAs) are an innovative class of medications primarily used to manage type 2 diabetes and obesity. These agents not only improve glycemic control but also promote significant weight loss and reduce cardiovascular risk.</p><p><strong>Summary: </strong>GLP-1RAs are associated with various dermatologic effects, including injection-site reactions and immune-mediated responses such as hypersensitivity, urticaria, and bullous pemphigoid. \"Ozempic face,\" a term describing facial fat loss, has gained media attention due to its cosmetic implications. Additionally, hair loss, particularly in the form of telogen effluvium, has been observed, potentially linked to rapid weight loss from GLP-1RA use. Emerging evidence also highlights the therapeutic potential of GLP-1RAs in enhancing wound healing and treating inflammatory skin conditions like psoriasis.</p><p><strong>Key messages: </strong>With the increasing use of GLP-1RAs for weight management, clinicians should remain alert to dermatologic side effects and consider appropriate dermatologic consultations when needed. Further research is essential to optimize the safe and effective use of GLP-1RAs, ensuring therapeutic benefits are maximized while minimizing adverse dermatologic outcomes.</p>","PeriodicalId":21844,"journal":{"name":"Skin Appendage Disorders","volume":"11 5","pages":"416-423"},"PeriodicalIF":1.3,"publicationDate":"2025-10-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12500303/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145245205","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}