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Çocukluk Çağı Vitiligosunun Demografik, Klinik ve Laboratuvar Özellikleri: 179 Hastanın Retrospektif Kesitsel Analizi

Yıl 2025, Cilt: 47 Sayı: 6, 964 - 974, 26.09.2025
https://doi.org/10.20515/otd.1733462

Öz

Vitiligo edinsel bir pigmentasyon bozukluğudur. Çocukluk çağı vitiligosu, erişkin başlangıçlı vitiligodan çeşitli açılardan farklılıklar gösterebilir. Bu çalışmada, çocuklardaki vitiligonun demografik ve klinik özellikleri ile laboratuvar sonuçlarının değerlendirilmesi amaçlandı. Vitiligo tanısı konmuş 18 yaş altı pediatrik hastalarda retrospektif, kesitsel bir çalışma yürütüldü. Demografik veriler, klinik özellikler ve tanı anındaki laboratuvar test sonuçları tıbbi kayıtlardan elde edildi. Vitiligo; non-segmental (NSV), segmental (SV) ve sınıflandırılamayan vitiligo olarak sınıflandırıldı. Toplam 179 hasta çalışmaya dahil edildi. Kadın/erkek oranı 1,2/1 idi. En yaygın form NSV (%87,7) olup, bunu SV (%7,3) izledi. NSV grubunda en yaygın alt tip, %42,5 ile jeneralize vitiligo olurken, bunu lokalize (%32,4) ve akrofasyal (%8,9) vitiligo izledi. Vitiligo, 156 (%88,6) hastada 12 yaş ve altında başlamıştı. NSV ve SV; cinsiyet, hastalığın başlangıç yaşı, hastalık süresi, halo nevüs ve Köbner fenomeni açısından anlamlı bir farklılık göstermedi (P > 0,05). Lökotrişi, SV grubunda (%84,6), NSV grubuna (%7,6) göre anlamlı derecede daha yaygındı (P < 0,001). En sık etkilenen vücut bölgesi yüzdü (%67,6). Nötrofil yüzdesi, ortalama trombosit hacmi (MPV), MPV/trombosit oranı, MPV/lenfosit oranı, nötrofil/lenfosit oranı (NLR), türetilmiş NLR ve sistemik inflamatuar yanıt indeksi, erken başlangıçlı (≤ 12 yaş) vitiligo hastalarında anlamlı olarak daha düşüktü; bu durum, küçük çocuklar ile ergenler arasındaki inflamatuar yanıt farklılığını gösterebilir. Dikkat çekici olarak, eozinofil sayısı, eozinofil/monosit oranı ve eozinofil/nötrofil oranı, kadın hastalarda anlamlı şekilde daha düşüktü. Bu durum, cinsiyet hormonlarının eozinofiller üzerindeki etkisini yansıtabilir. Bulgularımızı genişletmek için daha fazla çalışmaya ihtiyaç vardır.

Kaynakça

  • 1. Rodrigues M, Ezzedine K, Hamzavi I, Pandya AG, Harris JE. New discoveries in the pathogenesis and classification of vitiligo. J Am Acad Dermatol. 2017;77(1):1-13.
  • 2. Gandhi K, Ezzedine K, Anastassopoulos KP, Patel R, Sikirica V, Daniel SR, et al. Prevalence of Vitiligo Among Adults in the United States. JAMA Dermatol. 2022;158(1):43-50.
  • 3. Alikhan A, Felsten LM, Daly M, Petronic-Rosic V. Vitiligo: a comprehensive overview Part I. Introduction, epidemiology, quality of life, diagnosis, differential diagnosis, associations, histopathology, etiology, and work-up. J Am Acad Dermatol. 2011;65(3):473-91.
  • 4. Nicolaidou E, Mastraftsi S, Tzanetakou V, Rigopoulos D. Childhood Vitiligo. Am J Clin Dermatol. 2019;20(4):515-26.
  • 5. AL-smadi K, Imran M, Leite-Silva VR, Mohammed Y. Vitiligo: A Review of Aetiology, Pathogenesis, Treatment, and Psychosocial Impact. Cosmetics. 2023;10(3):84.
  • 6. Marchioro HZ, Silva de Castro CC, Fava VM, Sakiyama PH, Dellatorre G, Miot HA. Update on the pathogenesis of vitiligo. An Bras Dermatol. 2022;97(4):478-90.
  • 7. Ezzedine K, Lim HW, Suzuki T, Katayama I, Hamzavi I, Lan CC, et al. Revised classification/nomenclature of vitiligo and related issues: the Vitiligo Global Issues Consensus Conference. Pigment Cell Melanoma Res. 2012;25(3):E1-13.
  • 8. van Geel N, Speeckaert R, Taïeb A, Ezzedine K, Lim HW, Pandya AG, et al. Worldwide expert recommendations for the diagnosis and management of vitiligo: Position statement from the International Vitiligo Task Force Part 1: towards a new management algorithm. J Eur Acad Dermatol Venereol. 2023;37(11):2173-84.
  • 9. Bergqvist C, Ezzedine K. Vitiligo: A Review. Dermatology. 2020;236(6):571-92.
  • 10. Farajzadeh S, Khalili M, Mirmohammadkhani M, Paknazar F, Rastegarnasab F, Abtahi-Naeini B. Global clinicoepidemiological pattern of childhood vitiligo: a systematic review and meta-analysis. BMJ Paediatr Open. 2023;7(1):e001839.
  • 11. Weissmann S, Burrack N, Golan-Tripto I, Horev A. Determination of elevated eosinophil to lymphocyte ratio, eosinophil to neutrophil ratio, eosinophil to monocyte ratio and its association with severe vitiligo: A retrospective cohort study. PLoS One. 2024;19(2):e0296626.
  • 12. Temel B, Orenay O, Karaosmanoglu N. An Evaluation of the Hematological Markers of Systemic Inflammation and Oxidative Stress in Vitiligo: A Case-Control Study. Cureus. 2024;16(3):e56034.
  • 13. Demirbaş A, Elmas ÖF, Atasoy M, Türsen Ü, Lotti T. Can monocyte to HDL cholesterol ratio and monocyte to lymphocyte ratio be markers for inflammation and oxidative stress in patients with vitiligo? A preliminary study. Arch Dermatol Res. 2021;313(6):491-8.
  • 14. Solak B, Dikicier BS, Cosansu NC, Erdem T. Neutrophil to lymphocyte ratio in patients with vitiligo. Postepy Dermatol Alergol. 2017;34(5):468-70.
  • 15. Weissmann S, Babyev AS, Gordon M, Golan-Tripto I, Horev A. Decreased Neutrophil-to-lymphocyte Ratio in Patients with Vitiligo: National Data Analysis. Acta Derm Venereol. 2024;104:adv35406.
  • 16. Zahra FT, Amin SS, Adil M, Sarshar F, Pathak P. Clinico-Epidemiological Study of Childhood Vitiligo and its Associations: A Hospital-Based Cross-Sectional Study. Indian Journal of Paediatric Dermatology. 2022;23(2):116-22.
  • 17. Ahmed AA-A, Ahmed HS, Mohammed MH, Shanshal M. Childhood Vitiligo: A Retrospective Clinico-Epidemiological Study. medRxiv. 2020:2020.09.16.20195636.
  • 18. El-Husseiny R, Abd-Elhaleem A, Salah El-Din W, Abdallah M. Childhood vitiligo in Egypt: Clinico-epidemiologic Profile of 483 patients. J Cosmet Dermatol. 2021;20(1):237-42.
  • 19. Meiyun L, Li X, Xiaoyi L, Dan D. Epidemiologic and clinical differences between early-onset and later-onset childhood vitiligo: A retrospective cohort study. J Am Acad Dermatol. 2024;91(1):125-7.
  • 20. Aksoy F, Ersoy Evans S, Karaduman A. Childhood Vitiligo: A Prospective Analysis of 63 Patients. Turkiye Klinikleri J Dermatol. 2008;18(2):67-71.
  • 21. Akbas A, Kılınç F, Aktaş A. Clinical and Demographic Characteristics of Children with Vitiligo: Retrospective Analysis of 105 Cases. Turkish J Pediatr Dis. 2020;14(4):325-32.
  • 22. Arýcan O, Koç K, Ersoy L. Clinical characteristics in 113 Turkish vitiligo patients. Acta Dermatovenerol Alp Pannonica Adriat. 2008;17(3):129-32.
  • 23. Tarkowski B, Ławniczak J, Tomaszewska K, Kurowski M, Zalewska-Janowska A. Chronic Urticaria Treatment with Omalizumab-Verification of NLR, PLR, SIRI and SII as Biomarkers and Predictors of Treatment Efficacy. J Clin Med. 2023;12(7):2639.
  • 24. Bai X, Cheng L, Wang H, Deng Y, Tong X, Wen W, et al. The aggregate index of systemic inflammation (AISI) and the risk of all-cause, cardiovascular, and cardio-cerebrovascular mortality in congestive heart failure patients: results from NHANES 1999–2018. Sci Rep. 2025;15(1):18282.
  • 25. Nicolaidou E, Antoniou C, Miniati A, Lagogianni E, Matekovits A, Stratigos A, et al. Childhood- and later-onset vitiligo have diverse epidemiologic and clinical characteristics. J Am Acad Dermatol. 2012;66(6):954-8.
  • 26. Martins C, Hertz A, Luzio P, Paludo P, Azulay-Abulafia L. Clinical and epidemiological characteristics of childhood vitiligo: a study of 701 patients from Brazil. Int J Dermatol. 2020;59(2):236-44.
  • 27. Chakraborty AS, Agarwal R, Preethi P, Chandrashekar BS. Clinico-Epidemiological Profile of Childhood Vitiligo. Indian Dermatol Online J. 2024;15(4):683-4.
  • 28. Iannella G, Greco A, Didona D, Didona B, Granata G, Manno A, et al. Vitiligo: Pathogenesis, clinical variants and treatment approaches. Autoimmun Rev. 2016;15(4):335-43.
  • 29. Mazereeuw-Hautier J, Bezio S, Mahe E, Bodemer C, Eschard C, Viseux V, et al. Segmental and nonsegmental childhood vitiligo has distinct clinical characteristics: a prospective observational study. J Am Acad Dermatol. 2010;62(6):945-9.
  • 30. van Geel N, Speeckaert R. Segmental Vitiligo. Dermatol Clin. 2017;35(2):145-50.
  • 31. Ezzedine K, Diallo A, Léauté-Labrèze C, Mossalayi D, Gauthier Y, Bouchtnei S, et al. Multivariate analysis of factors associated with early-onset segmental and nonsegmental vitiligo: a prospective observational study of 213 patients. Br J Dermatol. 2011;165(1):44-9.
  • 32. Xu X, Jiang M, Zhang C, Qiao Z, Liu W, Le Y, et al. New insights into segmental vitiligo: A clinical and immunological comparison with nonsegmental vitiligo. Pigment Cell Melanoma Res. 2022;35(2):220-8.
  • 33. Lin X, Tang LY, Fu WW, Kang KF. Childhood vitiligo in China: clinical profiles and immunological findings in 620 cases. Am J Clin Dermatol. 2011;12(4):277-81.
  • 34. Agarwal S, Gupta S, Ojha A, Sinha R. Childhood vitiligo: clinicoepidemiologic profile of 268 children from the Kumaun region of Uttarakhand, India. Pediatr Dermatol. 2013;30(3):348-53.
  • 35. Nicolaidou E, Antoniou C, Miniati A, Lagogianni E, Matekovits A, Stratigos A, et al. Childhood- and later-onset vitiligo have diverse epidemiologic and clinical characteristics. J Am Acad Dermatol. 2012;66(6):954-8.
  • 36. Mogawer RM, Elmasry MF, Mostafa WZ. New insights into leukotrichia in nonsegmental vitiligo: A cross-sectional study. Indian J Dermatol Venereol Leprol. 2019;85(4):374-9.
  • 37. Lee JH, Ju HJ, Seo JM, Almurayshid A, Kim GM, Ezzedine K, et al. Comorbidities in Patients with Vitiligo: A Systematic Review and Meta-Analysis. J Invest Dermatol. 2023;143(5):777-89.e6.
  • 38. Tissera KA, Bitar RA, Hawryluk EB, Garza-Mayers AC. Comorbidities of pediatric vitiligo. JAAD Reviews. 2025;3:131-7.
  • 39. Speeckaert R, Caelenberg EV, Belpaire A, Speeckaert MM, Geel Nv. Vitiligo: From Pathogenesis to Treatment. J Clin Med. 2024;13(17):5225.
  • 40. Marra A, Bondesan A, Caroli D, Grugni G, Sartorio A. The neutrophil to lymphocyte ratio (NLR) positively correlates with the presence and severity of metabolic syndrome in obese adults, but not in obese children/adolescents. BMC Endocr Disord. 2023;23(1):121.
  • 41. Diny NL, Rose NR, Čiháková D. Eosinophils in Autoimmune Diseases. Front Immunol. 2017;8:484.
  • 42. Keselman A, Heller N. Estrogen Signaling Modulates Allergic Inflammation and Contributes to Sex Differences in Asthma. Front Immunol. 2015;6:568.
  • 43. Artham S, Chang CY, McDonnell DP. Eosinophilia in cancer and its regulation by sex hormones. Trends Endocrinol Metab. 2023;34(1):5-20.
  • 44. Niewoehner CB, Schorer AE. Gynaecomastia and breast cancer in men. BMJ. 2008;336(7646):709-13.
  • 45. Zhao L, Wu Y, Zhu H, Lin Y, Su H, Hu J, et al. Age, Sex, and Symptom-Dependent Variations in Total IgE and Eosinophils in Atopic Patients: A Five-Year Retrospective Study. J Asthma Allergy. 2025;18:915-26.

Demographics, Clinical and Laboratory Features of Childhood Vitiligo: A Retrospective Cross-sectional Analysis of 179 Patients

Yıl 2025, Cilt: 47 Sayı: 6, 964 - 974, 26.09.2025
https://doi.org/10.20515/otd.1733462

Öz

Vitiligo is an acquired pigmentation disorder. Childhood vitiligo can differ from adult-onset vitiligo in several aspects. We aimed to evaluate demographics, clinical features of vitiligo in children, and laboratory results. A retrospective, cross-sectional study was conducted on < 18-year-old pediatric patients with vitiligo. Demographics, clinical features, and laboratory test results performed at the time of diagnosis were retrieved from medical records. Vitiligo was classified as non-segmental (NSV), segmental (SV), and unclassified vitiligo. A total of 179 patients were included. The female/male ratio was 1.2/1. The most common form was NSV (87.7%), followed by SV (7.3%). Among NSV, generalized vitiligo was the most common subtype (42.5%), followed by localized (32.4%) and acrofacial (8.9%) vitiligo. Vitiligo began ≤ 12 years of age in 156 (88.6%) patients. NSV and SV were not significantly different in sex, age of disease onset, disease duration, halo nevi, or Koebner phenomenon. Leukotrichia was more common in SV (84.6%) than NSV (7.6%) (P < 0.001). Face (67.6%) was the most frequently involved body site. Neutrophil percentage, mean platelet volume (MPV), MPV/platelet ratio, MPV/lymphocyte ratio, neutrophil/lymphocyte ratio (NLR), derived NLR, and systemic inflammatory response index were significantly lower in patients with early-onset (≤ 12 years) vitiligo (P < 0.05), possibly indicating the differences in inflammatory response between young children and adolescents. It was noteworthy that eosinophil counts, eosinophil/monocyte ratio, and eosinophil/neutrophil ratio were significantly lower in female patients (P < 0.05), which might reflect the effect of sex hormones on eosinophils. Further studies are warranted to extend our results.

Kaynakça

  • 1. Rodrigues M, Ezzedine K, Hamzavi I, Pandya AG, Harris JE. New discoveries in the pathogenesis and classification of vitiligo. J Am Acad Dermatol. 2017;77(1):1-13.
  • 2. Gandhi K, Ezzedine K, Anastassopoulos KP, Patel R, Sikirica V, Daniel SR, et al. Prevalence of Vitiligo Among Adults in the United States. JAMA Dermatol. 2022;158(1):43-50.
  • 3. Alikhan A, Felsten LM, Daly M, Petronic-Rosic V. Vitiligo: a comprehensive overview Part I. Introduction, epidemiology, quality of life, diagnosis, differential diagnosis, associations, histopathology, etiology, and work-up. J Am Acad Dermatol. 2011;65(3):473-91.
  • 4. Nicolaidou E, Mastraftsi S, Tzanetakou V, Rigopoulos D. Childhood Vitiligo. Am J Clin Dermatol. 2019;20(4):515-26.
  • 5. AL-smadi K, Imran M, Leite-Silva VR, Mohammed Y. Vitiligo: A Review of Aetiology, Pathogenesis, Treatment, and Psychosocial Impact. Cosmetics. 2023;10(3):84.
  • 6. Marchioro HZ, Silva de Castro CC, Fava VM, Sakiyama PH, Dellatorre G, Miot HA. Update on the pathogenesis of vitiligo. An Bras Dermatol. 2022;97(4):478-90.
  • 7. Ezzedine K, Lim HW, Suzuki T, Katayama I, Hamzavi I, Lan CC, et al. Revised classification/nomenclature of vitiligo and related issues: the Vitiligo Global Issues Consensus Conference. Pigment Cell Melanoma Res. 2012;25(3):E1-13.
  • 8. van Geel N, Speeckaert R, Taïeb A, Ezzedine K, Lim HW, Pandya AG, et al. Worldwide expert recommendations for the diagnosis and management of vitiligo: Position statement from the International Vitiligo Task Force Part 1: towards a new management algorithm. J Eur Acad Dermatol Venereol. 2023;37(11):2173-84.
  • 9. Bergqvist C, Ezzedine K. Vitiligo: A Review. Dermatology. 2020;236(6):571-92.
  • 10. Farajzadeh S, Khalili M, Mirmohammadkhani M, Paknazar F, Rastegarnasab F, Abtahi-Naeini B. Global clinicoepidemiological pattern of childhood vitiligo: a systematic review and meta-analysis. BMJ Paediatr Open. 2023;7(1):e001839.
  • 11. Weissmann S, Burrack N, Golan-Tripto I, Horev A. Determination of elevated eosinophil to lymphocyte ratio, eosinophil to neutrophil ratio, eosinophil to monocyte ratio and its association with severe vitiligo: A retrospective cohort study. PLoS One. 2024;19(2):e0296626.
  • 12. Temel B, Orenay O, Karaosmanoglu N. An Evaluation of the Hematological Markers of Systemic Inflammation and Oxidative Stress in Vitiligo: A Case-Control Study. Cureus. 2024;16(3):e56034.
  • 13. Demirbaş A, Elmas ÖF, Atasoy M, Türsen Ü, Lotti T. Can monocyte to HDL cholesterol ratio and monocyte to lymphocyte ratio be markers for inflammation and oxidative stress in patients with vitiligo? A preliminary study. Arch Dermatol Res. 2021;313(6):491-8.
  • 14. Solak B, Dikicier BS, Cosansu NC, Erdem T. Neutrophil to lymphocyte ratio in patients with vitiligo. Postepy Dermatol Alergol. 2017;34(5):468-70.
  • 15. Weissmann S, Babyev AS, Gordon M, Golan-Tripto I, Horev A. Decreased Neutrophil-to-lymphocyte Ratio in Patients with Vitiligo: National Data Analysis. Acta Derm Venereol. 2024;104:adv35406.
  • 16. Zahra FT, Amin SS, Adil M, Sarshar F, Pathak P. Clinico-Epidemiological Study of Childhood Vitiligo and its Associations: A Hospital-Based Cross-Sectional Study. Indian Journal of Paediatric Dermatology. 2022;23(2):116-22.
  • 17. Ahmed AA-A, Ahmed HS, Mohammed MH, Shanshal M. Childhood Vitiligo: A Retrospective Clinico-Epidemiological Study. medRxiv. 2020:2020.09.16.20195636.
  • 18. El-Husseiny R, Abd-Elhaleem A, Salah El-Din W, Abdallah M. Childhood vitiligo in Egypt: Clinico-epidemiologic Profile of 483 patients. J Cosmet Dermatol. 2021;20(1):237-42.
  • 19. Meiyun L, Li X, Xiaoyi L, Dan D. Epidemiologic and clinical differences between early-onset and later-onset childhood vitiligo: A retrospective cohort study. J Am Acad Dermatol. 2024;91(1):125-7.
  • 20. Aksoy F, Ersoy Evans S, Karaduman A. Childhood Vitiligo: A Prospective Analysis of 63 Patients. Turkiye Klinikleri J Dermatol. 2008;18(2):67-71.
  • 21. Akbas A, Kılınç F, Aktaş A. Clinical and Demographic Characteristics of Children with Vitiligo: Retrospective Analysis of 105 Cases. Turkish J Pediatr Dis. 2020;14(4):325-32.
  • 22. Arýcan O, Koç K, Ersoy L. Clinical characteristics in 113 Turkish vitiligo patients. Acta Dermatovenerol Alp Pannonica Adriat. 2008;17(3):129-32.
  • 23. Tarkowski B, Ławniczak J, Tomaszewska K, Kurowski M, Zalewska-Janowska A. Chronic Urticaria Treatment with Omalizumab-Verification of NLR, PLR, SIRI and SII as Biomarkers and Predictors of Treatment Efficacy. J Clin Med. 2023;12(7):2639.
  • 24. Bai X, Cheng L, Wang H, Deng Y, Tong X, Wen W, et al. The aggregate index of systemic inflammation (AISI) and the risk of all-cause, cardiovascular, and cardio-cerebrovascular mortality in congestive heart failure patients: results from NHANES 1999–2018. Sci Rep. 2025;15(1):18282.
  • 25. Nicolaidou E, Antoniou C, Miniati A, Lagogianni E, Matekovits A, Stratigos A, et al. Childhood- and later-onset vitiligo have diverse epidemiologic and clinical characteristics. J Am Acad Dermatol. 2012;66(6):954-8.
  • 26. Martins C, Hertz A, Luzio P, Paludo P, Azulay-Abulafia L. Clinical and epidemiological characteristics of childhood vitiligo: a study of 701 patients from Brazil. Int J Dermatol. 2020;59(2):236-44.
  • 27. Chakraborty AS, Agarwal R, Preethi P, Chandrashekar BS. Clinico-Epidemiological Profile of Childhood Vitiligo. Indian Dermatol Online J. 2024;15(4):683-4.
  • 28. Iannella G, Greco A, Didona D, Didona B, Granata G, Manno A, et al. Vitiligo: Pathogenesis, clinical variants and treatment approaches. Autoimmun Rev. 2016;15(4):335-43.
  • 29. Mazereeuw-Hautier J, Bezio S, Mahe E, Bodemer C, Eschard C, Viseux V, et al. Segmental and nonsegmental childhood vitiligo has distinct clinical characteristics: a prospective observational study. J Am Acad Dermatol. 2010;62(6):945-9.
  • 30. van Geel N, Speeckaert R. Segmental Vitiligo. Dermatol Clin. 2017;35(2):145-50.
  • 31. Ezzedine K, Diallo A, Léauté-Labrèze C, Mossalayi D, Gauthier Y, Bouchtnei S, et al. Multivariate analysis of factors associated with early-onset segmental and nonsegmental vitiligo: a prospective observational study of 213 patients. Br J Dermatol. 2011;165(1):44-9.
  • 32. Xu X, Jiang M, Zhang C, Qiao Z, Liu W, Le Y, et al. New insights into segmental vitiligo: A clinical and immunological comparison with nonsegmental vitiligo. Pigment Cell Melanoma Res. 2022;35(2):220-8.
  • 33. Lin X, Tang LY, Fu WW, Kang KF. Childhood vitiligo in China: clinical profiles and immunological findings in 620 cases. Am J Clin Dermatol. 2011;12(4):277-81.
  • 34. Agarwal S, Gupta S, Ojha A, Sinha R. Childhood vitiligo: clinicoepidemiologic profile of 268 children from the Kumaun region of Uttarakhand, India. Pediatr Dermatol. 2013;30(3):348-53.
  • 35. Nicolaidou E, Antoniou C, Miniati A, Lagogianni E, Matekovits A, Stratigos A, et al. Childhood- and later-onset vitiligo have diverse epidemiologic and clinical characteristics. J Am Acad Dermatol. 2012;66(6):954-8.
  • 36. Mogawer RM, Elmasry MF, Mostafa WZ. New insights into leukotrichia in nonsegmental vitiligo: A cross-sectional study. Indian J Dermatol Venereol Leprol. 2019;85(4):374-9.
  • 37. Lee JH, Ju HJ, Seo JM, Almurayshid A, Kim GM, Ezzedine K, et al. Comorbidities in Patients with Vitiligo: A Systematic Review and Meta-Analysis. J Invest Dermatol. 2023;143(5):777-89.e6.
  • 38. Tissera KA, Bitar RA, Hawryluk EB, Garza-Mayers AC. Comorbidities of pediatric vitiligo. JAAD Reviews. 2025;3:131-7.
  • 39. Speeckaert R, Caelenberg EV, Belpaire A, Speeckaert MM, Geel Nv. Vitiligo: From Pathogenesis to Treatment. J Clin Med. 2024;13(17):5225.
  • 40. Marra A, Bondesan A, Caroli D, Grugni G, Sartorio A. The neutrophil to lymphocyte ratio (NLR) positively correlates with the presence and severity of metabolic syndrome in obese adults, but not in obese children/adolescents. BMC Endocr Disord. 2023;23(1):121.
  • 41. Diny NL, Rose NR, Čiháková D. Eosinophils in Autoimmune Diseases. Front Immunol. 2017;8:484.
  • 42. Keselman A, Heller N. Estrogen Signaling Modulates Allergic Inflammation and Contributes to Sex Differences in Asthma. Front Immunol. 2015;6:568.
  • 43. Artham S, Chang CY, McDonnell DP. Eosinophilia in cancer and its regulation by sex hormones. Trends Endocrinol Metab. 2023;34(1):5-20.
  • 44. Niewoehner CB, Schorer AE. Gynaecomastia and breast cancer in men. BMJ. 2008;336(7646):709-13.
  • 45. Zhao L, Wu Y, Zhu H, Lin Y, Su H, Hu J, et al. Age, Sex, and Symptom-Dependent Variations in Total IgE and Eosinophils in Atopic Patients: A Five-Year Retrospective Study. J Asthma Allergy. 2025;18:915-26.
Toplam 45 adet kaynakça vardır.

Ayrıntılar

Birincil Dil İngilizce
Konular Dermatoloji
Bölüm ORİJİNAL MAKALELER / ORIGINAL ARTICLES
Yazarlar

Özge Zorlu 0000-0001-5555-130X

Büşra Demirel 0009-0006-1006-814X

Hülya Albayrak 0000-0002-2022-578X

Sema Aytekin 0000-0003-1376-1573

Yayımlanma Tarihi 26 Eylül 2025
Gönderilme Tarihi 3 Temmuz 2025
Kabul Tarihi 4 Eylül 2025
Yayımlandığı Sayı Yıl 2025 Cilt: 47 Sayı: 6

Kaynak Göster

Vancouver Zorlu Ö, Demirel B, Albayrak H, Aytekin S. Demographics, Clinical and Laboratory Features of Childhood Vitiligo: A Retrospective Cross-sectional Analysis of 179 Patients. Osmangazi Tıp Dergisi. 2025;47(6):964-7.


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