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Lichen sclerosus clinically manifested in various age group girls

https://doi.org/10.17749/2313-7347/ob.gyn.rep.2026.574

Abstract

Aim: to study the features of lichen sclerosus (LS) clinically manifested in various age group girls.

Materials and Methods. A prospective observational study with 202 girls aged 0 to 18 years having verified LS clinical and histological diagnosis of LS was conducted. The age of LS onset was examined, determining the time from the appearance of the first symptoms to diagnosis was by analyzing most characteristic disease symptoms such as itching, changes in skin structure and color, the presence of cracks, constipation, dysuria, and lesion area related to childhood age period.

Results. It was found that 30 % LS girls noted the first disease symptoms at the age of 5–6 years (n = 67; 33.1 %). Among patients with vulvar LS, middle childhood (aged 3–5 years) girls predominated (n = 66, 32.7 %). Girls in early childhood (up to 2 years) and puberty period (13–17 years) were in minority comprising as few as 7 (3.5 %) and 19 (9.4 %) cases, respectively. The average LS duration before being properly diagnosed was 2.61 ± 0.13 years. In 27.7 % (n = 56) girls, the disease was asymptomatic, more often in younger patients aged 3–5 years (n = 10). Complaints of itching in the vulva, perineum and perianal area were reported in 58.9 % (n = 119) cases, but only five (2.48 %) girls had itching as a single complaint. In most cases, changes affected all 5 zones – the clitoris, labia minora, the inner surface of the labia majora, perineum and perianal area. A "figure eight"-like LS lesions of the genital tract were observed in 75.2 % (n = 152) girls, more often found in prepubertal (79.8 %; n = 79) and pubertal (82.9 %; n = 29) age.

Conclusion. LS incidence peaks during the transition from middle to late childhood. A more than nine-year observation was shown to shorten average duration of the disease before its diagnosis from 6 to 1.6 years. Analyzing pattern of complaints related to the age of girls allowed to conclude that LS exhibits no specific complaints, except for changes in vulvar skin structure and color, which are noticed only by 5 % patients. Itching in the vast majority of cases (n = 119; 58.9 %) is a consequence of arising complications such as cracks, ecchymosis and erosions.

About the Authors

L. Kh. Lukmanova
Republican Children's Clinical Hospital; Bashkir State Medical University, Ministry of Health of the Russian Federation
Russian Federation

Lina Kh. Lukmanova - MD.

98 Stepan Kuvykin Street, Ufa 450092; 3 Lenin Str., Ufa 450008



S. Yu. Muslimova
Bashkir State Medical University, Ministry of Health of the Russian Federation
Russian Federation

Sofya Yu. Muslimova - MD, Dr Sci Med.

3 Lenin Str., Ufa 450008



I. V. Sakhautdinova
Bashkir State Medical University, Ministry of Health of the Russian Federation
Russian Federation

Indira V. Sakhautdinova - MD, Dr Sci Med, Prof.

3 Lenin Str., Ufa 450008



References

1. Lichen sclerosus. ISSVD practical guide to diagnosis and management. Eds. T. Day, M. Mauskar, S. Amanda. Ad Médic, Lda, 2024. 212 p. https://doi.org/10.59153/adm.ls.001.

2. Orszulak D., Dulska A., Niziński K. et al. Pediatric vulvar lichen sclerosus – a review of the literature. Int J Environ Res Public Health. 2021;18(13):7153. https://doi.org/10.3390/ijerph18137153.

3. Singh N., Ghatage P. Etiology, clinical features, and diagnosis of vulvar lichen sclerosus: a scoping review. Obstet Gynecol Int. 2020;2020:7480754. https://doi.org/10.1155/2020/7480754.

4. Nerantzoulis I., Grigoriadis T., Michala L. Genital lichen sclerosus in childhood and adolescence – a retrospective case series of 15 patients: early diagnosis is crucial to avoid long-term sequelae. Eur J Pediatr. 2017;176:1429–32. https://doi.org/10.1007/s00431-017-3004-y.

5. Dendrinos M.L., Quint E.H. Lichen sclerosus in children and adolescents. Curr Opin Obstet Gynecol. 2013;25(5):370–4. https://doi.org/10.1097/GCO.0b013e328363a53c.

6. Liu L., He Y., Hu Q. et al. Vulvar lichen sclerosus in girls and adult females: A single-center retrospective study of 744 patients in China. J Dermatol. 2024;51(11):1470–5. https://doi:10.1111/1346-8138.17352.

7. Akbaş A., Kılınç F. Clinic and demographic characteristics of pediatric patients with Lichen sclerosus. Turk J Pediatr. 2021;63(1):126–35. https://doi.org/10.24953/turkjped.2021.01.015.

8. Wang M., Arlen A.M., Vash-Margita A. Characteristics among premenarchal girls with lichen sclerosus. J Low Genit Tract Dis. 2021;25(2):152–7. https://doi.org/10.1097/LGT.0000000000000584.

9. Focseneanu M.A., Gupta M., Squires K.C. et al. The course of lichen sclerosus diagnosed prior to puberty. J Pediatr Adolesc Gynecol. 2013;26(3):153–5. https://doi.org/10.1016/j.jpag.2012.12.002.

10. Powell J., Wojnarowska F. Childhood vulvar lichen sclerosus. The course after puberty. J Reprod Med. 2002;47(9):706–9.

11. van der Meijden W.I., Boffa M.J., Ter Harmsel B. et al. 2021 European guideline for the management of vulval conditions. J Eur Acad Dermatol Venereol. 2022;36(7):952–72. https://doi.org/10.1111/jdv.18102.

12. Topal İ.O., Sayılgan A.T., Kalçın, S. An uncommon cause of vulval pruritus in childhood: lichen sclerosus. Turk Pediatri Ars. 2014;49(1):86–7. https://doi.org/10.5152/tpa.2014.1365.

13. Kirtschig G., Becker K., Günthert A. et al. Evidence-based (S3) Guideline on (anogenital) lichen sclerosus. J Eur Acad Dermatol Venereol. 2015;29(10):e1–43. https://doi.org/10.1111/jdv.13136.

14. Pranteda G., Muscianese M., Grimaldi M. et al. Lichen sclerosus et atrophicus induced by carbamazepine: a case report. Int J Immunopathol Pharmacol. 2013;26(3):791–4. https://doi.org/10.1177/039463201302600326.

15. Cooper S.M., Gao X.H., Powell J.J., Wojnarowska F. Does treatment of vulvar lichen sclerosus influence its prognosis? Arch Dermatol. 2004;140(6):702–6. https://doi.org/10.1001/archderm.140.6.702.

16. Krapf J.M., Mitchell L., Holton M.A., Goldstein A.T. Vulvar lichen sclerosus: current perspectives. Int J Women's Health. 2020;12:11–20. https://doi.org/10.2147/IJWH.S191200.

17. Vaganov P.D., Yanovskaya E.Yu., Mandzhieva E.T. Periods of childhood. [Periody detskogo vozrasta]. Rossijskij medicinskij zhurnal. 2018;24(4):185–90. (In Russ.). https://doi.org/10.18821/0869-2106-2018-24-4-185-190.

18. Guarneri A.M., Kamboj M.K. Physiology of pubertal development in females. Pediatr Med. 2019;2:42. https://doi.org/10.21037/pm.2019.07.03.

19. Ngo M., Chang H., Carr C. et al. Patient questionnaire responses predict severe clinical signs in patients with vulvar lichen sclerosus: a retrospective cohort study. J Am Acad Dermatol. 2024;91(3):516–8. https://doi.org/10.1016/j.jaad.2024.04.046.

20. Papini M., Russo A., Simonetti O. et al. Mucous membrane disorders research group of SIDeMaST. Diagnosis and management of cutaneous and anogenital lichen sclerosus: recommendations from the Italian Society of Dermatology (SIDeMaST). Ital J Dermatol Venerol. 2021;156(5):519–33. https://doi.org/10.23736/S2784-8671.21.06764-X.

21. Singh N., Ghatage P. Etiology, clinical features, and diagnosis of vulvar lichen sclerosus: A scoping review. Obstet Gynecol. 2020;2020:7480754. https://doi.org/10.1155/2020/7480754.

22. De Luca D.A., Papara C., Vorobyev A. et al. Lichen sclerosus: The 2023 update. Front Med. 2023;16:10:1106318. https://doi.org/10.3389/fmed.2023.1106318.

23. Morrel B., Ewing-Graham P.C., van der Avoort I.A.M. et al. Structured analysis of histopathological characteristics of vulvar lichen sclerosus in a juvenile population. Hum Pathol. 2020;106:23–31. https://doi.org/10.1016/j.humpath.2020.09.003.


What is already known about this subject?

► The data regarding lichen sclerosus (LS) onset and peak incidence in girls are unequal.

► The most common complaints of LS patients are presented as itching, dyspareunia and apareunia; the disease is often asymptomatic. The main LS clinical signs are described.

► There were compared the epidemiological features, clinical manifestations and concomitant autoimmune diseases in girls and adult women with LS. However, LS clinical features in girls of different age groups were not assessed.

What are the new findings?

► LS is more often recorded in girls aged 5–6 years, at the transition from middle (3–5 years old)-to-late (6–8 years old) childhood.

► Asymptomatic LS is more common in younger age group (3–8 years old) girls.

How might it impact on clinical practice in the foreseeable future?

► Knowledge regarding LS incidence and its clinical features related to childhood age period may allow to correctly examine a pediatric patient, despite the lack of complaints to be diagnosed timely.

Review

For citations:


Lukmanova L.Kh., Muslimova S.Yu., Sakhautdinova I.V. Lichen sclerosus clinically manifested in various age group girls. Obstetrics, Gynecology and Reproduction. 2026;20(1):102-110. (In Russ.) https://doi.org/10.17749/2313-7347/ob.gyn.rep.2026.574

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ISSN 2313-7347 (Print)
ISSN 2500-3194 (Online)