Outcome Measures in Adult Vulvar Lichen Sclerosus: A Case Series of Women Diagnosed as Juveniles

Beth Morrel, Marianne J. Ten Kate-Booij, Charlotte van Dijk, Colette L.M. van Hees, Kiki M.G.J. Wigny, Curt W. Burger, Suzanne G.M.A. Pasmans, Irene A.M. van der Avoort

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Abstract

OBJECTIVES: Studies on the consequences of juvenile vulvar lichen sclerosus (JVLS) in adulthood are limited. A number of measuring tools are available for analyzing adult vulvar lichen sclerosus (VLS), but these have not been applied in studies on JVLS. The aim is to study physical findings, quality of life, sexual well-being, and self-image in adult women with a history of juvenile VLS. MATERIALS AND METHODS: Adult women with a biopsy proven history of JVLS were recruited to be examined and surveyed using available standardized measurement tools. This took place in an outpatient setting by physicians who were not involved in the treatment of participants. RESULTS: Twenty-seven women (median age 29 years) with a history of JVLS and median time since biopsy of 19.5 years were recruited. Of these women, 59% currently had symptoms, 63% had signs of active disease, and 85% had moderate to severe architectural changes. Despite these residual signs, vulvar specific-quality of life and vulvar self-image scored favorably while generic health-related quality of life was somewhat effected. CONCLUSIONS: JVLS has consequences in adulthood involving physical findings and vulvar quality of life. The use of standardized outcome measures for clinical practice and research purposes facilitates a better understanding of the sequelae to JVLS.

Original languageEnglish
Pages (from-to)295-299
Number of pages5
JournalJournal of Lower Genital Tract Disease
Volume28
Issue number3
DOIs
Publication statusPublished - 1 Jul 2024

Bibliographical note

Publisher Copyright:
© Lippincott Williams & Wilkins.

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