Evaluation of Skin Recovery after Fractional CO2 Laser Treatment of Vulvar Lichen Sclerosus Using Multimodal Optical Coherence Tomography
The aim of the study is to demonstrate the effect of fractional CO2 laser treatment on vulvar skin in lichen sclerosus using multimodal optical coherence tomography (MM OCT).
Materials and Methods. The study included 3 clinical cases of vulvar lichen sclerosus (VLS) (histologically classified as early, early with dermal edema, late) and 2 control cases without vulvar pathology. Patients with VLS underwent 3 procedures of fractional CO2 laser treatment with an interval of 30–40 days. In patients without vulvar pathology, the MM OCT examination was performed once, in patients with VLS it was done at the point of the greatest visible skin damage just before a punch biopsy, immediately after the first laser session, and 1 month after a full course of treatment.
Results. Analyzing the case series of vulvar skin recovery 1 month after fractional CO2 laser treatment, it has been found that the recovery depended on the dermal condition before the treatment. In early VLS and early VLS with dermal edema (clinical cases 1 and 2) before the treatment, the MM OCT examination has shown a decreased epidermal thickness, unclear contrast between the epidermis and dermis, a decrease in the values of the OCT signal attenuation coefficient in the dermis, and a sharp reduction in the density of blood and lymphatic vessels. After treatment, the MM OCT examination demonstrated a complete recovery of vulvar skin structure and all quantitative values reached the level characteristic of normal vulvar skin. Before the treatment, a homogenization zone (sclerosis) was clearly visible in the MM OCT images of the dermis in late VLS (clinical case 3). After the treatment, complete recovery of the vulvar skin structure was not observed; the area of sclerosis was preserved; however, visually, there was an increase in the density of blood and lymphatic vessels in the affected area, which almost reached the level of normal vulvar skin.
Conclusion. MM OCT can be proposed as a promising non-invasive method for monitoring skin recovery after fractional CO2 laser treatment of VLS.
- Kirillin M., Motovilova T., Shakhova N. Optical coherence tomography in gynecology: a narrative review. J Biomed Opt 2017; 22(12): 1–9, https://doi.org/10.1117/1.JBO.22.12.121709.
- Huisman B.W., Pagan L., Naafs R.G.C., Ten Voorde W., Rissmann R., Piek J.M.J., Damman J., Juachon M.J., Osse M., Niemeyer-van der Kolk T., van Hees C.L.M., van Poelgeest M.I.E. Dermatoscopy and optical coherence tomography in vulvar high-grade squamous intraepithelial lesions and lichen sclerosus: a prospective observational trial. J Low Genit Tract Dis 2023; 27(3): 255–261, https://doi.org/10.1097/LGT.0000000000000731.
- Xu L., Ma Q., Lin S., Ju J., Feng S., Shi Z., Bai Y., Song J., Du J., Wang B. Study on the application and imaging characteristics of optical coherence tomography in vulva lesions. Sci Rep 2022; 12(1): 3659, https://doi.org/10.1038/s41598-022-07634-1.
- Sudol N.T., Miao Y., Li Y., Chen J.J., Jing J.C., Zhu J., Tadir Y., Chen Z., Lane F. Optical vaginal biopsy using optical coherence tomography. Female Pelvic Med Reconstr Surg 2020; 26(2): 155–158, https://doi.org/10.1097/SPV.0000000000000839.
- Miao Y., Sudol N.T., Li Y., Chen J.J., Arthur R.A., Qiu S., Jiang Y., Tadir Y., Lane F., Chen Z. Optical coherence tomography evaluation of vaginal epithelial thickness during CO2 laser treatment: a pilot study. J Biophotonics 2022; 15(11): e202200052, https://doi.org/10.1002/jbio.202200052.
- Gubarkova E., Potapov A., Moiseev A., Kiseleva E., Krupinova D., Shatilova K., Karabut M., Khlopkov A., Loginova M., Radenska-Lopovok S., Gelikonov G., Grechkanev G., Gladkova N., Sirotkina M. Depth-resolved attenuation mapping of the vaginal wall under prolapse and after laser treatment using cross-polarization optical coherence tomography: a pilot study. Diagnostics (Basel) 2023; 13(22): 3487, https://doi.org/10.3390/diagnostics13223487.
- De Luca D.A., Papara C., Vorobyev A., Staiger H., Bieber K., Thaçi D., Ludwig R.J. Lichen sclerosus: the 2023 update. Front Med (Lausanne) 2023; 10: 1106318, https://doi.org/10.3389/fmed.2023.1106318.
- Apolikhina I.A., Sokolova A.V., Gumova Z.D. External genitalia lichen sclerosus and main causes, clinic, diagnostics and treatment. Meditsinskiy opponent 2018; 2: 77–82.
- Kirtschig G., Becker K., Günthert A., Jasaitiene D., Cooper S., Chi C.C., Kreuter A., Rall K.K., Aberer W., Riechardt S., Casabona F., Powell J., Brackenbury F., Erdmann R., Lazzeri M., Barbagli G., Wojnarowska F. Evidence-based (S3) guideline on (anogenital) lichen sclerosus. J Eur Acad Dermatol Venereol 2015; 29(10): e1–e43, https://doi.org/10.1111/jdv.13136.
- Apolikhina I.A., Plakhova K.I., Sokolova A.V., Chernukha L.V. Lichen sclerosus of the vulva. Akusherstvo i ginekologiya 2020; S9: 8–13.
- Lee A., Bradford J., Fischer G. Long-term management of adult vulvar lichen sclerosus: a prospective cohort study of 507 women. JAMA Dermatol 2015; 151(10): 1061–1067, https://doi.org/10.1001/jamadermatol.2015.0643.
- van Cranenburgh O.D., Nijland S.B.W., Lindeboom R., de Korte J., de Rie M.A., Ter Stege J.A., Prinsen C.A.C. Patients with lichen sclerosus experience moderate satisfaction with treatment and impairment of quality of life: results of a cross-sectional study. Br J Dermatol 2017; 176(6): 1508–1515, https://doi.org/10.1111/bjd.15125.
- Baggish M.S. Fractional CO2 laser treatment for vaginal atrophy and vulvar lichen sclerosus. Journal of Gynecologic Surgery 2016; 32(6): 309–317.
- Apolikhina I.A., Sokolova A.V., Balashov I.S., Chernukha L.V., Ermakova E.I. Treatment vulvar lichen sclerosus with fractional CO2-laser: cohort clinical study. Akusherstvo i ginekologiya: novosti, mneniya, obuchenie 2020; 8(2): 48–58.
- Burkett L.S., Siddique M., Zeymo A., Brunn E.A., Gutman R.E., Park A.J., Iglesia C.B. Clobetasol compared with fractionated carbon dioxide laser for lichen sclerosus: a randomized controlled trial. Obstet Gynecol 2021; 137(6): 968–978, https://doi.org/10.1097/AOG.0000000000004332.
- Balchander D., Nyirjesy P. Fractionated CO2 laser as therapy in recalcitrant lichen sclerosus. J Low Genit Tract Dis 2020; 24(2): 225–228, https://doi.org/10.1097/LGT.0000000000000512.
- Omi T., Numano K. The role of the CO2 laser and fractional CO2 laser in dermatology. Laser Ther 2014; 23(1): 49–60, https://doi.org/10.5978/islsm.14-RE-01.
- Orringer J.S., Sachs D.L., Shao Y., Hammerberg C., Cui Y., Voorhees J.J., Fisher G.J. Direct quantitative comparison of molecular responses in photodamaged human skin to fractionated and fully ablative carbon dioxide laser resurfacing. Dermatol Surg 2012; 38(10): 1668–1677, https://doi.org/10.1111/j.1524-4725.2012.02518.x.
- Dieter A.A., Iglesia C.B., Lee J.H., Etcheverry M.J., Gonzales M.K., Sokol A.I., Tefera E., Cardis M.A. A prospective pilot study to assess for histologic changes on vulvar biopsies in postmenopausal women with lichen sclerosus treated with fractionated CO2 laser therapy. Lasers Surg Med 2023; 55(6): 521–527, https://doi.org/10.1002/lsm.23669.
- Potapov A.L., Loginova M.M., Moiseev A.A., Radenska-Lopovok S.G., Kuznetsov S.S., Kuznetsova I.A., Mustafina N.N., Safonov I.K., Gladkova N.D., Sirotkina M.A. Cross-polarization optical coherence tomography for clinical evaluation of dermal lesion degrees in vulvar lichen sclerosus. Sovremennye tehnologii v medicine 2023; 15(1): 53, https://doi.org/10.17691/stm2023.15.1.06.
- Potapov A., Matveev L., Moiseev A., Sedova E., Loginova M., Karabut M., Kuznetsova I., Levchenko V., Grebenkina E., Gamayunov S., Radenska-Lopovok S., Sirotkina M., Gladkova N. Multimodal OCT control for early histological signs of vulvar lichen sclerosus recurrence after systemic PDT: pilot study. Int J Mol Sci 2023; 24(18): 13967, https://doi.org/10.3390/ijms241813967.
- Gorbunova E.A., Apolikhina I.A., Ramazanova M.O. Application of CO2-fraction laser photothermolysis in gynecological practice. Akusherstvo i ginekologiya 2023; 7: 155–161, https://doi.org/10.18565/aig.2023.176.
- Apolikhina I.A., Sokolova A.V., Plakhova K.I. Chernukha L.V., Saidova A.S. Method for the treatment of lichen sclerosus of the vulva in women. Patent RU 2755805C1. 2021.
- Gong P., Almasian M., van Soest G., de Bruin D., van Leeuwen T., Sampson D., Faber D. Parametric imaging of attenuation by optical coherence tomography: review of models, methods, and clinical translation. J Biomed Opt 2020; 25(4): 1–34, https://doi.org/10.1117/1.JBO.25.4.040901.
- Vermeer K.A., Mo J., Weda J.J., Lemij H.G., de Boer J.F. Depth-resolved model-based reconstruction of attenuation coefficients in optical coherence tomography. Biomed Opt Express 2013; 5(1): 322–337, https://doi.org/10.1364/BOE.5.000322.
- Moiseev A., Sherstnev E., Kiseleva E., Achkasova K., Potapov A., Yashin K., Sirotkina M., Gelikonov G., Matkivsky V., Shilyagin P., Ksenofontov S., Bederina E., Medyanik I., Zagaynova E., Gladkova N. Depth-resolved method for attenuation coefficient calculation from optical coherence tomography data for improved biological structure visualization. J Biophotonics 2023; 16(12):e202100392, https://doi.org/10.1002/jbio.202100392.
- Maslennikova A.V., Sirotkina M.A., Moiseev A.A., Finagina E.S., Ksenofontov S.Y., Gelikonov G.V., Matveev L.A., Kiseleva E.B., Zaitsev V.Y., Zagaynova E.V., Feldchtein F.I., Gladkova N.D., Vitkin A. In-vivo longitudinal imaging of microvascular changes in irradiated oral mucosa of radiotherapy cancer patients using optical coherence tomography. Sci Rep 2017; 7(1): 16505, https://doi.org/10.1038/s41598-017-16823-2.
- Potapov A.L., Konovalova E.A., Sirotkina M.A., Vagapova N.N., Safonov I.K., Timakova A.A., Radenska-Lopovok S.G., Kuznetsov S.S., Zagainova E.V., Kuznetsova I.A., Gladkova N.D. A new method of multimodal optical coherence tomography for the diagnosis of vulvar lichen sclerosus. Akusherstvo i ginekologiia 2020; 12: 169–176, https://doi.org/10.18565/aig.2020.12.169-176.
- Farage M.A., Maibach H.I. Morphology and physiological changes of genital skin and mucosa. Curr Probl Dermatol 2011; 40: 9–19, https://doi.org/10.1159/000321042.
- Latini A., Cota C., Orsini D., Cristaudo A., Tedesco M. Male and female genital lichen sclerosus. Clinical and functional classification criteria. Postepy Dermatol Alergol 2018; 35(5): 447–453, https://doi.org/10.5114/ada.2018.77236.
- Sokolova A.V., Apolikhina I.A., Zaitsev N.V., Chernukha L.V. Clinical and morphological stages vulvar lichen sclerosus. Gynecology 2020; 22(4): 22–27, https://doi.org/10.26442/20795696.2020.4.200278.
- Regauer S., Liegl B., Reich O. Early vulvar lichen sclerosus: a histopathological challenge. Histopathology 2005; 47(4): 340–347, https://doi.org/10.1111/j.1365-2559.2005.02209.x.
- Lei Y., Gold M.H., Ouyang H., Tan J. Fractional CO2 laser-assisted scar regeneration and repair: a review. Dermatological Reviews 2021; 2(1): 23–33, https://doi.org/10.1002/der2.61.