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Published in: Aesthetic Plastic Surgery 5/2022

20-01-2022 | Fat Grafting | Original Article

The Effect of Lipofilling and Platelet-Rich Plasma on Patients with Moderate–Severe Vulvar Lichen Sclerosus who were Non-Responders to Topical Clobetasol Propionate: A Randomized Pilot Study

Published in: Aesthetic Plastic Surgery | Issue 5/2022

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Abstract

Background

The first-line treatment for vulvar lichen sclerosus (VLS) is 3 months of topical corticosteroid therapy. However, limited evidence is available concerning the use of fat grafting and platelet-rich plasma as a second-line treatment for patients who do not respond to first-line treatment.

Methods

This prospective single-center randomized pilot trial included 20 patients with a clinical and histological diagnosis of moderate to severe VLS. The patients in the treatment group (TG) received two infiltrations (at 3-month intervals) of nanofat mixed with platelet-rich plasma (PRP) into the vulvar area, while the control group (CG) received standard topical corticosteroid therapy. Fat was aspirated from the medial thigh or lower abdomen regions. Microfat was obtained after centrifugation and was emulsified to obtain a nanofat suspension. Treatment efficacy was determined by measuring changes in the vulvar skin elasticity, histopathology, and clinical signs, symptoms, and patient quality of life at after 1 year.

Results

A total of 19 patients were finally assessed (9 TG and 10 CG). At the end of the study (1 year), there had been no significant improvement in vulvar skin elasticity. However, patients in the TG showed a significant improvement in their symptoms (itching, pain, burning, and dyspareunia) and clinical signs (cervical erosions, fissures, stenosis, and leukoderma). Analysis of skin biopsies revealed a significant decrease in all inflammatory cell types in the TG. No adverse events related to the autologous treatment were recorded.

Conclusions

Compared with topical corticosteroids, two infiltrations delivered 3 months apart decreased the inflammation of the vulva and improved most of the clinical signs and symptoms associated with VLS. Nonetheless, no improvement in vulvar skin elasticity was derived from the autologous treatment.

Level of Evidence I

This journal requires that authors assign a level of evidence to each article. For a full description of these Evidence-Based Medicine ratings, please refer to the Table of Contents or the online Instructions to Authors www.​springer.​com/​00266.
Literature
1.
go back to reference Meyrick Thomas RH, Ridley CM, McGibbon DH, Black MM (1988) Lichen sclerosus et atrophicus and autoimmunity–a study of 350 women. Br J Dermatol 118(1):41–46CrossRef Meyrick Thomas RH, Ridley CM, McGibbon DH, Black MM (1988) Lichen sclerosus et atrophicus and autoimmunity–a study of 350 women. Br J Dermatol 118(1):41–46CrossRef
2.
go back to reference Cox NH, Mitchell JN, Morley WN (1986) Lichen sclerosus et atrophicus in non-identical female twins. Br J Dermatol 115:743–746CrossRef Cox NH, Mitchell JN, Morley WN (1986) Lichen sclerosus et atrophicus in non-identical female twins. Br J Dermatol 115:743–746CrossRef
3.
go back to reference Sherman V, McPherson T, Baldo M, Salim A, Gao XH, Wojnarowska F (2010) The high rate of familial lichen sclerosus suggests a genetic contribution: an observational cohort study. J Eur Acad Dermatol Venereol 24:1031–1034PubMed Sherman V, McPherson T, Baldo M, Salim A, Gao XH, Wojnarowska F (2010) The high rate of familial lichen sclerosus suggests a genetic contribution: an observational cohort study. J Eur Acad Dermatol Venereol 24:1031–1034PubMed
4.
go back to reference Powell J, Wojnarowska F, Winsey S, Marren P, Welsh K (2000) Lichen sclerosus premenarche: autoimmunity and immunogenetics. Br J Dermatol 142:481–484CrossRef Powell J, Wojnarowska F, Winsey S, Marren P, Welsh K (2000) Lichen sclerosus premenarche: autoimmunity and immunogenetics. Br J Dermatol 142:481–484CrossRef
5.
go back to reference Oyama N, Chan I, Neill SM et al (2003) Autoantibodies to extracellular matrix protein 1 in lichen sclerosus. Lancet 362:118–123CrossRef Oyama N, Chan I, Neill SM et al (2003) Autoantibodies to extracellular matrix protein 1 in lichen sclerosus. Lancet 362:118–123CrossRef
6.
go back to reference Powell JJ, Wojnarowska F (1999) Lichen sclerosus. Lancet 353(9166):1777–1783CrossRef Powell JJ, Wojnarowska F (1999) Lichen sclerosus. Lancet 353(9166):1777–1783CrossRef
7.
go back to reference Goldstein AT, Marinoff SC, Christopher K, Srodon M (2005) Prevalence of vulvar lichen sclerosus in a general gynecology practice. J Reprod Med 50(7):477–480PubMed Goldstein AT, Marinoff SC, Christopher K, Srodon M (2005) Prevalence of vulvar lichen sclerosus in a general gynecology practice. J Reprod Med 50(7):477–480PubMed
8.
go back to reference Sadowsky LM, Schlosser BJ (2019) Vulvar squamous cell carcinoma in a patient with vulvar lichen sclerosus. JAMA Dermatol 155(7):844CrossRef Sadowsky LM, Schlosser BJ (2019) Vulvar squamous cell carcinoma in a patient with vulvar lichen sclerosus. JAMA Dermatol 155(7):844CrossRef
9.
go back to reference Lewis FM, Tatnall FM, Velangi SS, Bunker CB, Kumar A, Brackenbury F et al (2018) British association of dermatologists guidelines for the management of lichen sclerosus. Br J Dermatol 178(4):839–853CrossRef Lewis FM, Tatnall FM, Velangi SS, Bunker CB, Kumar A, Brackenbury F et al (2018) British association of dermatologists guidelines for the management of lichen sclerosus. Br J Dermatol 178(4):839–853CrossRef
10.
go back to reference Singh N, Mishra N, Ghatage P (2021) Treatment options in vulvar lichen sclerosus: a scoping review. Cureus 13(2):e13527PubMedPubMedCentral Singh N, Mishra N, Ghatage P (2021) Treatment options in vulvar lichen sclerosus: a scoping review. Cureus 13(2):e13527PubMedPubMedCentral
11.
go back to reference Ohshima H, Kinoshita S, Oyobikawa M, Futagawa M, Takiwaki H, Ishiko A et al (2013) Use of Cutometer area parameters in evaluating age-related changes in the skin elasticity of the cheek. Skin Res Technol 19(1):e238–e242CrossRef Ohshima H, Kinoshita S, Oyobikawa M, Futagawa M, Takiwaki H, Ishiko A et al (2013) Use of Cutometer area parameters in evaluating age-related changes in the skin elasticity of the cheek. Skin Res Technol 19(1):e238–e242CrossRef
12.
go back to reference Woo MS, Moon KJ, Jung HY, Park SR, Moon TK, Kim NS et al (2014) Comparison of skin elasticity test results from the Ballistometer(®) and Cutometer(®). Skin Res Technol 20(4):422–428CrossRef Woo MS, Moon KJ, Jung HY, Park SR, Moon TK, Kim NS et al (2014) Comparison of skin elasticity test results from the Ballistometer(®) and Cutometer(®). Skin Res Technol 20(4):422–428CrossRef
13.
go back to reference Günthert AR, Duclos K, Jahns BG, Krause E, Amann E, Limacher A et al (2012) Clinical scoring system for vulvar lichen sclerosus. J Sex Med 9(9):2342–2350CrossRef Günthert AR, Duclos K, Jahns BG, Krause E, Amann E, Limacher A et al (2012) Clinical scoring system for vulvar lichen sclerosus. J Sex Med 9(9):2342–2350CrossRef
14.
go back to reference Chren M-M (2012) The Skindex instruments to measure the effects of skin disease on quality of life. Dermatol Clin 30(2):231–236CrossRef Chren M-M (2012) The Skindex instruments to measure the effects of skin disease on quality of life. Dermatol Clin 30(2):231–236CrossRef
15.
go back to reference Jones-Caballero M, Peñas PF, García-Díez A, Chren MM, Badía X (2002) The Spanish version of Skindex-29 an instrument for measuring quality of life in patients with cutaneous diseases. Med Clin (Barc) 118(1):5–9CrossRef Jones-Caballero M, Peñas PF, García-Díez A, Chren MM, Badía X (2002) The Spanish version of Skindex-29 an instrument for measuring quality of life in patients with cutaneous diseases. Med Clin (Barc) 118(1):5–9CrossRef
16.
go back to reference Krapf JM, Mitchell L, Holton MA, Goldstein AT (2020) Vulvar lichen sclerosus: current perspectives. Int J Womens Health 12:11–20CrossRef Krapf JM, Mitchell L, Holton MA, Goldstein AT (2020) Vulvar lichen sclerosus: current perspectives. Int J Womens Health 12:11–20CrossRef
17.
go back to reference Renaud-Vilmer C, Cavelier-Balloy B, Porcher R, Dubertret L (2004) Vulvar lichen sclerosus: effect of long-term topical application of a potent steroid on the course of the disease. Arch Dermatol 140(6):709–712CrossRef Renaud-Vilmer C, Cavelier-Balloy B, Porcher R, Dubertret L (2004) Vulvar lichen sclerosus: effect of long-term topical application of a potent steroid on the course of the disease. Arch Dermatol 140(6):709–712CrossRef
18.
go back to reference Mojallal A, Lequeux C, Shipkov C, Breton P, Foyatier JL, Braye F et al (2009) Improvement of skin quality after fat grafting: clinical observation and an animal study. Plast Reconstr Surg 124(3):765–774CrossRef Mojallal A, Lequeux C, Shipkov C, Breton P, Foyatier JL, Braye F et al (2009) Improvement of skin quality after fat grafting: clinical observation and an animal study. Plast Reconstr Surg 124(3):765–774CrossRef
19.
go back to reference Eshtiaghi P, Sadownik LA (2019) Fact or fiction? adipose-derived stem cells and platelet-rich plasma for the treatment of vulvar lichen sclerosus. J Low Genit Tract Dis 23(1):65–70CrossRef Eshtiaghi P, Sadownik LA (2019) Fact or fiction? adipose-derived stem cells and platelet-rich plasma for the treatment of vulvar lichen sclerosus. J Low Genit Tract Dis 23(1):65–70CrossRef
20.
go back to reference Ersek RA (1991) Transplantation of purified autologous fat: a 3-year follow-up is disappointing. Plast Reconstr Surg 87(2):219–227CrossRef Ersek RA (1991) Transplantation of purified autologous fat: a 3-year follow-up is disappointing. Plast Reconstr Surg 87(2):219–227CrossRef
21.
go back to reference Casabona F, Priano V, Vallerino V, Cogliandro A, Lavagnino G (2010) New surgical approach to lichen sclerosus of the vulva: the role of adipose-derived mesenchymal cells and platelet-rich plasma in tissue regeneration. Plast Reconstr Surg 126(4):210e-e211CrossRef Casabona F, Priano V, Vallerino V, Cogliandro A, Lavagnino G (2010) New surgical approach to lichen sclerosus of the vulva: the role of adipose-derived mesenchymal cells and platelet-rich plasma in tissue regeneration. Plast Reconstr Surg 126(4):210e-e211CrossRef
22.
go back to reference Giuseppina Onesti M, Carella S, Ceccarelli S, Marchese C, Scuderi N (2016) The use of human adipose-derived stem cells in the treatment of physiological and pathological vulvar dystrophies. Stem Cells Int 2016:2561461CrossRef Giuseppina Onesti M, Carella S, Ceccarelli S, Marchese C, Scuderi N (2016) The use of human adipose-derived stem cells in the treatment of physiological and pathological vulvar dystrophies. Stem Cells Int 2016:2561461CrossRef
23.
go back to reference Boero V, Brambilla M, Sipio E, Liverani CA, Di Martino M, Agnoli B et al (2015) Vulvar lichen sclerosus: a new regenerative approach through fat grafting. Gynecol Oncol 139(3):471–475CrossRef Boero V, Brambilla M, Sipio E, Liverani CA, Di Martino M, Agnoli B et al (2015) Vulvar lichen sclerosus: a new regenerative approach through fat grafting. Gynecol Oncol 139(3):471–475CrossRef
24.
go back to reference La CL (2017) Perspectiva del paciente del ensayo clínico. Investig Rev Cubana Salud Pública 43(3):373–95 La CL (2017) Perspectiva del paciente del ensayo clínico. Investig Rev Cubana Salud Pública 43(3):373–95
26.
go back to reference Gause TM 2nd, Kling RE, Sivak WN, Marra KG, Rubin JP, Kokai LE (2014) Particle size in fat graft retention: a review on the impact of harvesting technique in lipofilling surgical outcomes. Adipocyte 3(4):273–279CrossRef Gause TM 2nd, Kling RE, Sivak WN, Marra KG, Rubin JP, Kokai LE (2014) Particle size in fat graft retention: a review on the impact of harvesting technique in lipofilling surgical outcomes. Adipocyte 3(4):273–279CrossRef
27.
go back to reference Andia I, Maffulli N (2013) Platelet-rich plasma for managing pain and inflammation in osteoarthritis. Nat Rev Rheumatol 9(12):721–730CrossRef Andia I, Maffulli N (2013) Platelet-rich plasma for managing pain and inflammation in osteoarthritis. Nat Rev Rheumatol 9(12):721–730CrossRef
29.
go back to reference Guillén MI, Platas J, Pérez Del Caz MD, Mirabet V, Alcaraz MJ (2018) Paracrine anti-inflammatory effects of adipose tissue-derived mesenchymal stem cells in human monocytes. Front Physiol 9:661CrossRef Guillén MI, Platas J, Pérez Del Caz MD, Mirabet V, Alcaraz MJ (2018) Paracrine anti-inflammatory effects of adipose tissue-derived mesenchymal stem cells in human monocytes. Front Physiol 9:661CrossRef
31.
go back to reference Ceserani V, Ferri A, Berenzi A, Benetti A, Ciusani E, Pascucci L et al (2016) Angiogenic and anti-inflammatory properties of micro-fragmented fat tissue and its derived mesenchymal stromal cells. Vasc Cell 8(1):1–2CrossRef Ceserani V, Ferri A, Berenzi A, Benetti A, Ciusani E, Pascucci L et al (2016) Angiogenic and anti-inflammatory properties of micro-fragmented fat tissue and its derived mesenchymal stromal cells. Vasc Cell 8(1):1–2CrossRef
32.
go back to reference Zuk PA, Zhu M, Ashjian P, De Ugarte DA, Huang JI, Mizuno H et al (2002) Human adipose tissue is a source of multipotent stem cells. Mol Biol Cell 13(12):4279–4295CrossRef Zuk PA, Zhu M, Ashjian P, De Ugarte DA, Huang JI, Mizuno H et al (2002) Human adipose tissue is a source of multipotent stem cells. Mol Biol Cell 13(12):4279–4295CrossRef
33.
go back to reference Heo SC, Jeon ES, Lee IH, Kim HS, Kim MB, Kim JH (2011) Tumor necrosis factor-α-activated human adipose tissue-derived mesenchymal stem cells accelerate cutaneous wound healing through paracrine mechanisms. J Investig Dermatol 131(7):1559–1567CrossRef Heo SC, Jeon ES, Lee IH, Kim HS, Kim MB, Kim JH (2011) Tumor necrosis factor-α-activated human adipose tissue-derived mesenchymal stem cells accelerate cutaneous wound healing through paracrine mechanisms. J Investig Dermatol 131(7):1559–1567CrossRef
34.
go back to reference Bendinelli P, Matteucci E, Dogliotti G, Corsi MM, Banfi G, Maroni P et al (2010) Molecular basis of anti-inflammatory action of platelet-rich plasma on human chondrocytes: mechanisms of NF-κB inhibition via HGF. J Cell Physiol 225(3):757–766CrossRef Bendinelli P, Matteucci E, Dogliotti G, Corsi MM, Banfi G, Maroni P et al (2010) Molecular basis of anti-inflammatory action of platelet-rich plasma on human chondrocytes: mechanisms of NF-κB inhibition via HGF. J Cell Physiol 225(3):757–766CrossRef
35.
go back to reference Sundman EA, Cole BJ, Karas V, Della Valle C, Tetreault MW, Mohammed HO et al (2014) The anti-inflammatory and matrix restorative mechanisms of platelet-rich plasma in osteoarthritis. Am J Sports Med 42(1):35–41CrossRef Sundman EA, Cole BJ, Karas V, Della Valle C, Tetreault MW, Mohammed HO et al (2014) The anti-inflammatory and matrix restorative mechanisms of platelet-rich plasma in osteoarthritis. Am J Sports Med 42(1):35–41CrossRef
36.
go back to reference Descalzi F, Ulivi V, Cancedda R, Piscitelli F, Luongo L, Guida F et al (2013) Platelet-rich plasma exerts antinociceptive activity by a peripheral endocannabinoid-related mechanism. Tissue Eng Part A 19(19–20):2120–2129CrossRef Descalzi F, Ulivi V, Cancedda R, Piscitelli F, Luongo L, Guida F et al (2013) Platelet-rich plasma exerts antinociceptive activity by a peripheral endocannabinoid-related mechanism. Tissue Eng Part A 19(19–20):2120–2129CrossRef
37.
go back to reference Goldstein AT, Mitchell L, Govind V, Heller D (2019) A randomized double-blind placebo-controlled trial of autologous platelet-rich plasma intradermal injections for the treatment of vulvar lichen sclerosus. J Am Acad Dermatol 80(6):1788–1789CrossRef Goldstein AT, Mitchell L, Govind V, Heller D (2019) A randomized double-blind placebo-controlled trial of autologous platelet-rich plasma intradermal injections for the treatment of vulvar lichen sclerosus. J Am Acad Dermatol 80(6):1788–1789CrossRef
Metadata
Title
The Effect of Lipofilling and Platelet-Rich Plasma on Patients with Moderate–Severe Vulvar Lichen Sclerosus who were Non-Responders to Topical Clobetasol Propionate: A Randomized Pilot Study
Publication date
20-01-2022
Published in
Aesthetic Plastic Surgery / Issue 5/2022
Print ISSN: 0364-216X
Electronic ISSN: 1432-5241
DOI
https://doi.org/10.1007/s00266-021-02718-1

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