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Licensed Unlicensed Requires Authentication Published by De Gruyter April 12, 2023

Case study of clinical improvement of atopic dermatitis in a patient treated with herbal-based parapharmaceuticals

  • Andrea Maraschio EMAIL logo , Katya Wulhfard and Luigi Monsellato

Abstract

Objectives

Atopic dermatitis (AD) is a chronic inflammatory skin disorder that has the immunoallergological characteristics of atopy and is characterised by itchy dermatitis with a recurrent-relapsing course and skin hyperreactivity. Official therapy involves topical anti-inflammatory and antimicrobial drugs for the skin but, as it is a recurrent and relapsing disease, the use of systemic anti-inflammatory and immunosuppressive drugs is eventually necessary to control the disease and prevent clinical exacerbation. However, systemic treatment may have a major impact on the patient, induce adverse reactions and not resolve the disease. The aim of the study is to establish whether the use of plant extracts may play a role in improving the quality of life of AD patients.

Case presentation

We describe the clinical case of a 27-year old Caucasian woman with dry, lichenified, slightly reddened and scaly skin lesions (EASI score 1.6), with anamnesis of atopy and multiple allergies, who was treated with an alternative therapeutic strategy to her previous ones, with three herbal-based parapharmaceuticals (Ribes nigrum L. buds, Piper longum L. fruits, Perilla frutescens L. Britton leaves and seeds in LUXFITOAL; Arctium lappa L. radix, Helychrisum italicum (Roth.) G. Don. flos, Viola tricolor L. herba cum floribus in LUXDERM; Trigonella foenum grecum seed extract, Hypericum perforatum extract in LUXTRIGONELLA cream). Two weeks after taking the drops and applying the cream the dry, lichenified skin lesions were no longer present and an eudermic state of the skin is restored (EASI score 0). Furthermore, six months after the beginning of the therapy, the good condition of the skin was maintained. The patient has never had such a long lapse of time without dermatitis reappearing on the anatomical sites observed at the first follow-up. After nine months, the patient was treated again for a dermatitis that had developed at another anatomical site, spreading frontally at the border between the lower margin of the neck and the upper margin of the thorax and at the chin (EASI value 3.2), achieving a marked improvement and a return of the eudermic state after two days (EASI value 0).

Conclusions

The patient was satisfied with the “clean hands” with no inflammation, with the resolution of the dermatitis in the other body sites and stated that the therapy has improved her perceived quality of life. These botanicals may be effective and play a role in improving the quality of life of a person with AD.


Corresponding author: Andrea Maraschio, Pharmacist, Second Level Master in Pharmacoepidemiology and Integrated Care Evaluation, Private Clinic, Via Mac Alister 31, Ferrara 44121, Italy, E-mail:

Acknowledgements

We would like to thank Dr. Eoghan O'Shaughnessy for his kind help in this study.

  1. Research funding: None declared.

  2. Author contributions: All authors have accepted responsibility for the entire content of this manuscript and approved its submission.

  3. Competing interests: The patient involved in the case report is being treated by Dr. Katya Wulhfard, an Internal Medicine physician and expert in Integrative Medicine. The case management and review of the scientific literature relevant to the case was carried out by Dr. Andrea Maraschio, pharmacist, pharmacoepidemiologist and by Dr. Luigi Monsellato, Orthopaedic physician, psychologist and psychotherapist, responsible for the discovery of the Omeosinergetic medical principles underlying the formulation of these herbal products. Dr. Andrea Maraschio declares that he is the scientific manager of Olos System srl, the company that owns the formulations of LUXFITOAL, LUXDERM, LUXTRIGONELLA products. The other authors declare no conflict of interest.

  4. Informed consent: Informed consent was obtained from all individuals included in this study.

  5. Ethical approval: Not applicable.

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Received: 2023-01-10
Accepted: 2023-03-14
Published Online: 2023-04-12

© 2023 Walter de Gruyter GmbH, Berlin/Boston

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