Efficacy of Polypodium leucotomos in pediatric patients with Xeroderma Pigmentosum
DOI:
https://doi.org/10.70099/BJ/2024.01.01.25Keywords:
Langerhans cells, Polypodium leucotomus, Xeroderma PigmentosumAbstract
Background: Xeroderma pigmentosum (XP) is a photosensitive genodermatotic to ultraviolet radiation, producing irreparable damage to DNA favoring carcinogenesis. Polypodium leucotomos (PL) decreases DNA mutation and improves carcinogenesis and immunosuppression by preserving Langerhans cells; there are no studies on using PL in patients with XP. Objective: To evaluate the efficacy of PL when comparing the incidence of cancer and improving immunosuppression in pediatric patients with XP through the differences in the measurement of Langerhans cells (CD1a) Methodology: A prospective, quasi-experimental study of one arm was carried out in 8 pediatric patients with a clinical diagnosis of XP at Hospital María Especialidades Pediatricas (HMEP) Tegucigalpa, Honduras (August 2017 - August 2018). PL 7.5 mg/kg was given in 2 doses for 1 year, and 2 separate measurements were made during this time. Results: We found 75% of the patients were women, clinically 62.5% were found in phase III or tumor; the main skin manifestations were hyperpigmentation, hypopigmentation and xerosis in 100% of the patients; photophobia and conjunctivitis in 100% and 87% of the cases. Significant differences were found in Langerhans cell measurements before (A) and after (B) the use of the PL extract, between epidermis A with a p-value of 0.029 and in dermis A and B with a p-value of (0.005 and 0.007), respectively. (p<0.05). Only 2 patients reported abdominal pain at the beginning of the study. Conclusion: Oral administration of PL demonstrated efficacy in pediatric patients with XP, as it preserves Langerhans cells, improves immunosuppression, and decreases carcinogenesis; it can be considered a preventive and palliative therapeutic alternative.
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