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1.
Arch Dermatol Res ; 316(6): 204, 2024 May 24.
Article in English | MEDLINE | ID: mdl-38787466

ABSTRACT

Plantar warts are common skin lesions that continue to represent a therapeutic challenge. They are still resistant to therapy and are highly recurrent, despite the diverse number of treatments available. Therapies targeting vasculature, such as pulsed dye laser, have been used successfully in the treatment of plantar warts. Polidocanol, a detergent sclerosant approved for the sclerotherapy of incompetent and dilated saphenous veins, has also been used as an off-label therapy for a wide range of skin conditions with vascular components such as hemangiomas and pyogenic granuloma. The current, open-label, prospective, pilot study aimed to evaluate the safety and efficacy of the intralesional polidocanol 3% in the treatment of plantar warts. Twenty patients (11 females and 9 males), with plantar warts, aged 12-50 years received biweekly sessions of intralesional polidocanol 3% until complete clearance or for a maximum of 6 sessions. Response to treatment was graded as complete (100% clearance), partial (50-99%), and no response (< 50%). At the end of the study, 12 (60%) patients achieved complete clearance of their warts after 1-5 sessions, 5 (25%) patients had only partial response, and 3 (15%) patients did not achieve any clearance of their warts. The procedure was largely tolerable by patients. Pain at the injection site and bruises were reported by 9 (45%) and 2 (10%) patients, respectively. Both side effects resolved spontaneously and completely within a few days. The findings of the current study suggest that intralesional injection of 3% polidocanol in biweekly sessions may be a safe, effective, and tolerable method for the treatment of plantar warts.


Subject(s)
Injections, Intralesional , Polidocanol , Sclerosing Solutions , Sclerotherapy , Warts , Humans , Polidocanol/administration & dosage , Pilot Projects , Female , Male , Adult , Sclerotherapy/methods , Sclerotherapy/adverse effects , Warts/therapy , Warts/drug therapy , Adolescent , Middle Aged , Treatment Outcome , Young Adult , Sclerosing Solutions/administration & dosage , Sclerosing Solutions/adverse effects , Prospective Studies , Child
2.
Dermatol Ther ; 35(11): e15815, 2022 11.
Article in English | MEDLINE | ID: mdl-36101002

ABSTRACT

Plantar warts continue to represent a therapeutic challenge due to treatment resistance and high recurrence rates. Intralesional methotrexate, a cytotoxic chemotherapeutic agent with in-vitro anti-viral properties has been used for many dermatological indications. Two previous studies evaluated intralesional injection of diluted methotrexate (in 0.5, 1, and 2 mg/ml dilutions) in the treatment of warts and found it poorly effective. The concentrations used in these studies were much lower than those used for other indications. The current, open-label, prospective, pilot study aimed to evaluate the safety and efficacy of the intralesional injection of full concentration (25 mg/ml) methotrexate in the treatment of plantar warts. Twenty patients with plantar warts, 10 (50%) males, and 10 (50%) females, with mean ± SD age of 28.45 ± 8.66 years (range, 18-46 years) received biweekly sessions of intralesional methotrexate (25 mg/ml) until complete clearance or for a maximum of 6 sessions. Complete clearance of warts was achieved in 2 (10%), 6 (30%), and 7 (35%) patients after 4, 5, and 6 sessions, respectively. Another 8 (40%) patients showed partial improvement after 6 sessions. The response rate did not correlate significantly with the number of warts. Nine (45%) patients did not report any side effects. Pain and bruises were reported by 8 (40%) and 6 (30%) patients, respectively. These findings suggest that biweekly sessions of full (25 mg/ml) concentration of methotrexate are a safe and effective treatment for plantar warts. It may be considered an alternative line of treatment for resistant cases.


Subject(s)
Methotrexate , Warts , Male , Female , Humans , Adolescent , Young Adult , Adult , Middle Aged , Pilot Projects , Methotrexate/adverse effects , Prospective Studies , Warts/diagnosis , Warts/drug therapy , Injections, Intralesional , Treatment Outcome
5.
Dermatol Ther ; 32(6): e13094, 2019 11.
Article in English | MEDLINE | ID: mdl-31580005

ABSTRACT

Pulsed-dye laser (PDL) is the treatment of choice for port wine stain (PWS), and the development of purpura is considered a therapeutic endpoint. Changes in PWS vasculature observed by dermoscopy immediately after laser irradiation have been suggested to predict the minimal effective fluence. The current study aimed at comparing these changes with purpura as a therapeutic endpoint. Fifty-six PWS patients, randomized into two groups, received five monthly PDL sessions (595 nm and 10 mm spot size). At the first visit, patients received multiple gradually increasing test irradiations. Patients in the first group were treated with the lowest dose that resulted in 24-hr-lasting purpura, while patients in the second group were treated with the lowest dose that resulted in vessel disappearance observed by dermoscope. No statistically significant differences were observed between the two groups (the dermoscopic and the purpuric) regarding mean average improvement (42.4 and 37.32%, respectively, p = .32), grade of improvement (p = .44), and the rate of side effects (0 and 13.79%, respectively, p = .13). In conclusion, the immediate post-irradiation vessel disappearance (detected by dermoscope) is comparable, in safety and efficacy, to purpura as a therapeutic endpoint and maybe more time-saving and more accepted cosmetically.


Subject(s)
Dermoscopy , Lasers, Dye/therapeutic use , Port-Wine Stain/therapy , Adolescent , Adult , Child , Child, Preschool , Female , Humans , Infant , Lasers, Dye/adverse effects , Male , Middle Aged , Port-Wine Stain/pathology , Prospective Studies , Treatment Outcome , Young Adult
6.
Andrologia ; 51(9): e13364, 2019 Oct.
Article in English | MEDLINE | ID: mdl-31304987

ABSTRACT

A cross-sectional survey was conducted in Egypt from November 2015 to June 2016. Sexually active adult men were interviewed by a questionnaire designed by the authors. All the participants were evaluated by the abridged 5-item version of the International Index of Erectile Function (IIEF). A total of 3,000 sexually active Egyptian males participated in this study, 946 (31.53%) reported using PDE5Is at least once, and 2054 (68.47%) have never used them. The majority of those who used PDE5Is obtained them for recreational purposes mainly for pleasure (58.35%) and to increase duration/frequency of the intercourse (15.6%). Only 26.05% used PDE5Is to treat ED. The main source of obtaining PDE5Is was friends, relatives and colleagues (62.79%); 25.16% of users obtained the drug by themselves, and 6.66% were prescribed the drug by a pharmacist. Only 5.39% of users obtained the drug after a specialist physician consultation. Sildenafil was the most commonly used PDE5I (90.6%), and most of the users (88.05%) used them in an occasional manner even in the presence of erectile dysfunction, while 11.95% used the drug in a regular manner for every intercourse. PDE5Is are frequently used by the Egyptian male population, and most of them seemed to take them as recreational medications.


Subject(s)
Coitus/psychology , Erectile Dysfunction/epidemiology , Phosphodiesterase 5 Inhibitors/therapeutic use , Pleasure , Adult , Cross-Sectional Studies , Egypt/epidemiology , Erectile Dysfunction/drug therapy , Humans , Male , Middle Aged , Patient Satisfaction/statistics & numerical data , Penile Erection/drug effects , Penile Erection/psychology , Phosphodiesterase 5 Inhibitors/pharmacology , Prevalence , Sildenafil Citrate/pharmacology , Sildenafil Citrate/therapeutic use , Surveys and Questionnaires/statistics & numerical data
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