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1.
Clin Exp Dermatol ; 44(5): e177-e180, 2019 Jul.
Article in English | MEDLINE | ID: mdl-30593710

ABSTRACT

The clinical characteristics associated with hidradenitis suppurativa (HS) severity are poorly understood. In this study, 124 patients with HS from 6 Italian dermatology centres participated in this study. Disease severity was assessed using the Hidradenitis Suppurativa Physician's Global Assessment score (HS-PGA) and Hurley score. The impact of clinical characteristics on disease severity was assessed by logistic regression. Clinical characteristics were similar between men (n = 53) and women (n = 71). Disease severity was also similar; 75% of the patients had Hurley stage II or III disease, and > 60% had moderate, severe or very severe HS as judged by HS-PGA. Lesions were more frequent in the gluteal region in men (32.3% in men vs. 8.7% in women, P < 0.001) and more frequent on the breast in women (16.3% in women vs. 4.6% in men, P = 0.02). Obesity was associated with increased disease severity as measured by HS-PGA (OR: 3.28, 95% CI 1.55-6.95, P < 0.01) and Hurley classification (OR: 3.22, 95% CI 1.34-7.31, P < 0.01). Although severity of HS is similar between the sexes, the localization of lesions is different.


Subject(s)
Hidradenitis Suppurativa/physiopathology , Adult , Axilla , Breast , Buttocks , Comorbidity , Female , Groin , Hidradenitis Suppurativa/epidemiology , Humans , Italy/epidemiology , Logistic Models , Male , Middle Aged , Obesity/epidemiology , Severity of Illness Index , Sex Factors , Young Adult
2.
J Eur Acad Dermatol Venereol ; 33 Suppl 6: 10-14, 2019 Oct.
Article in English | MEDLINE | ID: mdl-31535763

ABSTRACT

BACKGROUND: Ultrasound (US) is a real-time non-invasive technique that has been demonstrated to support an early diagnosis and a more precise assessment of hidradenitis suppurativa (HS). OBJECTIVES: To compare the clinical and US evaluation of a series of HS patients. METHODS: 434 HS patients (259 F, 175 M; mean age 33.82 ±13.31 years) observed across 19 Italian dermatology centres [members of the Italian Ultrasound Working Group (IUWG)] were enrolled in a retrospective study. Clinical staging was obtained by the Hidradenitis Suppurativa Physician's Global Assessment score (HS-PGA), while the ultrasonographic staging was determined by the US HS-PGA, based on the same scores as clinical HS-PGA but performed with the aid of US. RESULTS: At the end of the study, the mean clinical and US HS-PGA scores were 2.70 and 2.92, respectively. Direct comparison of clinical and ultrasonographic assessment revealed that a higher proportion of patients was classified as having moderate and very severe disease by US. In particular, 117 patients (26.96%) had a worse classification by US HS-PGA compared to clinical assessment. CONCLUSION: Our findings confirm that the use of clinical grading only to assess HS severity may underestimate the real disease severity. US examination can be considered an essential non-invasive imaging tool available to dermatologists for a more accurate diagnosis, staging, treatment planning and monitoring of HS and should be included in the pathway to an optimal standard of care of HS.


Subject(s)
Hidradenitis Suppurativa/diagnostic imaging , Physical Examination , Severity of Illness Index , Ultrasonography , Adult , Female , Hidradenitis Suppurativa/therapy , Humans , Male , Middle Aged , Retrospective Studies , Young Adult
3.
Photochem Photobiol Sci ; 16(9): 1471-1479, 2017 Sep 13.
Article in English | MEDLINE | ID: mdl-28812775

ABSTRACT

Polymorphic light eruption (PLE) is described as a delayed-type hypersensitivity reaction (DTHR) toward a de novo light-induced antigen, yet to be identified. In effect, the inflammatory pathways of PLE and allergic contact dermatitis (ACD) share common patterns in terms of the mediators involved from the innate and adaptive immune system participating in the DTHR. As we have previously highlighted the role of interleukin (IL)-1 family members in ACD, we hypothesised that the same mediators could have similar functions in PLE. Our research aimed to assess the expression of certain IL-1family members in PLE patients vs. controls, and to compare it with ACD. The study population comprised 17 patients with PLE, 5 affected by ACD and 10 healthy controls in the same age range. Lesional and healthy skin samples were collected respectively from patients and donors. IL-36α, IL-36ß, IL-36γ, IL-36 receptor antagonist (Ra), IL-1ß, IL-33 gene and protein expressions were evaluated through RT-PCR and immunohistochemistry. Circulating proteins in the PLE patients were analysed by using western blot. The IL-36γ gene expression was significantly increased in PLE lesions compared to that in healthy controls and ACD lesions (***p < 0.001; ##p < 0.01 respectively), whereas the other analyzed ILs were more expressed in ACD. Immunohistochemical analysis revealed that IL-36α and IL-36γ protein levels were increased in PLE lesions compared to those of the healthy samples (***p < 0.001). Furthermore the IL-36γ plasma level was increased in PLE patients vs. controls (*p < 0.05). Our findings indicate that the IL-1 family pro-inflammatory members are increased in PLE with distinct differences from those in ACD, in particular with regard to IL-36γ mRNA regulation. Their role as activators of the local, and perhaps systemic, immune response, or as inhibitors of the immune tolerance machinery, needs further investigation.


Subject(s)
Dermatitis, Allergic Contact/metabolism , Interleukin-1/metabolism , Photosensitivity Disorders/metabolism , Skin Diseases, Genetic/metabolism , Adult , Aged , Female , Humans , Interleukin-1/genetics , Male , Middle Aged
4.
Clin Exp Dermatol ; 41(1): 38-42, 2016 Jan.
Article in English | MEDLINE | ID: mdl-26053680

ABSTRACT

Acne is a common and complex skin disease, with a very complex pathogenesis. Although in women the relationship between acne and insulin resistance is well known, in particular in women with PCOS, in males this relationship has been poorly investigated. In total, 20 subjects with an altered metabolic profile were considered for this study and randomized as follows: 10 patients were treated with metformin plus a hypocaloric diet for 6 months (group A), while 10 patients did not receive any treatment with metformin and were only followed up (group B). All patients of group A, after 6 months of metformin therapy, had a statistically significant improvement compared with patients in group B. Our study reveals the importance of diet and insulin resistance in acne pathogenesis, and underlines the possible use of metformin and diet as possible adjuvant therapy for male patients with acne.


Subject(s)
Acne Vulgaris/therapy , Diet, Reducing , Hypoglycemic Agents/therapeutic use , Metformin/therapeutic use , Acne Vulgaris/pathology , Adolescent , Adult , Combined Modality Therapy , Glucose/metabolism , Glycemic Index , Humans , Insulin/metabolism , Insulin Resistance/physiology , Male , Young Adult
6.
Clin Exp Dermatol ; 39(3): 391-4, 2014 Apr.
Article in English | MEDLINE | ID: mdl-24635083

ABSTRACT

The isoflavones daidzein and genistein are natural compounds which have anti-inflammatory and photoprotective activities, and may be effective in the repair of ultraviolet (UV)-induced photodamage. In this study, an alcoholic solution of aglycone isoflavones with a genistein:daidzein ratio of 1:4 [Rottapharm (RPH)-aglycone] was examined for its effects on the repair of DNA damage induced by a single dose of UVB irradiation (20 mJ/cm(2)). For this purpose, human skin cells were first UVB-irradiated and then treated with RPH-aglycone. Comet assay analysis was used to estimate the UVB-induced DNA damage at different time points after treatment by measuring the tail moment parameter. We found that treatment with 10 µmol/L RPH-aglycone solution resulted in a significantly reduced tail moment at 1h after treatment, and 34-35% enhancement of damage repair at 4 h after treatment. These results suggest that isoflavone aglycones are protective against UVB-induced DNA damage.


Subject(s)
Anticarcinogenic Agents/pharmacology , DNA Damage/drug effects , Epidermal Cells , Epithelial Cells , Genistein/pharmacology , Isoflavones/pharmacology , Ultraviolet Rays/adverse effects , Cells, Cultured , Comet Assay , Epithelial Cells/drug effects , Epithelial Cells/radiation effects , Humans , Skin Aging/drug effects
9.
G Ital Dermatol Venereol ; 149(5): 581-5, 2014 Oct.
Article in English | MEDLINE | ID: mdl-25213385

ABSTRACT

AIM: The use of skin needling is believed to aid the transdermal delivery of drugs, even if it is mostly used for skin collagen induction. The aim of this paper was to use skin needling, combined with a local anesthetic EMLA (eutectic mixture of lidocaine and prilocaine), as a way to enhance transdermal drug penetration and optimize the analgesic effects of common local anesthesia. METHODS: We recruited 15 patients. For each patient of our study we defined a skin area of 3 cm2 from two forearms: on one side, we used skin needling first and immediately thereafter applied the EMLA in occlusion for 60 minutes; on the other one, we only applied EMLA in occlusion for 60 minutes. Then, pain was induced in each patient's forearm by introducing a 27 G needle into the skin 4 mm deep three times. Lastly, pain sensation measures were registered and a middle value was calculated. RESULTS: When skin needling is used in conjunction with EMLA applied in occlusion for 60 minutes on skin forearms, the level of pain sensation registered was significantly reduced on a Visual Analogue Scale compared to the application of EMLA alone. CONCLUSION: The use of skin needling can improve the transdermal delivery of an emulsion-like eutectic mixture of local anesthetics (EMLA) and can introduce the use of this method for delivering topical molecules in dermatology.


Subject(s)
Administration, Cutaneous , Anesthetics, Combined/administration & dosage , Anesthetics, Local/administration & dosage , Drug Delivery Systems/instrumentation , Lidocaine/administration & dosage , Needles , Prilocaine/administration & dosage , Adolescent , Adult , Anesthetics, Combined/pharmacokinetics , Anesthetics, Local/pharmacokinetics , Drug Delivery Systems/methods , Equipment Design , Female , Humans , Lidocaine/pharmacokinetics , Lidocaine, Prilocaine Drug Combination , Male , Middle Aged , Pain/prevention & control , Prilocaine/pharmacokinetics , Visual Analog Scale , Young Adult
10.
G Ital Dermatol Venereol ; 149(1): 123-30, 2014 Feb.
Article in English | MEDLINE | ID: mdl-24566573

ABSTRACT

AIM: The aim of the present study was to evaluate the efficacy and safety of narrowband UVB (NB-UVB) compared with tacrolimus ointment 0.1% in patients with bilateral vitiligo. METHODS: In this comparative study, four groups of patients were randomized. Each group was composed by 12 patients with bilateral vitiligo; in each group, every patient was irradiated with NB-UVB (length: 311 nm) twice a week for 9 months and applied tacrolimus ointment 0.1% twice a day on the other area in the same period. Before starting therapy and after 3, 6 and 9 months of therapy, a clinical and photographic evaluation of percentage of repigmentation was performed and Dermatology Life Quality Index Questionnaire was fulfilled. RESULTS: A repigmentation at least partial occurred in 71% of patients after 36 weeks of treatment with tacrolimus ointment 0.1%; in the whole sample, 14 patients (29%) showed no repigmentation at all, with 2 of them discontinuing the therapy because of side effects (erythema and folliculitis-like manifestations). A homogeneous repigmentation at least partial occurred in 69% of patients after 36 weeks of treatment with NB-UVB; in the whole sample 15 patients (31%) showed no repigmentation at all, with 1 of them discontinuing the therapy because of side effects. CONCLUSION: The present study confirmed that the efficacy of NB-UVB phototherapy in vitiligo is comparable to tacrolimus ointment 0.1% therapy. On the basis of our study, we may suggest tacrolimus ointment 0.1% as an alternative to NB-UVB therapy for treating vitiligo.


Subject(s)
Immunosuppressive Agents/therapeutic use , Tacrolimus/therapeutic use , Ultraviolet Therapy , Vitiligo/drug therapy , Vitiligo/radiotherapy , Adolescent , Adult , Aged , Child , Epidermis/pathology , Erythema/etiology , Folliculitis/etiology , Humans , Melanocytes/ultrastructure , Middle Aged , Prospective Studies , Skin Pigmentation , Surveys and Questionnaires , Vitiligo/complications , Vitiligo/pathology , Young Adult
11.
G Ital Dermatol Venereol ; 149(4): 441-5, 2014 Aug.
Article in English | MEDLINE | ID: mdl-25068233

ABSTRACT

AIM: The purpose of the study was to analyze the potential capacity of a dietary supplement, based on gamma linolenic acid, vitamin E, vitamin C, beta-carotene, coenzyme Q10 and Vitis Vitifera, to reduce side effects, in particular the dry skin, erythema and desquamation, due to treatment with oral isotretinoin, and evaluate the ability of the product to increase adherence to therapy in patients with acne. METHODS: Forty-eight patients with nodular acne (32 females and 16 males) were randomly divided into 2 groups: 24 received isotretinoin therapy (20-30 mg/day) for 6 months associated to dietary supplement (twice a day), while the other 24 patients received only isotretinoin (20-30 mg/day) for 6 months. For all patients the degree of acne severity, through GAGS (Global Acne Grading System), the sebum production by Sebutape, the hydration by Corneometer and the erythema by Mexameter, were measured. We have also evaluated the adherence to treatment, asking to patients how many days a week they follow the therapy. RESULTS: Patients treated with dietary supplement had lower side effects, with a less degree of erythema and dryness, and greater degree of hydration; a greater adherence to therapy was also reported. CONCLUSION: Thanks to antioxidant and moisturizing properties, the dietary supplement containing gamma linolenic acid, vitamin E, vitamin C, betacarotene, coenzyme Q10 and Vitis Vitifera, can be considered a useful supplement in the treatment and prevention of dry skin associated with the use of oral isotretinoin.


Subject(s)
Acne Vulgaris/drug therapy , Dermatologic Agents/administration & dosage , Dermatologic Agents/adverse effects , Dietary Supplements , Erythema/prevention & control , Isotretinoin/administration & dosage , Isotretinoin/adverse effects , Skin/drug effects , Acne Vulgaris/diagnosis , Administration, Oral , Adolescent , Adult , Ascorbic Acid/therapeutic use , Dose-Response Relationship, Drug , Erythema/chemically induced , Female , Humans , Italy , Male , Severity of Illness Index , Treatment Outcome , Ubiquinone/analogs & derivatives , Ubiquinone/therapeutic use , Vitamin E/therapeutic use , Vitamins/therapeutic use , Vitis , beta Carotene/therapeutic use , gamma-Linolenic Acid/therapeutic use
13.
Clin Exp Dermatol ; 38(2): 185-8, 2013 Mar.
Article in English | MEDLINE | ID: mdl-23397947

ABSTRACT

Ultraviolet (UV) radiation has profound effects on human skin, causing sunburn, inflammation, cellular-tissue injury, cell death, and skin cancer. Most of these effects are mediated by a number of cytokines produced by keratinocytes. In this study we investigated whether nicotinamide (NCT), the amide form of vitamin B3, might have a protective function in reducing the expression of interleukin (IL)-1ß, IL-6, IL-8, IL-10, monocyte chemoattractant protein (MCP)-1 and tumour necrosis factor (TNF)-α in UV-irradiated keratinocytes. HaCaT cells were treated with UVB in the presence or absence of NCT, and cytokine mRNA levels were examined by quantitative real-time PCR. NCT significantly downregulated IL-6, IL-10, MCP-1 and TNF-α mRNA expression, whereas it did not exert any significant effect on IL-1ß or IL-8 expression. Because of its ability to decrease these cytokine mediators after UV exposure, NCT is a possible therapy to improve or prevent conditions induced or aggravated by UV light.


Subject(s)
Cytokines/metabolism , Keratinocytes/drug effects , Niacinamide/pharmacology , Vitamin B Complex/pharmacology , Chemokine CCL2/genetics , Down-Regulation , Gene Expression Profiling , Humans , Interleukin-10/genetics , Interleukin-6/genetics , Keratinocytes/metabolism , Keratinocytes/radiation effects , RNA, Messenger/metabolism , Real-Time Polymerase Chain Reaction , Skin/drug effects , Skin/metabolism , Skin/radiation effects , Tumor Necrosis Factor-alpha/genetics , Ultraviolet Rays
19.
Dermatology ; 219(4): 322-8, 2009.
Article in English | MEDLINE | ID: mdl-19851060

ABSTRACT

BACKGROUND: Photodynamic therapy (PDT) with aminolevulinic acid (ALA) has been shown to be an effective treatment for acne. However, the effect of ALA PDT on comedo formation has never been objectively evaluated. Cyanoacrylate follicular biopsy (CFB), a noninvasive procedure, has been proposed as the most reliable tool for studying follicular casts. OBJECTIVE: To determine the possible effect of ALA and red light (550-700 nm) on macro- and microcomedones in acne patients. PATIENTS AND METHODS: 10 patients with mild-to-moderate facial and/or chest/back acne resistant to conventional therapies received ALA PDT at 2-week intervals in 3 sessions. The severity of acne had been estimated by a system of points, the Global Acne Grading System. The patients underwent PDT utilizing ALA 10% (face) or 15% (back/chest) and red light (15 J/cm(2) each session). CFBs were performed. RESULTS: Four weeks after their last PDT session, the patients showed an average global score reduction of 50%. CFBs demonstrated a reduction in the total area, the average area and the density of macrocomedones. CONCLUSION: The results obtained in this study using CFB evaluation demonstrate that ALA PDT exerts an action on the comedogenic phase as well.


Subject(s)
Acne Vulgaris/drug therapy , Acne Vulgaris/pathology , Aminolevulinic Acid/therapeutic use , Photochemotherapy/methods , Photosensitizing Agents/therapeutic use , Adolescent , Adult , Back/pathology , Biopsy , Face/pathology , Female , Humans , Male , Severity of Illness Index , Thoracic Wall/pathology , Treatment Outcome
20.
Dermatol Ther ; 21 Suppl 3: S29-32, 2008.
Article in English | MEDLINE | ID: mdl-19076629

ABSTRACT

Skin scars remain a therapeutic challenge to dermatologists. Over the past several decades, numerous surgical techniques have been used to improve the appearance of scarring. The objective of this study is to evaluate the efficacy of a local application of a (50%) concentration of trichloroacetic acid (TCA) for the treatment of atrophic acne scars (grade 3 in Goodman classification), as opposed to the higher (90%) TCA concentration used in previous studies, in order to reduce adverse local effects. The primary goal was the resolution of acne or chickenpox scars. Secondary goals were physician and subject assessments of scar improvement. Fifty percent TCA was applied locally to atrophic scars in five patients. Three patients had treated scars on the face and two patients had treated scars on the back. Wooden applicators were used to apply TCA locally and the treatment was repeated at 4-week intervals for a total of three sessions. Digital photographic analysis of lesions supported clinical observations. Histologic examination was performed only on two samples of patients with treated scars on the back. Clinical examination revealed cosmetic improvements in both depth and appearance of skin scars. We believe that the 50% TCA CROSS can be an effective technique for the treatment of atrophic scars.


Subject(s)
Acne Vulgaris/complications , Chemexfoliation/methods , Cicatrix/therapy , Dermatologic Agents/therapeutic use , Trichloroacetic Acid/therapeutic use , Acne Vulgaris/pathology , Acne Vulgaris/therapy , Adult , Cicatrix/etiology , Cicatrix/pathology , Female , Humans , Male , Patient Satisfaction , Pilot Projects , Time Factors , Treatment Outcome
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