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1.
Ital J Dermatol Venerol ; 156(3): 388-391, 2021 06.
Article in English | MEDLINE | ID: mdl-31804047

ABSTRACT

BACKGROUND: Erythroplasia of Queyrat (EQ) is a rare squamous cell carcinoma in situ, usually occurring on the glans penis, the prepuce, or the urethral meatus. Therapy is mandatory because it can progress to invasive carcinoma in up to 30% of cases. Treatment options include 5-fluorouracil, curettage, cryotherapy, radiotherapy, laser, partial or total penectomy, and microsurgery, as also with imiquimod and photodynamic therapies. METHODS: Between 2015 to 2018 we treated five patients, with histologically confirmed EQ, with ingenol mebutate (IM) 0.015% gel applied for 3 days consecutively. RESULTS: Three patients showed complete response at one year follow up. Two patients showed partial response after two months, so they received a second course of therapy with IM. At one-year follow-up, one of them showed complete response, the other partial response. CONCLUSIONS: Our experience demonstrated that IM may be considered as an effective and safe treatment option in EQ. IM offers various advantages such as easy and fast application, rapid complete remission, better compliance, few side effects and excellent cosmetical results. The authors call for further exploitation in bigger trials.


Subject(s)
Diterpenes , Erythroplasia , Penile Neoplasms , Photochemotherapy , Diterpenes/therapeutic use , Erythroplasia/drug therapy , Humans , Male , Penile Neoplasms/drug therapy
2.
Acta Dermatovenerol Croat ; 28(2): 93-101, 2020 Aug.
Article in English | MEDLINE | ID: mdl-32876034

ABSTRACT

Actinic keratosis (AK) is a common skin disease related to ultraviolet chronic exposure, that is now considered a squamous cell carcinoma in situ. Primary skin cancer prevention strategies should be recommended for high risk patients. There is a wide spectrum of treatment options available for AKs, and several variables should be taken into account regarding the best therapeutic choice for each patient. The purpose of this article is to review the current treatment strategies for AKs localized on the face and scalp, with a focus on the practical point of view that could be useful for choosing the best therapeutic option. The two main therapeutic approaches will be distinguished first: lesion-directed and field-directed. Afterwards, the treatment based on clinical type and patient comorbidity will be discussed.


Subject(s)
Carcinoma in Situ/therapy , Carcinoma, Squamous Cell/therapy , Face , Keratosis, Actinic/therapy , Precancerous Conditions/therapy , Scalp , Carcinoma in Situ/pathology , Carcinoma, Squamous Cell/pathology , Decision Making , Humans , Keratosis, Actinic/pathology , Precancerous Conditions/pathology
4.
Int J Dermatol ; 59(4): 406-411, 2020 Apr.
Article in English | MEDLINE | ID: mdl-31663126

ABSTRACT

Recent data support the theory of the involvement of IL-17 in the pathogenesis of several chronic inflammatory skin diseases (psoriasis, atopic dermatitis, acne, hidradenitis suppurativa) and autoimmune skin diseases (alopecia areata, vitiligo, bullous diseases). Even if the role of IL-17 in inflammatory and autoimmune diseases has been reported extensively, its role in tumor is still controversial. Some reports show that Th17 cells eradicate tumors, while others reveal that they promote the initiation and early growth of tumors. Herein, we review the role of IL-17 in the involvement of some common dermatologic diseases: psoriasis, atopic dermatitis, hidradenitis suppurativa, acne, vitiligo, melanoma, and nonmelanoma skin cancers.


Subject(s)
Autoimmunity , Carcinogenesis/immunology , Inflammation/immunology , Interleukin-17/metabolism , Skin Diseases/immunology , Th17 Cells/immunology , Animals , Disease Models, Animal , Humans , Mice , Review Literature as Topic , Skin/immunology , Skin/pathology , Skin Diseases/pathology , Th17 Cells/metabolism , Tumor Microenvironment/immunology
8.
Acta Dermatovenerol Croat ; 27(1): 22-27, 2019 Mar.
Article in English | MEDLINE | ID: mdl-31032787

ABSTRACT

Basal cell carcinoma (BCC) is the most frequent skin cancer and is characterized by slow growth, even if it can be locally invasive and rarely metastasizes. Many different phenotypic presentations and histopathologic subtypes have been described, and the current guidelines subdivide BCCs into low-risk (nodular and superficial) and high-risk subtypes (micronodular, infiltrating, and morphoeic BCC and those with squamous differentiation). Dermoscopy allows the identification of the features associated with these different subtypes. Compared with the low-risk forms of BCC, more aggressive ones tend to undergo more frequently incomplete surgical excision and perineural invasion, so the identification of these lesions before surgery is extremely important. The gold standard of treatment is surgery, particularly for the H region of the face and infiltrative lesions, but other options are available and selected according to many variables, including body area, age, comorbidities, and clinical, dermoscopic, and histopathological features of the lesion. Moreover, the possible complications of surgical approaches, namely healing defects, failure of skin grafts, and wound infection, should be considered. In this review we discuss the management of BCC localized on the face and scalp, according to the currently available treatment options.


Subject(s)
Carcinoma, Basal Cell/diagnosis , Carcinoma, Basal Cell/therapy , Facial Neoplasms/therapy , Scalp , Skin Neoplasms/diagnosis , Skin Neoplasms/therapy , Facial Neoplasms/diagnosis , Humans
9.
Dermatol Ther ; 29(6): 424-432, 2016 Nov.
Article in English | MEDLINE | ID: mdl-27424565

ABSTRACT

Androgenetic alopecia (AGA) is a genetically determined progressive hair-loss condition which represents the most common cause of hair loss in men. The use of the medical term androgenetic alopecia reflects current knowledge about the important role of androgens and genetic factors in its etiology. In addition to androgen-dependent changes in the hair cycle, sustained microscopic follicular inflammation contributes to its onset. Furthermore, Prostaglandins have been demonstrated to have the ability in modulating hair follicle cycle; in particular, PGD2 inhibits hair growth while PGE2/F2a promote growth. Due to the progressive nature of AGA, the treatment should be started early and continued indefinitely, since the benefit will not be maintained upon ceasing therapy. To date, only two therapeutic agents have been approved by the Food and Drug Administration and European Medicines Agency for the treatment of AGA: topical minoxidil and oral finasteride. Considering the many pathogenetic mechanisms involved in AGA, various treatment options are available: topical and systemic drugs may be used and the choice depends on various factors including grading of AGA, patients' pathological conditions, practicability, costs and risks. So, the treatment for AGA should be based on personalized therapy and targeted at the different pathophysiological aspects of AGA.


Subject(s)
5-alpha Reductase Inhibitors/administration & dosage , Alopecia/drug therapy , Finasteride/administration & dosage , Hair/drug effects , Minoxidil/administration & dosage , Scalp/drug effects , 5-alpha Reductase Inhibitors/adverse effects , Administration, Cutaneous , Administration, Oral , Alopecia/genetics , Alopecia/metabolism , Alopecia/physiopathology , Finasteride/adverse effects , Hair/growth & development , Hair/metabolism , Hair/transplantation , Humans , Minoxidil/adverse effects , Scalp/metabolism , Scalp/physiopathology , Treatment Outcome
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