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2.
Clin Case Rep ; 12(3): e8658, 2024 Mar.
Artículo en Inglés | MEDLINE | ID: mdl-38469131

RESUMEN

This report delineates two instances of dermatitis artefacta (DA), a psychodermatological condition marked by self-induced or exacerbated skin lesions. These cases, triggered by treatments from non-qualified practitioners, highlight the critical need for healthcare professionals to discern the potential repercussions of unsound medical guidance.

3.
Cureus ; 13(10): e18490, 2021 Oct.
Artículo en Inglés | MEDLINE | ID: mdl-34754651

RESUMEN

Chromoblastomycosis (CBM) is a rare chronic fungal infection caused by various dematiaceous fungi. This mycosis is mostly found in middle-aged males in tropical and subtropical countries. Only few cases of CBM in children have been reported. The diagnosis of CBM is often delayed due to the similarities with other dermatological diseases, such as cutaneous tuberculosis, mycetoma, leprosy, viral warts, psoriasis vulgaris, or malignancies. We report a case of an 11-year-old healthy boy having CBM. On his left knee, there were large erythematous plaques and tumors with scaly surfaces, some lesions appeared to be cauliflower-like. The patient denied pain and pruritus. The preliminary diagnosis was keloid; however, histopathological findings led to the final diagnosis, which was established as CBM. The patient was treated with oral itraconazole 100 mg daily. His lesions partially resolved within one month of treatment. Although uncommon in children, the differential diagnosis of CBM must be considered in any suspicious lesion(s). Itraconazole 100 mg daily gave a good response in children with CBM. Accurate diagnosis and early treatment are needed to achieve successful management of CBM in children.

4.
J Clin Aesthet Dermatol ; 11(12): 28-29, 2018 Dec.
Artículo en Inglés | MEDLINE | ID: mdl-30666276

RESUMEN

Background: Chronic exposure to solar ultraviolet irradiation can result in facial fine lines and wrinkles, poor texture, and sagging skin. Growth factors are polypeptides or proteins that play a key role in the regulation of a number of physiological processes. Topical application of growth factors also reduces signs of photoaging, promotes fibroblast and keratinocyte proliferation, and induces extracellular matrix formation. Objective: This study evaluated the efficacy of topical growth factor after microneedling treatment for the reduction of visual signs of facial photoaging in Fitzpatrick skin types III to IV. Methods: Eight patients applied 2mL of gel containing a mixture of four different growth factors to photodamaged facial skin after microneedling procedures. The gel contained a biosynthetic mixture of epidermal growth factor, fibroblast growth factor, hepatocyte growth factor, and insulin-like growth factor. This was performed every 10 days, with three treatments total. An independent physician evaluator used the Fitzpatrick wrinkle scale to evaluate clinical photographs that were taken pre- and posttreatment (at before treatment and after four weeks of treatment). Assessment of side effects was performed after the second and third treatments. Patient questionnaires were completed in the fourth week. Results: Based on the independent physician's clinical assessment, seven of the eight patients showed an improvement in texture, fine lines, and wrinkles, especially in the periorbital region. According to the patient questionnaire, four of the eight patients felt their wrinkles were improved, while all patients felt their skin texture was smoother. Five of the eight patients experienced slight redness at 1 to 2 days after treatment. Conclusion: The application of topical growth factors after microneedling can be useful to reduce visual signs of facial photoaging by improving skin texture and minimizing the appearance of fine lines and wrinkles.

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