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1.
An. bras. dermatol ; 96(4): 408-415, July-Aug. 2021. tab, graf
Article Dans Anglais | LILACS | ID: biblio-1285105

Résumé

Abstract Background: The ear is a region that has a high prevalence of cutaneous carcinomas and several guidelines indicate Mohs micrographic surgery as the first-choice treatment in such cases. Although the technique allows maximum preservation of healthy tissue, many auricular surgical wounds constitute a challenge due to the peculiar local anatomy, with evident curves and reliefs. Auricular reconstruction should prioritize function before aesthetics, but without leaving the latter aside, since postoperative distortions can have a significant psychological impact. Objective: To describe the authors' experience in auricular reconstruction after Mohs surgery and to evaluate the most frequently used repair methods. Methods: Retrospective study of consecutive cases submitted to Mohs surgery and auricular reconstruction, over a period of 3 years. Results: One hundred and one cases were included and the most common repair method was primary closure (n = 35), followed by full-thickness skin graft (n = 30) and flaps (n = 24). In thirty cases, reconstruction methods were associated. Seven patients had complications (partial graft necrosis, postoperative bleeding or infection). Study limitations: Retrospective design and the absence of long-term follow-up of some cases. Conclusions: The dermatologic surgeon should be familiarized with different options for auricular reconstruction. Primary closure and skin grafts were the most frequently used repair methods.


Sujets)
Tumeurs cutanées/chirurgie , Chirurgie de Mohs , Lambeaux chirurgicaux , Études rétrospectives , Transplantation de peau
2.
An. bras. dermatol ; 96(3): 263-277, May-June 2021. tab, graf
Article Dans Anglais | LILACS | ID: biblio-1285080

Résumé

Abstract Mohs micrographic surgery is a specialized form of skin cancer surgery that has the highest cure rates for several cutaneous malignancies. Certain skin cancers can have small extensions or "roots" that may be missed if an excised tumor is serially cross-sectioned in a "bread-loaf" fashion, commonly performed on excision specimens. The method of Mohs micrographic surgery is unique in that the dermatologist (Mohs surgeon) acts as both surgeon and pathologist, from the preoperative considerations until the reconstruction. Since Dr. Mohs's initial work in the 1930s, the practice of Mohs micrographic surgery has become increasingly widespread among the dermatologic surgery community worldwide and is considered the treatment of choice for many common and uncommon cutaneous neoplasms. Mohs micrographic surgery spares the maximal amount of normal tissue and is a safe procedure with very few complications, most of them managed by Mohs surgeons in their offices. Mohs micrographic surgery is the standard of care for high risks basal cell carcinomas and cutaneous squamous cell carcinoma and is commonly and increasingly used for melanoma and other rare tumors with superior cure rates. This review better familiarizes the dermatologists with the technique, explains the difference between Mohs micrographic surgery and wide local excision, and discusses its main indications.


Sujets)
Humains , Tumeurs cutanées/chirurgie , Carcinome basocellulaire/chirurgie , Carcinome épidermoïde/chirurgie , Mélanome/chirurgie , Chirurgie de Mohs
3.
An. bras. dermatol ; 93(5): 638-650, Sept.-Oct. 2018. tab, graf
Article Dans Anglais | LILACS | ID: biblio-949951

Résumé

Abstract: Fogo selvagem or endemic pemphigus foliaceus is an autoimmune acantholytic anti-cadherin bullous disease that primarily affects seborrheic areas, which might disseminate. Brazil has the world's largest number of patients, mainly in the Central-West region, but the disease has also been reported in other South American countries. It affects young people and adults who have been exposed to rural areas, with occurrence of familial cases. Anti-desmoglein-1 autoantibodies are directed against desmosomal structures, with loss of adhesion of the upper layers of the epidermis, causing superficial blisters. The etiology is multifactorial and includes genetic, immune, and environmental factors, highlighting hematophagous insect bites; drug-related factors are occasionally involved. Flaccid blisters readily rupture to yield erosive-crusty lesions that sometimes resemble seborrheic dermatitis, actinic keratosis, and chronic cutaneous lupus erythematosus. The clinical presentation varies from localized to disseminated lesions. Clinical suspicion should be confirmed with histopathological and immunofluorescence tests, among others. The progression is usually chronic, and therapy varies according to clinical presentation, but generally requires systemic corticosteroid therapy associated with adjuvant immunosuppressive treatment to decrease the adverse effects of corticosteroids. Once the disease is under control, many patients remain stable on low-dose medication, and a significant proportion achieve remission.


Sujets)
Humains , Pemphigus/étiologie , Pemphigus/épidémiologie , Maladies endémiques , Autoanticorps/immunologie , Brésil/épidémiologie , Photographie (méthode) , Pemphigus/diagnostic , Pemphigus/anatomopathologie , Desmogléines/immunologie
4.
An. bras. dermatol ; 93(4): 585-586, July-Aug. 2018. graf
Article Dans Anglais | LILACS | ID: biblio-949923

Résumé

Abstract: Harlequin syndrome is a rare condition in which one half of the face fails to flush and sweat due to damage of the sympathetic fibers on the ipsilateral side. The majority of cases are idiopathic, but may be iatrogenic or caused by space-occupying lesions or brainstem infarction. We report a case of idiopathic harlequin syndrome in a 34-year-old man with a 5-month history of unilateral facial flushing and sweating after exercise. Despite the rarity of this syndrome, dermatologists should be aware of this condition in order to diagnose properly and provide multidisciplinary assistance.


Sujets)
Humains , Mâle , Adulte , Maladies du système nerveux autonome/diagnostic , Rougeur de la face/diagnostic , Hypohidrose/diagnostic
5.
An. bras. dermatol ; 92(5,supl.1): 37-39, 2017. graf
Article Dans Anglais | LILACS | ID: biblio-887065

Résumé

Abstract: Bullous systemic lupus erythematosus (BSLE) is a rare autoimmune subepidermal blistering disease, with few cases described in childhood. It has different clinical-pathological features. We report a case of BSLE in a 10-year-old child with systemic lupus erythematosus, treated with prednisone and hydroxychloroquine. There was complete remission with dapsone, with no recurrence of skin lesions throughout one year of follow-up. We highlight the rarity and early age of occurrence.


Sujets)
Humains , Femelle , Enfant , Cloque/anatomopathologie , Lupus érythémateux disséminé/anatomopathologie , Membrane basale/anatomopathologie , Biopsie , Cloque/traitement médicamenteux , Technique d'immunofluorescence directe , Maladies rares/anatomopathologie , Maladies rares/imagerie diagnostique , Lupus érythémateux disséminé/traitement médicamenteux
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