Your browser doesn't support javascript.
loading
Mostrar: 20 | 50 | 100
Resultados 1 - 20 de 59
Filtrar
Más filtros

País/Región como asunto
Tipo del documento
País de afiliación
Intervalo de año de publicación
1.
J Cutan Pathol ; 2024 Jun 08.
Artículo en Inglés | MEDLINE | ID: mdl-38850220

RESUMEN

Circumscribed palmar hypokeratosis (CPH) is a localized disorder of epidermal keratinization that is presented as a well-delimited, depressed, erythematous plaque on the palms or on the soles. It is histopathologically characterized by an abrupt thinning of the corneal epidermal layer. CPH is considered a benign condition, but a few cases with dysplastic changes/carcinoma in situ in the hypokeratotic epidermis have been described. We report hereby a case of invasive squamous cell carcinoma developed within a plaque of CPH. The pathogenesis of the malignant changes in this disorder remains to be clarified. Clinicians should be aware of the potential for developing malignancy in CPH and carry out a closer follow-up of this disorder.

4.
Invest Clin ; 57(1): 59-65, 2016 Mar.
Artículo en Español | MEDLINE | ID: mdl-27382802

RESUMEN

We report the case of a 56 year-old male with an atypical leiomyoma in the context of a cutaneous leiomyomatosis and a family history of uterine leiomyomatosis. The genetic study revealed a mutation in the gene for the enzyme fumarate hydratase, but he has not had any renal malignancy so far. Atypical leiomyoma is a rare tumor that usually presents as a single lesion and is exceptional in patients with cutaneous leiomyomatosis. The relation between fumarate hydratase enzyme mutations with multiple leiomyomas, uterine leiomyomatosis and an increased risk of developing kidney cancer is widely known. However, the role of these mutations in the development of atypical leiomyomas is still impossible to clarify given the few cases reported in the literature.


Asunto(s)
Fumarato Hidratasa/genética , Leiomiomatosis/genética , Mutación , Neoplasias Cutáneas/genética , Humanos , Leiomioma/enzimología , Leiomioma/genética , Leiomioma/patología , Leiomiomatosis/enzimología , Leiomiomatosis/patología , Masculino , Persona de Mediana Edad , Neoplasias Cutáneas/enzimología , Neoplasias Cutáneas/patología
8.
Dermatol Online J ; 20(11)2014 Nov 15.
Artículo en Inglés | MEDLINE | ID: mdl-25419760

RESUMEN

Darier-White disease is an uncommon disorder, which presents in a localized pattern in about 10% of patients, usually without nail, mucosa, or acral involvement. Type-1 is the most common of the segmental Darier-White disease types: papules have unilateral distribution along Blaschko lines. A 36-year-old woman diagnosed with type-1 segmental Darier-White disease is reported herein.


Asunto(s)
Enfermedad de Darier/patología , Pared Abdominal , Adulto , Antiinflamatorios/uso terapéutico , Enfermedad de Darier/complicaciones , Enfermedad de Darier/tratamiento farmacológico , Quimioterapia Combinada , Femenino , Humanos , Queratolíticos/uso terapéutico , Metilprednisolona/análogos & derivados , Metilprednisolona/uso terapéutico , Ácidos Nicotínicos/uso terapéutico , Prurito/etiología
9.
Dermatol Online J ; 21(2)2014 Nov 16.
Artículo en Inglés | MEDLINE | ID: mdl-25756486

RESUMEN

Angioma serpiginosum (AS) is an unusual vascular disorder that typically affects female patients, begins in childhood and stabilizes in adulthood and not frequently involve acral skin. We herein present a 13 year-old girl with an asymptomatic erythematous punctuate first noticed on the right palm three years ago, with a proximal serpiginous progression up to the forearm. On examination there was a nonblanching erythematous punctuate on the palm and the inner aspect of right hand and forearm. Dermoscopy showed an erythematous parallel ridge pattern with some red globules and dots spreading on a linear arrangement, and the acrosyringia openings were not affected. Histopathological study showed dilated capillaries in the dermal papillae. This feature is consistent with angioma serpiginosum (AS). To the best of our knowledge, this is the first report that shows a dermoscopic image of a palmar AS. The dermoscopic pattern described in this case could aid in the diagnosis of AS and could add a value in the differential diagnosis with vascular lesions on acral skin.


Asunto(s)
Dermoscopía , Antebrazo/patología , Enfermedades Genéticas Ligadas al Cromosoma X/patología , Dermatosis de la Mano/patología , Enfermedades Cutáneas Vasculares/congénito , Adolescente , Femenino , Humanos , Enfermedades Cutáneas Vasculares/patología
10.
Dermatol Online J ; 20(3)2014 Mar 17.
Artículo en Inglés | MEDLINE | ID: mdl-24656271

RESUMEN

Acral persistent papular mucinosis is a subtype of localized lichen myxedematosus. It presents as acrally located papules with a benign, but persistent course. It is a scarcely reported disease. We present a female with both the clinical and histopathological described criteria.


Asunto(s)
Escleromixedema/diagnóstico , Brazo , Dermis/química , Diagnóstico Diferencial , Femenino , Dermatosis de la Mano/diagnóstico , Dermatosis de la Mano/patología , Humanos , Persona de Mediana Edad , Mucinas/análisis , Escleromixedema/patología
11.
Am J Dermatopathol ; 35(4): e57-9, 2013 Jun.
Artículo en Inglés | MEDLINE | ID: mdl-23334517

RESUMEN

In the skin, the antigen-presenting cells are mainly represented by Langerhans cells, indeterminate cells, and interstitial dendritic cells, which show distinctive immunophenotype and/or ultrastructure. We report a case of a cutaneous-limited self-regressing histiocytosis with a peculiar immunohistochemical profile (CD1a-positive and S100 protein-negative) that is not observed in any of the known cutaneous antigen-presenting cell or nowadays recognized neoplasm. This lesion is probably related to indeterminate dendritic cell tumors, but very few cases with such immunoprofile have been reported up-to-date, and their exact nosologic position and outcome remain to be clarified.


Asunto(s)
Antígenos CD1/análisis , Histiocitosis/inmunología , Proteínas S100/análisis , Enfermedades de la Piel/inmunología , Biomarcadores/análisis , Biopsia , Proliferación Celular , Femenino , Histiocitosis/patología , Humanos , Inmunohistoquímica , Inmunofenotipificación , Persona de Mediana Edad , Remisión Espontánea , Enfermedades de la Piel/patología
12.
J Cosmet Laser Ther ; 15(2): 98-101, 2013 Apr.
Artículo en Inglés | MEDLINE | ID: mdl-23383859

RESUMEN

Depilation techniques have gain popularity in the last few decades. Nowadays there are available a wide variety of lasers as well as intense pulsed light for depilation. However, little is known about the long-term effects of these procedures when melanocytic nevi are affected by them. We report the cases of three patients where we observed clinical, dermoscopic and histopathological changes secondary to laser therapy and intense pulsed light depilation, respectively. We believe that it is necessary to perform further studies to prove the absence of malignant transformation so that we will be able to set up recommendations in those patients with a personal or family history of malignant melanoma and/or dysplastic nevi.


Asunto(s)
Remoción del Cabello/instrumentación , Terapia por Luz de Baja Intensidad/instrumentación , Nevo Pigmentado/patología , Remoción del Cabello/efectos adversos , Humanos , Terapia por Luz de Baja Intensidad/efectos adversos , Masculino , Persona de Mediana Edad
13.
Wound Repair Regen ; 20(6): 815-21, 2012.
Artículo en Inglés | MEDLINE | ID: mdl-23110444

RESUMEN

The objective of this 6-week, 120-patient, double-blind, randomized, controlled trial was to investigate if a foam dressing with ibuprofen provided clinically relevant pain relief (PAR) for exuding, painful venous leg ulcers in comparison with a similar foam dressing without ibuprofen. Primary outcome parameter was PAR compared with baseline pain during the first 5 days of the investigation. PAR was registered by the patient morning and evening. Main end point was proportion of patients reporting a summed PAR score of at least 50% of the total maximum PAR (i.e., responders) and the corresponding number needed to treat (NNT). Wound-related parameters such as ulcer healing, ulcer area reduction, and peri-ulcer skin condition as well as adverse events were recorded during all 6 weeks of the investigation. PAR was significantly greater in the ibuprofen foam group than the comparator group (p = 0.0438). There were 34% responders in the ibuprofen foam group vs. 19% in the comparator group (NNT = 6.8). When evening data were analyzed separately to evaluate PAR over daytime, NNT was 5.3. Wound healing parameters and adverse events were comparable. In conclusion, in this study, the ibuprofen foam dressing provided clinically relevant PAR for patients with exuding, painful venous ulcers.


Asunto(s)
Analgésicos no Narcóticos/administración & dosificación , Antiinflamatorios no Esteroideos/administración & dosificación , Ibuprofeno/administración & dosificación , Dolor/tratamiento farmacológico , Úlcera Varicosa/tratamiento farmacológico , Cicatrización de Heridas , Administración Cutánea , Anciano , Vendajes , Método Doble Ciego , Europa (Continente) , Exudados y Transudados , Femenino , Humanos , Masculino , Dolor/etiología , Dolor/patología , Satisfacción del Paciente , Resultado del Tratamiento , Úlcera Varicosa/patología , Sustancias Viscoelásticas
14.
Photodermatol Photoimmunol Photomed ; 28(2): 102-4, 2012 Apr.
Artículo en Inglés | MEDLINE | ID: mdl-22409714

RESUMEN

Folliculitis decalvans is a chronic form of deep folliculitis that occurs on the scalp as patches of scarring alopecia at the expanding margins of which are follicular pustules. Treatment of folliculitis decalvans is extremely difficult with a resultant poor prognosis. Photodynamic therapy has been reported to be effective in disorders as acne or folliculitis. We report one patient with folliculitis decalvans who was successfully treated with photodynamic therapy.


Asunto(s)
Foliculitis/tratamiento farmacológico , Fotoquimioterapia , Adulto , Femenino , Humanos , Pronóstico
16.
Dermatol Online J ; 18(9): 7, 2012 Sep 15.
Artículo en Inglés | MEDLINE | ID: mdl-23031374

RESUMEN

Human leishmaniasis produced by Leishmania infantum is endemic in Mediterranean countries. In the context of a leishmaniasis outbreak in the town of Fuenlabrada, Madrid, Spain, we had two patients with cutaneous leishmaniasis that developed non-necrotizing cutaneous granulomas. They had both been receiving anti-TNF treatment with adalimumab for rheumatic diseases. Neither of them developed visceral disease and did not require anti-TNF treatment withdrawal to control the cutaneous disease. It is well known that anti-TNF therapy is associated with opportunistic diseases, especially with those in which granuloma formation is an important part of the host defence, as in tuberculosis. We think that granuloma formation through activation of Toll-like receptor-9 and via induction of a Th17 response may be precipitated by the parasites in the dermis.


Asunto(s)
Anticuerpos Monoclonales Humanizados/efectos adversos , Artritis Psoriásica/tratamiento farmacológico , Artritis Reumatoide/tratamiento farmacológico , Granuloma/etiología , Granuloma/patología , Leishmaniasis Cutánea/etiología , Leishmaniasis Cutánea/patología , Adalimumab , Anticuerpos Antinucleares/sangre , Anticuerpos Monoclonales Humanizados/uso terapéutico , Quimioterapia Combinada , Femenino , Humanos , Meglumina/uso terapéutico , Antimoniato de Meglumina , Metotrexato/uso terapéutico , Persona de Mediana Edad , Compuestos Organometálicos/uso terapéutico
18.
Photodermatol Photoimmunol Photomed ; 26(3): 156-8, 2010 Jun.
Artículo en Inglés | MEDLINE | ID: mdl-20584256

RESUMEN

Discoid lupus erythematosus (DLE) can be a therapeutic challenge. Antimalarials and topic steroids are the first-line standard therapies, while systemic steroids, immunomodulators (as azathioprine, methotrexate, cyclosporine), retinoids (acitretin), thalidomide, auranofin and dapsone are used as second-line therapies. We report two patients with recalcitrant DLE who were treated with three and two sessions of 5-aminolevulinic photodynamic therapy without an improvement and with a bad tolerance to the therapy.


Asunto(s)
Lupus Eritematoso Discoide/tratamiento farmacológico , Fotoquimioterapia , Femenino , Humanos , Masculino , Persona de Mediana Edad , Resultado del Tratamiento
20.
Dermatol Online J ; 16(6): 15, 2010 Jun 15.
Artículo en Inglés | MEDLINE | ID: mdl-20579470

RESUMEN

Erythrodermic psoriasis is a chronic condition that is difficult to treat. Biological agents offer a new alternative, but there are no controlled trials to support their use; there are a few reports of patients treated with these agents, but often only with short term results. We report a 68-year-old man with erythrodermic psoriasis and ankylosing spondylitis, treated with infliximab for 48 weeks and then low-dose etanercept monotherapy for 34 additional months. Excellent results were obtained for both conditions without significant side effects. We think etanercept can be a good therapeutic option for long-term control of erythrodermic psoriasis.


Asunto(s)
Dermatitis Exfoliativa/tratamiento farmacológico , Fármacos Dermatológicos/uso terapéutico , Inmunoglobulina G/uso terapéutico , Psoriasis/tratamiento farmacológico , Receptores del Factor de Necrosis Tumoral/uso terapéutico , Espondilitis Anquilosante/tratamiento farmacológico , Factor de Necrosis Tumoral alfa/antagonistas & inhibidores , Anciano , Anticuerpos Monoclonales/uso terapéutico , Etanercept , Humanos , Infliximab , Masculino , Resultado del Tratamiento
SELECCIÓN DE REFERENCIAS
DETALLE DE LA BÚSQUEDA