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5.
Med. cután. ibero-lat.-am ; 37(1): 33-37, ene. -feb. 2009. ilus
Article in Spanish | IBECS | ID: ibc-80150

ABSTRACT

El Granuloma Anular Subcutáneo (GAS) es una forma clínica poco frecuente, de granuloma anular, más común en la infancia. Clínicamente, se caracterizapor la presencia de nódulos subcutáneos, indoloros, localizados en cuero cabelludo o en extremidades. El diagnóstico se basa en la historia y lapresentación clínica, y en el estudio histopatológico. El diagnóstico diferencial se plantea sobre todo, con los nódulos cutáneos de la artritis reumatoide.El proceso tiende a ser autolimitado.Presentamos el caso de una paciente, de 16 años, tratada con éxito con isotretinoina oral (AU)


Subcutaneous Granuloma Annulare (SGA) is a rare clinical form of granuloma annulare, more common in childhood. The clinical presentation is apainless subcutaneous nodules located in scalp or extremities. Diagnosis is based on medical history, clinical findings and histopathology. Differentialdiagnosis is necessary with respect to nodular lesions of rheumatoid arthritis. Lesions tend to be self-limiting.Here we report a case of a female patient, of 16 years old, treated with oral isotretinoin successfully (AU)


Subject(s)
Humans , Female , Adolescent , Dermatologic Agents/therapeutic use , Isotretinoin/therapeutic use , Granuloma Annulare/diagnosis , Granuloma Annulare/drug therapy , Granuloma Annulare/pathology , Biopsy
6.
Med. cután. ibero-lat.-am ; 36(4): 199-202, mayo-jun. 2008. ilus
Article in Spanish | IBECS | ID: ibc-60935

ABSTRACT

Los angiosarcomas cutáneos, son tumores malignos vasculares, poco frecuentes, que afectan sobre todo a personas mayores, de raza blanca. Sonmuy agresivos, por lo cual su detección precoz, es lo único que puede modificar su pronóstico.Describimos el caso de una mujer anciana, con angiosarcoma del cuero cabelludo. La paciente recibió tratamiento con radioterapia de electrones.Desafortunadamente, a los 3 meses del diagnóstico falleció (AU)


Cutaneous angiosarcoma is a rare malignant vascular tumor, most often occurs in white elderly people. It´s very agressive, only early detection canmodify the prognosis.An old woman, who was diagnosed of angiosarcoma of the scalp is reported. The patient was treated by electron-beam radiotherapy. Unfortunatelyshe died 3 months after the diagnosis (AU)


Subject(s)
Humans , Female , Aged, 80 and over , Hemangiosarcoma/diagnosis , Hemangiosarcoma/radiotherapy , Hemangiosarcoma/pathology , Immunohistochemistry , Fatal Outcome
7.
Neurologia ; 9(2): 69-71, 1994 Feb.
Article in Spanish | MEDLINE | ID: mdl-8204252

ABSTRACT

We present a patient with slowly progressing optic atrophy, sensorineural deafness and sensory neuropathy. Clinical examination and testing revealed the exclusively sensorineural nature of this syndrome. Nerve biopsy pointed to primary degeneration. Our review of the literature indicates that this syndrome is categorized as heredo-degenerative.


Subject(s)
Hearing Loss, Sensorineural/complications , Hereditary Sensory and Motor Neuropathy/pathology , Optic Atrophy/pathology , Adolescent , Audiometry , Axons/pathology , Female , Hearing Loss, Sensorineural/diagnosis , Hereditary Sensory and Motor Neuropathy/diagnosis , Humans , Optic Atrophy/complications , Optic Atrophy/diagnosis , Sural Nerve/physiopathology , Sural Nerve/ultrastructure
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