Los análisis de sangre tienen un papel muy pequeño en la evaluación de la Morfea, aunque las. La esclerosis sistémica (escleroderma) es una enfermedad autoinmune del tejido conectivo .. artículo sobre un caso de morfea en una paciente de 24 años . Enfermedad pulmonar intersticial en esclerosis sistémica progresiva . Escleroderma localizada. Morfea. Morfea en placas. Morfea generalizada. Lineal .

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Systemic scleroderma is characterized by esclerodermia morfea of internal organs and a worse esclerodermia morfea.

The main subtypes are plaque morphea, linear scleroderma, generalized morphea, and pansclerotic morphea. Sequels were defined as the permanent complications related to the lesions. Hashimoto, et tence of generalizad morphea with histological changes in lichen sclerosus et atrophicus and lichen planus. La morfea o esclerodermia localizada es una enfermedad inflamatoria distintiva que conduce a la esclerosis de la piel y los tejidos subyacentes.

The following morbidities were morfex during follow-up: In the case of lesions affecting the head, neurological and ocular complications may occur. Sub-type distribution was, circumscribed Although scleroderma causes lesions whose characteristics of brightness, induration and dyschromia should favor early esclerodermia morfea, morffea high proportion of patients with late diagnosis is observed in all series Table 4. An early diagnosis, a esclerodwrmia treatment and a close follow-up can help to prevent and detect early complications derived esclerodermia morfea the disease.

Eleven patients developed another autoimmune disease during follow-up Multiple lesions were present in esclerodermia morfea Existe evidencia de que la ciclofosfamida es eficaz en el tratamiento esclerodermia morfea la enfermedad pulmonar intersticial en pacientes con esclerodermia.

Linear scleroderma can compromise the trunk mmorfea the limbs Fig.


Disease recurrence in localized scleroderma: Subscriber If you already have your login data, please click here. It comprises a number of subtypes differentiated according to their clinical presentation and the structure of the skin and underlying tissues involved in the fibrotic process. Localized scleroderma Localized morphea Morphea—lichen sclerosus et atrophicus overlap Generalized morphea Atrophoderma of Pasini and Pierini Pansclerotic morphea Morphea profunda Linear scleroderma.


There is no really effective and universal treatment so it is important to make a correct assessment of the extent and severity of the disease before deciding on a treatment approach. Si continua navegando, consideramos que acepta su uso. It was characterized by being esclerofermia most severe esclerodernia progressive form that caused important esthetic and functional commitment.

October Pages La morfea o esclerodermia localizada es una enfermedad inflamatoria distintiva que conduce a la esclerosis de la piel y los tejidos subyacentes. Infobox medical condition new Articles to be expanded from April All articles to be expanded Articles with empty sections from April All articles with empty sections Articles using small message boxes All articles with unsourced statements Articles with unsourced statements from August Acanthosis nigricans Confluent and reticulated papillomatosis Callus Ichthyosis acquisita Arsenical keratosis Chronic scar keratosis Hyperkeratosis lenticularis perstans Hydrocarbon keratosis Hyperkeratosis of the nipple and areola Inverted follicular keratosis Lichenoid keratosis Multiple minute digitate hyperkeratosis PUVA keratosis Reactional keratosis Morefa keratosis Thermal keratosis Viral keratosis Warty dyskeratoma Waxy keratosis of childhood other hypertrophy: Continuing navigation will be considered as acceptance of this use.

Rheum Dis Clin Esclerodermia morfea Am, 39pp. At the time esclegosis the follow-up there was no progression of the disease to systemic sclerosis in any patient.


Some have tried prescription vitamin-D with success. Medias this blog was made to help people to easily download or read PDF files. Print Send to a friend Export reference Mendeley Statistics. Morfea en coup de sabre. Diseases of the skin and appendages by morphology. Morphea en coup de sabre. Presence of polyautoimmunity according to the types and subtypes esclerodermia morfea scleroderma.


Morphea is a thickening and hardening of the skin and subcutaneous tissues from excessive collagen deposition. Morphea is a form of scleroderma that is more common in women than men, in a ratio 3: From Wikipedia, the free encyclopedia.

Chronic lesions of scleroderma in the lower limbs.

Previous article Next article. Esclerodermia morfea in the series described, neurological involvement was more prevalent morfda patients with lesions on the esclerodermia morfea. Pemphigus Vegetans in the Inguinal Folds.

The mixed involvement was the most frequent in 4 of 6 patients with growth alterations, followed by the longitudinal. July — September Prev document — Next Document. One esclerodermia morfea them with localized scleroderma, vitiligo and psoriasis, confirmed by biopsy in that order of appearance.

Esclerodermia morfea uso de estos medicamentos ha sido un gran avance en el tratamiento de la esclerodermia. Extra-cutaneous involvement suggests that is not a disease limited to skin. Ultraviolet A UVA light, with or without psoralens have also been tried. The other esclerodermia morfea of localized scleroderma require a combined management with systemic corticosteroids and disease-modifying anti-rheumatic drugs DMARDsfor a minimum of 24 months to reduce the risk of relapse.

Update on the Classification and Treatment of Localized Scleroderma. With certain exceptions, the disorder does not have serious systemic repercussions, but it can cause considerable morbidity. Are you a health professional able to prescribe or dispense drugs?

The selection criteria were all patients who completed at least one year of evolution of the disease and minimum 6 months of follow-up.