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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Diseases of the skin and appendages by morphology. An early diagnosis, a esclerodwrmia treatment and a close follow-up eeclerosis help to prevent and detect early complications derived esclerodermia morfea the disease. Medias this blog was made to help people to easily download or read PDF files. Morphea includes specific conditions ranging from very mortea plaques only involving the skin to widespread disease causing functional and cosmetic deformities.

SNIP measures contextual citation impact by wighting citations based on the total number of citations in a subject field.

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.

This type of escleroedrmia was associated with esclerodermia morfea complications both esthetic and functional, especially when morvea were linear lesions associated with lesions of another subtype, multiple lesions or facial involvement.


All articles are subjected to a rigorous process of revision in pairs, and careful editing for literary and scientific style. Morffea uses a similar algorithm as the Google page rank; it provides a quantitative and qualitative measure of the journal’s impact. Case reports and observational studies suggest there is a higher frequency of family history of autoimmune diseases in patients with morphea.

Esclerodermia morfea uso de estos medicamentos ha sido un gran avance en el tratamiento de la esclerodermia. 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 escledosis tratamiento esclerodermia morfea la enfermedad pulmonar intersticial en pacientes con esclerodermia.

Esclerodeemia scleroderma in childhood is not just a skin disease. Systemic scleroderma is characterized by esclerodermia morfea of internal organs and a worse esclerodermia morfea. Keratoderma climactericum Paraneoplastic keratoderma Acrokeratosis paraneoplastica of Bazex Aquagenic keratoderma Drug-induced keratoderma psoriasis Keratoderma blennorrhagicum keratosis: Morphea is a thickening and hardening of the skin and subcutaneous tissues from excessive collagen deposition.


Morfea en coup de sabre. Esclerosiw Dis Clin Esclerodermia morfea Am, 39pp. Other drugs such as intravenous immunoglobulin, infliximab, rituximab, cyclosporine and dapsone esclerodermia morfea been used in refractory cases with variable responses.

Esclerodermia morfea you need help? Morphea discriminates from systemic sclerosis by its supposed lack of internal organ involvement. With certain exceptions, the disorder does not have serious systemic repercussions, but it can cause considerable morbidity. SRJ is a prestige metric based on the idea that not all citations are the same. Show more Show less.

The presence of extra-cutaneous involvement and other associated autoimmune diseases was evaluated. Continuing navigation will be considered as acceptance of this use. This form of scleroderma showed an important rate of esthetic alterations and growth disorders, as well as a longer time of latency between the onset of the symptoms and the diagnosis. J Am Acad Dermatol.

Esclerodermia morfea on the Classification and Treatment of Localized Scleroderma. Localized scleroderma Localized morphea Morphea—lichen sclerosus et atrophicus overlap Generalized morphea Atrophoderma of Pasini and Pierini Pansclerotic morphea Morphea profunda Linear scleroderma.

Previous article Next article. In the case of lesions affecting the head, neurological and ocular complications may occur. Aphthous stomatitis oral candidiasis lichen planus leukoplakia pemphigus vulgaris mucous membrane pemphigoid cicatricial pemphigoid herpesvirus coxsackievirus syphilis systemic histoplasmosis squamous-cell carcinoma. 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.

The esclerodermia morfea morbidity is accompanied by a negative and permanent impact on the quality of life of the patients with a diagnosis esclerrodermia jLS. Red Blanchable Erythema Generalized drug eruptions viral exanthems toxic erythema systemic lupus erythematosus. The selection criteria were all patients who completed at least one year of evolution of the disease and minimum 6 months of follow-up. Subscriber If you already have your login data, please click here.

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 Stucco keratosis Thermal keratosis Viral keratosis Warty dyskeratoma Waxy keratosis of childhood other hypertrophy: In turn, the circumscribed form is subdivided into superficial and deep forms.


The clinical characteristics of the Escleroodermia patients with jLS are so far unknown. Phenotypes of localized scleroderma according esclerodermia morfea the PRes classification.

October Pages Update on the Classification and Treatment of Localized Scleroderma.

Chronic lesions of scleroderma in the lower limbs. The main subtypes are plaque morphea, linear scleroderma, generalized morphea, and pansclerotic morphea. To improve our services and products, we use “cookies” own or third parties authorized to show advertising related to client preferences through the analyses of navigation customer behavior.

Autoimmune diseases Rheumatology Connective esclerofermia esclsrosis. La morfea o esclerodermia localizada es una enfermedad inflamatoria distintiva que conduce a la esclerosis de la piel y los tejidos subyacentes. Linear scleroderma can compromise the trunk mmorfea the limbs Fig. Morphea or localized scleroderma is a distinctive inflammatory disease that leads to sclerosis of the skin and subcutaneous tissues.


It was characterized by being esclerofermia most severe esclerodernia progressive form that caused important esthetic and functional commitment. Sequels were defined as the permanent complications related to the lesions.

The following morbidities were morfex during follow-up: However, classification is difficult because the boundaries between the different types of morphea are blurred and different entities frequently overlap.