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1.
Med Cutan Ibero Lat Am ; 7(1-3): 19-26, 1979.
Article in Spanish | MEDLINE | ID: mdl-398932

ABSTRACT

Preceded by a brief commentary about the clinical characteristics of actinic prurigo, the qualities of anantifibrinolytic medication and its possible machanism of action in allergic conditions and atopias are analysed. An earlier experience with five familiar cases of actinic prurigo given 1 g of tranexamic acid or 3 g E. ACA, within a period of three months has been effective remarkally exceeding the results obtained with other therapeutic agents. The proposed therapeutic scheme may or may not be, modified, according to the response to the response of each individual case.


Subject(s)
Antifibrinolytic Agents/therapeutic use , Facial Dermatoses/etiology , Prurigo/drug therapy , Sunlight , Adolescent , Adult , Aminocaproic Acid/therapeutic use , Dermatitis, Atopic/drug therapy , Dermatitis, Atopic/genetics , Drug Evaluation , Drug Therapy, Combination , Facial Dermatoses/drug therapy , Facial Dermatoses/genetics , Female , Humans , Male , Prurigo/etiology , Prurigo/genetics , Tranexamic Acid/therapeutic use
2.
Med Cutan Ibero Lat Am ; 5(3): 159-65, 1977.
Article in Spanish | MEDLINE | ID: mdl-357857

ABSTRACT

Two cases of naevus lipomatosus superficialis (Hoffmann and Zurhelle) are described by the authors. The main clinical characteristics and histological peculiarities are reviewed. Both cases were disseminated and had typical localisation (pelvic area). The histological examination showed ectopic adipocytes in the dermis. The authors mare a reference to the different hypotheses on the pathogenesis of these lesions.


Subject(s)
Lipoma/pathology , Skin Neoplasms/pathology , Adolescent , Diagnosis, Differential , Female , Humans
3.
Med Cutan Ibero Lat Am ; 3(6): 415-22, 1975.
Article in Spanish | MEDLINE | ID: mdl-1241699

ABSTRACT

A new case of hereditary acrokeratotic poikiloderma of Weary is presented by the authors. There was no eczematoid dermatitis and the patient was the only member of the family affected. There were similarities with the cases published by Piñol Aguadé and co-workers. The authors suggest that this disease can appear in two forms; a complete form (Weary type) and an incomplete form (Piñol type). The histology of the keratotic lesions is reported for the first time. The lesions are very similar in the 15 cases published up to 1975, and the authors believe that it constitutes a well defined entity.


Subject(s)
Rothmund-Thomson Syndrome , Skin Diseases , Adolescent , Female , Humans , Rothmund-Thomson Syndrome/genetics , Rothmund-Thomson Syndrome/pathology , Skin/pathology , Skin Diseases/genetics
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