PubMed HealthSearch

Biomedical subjects

R Naranjo Sintes

Publications and source records attributed to R Naranjo Sintes.

18 recordsLinked to original sources

[Angiokeratoma. Apropos of 93 cases].

A description of 93 cases of angiokeratoma [Mibelli (3 cases), Fordyce (13 cases), circumscriptum naeviformis (12 cases) and solitary (65 cases)], confirmed histologically and observed during the last 30 years (1955-1985) in the Department of Medicine and Surgery of the School of Medicine of the University of Granada is presented. We carry out a detailed histological and ultrastructural study.

Angiokeratoma

[Dermatosis with the phenomenon of transepidermal elimination].

A revision was carried out on all cases of dermatosis involving transepidermal elimination seen in the last 25 years in the Department of Medical Surgical Dermatology and Venereology, School of Medicine, University of Granada. The study included clinical-statistical, therapeutic, histopathologic and evolutional aspects. In the discussion the low incidence of perforating dermatoses in the Eastern Andalusian area is emphasized.

Adult

[23 observations of subungual exostosis].

Twenty-three cases of subungual exostosis are described, representing an incidence of 0.031% in our setting. Children and adolescents were most frequently affected, with a clear predominance of females. Eight lesions were observed in exceptional locations, three on the fingers and five on the third and fourth toes. The results of the surgical technique employed to excise the exostosis are evaluated.

Adolescent

[Epidermodysplasia verruciformis and achondroplasia].

We are presenting a new case of EV which has association with three diseases: Epilepsy, achondroplasia and endocrine disturbances. We are considering that it is very much interesting the association existing between the previously mentioned diseases (all conditioned by genetic factors) and EV which is characterized by a generalized viral infection also conditioned by genetic factors.

Achondroplasia

[Infantile acro-localized papulo-vesicular syndromes].

Seven observations of papulo-vesicular acrolocated syndromes in males between 6 months and three years age. Clinical, histological and nosological aspects are commented in according to Gianotti's words and last reports about this disease.

Acrodermatitis

[Eosinophilic pustular folliculitis (Ofuji syndrome)].

The first observation in Occident of "eosinophilic pustular folliculitis (Ofuji)" is reported. The condition is characterized by pruritic follicular sterile papulopustules on indurated erythematous plaque in the face. They extended centrifugally and the plaque proceeds with remission and exacerbations with leukocytosis and numerous eosinophils. Histological features are pustular folliculitis from the ostium to the sebaceous gland, chiefly composed of polymorphs and many eosinophiles. The treatment are corticosteroids by long-term. It is the first case studied by electron microscopy.

Administration, Oral

[Cowden's syndrome].

Explore the source record for details and available documents.

Abnormalities, Multiple