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Biomedical subjects

Andrés Sanz

Publications and source records attributed to Andrés Sanz.

5 recordsLinked to original sources

[Linear Darier disease].

Darier disease is a genodermatosis with a pattern of autosomal dominant inheritance, which occasionally presents by following a linear or segmental pattern. We present the case of a 22-year-old woman who had presented for three years with small, linearly distributed, yellowish-brown papules on the right lower extremity, with no other skin, mucous membrane or appendage involvement. She had no personal or family history of any interest. Histologically, suprabasal acantholysis and abundant dyskeratotic cells were seen. All of this data led to the diagnosis of linear Darier disease.

Adult↗

[Spindle-cell carcinoma in situ treated with 5% imiquimod].

We present the case of a 70-year-old woman with no personal history of interest who presented to her physician with a plaque in the right infraumbilical region whose largest diameter measured nine centimeters. The clinical and histological diagnosis was Bowen's disease. She was treated with 5 % imiquimod cream, once a day, four times a week, for eight weeks, with an excellent response. One year after treatment, no new lesions have appeared in the treated area.

Administration, Cutaneous↗

Cutaneous mixed tumor with lipomatous stroma.

AIM: Mixed tumors are usually composed of two components, one epithelial and the other mesenchymal. The latter component is commonly myxoid or myxochondroid; a massively lipomatous stroma is very unusual. To date, only two cases of mixed tumor of the skin have been reported with this type of stroma. METHODS AND RESULTS: We report the case of a 61-year-old man with a mixed tumor situated on the hand, an unusual site for these tumors, with over 90% of the tumor composed of adipose tissue. The tumor was a well-circumscribed, 4.5-cm mass, with the gross appearance of a lipoma. The lipomatous stroma contained nests and ribbons of epithelial cells, with occasional tubular structures, surrounded by a scarce amount of fibromyxoid tissue. Immunohistochemical study showed findings similar to those seen in classic mixed tumors. CONCLUSION: Together with a few other cases in the skin and parotid gland, this report shows how massive adipose differentiation can arise in a mixed tumor of the skin.

Adipose Tissue↗

[Epidermodysplasia verruciformis].

We present the case of a 50-year-old Latin American woman who consulted her physician because of recent pruritic lesions on her arms and thighs. During the examination, we observed multiple flat papules on the limbs, as well as hypopigmented macules on the trunk which, according to the patient, began to appear during childhood. A histological study was performed on both types of lesions, and showed some enlarged keratinocytes with light blue cytoplasm in the upper layers of the epidermis. More than 20 types of HPV associated with EV (HPV-EV) have been described. Although it was previously thought that these were specific to EV, new molecular biology techniques have made it possible to isolate HPV-EV sequences in skin diseases, both benign and malignant, with epidermal hyperproliferation in the immunocompetent population.

Epidermodysplasia Verruciformis↗