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J J Vilata Corell

Publications and source records attributed to J J Vilata Corell.

7 recordsLinked to original sources
PubMed1986

[Lupus-pemphigus].

A case of a woman of 23 years old with lesions in the exposed areas of the skin (face and lower neck) is presented. The histological study was compatible with pemphigus (subcorneal acantholysis and acantholytic cells). The direct immunofluorescence revealed the presence of IgG in intercellular spaces on all the surfaces of the epidermis. In the indirect immunofluorescence ANA (1/800), anti-DNA (1/200) and anti-ICS (1/200) was found. The rest of the analysis clearly showed thrombocytopenia and C4 consumption. The interesting aspect of this case rests in the coexistence of clinical and analytical findings of each of these of autoimmune diseases.

Adult↗
PubMed1984

[Reiter-Fiessinger-Leroy syndrome].

A patient with Reiter- Fiessinger - Leroy disease is described. He presented all the symptoms: urethritis , conjunctivitis , arthritis, balanitis circinata and keratodermia. The antigen reward HLA-B27 lean up on the diagnostic. The treatment with methotrexate disappeared the clinical manifestations.

Adult↗
PubMed1984

[Benign late syphilis: 2 cases, gummatous syphilis and nodular syphilis].

Two mild syphilis cases are hereby described. Their clinical and morphological characteristics differ. The first case showed syphilitic gums on the right eyebrow rim and tuberous lesions, some of which ulcerated. They made up plaques like archs on limbs. The second case showed nodular lesions distribute on practically all the cutaneous tegument. The specific and non-specific syphilitic tests were positive. The CRL study on the cellular and serological aspects was normal. The histopathologic pieces were compatible with the clinical diagnosis. Lesions evolved to a quick disappearance with the penicillin G benzatine treatment established. Attention is drawn to the possibility of noticing new cases of mild syphilis due to the present high incidence of the sexually transmitted diseases.

Adult↗
PubMedDate not supplied

Phacomatosis pigmentokeratotica: a 20-year follow-up with malignant degeneration of both nevus components.

Phacomatosis pigmentokeratotica is a rare syndrome defined by the association of an organoid nevus occasionally with sebaceous differentiation, a speckled lentiginous nevus, and other extracutaneous anomalies. The disorder is a consequence of the so-called twin spot genetic mechanism. We describe the first occurrence involving malignant degeneration of both nevus components, giving rise to three basal cell carcinomas over the sebaceous nevus and a malignant melanoma of the superficial spreading type over the speckled lentiginous nevus. This observation, in concert with the other instances reported in the literature, points to the need for adequate patient follow-up to ensure early detection and treatment of any possible associated malignant degeneration.

Adult↗