Publications by authors named "J E Arrese-Estrada"

Article Synopsis
  • Leishmaniasis is a disease caused by Leishmania parasites transmitted by sandflies, and can manifest as cutaneous, mucocutaneous, or visceral forms, making diagnosis difficult due to similarity with other diseases.
  • A 52-year-old immunosuppressed Belgian woman with rheumatoid arthritis was diagnosed with visceral leishmaniasis and treated successfully, but later experienced relapses and progressed to cutaneous forms and lymphadenopathy.
  • Clinicians should consider the possibility of multiple forms of leishmaniasis in immunosuppressed patients, as demonstrated by the patient's complex case and eventual complications leading to her death.
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Corneofungimetry is a bioassay in dermatomycology evaluating the antifungal effect of drugs. It is based on the method of culture of fungi on human stratum corneum harvested by cyanoacrylate skin surface strippings. Using corneofungimetry, it is possible to establish a classification of topical antifungals according to their spectrum of activity and their fungitoxicity.

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Kufs' disease is the adult form of a group of disorders referred to as neuronal ceroid-lipofuscinosis or Batten's disease. We report here the clinical and anatomopathological features of two young brothers presenting with a progressive myoclonic epilepsy corresponding to type A of the disease according to Berkovic. The first clinical manifestations occurred before 20 years of age.

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Fungal infections account for approximately 20% of all nail diseases, and the incidence of onychomycosis is increasing. Traditional therapies are often ineffective. The activity, clinical efficacy, pharmacokinetics, and patient acceptability of griseofulvin and ketoconazole, the two "traditional" oral agents, are reviewed and compared with two new agents, terbinafine and itraconazole.

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This report is the first to study histological, immunopathological, ultrastructural, and morphometric aspects of the abnormal structure of the dermis in Ehlers-Danlos syndrome, type VIIc. This disease, resulting from a defect in procollagen peptidase, resembles dermatosparaxis in animals. Dermal cells were abnormal in many aspects, including their large number, their strong argent affinity, and the occasional presence of oligocilia.

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