Résumé
Systemic fungal infections are rare. In pregnancy, treatment is problematic because of the risk of possible teratogenic effects of the antifungal drugs. We present the case of a 32 year-old woman who presented during pregnancy with a two-month history of painless subcutaneous nodules. Excision biopsy of one lesion showed dematiaceous fungal elements. Anti-fungal treatment was deferred and the pregnancy proceeded uneventfully. The remaining nodules were excised at the time of caesarean section delivery. Three weeks into the puerperium, she developed generalised seizures and investigations indicated systemic fungal infection with positive cultures for Aureobasidium spp which responded to appropriate antifungal therapy of flucytosine and itraconazole.
Sujets)
Adulte , Femelle , Humains , Grossesse , Complications infectieuses de la grossesse/diagnostic , Infection puerpérale/diagnostic , Ascomycota/isolement et purification , Mycosis fongoïde/diagnostic , Complications infectieuses de la grossesse/traitement médicamenteux , Infection puerpérale/traitement médicamenteux , Peau/anatomopathologie , Tomodensitométrie , Itraconazole/usage thérapeutique , Flucytosine/usage thérapeutique , Mycoses/traitement médicamenteux , Antifongiques/usage thérapeutiqueRésumé
A case of angiomyofibroblastoma of the vulva in a 23-year-old woman is presented. Clinical, histological and immunohistochemical features as well as the differential diagnosis and prognosis of this rare but distinct entity are discussed. Only about 65 cases are documented in the literature and to our knowledge this is the first case to be reported from the Caribbean.