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zoonoses and communicable diseases common to ... - PAHO/WHO

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ZYGOMYCOSIS 357Occurrence in Animals: It occurs sporadically in many animal species, such asdomestic <strong>and</strong> wild mammals (including marine mammals), birds, reptiles, amphibians,<strong>and</strong> fish. There was a significant epizootic outbreak in New South Wales <strong>and</strong>Queensl<strong>and</strong>, Australia, affecting 52 sheep farms; 700 sheep died in three months. Thecausal agent was Conidiobolus incongruens of the order En<strong>to</strong>mophthorales (Carriganet al., 1992).The Disease in Man: The agents of mucormycoses are potential pathogens thatare classified as opportunistic, since they invade the tissues of patients debilitated byother <strong>diseases</strong> or treated for a long time with antibiotics or corticosteroids. About40% of the cases have been associated with diabetes mellitus. In contrast, in Africa<strong>and</strong> Asia en<strong>to</strong>mophthoromycoses occur in individuals without his<strong>to</strong>ries of preexistingillness (Bittencourt et al., 1982).The mucormycoses are caused by fungi of the genera Absidia, Mucor, Rhizopus,Cunninghamella, Rhizomucor, <strong>and</strong> several others. The infection begins in the nasalmucosa <strong>and</strong> paranasal sinuses, where the fungi may multiply rapidly <strong>and</strong> spread <strong>to</strong>the eye sockets, meninges, <strong>and</strong> brain. The clinical forms caused by these fungi arerhinocerebral, pulmonary, gastrointestinal, disseminated, cutaneous, <strong>and</strong> subcutaneousmucormycoses. The rhinocerebral form appears mainly in diabetes mellituspatients with acidosis <strong>and</strong> in leukemia patients with prolonged neutropenia. Patientshave fever, facial pain, <strong>and</strong> headache. As rhinocerebral mucormycosis progresses,there may be loss of vision, p<strong>to</strong>sis, <strong>and</strong> pupillary dilatation. This form of the diseaseis highly fatal. Patients with a malignant blood disease <strong>and</strong> those receiving immunosuppressantsprimarily suffer from pulmonary or disseminated mucormycoses <strong>and</strong>,less frequently, from the rhinocerebral form. The gastrointestinal form has occurredin a few cases in malnourished children <strong>and</strong> in adult patients with advanced malnutrition;it is generally diagnosed postmortem. The cutaneous <strong>and</strong> subcutaneous formmay be due <strong>to</strong> deep burns, injections, <strong>and</strong> application of contaminated b<strong>and</strong>ages.Mucormycosis is characterized by vascular occlusion with fungal hyphae, thrombosis,<strong>and</strong> necrosis.Localized mucormycosis may disseminate (disseminated mucormycosis) <strong>to</strong> variousorgans <strong>and</strong> systems. The underlying <strong>diseases</strong> are generally leukemia, solid neoplasias,chronic renal deficiency (dialysis treatment with deferoxamine seems <strong>to</strong>predispose the patient <strong>to</strong> mucormycosis, particularly <strong>to</strong> Rhisopus spp.), hepatic cirrhosis,organ transplants (particularly bone marrow transplants), <strong>and</strong> diabetes. Thelargest group of disseminated mucormycoses involves cancer patients (51% of 185cases analyzed) (Ingram et al., 1989).Treatment consists of controlling the underlying disease, controlling hyperglycemia<strong>and</strong> acidosis in diabetics, <strong>and</strong> reducing immunosuppressant use in othercases. Surgical intervention <strong>and</strong> systemic administration of amphotericin B yieldedfavorable results in pulmonary <strong>and</strong> rhinocerebral mucormycosis when diagnosisoccurred early. In primary cutaneous mucormycosis, débridement <strong>and</strong> <strong>to</strong>pical treatmentwith amphotericin B are indicated. Generally, the earlier the infection isdetected, the smaller the amount of dead tissue that will have <strong>to</strong> be removed <strong>and</strong> thegreater the chances for avoiding major tissue damage (Sugar, 1990).Treatment of en<strong>to</strong>mophthoromycosis consists primarily of surgical excision of thesubcutaneous nodules (Basidiobolus) or corrective surgery (Conidiobolus) of thenose <strong>and</strong> other parts of the face. It is advisable at the same time <strong>to</strong> treat the patient

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