In one case, the disease was associated with acute lymphocytic leukaemia (ALL),

and in the second, the disease was associated with severe malnutrition. In both cases, primary cutaneous mucormycosis originated after the nasogastric tube was inserted and secured with adhesive bandages, and the disease then progressed to the rhinocerebral type. Both cases were counted find protocol as having primary cutaneous mucormycosis because it was the initial manifestation. With regard to the mycological data, the 22 cases showed aseptate, dichotomous hyphae on direct examination. Cultures were developed from 21/22 cases, and the remaining case had a positive direct examination and biopsy allowing for inclusion in the study. Due to the patients’ conditions (thrombocytopenia, severe neutropenia or critical illness), biopsies were performed in only 8/22 cases. The results reported thrombotic processes with multiple tissue infarctions and fungal structures similar to observed on direct examination. Better

results were achieved when GMS staining was used. Table 3 displays the morphological identification of the 21 positive cultures. Because this was a retrospective study, only 10/21 strains (47.61%) were identified by molecular biology and these results are shown in the same table. The main isolated agents were Rhizopus arrhizus in 13/22 cases (59.1%) and Lichteimia corymbifera in 5/22 cases (10.3%). The rest of the microorganisms SAR245409 nmr were isolated from one case each. Rhizopus arrhizus (formerly R. oryzae) (6 strains, HGM-Z-01 al 06) Lichtheimia corymbifera (1 strain, HGM-Z-39) Rhizopus arrhizus (1 strain, No HGM-Z-33) Mucor circinelloides (1 strain, HGM-Z-09) Cunninghamella bertholletiae (1 strain, HGM-Z-18) All the patients received amphotericin B deoxycholate and management for the overlying conditions, Quinapyramine with metabolic regulation and haematological improvement. A clinical cure and mycological cure were accomplished in 6/22 cases (27.3%). Of these six cases, four patients had the primary cutaneous pattern and two patients had the rhinocerebral

pattern.[11] Mucormycosis in children is a rare disease. Most reports of mucormycosis are of isolated cases, and there are few cases series in the literature. HM is the major underlying disease in these patients.[12-18] This study examines the paediatric mucormycosis cases of a larger cases series at a single centre. Of the 158 confirmed cases of mucormycosis, 14% were children. In accordance with previous reports, patients with ages from 6 months to 18 years were enrolled, and the mean age was 10.3 years.[12, 13, 16] A slight male predominance was noted during the study; however, the gender difference was not significant. This male predominance agrees with previous reports.[10, 15, 16] Some authors have correlated this tendency to the protective influence of oestrogens, but this correlation may not be valid in children younger than 12 years of age.