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Plasmodium falciparum (P. falciparum) malaria continues to pose a significant threat to public health worldwide, particularly in endemic areas. While the majority of cases can be effectively treated and cured, recurrences of P. falciparum malaria are not uncommon and can occur years following initial exposure. This phenomenon adds a new level of complexity to the management and prevention of the disease. The present study describes the compelling clinical case of a patient who contracted malaria despite not having been in an endemic region for over a decade. The patient had previously been infected and treated for the same disease. With low parasitemia, the patient was successfully treated with anti-malarial drugs; however, certain aspects of his medical history remained unclear. The present study also discusses the possibility that this case represents P. falciparum recrudescence or cryptic malaria, drawing on existing literature to contextualize the findings. The case presented herein highlights the need for continued vigilance in the diagnosis and treatment of P. falciparum malaria, particularly in instances of recurrence. Furthermore, it underscores the ongoing challenges posed by this persistent and insidious disease. [ABSTRACT FROM AUTHOR]

Human autochthonous myiasis is uncommonly reported in Europe. This report describes a case of myiasis of a wound caused by Sarcophaga spp. Suffering from cutaneous lymphoma, the patient showed, at the level of his scalp lesions, the presence of larvae that were removed during curettage surgery; they were subsequently identified as belonging to the genus Sarcophaga. Preservation of these larvae in 10% formalin did not allow identification at the species level using molecular methods.