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Stran 1 iz 28 rezultatov
Fever in aspergillus mycetoma.
Samo registrirani uporabniki lahko prevajajo članke
Prijava / prijava
Giant Candida mycetoma in an ascending aorta tubular graft.
Samo registrirani uporabniki lahko prevajajo članke
Prijava / prijava
We report the case of a 46-year-old male hospitalized for abdominal pain and fever with history of a David procedure followed by an aortic valve replacement due to severe aortic regurgitation. Transesophageal echocardiography (TEE) and computed tomography showed a large mass floating in the aorta.
[Mycetoma-like manifestations in invasive pulmonary aspergillosis].
Samo registrirani uporabniki lahko prevajajo članke
Prijava / prijava
Invasive pulmonary aspergillosis is characterized by radiological signs allowing a correct diagnosis, including differentiation from pulmonary candidiasis, when they are associated with appropriate clinical symptoms (neutropenia and fever persisting despite broad-spectrum antibiotics). In particular
The first Korean case of disseminated mycetoma caused by Nocardia pseudobrasiliensis in a patient on long-term corticosteroid therapy for the treatment of microscopic polyangiitis.
Samo registrirani uporabniki lahko prevajajo članke
Prijava / prijava
Nocardia pseudobrasiliensis is predominantly associated with invasive infections in immunocompromised patients. We report a case of disseminated mycetoma caused by N. pseudobrasiliensis in a 57-yr-old woman with microscopic polyangiitis, who was treated for 3 months with corticosteroids. The same
[Mycetoma: attempt at intra-arterial management].
Samo registrirani uporabniki lahko prevajajo članke
Prijava / prijava
A 28 year old African student had acquired a mycetoma of his left foot after an injury in 1975. As the surgical and antimycotic therapy had no effect, he was brought to Düsseldorf for the amputation of his foot. Madurella mycetomi was isolated from the skin, pus and bone. Before the amputation was
Scedosporium apiospermum mycetoma with bone involvement successfully treated with voriconazole.
Samo registrirani uporabniki lahko prevajajo članke
Prijava / prijava
Treatment of Scedosporium apiospermum mycetoma usually requires limb amputation. A 49-year-old woman, from Ivory Coast, was diagnosed with Madura foot in 1995. She failed to respond to several treatments including itraconazole, fluconazole and co-trimoxazole, and refused limb amputation. In December
Eumycotic mycetoma caused by Pseudallescheria boydii in the abdominal cavity of a dog.
Samo registrirani uporabniki lahko prevajajo članke
Prijava / prijava
An abdominal eumycotic mycetoma with multiorgan dissemination was diagnosed in a 2-year-old dog. Clinical signs included fever, vomiting, diarrhea, weight loss, and a palpable abdominal mass. The dog developed disseminated intravascular coagulation and died. Pseudallescheria boydii was isolated from
Eumycotic mycetoma caused by Pseudallescheria boydii in a dog.
Samo registrirani uporabniki lahko prevajajo članke
Prijava / prijava
Abdominal eumycotic mycetoma caused by Pseudallescheria boydii was diagnosed in a 3-year-old male Siberian Husky. The dog was examined because of weight loss and signs of depression. Initially, pyrexia was the only clinical finding. Antibiotic and corticosteroid treatment was ineffective. Two weeks
Unusual Presentation of Mycetoma of the Foot: A Rare Case Report.
Samo registrirani uporabniki lahko prevajajo članke
Prijava / prijava
BACKGROUND
Mycetoma is a chronic granulomatous infection. It is caused by actinomycetes or fungi. It is common in tropical countries and males. Predisposing conditions include malnutrition, poor hygiene, history of trauma, wounds on barefeet, and systemic infections. Eumycotic mycetoma commonly
Case report: Eumycetoma and mycotic arthritis of the knee caused by Arthrographis kalrae.
Samo registrirani uporabniki lahko prevajajo članke
Prijava / prijava
A 33-year-old male presents following a penetrating injury to his right knee. Clinically he demonstrated pain, an effusion and fevers. At diagnostic arthroscopy, no microbiological growth was cultured. Delayed growth yielded the fungus Arthrographis kalrae. He was treated with a three-stage total
Case 249: Intramuscular Mycetoma.
Samo registrirani uporabniki lahko prevajajo članke
Prijava / prijava
History A 21-year-old man presented with swelling of the medial aspect of the left thigh of 1-month duration. There was no history of fever or penetrating injury in the left thigh. The patient had undergone renal transplantation 7 years earlier and had been taking immunosuppressants since
Deep fungal infection in systemic lupus erythematosus - three cases reported, literature reviewed.
Samo registrirani uporabniki lahko prevajajo članke
Prijava / prijava
Three patients with systemic lupus erythematosus (SLE) and deep fungal infection are described. Two patients had disseminated cryptococcal infection and the third disseminated histoplasmosis. Allwere receiving corticosteroids at the time fungal infection developed. One patient with disseminated
[A case of lung scedosporiosis successfully treated with monitoring of plasma voriconazole concentration level].
Samo registrirani uporabniki lahko prevajajo članke
Prijava / prijava
A 71-year-old man was referred because of fever and productive cough. His chest radiograph showed a large cavitary mass with an intracavitary mycetoma-like lesion in the left middle lung field. We undertook bronchoscopy and CT-guided biopsy, and both bronchial lavage fluid culture and CT-guided
Pulmonary aspergilloma.
Samo registrirani uporabniki lahko prevajajo članke
Prijava / prijava
BACKGROUND
Aspergillosis is a serious pathologic condition caused by Aspergillus organisms and is frequently seen in immunocompromised patients. Aspergillus species causes a variety of pulmonary diseases such as saphrophyticus (aspergilloma/mycetoma), hypersensitivity reaction (allergic
Intracranial Fungal Granulomas: A Single Institutional Clinicopathologic Study of 66 Patients and Review of the Literature.
Samo registrirani uporabniki lahko prevajajo članke
Prijava / prijava
BACKGROUND
Fungal granulomas of the central nervous system are rare and have a high rate of mortality and morbidity, irrespective of treatment. The authors report their experience of managing 66 patients during 15 years and discuss the clinical, radiological, surgical, and pathologic findings. This
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