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1.
Saudi J Kidney Dis Transpl ; 34(Suppl 1): S226-S229, 2023 Dec 01.
Article in English | MEDLINE | ID: mdl-38995288

ABSTRACT

Pulmonary mucormycosis is rare in kidney transplant recipients and has a high mortality rate. We report a case of pulmonary mucormycosis presenting as round pneumonia 1 year and 1 month after the transplant. The diagnosis was confirmed by a percutaneous lung biopsy. A complete resection of the lung mass, followed by intravenous liposomal amphotericin B therapy, saved the life of the patient. In conclusion, early and prompt diagnosis followed by complete resection of the lesion in pulmonary mucormycosis is lifesaving.


Subject(s)
Amphotericin B , Antifungal Agents , Kidney Transplantation , Lung Diseases, Fungal , Mucormycosis , Pneumonectomy , Humans , Mucormycosis/diagnosis , Mucormycosis/drug therapy , Mucormycosis/surgery , Kidney Transplantation/adverse effects , Lung Diseases, Fungal/drug therapy , Lung Diseases, Fungal/diagnosis , Lung Diseases, Fungal/microbiology , Lung Diseases, Fungal/surgery , Antifungal Agents/therapeutic use , Amphotericin B/therapeutic use , Male , Treatment Outcome , Pneumonia/microbiology , Pneumonia/drug therapy , Pneumonia/diagnosis , Biopsy , Tomography, X-Ray Computed , Middle Aged , Immunocompromised Host
2.
Trop Doct ; 50(4): 346-349, 2020 Oct.
Article in English | MEDLINE | ID: mdl-32576098

ABSTRACT

A young Indian man presented elsewhere with a short history of haematuria and cough. Investigations revealed renal and pulmonary lesions. Histopathology of these lesions was reported as mucormycosis. He consulted us two months after onset of symptoms, asymptomatic and clinically well, having received no treatment. In view of clinico-histopathological discordance, a review of the biopsy slides was advised but the patient refused further work-up at that time. One week later, however, he was admitted with left hemiparesis. Brain imaging showed an abscess. He underwent surgical excision of the brain abscess and nephrectomy. Review of previous slides showed septate fungal filaments with granulomatous inflammation. Intraoperative cultures grew Aspergillus flavus. He received voriconazole for one year and is well at his two-year follow-up. His immunological work-up was negative for immunodeficiency. This case illustrates that granulomatous aspergillosis may be an indolent infection in apparently normal individuals and reiterates the importance of interpreting diagnostic reports in conjunction with clinical features.


Subject(s)
Aspergillosis/pathology , Aspergillosis/therapy , Adult , Antifungal Agents/therapeutic use , Aspergillosis/diagnosis , Aspergillosis/microbiology , Aspergillus flavus/isolation & purification , Brain/diagnostic imaging , Brain/microbiology , Brain/pathology , Brain/surgery , Humans , Kidney/diagnostic imaging , Kidney/microbiology , Kidney/pathology , Lung/diagnostic imaging , Lung/microbiology , Lung/pathology , Lung/surgery , Male , Treatment Outcome
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