Gastrointestinal basidiobolomycosis: An emerging mycosis difficult to diagnose but curable. Case report and review of the literature

Gastrointestinal basidiobolomycosis (GIB) is a rare mycosis affecting almost exclusively immunocompetent subjects. We describe a case of GIB caused by Basidiobolus ranarum in a 25-year-old Italian immunocompetent man resident in Ireland who presented a 2-month history of epigastric pain. Suspecting...

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Published inTravel medicine and infectious disease Vol. 31; p. 101378
Main Authors Pezzani, Maria Diletta, Di Cristo, Valentina, Parravicini, Carlo, Sonzogni, Angelica, Tonello, Cristina, Franzetti, Marco, Sollima, Salvatore, Corbellino, Mario, Galli, Massimo, Milazzo, Laura, Antinori, Spinello
Format Journal Article
LanguageEnglish
Published Netherlands Elsevier Ltd 01.09.2019
Elsevier Limited
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Summary:Gastrointestinal basidiobolomycosis (GIB) is a rare mycosis affecting almost exclusively immunocompetent subjects. We describe a case of GIB caused by Basidiobolus ranarum in a 25-year-old Italian immunocompetent man resident in Ireland who presented a 2-month history of epigastric pain. Suspecting colon cancer he underwent a right hemicolectomy subsequently leading to a diagnosis of GIB by means of molecular biology. After surgery a 9-month therapy with itraconazole was employed with a good outcome. A review of medical literature regarding GIB cases published in the period 1964–2017 is presented. One-hundred and two cases of GIB were included in this analysis. The disease was observed predominantly in male gender (74.5%) and children (41.2%). Abdominal pain was the single most common complaint (86.3%) followed by fever (40.2%) and evidence of an abdominal mass (30.4%). Peripheral blood eosinophilia was detected in 85.7% of cases. Most of the patients were diagnosed in Saudi Arabia (37.2%) followed by USA (21.6%) and Iran (20.6%). Surgery plus antifungal therapy was employed in the majority of patients (77.5%). An unfavourable outcome was documented globally in 18.6% of patients. GIB seems to be an emerging intestinal mycosis among immunocompetent patients living in the Middle East and Arizona.
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ISSN:1477-8939
1873-0442
1873-0442
DOI:10.1016/j.tmaid.2019.01.013