<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>15</volume><submitter>Welfringer A</submitter><pubmed_abstract>We report a rare case of phaehyphomycosis in a 71-year-old heart transplant recipient Togo native patient. Four months after the transplant, he presented painless nodules on the right heel with superficial ulceration. The polyphasic identification uncovered a rare cause of phaehyphomycose: V. botryosa. The treatment combined surgical excision of the lesions and anti-fungal therapy with posaconazole. We discussed eleven reported cases in literature since 1990.</pubmed_abstract><journal>Medical mycology case reports</journal><pagination>21-24</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC5300299</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>A rare fungal infection: Phaehyphomycosis due to &lt;i>Veronaea botryosa&lt;/i> and review of literature.</pubmed_title><pmcid>PMC5300299</pmcid><pubmed_authors>Vuong V</pubmed_authors><pubmed_authors>Argy N</pubmed_authors><pubmed_authors>Chochillon C</pubmed_authors><pubmed_authors>Welfringer A</pubmed_authors><pubmed_authors>Harent S</pubmed_authors><pubmed_authors>Vindrios W</pubmed_authors><pubmed_authors>Descamps V</pubmed_authors><pubmed_authors>Rollin G</pubmed_authors><pubmed_authors>Deschamps L</pubmed_authors><pubmed_authors>Joly V</pubmed_authors></additional><is_claimable>false</is_claimable><name>A rare fungal infection: Phaehyphomycosis due to &lt;i>Veronaea botryosa&lt;/i> and review of literature.</name><description>We report a rare case of phaehyphomycosis in a 71-year-old heart transplant recipient Togo native patient. Four months after the transplant, he presented painless nodules on the right heel with superficial ulceration. The polyphasic identification uncovered a rare cause of phaehyphomycose: V. botryosa. The treatment combined surgical excision of the lesions and anti-fungal therapy with posaconazole. We discussed eleven reported cases in literature since 1990.</description><dates><release>2017-01-01T00:00:00Z</release><publication>2017 Mar</publication><modification>2024-12-03T17:47:22.949Z</modification><creation>2019-03-27T02:36:11Z</creation></dates><accession>S-EPMC5300299</accession><cross_references><pubmed>28217435</pubmed><doi>10.1016/j.mmcr.2017.02.001</doi></cross_references></HashMap>