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. 2020 Sep;26(9):2022–2030. doi: 10.3201/eid2609.200276

Table 2. Clinical and laboratory characteristics of invasive infections with Nannizziopsis obscura as previously reported in the literature*.

Year of diagnosis Sex/age, y Underlying risk factors Country of birth/time since last travel in Africa Clinical, radiologic, and biologic findings Direct examination Serum β-D-glucan (Fungitell) Suspected identification at diagnosis Treatment (duration) Outcome Ref
Before 1982 (reported in 1984) M/24 HIV, osteomyelitis Africa/7 y Tibia (abscess) Septate hyphae and budding yeasts Not done Geotrichum sp. and then Chrysosporium sp. Amphotericin B (4 mo) Persistent lytic area in the distal tibia after 2 y (3)
2005 M/38 HIV Nigeria (living in Germany)/NA Brain (abscess, needle aspiration); lung (nodules) Not available Not done Chrysosporium anamorph of Nannizziopsis vriesii Voriconazole Recovery without sequelae after 4 mo (4)
2015 F/63 T-cell prolymphocytic leukemia (2014) France/6 mo (Senegal) Blood (blood culture, positive PCR on CSF, ascites fluid) Septate hyphae, arthroconidia Not done N. obscura Not treated Dead before diagnosis (6)
2015 M/34 Renal transplant (2008) Gambia/3 mo Back (paraspinal abscesses); lymph nodes (needle aspiration) Aleurioconidia and arthroconidia in chains Not done N. obscura Posaconazole Recovery after 10 mo of azole therapy (7)
2017 F/52 AIDS Mali/resident Brain (abscess), lung (nodule), β-D-glucan+ Not done 953 pg/mL N. obscura LAMB (1 mo), craniotomy, then voriconazole Recovery but neurologic sequelae after 2 mo (6)

*CSF, cerebrospinal fluid; LAMB, liposomal amphotericin B; Ref, reference.