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A Case of Magnusiomyces capitatus Peritonitis Without Underlying Malignancies

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Magnusiomyces capitatus is a rare cause of fungal infection in immunocompromised patients, mainly seen in hematological malignancies. M capitatus infections are extremely rare in immunocompetent patients, as it is part of normal human microbial flora. We are presenting an extremely rare case of M capitatus peritonitis in an otherwise immunocompetent patient who suffered from gastrointestinal leakage due to pancreatitis. Fungal identification was performed at reference laboratory by phenotypic characteristics and DNA sequencing of target internal transcribed spacer region of the rRNA gene and the D1-D2 domain of the large-subunit rRNA gene and susceptibility testing by Clinical and Laboratory Standards Institute guidelines (document M27-S4) broth dilution method. He was successfully treated with a combination of surgical repair and voriconazole single therapy.
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https://doi.org/10.1177/2324709618795268
Journal of Investigative Medicine High
Impact Case Reports
Volume 6: 1–4
© 2018 American Federation for
Medical Research
DOI: 10.1177/2324709618795268
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Case Report
Introduction
Magnusiomyces capitatus, previously known as Geotrichum
capitatum, Dipodascus capitatus, Trichosporon captiatum,
Saprochaete capitata, or Blastoschizomyces capitatus,1 is a
rare cause of fungal infection in immunocompromised
patients, mainly seen in hematological malignancies.2-17 M
capitatus is extremely rare in immunocompetent patients, as
it is part of normal human microbial flora.18 Presented here is
a case of peritonitis infection with M capitatus without
underlying malignancies.
Case Report
A 32-year-old alcoholic male with liver steatosis presented
with hemorrhagic necrotizing pancreatitis with peritonitis
and retroperitoneum involvement. He was started on conser-
vative therapy and percutaneous irrigation and drainage.
Unfortunately, he rapidly deteriorated on hospital day 4 into
acute abdominal compartment syndrome with acute respira-
tory distress. He was intubated and underwent damage con-
trol laparotomy resulting in pancreatic necrosectomy with
subtotal pancreatectomy, splenectomy, repair of superior
mesenteric vein, and wedge liver biopsy. Intraoperatively,
peripancreatic necrosis was noted to extend proximally to
diaphragm with extensive dissection throughout the retro-
peritoneum and at the root of the small bowel retroperitoneal
area. During his second relaparotomy on hospital day 5 for
removal of abdominal packing, incidental duodenal and gas-
tric enterotomies were noted and repaired. Retroperitoneal
edema was much improved. Cholecystectomy was per-
formed for eosinophilic cholecystitis. Large Davol sump
drains were placed for postoperative irrigation. Whittman
patch and wound vacuum-assisted closure were placed. He
required prolonged intensive care unit (ICU) admission with
mechanical ventilation. Four additional operations were
required to reapproximate his abdominal fascia. Skin was
eventually closed on hospital day 17.
795268HICXXX10.1177/2324709618795268Journal of Investigative Medicine High Impact Case ReportsD’Assumpcao et al
case-report20182018
1Ross University, Miramar, FL, USA
2Kern Medical—University of California Los Angeles, Bakersfield, CA,
USA
Received April 18, 2018. Revised July 16, 2018. Accepted July 22, 2018.
Corresponding Author:
Carlos D’Assumpcao, MD, Kern Medical—UCLA, 1700 Mount Vernon
Avenue, Bakersfield, CA 93306, USA.
Email: cdassumpcao@gmail.com
A Case of Magnusiomyces capitatus
Peritonitis Without Underlying
Malignancies
Carlos D’Assumpcao, MD1,2 , Benson Lee, DO2,
and Arash Heidari, MD2
Abstract
Magnusiomyces capitatus is a rare cause of fungal infection in immunocompromised patients, mainly seen in hematological
malignancies. M capitatus infections are extremely rare in immunocompetent patients, as it is part of normal human microbial
flora. We are presenting an extremely rare case of M capitatus peritonitis in an otherwise immunocompetent patient who
suffered from gastrointestinal leakage due to pancreatitis. Fungal identification was performed at reference laboratory by
phenotypic characteristics and DNA sequencing of target internal transcribed spacer region of the rRNA gene and the
D1-D2 domain of the large-subunit rRNA gene and susceptibility testing by Clinical and Laboratory Standards Institute
guidelines (document M27-S4) broth dilution method. He was successfully treated with a combination of surgical repair and
voriconazole single therapy.
Keywords
Magnusiomyces capitatus, Geotrichum capitatum, Dipodascus capitatus, Trichosporon captiatum, Saprochaete capitata,
Blastoschizomyces capitatus, peritonitis
2 Journal of Investigative Medicine High Impact Case Reports
His course was also complicated by pleural effusions, pul-
monary embolism, and persistent fevers and leukocytosis.
Pleural effusions were therapeutically drained and were cul-
ture negative. Heparin was bridged to warfarin for his pul-
monary embolism. Meropenem, linezolid, and micafungin
were started empirically on hospital day 19.
Peritoneal fluid was collected on hospital day 19 and sent
for culture, which grew Klebsiella oxytoca and vancomy-
cin-resistant Enterococcus faecium (VITEK2, bioMérieux,
Durham, NC). There was suspicion of incomplete drainage
of intraabdominal fluid, and so a retroperitoneal drain was
placed by interventional radiology on hospital day 31.
Culture of this retroperitoneal fluid grew vancomycin-resis-
tant enterococci E faecium (VITEK2, bioMérieux) and M
capitatus (identification by phenotypic characterization and
DNA sequencing of targets internal transcribed spacer region
of the rRNA gene and the D1-D2 domain of the large-subunit
rRNA gene and the D1-D2 domain of the large-subunit rRNA
gene by University of Texas Health Science, San Antonio,
TX; see Figures 1-3). Peritoneal fluid was collected again
from hospital day 40, and it grew M capitatus, K oxytoca,
and Streptococcus sanguinis (VITEK2, bioMérieux). He
also developed eosinophilia (absolute eosinophil count of
800) on hospital days 42 to 46.
Meropenem was de-escalated to a 2-week course of cef-
triaxone on hospital day 45 (changed to ciprofloxacin at dis-
charge). Linezolid was discontinued after a 2-week course
was completed. A 12-week course of voriconazole (mini-
mum inhibitory concentration = 0.25 µg/mL by Clinical and
Laboratory Standards Institute broth dilution M27-S4
method by the University of Texas Health Science, San
Antonio, TX; see Table 1) was started on hospital day 45.
Warfarin for his pulmonary embolism was switched to
enoxaparin due to drug-drug interaction of warfarin with
voriconazole. He started to improve and was eventually dis-
charged home on hospital day 50 with follow-up in outpa-
tient clinic, ambulating and tolerating food.
At 12-week follow-up, the patient reported abstinence
from alcohol since initial hospital admission. The patient’s
wife was supportive during the entire hospital stay as well
as the post hospital recovery, ensuring wound dressing
changes and medication compliance. Liver function was
monitored every 3 to 4 weeks as an outpatient throughout
the 12-week course of voriconazole. Liver function was
within normal limits. He completed a 90-day course of
anticoagulation.
Figure 1. Magnusiomyces capitatus, peritoneal fluid, 5-day culture
on Sabouraud Dextrose Agar, Emmons media (Thermo Scientific,
Remel, Lenexa, KS).
Figure 2. Magnusiomyces capitatus, peritoneal fluid, 2-day culture,
lactophenol cotton blue stain, 40× magnification.
Figure 3. Magnusiomyces capitatus, retroperitoneal fluid, 7-day
culture, lactophenol cotton blue stain, 40× magnification.
D’Assumpcao et al 3
Discussion
To our knowledge, this is an extremely rare case of M capi-
tatus peritonitis in an otherwise immunocompetent patient
who suffered from gastrointestinal leakage due to pancreati-
tis, likely from the gastric and duodenal enterotomies found
and repaired on hospital day 5. He was successfully treated
with a combination of surgical repair and voriconazole.
Literature review suggests an intrinsic resistance to echino-
candins19; however, in vitro and in vivo activity of antifungals
may differ. Liposomal amphotericin B and azoles, specifically
voriconazole and posaconazole, have had reported clinical
success.7,16,20 In vitro studies with flucytosine, fluconazole,
and itraconazole showed poor susceptibilities.21 No suscepti-
bility break points have been determined yet.
The newest triazole, isavuconazole, demonstrated excel-
lent in vitro activity against M capitatus.22 In the SECURE
trial, a phase 3, randomized, controlled, noninferiority clini-
cal trial against aspergillus and other filamentous fungi, isa-
vuconazole was equally tolerable but had better
pharmacokinetics and fewer drug-related adverse events
compared with voriconazole.23 Due to identical minimum
inhibitory concentration of our patient’s isolate to voricon-
azole and isavuconazole (see Table 1), voriconazole was
selected as the initial triazole antifungal therapy so that isa-
vuconazole could be reserved for rescue therapy in the event
that voriconazole did not improve clinical status. Recently,
ICU admissions have been linked to the development of M
capitatus infection. In Italy, a non-neutropenic patient in the
ICU after cardiac surgery developed M capitatus fungemia.24
In Croatia, a fatal M capitatus respiratory tract infection was
diagnosed posthumously in a patient who became febrile 7
days into his ICU admission for polytrauma.25 Moreover, a
recent survey of M capitatus infections in the ICU and hema-
tology-oncology unit within a single hospital in Turkey
found the strains to be genetic clones. However, microbio-
logical investigations of the hospital environment failed to
find the isolate.26 While M capitatus is considered a ubiqui-
tous environmental organism and part of the normal human
gastrointestinal flora,18 to the authors’ knowledge, there has
not been any case reports or studies tracing M capitatus to a
hospital fomite. More studies are needed to determine a true
correlation between ICU admissions and M capitatus
infections.
Vancomycin-resistant E faecium, S sanguinis, and K oxy-
toca likely had a gastrointestinal instead of a cutaneous
source. While coinfection may have caused peritonitis in this
patient, his clinical status did not improve until the addition
of the appropriate antifungal covering this particular strain of
M capitatus.
Authors’ Note
This case report was presented as a poster at the Solomon Scholars
Research Program at UCLA Department of Medicine, in June 2017;
American College of Physicians Southern California Chapters
Regions I, II, and III at Marina del Rey, California, in September
2017; as well as American Federation for Medical Research Western
Medical Research Conference in Carmel, California, in January 2018.
Acknowledgments
The authors wish to acknowledge the contributions of the follow-
ing: Danna Mejia, Jocelyn Oats, and Joan Buddecke.
Declaration of Conflicting Interests
The authors(s) declared no potential conflicts of interest with respect
to the research, authorship, and/or publication of this article.
Funding
The authors(s) received no financial support for the research,
authorship, and/or publication of this article.
Ethics Approval
Ethical approval to report this case was obtained from the Kern
Medical Center Institutional Review Board (Study #17037).
Informed Consent
Informed consent for patient information to be published in this
article was not obtained because patient or legal representative was
not available in time for publication. The information in the inves-
tigator’s written request for “Waiver of Consent” coupled with the
written research proposal disclosing the data use plan were reviewed
by the Kern Medical Center Institutional Review Board to deter-
mine that under the conditions of study approval, there should be
minimal or less risk for exposure of patient identity. The Kern
Medical Center Institutional Review Board approved the request
for the Waiver of Consent as part of its ethics approval of the study.
ORCID iD
Carlos D’Assumpcao https://orcid.org/0000-0001-9967-9612
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Isavuconazole 0.25 µg/mL
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... S. capitata may be found in colonization in the skin, digestive, and respiratory tracts of healthy people [1,3]. S. capitata IFI are very rare in immunocompetent patients [7]. In immunocompromised patients, S. capitata is an emerging yeast responsible for life-threatening IFI, particularly in neutropenic hematological patients [3,5]. ...
... D'Assumpcao et al. have reported a case of S. capitata peritonitis without underlying malignancies in an adult man with necrotizing pancreatitis who survived after appropriate antifungal therapy [7]. To our knowledge, this is the first reported case of S. capitata peritonitis with a fatal outcome in a patient without neutropenia or associated malignancy. ...
Article
Full-text available
Saprochaete capitata (S. capitata) is an opportunistic arthroconidial yeast-like fungus causing invasive infections in immunocompromised patients, mainly those with hematological malignancies and severe neutropenia. However, infections due to S. capitata are extremely rare in immunocompetent and non-neutropenic patients. Saprochaete spp. are microscopically characterized by arthroconidia with hyaline-septated hyphae. S. capitata is known to be intrinsically resistant to echinocandins and highly resistant to fluconazole. It is suggested to use amphotericin B or voriconazole (in monotherapy or in combination) as the gold standard treatment for S. capitata systemic infections. We report a rare case of S. capitata peritonitis with fatal outcome in a non-neutropenic patient without underlying malignancies. This case report highlights the value of direct microscopic examination and stained smears in a prompt preliminary diagnosis of S. capitata invasive fungal infections. We also aim to emphasize the importance of early initiation of appropriate antifungal treatment in patients with S. capitata systemic infections, thus improving their therapeutic outcome.
... They have also been reported in other areas of Europe (Slovakia, Switzerland, and the Czech Republic) [4] and in Asia (India, Nepal, Kuwait, and China) [21][22][23]. In the Americas, M. capitatus was recently isolated from an alcoholic male patient in the United States [24]. ...
... Therefore, phylogenetic reconstruction methods were employed for the characterization of the fungal strain. Molecular identification and phylogeny have been used previously for the detection of M. capitatus and its differentiation from closely related species such as S. clavata [24][25][26]. These techniques were instrumental for recognizing M. capitatus ENCB-HI-834 as the agent of the present systemic infection. ...
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Magnusiomyces capitatus (also denominated “Geotrichum capitatum” and “the teleomorph stage of Saprochaete capitata”) mainly affects immunocompromised patients with hematological malignancies in rare cases of invasive fungal infections (IFIs). Few cases have been reported for pediatric patients with acute lymphoblastic leukemia (ALL), in part because conventional diagnostic methods do not consistently detect M. capitatus in infections. The current contribution describes a systemic infection in a 15-year-old female diagnosed with ALL. She arrived at the Children’s Hospital of Mexico City with a fever and neutropenia and developed symptoms of septic shock 4 days later. M. capitatus ENCB-HI-834, the causal agent, was isolated from the patient’s blood, urine, bile, and peritoneal fluid samples. It was identified with matrix-assisted laser desorption/ionization time-of-flight mass spectrometry (MALDI-TOF MS) and a phylogenetic reconstruction using internal transcribed spacer (ITS) and 28S ribosomal sequences. The phylogenetic sequence of M. capitatus ENCB-HI-834 clustered with other M. capitatus-type strains with a 100% identity. In vitro antifungal testing, conducted with the Sensititre YeastOne susceptibility system, found the following minimum inhibitory concentration (MIC) values (μg/mL): posaconazole 0.25, amphotericin B 1.0, fluconazole > 8.0, itraconazole 0.25, ketoconazole 0.5, 5-flucytosine ≤ 0.06, voriconazole 0.25, and caspofungin > 16.0. No clinical breakpoints have been defined for M. capitatus. This is the first clinical case reported in Mexico of an IFI caused by M. capitatus in a pediatric patient with ALL. It emphasizes the importance of close monitoring for a timely and accurate diagnosis of neutropenia-related IFIs to determine the proper treatment with antibiotics, antifungals, and chemotherapy for instance including children with ALL.
... M. capitatus can cause invasive infections among immunosuppressed patients especially those with hematologic disorders [2,3] (Mazzcato et al., 2015; Tanuskova et al., 2017). It can also infect non-neutropenic and immunocompetent patients [4,5] (Shah, 2017;D'Assumpcao et al., 2018). In immunocompromised patients, infections with M. capitatus are associated with increased risk of dissemination and high rates of mortality. ...
... M. capitatus can cause invasive infections among immunosuppressed patients especially those with hematologic disorders [2,3] (Mazzcato et al., 2015; Tanuskova et al., 2017). It can also infect non-neutropenic and immunocompetent patients [4,5] (Shah, 2017;D'Assumpcao et al., 2018). In immunocompromised patients, infections with M. capitatus are associated with increased risk of dissemination and high rates of mortality. ...
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Two cases of fungemia caused by Magnusiomyces capitatus, an arthroconidial yeast-like fungus, in non-hematologic immunocompromised patients are described. Both patients died before definite diagnosis of M. capitatus was made. The report highlights that pending confirmation of the isolate by phenotypic and/or molecular methods, the characteristic morphologic features observed in Gram-stained smears of blood culture positive bottles can lead to early preliminary diagnosis, thus significantly reducing time required for initiating appropriate antifungal therapy.
... The patient passed away unfortunately five days into admission [11]. In the second case, the patient was much younger and had isolated intraperitoneal positive cultures identifying S. capitata without disseminated diseases, which were all favorable to the outcome, and the patient, fortunately, survived [12]. However, given our patient's complex hospital course, pre-existing comorbidities, severe multi-organ damage, and disseminated intravascular coagulation, there was no adequate therapeutic response even with targeted therapy. ...
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Saprochaete capitata is an uncommon yeast species; its impact on non-neutropenic patients appears to be on the rise. We describe a case of S. capitata fungemia in a critically ill end-stage kidney disease (ESKD) patient on peritoneal dialysis. The patient presented with mesenteric ischemia and underwent several laparotomies during hospitalization. His hospital stay was complicated as fungemia developed and spread to multiple sites, which resulted in severe complications and ultimately led to fatal outcomes. S. capitata's diagnostic delay is a concern, but matrix-assisted laser desorption/Ionization time-of-flight (MALDI-TOF) mass spectrometry may help provide accurate identification. Our case highlights the need for prompt diagnosis and tailored antifungal therapy, especially when managing this challenging infection in immunocompromised patients.
... In this review, 82% (61/74) of the publications reported peritoneal dialysis-related peritonitis. When data were available, other risk factors for peritonitis were underlying neoplasia [118], gastric and duodenal ulcer perforation [119], recent digestive surgery [120][121][122][123][124], severe immunosuppression [125,126], and pancreatitis [127]. In some cases, infection of the peritoneum, as well as other unusual infection sites including the biliary tract (9 publications), gastric tract (12 publications), and spleen (19 publications), may also be a secondary condition to the haematogenous dissemination of yeasts [128]. ...
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Invasive fungal diseases are a public health problem. They affect a constantly increasing number of at-risk patients, and their incidence has risen in recent years. These opportunistic infections are mainly due to Candida sp. but less common or rare yeast infections should not be underestimated. These so-called “less common” yeasts include Ascomycota of the genera Candida (excluding the five major Candida species), Magnusiomyces/Saprochaete, Malassezia, and Saccharomyces, and Basidiomycota of the genera Cryptococcus (excluding the Cryptococcus neoformans/gattii complex members), Rhodotorula, and Trichosporon. The aim of this review is to (i) inventory the less common yeasts isolated in humans, (ii) provide details regarding the specific anatomical locations where they have been detected and the clinical characteristics of the resulting infections, and (iii) provide an update on yeast taxonomy. Of the total of 239,890 fungal taxa and their associated synonyms sourced from the MycoBank and NCBI Taxonomy databases, we successfully identified 192 yeasts, including 127 Ascomycota and 65 Basidiomycota. This repertoire allows us to highlight rare yeasts and their tropism for certain anatomical sites and will provide an additional tool for diagnostic management.
... Other risk factors include the duration of neutropenia, recent chemotherapy, use of broadspectrum antibiotics, and the presence of a central venous catheter (3,4) . However, fungal infection due to Saprochaete capitata has been reported in several case reports in patients without any significant immunosuppression (5,6) . It is noteworthy that in our case series, five patients did not have malignancy or neutropenic course. ...
Article
Full-text available
Introduction: Saprochaete capitata is a rare cause of invasive fungal infection. Patients with hematological malignancies and those with severe neutropenia are at high risk. It has been generally reported as case reports or small case series in the literature. Here, we report 17 cases of Saprochaete capitata infection detected in our center over a five-year period. Materials and Methods: Culture results were evaluated retrospectively between 2014 and 2019. Blood samples were cultured in BACTEC 9240 (Becton Dickinson, Diagnostic Instrument System, Sparks, USA) fully automated blood culture system. Yeast colonies were identified as Saprochaete capitata by Phoenix™-100 (Becton Dickinson, Diagnostic Instrument System, Sparks, USA) automated system. Antifungal susceptibility of isolates was evaluated by colorimetric microdilution using Sensititre Yeast One Panel (TREK Diagnostic Systems, USA). Results: The most common isolated sites were blood culture (n=7) and urine culture (n=7). 11 patients had a history of underlying malignancy, while six patients did not have any immunosuppression. Eight patients were neutropenic at diagnosis. The median neutrophil count was 57/mm3 (0-550) and the median duration of neutropenia was 25.5 days (14-43). Voriconazole or amphotericin B were the first choices in the treatment. 13 patients died during the follow-up. In six of them (35.3%) the main cause of death was attributed to S.capitata. Conclusion: There has been an increase in the number of S.capitata infections in recent years. It has been reported mainly from Mediterranean countries, including Turkey. Recommendations as to appropriate treatment regimens and breakpoints for antifungal agents are unclear. Voriconazole or amphotericin B alone or in combination seems to be effective. Further studies are warranted in order to contribute to the management of the infection.
... Timely administration of antifungal agents and source control (e.g., drainage of an empyema or retroperitoneal fluid collection) are a mainstay for the treatment of invasive Saprochaete spp. Infections [3,74,75]. Recovery from immunosuppression likely plays a crucial role in successful treatment [11,31]. The use of granulocyte stimulating factor (G-CSF) or Interferon-gamma in combination with antifungal therapy has been successful in eliminating the infection in some patients [29,76]; however, the impact of these regimens on clinical outcomes remains unclear. ...
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Magnusiomyces capitatus (previously known as Geotrichum capitatum or Blastoschizomyces capitatus or Trichosporon capitatum) is a rare cause of fungal infection in immunocompromised patients. Most of these cases (87%) have been reported from the Mediterranean region, as it is extremely rare to recognize it in other regions. Here we report a first case of disseminated M. capitatus infection in Slovakia. The patient – 19 year old woman with myelodysplastic syndrome was diagnosed with M. capitatus fungemia after allogeneic stem cell transplantation. The infection occurred despite antifungal prophylaxis with micafungin, which was in vitro sensitive to the yeast. The treatment according to minimal inhibitory concentrations (micafungin, voriconazol) and granulocyte transfusions were administered. M. capitatus was cleared out from the bloodstream. However, patient died of multiple organ failure. Autopsy showed multiple lesions in organs, but did not prove presence of yeast by histopathology. M. capitatus was confirmed by polymerase chain reaction from all tested organs: heart, brain, lungs, spleen, liver and kidneys. We present the post mortem pictures showing the yeast lesions in affected organs. 2012 Elsevier Ltd. All rights reserved.
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Geotrichum capitatum is a rare pathogen that causes opportunistic fungal infections in immunocompromised patients, particulary in patients with hematological malignancies. We report the case of a 72 year patient with polytrauma whose outcome was fatal. During his stay in the intensive care unit (ICU), he received a broad-spectrum antimicrobial therapy and underwent different invasive procedures. After becoming febrile on the 7th day of admission, two consecutive bronchoalveolar lavage (BAL) specimens were taken for microbiological analysis. The isolated species came as G. capitatum, that was identified using VITEK 2. Unfortunately, patient died before fungal identification, so the antifungal therapy wasn’t administered. This case presentation emphasizes the importance of Geotrichum capitatum as an emerging fungal pathogen, as well as the significance of the predisponing factors that contributed to development of infection. © 2015, EDIMES Edizioni Medico Scientifiche. All rights Reserved.
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Empirical antifungal therapy is most often given to patients with leukemia. However breakthrough fungal infections under antifungal therapy are not uncommon. Four children, with hematologic malignant disease developed mycotic breakthrough infections while on empirical caspofungin treatment for a median of 14 (range 11-19) days. Trichosporon asahii was detected in the blood culture of two patients and Geotrichum capitatum in the other two (one patient also had positive cerebrospinal fluid culture). Because the patients' clinical situation worsened, voriconazole was empirically added for two patients three and five days before the agent was detected. The first sterile blood culture was obtained 3-7 days of voriconazole treatment. All patients reached clear cultures but one patient died. One patient with central nervous system infection with G. capitatum had severe neurological sequelae. Very severe fungal infections can occur during empirical caspofungin therapy. Therefore, patients should be followed closely. Copyright © 2015 Elsevier Editora Ltda. All rights reserved.
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The majority of invasive fungal infections observed in non-neutropenic patients hospitalized in an intensive care unit are caused by Candida spp and current guidelines recommend echinocandins as the first-line treatment. Fungemias caused by filamentous or arthrosporic fungi such as Saprochaete capitata (previously named Geotrichum capitatum) are extremely rare. In fact, invasive infections due to S. capitata have been reported almost exclusively in neutropenic oncohematological patients. In this report, we describe a case of fungemia caused by S. capitata in a non-neutropenic patient hospitalized in an intensive care unit after aortic valve replacement. The prompt identification of S. capitata is extremely important because of its intrinsic resistance to echinocandins.
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Background: Saprochaete capitata isolates have emerged as important nosocomial pathogens, among immunosuppressed or neutropenic patients, and a rare cause of nosocomial infection in the hematology-bone marrow unit (HBMU) and the intensive care unit (ICU). The purpose of this study was to molecular epidemiology and antifungal susceptibility of S. capitata (Blastoschizomyces capitatus) isolates causing nosocomial infection at Kayseri in Turkey. Methods: During a period from 2012 to 2015, a total of 20 S. capitata strains were obtained from patients hospitalized at Erciyes University Hospital. The identification of S. capitata was performed by phenotypic and biochemical methods; this was confirmed by molecular methods by DNA sequencing analysis. Genotyping of S.capitata isolates from different patients was determined to by the repetitive sequence PCR (repPCR) using the DiversiLab System (BioMerieux). Results: More than half of the patients with S. capitata infections were hospitalized in the hematology-oncology unit (60%). The patients mainly included those using intravascular devices (90%), and receiving parenteral antibiotics (85%); the mortality rate was 55%. The microbiological investigation failed to identify S. capitata in the hospital environment. All isolates were resistant to caspofungin (>32). However, the MIC90 values for voriconazole, amphotericin B, and fluconazole against all of the isolates were 0.125, 0.25, and 1μg/ml, respectively. The S. capitata strains belonged to five clones (A-E) which were determined by the use of rep-PCR and Clone C was found to be predominant. Conclusions: S. capitata isolates are an important cause of nosocomial infection in the HBMU and ICUs.
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Background: Isavuconazole is a novel triazole with broad-spectrum antifungal activity. The SECURE trial assessed efficacy and safety of isavuconazole versus voriconazole in patients with invasive mould disease. Methods: This was a phase 3, double-blind, global multicentre, comparative-group study. Patients with suspected invasive mould disease were randomised in a 1:1 ratio using an interactive voice-web response system, stratified by geographical region, allogeneic haemopoietic stem cell transplantation, and active malignant disease at baseline, to receive isavuconazonium sulfate 372 mg (prodrug; equivalent to 200 mg isavuconazole; intravenously three times a day on days 1 and 2, then either intravenously or orally once daily) or voriconazole (6 mg/kg intravenously twice daily on day 1, 4 mg/kg intravenously twice daily on day 2, then intravenously 4 mg/kg twice daily or orally 200 mg twice daily from day 3 onwards). We tested non-inferiority of the primary efficacy endpoint of all-cause mortality from first dose of study drug to day 42 in patients who received at least one dose of the study drug (intention-to-treat [ITT] population) using a 10% non-inferiority margin. Safety was assessed in patients who received the first dose of study drug. This study is registered with ClinicalTrials.gov, number NCT00412893. Findings: 527 adult patients were randomly assigned (258 received study medication per group) between March 7, 2007, and March 28, 2013. All-cause mortality from first dose of study drug to day 42 for the ITT population was 19% with isavuconazole (48 patients) and 20% with voriconazole (52 patients), with an adjusted treatment difference of -1·0% (95% CI -7·8 to 5·7). Because the upper bound of the 95% CI (5·7%) did not exceed 10%, non-inferiority was shown. Most patients (247 [96%] receiving isavuconazole and 255 [98%] receiving voriconazole) had treatment-emergent adverse events (p=0·122); the most common were gastrointestinal disorders (174 [68%] vs 180 [69%]) and infections and infestations (152 [59%] vs 158 [61%]). Proportions of patients with treatment-emergent adverse events by system organ class were similar overall. However, isavuconazole-treated patients had a lower frequency of hepatobiliary disorders (23 [9%] vs 42 [16%]; p=0·016), eye disorders (39 [15%] vs 69 [27%]; p=0·002), and skin or subcutaneous tissue disorders (86 [33%] vs 110 [42%]; p=0·037). Drug-related adverse events were reported in 109 (42%) patients receiving isavuconazole and 155 (60%) receiving voriconazole (p<0·001). Interpretation: Isavuconazole was non-inferior to voriconazole for the primary treatment of suspected invasive mould disease. Isavuconazole was well tolerated compared with voriconazole, with fewer study-drug-related adverse events. Our results support the use of isavuconazole for the primary treatment of patients with invasive mould disease. Funding: Astellas Pharma Global Development, Basilea Pharmaceutica International.
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A taxonomic revision is presented of all filamentous Hemiascomycetes that reproduce with predominantly arthric conidiogenesis. On the basis of SSU rDNA data, two widely divergent groups (1 and 2) are known to exist. Both are distantly related to the Hemiascomycetes, and show remarkable diversity in ITS rDNA, leading to the supposition that phylogenetically ancient fungi are concerned. The teleomorph / anamorph genera occurring in Groups 1 vs. 2 are classified in (1) Galactomyces and Dipodascus with Geotrichum anamorphs, vs. (2) Magnusiomyces with Saprochaete anamorphs. Taxonomy at the species level is based on ITS rDNA sequences and nDNA/DNA reassociation data. In total, 32 taxa are recognized. The phenetic data set applied is nutritional physiology. A key to the species is provided.
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Emerging fungal pathogens, such as Geotrichum capitatum, are often associated with poor prognosis and represent a new challenge in modern medicine. Invasive Geotrichum capitatum infection is rare and has been reported exclusively in patients who showed signs of severe immunodeficiency, particularly those affected by haematological malignancies. The optimal therapy against systemic geotricosis has not yet been identified due to limited data about its antifungal susceptibility. The use of several therapeutic strategies and the low number of cases treated does not allow identification of specific therapeutic protocols. Furthermore, in spite of antifungal therapy, mortality rates reach very high levels. We report a case of systemic Geotrichum capitatum infection in a 78-year-old male treated with salvage therapy after acute myeloid leukaemia (AML) relapse. Geotrichum capitatum was isolated from his blood culture and identified by using Vitek 2 and Maldi time-of-flight system (MALDI-TOF). The infection was unsuccessfully treated, despite in vitro susceptibility, with micafungin and liposomal amphotericin B.
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Geotrichum capitatum is an uncommon cause of invasive infections in immunocompromised patients, particularly those with hematological malignancies and severe neutropenia. The aim of this study was to report the cases of invasive geotrichosis in our hospital. It is a retrospective study of invasive geotrichosis diagnosed in the Laboratory of Parasitology-Mycology of the UH Habib Bourguiba, Sfax, from January 2005 to August 2013. Six cases of invasive Geotrichum infections were diagnosed. There were three men and three women. The mean age was 35 years. Five patients have acute myeloid leukemia with a profound neutropenia, and one patient was hospitalized in the intensive care unit for polytraumatism. Clinically, the prolonged fever associated with pulmonary symptoms was the predominant symptom (n = 5). Geotrichum capitatum was isolated in one or more blood culture. Two patients had urinary tract infections documented by multiple urine cultures positive for G. capitatum. Five patients received conventional amphotericin B alone or associated with voriconazole. The outcome was fatal in four cases. Invasive geotrichosis is rare, but particularly fatal in immunocompromised patients. Approximately, 186 cases have been reported in the literature. The prognostic is poor with mortality over 50 %. So, early diagnosis and appropriate management are necessary to improve prognosis.