Semin Respir Crit Care Med 2011; 32(6): 703-716
DOI: 10.1055/s-0031-1295718
© Thieme Medical Publishers

Pneumonia and Lung Infections due to Emerging and Unusual Fungal Pathogens

Sharon C.-A. Chen1 , 2 , Christopher C. Blyth3 , Tania C. Sorrell1 , 2 , Monica A. Slavin4
  • 1Centre for Infectious Diseases and Microbiology, Westmead Hospital, Westmead, Australia
  • 2Sydney Emerging Infectious Diseases Institute, University of Sydney, Sydney, Australia
  • 3Department of Paediatrics and Child Health, University of Western Australia, Perth, Australia
  • 4Department of Infectious Diseases, Peter MacCallum Cancer Centre, Melbourne, Australia
Further Information

Publication History

Publication Date:
13 December 2011 (online)

ABSTRACT

Invasive mold infections affecting the lungs are increasing in incidence and diversity. Severely immunocompromised patients are particularly vulnerable to infection from unusual, normally nonpathogenic fungi that are found naturally in the environment. Certain fungi such as Scedosporium and the dematiaceous fungi also cause lung disease in hosts without overt immune compromise. The impacts of these emerging pathogens range from airway colonization to locally invasive lung, and disseminated, disease. Diagnosis requires isolation and identification of the etiologic agent by either or both phenotypic and molecular biology methods. Evidence of tissue invasion on histopathology is often required to distinguish infection from colonization. Diagnostic imaging techniques are nonspecific, and there are no reliable serological biomarkers of infection. Many rare molds and yeasts demonstrate reduced in vitro susceptibility to antifungal agents. Although amphotericin B formulations remain clinically useful for many of these infections, voriconazole and posaconazole are more effective for some of these difficult-to-treat pathogens. Surgical resection of diseased tissue and support of the host immune system are often required to optimize outcomes.

REFERENCES

  • 1 Pfaller M A, Diekema D J. Epidemiology of invasive mycoses in North America.  Crit Rev Microbiol. 2010;  36 (1) 1-53
  • 2 Ben-Ami R, Lewis R E, Kontoyiannis D P. Invasive mould infections in the setting of hematopoietic cell transplantation: current trends and new challenges.  Curr Opin Infect Dis. 2009;  22 (4) 376-384
  • 3 Neofytos D, Horn D, Anaissie E et al.. Epidemiology and outcome of invasive fungal infection in adult hematopoietic stem cell transplant recipients: analysis of Multicenter Prospective Antifungal Therapy (PATH) Alliance registry.  Clin Infect Dis. 2009;  48 (3) 265-273
  • 4 Pappas P G, Alexander B D, Andes D R et al.. Invasive fungal infections among organ transplant recipients: results of the Transplant-Associated Infection Surveillance Network (TRANSNET).  Clin Infect Dis. 2010;  50 (8) 1101-1111
  • 5 Malani A N, Kauffman C A. Changing epidemiology of rare mould infections: implications for therapy.  Drugs. 2007;  67 (13) 1803-1812
  • 6 Pfaller M A, Diekema D J. Azole antifungal drug cross-resistance: mechanisms, epidemiology and clinical significance.  J Invasive Fungal Infect. 2007;  1 74-92
  • 7 Cortez K J, Roilides E, Quiroz-Telles F et al.. Infections caused by Scedosporium spp.  Clin Microbiol Rev. 2008;  21 (1) 157-197
  • 8 Revankar S G, Sutton D A. Melanized fungi in human disease.  Clin Microbiol Rev. 2010;  23 (4) 884-928
  • 9 Naggie S, Perfect J R. Molds: hyalohyphomycosis, phaeohyphomycosis, and zygomycosis.  Clin Chest Med. 2009;  30 (2) 337-353, vii–viii
  • 10 Nucci M, Anaissie E. Fusarium infections in immunocompromised patients.  Clin Microbiol Rev. 2007;  20 (4) 695-704
  • 11 Heath C H, Slavin M A, Sorrell T C Australian Scedosporium Study Group et al. Population-based surveillance for scedosporiosis in Australia: epidemiology, disease manifestations and emergence of Scedosporium aurantiacum infection.  Clin Microbiol Infect. 2009;  15 (7) 689-693
  • 12 Gilgado F, Gené J, Cano J, Guarro J. Heterothallism in Scedosporium apiospermum and description of its teleomorph Pseudallescheria apiosperma sp. nov.  Med Mycol. 2010;  48 (1) 122-128
  • 13 Ben-Ami R, Lewis R E, Raad I I, Kontoyiannis D P. Phaeohyphomycosis in a tertiary care cancer center.  Clin Infect Dis. 2009;  48 (8) 1033-1041
  • 14 Labbé A C, Su S H, Laverdière M et al.. High incidence of invasive aspergillosis associated with intestinal graft-versus-host disease following nonmyeloablative transplantation.  Biol Blood Marrow Transplant. 2007;  13 (10) 1192-1200
  • 15 Husain S, Muñoz P, Forrest G et al.. Infections due to Scedosporium apiospermum and Scedosporium prolificans in transplant recipients: clinical characteristics and impact of antifungal agent therapy on outcome.  Clin Infect Dis. 2005;  40 (1) 89-99
  • 16 Husain S, Alexander B D, Munoz P et al.. Opportunistic mycelial fungal infections in organ transplant recipients: emerging importance of non-Aspergillus mycelial fungi.  Clin Infect Dis. 2003;  37 (2) 221-229
  • 17 Pagano L, Akova M, Dimopoulos G, Herbrecht R, Drgona L, Blijlevens N. Risk assessment and prognostic factors for mould-related diseases in immunocompromised patients.  J Antimicrob Chemother. 2011;  66 (Suppl 1) i5-i14
  • 18 Nucci M, Marr K A, Queiroz-Telles F et al.. Fusarium infection in hematopoietic stem cell transplant recipients.  Clin Infect Dis. 2004;  38 (9) 1237-1242
  • 19 Neofytos D, Fishman J A, Horn D et al.. Epidemiology and outcome of invasive fungal infections in solid organ transplant recipients.  Transpl Infect Dis. 2010;  12 (3) 220-229
  • 20 Garcia-Vidal C, Upton A, Kirby K A, Marr K A. Epidemiology of invasive mold infections in allogeneic stem cell transplant recipients: biological risk factors for infection according to time after transplantation.  Clin Infect Dis. 2008;  47 (8) 1041-1050
  • 21 Safdar A, Rodriguez G H, De Lima M J et al.. Infections in 100 cord blood transplantations: spectrum of early and late posttransplant infections in adult and pediatric patients 1996–2005.  Medicine (Baltimore). 2007;  86 (6) 324-333
  • 22 Mihu C N, King E, Yossepovitch O et al.. Risk factors and attributable mortality of late aspergillosis after T-cell depleted hematopoietic stem cell transplantation.  Transpl Infect Dis. 2008;  10 (3) 162-167
  • 23 van Burik J A, Carter S L, Freifeld A G et al.. Higher risk of cytomegalovirus and Aspergillus infections in recipients of T cell-depleted unrelated bone marrow: analysis of infectious complications in patients treated with T cell depletion versus immunosuppressive therapy to prevent graft-versus-host disease.  Biol Blood Marrow Transplant. 2007;  13 (12) 1487-1498
  • 24 Tsiodras S, Samonis G, Boumpas D T, Kontoyiannis D P. Fungal infections complicating tumour necrosis factor alpha blockade therapy.  Mayo Clin Proc. 2008;  83 (2) 181-194
  • 25 Marr K A, Carter R A, Crippa F, Wald A, Corey L. Epidemiology and outcome of mould infections in hematopoietic stem cell transplant recipients.  Clin Infect Dis. 2002;  34 (7) 909-917
  • 26 Kontoyiannis D P, Marr K A, Park B J et al.. Prospective surveillance for invasive fungal infections in hematopoietic stem cell transplant recipients, 2001-2006: overview of the Transplant-Associated Infection Surveillance Network (TRANSNET) Database.  Clin Infect Dis. 2010;  50 (8) 1091-1100
  • 27 Marr K A, Carter R A, Boeckh M, Martin P, Corey L. Invasive aspergillosis in allogeneic stem cell transplant recipients: changes in epidemiology and risk factors.  Blood. 2002;  100 (13) 4358-4366
  • 28 Campo M, Lewis R E, Kontoyiannis D P. Invasive fusariosis in patients with hematologic malignancies at a cancer center: 1998-2009.  J Infect. 2010;  60 (5) 331-337
  • 29 Carneiro H A, Coleman J J, Restrepo A, Mylonakis E. Fusarium infection in lung transplant patients: report of 6 cases and review of the literature.  Medicine (Baltimore). 2011;  90 (1) 69-80
  • 30 Groll A H, Walsh T J. Uncommon opportunistic fungi: new nosocomial threats.  Clin Microbiol Infect. 2001;  7 (Suppl 2) 8-24
  • 31 Backman K S, Roberts M, Patterson R. Allergic bronchopulmonary mycosis caused by Fusarium vasinfectum.  Am J Respir Crit Care Med. 1995;  152 (4 Pt 1) 1379-1381
  • 32 Saini S K, Boas S R, Jerath A, Roberts M, Greenberger P A. Allergic bronchopulmonary mycosis to Fusarium vasinfectum in a child.  Ann Allergy Asthma Immunol. 1998;  80 (5) 377-380
  • 33 Sahi H, Avery R K, Minai O A et al.. Scedosporium apiospermum (Pseudoallescheria boydii) infection in lung transplant recipients.  J Heart Lung Transplant. 2007;  26 (4) 350-356
  • 34 Symoens F, Knoop C, Schrooyen M et al.. Disseminated Scedosporium apiospermum infection in a cystic fibrosis patient after double-lung transplantation.  J Heart Lung Transplant. 2006;  25 (5) 603-607
  • 35 Tamm M, Malouf M, Glanville A. Pulmonary Scedosporium infection following lung transplantation.  Transpl Infect Dis. 2001;  3 (4) 189-194
  • 36 Katragkou A, Dotis J, Kotsiou M, Tamiolaki M, Roilides E. Scedosporium apiospermum infection after near-drowning.  Mycoses. 2007;  50 (5) 412-421
  • 37 Blyth C C, Middleton P G, Harun A, Sorrell T C, Meyer W, Chen S C. Clinical associations and prevalence of Scedosporium spp. in Australian cystic fibrosis patients: identification of novel risk factors?.  Med Mycol. 2010;  48 (Suppl 1) S37-S44
  • 38 Varkey J B, Perfect J R. Rare and emerging fungal pulmonary infections.  Semin Respir Crit Care Med. 2008;  29 (2) 121-131
  • 39 Pastor F J, Guarro J. Clinical manifestations, treatment and outcome of Paecilomyces lilacinus infections.  Clin Microbiol Infect. 2006;  12 (10) 948-960
  • 40 Castro L G, Salebian A, Sotto M N. Hyalohyphomycosis by Paecilomyces lilacinus in a renal transplant patient and a review of human Paecilomyces species infections.  J Med Vet Mycol. 1990;  28 (1) 15-26
  • 41 Byrd Jr R P, Roy T M, Fields C L, Lynch J A. Paecilomyces variotii pneumonia in a patient with diabetes mellitus.  J Diabetes Complications. 1992;  6 (2) 150-153
  • 42 Pastorino A C, Menezes U P, Marques H H et al.. Acremonium kiliense infection in a child with chronic granulomatous disease.  Braz J Infect Dis. 2005;  9 (6) 529-534
  • 43 Gutiérrez F, Masiá M, Ramos J, Elía M, Mellado E, Cuenca-Estrella M. Pulmonary mycetoma caused by an atypical isolate of Paecilomyces species in an immunocompetent individual: case report and literature review of Paecilomyces lung infections.  Eur J Clin Microbiol Infect Dis. 2005;  24 (9) 607-611
  • 44 Chouaki T, Lavarde V, Lachaud L, Raccurt C P, Hennequin C. Invasive infections due to Trichoderma species: report of 2 cases, findings of in vitro susceptibility testing, and review of the literature.  Clin Infect Dis. 2002;  35 (11) 1360-1367
  • 45 Alanio A, Brethon B, Feuilhade de Chauvin M et al.. Invasive pulmonary infection due to Trichoderma longibrachiatum mimicking invasive Aspergillosis in a neutropenic patient successfully treated with voriconazole combined with caspofungin.  Clin Infect Dis. 2008;  46 (10) e116-e118
  • 46 Mouri M, Nambu Y, Horii H et al.. Case report and review of literature on seasonal distribution and pathogenesis of acute eosinophilic pneumonia in Japan [in Japanese].  Nihon Kyobu Shikkan Gakkai Zasshi. 1993;  31 (12) 1578-1584
  • 47 Machouart M, Garcia-Hermoso D, Rivier A et al.. Emergence of disseminated infections due to Geosmithia argillacea in patients with chronic granulomatous disease receiving long-term azole antifungal prophylaxis.  J Clin Microbiol. 2011;  49 (4) 1681-1683
  • 48 De Ravin S S, Challipalli M, Anderson V et al.. Geosmithia argillacea: an emerging cause of invasive mycosis in human chronic granulomatous disease.  Clin Infect Dis. 2011;  52 (6) e136-e143
  • 49 Revankar S G, Patterson J E, Sutton D A, Pullen R, Rinaldi M G. Disseminated phaeohyphomycosis: review of an emerging mycosis.  Clin Infect Dis. 2002;  34 (4) 467-476
  • 50 Shoham S, Pic-Aluas L, Taylor J et al.. Transplant-associated Ochroconis gallopava infections.  Transpl Infect Dis. 2008;  10 (6) 442-448
  • 51 Boyce R D, Deziel P J, Otley C C et al.. Phaeohyphomycosis due to Alternaria species in transplant recipients.  Transpl Infect Dis. 2010;  12 (3) 242-250
  • 52 Girmenia C, Pagano L, Martino B GIMEMA Infection Program et al. Invasive infections caused by Trichosporon species and Geotrichum capitatum in patients with hematological malignancies: a retrospective multicenter study from Italy and review of the literature.  J Clin Microbiol. 2005;  43 (4) 1818-1828
  • 53 Ruan S Y, Chien J Y, Hsueh P R. Invasive trichosporonosis caused by Trichosporon asahii and other unusual Trichosporon species at a medical center in Taiwan.  Clin Infect Dis. 2009;  49 (1) e11-e17
  • 54 Matsue K, Uryu H, Koseki M, Asada N, Takeuchi M. Breakthrough trichosporonosis in patients with hematologic malignancies receiving micafungin.  Clin Infect Dis. 2006;  42 (6) 753-757
  • 55 Wolf D G, Falk R, Hacham M et al.. Multidrug-resistant Trichosporon asahii infection of nongranulocytopenic patients in three intensive care units.  J Clin Microbiol. 2001;  39 (12) 4420-4425
  • 56 Cuenca-Estrella M, Bassetti M, Lass-Flörl C, Rácil Z, Richardson M, Rogers T R. Detection and investigation of invasive mould disease.  J Antimicrob Chemother. 2011;  66 (Suppl 1) i15-i24
  • 57 De Pauw B, Walsh T J, Donnelly J P European Organization for Research and Treatment of Cancer/Invasive Fungal Infections Cooperative Group et al. Revised definitions of invasive fungal disease from the European Organization for Research and Treatment of Cancer/Invasive Fungal Infections Cooperative Group and the National Institute of Allergy and Infectious Diseases Mycoses Study Group (EORTC/MSG) Consensus Group.  Clin Infect Dis. 2008;  46 (12) 1813-1821
  • 58 Hayden R T, Isotalo P A, Parrett T et al.. In situ hybridization for the differentiation of Aspergillus, Fusarium, and Pseudallescheria species in tissue section.  Diagn Mol Pathol. 2003;  12 (1) 21-26
  • 59 Lau A, Chen S, Sorrell T et al.. Development and clinical application of a panfungal PCR assay to detect and identify fungal DNA in tissue specimens.  J Clin Microbiol. 2007;  45 (2) 380-385
  • 60 Harun A, Blyth C C, Gilgado F, Middleton P, Chen S C, Meyer W. Development and validation of a mulitplex PCR for detection of Scedosporium spp. in respiratory tract specimens from patients with cystic fibrosis.  J Clin Microbiol. 2011;  49 (4) 1508-1512
  • 61 Ahmad S, Khan Z U, Theyyathel A M. Development of a nested PCR assay for the detection of Fusarium solani DNA and its evaluation in the diagnosis of invasive fusariosis using an experimental mouse model.  Mycoses. 2010;  53 (1) 40-47
  • 62 De Hoog G S, Guarro J, Gene J et al.. Atlas of Clinical Fungi. Utrecht/Reus: Centraalbureau voor Schimmelcultures/Universität Rovira i Virgili; 2000
  • 63 Herbrecht R, Letscher-Bru V, Fohrer C et al.. Acremonium strictum pulmonary infection in a leukemic patient successfully treated with posaconazole after failure of amphotericin B.  Eur J Clin Microbiol Infect Dis. 2002;  21 (11) 814-817
  • 64 Silveira F P, Kwak E J, Paterson D L, Pilewski J M, McCurry K R, Husain S. Post-transplant colonization with non-Aspergillus molds and risk of development of invasive fungal disease in lung transplant recipients.  J Heart Lung Transplant. 2008;  27 (8) 850-855
  • 65 Lionakis M S, Kontoyiannis D P. The significance of isolation of saprophytic molds from the lower respiratory tract in patients with cancer.  Cancer. 2004;  100 (1) 165-172
  • 66 Balajee S A, Borman A M, Brandt M E et al.. Sequence-based identification of Aspergillus, fusarium, and mucorales species in the clinical mycology laboratory: where are we and where should we go from here?.  J Clin Microbiol. 2009;  47 (4) 877-884
  • 67 Wang H, Xiao M, Kong F R et al.. Accurate and practical identification of 20 Fusarium species by seven-locus sequence analysis and reverse line blot hybridization, and an in vitro antifungal susceptibility study.  J Clin Microbiol. 2011;  49 (5) 1890-1898
  • 68 Barnett J A, Payne R W, Yarrow D. Yeasts: Characteristics and Identification. 3rd ed. Cambridge: Cambridge University Press; 2000
  • 69 Lau A, Chen S, Sleiman S, Sorrell T. Current status and future perspectives on molecular and serological methods in diagnostic mycology.  Future Microbiol. 2009;  4 (9) 1185-1222
  • 70 O’Donnell K, Sutton D A, Rinaldi M G et al.. Internet-accessible DNA sequence database for identifying fusaria from human and animal infections.  J Clin Microbiol. 2010;  48 (10) 3708-3718
  • 71 Hennequin C, Abachin E, Symoens F et al.. Identification of Fusarium species involved in human infections by 28S rRNA gene sequencing.  J Clin Microbiol. 1999;  37 (11) 3586-3589
  • 72 Nilsson R H, Ryberg M, Kristiansson E, Abarenkov K, Larsson K H, Kõljalg U. Taxonomic reliability of DNA sequences in public sequence databases: a fungal perspective.  PLoS ONE. 2006;  1 e59
  • 73 Mennink-Kersten M A, Ruegebrink D, Klont R R et al.. Bifidobacterial lipoglycan as a new cause for false-positive platelia Aspergillus enzyme-linked immunosorbent assay reactivity.  J Clin Microbiol. 2005;  43 (8) 3925-3931
  • 74 Viscoli C, Machetti M, Cappellano P et al.. False-positive galactomannan platelia Aspergillus test results for patients receiving piperacillin-tazobactam.  Clin Infect Dis. 2004;  38 (6) 913-916
  • 75 Yoshida M, Obayashi T, Iwama A et al.. Detection of plasma (1 —>3)-beta-D-glucan in patients with Fusarium, Trichosporon, Saccharomyces and Acremonium fungaemias.  J Med Vet Mycol. 1997;  35 (5) 371-374
  • 76 Ostrosky-Zeichner L, Alexander B D, Kett D H et al.. Multicenter clinical evaluation of the (1—>3) beta-D-glucan assay as an aid to diagnosis of fungal infections in humans.  Clin Infect Dis. 2005;  41 (5) 654-659
  • 77 Karageorgopoulos D E, Vouloumanou E K, Ntziora F, Michalopoulos A, Rafailidis P I, Falagas M E. β-D-glucan assay for the diagnosis of invasive fungal infections: a meta-analysis.  Clin Infect Dis. 2011;  52 (6) 750-770
  • 78 Alexander B D, Smith P B, Davis R D, Perfect J R, Reller L B. The (1,3)beta-D-glucan test as an aid to early diagnosis of invasive fungal infections following lung transplantation.  J Clin Microbiol. 2010;  48 (11) 4083-4088
  • 79 Marom E M, Holmes A M, Bruzzi J F, Truong M T, O’Sullivan P J, Kontoyiannis D P. Imaging of pulmonary fusariosis in patients with hematologic malignancies.  AJR Am J Roentgenol. 2008;  190 (6) 1605-1609
  • 80 Althoff Souza C, Müller N L, Marchiori E, Escuissato D L, Franquet T. Pulmonary invasive aspergillosis and candidiasis in immunocompromised patients: a comparative study of the high-resolution CT findings.  J Thorac Imaging. 2006;  21 (3) 184-189
  • 81 Tashiro T, Nagai H, Nagaoka H, Goto Y, Kamberi P, Nasu M. Trichosporon beigelii pneumonia in patients with hematologic malignancies.  Chest. 1995;  108 (1) 190-195
  • 82 Houbraken J, Verweij P E, Rijs A J, Borman A M, Samson R A. Identification of Paecilomyces variotii in clinical samples and settings.  J Clin Microbiol. 2010;  48 (8) 2754-2761
  • 83 Ananda-Rajah M R, Grigg A, Slavin M A. Breakthrough disseminated Scedosporium prolificans infection in a patient with relapsed leukaemia on prolonged voriconazole followed by posaconazole prophylaxis.  Mycopathologia. 2008;  166 (2) 83-86 Epub 2008 May 30
  • 84 Liu J Y, Chen W T, Ko B S et al.. Combination antifungal therapy for disseminated fusariosis in immunocompromised patients: a case report and literature review.  Med Mycol. 2011;  49 (8) 872-878
  • 85 Henrich T J, Marty F M, Milner Jr D A, Thorner A R. Disseminated Geotrichum candidum infection in a patient with relapsed acute myelogenous leukemia following allogeneic stem cell transplantation and review of the literature.  Transpl Infect Dis. 2009;  11 (5) 458-462
  • 86 Rodriguez-Tudela J L, Berenguer J, Guarro J et al.. Epidemiology and outcome of Scedosporium prolificans infection, a review of 162 cases.  Med Mycol. 2009;  47 (4) 359-370
  • 87 Perfect J R, Marr K A, Walsh T J et al.. Voriconazole treatment for less-common, emerging, or refractory fungal infections.  Clin Infect Dis. 2003;  36 (9) 1122-1131
  • 88 Raad I I, Hachem R Y, Herbrecht R et al.. Posaconazole as salvage treatment for invasive fusariosis in patients with underlying hematologic malignancy and other conditions.  Clin Infect Dis. 2006;  42 (10) 1398-1403
  • 89 Troke P, Aguirrebengoa K, Arteaga C Global Scedosporium Study Group et al. Treatment of scedosporiosis with voriconazole: clinical experience with 107 patients.  Antimicrob Agents Chemother. 2008;  52 (5) 1743-1750
  • 90 Lortholary O, Obenga G, Biswas P French Mycoses Study Group et al. International retrospective analysis of 73 cases of invasive fusariosis treated with voriconazole.  Antimicrob Agents Chemother. 2010;  54 (10) 4446-4450
  • 91 Castelli M V, Alastruey-Izquierdo A, Cuesta I et al.. Susceptibility testing and molecular classification of Paecilomyces spp.  Antimicrob Agents Chemother. 2008;  52 (8) 2926-2928
  • 92 Mattei D, Mordini N, Lo Nigro C et al.. Successful treatment of Acremonium fungemia with voriconazole.  Mycoses. 2003;  46 (11-12) 511-514
  • 93 Suzuki K, Nakase K, Kyo T et al.. Fatal Trichosporon fungemia in patients with hematologic malignancies.  Eur J Haematol. 2010;  84 (5) 441-447
  • 94 Alastruey-Izquierdo A, Cuenca-Estrella M, Monzón A, Mellado E, Rodríguez-Tudela J L. Antifungal susceptibility profile of clinical Fusarium spp. isolates identified by molecular methods.  J Antimicrob Chemother. 2008;  61 (4) 805-809
  • 95 Shalit I, Shadkchan Y, Mircus G, Osherov N. In vitro synergy of caspofungin with licensed and novel antifungal drugs against clinical isolates of Fusarium spp.  Med Mycol. 2009;  47 (5) 457-462
  • 96 Nucci M, Anaissie E J, Queiroz-Telles F et al.. Outcome predictors of 84 patients with hematologic malignancies and Fusarium infection.  Cancer. 2003;  98 (2) 315-319
  • 97 Neuburger S, Massenkeil G, Seibold M et al.. Successful salvage treatment of disseminated cutaneous fusariosis with liposomal amphotericin B and terbinafine after allogeneic stem cell transplantation.  Transpl Infect Dis. 2008;  10 (4) 290-293
  • 98 Ho D Y, Lee J D, Rosso F, Montoya J G. Treating disseminated fusariosis: amphotericin B, voriconazole or both?.  Mycoses. 2007;  50 (3) 227-231
  • 99 Meletiadis J, Mouton J W, Meis J F, Verweij P E. In vitro drug interaction modeling of combinations of azoles with terbinafine against clinical Scedosporium prolificans isolates.  Antimicrob Agents Chemother. 2003;  47 (1) 106-117
  • 100 Cuenca-Estrella M, Alastruey-Izquierdo A, Alcazar-Fuoli L et al.. In vitro activities of 35 double combinations of antifungal agents against Scedosporium apiospermum and Scedosporium prolificans.  Antimicrob Agents Chemother. 2008;  52 (3) 1136-1139
  • 101 Kesson A M, Bellemore M C, O’Mara T J, Ellis D H, Sorrell T C. Scedosporium prolificans osteomyelitis in an immunocompetent child treated with a novel agent, hexadecylphospocholine (miltefosine), in combination with terbinafine and voriconazole: a case report.  Clin Infect Dis. 2009;  48 (9) 1257-1261
  • 102 Schell W A, Perfect J R. Fatal, disseminated Acremonium strictum infection in a neutropenic host.  J Clin Microbiol. 1996;  34 (5) 1333-1336
  • 103 Pfaller M A, Messer S A, Hollis R J, Jones R N. SENTRY Participants Group . Antifungal activities of posaconazole, ravuconazole, and voriconazole compared to those of itraconazole and amphotericin B against 239 clinical isolates of Aspergillus spp. and other filamentous fungi: report from SENTRY Antimicrobial Surveillance Program, 2000.  Antimicrob Agents Chemother. 2002;  46 (4) 1032-1037
  • 104 Perfect J R. Treatment of non-Aspergillus moulds in immunocompromised patients, with amphotericin B lipid complex.  Clin Infect Dis. 2005;  40 (Suppl 6) S401-S408
  • 105 Fianchi L, Montini L, Caira M et al.. Combined voriconazole plus caspofungin therapy for the treatment of probable Geotrichum pneumonia in a leukemia patient.  Infection. 2008;  36 (1) 65-67
  • 106 Etienne A, Datry A, Gaspar N et al.. Successful treatment of disseminated Geotrichum capitatum infection with a combination of caspofungin and voriconazole in an immunocompromised patient.  Mycoses. 2008;  51 (3) 270-272

Sharon C.-A. ChenPh.D. 

Centre for Infectious Diseases and Microbiology

Westmead Hospital, Darcy Road, Westmead NSW 2145, Australia

Email: sharon.chen@swahs.health.nsw.gov.au

    >