Mucormycosis diagnostic criteria: Difference between revisions
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==Diagnostic Criteria== | ==Diagnostic Criteria== | ||
* | Mucormycosis may be diagnosed using the definitions and criteria provided by 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. It classifies invasive fungal infection as: | ||
* Proven invasive fungal disease except endemic mycosis | |||
* Probable invasive fungal disease except endemic mycosis | |||
* Criteria for diagnosis of endemic mycosis | |||
'''Criteria for proven invasive fungal disease except for endemic mycoses''' | |||
{| class="wikitable" | |||
! colspan="1" rowspan="1" |Analysis and specimen | |||
! colspan="1" rowspan="1" |Molds | |||
! colspan="1" rowspan="1" |Yeasts | |||
| colspan="1" rowspan="1" |Microscopic analysis: sterile material | |||
| colspan="1" rowspan="1" |Histopathologic, cytopathologic, or direct microscopic examination of a specimen obtained by needle aspiration or biopsy in which hyphae or melanized yeast-like forms are seen accompanied by evidence of associated tissue damage | |||
| colspan="1" rowspan="1" |Histopathologic, cytopathologic, or direct microscopic examinationb of a specimen obtained by needle aspiration or biopsy from a normally sterile site (other than mucous membranes) showing yeast cells—for example, ''Cryptococcus'' species indicated by encapsulated budding yeasts or ''Candida'' species showing pseudohyphae or true hyphaec | |||
|- | |||
| colspan="1" rowspan="1" |Sterile material | |||
| colspan="1" rowspan="1" |Recovery of a mold or “black yeast” by culture of a specimen obtained by a sterile procedure from a normally sterile and clinically or radiologically abnormal site consistent with an infectious disease process, excluding bronchoalveolar lavage fluid, a cranial sinus cavity specimen, and urine | |||
| colspan="1" rowspan="1" |Recovery of a yeast by culture of a sample obtained by a sterile procedure (including a freshly placed [<24 h ago] drain) from a normally sterile site showing a clinical or radiological abnormality consistent with an infectious disease process | |||
|- | |||
| colspan="1" rowspan="1" |Blood | |||
| colspan="1" rowspan="1" |Blood culture that yields a mold (e.g., ''Fusarium'' species) in the context of a compatible infectious disease process | |||
| colspan="1" rowspan="1" |Blood culture that yields yeast (e.g., ''Cryptococcus'' or ''Candida'' species) or yeast-like fungi (e.g., ''Trichosporon'' species) | |||
|- | |||
| colspan="1" rowspan="1" |Serological analysis: CSF | |||
| colspan="1" rowspan="1" |Not applicable | |||
| colspan="1" rowspan="1" |Cryptococcal antigen in CSF indicates disseminated cryptococcosis | |||
|} | |||
'''Criteria for probable invasive fungal disease except for endemic mycoses''' | |||
'''Host factors:''' | |||
* Recent history of neutropenia (<0.5 × 109 neutrophils/L [<500 neutrophils/mm3] for >10 days) temporally related to the onset of fungal disease | |||
* Receipt of an allogeneic stem cell transplant | |||
* Prolonged use of corticosteroids (excluding among patients with allergic bronchopulmonary aspergillosis) at a mean minimum dose of 0.3 mg/kg/day of prednisone equivalent for >3 weeks | |||
* Treatment with other recognized T cell immunosuppressants, such as cyclosporine, TNF-α blockers, specific monoclonal antibodies (such as alemtuzumab), or nucleoside analogues during the past 90 days | |||
* Inherited severe immunodeficiency (such as chronic granulomatous disease or severe combined immunodeficiency) | |||
'''Clinical criteria''' | |||
* Lower respiratory tract fungal disease | |||
* The presence of 1 of the following 3 signs on CT: | |||
*# Dense, well-circumscribed lesions(s) with or without a halo sign | |||
*# Air crescent sign | |||
*# Cavity | |||
* Tracheobronchitis | |||
* Tracheobronchial ulceration, nodule, pseudomembrane, plaque, or eschar seen on bronchoscopic analysis | |||
* Sino-nasal infection | |||
* Imaging showing sinusitis plus at least 1 of the following 3 signs: | |||
# Acute localized pain (including pain radiating to the eye) | |||
# Nasal ulcer with black eschar | |||
# Extension from the paranasal sinus across bony barriers, including into the orbit | |||
* CNS infection | |||
* 1 of the following 2 signs: | |||
# Focal lesions on imaging | |||
# Meningeal enhancement on MRI or CT | |||
# Disseminated candidiasis | |||
* At least 1 of the following 2 entities after an episode of candidemia within the previous 2 weeks: | |||
# Small, target-like abscesses (bull's-eye lesions) in liver or spleen | |||
# Progressive retinal exudates on ophthalmologic examination | |||
'''Mycological criteria''' | |||
* Direct test (cytology, direct microscopy, or culture) | |||
* Mold in sputum, bronchoalveolar lavage fluid, bronchial brush, or sinus aspirate samples, indicated by 1 of the following: | |||
# Presence of fungal elements indicating a mold | |||
# Recovery by culture of a mold (e.g., Aspergillus, Fusarium, Zygomycetes, or Scedosporium species) | |||
* Indirect tests (detection of antigen or cell-wall constituents) | |||
* Aspergillosis | |||
** Galactomannan antigen detected in plasma, serum, bronchoalveolar lavage fluid, or CSF | |||
* Invasive fungal disease other than cryptococcosis and zygomycoses | |||
** β-d-glucan detected in serum | |||
==References== | ==References== |
Revision as of 16:14, 5 June 2017
Mucormycosis Microchapters |
Diagnosis |
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Treatment |
Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief: Syed Hassan A. Kazmi BSc, MD [2]
Overview
Diagnostic Criteria
Mucormycosis may be diagnosed using the definitions and criteria provided by 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. It classifies invasive fungal infection as:
- Proven invasive fungal disease except endemic mycosis
- Probable invasive fungal disease except endemic mycosis
- Criteria for diagnosis of endemic mycosis
Criteria for proven invasive fungal disease except for endemic mycoses
Analysis and specimen | Molds | Yeasts | Microscopic analysis: sterile material | Histopathologic, cytopathologic, or direct microscopic examination of a specimen obtained by needle aspiration or biopsy in which hyphae or melanized yeast-like forms are seen accompanied by evidence of associated tissue damage | Histopathologic, cytopathologic, or direct microscopic examinationb of a specimen obtained by needle aspiration or biopsy from a normally sterile site (other than mucous membranes) showing yeast cells—for example, Cryptococcus species indicated by encapsulated budding yeasts or Candida species showing pseudohyphae or true hyphaec |
---|---|---|---|---|---|
Sterile material | Recovery of a mold or “black yeast” by culture of a specimen obtained by a sterile procedure from a normally sterile and clinically or radiologically abnormal site consistent with an infectious disease process, excluding bronchoalveolar lavage fluid, a cranial sinus cavity specimen, and urine | Recovery of a yeast by culture of a sample obtained by a sterile procedure (including a freshly placed [<24 h ago] drain) from a normally sterile site showing a clinical or radiological abnormality consistent with an infectious disease process | |||
Blood | Blood culture that yields a mold (e.g., Fusarium species) in the context of a compatible infectious disease process | Blood culture that yields yeast (e.g., Cryptococcus or Candida species) or yeast-like fungi (e.g., Trichosporon species) | |||
Serological analysis: CSF | Not applicable | Cryptococcal antigen in CSF indicates disseminated cryptococcosis |
Criteria for probable invasive fungal disease except for endemic mycoses
Host factors:
- Recent history of neutropenia (<0.5 × 109 neutrophils/L [<500 neutrophils/mm3] for >10 days) temporally related to the onset of fungal disease
- Receipt of an allogeneic stem cell transplant
- Prolonged use of corticosteroids (excluding among patients with allergic bronchopulmonary aspergillosis) at a mean minimum dose of 0.3 mg/kg/day of prednisone equivalent for >3 weeks
- Treatment with other recognized T cell immunosuppressants, such as cyclosporine, TNF-α blockers, specific monoclonal antibodies (such as alemtuzumab), or nucleoside analogues during the past 90 days
- Inherited severe immunodeficiency (such as chronic granulomatous disease or severe combined immunodeficiency)
Clinical criteria
- Lower respiratory tract fungal disease
- The presence of 1 of the following 3 signs on CT:
- Dense, well-circumscribed lesions(s) with or without a halo sign
- Air crescent sign
- Cavity
- Tracheobronchitis
- Tracheobronchial ulceration, nodule, pseudomembrane, plaque, or eschar seen on bronchoscopic analysis
- Sino-nasal infection
- Imaging showing sinusitis plus at least 1 of the following 3 signs:
- Acute localized pain (including pain radiating to the eye)
- Nasal ulcer with black eschar
- Extension from the paranasal sinus across bony barriers, including into the orbit
- CNS infection
- 1 of the following 2 signs:
- Focal lesions on imaging
- Meningeal enhancement on MRI or CT
- Disseminated candidiasis
- At least 1 of the following 2 entities after an episode of candidemia within the previous 2 weeks:
- Small, target-like abscesses (bull's-eye lesions) in liver or spleen
- Progressive retinal exudates on ophthalmologic examination
Mycological criteria
- Direct test (cytology, direct microscopy, or culture)
- Mold in sputum, bronchoalveolar lavage fluid, bronchial brush, or sinus aspirate samples, indicated by 1 of the following:
- Presence of fungal elements indicating a mold
- Recovery by culture of a mold (e.g., Aspergillus, Fusarium, Zygomycetes, or Scedosporium species)
- Indirect tests (detection of antigen or cell-wall constituents)
- Aspergillosis
- Galactomannan antigen detected in plasma, serum, bronchoalveolar lavage fluid, or CSF
- Invasive fungal disease other than cryptococcosis and zygomycoses
- β-d-glucan detected in serum