Table 1.
Clinical presentation of and host reaction to the more common mycoses
| Fungus(i) | Clinical presentation | Host responsea | Comment(s) |
|---|---|---|---|
| Blastomyces dermatitidis | Asymptomatic | Tissue descriptions unavailable | Epidemiologic evidence |
| Acute pneumonia | Mixed suppurativeb inflammation | Seen in areas of endemicity | |
| Chronic pneumonia | Mixed suppurative and granulomatousc inflammation | Most frequently diagnosed | |
| ARDS | Diffuse alveolar damage | Can be fatal | |
| Disseminated | Various inflammatory responses depending on immune status | Skin, soft tissue, bone, GU, or CNS is primarily involved | |
| Cutaneous | Mixed suppurative and granulomatous inflammation | Rare, due to direct cutaneous inoculation | |
| Cryptococcus spp. | Asymptomatic | Minimal reaction | Rare, epidemiologic evidence |
| Pneumonia | Predominantly granulomatous inflammation, can have abundant fibrosis | More frequent in immunocompetent individuals | |
| Cryptococcoma | Granuloma with various degrees of necrosis and fibrosis | More frequent with C. gattii | |
| Pleural effusion | Various inflammatory responses depending on immune status | More frequent in immunosuppressed patients | |
| Disseminated | Various inflammatory responses depending on immune status, abundant extracellular yeasts may efface tissue architecture, necrosis may be present | Frequent in immunosuppressed patients; involves the CNS (producing meningitis or cryptococcomas), skin, bones, or other tissues | |
| Histoplasma capsulatum | Asymptomatic | Tissue descriptions not available | Occurs when low numbers of microconidia are inhaled |
| Acute pneumonia | Nodules showing vascular necrosis associated with lympho-histiocytic vasculitis and rare granulomatous inflammation | Occurs when high numbers of microconidia are inhaled | |
| ARDS | Diffuse alveolar damage | Can be fatal | |
| Mediastinitis | Granulomatous inflammation | Occurs upon initial inhalation of the microconidia | |
| Chronic pneumonia | Granulomas with various degrees of necrosis and calcification | Can present as a nodule or cavity | |
| Disseminated | Various inflammatory responses depending on immune status, abundant intracellular yeasts may efface tissue architecture, necrosis may be present | Seen upon initial infection or as reactivation of latent disease in patients with T-cell deficiencies; can involve skin, GI tract, liver, spleen, and bone marrow | |
| Coccidioides immitis/posadasii | Asymptomatic | Tissue descriptions unavailable | Epidemiologic evidence |
| Acute pneumonia | Suppurative and granulomatous inflammation | Presents as lobar infiltrates and adenopathy | |
| Chronic pneumonia | Mixed suppurative (including eosinophils) and granulomatous inflammation with a rim of lymphocytes, Splendore-Höeppli phenomenon likely | Can present as a nodule or cavity | |
| Disseminated | Various inflammatory responses depending on immune status | Occurs in certain risk groups (those with diabetes, use of steroids, and others); can involve skin, lymph nodes, bones, joints, and CNS | |
| Cutaneous | Mixed suppurative and granulomatous inflammation | Rare, due to direct cutaneous inoculation | |
| Candida spp. | Superficial infections | Minimal to suppurative inflammation depending on immune status of individual | Skin and mucous membranes of GI and GU tracts in immunocompetent and immunosuppressed individuals |
| Invasive disease | Various inflammatory responses depending on immune status, primarily suppurative inflammation with rare granulomas, invasion of blood vessels, necrotizing vasculitis | Occurs primarily as a health care-associated infection (patients with vascular access devices, with recent surgeries, receiving broad-spectrum antibiotics, or immunosuppressed), can involve all organs | |
| Pneumocystis jirovecii | Asymptomatic | Minimal reaction | Has been found in the lungs of children |
| Pneumonia | Minimal reaction; rarely atypical reactions such as fibrosis, granulomas, and others | Affects immunosuppressed patients | |
| Disseminated | Minimal reaction; rarely atypical reactions such as fibrosis, granulomas, and others | Rare, affects immunosuppressed patients | |
| Sporothrix schenckii | Cutaneous | Mixed suppurative (including eosinophils) and granulomatous inflammation, Splendore-Höeppli phenomenon frequent, presence of asteroid bodies, epidermis with pseudoepitheliomatous hyperplasia | Associated with handling contaminated soil or animals, draining lymph nodes are frequently affected |
| Disseminated | Various inflammatory responses depending on immune status | Affects bone, joints, meninges, and other organs | |
| Penicillium marneffei | Cutaneous | Mixed suppurative and granulomatous inflammation with various degrees of necrosis | Seen mostly in Southeast Asia |
| Disseminated | Various inflammatory responses depending on immune status, may consist only of necrosis and infected macrophages | Seen mostly in Southeast Asia; P. marneffei infection represents the most frequent AIDS-defining illness | |
| Paracoccidioides brasiliensis | Acute pneumonia | Mixed suppurative and granulomatous inflammation | Correlates with hormonal, genetic, immunologic, and nutritional status |
| Chronic pneumonia | Mixed suppurative and granulomatous inflammation surrounded by fibrosis | Correlates with hormonal, genetic, immunologic, and nutritional status; if organism is swallowed, can cause GI disease | |
| Disseminated | Mixed suppurative and granulomatous inflammation, bone may show osteonecrosis | Involvement of bone marrow, adrenal glands, CNS, and other tissues | |
| Cutaneous | Mixed suppurative and granulomatous inflammation, epidermis with epitheliomatous hyperplasia | Rare, due to direct cutaneous inoculation | |
| Rhinosporidium seeberid | Nose, nasopharynx, ocular areas | Granulomatous inflammation with fibrosis and granulation tissue | Presents as a mass or polyp |
| Disseminated | Chronic and granulomatous inflammation | Rare, can involve other mucous membranes or cutaneous sites and internal organs | |
| Aspergillus spp. | Allergic bronchopulmonary aspergillosis | Allergic mucous with eosinophils, Curshmann's spirals, Charcot-Leyden crystals; mucosa with suppurative and granulomatous inflammation, vasculitis, and fibrosis | Hypersensitivity reaction to fungi, most frequently A. fumigatus; seen frequently in patients with cystic fibrosis or steroid-dependent asthma |
| Allergic fungal rhinosinusitis | Similar to that for allergic bronchopulmonary aspergillosis | Hypersensitivity reaction to fungi similar to that for allergic bronchopulmonary aspergillosis | |
| Chronic pulmonary aspergillosis | The wall surrounding the fungus ball consists of fibrosis | Occurs in immunocompetent individuals with a variety of lung conditions (tuberculosis, emphysema, and others) in which the cavity or lesion is colonized and then a “fungus ball” or aspergilloma forms | |
| Chronic necrotizing pulmonary aspergillosis | The wall surrounding the fungus ball consists of a layer of necrosis, granulation tissue, granulomatous inflammation, and fibrosis | Occurs in immunosuppressed individuals with chronic pulmonary aspergillosis, where the fungus is invading the tissues locally | |
| Invasive disease | Angioinvasion by hyphae with consequent necrosis or hemorrhage of surrounding tissue | Seen in severely immunosuppressed patients, involves the lungs, CNS, and other tissues | |
| Mucorales genera | Cutaneous | Angioinvasion by hyphae with consequent necrosis or hemorrhage of surrounding tissue; inflammation, if present, is frequently suppurative, less commonly granulomatous, but varies depending on immune status | Necrotic (black) skin lesion in immunosuppressed patients |
| Rhinocerebral | Similar to that for cutaneous disease | Particularly frequent in diabetic patients but can occur in any immunosuppressed patient | |
| Pulmonary | Similar to that for cutaneous disease | Multiple pulmonary nodules and pleural effusions in immunosuppressed patients | |
| Invasive disease | Similar to that for cutaneous disease | Risk factors include cancer chemotherapy and stem cell transplantation | |
| Entomophthorales | Mucocutaneous | Fibrosis, granulation tissue, mixed eosinophilic and granulomatous inflammation; Splendore-Höeppli phenomenon present | Presents as a mass in immunocompetent individuals, the lesion can be in the GI tract |
| Hyaline septated molds (Fusarium spp., Scedosporium spp., Trichoderma spp., Paecilomyces spp., and others) | Superficial infections | Mild inflammation | Occur in skin, cornea, and nails; Fusarium spp. are the most common of these organisms in causing superficial infections |
| Range of diseases similar to that for Aspergillus: allergic, chronic pulmonary, and invasive | Similar to that for Aspergillus | Some organisms have some peculiarities (for example, Scedosporium spp. are associated with pneumonia after near drowning, and Trichoderma spp. have been observed in patients undergoing dialysis) | |
| Dematiaceous fungi (Madurella spp., Fonsecaea spp., Cladophialophora spp., Exophiala spp., Curvularia spp., Bipolaris spp., and others) | Superficial infections | Mild inflammation | Occur in skin, cornea, and nails |
| Deep skin infections | Mixed suppurative and granulomatous inflammation with reactive epidermal changes, including pseudoepitheliomatous hyperplasia and draining sinuses | See Table 3 | |
| Range of diseases similar to that for Aspergillus: allergic, chronic pulmonary, and invasive | Similar to that for Aspergillus | Bipolaris and Curvularia are most frequently associated with eosinophilia and allergic sinusitis or allergic bronchopulmonary mycosis, Cladophialophora bantiana is most frequently associated with brain abscesses |
Suppurative inflammation refers to presence of congestion, edema, necrosis, and an inflammatory infiltrate with a predominance of neutrophils.
Granulomatous inflammation refers to presence of epithelioid macrophages including multinucleated giant cells, lymphocytes, and necrosis.
R. seeberi is not a fungus but is included for purposes of contrast with fungi that have similar morphology.