- 1.1 Parasite Classification |
- 1.2 Body Site, Specimens, Procedures, Parasites, Comments |
- 1.3 STAT Testing in Parasitology |
- 1.4 Test Issues and Reports: Computer Report Comments|
- 1.5 Rapid Diagnostic Testing
- 2.1 Stool Testing Order Recommendations |
- 2.2 Fecal specimens for parasites: options for collection and processinga2 |
- 2.3 Preservatives used for Stool Specimens
- 3.1 Body Sites and Specimen Collection | - 3.2 Body sites and the most common parasites recovered | - 3.3 Body Site, Specimens and Recommended Stain | - 3.4 Examination of tissues and body fluids | - 3.5 Parasitic Infections: Clinical Findings Healthy/Compromised Hosts | - 3.6 Microscope Calibration | - 3.7 Serologic, Antigen, and Probe Tests for Parasite Diagnosis
- 4.1 Protozoa: Intestinal Tract, Urogenital System: Key Characteristics | - 4.2 Tissue Protozoa: Characteristics |
- 4.3 Tips on Performance of Fecal Immunoassays for Intestinal Protozoa
5.1 Helminths: Key Characteristics | 5.2 Helminth Parasites Associated with Eosinophilia
6.1 Reference Laboratory for Parasite Blood Testing | 6.2 Parasites Found in Blood: Characteristics
7.1 Malaria (5 Species) (2 P. ovale subspecies) | 7.2 Malaria (5 Species, Images) | 7.3 Rapid Malaria Testing (BinaxNOW Malaria Test) | 7.4 Malaria Parasitemia Method |
7.5 Malaria Parasitemia Interpretation
- USE OF A REFERENCE LABORATORY FOR PARASITE BLOOD DIAGNOSTIC
TESTING (Including the Binax Rapid Test and Report Comments)
- HELMINTH PARASITES ASSOCIATED WITH EOSINOPHILIA |
- Histology: Staining Characteristics - Table 1 |
- Histological Identification of Parasites - Table 2 |
- Microscope Calibration |
- Figures for Histology Identification Table 2 |
3.4 Examination of tissues and body fluids |
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Suspect causative agent(s) |
Disease(s) |
Appropriate test(s)a |
Positive result |
Protozoa |
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Naegleria fowleri |
Primary amebic meningoencephalitis |
1. Wet examination of CSF (not in counting chamber) |
Trophozoites present and identified |
Acanthamoeba spp. |
Amebic keratitis, chronic meningoencephalitis |
1. Culture or stained smears |
Trophozoites and/or cysts present and identified |
Balamuthia mandrillaris |
Chronic/subacute meningoencephalitis (granulomatous amebic encephalitis) |
1. Calcofluor (cysts only) |
Trophozoites and/or cysts present and identified |
Entamoeba histolytica Giardia duodenalis (G. lamblia, G. intestinalis) |
Amebiasis |
Biopsy or routine histology |
|
Giardiasis |
1. Duodenal aspirate |
Trophozoites present and identified |
|
Leishmania spp. (cutaneous lesions) |
Cutaneous leishmaniasis |
1. Material from under bed of ulcer a. Smear b. Culture c. Animal inoculation 2. Punch biopsy at edge of lesion a. Routine histology b. Squash preparation c. Culture d. NAAT |
Amastigotes recovered in macrophages of skin or from animal inoculation; other stages recovered in culture |
Leishmania spp. (mucocutaneous lesions) |
Mucocutaneous leishmaniasis |
As for cutaneous leishmaniasis |
Amastigotes recovered in macrophages of skin and mucous membranes or from animal inoculation; other stages recovered in culture |
Leishmania spp. (visceral) |
Visceral leishmaniasis (kala-azar) |
1. Buffy coat a. Stain b. Culture c. Animal inoculation 2. Bone marrow a. Stain b. Culture c. Animal inoculation 3. Liver or spleen biopsy with routine histology a. Stain b. Culture c. Animal inoculation |
Amastigotes recovered in cells of reticuloendothelial system |
Toxoplasma gondii |
Toxoplasmosis |
1. Lymph node biopsy 1. Lymph node biopsy a. Routine histology b. Tissue culture isolation c. Animal inoculation 2. Serology */ |
Identification of organisms plus appropriate serological test results |
Cryptosporidium spp. |
Cryptosporidiosis |
1. Duodenal scrapin 2. Duodenal biopsy a. Stain b. Routine histology 3. Punch biopsy a. Routine histology b. Squash preparation 4. Sputum 5. Immunoassays |
Identification of organisms in microvillus border or other tissues (lung and gallbladder have also been involved); routine stains or monoclonal antibody reagents to identify oocysts in stool |
Microsporidia |
Microsporidiosis |
NAAT, routine histology; modified trichrome, tissue Gram stains, silver, periodic acid-Schiff, and Giemsa stains recommended (spores); animal inoculation not recommended/latent infections |
These organisms (spores) have been found as insect or other animal parasites; route of infection is probably ingestion. Human cases involve muscle, CSF (AIDS); other body sites have also been documented. |
Trachipleistophora spp |
Electron microscopy may be necessary for confirmation. |
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Helminths |
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|
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Larvae (Ascaris and Strongyloides spp.) |
“Pneumonia” |
Sputum, wet preparation |
This is an incidental finding but has been reported in severe infections. |
Eggs (Paragonimus spp.) |
Paragonimiasis |
Sputum, wet preparation |
Eggs will be coughed up and appear as “iron filings”; eggs could also be found in stool. |
Hooklets (Echinococcus spp.) |
Hydatid disease |
Sputum, wet preparation |
Rare finding, but protoscolices and hooklets can be found when the hydatid cyst is in the lung. |
Onchocerca volvulus |
Onchocerciasis |
Skin snips |
Skin snips examined in saline; microfilariae may be present; presence of adult worms in routine histology of nodules |
Mansonella streptocerca |
Streptocerciasis |
Skin snips |
Skin snips examined in saline; microfilariae may be present. |
Schistosoma spp. |
Schistosomiasis |
1. Rectal valve biopsy |
Eggs present and identified |
a NAAT and other molecular tests are available for many of the organisms mentioned in this table; however, test options may be limited to research and/or reference laboratories.