Introduction to Parasitic Infections¶
Part 5: Infectious Diseases | Part 5 – Infectious Diseases: Parasitic · Part 5 – Infectious Diseases: Parasitic · Chapter 228
Key Clinical Points¶
- Parasites are eukaryotic organisms (helminths and protozoa) distinct from bacteria and viruses.
- Helminths are multicellular (worms); Protozoans are single-celled and can multiply within the human host.
- Travel history is the critical component of diagnosis for parasitic infections in non-endemic areas.
- Malaria (Plasmodium falciparum) is the most common parasitic infection with higher mortality than any other parasite.
- Immunocompromised hosts are at high risk for disseminated protozoan infections (Leishmania, Toxoplasma, Cryptosporidium) and Strongyloides.
- Fever onset timing: >10–14 days post-travel → Malaria likely; <10 days → Dengue/Chikungunya/Zika more probable.
- Duffy antigen negativity → resistance to Plasmodium vivax and ovale.
- Strongyloides infection can persist for decades → risk of dissemination during immune compromise.
- Table 228-1 provides a comprehensive mapping of parasites by organ system, symptoms, and geography.
- Specific clinical markers include: Ring-enhancing CNS lesions (Toxoplasma), Amastigotes (Leishmania), and Calcified cysts (>1cm) (Echinococcus).
1. DEFINITION & OVERVIEW¶
• Etymology: Parasites derived from Greek 'para' (beside) and 'sitos' (food); organisms living at another’s expense. • Biological Distinction: Unlike bacteria/viruses, parasites are eukaryotic; their structure resembles human cells, complicating drug development.
• Classification of Internal Parasites: • Helminths: Multicellular worms. • Two phyla: Platyhelminthes (flatworms) and Nemathelminthes (roundworms). • Life Cycle: Often require intermediate hosts; Exceptions: Strongyloides and Capillaria complete life cycles in humans. • Protozoa: Microscopic single-celled organisms. • Pathogenesis: Utilize mechanisms like antigenic variation (Trypanosoma) or intracellular survival (Plasmodium, Toxoplasma). • Risk Factor: Immunocompromised hosts lack partial immunity → severe disease.
1.1 Helminths vs. Protozoa¶
• Helminths: - Multicellular organisms visible to the naked eye. - Two phyla: Platyhelminthes (flatworms) and Nemathelminthes (roundworms). - Humans as definitive hosts for intestinal helminths; intermediate hosts for tissue-invading species. - Exceptions: Strongyloides and Capillaria complete life cycles in humans.
• Protozoa: - Microscopic single-celled organisms capable of intracellular replication. - Major pathogenic mechanisms include immune evasion via antigenic variation (Trypanosoma) or intracellular survival (Plasmodium, Toxoplasma). - Immunocompromised hosts experience severe disease due to lack of partial immunity.
2. EPIDEMIOLOGY¶
• Prevalence: Intestinal roundworm infections are the most common globally; prevalent in resource-poor regions with poor sanitation. • Travel Risk: Low risk for general travelers unless exposed to high-risk environments (war zones, refugee camps). • Malaria: Highest mortality rate among all parasitic infections.
• Risk Factors: • Prolonged exposure to endemic regions. - Immunocompromise (HIV, organ transplant) → risk of disseminated infection (Leishmania, Toxoplasma). - Adventure travel, rural exposure, or refugee settings. - Immigrant status from developing countries.
• Prevention: First-generation P. falciparum vaccine targets children in high-prevalence regions.
3. ETIOLOGY & PATHOPHYSIOLOGY¶
• Helminth Classification: • Tapeworms (Cestodes): Taenia saginata (beef), T. solium (pork), Diphyllobothrium latum (fish); Echinococcus granulosus (hydatid disease); Echinococcus multilocularis (sub-Arctic). • Flukes (Trematodes): Clonorchis sinensis, Opisthorchis spp., Fasciola hepatica (liver flukes); Paragonimus spp. (lung flukes); Schistosoma spp. (blood flukes: S. mansoni, S. haematobium, S. japonicum). • Roundworms (Nematodes): Ascaris lumbricoides, hookworms, Strongyloides stercoralis; Filariasis (Wuchereria bancrofti, Onchocerca volvulus, Loa loa); Trichinella spiralis, Gnathostoma spp., Angiostrongylus spp.
• Protozoan Classification: • Intestinal Protozoa: Entamoeba histolytica (amebic dysentery, liver abscesses); Cryptosporidium (waterborne, severe in AIDS); Giardia lamblia (foul-smelling stool/steatorrhea); Microsporidia (chronic diarrhea in AIDS). • Blood/Tissue Protozoa: Plasmodium falciparum (cerebral malaria, highest mortality); Trypanosoma cruzi (Chagas disease, cardiomyopathy); Leishmania spp. (visceral leishmaniasis, AIDS-defining); Toxoplasma gondii (reactivation in immunocompromise); Free-living amoebae (Acanthamoeba keratitis, Naegleria meningitis).
3.1 Helminth Classification¶
• Tapeworms (Cestodes): - Taenia saginata (beef), T. solium (pork), Diphyllobothrium latum (fish). - Echinococcus granulosus (hydatid disease from dog feces); - Echinococcus multilocularis (sub-Arctic regions, fox/dog transmission).
• Flukes (Trematodes): - Clonorchis sinensis, Opisthorchis spp., Fasciola hepatica (liver flukes); - Paragonimus spp. (lung flukes); - Schistosoma spp. (blood flukes: S. mansoni, S. haematobium, S. japonicum).
• Roundworms (Nematodes): - Ascaris lumbricoides, hookworms, Strongyloides stercoralis; - Filariasis (Wuchereria bancrofti, Onchocerca volvulus, Loa loa); - Trichinella spiralis, Gnathostoma spp., Angiostrongylus spp.
3.2 Protozoan Classification¶
• Intestinal Protozoa: - Entamoeba histolytica (amebic dysentery, liver abscesses); - Cryptosporidium (waterborne, severe diarrhea in AIDS); - Giardia lamblia (foul-smelling stools); - Microsporidia (chronic diarrhea in AIDS).
• Blood/Tissue Protozoa: - Plasmodium falciparum (cerebral malaria, highest mortality); - Trypanosoma cruzi (Chagas disease, cardiomyopathy); - Leishmania spp. (visceral leishmaniasis, AIDS-defining illness); - Toxoplasma gondii (reactivation in immunocompromise); - Free-living amoebae (Acanthamoeba keratitis, Naegleria meningitis).
4. CLINICAL FEATURES¶
• General Presentation: Varies by parasite and organ involvement; includes cutaneous lesions, CNS symptoms, ocular findings, and systemic complications.
• Patient Assessment: - Travel History: Critical for diagnosis in non-endemic areas; duration of stay correlates with risk. - Immune Status: Immunocompromise increases severity (e.g., disseminated Strongyloides, Toxoplasma). - Timing of Fever Decision Pathway: - If fever onset is >10–14 days post-travel → Malaria likely. - If fever onset is <10 days post-travel → Dengue/Chikungunya/Zika more probable. - Duration of Diarrhea: Persistent traveler's diarrhea (>2 weeks) → suggests parasitic etiology (Cryptosporidium, Giardia). - Physical Exam: Focus on organ-specific signs (e.g., hepatosplenomegaly, skin nodules).
5. DIFFERENTIAL DIAGNOSIS¶
• Amebiasis vs. Bacterial Diarrhea: Amebiasis features slower onset and potential liver abscesses; E. histolytica is indistinguishable from noninvasive E. dispar. • Malaria vs. Other Fevers: Malaria must be considered first in febrile post-travel patients; timing of fever (10–14 days) helps differentiate from Dengue/Chikungunya/Zika. • Traveler's Diarrhea: Acute bacterial/viral → resolves quickly; Chronic (>2 weeks) → parasitic (Cryptosporidium, Giardia). • Bacterial vs. Parasitic Jaundice: Hepatitis A/B unlikely in immunized patients; Malaria possible despite chemoprophylaxis due to drug resistance.
6. INVESTIGATIONS & DIAGNOSIS¶
- Travel History Assessment:
- Duration of stay in endemic areas.
- Adherence to chemoprophylaxis.
- Timing of symptom onset relative to travel return.
- Laboratory & Imaging Findings:
- E. histolytica: Trophozoites/cysts (indistinguishable from noninvasive E. dispar).
- Leishmania: Amastigotes in tissue biopsies.
- Onchocerca: Microfilariae in skin snips.
- Naegleria: Motile trophozoites in CSF.
- Toxoplasma: Ring-enhancing lesions on CT.
- Taenia solium: Calcified cysts on imaging.
- Echinococcus: Liver > lung cysts; cysts >1cm.
- Cryptosporidium: Watery diarrhea in AIDS patients.
- Giardia: Foul-smelling stool with steatorrhea.
- Schistosoma haematobium: Hematuria with negative cultures; potential for bladder cancer.
6.1 Table 228-1: Parasitic Infections by Organ System¶
Table 228-1 provides a comprehensive mapping of parasites to clinical findings:
• Eosinophilic Meningitis: - Angiostrongylus (most common cause globally; spontaneous resolution). - Gnathostoma (migratory nodules). • Eyes: - Acanthamoeba (corneal opacification/ulcers). - Toxoplasma (retinal mass). - Onchocerca & L. loa (worms may cross eye during migration). • Heart: - P. falciparum (pulmonary edema as end-organ damage from severe malaria). - Trypanosoma cruzi (cardiomegaly, arrhythmias). • Gastrointestinal Tract: - Entamoeba histolytica (bloody diarrhea, liver abscesses; acute with fever/RUQ pain or chronic with enlarged liver/abscesses). - Schistosoma mansoni (portal obstruction, cirrhosis, varices). - Leishmania donovani complex (visceral leishmaniasis; AIDS-defining infection). - Echinococcus & Fasciola (common in sheep-raising areas). - Clonorchis (recurrent cholangitis and late cholangiocarcinoma). - Cryptosporidium (watery diarrhea, severe in immunocompromised). - Giardia (foul-smelling stool with steatorrhea). - Isospora belli (fever, abdominal pain, chronic diarrhea). - Microsporidia (chronic diarrhea in AIDS). - Capillaria (malabsorption, wasting; Southeast Asia/Egypt). - Pinworm (anal itching; eggs rarely detected by O&P). - Trichuris (rectal prolapse with heavy infection in children). - T. solium or Taenia saginata (passage of tapeworm segments >6 cm). - Diphyllobothium latum (pernicious anemia in genetically predisposed Scandinavians). • Genitourinary System: - Trichomonas vaginalis (common STD). - Schistosoma haematobium (hematuria with negative cultures; potential for bladder cancer).
7. MANAGEMENT & TREATMENT¶
- Malaria: Artemisinin-based combination therapies (ACTs) for P. falciparum.
- Leishmania: Liposomal amphotericin B.
- Toxoplasma: Pyrimethramine + sulfadiazine.
- Strongyloides: Ivermectin (primaquine for liver forms).
- Schistosomiasis: Praziquantel.
• Special Considerations: - Immunocompromised patients require prolonged therapy. - Drug resistance in malaria necessitates ACTs. - Vaccine availability limited to P. falciparum.
8. PROGNOSIS & COMPLICATIONS¶
• Malaria (P. falciparum): Highest mortality among parasites; can cause end-organ damage like pulmonary edema. • Immunocompromised Patients: Disseminated infections (Toxoplasma, Cryptosporidium) are often fatal without treatment. • Chronic Helminth Damage: Schistosomiasis leads to portal hypertension and cirrhosis. • Strongyloides: Can persist for decades → risk of dissemination during immune compromise.
9. SPECIAL CONSIDERATIONS¶
• Geographic Variation: - Malaria: Sub-Saharan Africa (P. falciparum), Southeast Asia (P. vivax). - Schistosomiasis: Africa, China. - Leishmaniasis: India, Brazil. - Toxoplasma: Global; severe in immunocompromised.
• Diagnostic Clues: - Migratory skin nodules → Loa loa, Gnathostoma. - Ring-enhancing CNS lesions → Toxoplasma. - Calcified liver cysts → Echinococcus. - Serpentine rash/anemia → Hookworm. - Foul-smelling stool with steatorrhea → Giardia. - Hematuria with negative cultures → Schistosoma haematobium.
Reference Tables¶
TABLE 228-1 Parasitic Infections, by Organ System and Signs/Symptoms a¶
Harrison's 22e, p.1739
| ORGAN SYSTEM, MAJOR SIGN(S)/SYMPTOM(S) |
PARASITE(S) | GEOGRAPHIC DISTRIBUTION | COMMENTS |
|---|---|---|---|
| Naegleria | Worldwide | ||
| Eosinophilic meningitis | Angiostrongylus (rat lung worm) |
Southeast Asia, Pacific, Caribbean |
Most common cause globally of eosinophilic meningitis; spontaneous resolution |
| Gnathostoma | Southeast Asia and China | Migratory nodules | |
| Eyes | |||
| Acanthamoeba | Worldwide | ||
| Corneal opacification | Onchocerca | Mexico, Central/South America, Africa |
Immune response to microfilaria in cornea |
| Toxoplasma | Worldwide | ||
| Retinal mass | Toxocara | Worldwide | Ocular larva migrans |
| Visible roundworm in eye | Onchocerca | Mexico, Central/South America, Africa |
Worms may cross eye during migration. |
| L. loa | Western and central Africa | Worms may cross eye during migration. | |
| Gnathostoma | Southeast Asia and China | ||
| Lungs | |||
| Pulmonary nodule/abscess | Paragonimus | Far East, Africa, Americas | Ectopic migration to abdomen or central nervous system |
| Migrating helminths | Worldwide | ||
| Heart | |||
| Pulmonary edema | P. falciparum (complication) | Tropics and subtropics | End-organ damage from severe malaria |
| Trypanosoma cruzi | Mexico, Central/South America | ||
| Gastrointestinal Tract | |||
| Hepatosplenomegaly | Malaria (multiple episodes) | Tropics and subtropics | Splenomegaly with anemia and recurrent fever are hallmarks of malaria. |
| S. mansoni | Africa, Central/South America | Portal obstruction with cirrhosis and late varices | |
| Leishmania donovani complex | Tropics and subtropics | Visceral leishmaniasis; AIDS-defining infection | |
| Entamoeba histolytica | Tropics | ||
| Echinococcus | Sheep-raising areas | ||
| Fasciola | Sheep-raising areas | ||
| Cholangitis | Clonorchis | China, Southeast Asia | Recurrent cholangitis and late cholangiocarcinoma |
| Microsporidia | Worldwide | AIDS | |
| Cryptosporidium | Worldwide | AIDS-defining infection | |
| E. histolytica | Tropics | ||
| S. mansoni | Africa, Central/South America | ||
| S. japonicum | Far East | ||
| Watery diarrhea | Cryptosporidium | Worldwide | Severe in immunocompromised patients |
| Giardia | Worldwide | Foul-smelling stool with steatorrhea | |
| Isospora belli | Worldwide | Fever, abdominal pain, chronic diarrhea | |
| Microsporidia | Worldwide | Chronic diarrhea with AIDS | |
| Capillaria | Southeast Asia, Egypt | Malabsorption, wasting | |
| Ascaris | Worldwide | ||
| Small roundworms visible around anus |
Pinworm | Worldwide | Anal itching; eggs rarely detected by ova and parasite (O&P) exam |
| Trichuris | Worldwide | Rectal prolapse with heavy infection in children | |
| T. solium or Taenia saginata | Worldwide | ||
| Diphyllobothrium latum | Worldwide | ||
| Genitourinary System | |||
| Itchy discharge | Trichomonas vaginalis | Worldwide | Common sexually transmitted disease of both sexes |
| Schistosoma haematobium | Africa |