Uploaded by mohamed abdelmonem (Jinx)

Parasites affecting renal system

advertisement
Parasites affecting renal system:
Helminthes:
 Schistosomiasis
 Hydatid disease
 Filariasis
Protozoa:
 Malaria
 Babesiosis
 Leishmaniasis
Schistosomiasis:
Schistosoma haematobium (Urinary schistosomiasis)
Geographical distribution:
- Africa: scattered areas. In Egypt, it is prevalent all over the Nile Valley.
Some area in Asia and Europe
- Habitat: Schistosoma haematobium adults live in the vesical and pelvic
venous plexuses in man surrounding the kidney, pelvis, urinary bladder,
urethra, prostate, seminal vesicles, lower 1/3 of uterus and vagina.
- Definitive host: man.
- Intermediate host: snail Bulinus truncatus in Egypt.
- Reservoir host: no reservoir host.
- Diagnostic stage: Large sized egg with terminal spine (in urine)
- Infective stage: furcocercus cercaria.
- Stages in life cycle: egg → miracidium→ sporocyst→ furcocercus
cercaria→ adult.
- Mode of infection: Infection occurs by skin penetration.
- Drinking water may lead to infection when cercaria penetrates the mucus
membrane of the mouth.
- schistosomulum is carried by the blood → left side of the heart →
systemic circulation→ intestinal capillary bed→ intra-hepatic branches of
the portal vein where it matures → Then male carries the female→
migrates out of the liver in the portal vein against the blood stream to reach
the vesical and pelvic plexuses to deposit the eggs→ Eggs appear in urine 10
weeks after infection.
Schistosoma mansoni
(Intestinal schistosomiasis)
- Geographical distribution: It is widespread in Africa.
- In Egypt, Nile delta, but after construction of the high dam, it invaded Upper
Egypt. It is found in Saudi Arabia, Yemen and Tropical America.
- Habitat: the inferior mesenteric vein draining the large intestine, and in the
portal system.
- Definitive host: man.
- Intermediate host: snail Biomphalaria alexandrina in Egypt.
- Reservoir host: monkeys and rodents.
- Diagnostic stage: Large sized egg with lateral spine (in stool)
- Infective stage, life cycle and mode of infection like S. haematobium
Effect of schistosoma haematobium and mansoni on renal system:
- Renal involvement occurs due to precipitation of immune complexes in the
glomerular vascular bed leading to end-stage renal failure.
- Schistosoma haematobium gives rise to renal problems as a result of direct
invasion of the urinary tract. Egg deposition may induce chronic bladder
infection, calcification and fibrosis with extension to the ureters, and
carcinoma of the bladder, especially squamous cell carcinoma. The fibrosis
may lead to irregular ureteral stenoses and eventually to dilatation, resulting
in either hydronephrosis or reflux nephropathy.
- Schistosoma mansoni and S. haematobium can cause portal hypertension
and an enlarged spleen (hepatosplenic schistosomiasis) have an increased
frequency (15%) of renal disease; this infection is clinically characterized by
variable proteinuria ranging from asymptomatic to nephrotic syndrome
- Both types can cause nephrotic syndrome.
Treatment: praziquantel
Echinococcus granulosus (Hydatid disease)
 Distribution:
Worldwide, where dogs are used as pets or as guards or for herding.
 Hosts:
Definitive hosts are dogs, wolfs, wild canines.
Intermediate hosts are grazing herbivorous animals, and accidentally
man.
 Habitat:
Small intestine of dogs
 Infective stage:
swallowing egg with food or drink
Effect on renal system:
- most hydatid cysts occur in the liver and lungs, some cysts involve other
sites such as the kidneys (2%).
- Also can cause nephrotic syndrome
Wuchereria bancrofti
 Disease:
Bancroftian filariasis, wuchereriasis, and elephantiasis.
 Distribution:
Tropical and sub tropical countries including some foci in Egypt.
 Host:
Final host: In nature, only mankind.
Intermediate host: Female mosquitoes of the genera Culex, Aedes, and
Anopheles.
1- Habitate: The adults live in the affarent lymphatics close to the lymph nodes
of man.
 Life cycle: as in diagram
Effect on renal system:
- Glomerular disease associated with filariasis is thought to be immune
complex mediated.
- It causes nephrotic syndrome.
- Also treatment of wucheraria can increase the incidence of nephrotic
syndrom in those patients
Malaria
Hosts:
- The definitive host : female anopheles mosquitoes.
- The intermediate host : man.
Infective stage:
- Sporozoite from bite of female anopheles mosquito
Diagnosis:
- blood film, and serology
Life cycle as in following diagram
Type species and morphology:
- Plasmodium malariae: It causes quartan malaria with paroxysms
every 72 hours.
- Plasmodium vivax: It is the cause of benign tertian malaria or
vivax malaria. It is called tertian because its erythocytic cycle, and
hence the paroxysms every third day.
-
Plasmodium ovale: this species causes ovale, or mild, tertian
malaria
- Plasmodium falciparum: It is the cause of malignant tertian and
subtertian malaria. It is the most virulent Plasmodium spp. in man.
The above picture shows some effects of malaria on human
Effect on renal system
 Only two types of the malaria parasites, namely, P. malariae (quartan
malaria) and P. falciparum (falciparum malaria), are clearly associated
with renal disease, and this occurs only in a small percentage of patients.
 Plasmodium malariae
- Renal involvement in the course of quartan malaria is generally
characterized by nephrotic syndrome. A membranoproliferative
type of glomerulonephritis
 Plasmodium falciparum
- Nephrotic syndrome or proteinuria is rare and, if present, is usually
associated with the same type of glomerular lesions as in quartan
malaria.
- renal involvement in falciparum malaria is usually transient and
disappears when the infection is brought under control. A striking
feature of falciparum malaria is the occurrence of acute renal
failure with or without overt hemoglobinuria.
- The pathology in this context consists of tubulointerstitial damage
such as tubular necrosis, hemoglobin and cellular casts in tubuli,
and interstitial edema
- These lesions seem to be due to impaired blood flow in the
microcirculation as a consequence of increased rigidity and
adhesiveness of erythrocytes, hypovolemia, intravascular
coagulation, and hemolysis.
Babesiosis
 Babesia is a tick-borne intraerythrocytic parasite. In Europe, Babesia
bovis and Babesia divergens are transmitted from cattle to humans.
Asplenic persons are particularly susceptible to this disease. In the
United States, most infections are caused by a rodent parasite, Babesia
microti, usually in patients with intact spleens.
 In severe cases involving massive hemolysis, renal involvement,
resulting in acute renal failure is seen.
LEISHMANIASIS
- Infective stage:
Infection occurs by bite of female sand fly (flebbotomus papatassi)
injecting promastigote of visceral leishmaniasis (leishmania
donovani) into the blood
- Diagnosis:
Blood film, splenic smear and serology
- Life cycle : as in diagram.
Effect on renal system:
- Glomerular lesions are observed with visceral leishmaniasis (kalaazar) caused by Leishmania donovani.
- Cutaneous or mucocutaneous leishmaniasis caused by other
Leishmania species (Leishmania tropica, Leishmania mexicana,
etc.) are not associated with renal disease
- The pathological picture is nephrotic syndrom
- Amyloidosis can be a complication of kala-azar.
- Kala-azar is usually associated with hyperimmunoglobulinemia
with high IgG levels and circulating immune complexes.
References:
1- Paniker’s Textbook of parasitology.
2- - Garcia, LS. & Bruckner, DA. (eds.), 2016 : Diagnostic Medical Parasitology 6th edition.
Wiley.
3- - Roberts, LS. & Janovy, JJ. (eds.), and Nadler Steve, 2012: Foundations of Parasitology. 9th
edition McGraw hill.
Some internet sites useful in Parasitology:
1- http://www.parasitesonline.net.
2- http://www.Freebooks4doctors.com.
3- http://www.cdfound.to.it/HTML/atlas.htm
4- http://www.bhj.org/books/liver/contents.htm
5- http://www.nlm.nih.gov/tsd/acquisitions/cdm/subjects76.html
6- http://www.nlm.nih.gov/tsd/acquisitions/cdm/subjects52.html
7- http://www.nlm.nih.gov/mimcom/reference.html
8- http://www.nlm.nih.gov/mesh/subhierarchy2003.html
9- http://www.nlm.nih.gov/mimcom/news/tropmedwg.html
10- http://www.cdc.gov/
11- http://pathmicro.med.sc.edu/book/parasit-sta.htm
12- http://www.dpd.cdc.gov/dpdx/
13- http://www.diplectanum.dsl.pipex.com/purls/
14- http://www.aber.ac.uk/~mpgwww/Edu/EduIndex.html
15- http://www.k-state.edu/parasitology/
16- http://www.cvm.okstate.edu/~users/jcfox/htdocs/clinpara/Index.htm
17- http://www.sciencedirect.com/science/journal/00144894
18- http://www.parasite.org.au/
19- http://www.parasitology.com/
20- http://www.udel.edu/medtech/dlehman/medt372/images.html
21- http://www.parasitologyindia.org/
22- http://www.parasitesonline.net/
23- http://compepid.tuskegee.edu/syllabi/pathobiology/pathology/parasitology/in
dex.htm
24- http://www.livjm.ac.uk/parasitology/
25- http://www.med.nyu.edu/parasitology/
Download