1. SCHISTOSOMIASIS BILHARIZIASIS

2. Is a human disease syndrome due to infestation by Schistosoma
Most human schistosomiasis is caused by
1. Schistosoma haematobium discovered by Theodor Bilharz in Cairo in 1861 (mainly UTS).
2. Schistosoma mansoni (mainly GIT).
3. Schistosoma japonicum (mainly GIT).

3. EPIDEMIOLOGY

5. NILE RIVER

6. Schistosomiasis is a major source of morbidity and mortality.
The endemic areas are limited to tropical and subtropical zones, which exist around the world.
The spread continues because of
a. water resource contamination in developing countries
b. the migration of infected populations.

7. At least 200 million people in at least 74 countries have active schistosomal infection. Of these, approximately 120 million people have symptoms, and 20 million are severely ill.
Disease prevalence tends to be worse in areas with poor sanitation, increased freshwater irrigation usage, and heavy schistosomal infestation of human and/or snail populations.

8. S mansoni and S haematobium infections predominate in sub-Saharan Africa.
S mansoni is endemic in parts of South America and the Caribbean.
S japonicum is common in China, Indonesia, and the Philippines.

9. GLOBAL DISTRIBUTION

10. LIFE CYCLE
The ovum is passed in the urine or faeces of infected individuals and gains access to fresh water where the ciliated miracidium inside it is liberated; it enters its intermediate host, a species of freshwater snail, in which it multiplies .
Large numbers of fork-tailed cercariae are then liberated into the water, where they may survive for 2-3 days.

11. Cercariae can penetrate the skin or the mucous membrane of the mouth of their definitive host, humans. They transform into schistosomulae and moult as they pass through the lungs and are carried by the blood stream to the liver and so to the portal vein where they mature.

12. The male worm is up to 20 mm in length and the more slender cylindrical female, usually enfolded longitudinally by the male, is rather longer .
Within 4-6 weeks of infection they migrate to the venules draining the pelvic viscera, where the females deposit ova.

13. LIFE CYCLE

17. PATHOLOGY
The pathological changes and symptoms depend on species and stage of infection.
Most of the disease is due to the passage of eggs through mucosa and to the granulomatous reaction to eggs deposited in tissues.
The eggs of S. haematobium pass mainly through the wall of the bladder, but may also involve rectum, seminal vesicles, vagina, cervix and uterine tubes.

18. S. mansoni and S. japonicum eggs pass mainly through the wall of the lower bowel or are carried to the liver.
The most serious, although rare, consequences of the ectopic deposition of eggs are transverse myelitis and paraplegia.
Granulomas are composed of macrophages, eosinophils, epithelioid and giant cells around an ovum.

19. Later there is fibrosis and eggs calcify, often
in sufficient numbers to become radiologically
visible.
Eggs of S. haematobium, and of the other
two species after the development of portal
hypertension, may reach the lungs.

20. CLINICAL MANIFESTATION 1. URINARY TRACT 2. GIT AND LIVER 3
CLINICAL MANIFESTATION URINARY TRACT GIT AND LIVER GENITAL TRACT PULMONARY HYPERTENTION SPINAL CORD

21. Patients with acute schistosomiasis (Katayama fever)
During the early stages of infection there may be
itching lasting 1-2 days at the site of cercarial
penetration.
After a symptom-free period of 3-5 weeks,
acute schistosomiasis (Katayama syndrome) may
present with allergic manifestations such as
urticaria, fever, muscle aches, abdominal pain,
headaches, cough and sweating.

22. On examination
Hepatomegaly, splenomegaly,lymphadenopathy
and pneumonia may be present. There is
eosinophilia and schistosomiasis serology may
be positive. These allergic phenomena may be
severe in infections with S. mansoni and S.
japonicum but are rare with S. haematobium.
The features subside after 1-2 weeks.

23. Chronic schistosomiasis
is due to egg deposition and occurs months
to years after infection. The symptoms and
signs depend upon the intensity of infection
and the species of infecting schistosome.

24. S. haematobium Humans are the only natural hosts of S.
haematobium, which is highly endemic in
Egypt and East Africa, and occurs
throughout Africa and the Middle East .
Infection can be acquired after a brief
exposure such as swimming in freshwater
lakes in Africa.

25. Painless terminal haematuria is usually the first and most common symptom.
Frequency of micturition follows, due to bladder neck obstruction.
Later the disease may be complicated by frequent urinary tract infections, bladder or ureteric stone formation, hydronephrosis, renal functional abnormalities
and ultimately renal failure with a contracted calcified bladder.

26. Pain in the iliac fossa or in the loin and radiates to the groin.
association of S. haematobium infection with squamous cell carcinoma of the bladder.
Disease of the seminal vesicles may lead to haemospermia. Females may develop schistosomal papillomas of the vulva, and schistosomal lesions of the cervix may be mistaken for cancer. Intestinal symptoms may follow involvement of the bowel wall.

27. Ectopic worms cause skin or cord lesions.
The severity of S. haematobium infection varies greatly, and many with a light infection are asymptomatic. However, as adult worms can live for 20 years or more and lesions may progress, these patients should always be treated.

28. LIVER AND GIT (Mainly S. Mansoni and Japanicum

29. Bloody diarrhea
Abdominal pain: RUQ pain, cramping
Hematemesis (with portal hypertension)
Ascites (with portal hypertension)
Vulvar or perianal lesions
On examination: Hepatosplenomegaly
Abdominal tenderness
Heme-positive stool and/or bloody diarrhea
Ascites

32. Note: Hepatic failure and jaundice are not features of hepatic schistosomiasis

33. OTHER SITES AFFECTED BY SCHISTOSOMIASIS

34. Pulmonary hypertension Dyspnea on exertion . Cough . Palpitations .
Atypical chest pain .
Pedal edema (with right heart failure)
Central nervous system (CNS)
Seizures and/or mental status changes (with cerebral involvement)
Paralysis (with spinal cord involvement)
Skin

35. DIAGNOSIS CLINICAL HEMATOLOGICAL, BIOCHEMICAL CONFIRMED BY
Detection of ova in urine deposit of terminal stream (especially after exercise) or from stool, biopsy or snip from rectum and bladder wall. Ovum has terminal spine in S. Hematobium and lateral spine in S. mansoni
Serological tests ELISA for screening
4. Radiological and scope examination

36. SPECIFIC TREATMENT
Aim to stop egg-laying and reduce adult worm load up to 90%
Three main drugs
Praziquantel 40mg /kg for all types and as a single dose is treatment of choice. Induce parasitological cure in 80% of people and over 90% reduction in egg count in the remaining individuals. Side effects like nausea and abdominal pain are uncommon. Early therapy reverse pathological changes like hepatomegaly and bladder wall thickening and even large granuloma.

37. Oxamniquine (old drug not used)15mg/kg/12hr for 2 days in S.mansoni
Metrifonate (old drug not used) 7.5mg/kg every 2ws (1month)
Surgery in special circumstances and for some complications like ureteric stricture, and small fibrotic urinary bladder. Diathermy for rectal papiloma removal. Neurosurgical procedures may be needed for neurological complications if chemotherapy is ineffective.

38. COMPLICATIONS OF SCHISTOSOMIASIS BILHARIZIASISIN GENERAL
1. Pulmonary hypertension
2. Cor pulmonale
3. Portal hypertension.
4. Obstructive uropathy.
5. Squamous cell carcinoma of the bladder.
6. Gastrointestinal bleeding
7. Carrier for salmonella
8. Neurological complications

39. Prognosis Almost all patients improve with treatment.
Most patients with early disease or without severe end-organ complications recover completely.
Surprisingly, patients with hepatic and urinary disease, even with fibrosis, may improve significantly over months or years following treatment.
Resolution of pulmonary disease is less well documented.

40. Patients with heavier worm burdens are less likely to improve and are more likely to require re-treatment.
Treatment is indicated for patients with end-stage complications of portal hypertension and severe pulmonary hypertension, but these patients are much less likely to benefit.
Co-infection (with malaria, HIV, or hepatitis
worsens the prognosis.

41. PREVENTION
Travelers to endemic areas should avoid exposure to freshwater that is likely to be contaminated.
No accepted prophylactic regimens have been developed.
No vaccines are currently available, although vaccine development is increasingly promising.
Early treatment after high-risk exposures should minimize morbidity.

42. Prevention for groups residing in endemic areas is more difficult than prevention for travelers.
Improved sanitation to decrease freshwater contamination with sewage should decrease disease prevalence.

43. Decrease occupational and recreational contact with contaminated water may be useful. These interventions are particularly problematic with children.
Molluscicides to decrease the prevalence of the snail hosts have some usefulness but require frequent reapplication and are used less frequently now than in the past.

44. Mass treatment of targeted populations with the newer less toxic antischistosomal agents may have utility. It can be combined with molluscicide treatment if needed.
Vaccines hold the promise of significantly reducing infection in endemic areas