SCHISTOSOMIASIS
KAMPALA INTERNATIONAL
UNIVERSITY, Lira teaching site
PRESENTED BY:
SSEKABIRA ABUD RASHID
2022-01-07616
outline
 Introduction
 Pathophysiology
 Clinical presentation
 Investigations
 Diagnosis
 Management
 Follow up and
prognosis
 References
Introduction
 Dfn:- An acute and chronic debilitating
disease caused by infection with
parasitic blood flukes/ trematode worms
of the genus schistosoma.
 Also known as Bilharziasis after Theodor
Bilharz-identified the parasite in 1852
Epidemiology
 A tropically neglected disease
 Atleast 300 million people are affected, 700 million
people at risk, especially children and young adults.
 Second most disabling parasitic disease after malaria,
with increasing prevalence due to population density
and new irrigation- increases snail vector density
 Majority in Africa, over 4 million in Uganda
Epid…
 Prevalent in tropical and subtropical areas, poor
communities without access to safe water and proper
sanitation
 Children are more vulnerable due to lack of hygiene,
play habbits like swimming/ fishing in infested waters
 Especially school going and pre-school children.
pathophysiology
Paediatric Schistosomiasis majorly
takes on one of two forms;
Intestinal (S. mansoni or S.
japonicum), Urogenital (S.
haematobium)
 Different schistoma species are
prevalent in different geographical
regions
Species and distribution
SPECIES DISTRIBUTION
Intestinal
schistosomiasis
S. mansoni Africa, the Middle East, the
Caribbean, Brazil, Venezuela
and Suriname
S. Japonicum China, indonesia, philippines
S. Mekongi D.R.C, Cambodia
S. guineensis, S.
intercalatum
Central Africa
Urogenital
schistosomiasis
S. Haematobium Africa, middle East, France
Life cycle
 Schistosomes are digenetic, with two hosts,
man(definitive host for sexual reproduction) and
some snail species as the intermediate host for
asexual reproduction.
 byHuman become infected through penetration of
the skin cercariae rather than through oral
ingestion.
 The cerceriae, motile, forked-tail organisms
emerge from infected snails to penetrate intact
human skin.
Life cycle cont…
 Adult worms migrate to specific
anatomic sites characteristic of
each schistosome species:
 The human scistosomes can
infect other vertebrates and
provide an animal reservoir of
infection (S.japonicum)
Life cycle cont…
 Schistosoma eggs are eliminated with feces or
urine, depending on species.
 Eggs hatch and release miracidia, which swim and
penetrate specific snail intermediate hosts-two
generations of sporocysts and the production of
cercariae in the snail.
 The infective cercariae are released(4-12 wks),
swim, penetrate the skin of the human host , and
shed their forked tails, becoming schistosomulae.
Life Cycle Cont…
 Schistosomulae migration: via venous circulation
to lungs, heart, and then develop in the liver,&
exit via the portal vein system when mature.
 Sexual stage: Male and female adult worms
copulate and reside in the mesenteric venules (S.
japonicum -superior mesenteric veins draining
the SI, S. mansoni-inferior mesenteric veins of
the LI, S. mansoni- pelvic pexus of the UB)
Cont…
 The eggs are moved progressively
toward the lumen of the intestine (S.
mansoni,S. japonicum, S. mekongi, S.
intercalatum/guineensis) and of the
bladder and ureters (S. haematobium),
and are eliminated with feces or urine,
respectively,
 THE CYCLE CONTINUES!!!!!!!
Granuloma formation
 Not all schistosome eggs are excreted from the
body
 50% can embolize to other body areas forming
granulomas, causing ulceration in host
tissues(bladder and intestine)
 Most common sites are the liver and the bladder
 Other less affected sites are the lungs, CNS and
kidneys
 They involve the delayed hypersensitivity type of
Type 1 (Th1) and Type 2(Th2) helper cell responses
with local cytokine production
Life cycle
Clinical presentation
 Symptoms of schistosomiasis are not caused
by the worms themselves but by the body’s
reaction to the eggs.
 Takes two clinical syndromes;
Intestinal (S. mansoni or S.
japonicum)
Urogenital (S. haematobium)
 Incubation period 14-84 days
 Many infections are asymptomatic.
Clinical Cont…
 Schistosomal dermatitis/ swimmer’s
itch A local cutaneous hypersensitivity
reaction with itchy maculopapular
lesions occurs following skin
penetration by cercariae
 Occasionally, systemic hypersensitivity
reaction may occur weeks after the
initial infection(Katayama fever),
especially by S. mansoni and S.
japonicum
Swimmer's itch
Katayama fever
 A.k.a acute schistosomiasis, mostly
in heavily infested individuals, 4-8
weeks after exposure.
 Is a febrile illness due to
oviposition and early infection
 Characterised by a serum- like
syndrome with acute onset of fever,
cough, chills, sweating, abdominal
pain, lymphadenopathy,
hepatomegaly and eosinophilia.
chronic Intestinal
presentation
 Colicy abdominal pain
 Bloody diarhhoea
 Hematemesis
 Hepatomegaly
 Portal hypertension
 Ascites
 Melana
Non- organ specific symptoms
 Anaemia
 Chronic pain
 Diarhhoea
 Exercise intolerance
 Chronic under nutrition(growth
stunting)
Chronic Urogenital
presentation
 Urinary frequency, dysuria,
terminal hematuria
 Referrred suprapubic/perineal
pain
Clinical picture continued
Child with hepatosplenic
schistosomiasis
Complications
 Female genital schistosomiasis-
granulomatous inflammatory
response,contact bleeding, pain and
infertility- starts at 10 years
 Male schistosomiasis- hematospermia,
pain, lumpy semen.
 Liver disease- due to granuloma formation
and periportal fibrosis.
 Eggs in lungs causes pulmonary HTN and
cor pulonale.
 CNS seizures due to CNS migration of eggs.
NOTE
 Advanced stages of urogenital
schistosomiasis are associated
with chronic renal failure,
secondary infections and
squamous carcinoma of the
bladder
Investigations
 Urinalysis- around 10 mls of urine colected at
midday(time of maximum egg deposition)
 Stool analysis (blood, melena, eggs depending on
worm burden)
 CBC (eosinophilia, thrombocytopenia, anemia)
 Prolonged PT
 Normal or slightly elevated serum bilirubin and
transaminases
Lab cont…
 The unique schistosome antigens
circulating anodic antigen (CAA) and
circulating cathodic antigen (CCA) may
also be detected in the urine or
plasma.
 PCR assays- 99.9% specific, 94.4%
sensitive for the diagnosis of
schistosomiasis.
Imaging.
 CT ( R/O pulmonary disease and
brain involvement)
 Ultrasonography
 MRI (granulomas in brain,
lungs,liver, spinalcord—ring
enhancing lesions)
Imaging cont…
 IV pyelography (hydronephrosis,
calcifications and filing defects)
 Endoscopy, sigmoidoscopy,
bronchoscopy, colonoscopy
 Histology of liver biopsy
Management(pharmacological
)
 Praziquantel 20mg/kg BD on day 1
for S.haematobium, S intercalatum,and S
mansoni
 20 mg/kg orally TDS on day 1 for S japonicum and
S mekongi.
 Children <5 years may need 60mg/kg/day to
achieve clearence
Mgt cont…
 Monitor patients for seizures or
neurologic sequelae
 Corticosteroids to control post
treatment inflammation
 Give second dose of drug 4-6weeks
after 1st
dose because immature
forms are less susceptible
Surgical management
 Surgery (resection of bladder and colonic
polyps)
 Correction of obstructive uropathy
 Partial colectomy for intestinal polyps
 Resection of cerebral cortical granulomas
after failure of chemotherapy
Surgical mgt cont…
 Placement of a distal spleno-renal
shunt for reversal of Portal
Hypertension
 Consult with other specialits…
Follow up and prognosis.
 Prognosis is generally good
 Acute schistosomiasis is associated with a
mortality rate of up to 25% in some series
 Repeat stool and urinalysis for 1 year post
treatment for decreased egg excretion
 Monitor antigen levels
Prevention.
 Currently no vaccine against schistosomiasis
 Prevention can be achieved by reducing the
parasite load in the population by single dose anti
parasitics.
 Focal application of molluscicidals
 Animal vaccination
 Creating awareness about the risks and access to
clean water and proper sanitation are the best
prevention measures to overcome the burden.
 Reduce exposure to contaminated water
references
 Kleigman.R.M, ST Geme III.J.W, Blum.N,2019. Nelson
Textbook of Paediatrics 21st
Edition, Pg 7515-7522
 World Health Organisation. (2023, February,1st
).
Schistosomiasis. Retrieved from
https://www.who.int/news-room/fact-sheets/detail/sc
histosomiasis#:~:text=Schistosomiasis%20is%20an%20acu
te%20and%20chronic%20parasitic%20disease%20caused%
20by,will%20reduce%20and%20prevent%20morbidity
.
 Center for Disease Control. (2020,October, 28th
).
Parasites- Schistosomiasis. Retrieved from
https://www.cdc.gov/parasites/schistosomiasis/health_
professionals/index.html#:~:text=If%20the%20pre%2Dtre
atment%20stool,to%20help%20confirm%20successful%20c
ure
.

SCHISTOSOMIASIS presentation, investigations to management.pptx

  • 1.
    SCHISTOSOMIASIS KAMPALA INTERNATIONAL UNIVERSITY, Lirateaching site PRESENTED BY: SSEKABIRA ABUD RASHID 2022-01-07616
  • 2.
    outline  Introduction  Pathophysiology Clinical presentation  Investigations  Diagnosis  Management  Follow up and prognosis  References
  • 3.
    Introduction  Dfn:- Anacute and chronic debilitating disease caused by infection with parasitic blood flukes/ trematode worms of the genus schistosoma.  Also known as Bilharziasis after Theodor Bilharz-identified the parasite in 1852
  • 4.
    Epidemiology  A tropicallyneglected disease  Atleast 300 million people are affected, 700 million people at risk, especially children and young adults.  Second most disabling parasitic disease after malaria, with increasing prevalence due to population density and new irrigation- increases snail vector density  Majority in Africa, over 4 million in Uganda
  • 5.
    Epid…  Prevalent intropical and subtropical areas, poor communities without access to safe water and proper sanitation  Children are more vulnerable due to lack of hygiene, play habbits like swimming/ fishing in infested waters  Especially school going and pre-school children.
  • 6.
    pathophysiology Paediatric Schistosomiasis majorly takeson one of two forms; Intestinal (S. mansoni or S. japonicum), Urogenital (S. haematobium)  Different schistoma species are prevalent in different geographical regions
  • 8.
    Species and distribution SPECIESDISTRIBUTION Intestinal schistosomiasis S. mansoni Africa, the Middle East, the Caribbean, Brazil, Venezuela and Suriname S. Japonicum China, indonesia, philippines S. Mekongi D.R.C, Cambodia S. guineensis, S. intercalatum Central Africa Urogenital schistosomiasis S. Haematobium Africa, middle East, France
  • 9.
    Life cycle  Schistosomesare digenetic, with two hosts, man(definitive host for sexual reproduction) and some snail species as the intermediate host for asexual reproduction.  byHuman become infected through penetration of the skin cercariae rather than through oral ingestion.  The cerceriae, motile, forked-tail organisms emerge from infected snails to penetrate intact human skin.
  • 10.
    Life cycle cont… Adult worms migrate to specific anatomic sites characteristic of each schistosome species:  The human scistosomes can infect other vertebrates and provide an animal reservoir of infection (S.japonicum)
  • 11.
    Life cycle cont… Schistosoma eggs are eliminated with feces or urine, depending on species.  Eggs hatch and release miracidia, which swim and penetrate specific snail intermediate hosts-two generations of sporocysts and the production of cercariae in the snail.  The infective cercariae are released(4-12 wks), swim, penetrate the skin of the human host , and shed their forked tails, becoming schistosomulae.
  • 14.
    Life Cycle Cont… Schistosomulae migration: via venous circulation to lungs, heart, and then develop in the liver,& exit via the portal vein system when mature.  Sexual stage: Male and female adult worms copulate and reside in the mesenteric venules (S. japonicum -superior mesenteric veins draining the SI, S. mansoni-inferior mesenteric veins of the LI, S. mansoni- pelvic pexus of the UB)
  • 15.
    Cont…  The eggsare moved progressively toward the lumen of the intestine (S. mansoni,S. japonicum, S. mekongi, S. intercalatum/guineensis) and of the bladder and ureters (S. haematobium), and are eliminated with feces or urine, respectively,  THE CYCLE CONTINUES!!!!!!!
  • 16.
    Granuloma formation  Notall schistosome eggs are excreted from the body  50% can embolize to other body areas forming granulomas, causing ulceration in host tissues(bladder and intestine)  Most common sites are the liver and the bladder  Other less affected sites are the lungs, CNS and kidneys  They involve the delayed hypersensitivity type of Type 1 (Th1) and Type 2(Th2) helper cell responses with local cytokine production
  • 17.
  • 18.
    Clinical presentation  Symptomsof schistosomiasis are not caused by the worms themselves but by the body’s reaction to the eggs.  Takes two clinical syndromes; Intestinal (S. mansoni or S. japonicum) Urogenital (S. haematobium)  Incubation period 14-84 days  Many infections are asymptomatic.
  • 19.
    Clinical Cont…  Schistosomaldermatitis/ swimmer’s itch A local cutaneous hypersensitivity reaction with itchy maculopapular lesions occurs following skin penetration by cercariae  Occasionally, systemic hypersensitivity reaction may occur weeks after the initial infection(Katayama fever), especially by S. mansoni and S. japonicum
  • 20.
  • 21.
    Katayama fever  A.k.aacute schistosomiasis, mostly in heavily infested individuals, 4-8 weeks after exposure.  Is a febrile illness due to oviposition and early infection  Characterised by a serum- like syndrome with acute onset of fever, cough, chills, sweating, abdominal pain, lymphadenopathy, hepatomegaly and eosinophilia.
  • 22.
    chronic Intestinal presentation  Colicyabdominal pain  Bloody diarhhoea  Hematemesis  Hepatomegaly  Portal hypertension  Ascites  Melana
  • 23.
    Non- organ specificsymptoms  Anaemia  Chronic pain  Diarhhoea  Exercise intolerance  Chronic under nutrition(growth stunting)
  • 24.
    Chronic Urogenital presentation  Urinaryfrequency, dysuria, terminal hematuria  Referrred suprapubic/perineal pain
  • 25.
  • 26.
  • 27.
    Complications  Female genitalschistosomiasis- granulomatous inflammatory response,contact bleeding, pain and infertility- starts at 10 years  Male schistosomiasis- hematospermia, pain, lumpy semen.  Liver disease- due to granuloma formation and periportal fibrosis.  Eggs in lungs causes pulmonary HTN and cor pulonale.  CNS seizures due to CNS migration of eggs.
  • 28.
    NOTE  Advanced stagesof urogenital schistosomiasis are associated with chronic renal failure, secondary infections and squamous carcinoma of the bladder
  • 29.
    Investigations  Urinalysis- around10 mls of urine colected at midday(time of maximum egg deposition)  Stool analysis (blood, melena, eggs depending on worm burden)  CBC (eosinophilia, thrombocytopenia, anemia)  Prolonged PT  Normal or slightly elevated serum bilirubin and transaminases
  • 30.
    Lab cont…  Theunique schistosome antigens circulating anodic antigen (CAA) and circulating cathodic antigen (CCA) may also be detected in the urine or plasma.  PCR assays- 99.9% specific, 94.4% sensitive for the diagnosis of schistosomiasis.
  • 31.
    Imaging.  CT (R/O pulmonary disease and brain involvement)  Ultrasonography  MRI (granulomas in brain, lungs,liver, spinalcord—ring enhancing lesions)
  • 32.
    Imaging cont…  IVpyelography (hydronephrosis, calcifications and filing defects)  Endoscopy, sigmoidoscopy, bronchoscopy, colonoscopy  Histology of liver biopsy
  • 33.
    Management(pharmacological )  Praziquantel 20mg/kgBD on day 1 for S.haematobium, S intercalatum,and S mansoni  20 mg/kg orally TDS on day 1 for S japonicum and S mekongi.  Children <5 years may need 60mg/kg/day to achieve clearence
  • 34.
    Mgt cont…  Monitorpatients for seizures or neurologic sequelae  Corticosteroids to control post treatment inflammation  Give second dose of drug 4-6weeks after 1st dose because immature forms are less susceptible
  • 35.
    Surgical management  Surgery(resection of bladder and colonic polyps)  Correction of obstructive uropathy  Partial colectomy for intestinal polyps  Resection of cerebral cortical granulomas after failure of chemotherapy
  • 36.
    Surgical mgt cont… Placement of a distal spleno-renal shunt for reversal of Portal Hypertension  Consult with other specialits…
  • 37.
    Follow up andprognosis.  Prognosis is generally good  Acute schistosomiasis is associated with a mortality rate of up to 25% in some series  Repeat stool and urinalysis for 1 year post treatment for decreased egg excretion  Monitor antigen levels
  • 38.
    Prevention.  Currently novaccine against schistosomiasis  Prevention can be achieved by reducing the parasite load in the population by single dose anti parasitics.  Focal application of molluscicidals  Animal vaccination  Creating awareness about the risks and access to clean water and proper sanitation are the best prevention measures to overcome the burden.  Reduce exposure to contaminated water
  • 39.
    references  Kleigman.R.M, STGeme III.J.W, Blum.N,2019. Nelson Textbook of Paediatrics 21st Edition, Pg 7515-7522  World Health Organisation. (2023, February,1st ). Schistosomiasis. Retrieved from https://www.who.int/news-room/fact-sheets/detail/sc histosomiasis#:~:text=Schistosomiasis%20is%20an%20acu te%20and%20chronic%20parasitic%20disease%20caused% 20by,will%20reduce%20and%20prevent%20morbidity .  Center for Disease Control. (2020,October, 28th ). Parasites- Schistosomiasis. Retrieved from https://www.cdc.gov/parasites/schistosomiasis/health_ professionals/index.html#:~:text=If%20the%20pre%2Dtre atment%20stool,to%20help%20confirm%20successful%20c ure .