eMedicine Specialties > Infectious Diseases > Parasitic Infections

Schistosomiasis: Differential Diagnoses & Workup

Author: Palaniandy Kogulan, MBBS, MD, Assistant Director of Internal Medicine, Synergy Medical Education Alliance; Assistant Professor of Medicine, Michigan State University College of Human Medicine
Coauthor(s): Daniel R Lucey, MD, MPH, Chief, Fellowship Program Director, Department of Internal Medicine, Division of Infectious Diseases, Washington Hospital Center; Professor, Department of Internal Medicine, Uniformed Services University of the Health Sciences
Contributor Information and Disclosures

Updated: Feb 26, 2010

Differential Diagnoses

Hepatitis, Viral
Typhoid Fever
Leishmaniasis
Urethral Cancer
Malaria
Myeloproliferative Disease
Peptic Ulcer Disease

Other Problems to Be Considered

Acute nephritis
Acute viral syndrome (including HIV)
Cancer of the urogenital tract
Drug reactions
Epilepsy
Helminthic parasitic diseases
Pancreatitis
Renal tuberculosis
Space-occupying lesion
Tropical splenomegaly
Visceral leishmaniasis

Workup

Laboratory Studies

  • Stool or urine analysis
    • Identify and speciate the eggs in the stool or urine.
    • Urinary excretion of eggs is not uniform. The urine is most likely to be positive for S hematobium from 10 am until 2 pm.
    • Quantification of the egg excretion is calculated by collecting 24-hour urine or stool, homogenizing the sample, and counting the eggs in a measured sample.
    • Urine or stool egg count in a 24-hour collection quantitates the severity of the infection.
    • Fewer than 100 eggs per gram indicates a light infection, 100-400 eggs per gram indicates a moderate infection, and more than 400 eggs per gram indicates a heavy infection.
  • Egg viability test
    • This test is important for assessing the effectiveness of treatment.
    • It requires mixing the stools or urine with room-temperature distilled water and observing for hatching miracidia.
    • An active infection produces viable eggs, while treated or past infection results in nonviable eggs and an absence of miracidia.
  • Acute illness is often associated with eosinophilia in the blood and tissues.
  • With chronic illness, peripheral eosinophilia may be minimal or absent while tissue eosinophilia persists.
  • Urinary schistosomiasis (occurs with chronic disease)
    • Urine syringe filtration techniques provide a quantitative estimate of eggs in the urine.
    • Urine analysis and culture for hematuria, proteinuria, leukocyturia, and associated urinary infections
    • A Salmonella urinary tract infection should always lead to suspicion of schistosomiasis.
    • Blood chemistries, including renal function tests
    • Blood cultures for salmonella bacteremia
    • CBC count for anemia and eosinophilia
  • Intestinal and liver schistosomiasis (chronic disease)
    • Direct stool examination is not a sensitive test.
    • Concentration techniques such as a Kato-Katz thick smear are needed. This demonstrates the number of eggs excreted per day.
    • Blood in the stool should be ruled out.
    • CBC for anemia and eosinophilia
    • Additional testing for HIV and HPV should be considered in female genital schistosomiasis (FGS).
    • Liver function test results usually are within the reference range until the end stage of disease. An exception may include a mild elevation of alkaline phosphatase levels. If liver function test results are abnormal, look for other co-infections or diseases.
    • Diagnostic tests for hepatitis B and C should be considered in liver schistosomiasis.
  • Serology
    • The antibody test is a useful epidemiological tool but cannot be used to differentiate active and past illness.
    • It does not allow quantification of egg burden.
    • Serology findings can be used to reach a diagnosis in a patient from a nonendemic area because a negative antibody test result would be expected.
    • Detecting antibodies specific to S mansoni, S hematobium, and S japonicum adult worm microsomal antigens (ie, Mansoni adult worm microsomal antigen [MAMA], hematobium adult worm microsomal antigen [HAMA], japonicum adult worm microsomal antigen [JAMA]) have been reported to be highly specific for all 3 species when used in the Falcon assay screening test (FAST), enzyme-linked immunoassay (ELISA), and immunoblot assays.3

Imaging Studies

  • With acute schistosomiasis, a chest radiograph sometimes demonstrates a generalized increase in vascular and interstitial marking and mild lymphadenopathy.
  • Urinary schistosomiasis (occurs with chronic disease)
    • Plain abdominal radiographs may demonstrate bladder and ureteral calcifications.
    • On a sonogram, hydronephrosis, hydroureters, and bladder wall irregularities may be visible.
    • Urography may demonstrate abnormalities in the ureter and bladder wall.
  • Liver and intestinal schistosomiasis (chronic disease)
    • Ultrasonography of liver and spleen is used to reach an early and accurate diagnosis of periportal fibrosis and a diagnosis of hepatosplenomegaly and ascites.
    • On CT scan of the liver, calcified capsules and septa are visible.
    • Mucosal irregularities are revealed by contrast studies of the intestine.
  • Lung schistosomiasis (chronic disease)
    • CT scan of the lungs may demonstrate early interstitial fibrosis.
    • Findings on echocardiogram reflect pulmonary hypertension due to egg emboli to pulmonary vasculature.
  • CNS schistosomiasis also occurs with chronic disease, and a CT scan and MRI scan of the brain and spinal cord may show lesions.

Other Tests

  • Detecting circulating antigen
    • Because these tests measure parasite antigen as opposed to host antibody response, they reflect active infection. The tests are still investigational.
    • With effective treatment, a reduction in antigenemia is expected.
    • The 2 proteoglycan gut-associated antigens that appear most promising are circulating anodic antigen (CAA) and circulating cathodic antigen (CCA). These antigens can be found in urine or serum.
    • Studies are underway to evaluate the sensitivity and specificity of these investigational antigen tests.

Procedures

  • Rectal biopsy or bladder mucosal biopsy
    • Mucosal biopsy is effective for visualizing eggs.
    • Biopsy is helpful when stool sample findings are negative or in light infection.
    • Obtain multiple biopsy samples and crush them between slides (to increase egg-detecting sensitivity).
  • Sigmoidoscopy/proctoscopy
    • To obtain mucosal biopsies (including rectal)
    • For diagnosis and to identify complications such as pedunculated and sessile polyps
  • Upper endoscopy
    • Assess for esophageal varices.
    • Treat upper intestinal bleeding with endoscopic sclerotherapy.
  • Cystoscopy
    • To obtain mucosal biopsy for diagnosis
    • To assess complications such as bladder cancer
  • Surgical biopsy findings may be used to diagnose ectopic schistosomiasis.

More on Schistosomiasis

Overview: Schistosomiasis
Differential Diagnoses & Workup: Schistosomiasis
Treatment & Medication: Schistosomiasis
Follow-up: Schistosomiasis
Multimedia: Schistosomiasis
References
Further Reading

References

  1. Mosunjac MB, Tadros T, Beach R, et al. Cervical schistosomiasis, human papilloma virus (HPV), and human immunodeficiency virus (HIV): a dangerous coexistence or coincidence?. Gynecol Oncol. Jul 2003;90(1):211-4. [Medline].

  2. Friedman JF, Mital P, Kanzaria HK, Olds GR, Kurtis JD. Schistosomiasis and pregnancy. Trends Parasitol. Apr 2007;23(4):159-64. [Medline].

  3. Al-Sherbiny MM, Osman AM, Hancock K, et al. Application of immunodiagnostic assays: detection of antibodies and circulating antigens in human schistosomiasis and correlation with clinical findings. Am J Trop Med Hyg. Jun 1999;60(6):960-6. [Medline][Full Text].

  4. N'Goran EK, Utzinger J, Gnaka HN, et al. Randomized, double-blind, placebo-controlled trial of oral artemether for the prevention of patent Schistosoma haematobium infections. Am J Trop Med Hyg. Jan 2003;68(1):24-32. [Medline][Full Text].

  5. Utzinger J, Keiser J, Shuhua X, et al. Combination chemotherapy of schistosomiasis in laboratory studies and clinical trials. Antimicrob Agents Chemother. May 2003;47(5):1487-95. [Medline][Full Text].

  6. World Health Organization. Preventive chemotherapy in human helminthiasis. Geneva: World Health Organization; November, 2006. [Full Text].

  7. Andrade ZA. Schistosomiasis and liver fibrosis. Parasite Immunol. Nov 2009;31(11):656-63. [Medline].

  8. Barsoum RS. Schistosomiasis and the kidney. Semin Nephrol. Jan 2003;23(1):34-41. [Medline].

  9. Bergquist NR, Leonardo LR, Mitchell GF. Vaccine-linked chemotherapy: can schistosomiasis control benefit from an integrated approach?. Trends Parasitol. Mar 2005;21(3):112-7. [Medline].

  10. Brown M, Mawa PA, Joseph S, et al. Treatment of Schistosoma mansoni infection increases helminth-specific type 2 cytokine responses and HIV-1 loads in coinfected Ugandan adults. J Infect Dis. May 15 2005;191(10):1648-57. [Medline].

  11. Corachan M. Schistosomiasis and international travel. Clin Infect Dis. Aug 15 2002;35(4):446-50. [Medline].

  12. Cunha BA. Antibiotic Essentials. Royal Oak, Mich: Physicians Press; 2005.

  13. de Villiers KA, Egan TJ. Recent advances in the discovery of haem-targeting drugs for malaria and schistosomiasis. Molecules. Aug 4 2009;14(8):2868-87. [Medline].

  14. Dzeing-Ella A, Mechaï F, Consigny PH, Zerat L, Viard JP, Lecuit M, et al. Cervical schistosomiasis as a risk factor of cervical uterine dysplasia in a traveler. Am J Trop Med Hyg. Oct 2009;81(4):549-50. [Medline].

  15. Hagan P. Schistosomiasis--a rich vein of research. Parasitology. Oct 2009;136(12):1611-9. [Medline].

  16. King CH, Mahmoud AAF. Schistosomiasis. In: Guerrant RL, Walker DH, Weller PF, eds. Tropical Infectious Diseases: Principals, Pathogen, & Practice. Vol 2. ed. Philadelphia, Pa: Churchill Livingstone; 1999:1031-8.

  17. Lucey DR, Maguire JH. Schistosomiasis. Infect Dis Clin North Am. Sep 1993;7(3):635-53. [Medline].

  18. MMWR. Acute schistosomiasis with transverse myelitis in American students returning from Kenya. MMWR Morb Mortal Wkly Rep. Aug 10 1984;33(31):445-7. [Medline].

  19. Mwanakasale V, Siziya S, Mwansa J, Koukounari A, Fenwick A. Impact of iron supplementation on schistosomiasis control in Zambian school children in a highly endemic area. Malawi Med J. Mar 2009;21(1):12-8. [Medline].

  20. Pearce EJ. Progress towards a vaccine for schistosomiasis. Acta Trop. May 2003;86(2-3):309-13. [Medline].

  21. Ross AG, Bartley PB, Sleigh AC, et al. Schistosomiasis. N Engl J Med. Apr 18 2002;346(16):1212-20. [Medline].

  22. Shoff WH, Chen EH, Shepherd SM. Shistosomiasis (part I and II). Infect Dis Pract. 2005;29:419-36.

  23. Vennervald BJ, Dunne DW. Morbidity in schistosomiasis: an update. Curr Opin Infect Dis. Oct 2004;17(5):439-47. [Medline].

  24. Wang LD, Guo JG, Wu XH, Chen HG, Wang TP, Zhu SP, et al. China's new strategy to block Schistosoma japonicum transmission: experiences and impact beyond schistosomiasis. Trop Med Int Health. Dec 2009;14(12):1475-83. [Medline].

  25. WHO Expert Committee. Prevention and control of schistosomiasis and soil-transmitted helminthiasis. World Health Organ Tech Rep Ser. 2002;912:i-vi, 1-57, back cover. [Medline].

  26. Wilson RA, Coulson PS. Immune effector mechanisms against schistosomiasis: looking for a chink in the parasite's armour. Trends Parasitol. Sep 2009;25(9):423-31. [Medline].

Keywords

schistosomiasis, bilharzia, Schistosoma hematobium, Schistosoma mansoni, Schistosoma japonicum, Schistosoma intercalatum, Schistosoma mekongi, S hematobium, S mansoni, S japonicum, S intercalatum, S mekongi, blood flukes, Katayama fever, acute schistosomiasis, chronic schistosomiasis, gastrointestinal schistosomiasis, periportal fibrosis, Symmers clay pipestem fibrosis, urinary tract schistosomiasis, female genital schistosomiasis, FGS, schistosomal cor pulmonale, CNS schistosomiasis, transverse myelitis, hepatic schistosomiasis, cardiopulmonary schistosomiasis, liver schistosomiasis

Contributor Information and Disclosures

Author

Palaniandy Kogulan, MBBS, MD, Assistant Director of Internal Medicine, Synergy Medical Education Alliance; Assistant Professor of Medicine, Michigan State University College of Human Medicine
Palaniandy Kogulan, MBBS, MD is a member of the following medical societies: American College of Physicians, Infectious Diseases Society of America, and Michigan State Medical Society
Disclosure: Nothing to disclose.

Coauthor(s)

Daniel R Lucey, MD, MPH, Chief, Fellowship Program Director, Department of Internal Medicine, Division of Infectious Diseases, Washington Hospital Center; Professor, Department of Internal Medicine, Uniformed Services University of the Health Sciences
Daniel R Lucey, MD, MPH is a member of the following medical societies: Alpha Omega Alpha and American College of Physicians
Disclosure: Nothing to disclose.

Medical Editor

Wesley W Emmons, MD, FACP, Assistant Professor, Department of Medicine, Thomas Jefferson University; Consulting Staff, Infectious Diseases Section, Department of Internal Medicine, Christiana Care, Newark, DE
Wesley W Emmons, MD, FACP is a member of the following medical societies: American College of Physicians, American Medical Association, American Society of Tropical Medicine and Hygiene, Infectious Diseases Society of America, and International AIDS Society
Disclosure: Nothing to disclose.

Pharmacy Editor

Francisco Talavera, PharmD, PhD, Senior Pharmacy Editor, eMedicine
Disclosure: eMedicine Salary Employment

Managing Editor

Joseph F John Jr, MD, FACP, FIDSA, FSHEA, Clinical Professor of Medicine, Molecular Genetics and Microbiology, Medical University of South Carolina; Associate Chief of Staff for Education, Ralph H Johnson Veterans Affairs Medical Center
Disclosure: BioMerieux Honoraria Review panel membership; Cubist Honoraria Review panel membership; Pfizer Honoraria Speaking and teaching; Merck Stock dividends stock holdings

CME Editor

Eleftherios Mylonakis, MD, Clinical and Research Fellow, Department of Internal Medicine, Division of Infectious Diseases, Massachusetts General Hospital
Eleftherios Mylonakis, MD is a member of the following medical societies: American Association for the Advancement of Science, American College of Physicians, American Society for Microbiology, and Infectious Diseases Society of America
Disclosure: Nothing to disclose.

Chief Editor

Burke A Cunha, MD, Professor of Medicine, State University of New York School of Medicine at Stony Brook; Chief, Infectious Disease Division, Winthrop-University Hospital
Burke A Cunha, MD is a member of the following medical societies: American College of Chest Physicians, American College of Physicians, and Infectious Diseases Society of America
Disclosure: Nothing to disclose.

 
 
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