Isosporiasis Workup

  • Author: Robert W Tolan Jr, MD; Chief Editor: Michael Stuart Bronze, MD   more...
 
Updated: Jun 29, 2011
 

Approach Considerations

The diagnosis of isosporiasis is based on a combination of clinical, epidemiologic, and diagnostic tests. Routine laboratory tests are not diagnostic, but peripheral eosinophilia is an important clue, seen in about one half of patients. Serologic tests for isosporiasis are not available.

Because isosporiasis is an AIDS-defining illness, an appropriate workup for HIV infection should be performed, if necessary.

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Stool Examination

Stool examination for ova and parasites is the test of choice for isosporiasis. Multiple specimens or specimen concentration increases diagnostic yield. Zinc sulfate or sugar flotation is the most sensitive stool concentration technique.

Mature oocysts measure 30 × 12 µm and have a thin translucent wall and 2 round sporocysts, each of which has 4 crescentic sporozoites. Auramine-rhodamine fluorescent, modified Kinyoun acid-fast, hematoxylin/eosin, Giemsa, and/or carbol fuchsin staining may be helpful in identifying the translucent oocysts (see the image below). Oocysts autofluoresce under ultraviolet epifluorescence illumination using a 450- to 490-nm excitation filter.

Oocyst of Isospora belli with 2 sporoblasts. From Oocyst of Isospora belli with 2 sporoblasts. From the Image Library, Division of Parasitic Diseases at the National Center for Infectious Diseases, Centers for Disease Control and Prevention (CDC), Atlanta, Georgia.

Charcot-Leyden crystals and high fat content are often observed in stool specimens. Polymorphonuclear leukocytes (PMNs) are not observed in fecal specimens.

Studies suggest that real-time polymerase chain reaction (PCR) testing is promising for the detection of I belli in stool samples.[4]

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Radiography

A double-contrast barium upper gastrointestinal (GI) series with small-bowel follow-through may be helpful. Nonspecific radiographic findings (eg, prominent mucosal folds, thickening of intestinal wall) may be observed.

The severity of radiographic findings seems to depend on duration of illness and to correlate with the degree of villous atrophy noted on biopsy findings (see Tissue Analysis and Histologic Findings). Short-term disease (< 1 y) seems to result in minimal or irregular thickening of mucosal folds. Long-term disease seems to correlate with markedly granular mucosal appearance with effacement of the folds.

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Other Tests

String test

The Entero-Test (swallowed string test to provide a duodenal sample) may yield a positive specimen, if stool study results are negative.

Upper GI endoscopy

Upper GI endoscopy may provide useful specimens for examination, if the following test results are negative:

  • Duodenal aspirate for ova and parasite examination
  • Small bowel biopsy for histopathology

Electron microscopy

If performed as a part of workup for malabsorption, I belli may be observed with electron microscopy of tissue specimens.

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Tissue Analysis and Histologic Findings

A small-bowel biopsy is not a routine test for diagnosis of isosporiasis. Nonspecific findings of isosporiasis observed in small-bowel biopsy specimens include mucosal atrophy, shortened villi, hypertrophic crypts, and lamina propria infiltrated with eosinophils. I belli may be observed in the cytoplasm of enterocytes with electron microscopy.

Histologic findings appear to correlate with the severity of the symptoms observed. Focal-to-widespread mucosal changes are associated with severe symptoms. In mild cases, the only findings may range from flattened villi to mild, nonspecific alterations and increased inflammatory cells in the lamina propria.

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Contributor Information and Disclosures
Author

Robert W Tolan Jr, MD  Chief, Division of Allergy, Immunology and Infectious Diseases, The Children's Hospital at Saint Peter's University Hospital; Clinical Associate Professor of Pediatrics, Drexel University College of Medicine

Robert W Tolan Jr, MD is a member of the following medical societies: American Academy of Pediatrics, American Medical Association, American Society for Microbiology, American Society of Tropical Medicine and Hygiene, Infectious Diseases Society of America, Pediatric Infectious Diseases Society, Phi Beta Kappa, and Physicians for Social Responsibility

Disclosure: Novartis Honoraria Speaking and teaching

Coauthor(s)

Venkat R Minnaganti, MD  Consulting Staff, Department of Medicine, Winthrop University Hospital; Clinical Instructor, Department of Internal Medicine, Division of Infectious Disease, State University of New York School of Medicine at Stony Brook

Venkat R Minnaganti, MD is a member of the following medical societies: All India Ophthalmological Society, American College of Physicians, American Medical Association, American Society for Microbiology, and Infectious Diseases Society of America

Disclosure: Nothing to disclose.

Glenn Fennelly, MD, MPH  Director, Division of Infectious Diseases, Lewis M Fraad Department of Pediatrics, Jacobi Medical Center; Clinical Associate Professor of Pediatrics, Albert Einstein College of Medicine

Glenn Fennelly, MD, MPH is a member of the following medical societies: Pediatric Infectious Diseases Society

Disclosure: Nothing to disclose.

Specialty Editor Board

Klaus-Dieter Lessnau, MD, FCCP  Clinical Associate Professor of Medicine, New York University School of Medicine; Medical Director, Pulmonary Physiology Laboratory; Director of Research in Pulmonary Medicine, Department of Medicine, Section of Pulmonary Medicine, Lenox Hill Hospital

Klaus-Dieter Lessnau, MD, FCCP is a member of the following medical societies: American College of Chest Physicians, American College of Physicians, American Medical Association, American Thoracic Society, and Society of Critical Care Medicine

Disclosure: Nothing to disclose.

Francisco Talavera, PharmD, PhD  Adjunct Assistant Professor, University of Nebraska Medical Center College of Pharmacy; Editor-in-Chief, Medscape Drug Reference

Disclosure: Medscape Salary Employment

John W King, MD  Professor of Medicine, Chief, Section of Infectious Diseases, Director, Viral Therapeutics Clinics for Hepatitis, Louisiana State University Health Sciences Center; Consultant in Infectious Diseases, Overton Brooks Veterans Affairs Medical Center

John W King, MD is a member of the following medical societies: American Association for the Advancement of Science, American College of Physicians, American Federation for Medical Research, American Society for Microbiology, Association of Subspecialty Professors, Infectious Diseases Society of America, and Sigma Xi

Disclosure: emedicine $50.00 Author of chapter; MERCK None Other

Russell W Steele, MD  Head, Division of Pediatric Infectious Diseases, Ochsner Children's Health Center; Clinical Professor, Department of Pediatrics, Tulane University School of Medicine

Russell W Steele, MD is a member of the following medical societies: American Academy of Pediatrics, American Association of Immunologists, American Pediatric Society, American Society for Microbiology, Infectious Diseases Society of America, Louisiana State Medical Society, Pediatric Infectious Diseases Society, Society for Pediatric Research, and Southern Medical Association

Disclosure: Nothing to disclose.

Chief Editor

Michael Stuart Bronze, MD  Professor, Stewart G Wolf Chair in Internal Medicine, Department of Medicine, University of Oklahoma Health Science Center

Michael Stuart Bronze, MD is a member of the following medical societies: Alpha Omega Alpha, American College of Physicians, American Medical Association, Association of Professors of Medicine, Infectious Diseases Society of America, Oklahoma State Medical Association, and Southern Society for Clinical Investigation

Disclosure: Nothing to disclose.

References
  1. Woodcock HM. Notes on Protozoan parasites in the excreta. BMJ. 1915;2:709..

  2. Goodgame R. Emerging Causes of Traveler's Diarrhea: Cryptosporidium, Cyclospora, Isospora, and Microsporidia. Curr Infect Dis Rep. Feb 2003;5(1):66-73. [Medline].

  3. Sasaki M, Tanaka A, Nishimura T, Tsujikawa T, Andoh A, Ishizuka I, et al. A case of malabsorption syndrome caused by isosporiasis in an immunocompetent patient. J Gastroenterol. Jan 2004;39(1):88-9. [Medline].

  4. ten Hove RJ, van Lieshout L, Brienen EA, Perez MA, Verweij JJ. Real-time polymerase chain reaction for detection of Isospora belli in stool samples. Diagn Microbiol Infect Dis. Jul 2008;61(3):280-3. [Medline].

  5. Malik S, Samantaray JC, Bagga A, Das A. Refractory isosporiasis. Indian J Pediatr. May 2005;72(5):437-9. [Medline].

  6. Sorvillo FJ, Lieb LE, Seidel J, Kerndt P, Turner J, Ash LR. Epidemiology of isosporiasis among persons with acquired immunodeficiency syndrome in Los Angeles County. Am J Trop Med Hyg. Dec 1995;53(6):656-9. [Medline].

  7. Rowe JS, Shah SS, Motlhagodi S, Bafana M, Tawanana E, Truong HT, et al. An epidemiologic review of enteropathogens in Gaborone, Botswana: shifting patterns of resistance in an HIV endemic region. PLoS One. Jun 2 2010;5(6):e10924. [Medline]. [Full Text].

  8. DeHovitz JA, Pape JW, Boncy M, Johnson WD Jr. Clinical manifestations and therapy of Isospora belli infection in patients with the acquired immunodeficiency syndrome. N Engl J Med. Jul 10 1986;315(2):87-90. [Medline].

  9. Limson-Pobre RN, Merrick S, Gruen D, Soave R. Use of diclazuril for the treatment of isosporiasis in patients with AIDS. Clin Infect Dis. Jan 1995;20(1):201-2. [Medline].

  10. Fox LM, Saravolatz LD. Nitazoxanide: a new thiazolide antiparasitic agent. Clin Infect Dis. Apr 15 2005;40(8):1173-80. [Medline].

  11. Gilles HM, Hoffman PS. Treatment of intestinal parasitic infections: a review of nitazoxanide. Trends Parasitol. Mar 2002;18(3):95-7. [Medline].

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Oocyst of Isospora belli with 2 sporoblasts. From the Image Library, Division of Parasitic Diseases at the National Center for Infectious Diseases, Centers for Disease Control and Prevention (CDC), Atlanta, Georgia.
 
 
 
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