[Bowel parasites and faecal eosinophilia]

J C Petithory1, F G Ardoin

  • 1Qualité en parasitologie et biologie, Département de biologie médicale Emile-Brumpt, Centre hospitalier, 95500 Gonesse, France. petithory.parasito@wanadoo.fr

Insights

A new staining method for fecal polynuclear eosinophils (PE) offers advantages over traditional techniques. This method aids in diagnosing parasitic infections and intestinal allergies by detecting tissue eosinophilia.

Area of Science:

  • Medical Parasitology
  • Gastroenterology
  • Clinical Pathology

Background:

  • Traditional May-Grünwald-Giemsa staining for fecal polynuclear eosinophils (PE) has limitations.
  • These include bacterial overstaining, lipid dissolution, and sensitivity to stool pH.
  • A need exists for a more robust and informative staining technique.

Purpose of the Study:

  • To evaluate an adapted Wheatley staining technique for fecal polynuclear eosinophils (PE).
  • To compare its advantages against the May-Grünwald-Giemsa method.
  • To explore the diagnostic utility of fecal PE in various gastrointestinal conditions.

Main Methods:

  • Adaptation of the Wheatley staining technique for fecal samples.
  • Comparison of staining characteristics with May-Grünwald-Giemsa.
  • Analysis of fecal PE presence in patients with helminthiasis, intestinal coccidiosis, other protozoal infections, and intestinal allergies.

Main Results:

  • The adapted Wheatley stain shows advantages: less bacterial staining, preserved lipids, and reduced pH dependency.
  • Fecal polynuclear eosinophils (PE) are preserved for over a year in stool samples.
  • PE are detected in approximately 50% of helminthiasis and intestinal coccidiosis cases, and in intestinal allergies, but not other protozoal infections.

Conclusions:

  • The adapted Wheatley staining method for fecal polynuclear eosinophils (PE) is advantageous for diagnosing gastrointestinal conditions.
  • Faecal eosinophilia, detected by this method, indicates tissue eosinophilia and is linked to parasitic infections and allergies.
  • This technique allows observation of eosinophilia mechanisms not evident in blood eosinophilia.

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