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溶组织内阿米巴

溶组织内阿米巴. 溶组织内阿米巴 Entamoeba histolytica. 前言 形态 生活史 致病 实验诊断 流行与防治. 山东大学寄生虫学教研室 何深一. Introduction. 1. The only pathogenic amoeba among all of the intestinal amoebae 2. Infecting perhaps 10% of the world's population. 3. Lead to invasive amoebiasis.

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溶组织内阿米巴

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  1. 溶组织内阿米巴 溶组织内阿米巴Entamoeba histolytica • 前言 • 形态 • 生活史 • 致病 • 实验诊断 • 流行与防治 山东大学寄生虫学教研室 何深一

  2. Introduction 1. The only pathogenic amoeba among all of the intestinal amoebae 2. Infecting perhaps 10% of the world's population. 3. Lead to invasive amoebiasis.

  3. Entamoeba histolyticaEntamoeba dispar • Major pathogen • world-wide distribution (10%) • 5% in some developed countries • 100 deaths in Chicago 1930 • Trophozoite & Cyst • oral-faecal transmission

  4. Morphology • Pay your attention to stages that have diagnostic valueParasites stained with hematoxylin is described here.

  5. Trophozoite (active form) • (1) Size: 10-40 micrometers in diameter, some are above 60 micrometers. • (2) Pseudopodium(ectopalsmic protrusion):    A. broad or finger-like in form    B. thrust out quickly    C. firstly, formed with ectoplasm, secondly, endoplasm flows slowly into it.    D. motility is progressive and directional.

  6. Trophozoite (active form) • (3) Endoplasm: red blood cells may be found in it. • (4) Nucleus (vesicular type)      It is not visible in an unstained specimen; but its clear structure can be seen when stained with hematoxylin.  A: membrane: distinct line  B: chromatin granules: fine and uniformly arranged in the inner surface of the nuclear membrane.  C: karyosome: small and centrally located.

  7. Phase contrast photomicrograph of cultured Entamoeba histolytica trophozoites. 

  8. Charcot Leyden Crystal • These diamond shaped crystals are often seen in amoebic dysentery faeces and may also be present in other parasitic infections. They are absent in bacillary dysentery. Interference contrast. ×400. Enlarged by 9.6

  9. Movement of E. histolytica 进行性和定向阿米巴运动 progressive and directional

  10. Cyst (non-motile) (1) 10-20 mocrometers in size • (2) spherical in shape • (3) 1-2 nuclei (immature cyst); 4 nuclei (mature cyst-infective stage). • (4) inclusions:(become smaller and smaller as the cyst ages)      glycogen vacuole  appears as a clear space; food reservoir    chromatoid body  dark blue rods or dots; its function is not known

  11. The single nucleus with its central endosome and regularly distributed chromatin is visible.  The dark "rods" in the cytoplasm are the chromatoid bars; approximate size = 18 µm.

  12. This is a mature cyst and contains four nuclei.  However, only two nuclei are visible in this plane of focus, and a chromatoid bar is still present; approximate size = 17 µm.

  13. Entamoeba coli • Gut commensal • Trophozoite & cyst • Slow “lazy” movement • Oral-faecal transmission

  14. E. histolytica v E. coli • Trophozoite • 10-40um • delicate nuclear structure • Cyst • 9.5-15.5um • 4 nuclei • Broad, blunt chromatid bodies • 15-30um • coarse nuclear structure • 10-30um • 8 nuclei • thin, sharp chromatid bodies

  15. Entamoeba coli

  16. Entamoeba coli

  17. Life Cycle • 1  infective stage: mature cyst • 2  access:  mouth • 3  ecological niches:  large intestine; liver, lung and other organs. • 4  pathogenic stage:  trophozoite • 5  diagnostic stage:  cyst; trophozoites

  18. Pathogenic factors • 1. Toxicity of parasites  pathogenic- nonpathogenic complex. • Entamoeba histolytica    Entamoeba dispar • 2. Symbiotic bacteria • 3. Defence barrier  immunity

  19. This cytolytic event is a result of incorporation in the host cell membrane of an ameba-produced, pore-forming protein, Amoebapore. • This protein forms ion channels in lipid cell membranes and results in cell death within minutes of cell contact with the ameba. Amoebapore has been isolated, synthesized and well characterized. Non-pathogenic strains of E. histolytica can also produce amoebapore but are much less efficient at its production and the molecule is not exactly similar to that produced by virulent strains.

  20. Pathology and Clinical Manifestation • Pinpoint lesion on mucous membrane • Flask-shaped crateriform ulcers

  21. Clinical classification • Asymptomatic infection (carrier)  >90% cases (E. dispar?) • Sympomatic cases <10% • 8-10% dysentery, colitis, etc • 2% invasive amoebiasis • 0.1% deaths

  22. A. Intestinal amoebiasis • a. dysentery:dysenteric stools (pus and blood without feces). fever, dehydration, and electrolyte abnormalities. Tenesmus and abdominal tenderness. • b. non-dysenteric colitis • c. appendicitis • d. amoeboma:may become the leading point of an intussusception or may cause intestinal obstruction.

  23. Histopathology of a typical flask-shaped ulcer of intestinal amebiasis

  24. A Micro Abscess in the submucosa . • Containing a large number of E. histolytica trophozoites mostly at the periphery .H and E. ×400. Enlarged by 5.4.

  25. B. Extra-intestinal amoebiasis •   a. Hepatic  •     (1) acute non-suppurative •     (2) liver abscess: right upper quadrant pain, referred to the right shoulder. tender. •   b. Pulmonary

  26. B. Extra-intestinal amoebiasis •   c. Brain •   d. Skin, perianal infection •   e. Other extra-intestinal amoebiasis

  27. Amoebic Liver Abscess

  28. Gross pathology of liver containing amebic abscess

  29. Gross pathology of amebic abscess of liver. Tube of "chocolate" pus from abscess. 

  30. An Amoebic Liver Abscess Being Aspirated. • Note the reddish brown color of the pus (‘anchovy-sauce’). This color is due to the breakdown of liver cells. Enlarged by 5.4

  31. X-ray of a Large Amoebic Liver Abscess. • A fluid level has formed after aspiration due to entry of air

  32. trophozoite cyst specimen feces feces method direct smear with normal saline direct smear with iodine stain diseases amoebic dysentery chronic intestinal amoebiasis or carriers remarks 1.container must clean2.examined soon after they have been passed.3.select bloody and mucous portion. 4.keep specimen warm. 5.drug using histry. Diagnosis1.Stool examination

  33. Diagnosis • 2. Serologic studies: indirect hemagglutination, skin tests, ELISA and latex agglutination. • 3.Tissue examination: sigmoidoscopic biopsy, aspiration • 4. DNA probe

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