A random specimen of stool (at least 4 ml or 4 cm³) is collected in a clean, dry, container with a tightly fitting lid (a tin box, plastic box, glass jar, or waxed cardboard box) and transported immediately to the laboratory (this is because trophozoites of Entameba histolytica rapidly degenerate and alter in morphology). About 20-40 grams of formed stool or 5-6 tablespoons of watery stool should be collected. Stool should not be contaminated with urine, water, soil, or menstrual blood. Urine and water destroy trophozoites; the soil will introduce extraneous organisms and also hinder proper examination. Parasites are best detected in warm, freshly passed stools and therefore stools should be examined as early as possible after receipt in the laboratory (preferably within 1 hour of collection). If a delay in the examination is anticipated, the sample may be refrigerated. A fixative containing 10% formalin (for the preservation of eggs, larvae, and cysts) or polyvinyl alcohol (for the preservation of trophozoites and cysts, and for permanent staining) may be used if the specimen is to be transported to a distant laboratory.
|Parameter||Amebic dysentery||Bacillary dysentery|
|1. Cause||Entamoeba histolytica||Shigella (most common)|
|3. Fever/vomiting||Not significant||Significant|
|4. Appearance of fecal sample||Unformed with blood and mucus||Unformed with blood, mucus, and pus|
|5. Microscopic examination of stool|
|• Red cells||Clumps||Discrete|
|• Pus cells||Nil or few||Numerous|
|• Macrophages||Not seen||Many, some with ingested red cells|
|• Charcot-Leyden crystals||May be present||Not seen|
|• Trophozoites of E. histolytica||Present||Not seen|
|• Bacteria||Many, motile||Few, nonmotile|
|6. Antigen test for E. histolytica||Positive||Negative|
|7. Stool culture||Negative||Positive for Shigella|
E. histolytica is worldwide in distribution and endemic in tropical and subtropical countries. It is transmitted by the fecal-oral route (ingestion of food or water contaminated by cysts of E. histolytica).
Infection by E. histolytica may be asymptomatic or may cause amebic dysentery or amebic liver abscess. Amebic trophozoites invade the large intestinal mucosa, multiply in the submucosa, spread laterally and produce flask-shaped ulcers. Symptoms include low-grade fever, diarrhea with blood and mucus, weight loss, and cramping abdominal pain. The cecum, ascending colon, and rectosigmoid are commonly affected. Excessive granulation tissue may form in the intestine at the site of lesion (ameboma) to produce constriction, which may be mistaken clinically for a neoplasm.
In some cases, amebae penetrate the portal vessels and are transported to the liver where they form the liver abscess. Amebic abscesses can also form in lungs or brain.
Life cycle of E. histolytica
Infection is acquired by ingestion of food or water contaminated with infective (quadrinucleate) cysts of E. histolytica. Dissolution of cyst wall in the small intestine occurs with formation of trophozoites. Actively motile trophozoites invade large intestinal mucosa, lodge in the submucosa, multiply, and cause disease (colitis).
Extraintestinal spread to the liver and other sites can occur.
Under unfavorable conditions, encystation of trophozoites leads to the formation of cysts in the intestinal lumen. Cysts are discharged in feces and can survive in moist environmental conditions for weeks to months and propagate the life cycle by the further fecal-oral spread.
1. Identification of trophozoites and cysts on stool examination:
Demonstration of trophozoites of E. histolytica in fecal specimens is required for the diagnosis of amebic dysentery. For diagnosis, at least three fresh stool samples should be examined to increase sensitivity. Trophozoites vary from 15 to 40 μ in diameter. In saline wet mounts, trophozoites show motility in one direction via pseudopodia, which form rapidly. Cytoplasm shows outer transparent ectoplasm and inner finely granular endoplasm. The diagnostic feature of E. histolytica trophozoites is the presence of ingested red cells. The nucleus is visible in the iodine preparation (Figure 1181.1). Fine granules of peripheral nuclear chromatin are evenly distributed along the nuclear membrane. Karyosome is small and centrally placed (Motility is lost in iodine mount).
Cysts of E. histolytica are spherical and measure 10-15 μ in diameter. Nuclei are 1, 2, 3, or 4 and are similar in morphology to trophozoite nucleus (mature cyst contains 4 nuclei). The nuclear membrane is regular and thin with finely granular peripheral chromatin. Karyosome is small and central. Immature cysts may show chromatoid bodies (aggregates of ribosomes) that are oblong structures with rounded ends, and glycogen clumps (Figure 1181.2).
Entameba dispar is a morphologically identical organism; however, it is non-pathogenic. If red blood cells are identified within trophozoites, then the species is E. histolytica. However, there is no morphologic feature to distinguish between the cysts of these two organisms. Therefore, if only cysts are identified on stool examination, they are reported as “Cysts of E. histolytica/dispar”. Asymptomatic infections with E. histolytica reported in the past are now known to be due to E. dispar. Monoclonal antibodies can distinguish between these two organisms.
Entamoeba histolytica can be definitively identified in saline wet mount if it shows definite directional motility and contains ingested red cells.
It is also necessary to distinguish E. histolytica from other non-pathogenic amebae found in stools like Entamoeba coli, Entamoeba hartmanii, Endolimax nana, and Iodameba butschlii.
Wet mount examination of stool has low sensitivity (25-60%) and also false-positivity due to E. dispar. For identification of trophozoites, stool smears can be prepared and stained with trichrome stain (Figure 1181.3).
2. Other findings on stool examination:
Plenty of red cells and very few white cells are helpful in differentiating amebic from bacillary dysentery. Charcot-Leyden crystals may be seen. Differences between amebic and bacillary dysentery are listed in Table 1181.1.
3. Detection of the antigen of E. histolytica in stools:
Direct detection of antigen-specific to E. histolytica is possible by commercially available tests based on enzyme immunoassay. These tests are specific and sensitive (90%) and can differentiate E. histolytica from E. dispar. These tests are indicated if direct stool examination is negative for organisms and intestinal amebiasis is suspected clinically.
4. Detection of DNA specific to E. histolytica:
It is possible by polymerase chain reaction-based assays.
5. Serologic tests:
Serologic tests, which detect antibodies to E. histolytica, are performed to support the diagnosis of invasive amebiasis (i.e. colitis, liver abscess, or ameboma) when organisms cannot be demonstrated on stool examination. Various tests are available like latex agglutination test, indirect hemagglutination test, enzyme immunoassay, and counterimmunoelectrophoresis. Enzyme immunoassay is the method of choice since it is most sensitive and specific. Serologic tests, however, remain positive for many years after infection and thus cannot distinguish between recent and past infections.
6. Endoscopic biopsy of ulcer in the intestine:
This can demonstrate trophozoites of E. histolytica in 50% of cases. Staining with periodic acid Schiff stain facilitates identification of parasites.
Giardia intestinalis (lamblia)
G. intestinalis (lamblia), a pathogenic intestinal protozoan, has a worldwide distribution. It is transmitted by the fecal-oral route and is usually water-borne. Giardia is resistant to chlorine levels in tap water and is commonly found in cold mountain streams. Giardiasis frequently occurs in persons who spend time camping outdoors or in woods and is also called as “Backpacker’s diarrhea” or “beaver fever”. It can cause asymptomatic infection, mild diarrhea, or a severe disease with diarrhea, malabsorption, weight loss and steatorrhea.
Life cycle of Giardia intestinalis (lamblia)
There are two stages in the life cycle, cyst, and trophozoite. After ingestion of cysts, excystation occurs due to the action of gastric acid, and trophozoites are released which migrate to the duodenum and proximal jejunum where they attach to the mucosa and replicate.
1. Demonstration of trophozoites or cysts:
G. lamblia trophozoites are found in fresh liquid stools, particularly in flakes of mucus. They often occur in clusters. Cysts are more likely to be found in formed or loose stools.
Duodenal aspirates may be obtained if repeated fecal examinations are negative for G. lamblia and there is a strong clinical suspicion of giardiasis. However, the test is invasive and is usually not necessary for diagnosis.
Trophozoites of G. lamblia are pear-shaped, 12-15 μ in diameter, have 4 pairs of flagella, 2 large and oval nuclei, 2 axonemes (axial filaments of flagella), and 1 or 2 curved median bodies. Motility is likened to that of “falling leaf”.
Cysts of G. lamblia are 8-12 μ in diameter, oval, and contain 4 nuclei, axonemes, median bodies, and remains of flagella (Figure 1181.4).
2. Detection of the antigen of G. lamblia in stool sample:
The antigen of G. lamblia can be demonstrated by enzyme immunoassay technique with high sensitivity (90-99%) and specificity (95-100%). This test can be used as the initial test for diagnosis of giardiasis; however, stool examination is still important for detection of other concomitant parasite infections.
3. Direct fluorescent antibody assay:
This test is available commercially in a kit form and is highly sensitive and specific. Cysts are labeled with immunofluorescent antibodies and are detected under the fluorescence microscope.
Isospora belli, Cryptosporidium parvum, and Cyclospora cayetanensis are human intestinal coccidia. They have a worldwide distribution. Transmission is by the fecal-oral route (ingestion of infective oocysts). These protozoan organisms cause self-limited, mild diarrheal illness; however, in immunocompromised patients (such as patients with acquired immunodeficiency syndrome) they can induce severe and protracted diarrhea, which may sometimes be life-threatening.
Life cycle of Coccidia
Ingestion of infective oocysts by humans leads to infection. The release of sporozoites from oocysts occurs which infect intestinal epithelial cells. Sporozoites multiply within epithelial cells with formation of merozoites (asexual reproduction by fission or schizogony), which infect other epithelial cells. Some merozoites develop into male and female gametes. Fertilization of male and female gametes produces a zygote.
Oocyst is formed by encystation around the conjugating gametes. Sporozoites form within oocysts by sexual reproduction or sporogony. Oocysts are excreted in feces and contaminate food or water.
1. Examination of stools for the demonstration of oocysts of I. belli, C. parvum, or C. cayetanensis:
Isospora belli: Oocysts of I. belli can usually be found in direct wet mounts of feces (unstained). Formalin-ether concentration technique may sometimes be necessary. Oocysts of I. belli are oval and about 32 × 16 μ in size. Immature oocysts contain a granular zygote. Mature oocysts contain two sporocysts, each with four sporozoites. With modified Ziehl-Neelsen stain (on a fecal smear prepared from the sediment after formalin-ether concentration), oocysts stain uniform red-pink. Under ultraviolet light, oocysts show autofluorescence.
Cryptosporidium parvum: Oocysts of C. parvum are difficult to demonstrate in direct fecal wet mounts. They are demonstrated either by modified Ziehl-Neelsen staining of concentrated fecal smear or by immunofluorescence technique. They are 4-6 μ in size, round to oval, and stain pink-red.
Cyclospora cayetanensis: In direct wet mounts of feces, oocysts measure 8-10 μ in diameter, and contain a cluster of refractile globules (morula-like appearance). With modified Ziehl-Neelsen stain, they appear similar to C. parvum but are larger. Under ultraviolet light (365 nm), oocysts show intense blue autofluorescence.
2. Detection of antigen in stool samples:
Enzyme immunoassay for detection of specific antigen of C. parvum is available. It is more sensitive and specific than Ziehl-Neelsen staining.
3. Direct fluorescent antibody assay:
This assay is available for Cryptosporidium parvum and is highly sensitive and specific. Oocysts of Cryptosporidium labeled with fluorescent antibody are readily detected under the fluorescence microscope.
Microsporidia are obligate intracellular protozoa, which cause opportunistic infection in immunocompromised patients leading to persistent diarrhea and weight loss. Common species causing infection in humans are Enterocytozoon bieneusi, Encephalitozoon intestinalis, and Encephalitozoon hellem.
Transmission of infection is by ingestion of spores. The organisms develop and multiply in intestinal cells and form infective spores; rupture of host cells releases spores some of which infect newer cells while others are excreted in feces.
Some microsporidia can cause keratoconjunctivitis, hepatitis, peritonitis, respiratory infection, and kidney disease. Microsporidia cannot be demonstrated on wet mounts because of their very small size.
1. Modified trichrome stain of stool sample:
Spores are very small (1-5 μ), stain red, and may show a transverse band.
2. Small intestinal biopsy for the demonstration of spores within intestinal cells.
Ascaris lumbricoides (Roundworm)
This is the most common helminthic infection in humans. Children are more commonly affected than adults. Mode of transmission is the fecal-oral route (ingestion of infective eggs). Adult worms live in the small intestine (duodenum and jejunum) of the host. Eggs are laid by adult female worms (about 200,000 per day), which are excreted in feces. Eggs can remain viable in the soil for many years. Contamination can occur when untreated human feces are used as a fertilizer or by soiling of hands of playing children. Adult worms can live in the intestine for 1-2 years.
Life cycle of Ascaris lumbricoides (Roundworm)
Infection is acquired by ingestion of infective eggs via contaminated food or hands. Eggs hatch to release larvae in the intestine. Larvae penetrate the mucosa and enter the bloodstream. Larvae circulate, reach lungs and penetrate alveolar walls to enter the respiratory tree.
Larvae migrate up the trachea to the epiglottis from where they are swallowed. Maturation of larvae to adult worms occurs in the small intestine. Female worms lay down eggs, which are excreted in feces. Eggs become embryonated (infective) in 4-6 weeks in a favorable environment.
- Asymptomatic if the infection is light.
- Loeffler’s syndrome: Migration of larvae through the lungs can induce a cough, wheezing, eosinophilia, and bilateral, irregular pulmonary densities.
- Local effects: These include abdominal pain, diarrhea, intestinal obstruction due to a large mass of worms, and intestinal perforation. Sometimes worms can invade pancreatic duct or common bile duct and cause obstruction; this can lead to pancreatitis or obstructive jaundice respectively. From the bile duct, adult worms can reach the liver and cause an abscess. Adult worms can migrate to the appendix to cause appendicitis.
1. Demonstration of eggs of A. lumbricoides:
Diagnosis of A. lumbricoides infection is made by demonstration of eggs on stool examination. Eggs can be demonstrated in the direct wet mount of feces in moderate to heavy infections. The recommended procedure is formol-ethyl acetate sedimentation technique for the concentration of eggs. In feces, four types of eggs are found: fertilized (double-shelled or decorticated) and unfertilized (double-shelled or decorticated).
Fertilized eggs: These are oval, yellow-brown, and about 70 μ × 50 μ in size. They have outer and inner shells. The outer shell is uneven, brown (due to staining by bile), and rough (mamillated), while the inner shell is thick, smooth, and colorless. The egg contains a single central granular mass (fertilized ovum).
Unfertilized eggs: Single female worms discharge these eggs. They are slightly larger and more elongated than the fertilized eggs (90 μ in length). The outer shell is dark brown and more irregular, while the inner shell is thinner. This egg is filled with a mass of large refractile granules (Figure 1181.5).
Decorticated eggs do not have the outer uneven shell and resemble the hookworm eggs.
2. Identification of adult worms:
Occasionally adult worms are passed spontaneously in the feces and brought to the laboratory for identification. Adult Ascaris worms are cylindrical or round, pinkish, and measure about 15 cm (male) or 30 cm (female) in length. Diameter is about 0.5 cm and the tail is curved (male) or straight (female). There are three lips at the anterior end (mouth).
The hookworms are Ancylostoma duodenale (old world hookworm) and Necator americanus (new world hookworm).
Life cycle of hookworms
Infection occurs when there is penetration of the skin of foot by filariform larvae present in the soil. Larvae enter the circulation, and through veins are carried to the heart and then reach lungs, migrate up the respiratory tree and are swallowed. Maturation of larvae to the adult worms occurs in the small intestine. Adult worms attach to the mucosa and suck blood. Adult female worms produce eggs, which are excreted in feces. Rhabditiform larvae are released from eggs into the soil and mature into infective filariform larvae. Both A. duodenale and N. americanus infection are acquired when infective filariform larvae penetrate the skin. A. duodenale infection is also acquired by ingestion of infective larvae.
Hookworm infection can cause:
- “Ground itch”: This is inflammation and marked itching on the skin at the site of larval penetration.
- Loeffler’s syndrome: This is due to migration of larvae through the lungs.
- Iron deficiency anemia due to chronic blood loss: This is a well-known and most common complication of hookworm infection. Adult worms attach themselves to the small intestinal mucosa by teeth-like structures or cutting plates, and suck blood. They then change their sites of attachment (every 4-8 hours) while blood continues to ooze from the previous site. One adult A. duodenale causes loss of 0.15 ml of blood while one N. americanus causes loss of 0.03 ml per day.
- Abdominal pain and diarrhea if worm load is high.
1. Demonstration of hookworm eggs:
Diagnosis is based on the identification of hookworm eggs on stool examination. The technique of formol-ethyl acetate sedimentation is preferred; if not available, a direct wet mount of a fecal sample can demonstrate eggs in moderate to heavy infections. Eggs of A. duodenale and N. americanus are morphologically similar. They are 50-75 μ in length and 40 μ in width, oval, colorless, and have a thin shell. In fresh stools, eggs show 4-8 gray, granular cells (Figure 1181.6). If the stool is more than 12 hours old, eggs will show a rhabditiform larva folded upon itself. Such an egg is called as embryonated. If feces are more than 24 hours old, then free rhabditiform larvae will be seen. This should be differentiated from larvae of Strongyloides stercoralis (buccal cavity of hookworm larva is longer).
2. Other laboratory features:
Infection is acquired by ingestion of infective eggs. Larvae, which are released, develop into adult worms and attach to the mucosa. Released eggs are excreted in feces, and mature in the soil to the infective stage under suitable conditions. Heavy infection can cause diarrhea with blood and mucus in stools, iron deficiency anemia, or rectal prolapse.
Diagnosis depends on identification of typical eggs on stool examination. Eggs measure 50 × 25 μ in size, are yellow-brown and barrel-shaped. A rounded, transparent plug is present at both poles (Figure 1181.7). Eggs contain central, uniformly granular mass. Eggs are often quantitated to assess the severity of an infection.
Life cycle of Strongyloides stercoralis
The life cycle is more complex than that of other nematodes. Penetration of skin by infective filariform larvae in the soil causes infection. Larvae enter the circulation and migrate to the lungs, penetrate the alveolar spaces, move up the trachea, and are swallowed. Maturation to adult worms occurs in the small intestine. Female worms lay down eggs (parthenogenesis). Eggs hatch to release rhabditiform larvae in the small intestine, which are excreted along with feces (Sometimes, rhabditiform larvae can mature into filariform larvae, which penetrate mucosa, or perianal skin and enter the circulation; this is called as autoinfection). Maturation of rhabditiform larvae to infective filariform larvae occurs in soil, which can penetrate the skin and cause infection. If this does not happen, larvae develop into adult male and female worms which mate and lay down eggs, from which rhabditiform larvae are released which further mature into infective filariform larvae.
- Redness and itching at the site of penetration of filariform larva.
- Loeffler’s syndrome due to the migration of the larva through the lungs.
- Heavy infection can cause abdominal pain, diarrhea, and malabsorption.
- Chronic infection causes abdominal pain, diarrhea, and urticaria.
- In immunocompromised persons, potentially fatal hyper-infection (secondary to auto-infection) can occur causing severe pneumonia, neurologic complications, abdominal pain, shock, and septicemia.
Identification of larvae of S. stercoralis:
Diagnosis of S. stercoralis infection depends on the demonstration of rhabditiform larvae in fresh stool specimens. Eggs of S. stercoralis are rarely seen in stool samples because they hatch and release rhabditiform larvae in the intestine. Rhabditiform larvae are 200-300 μ in length and 15 μ in width and are actively motile. They have two esophageal swellings, a prominent genital primordium, and a short buccal cavity. Sometimes, in old fecal samples, rhabditiform larvae of hookworms are seen which resemble those of S. stercoralis; the differentiating feature is the longer buccal cavity of the former.
Excretion of larvae is often irregular and their number may be few. Therefore, a fecal examination may yield the negative result. In suspected cases, concentration technique (formol-ethyl acetate) is helpful.
Duodenal fluid can be aspirated for detection of larvae or Entero-test (String test) can be performed. (Entero-test: A commercially available gelatin capsule consists of a textured string. One end of the string is attached or taped to the cheek and the capsule is then swallowed. The end of the string reaches and is exposed in the duodenum after several hours. After removal, the terminal part of the string should be bile-stained. The mucus from the end of the string is wiped onto a glass slide and examined for larvae). In disseminated infection, larvae may be detected in sputum.
Enzyme immunoassay test that detects IgG antibodies to S. stercoralis is available and is indicated if the organism is not detected in feces, duodenal aspirate, or string test and clinical suspicion is strong. It cannot differentiate between recent and past infection.
E. vermicularis is also called as pinworm, seatworm, or oxyurids. It is distributed worldwide. Infection is common in children. Mode of transmission is ingestion of food or water contaminated with infective eggs through fingers.
Life cycle of E. vermicularis
After ingestion, eggs hatch to release larvae in the intestine. Larvae mature to the adult worms in the cecum or appendix. Female worms migrate at night to the perianal skin to deposit up to 15,000 eggs. Marked irritation at the site leads to contamination of fingers through scratching which causes self-infection by transferring eggs to the mouth. Enterobiasis can also be acquired by handling contaminated clothes, linen, etc.
Intense nocturnal perineal or perianal itching is usual. Acute appendicitis can occur due to the presence of the worm in the appendix. Sometimes, the worm can invade female genital tract leading to vulvovaginitis, and formation of pelvic and peritoneal granulomas.
Special technique for collection and demonstration of pinworm eggs: Adult female pinworm migrates at night from the intestine (cecum) to the perianal skin and deposits eggs. Pinworm eggs are, therefore, detected in perianal skin folds and are often not found on routine stool examination. Pinworm eggs can be collected either by a transparent adhesive tape (“cellophane tape test”) or by anal swab. Specimen should preferably be collected late into the night or early morning before patient passes urine, feces, or takes a bath.
A transparent adhesive tape is folded over the end of a glass slide, spoon handle or a wooden tongue depressor (sticky surface outwards). Patient’s buttocks are separated and the slide or spoon handle covered with tape is pressed over the perianal skin at many sites. The tape is then spread over a glass slide with adhesive side down and pressed flat onto the slide surface. Slide covered with tape is then examined under the microscope.
In another method, a cotton swab is rubbed around the anus and then rinsed in a test tube containing 0.5 ml saline. The fluid is drawn in a pipette; a drop is placed on a glass slide and observed under the microscope with reduced illumination.
Diagnosis depends on the demonstration of eggs in samples collected from perianal skin (transparent adhesive tape method) or demonstration of adult worms. Eggs of E. vermicularis measure 60 μ × 30 μ in size, are oval and flattened on one side. They are colorless, transparent with a double-lined smooth shell, and contain a small granular mass (Figure 1181.8) or a larva. Adult pinworms may be recovered from perianal skin folds (by adhesive tape) or may be found in children’s feces. They are white, motile, and small in size (male: 0.5 cm; female: 1 cm).
T. solium occurs mainly in India, Pakistan, China, S. Africa, and Latin America. It is transmitted by ingestion of raw or undercooked pork containing infective cysticercus larvae (cysticercus cellulose).
Life cycle of T. solium
Infection is acquired by ingestion of raw or undercooked pork containing infective encysted cysticercus larva by a man who is a definitive host. Scolex of cysticercus is freed and attaches to the wall of the intestine by its suckers and hooks. Development of cysticercus into an adult tapeworm occurs by addition of multiple segments or proglottids to the scolex. Length of the adult tapeworm is about 2-7 meters. Each proglottid is a functional hermaphroditic reproductive unit, which produces numerous eggs. The egg-filled segment at the end of the worm detaches itself from the worm and releases eggs in feces; segment is also excreted. Eggs contaminate the soil and are ingested by the pigs (intermediate hosts) while feeding. Embryo (released from the egg) penetrates the intestinal wall of the pig and is carried through the bloodstream to the muscles where it develops into infective cysticercus larvae.
Man can become an intermediate host if he eats food contaminated with eggs or if there is self-contamination (through contaminated fingers). In such an event, embryo enters the bloodstream and cysticercus develops at any body site.
- Intestinal infection: Clinical features are usually insignificant. The patient may notice the passage of a flat segment of the worm in feces.
- Cysticercosis: This occurs if the man accidentally ingests food contaminated with T. solium eggs (or if there is autoinfection). Nodules containing cysticercus develop in skeletal muscle, subcutaneous tissue, heart, liver, brain, etc. Cysticercus (or bladder worm) is a small cyst (< 1.5 cm) containing clear fluid and inverted scolex.
- Involvement of brain (neurocysticercosis) can cause seizures (neurocysticercosis is a common cause of epilepsy in endemic areas in children), raised intracranial tension (due to obstruction to cerebrospinal fluid flow by intraventricular cysts), psychiatric disturbances, and localizing signs; sometimes sudden death can occur.
1. Examination of feces:
- Identification of eggs: Morphologically, eggs of T. solium and T. saginata are identical. The distinction between the two species requires examination of proglottids or scolices. Egg measures 30-40 μ in diameter, is round to oval and has a thick, brown wall with transverse lines. The egg contains an embryo, which is a round granular mass containing 3 pairs of hooklets and surrounded by a fine membrane (Figure 1181.9). Occasionally, the egg is enclosed in a clear sac. Eggs are discharged intermittently by the tapeworm and therefore may not be detected easily. Repeated stool examinations and formol-ether concentration technique are often required for their demonstration.
- Identification of gravid segments or proglottids: This allows identification of species. The segment is flattened between two glass slides and examined under a magnifying glass. Gravid segment is 13 mm × 8 mm in size, translucent, and pale blue. It has a central uterine stem with 8-13 lateral branches. (Uterine branches are >13 in T. saginata).
- Identification of scolex (head): Scolex of a tapeworm is very small (pinhead size) and is rarely seen. When examined with a magnifying glass, scolex of T. solium shows 4 suckers and a crown of hooklets.
2. Diagnosis of cysticercosis:
Cysticercosis can be diagnosed by serologic tests, radiologic studies, and biopsy of the lesion.
Indirect hemagglutination assay has the sensitivity of about 80%. A titer of ≥ 1:64 indicates cysticercosis. Newer glycoprotein immunoblot assay is more sensitive and specific for the diagnosis of neurocysticercosis. X-ray is helpful in detecting calcified cysts. Computed tomography scans are helpful in diagnosing neurocysticercosis.
T. saginata (beef tapeworm) has the worldwide distribution with particularly high prevalence in the Middle East, Africa, Asia, and Latin America. Mode of transmission is eating raw or undercooked beef (containing infective cysticercus bovis larvae).
Life cycle is similar to that of T. solium except (i) animal host is cattle, (ii) eggs are not infectious to humans and therefore human cysticercosis does not occur after ingestion of eggs, and (iii) segments of T. saginata also migrate to the perianal skin and deposit eggs.
These are usually insignificant. Sometimes abdominal pain and diarrhea can occur.
- Identification of eggs: Eggs of T. saginata can be identified in feces and perianal skin. They are morphologically similar to those of T. solium.
- Identification of gravid segments: Segments measure 20 mm × 6 mm in size, and are ivory white. They contain a central uterine stem with more than 13 side branches (i.e. 15-20 branches).
- Identification of head or scolex: Scolex of T. saginata has 4 suckers but no hooklets. It measures 2 mm in width. Various laboratory tests for diagnosis of parasitic infection of intestine are summarized in Table 1181.2.
|1. Direct saline mount||Trophozoites, cysts, ova, and larvae|
|2. Direct iodine mount||Protozoal cysts|
|3. Faecal concentration||Recovery of protozoal cysts, helminth ova and larvae|
|4. Cellophane tape technique||Ova of Enterobius vermicularis|
|5. Trichrome stain of fecal smear||Protozoal cysts and trophozoites|
|6. AFB stain of fecal smear||Oocysts of Cryptosporidium, Cyclospora, and Isospora|
|7. Detection of antigen in random stool sample||E. histolytica, G. lamblia, Cryptosporidium|
|8. Molecular methods based on polymerase chain reaction on stool sample||E. histolytica, G. lamblia, Cryptosporidium, Microsporidia, Cyclospora|
|9. Serologic methods||E. histolytica, S. stercoralis, Cysticercus|