Q4
LONG ANSWER
10M
★ High-yield
Describe lymphatic filariasis with its life cycle, clinical features, laboratory diagnosis and control.
The Parasites and Their Vectors
| Parasite | Vector | Disease and distribution |
|---|---|---|
| wuchereria bancrofti | CULEX quinquefasciatus, which breeds in dirty stagnant water, drains and cesspits — hence its association with poor urban sanitation | Lymphatic filariasis; over 95% of Indian cases. Endemic across Uttar Pradesh, Bihar, Jharkhand, Odisha, Andhra Pradesh, Tamil Nadu and West Bengal |
| BRUGIA malayi | Mansonia, which breeds in ponds with aquatic vegetation such as Pistia | Lymphatic filariasis, chiefly below the knee; Kerala, Tamil Nadu and coastal areas |
| onchocerca volvulus | Blackfly (Simulium), breeding in fast-flowing rivers | "river blindness" — subcutaneous nodules, severe itching and keratitis; Africa, not India |
| Loa loa | Deer fly (Chrysops) | Calabar swellings; the adult worm visibly crosses the conjunctiva; West Africa |
| Dracunculus medinensis | Cyclops in water | Guinea worm — eradicated from India in 2000 |
- Man is the only definitive host of W. Bancrofti, and there is no animal reservoir — which is exactly what makes elimination feasible
- Nocturnal periodicity — microfilariae appear in the peripheral blood between about 10 pm and 2 am and are sequestered in the pulmonary capillaries by day. This coincides with the biting habit of Culex, and it dictates that blood for microfilariae must be collected at night — a major practical constraint on surveys
- The adult worms live in the lymphatics, particularly the lower limb, inguinal and scrotal vessels, for 5 to 10 years, releasing microfilariae into the blood
- wolbachia, an endosymbiotic bacterium within the worm, is essential to its fertility and survival, and contributes to the inflammatory response. This is why doxycycline — an antibiotic — is an effective antifilarial, killing the symbiont and sterilising the adult worm
CLINICAL PEARL
An antibiotic kills a worm because the worm cannot live without its bacterium. Wolbachia lives inside the filarial worm and is required for its fertility and long-term survival. A course of doxycycline therefore sterilises and eventually kills the adult worm — something no conventional antifilarial does well — and does so gradually, avoiding the violent reaction that follows rapid microfilarial death.
Clinical Features
| Stage | Features |
|---|---|
| Asymptomatic microfilaraemia | The commonest state by far. The person is well but is the reservoir that infects mosquitoes. Subclinical lymphatic damage is already present and demonstrable by lymphoscintigraphy |
| Acute adenolymphangitis (ADL) | Recurrent episodes of fever with painful lymphadenitis and retrograde lymphangitis — spreading down the limb from the node, unlike bacterial lymphangitis which spreads UP. Funiculitis, epididymo-orchitis and orchitis. Most acute episodes are in fact precipitated by secondary bacterial infection of damaged skin |
| Chronic obstructive disease | Develops after years: lymphoedema progressing to elephantiasis of the leg, scrotum, arm or breast; hydrocele, which is the commonest chronic manifestation of W. Bancrofti; chyluria from rupture of lymphatics into the urinary tract; and lymph scrotum |
| Tropical pulmonary eosinophilia (TPE) | A hypersensitivity response to microfilariae trapped in the lungs. Nocturnal cough and wheeze mimicking asthma, with massive eosinophilia (often above 3,000/mm3), very high IgE and filarial antibody, and miliary mottling on the chest radiograph. Microfilariae are absent from the blood, because they are all being destroyed in the lung. It responds dramatically to diethylcarbamazine, which is diagnostic in itself |
- Elephantiasis is caused by the host response, not by the worm obstructing the vessel — repeated inflammation, lymphangiectasia, incompetent valves and secondary bacterial infection produce progressive fibrosis. This is why killing the worms does not reverse established elephantiasis, and why management of the chronic stage is hygiene and physiotherapy rather than drugs
Laboratory Diagnosis
- Blood film for microfilariae, taken at night; a thick film stained with Giemsa. Distinguishing the species depends on the sheath and the arrangement of nuclei in the tail: W. Bancrofti is sheathed with NO nuclei in the tail tip, whereas B. Malayi is sheathed with two separate terminal nuclei
- Concentration methods — the KNOTT technique (centrifugation in 2% formalin) and membrane filtration, both far more sensitive than a direct film
- DEC provocation test — a small daytime dose of diethylcarbamazine draws microfilariae into the peripheral blood within an hour, allowing a daytime specimen
- Circulating filarial antigen (ICT card test, Og4C3) — detects adult worm antigen, is positive whether or not microfilariae are present, and can be done at any time of day. It has replaced night blood surveys in the elimination programme and is the most important practical advance
- Ultrasound — the "filarial dance sign", the characteristic writhing movement of live adult worms within a dilated scrotal lymphatic, which is diagnostic and allows treatment to be monitored
- Other — PCR; lymphoscintigraphy; eosinophilia and raised IgE; demonstration of microfilariae in hydrocele fluid, chylous urine or a node aspirate
Differentiating the Microfilariae
| Feature | W. Bancrofti | B. Malayi | Onchocerca |
|---|---|---|---|
| Sheath | Present | Present, staining pink with Giemsa | Absent |
| Nuclei in the tail tip | Absent — the tail tip is free of nuclei | Two distinct terminal nuclei, separated from the rest | Absent |
| Body curve | Graceful, sweeping curves | Kinked, with secondary crinkles | Sharply bent tail |
| Periodicity | Nocturnal | Nocturnal (a subperiodic form exists) | None — found in skin snips, not blood |
| Vector | Culex | Mansonia | Simulium blackfly |
| Site of adult | Lymphatics | Lymphatics | Subcutaneous nodules (onchocercomas) |
Treatment, Control and Applied Aspects
- Diethylcarbamazine (DEC) is the mainstay in India, killing microfilariae rapidly and adults partially; ivermectin is microfilaricidal; albendazole is added for its effect on adults; and doxycycline for 4 to 6 weeks kills Wolbachia and with it the adult worm
- Rapid microfilarial death provokes a reaction — the mazzotti reaction with fever, headache, itching and lymphadenitis; it is managed with antihistamines and analgesics and is not an allergy to the drug
- DEC is contraindicated where onchocerciasis or loiasis may coexist, because rapid microfilarial death causes blindness in the former and fatal encephalopathy in the latter — which is why African programmes use ivermectin instead
- Mass drug administration (MDA) — annual single-dose DEC plus albendazole to the entire population at risk, for at least 5 years, aiming to suppress microfilaraemia below the level that sustains transmission. This is the core of India's National Filaria Elimination Programme, together with DEC-fortified salt in some areas
- Morbidity management is the other half of the programme, and it is what helps those already affected: washing the limb daily with soap and water, careful skin and nail care, treating entry lesions and fungal infection, elevation, exercise and compression — all of which reduce acute attacks substantially, because most attacks are bacterial. Hydrocelectomy is offered surgically
- Vector control — improving drainage and sanitation to deny Culex its breeding sites, and removing aquatic weed for Mansonia; personal protection with nets and repellents
- Elimination is achievable because man is the only host, an effective single-dose regimen exists, and a field antigen test allows mapping; India has made substantial progress and many districts have stopped mass drug administration after passing transmission assessment surveys
- Limb hygiene reduces acute attacks more than any drug, because most acute episodes are bacterial infections of damaged skin rather than filarial activity — and washing with soap and water costs nothing
- Killing the worms does not reverse elephantiasis; patients must be told this honestly, and offered morbidity management rather than repeated courses of DEC
- The antigen test can be done by day, which removed the single greatest practical obstacle to filariasis surveys and made mapping feasible at scale
- Consider tropical pulmonary eosinophilia in nocturnal asthma with a very high eosinophil count and no microfilariae; the response to DEC is dramatic and confirms the diagnosis
- Hydrocele is the commonest chronic manifestation in India and is surgically curable, so filariasis programmes include hydrocelectomy alongside drug distribution
- Retrograde lymphangitis distinguishes filarial from bacterial lymphangitis — the filarial streak spreads down the limb from the node, the bacterial one spreads UP toward it
- DEC must not be used where onchocerciasis or loiasis is possible, which matters for Indians returning from work in Africa; ivermectin is used instead
- Collect night blood or use the antigen card; a daytime blood film for microfilariae is a wasted specimen unless the DEC provocation test is used
- The filarial dance sign on scrotal ultrasound shows living adult worms and is both diagnostic and a way of confirming that treatment has worked
- Doxycycline works by killing the worm’s bacterial symbiont, and is the only widely available agent that reliably kills adult worms — slowly enough to avoid a severe reaction
- Asymptomatic microfilaraemic people are the reservoir, which is why mass drug administration treats everyone rather than only those with symptoms
- The Mazzotti reaction is not a drug allergy but the response to dying microfilariae; it is managed symptomatically and does not contraindicate future treatment
- Culex breeds in dirty stagnant water, so filariasis control is a sanitation and drainage problem as much as a drug problem
- Five annual rounds of mass drug administration with adequate coverage are needed before transmission assessment surveys can be attempted, so programme continuity matters more than intensity in any single year
All questions in Parasitology II — Helminths
- Q1Classify the helminths and describe their general features. Describe the intestinal tapeworms with their diagnosis and treatment. ★
- Q2Describe cysticercosis and hydatid disease with their pathogenesis, diagnosis and management. ★
- Q3Describe the intestinal nematodes with their life cycles, clinical features and treatment. ★
- Q4Describe lymphatic filariasis with its life cycle, clinical features, laboratory diagnosis and control. ★
- Q5Describe the trematodes with their general features. Discuss schistosomiasis and the food-borne flukes. ★
- SN1Describe Enterobius vermicularis with its transmission, diagnosis and treatment. ★
- SN2Describe cutaneous and visceral larva migrans with their causes and management. ★
- SN3Describe Trichinella spiralis with its life cycle, clinical features and diagnosis. ★
- SN4Describe Dracunculus medinensis and the eradication of guinea worm from India. ★
- SN5Describe the soil-transmitted helminths and the national deworming programme. ★
- SN6Describe eosinophilia in helminth infection and the approach to a patient with eosinophilia. ★
- SN7Describe eosinophilic meningitis and the food-borne zoonotic helminths.