Cutaneous larva migrans
Salient features
·
Due to larvae of animal hookworms (intestinal nematodes)
·
Skin lesions are serpiginous and pruritic, representing the
paths of migration of organisms within the epidermis
·
The rate of migration is 1–2 cm per day
·
Self-limited disease
Introduction
Cutaneous larva migrans is a
serpiginous cutaneous eruption caused by the accidental penetration and
migration of animal hookworm larvae through the epidermis. The prime features,
as the name suggests, are that the lesions creep or migrate, and that they are
due to the presence of moving parasites in the skin. The infection has a
worldwide distribution and occurs most frequently in warmer climates. The skin
lesions are usually self-limited.
Causative
organisms
Cutaneous larva migrans is caused
by the larvae of hookworms that infect domestic dogs and cats, most often Ancylostoma braziliense or A. caninum and occasionally Uncinaria stenocephala or Bunostomum phlebotomum.
Adult hookworms live in the
intestines of dogs and cats, and their ova are deposited in the animals’ feces.
Under favorable conditions of humidity and temperature, the ova hatch into
infective larvae, which will penetrate human skin. The infection is usually
acquired by walking barefoot on ground contaminated with animal feces, but the
buttock or other body sites can become infected via contact with contaminated
soil or sand. The larvae enter the skin and begin a prolonged process of
migration within the epidermis. With rare exceptions, the parasite remains
confined to the epidermis, producing visible tracts and intense pruritus. The
parasite lacks collagenase, which is necessary to disrupt the basement
membrane.
Clinical
features
The larvae may cause a pruritic erythematous papule in a few hours at the point of entry where
the skin has been in contact with infected soil. This is commonly the feet,
hands and buttocks. They can then lie quiet for weeks or months, or immediately
begin creeping activity with the production of a wandering thread‐like serpiginous “tracts”. Typically
one to three such serpiginous lesions, 3 mm wide and up to 20 cm in length are
present. This is exceedingly itchy, slightly raised, flesh‐colored or pink. In severe
infections, hundreds of such lesions may be found on a single patient. The pathognomonic garland or zigzag-shaped
inflammatory stripes becomes visible at the beginning of larval migration.
The larvae advance at a rate of a few millimeters
to a few centimeters daily, and in some a
blister is seen that marks the head of the tract. If untreated, a single larval
tract may progress, then disappear for a few days, reappear, advance some more,
and so on, for weeks or months, after which time it will spontaneously resolve.
The wanderings of an individual larva are usually confined to a relatively
small area, but exceptionally it travels much further. Due to intense pruritus
and scratching, superimposed bacterial infections and dermatitis may complicate
the clinical picture. In later stages, these tracks are difficult to see, the
path being marked by small itchy nodules.
The
disease is self‐limiting. Estimates for the natural duration of the disease
vary considerably. This variation almost certainly depends on the species of
larva observed, and this is usually unknown.
Larva migrans can be accompanied by Loeffler syndrome of pulmonary eosinophilia, particularly in severe infestations.
Differential
diagnosis
The
main differential diagnosis is the larva currens (‘running larva’) of
strongyloidiasis. The main distinguishing factor between the two diseases is
the speed at which the larvae travel. Larva currens is
known for its distinct rapidity, with the larval track progressing at
approximately 0.2 cm/min, with cutaneous lesions progressing up to 5–15 cm/h.
In cutaneous larva migrans, the larval track progresses at approximately 1 cm/h
with cutaneous lesions only progress a few millimeters to a few centimeters daily.
Diagnosis
The classic clinical picture of
wandering, advancing, serpentine and itchy lesions is easily recognized, but
may be atypical, hidden by vesicles and scaling, or spoiled by scratching and
secondary infection.
Biopsy in larva migrans is of little value, as the larvae
have advanced beyond the clinical lesions.
Treatment
Although cutaneous larva migrans is
self-limited, its potential complications (e.g. impetigo and allergic
reactions), together with the intense pruritus and the significant duration of
the disease (sometimes several months), usually necessitate treatment.
Antihelminthic treatment is warranted
to relieve symptoms and reduce the likelihood of secondary bacterial infection.
Ivermenctin is the preferred treatment, and is given at 200 μg/kg PO × 1 or 2
days. Albendazole 400 mg/day PO to adults and children >2
years of age for 3 days is also effective,
although in some cases the responses are poor.
Topical 10–15% thiabendazole solution may have benefit for
localized disease, but it requires application three times daily for at least
15 days. This therapy
leads to healing in 90% of cases. The local treatment must be carried out over
a large area beyond the larval duct, as the larvae often sit in front of the
visible duct.
Freezing the
leading edge of the skin track (cryotherapy) has been suggested, but this
modality is rarely sufficient.
Therapeutic ladder
First line
·
Ivermectin 200 μg/kg orally once
daily for 1 or 2 days
Second line
·
Albendazole 400 mg orally for 3 days