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The New Zealand Medical Journal

 Journal of the New Zealand Medical Association, 31-March-2006, Vol 119 No 1231

Cutaneous larva migrans (hookworm) acquired in Christchurch, New Zealand
Laurens Manning, Stephen Chambers, Graeme Paltridge, Paul Maurice
Abstract
A case of cutaneous larva migrans is presented. The patient acquired the parasite in a suburban Christchurch property. A biopsy confirmed the clinical diagnosis. Cutaneous larva migrans is common in returned travellers from the tropics. It is rare in New Zealand, however. Presumably there were very specific, favourable local factors to allow maturation and transmission of the larva in this case.

Case report

An 80-year-old woman presented to the outpatient clinic with a 4-month history of an itchy migrating lesion on the skin of her right buttock. Five months prior to presentation, she noticed an intensely pruritic lesion on her buttock. This moved superiorly over the next 2 weeks before disappearing spontaneously. A similar lesion appeared 3 weeks later. There was no response to topical steroids or antifungals and 3 months later she was seen in our clinic with ongoing symptoms. The patient kept no pets of her own. She had not travelled overseas for more than 10 years, nor had she travelled to the North Island recently. There were no serious coexisting chronic illnesses. She was systemically well.
Examination revealed a linear, serpiginous lesion on the upper right buttock. The terminal portion of the lesion was marked by a raised 3–4 mm vesicle (Figure 1).
Figure 1. Serpiginous lesion of cutaneous larva migrans (hookworm) on the buttock
The patient was a keen gardener and had moved into a residence in suburban Christchurch 9 months previously. The house had a substantial vegetable garden that previous owners had covered with pea straw. Since moving into the house she had spent considerable time in the garden. Whilst kneeling on a garden cushion she would regularly rock back so that her buttocks would rest on her shoes or the ground.
A diagnosis of cutaneous larva migrans (CLM) was made. Strongyloides stercoralis and Toxocara canis serology was negative. There was no blood eosinophilia. The lesion was biopsied close to the terminal portion of the serpiginous lesion and she was given a course of oral albendazole, 400 mg daily for 3 days. The patient reported complete resolution of her symptoms and her lesion was not present 2 weeks later.
Microscopy of the skin biopsy (Figure 2) revealed a cross-section and longitudinal section of a larva in the epidermis. This was thought to be a single coiled larva. There was dermal oedema and an inflammatory infiltrate consisting mainly of lymphocytes and eosinophils.
The parasite measured 34 by 20 microns in cross section and 93 by 22 microns in longitudinal section. The cross section of the larva showed an intestine with a lumen, distinguishing it from infectious third-stage Strongyloides larvae that do not have an intestine. The longitudinal section revealed two alae. These are longitudinal ridges seen on the lateral aspect of the larva. The presence of double alae rather than a single ala excludes Toxocara as a cause for the lesion (G Paltridge, personal communication with MD Little, 2005).
The most likely pathologic diagnosis was the larva of an animal hookworm, but further speciation was not possible.

Discussion

Cutaneous larva migrans is caused by the third-stage larva of an animal hookworm that penetrates the epidermis after maturation in the soil. CLM usually presents in returning travellers from tropical and subtropical areas, particularly Africa, South East Asia, South America, the Caribbean, and Florida.1 However CLM can be acquired in more temperate climates where the soil and weather conditions are usually less favourable for larval survival and development.2 Indeed, cases and outbreaks have been described in Italy,1 England,3 Scotland,4 and Germany.5
In New Zealand (NZ), home-grown acquisition of CLM is rarely reported. Two cases of clinically diagnosed CLM in young children have been described in the northern town of Kaitaia.6 To our knowledge, no cases have been previously described in the cooler southern parts of the country.
Our patient acquired her infection in Christchurch and we assume there were very specific local factors to encourage the presence and survival of hookworm larvae. The pea straw mulch may have provided conditions suitable to the maturation of third-stage larvae, particularly if roaming dogs had defecated in this area. Whatever the origin of the larva, the patient had significant skin-to-soil exposure in her garden to account for the acquisition of CLM.
The exact causative organism remains uncertain as microscopic identification of hookworm larvae is difficult. There is limited literature regarding the prevalence of animal hookworms in NZ. Ancylostoma braziliense has not been identified in NZ dogs. Ancylostoma caninum was first identified in NZ dogs in 1976,7 but is only rarely identified in the faeces of dogs in northern areas. Uncinaria stenocephala is a relatively common infection of dogs in NZ especially where moist conditions around kennels encourage transmission. Infection of cats has not been reported in NZ.8
Whilst not life-threatening, CLM causes considerable distress and medical practitioners should be aware that the condition can occasionally be acquired in NZ.
Author information: Laurens Manning, Infectious Diseases Registrar, Chrsitchurch Hospital; Stephen Chambers, Infectious Disease Physician, Christchurch Hospital; Graeme Paltridge, Section Head, Bacteriology and Parasitology Laboratory, Canterbury Health Laboratories; Paul Maurice, Dermatologist, Christchurch Hospital; Christchurch
Acknowledgment: We gratefully acknowledge Dr M Dale Little (Emeritus Professor, Department of Tropical Medicine, Tulane University, New Orleans, USA) for assistance with hookworm larva identification.
Correspondence: Dr Laurens Manning, Infectious Diseases Registrar, Christchurch Hospital, Private Bag 4710, Christchurch. Fax: (03) 364 0952; email: laurens.manning@cdhb.govt.nz
References:
  1. Galanti B, Fusco FM, Nardiello S. Outbreak of cutaneous larva migrans in Naples, southern Italy. Trans R Soc Trop Med Hyg. 2002;96:491–2.
  2. Edelglass JW, Douglass MC, Stiefler R, Tessler M. Cutaneous larva migrans in northern climates. A souvenir of your dream vacation. J Am Acad Dermatol. 1982;7:353–8.
  3. Patterson CR, Kersey PJ. Cutaneous larva migrans acquired in England. Clin Exp Dermatol. 2003;28:671–2.
  4. Beattie PE, Fleming CJ. Cutaneous larva migrans in the west coast of Scotland. Clin Exp Dermatol. 2002;27:248–9.
  5. Klose C, Mravak S, Geb M, et al. Autochthonous cutaneous larva migrans in Germany. Trop Med Int Health. 1996;1:503–4.
  6. Bradley J. Home-grown cutaneous larva migrans. N Z Med J. 1999;112:241–2.
  7. Smith CF, Hooke FG. Letter: Ancylostoma in dogs. N Z Vet J. 1976;24:95–6.
  8. Wilks CR, Humble MW. Zoonoses in New Zealand: A combined veterinary and medical perspective. 2nd ed. Palmerston North: Publication No. 178 Veterinary Continuing Education, Massey University; 1997, p61.
     
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