ARTICLE
A 27-year-old Caucasian woman was admitted to our Institute because of
a nodular lesion localized on the sole of the left foot. The patient stated
that she was in good general health, that she was not on any medication
and that she had just returned a few days earlier from a trip to Madagascar,
where the nodular lesion had probably developed. The lesion was round,
0.5 cm in diameter, yellowish in colour, with well-defined borders (Fig.
1), hard in consistency and painful. It was diagnosed by the patient's
general doctor as a viral wart.
Tungiasis
A close examination of the lesion revealed a tiny central opening (Fig.
1), from which a small amount of sero-haematic fluid oozed: it
contained numerous oval-shaped, white "bodies" that, on direct microscopic
examination, were found to be eggs of Tunga penetrans L. (Fig.
2). Enlarging the opening by means of the tip of a scalpel, it
was possible to remove portions of the body of the flea, numerous other
eggs and necrotic material. The residual cavity was subjected to surgical
debridement. Topical gentamicin (twice a day for 10 days) was prescribed.
The lesion healed without any sequelae.
Discussion
Tunga penetrans L. is a flea that lives in Central and South
America, sub-Saharan Africa and Central Asia. In Europe, only imported
cases of tungiasis have been described so far [1-17], the majority of
which by French [2, 4-6, 13, 16], German [1, 7-9] and Italian authors
[10-12, 17].
The natural habitat of Tunga penetrans L. is represented by the
sandy and warm soil of deserts and beaches; furthermore, the flea lives
in stables and stock farms, as well as in soil and dust close to farms.
Tunga penetrans L. is a parasite of the skin. Apart from man,
this flea can also infest pigs, dogs, cats, sheep, horses, mules, cattle,
rats, mice and even gorillas in captivity.
Both the male and female are haematophagous.
After coupling, the male dies. To complete the life cycle, which lasts
just over one month and consists of four stages (egg, larva, pupa, adult),
the fertilized female penetrates the skin. The mechanism by which the
flea penetrates is not known: it is assumed that the flea liberates keratolytic
enzymes. In the skin the flea burrows a cavity with the head turned towards
the upper dermis, in order to feed on the host's blood, by means of a
well-developed buccal apparatus. Only the end portion of the abdomen extrudes.
Soon after penetration, the flea begins to produce eggs; the abdomen enlarges
markedly: it can reach a diameter of 1 cm (the male and the non-fertilized
female are about 1 mm long). Ovaries contain up to 200 eggs. Eggs and
excrements are eliminated to the outside through a small foramen in the
epidermis, in the proximity of the insect's anal opening; this foramen
also allows respiration. The eggs are laid on the ground, where they natch
in 3-4 days, liberating larvae. At this stage, the adult dies. After 10-15
days, the larvae develop into pupae, that after 7-15 days become adults.
Characteristic localizations of tungiasis are toes, particularly peri-
and subungual folds, interdigital spaces, sole and heel. Walking may be
markedly limited. Other possible sites of infestations are the legs, knees,
thighs and hands. All the other sites are rare.
Infestation by Tunga penetrans L. is
characterized clinically by the slow appearance of papular or nodular
lesions, either single or multiple (very rare cases with hundreds of lesions
have been described), white or greyish or yellowish in colour, with a
brown-black central tip that corresponds to the posterior portion of the
flea. These lesions may be more or less erythematous, occasionally covered
by brownish-black crusts; sometimes they are ulcerative or pustular d'emblée.
The penetration of the tunga is asymptomatic: only when the insect increases
in size do inflammatory and necrotic phenomena develop leading to pruritus
and/or pain.
As shown by this case and others [14], the differential diagnosis includes
mainly viral warts: a biopsy for histopathological examination is sometimes
necessary.
With the exception of superinfections, mainly caused by Staphylococcus
aureus and Gram negative bacteria, and the risk of tetanus, complications
of tungiasis are uncommon: however, cases of gangrene, spontaneous amputation
of the toes, lymphangitis, lymphadenitis and sepsis have been described.
Histopathological examination shows hyperkeratosis and acanthosis. The
body of the insect is localized in the epidermis and upper dermis: it
is enclosed in a pseudocystic cavity. Inside the cavity, annular-shaped
digestive and respiratory organs and egg-laden ovaries are present. Eggs
are round or oval, with a thickened wall and a pale centre. A perilesional
inflammatory infiltrate with lymphocytes, neutrophils and, especially
eosinophils is present.
Treatment consisting the surgical removal of the papular/nodular lesion
or removal of the flea, possibly intact, by enlarging the orifice with
a needle or the tip of a scalpel and exerting pressure at the sides. The
residual cavity should then undergo surgically cleaned. Thereafter, it
is necessary to apply a topical antibiotic. Also useful is anti-tetanus
prophylaxis. Systemic antibiotics are necessary if numerous and/or pustular
lesions are present. Fairly good results have also been reported with
electrodesiccation and cryotherapy, while the application of chloroform,
ether, formaldehyde and petrolatum is anecdotal. Prophylaxis consists
in avoiding walking barefoot in endemic areas and the use of insecticides.
CONCLUSION
1. Borelli S, Müller E. Tungiasis in der poliklinischen Sprechstunde
in München. Hautartz 1962; 13: 23-5.
2. Bazex A, Salvador R, Dupré A, Vitas P, Balas D. Sarcopsyllose
(Tungiasis) ou puce chique d'origine péruvienne. Bull Soc Fr
Dermatol Syphil 1968; 75: 143-6.
3. Tan-Lim KN, Pluis AHG. Tungiasis. Dermatologica 1971; 143:
245-6.
4. Lèques B, Comby F, Seurat P, Bullier R, Josseran R. Présentation
de photos cliniques et parasitologiques d'un cas bordelais importé
de Tungose. Bull Soc Fr Dermatol Syphil 1973; 80: 152-3.
5. Laugier P. Tungose africaine. Bull Soc Fr Dermatol Syphil
1974; 81: 597-8.
6. Laugier P, Hunziker N, Orusco M, Brun R, Reiffers J, Posternak F.
Tungose africaine. Dermatologica 1975; 150: 222.
7. Bäurle G, Stroothenke M. Tungiasis eine "Urlaubsdermatose".
Hautarzt 1981; 32: 372-3.
8. Peschlow I, Schlenzka K, Merk G, Neumann HJ. Tropendermatosen aktuell
Tungiasis, Ulcus tropicum, Leishmaniase Beobachtungen aus der Praxis.
Dermatol Monatsschr 1983; 169: 120-4.
9. Schuller-Petrovic S, Mainitz M, Böhler-Sommeregger K. Tungiasis
eine immer häufigere Urlaubsdermatose. Hautarzt 1987;
38: 162-4.
10. Fimiani M, Reimann R, Alessandrini C, Miracco C. Ultrastructural
findings in tungiasis. Int J Dermatol 1990; 29: 220-2.
11. Trevisan G, Pauluzzi P, Kokelj F. Tungiasis: report of a case. J
Eur Acad Dermatol Venereol 1992; 1: 73-5.
12. Carabelli A, Di Vincenzo R, Vanotti P, Bertani E. La tungose. Nouv
Dermatol 1992; 11: 826.
13. Bolzinger T, Beylot-Barry M, Babin B, Beylot C. Cas pour diagnostic.
Ann Dermatol Venereol 1994; 121: 55-6.
14. Wardhaugh AD, Norris JF. A case of imported tungiasis in Scotland
initially mimicking verrucae vulgaris. Scott Med J 1994; 39: 146-7.
15. Douglas-Jones AG, Llewelyn MB, Mills CM. Cutaneous infection with
Tunga penetrans. Br J Dermatol 1995; 133: 125-7.
16. Caumes E, Carriere J, Guermonprez G, Bricaire F, Danis M, Gentilini
M. Dermatoses associated with travel to tropical countries: a prospective
study of the diagnosis and management of 269 patients presenting to a
tropical disease unit. Clin Infect Dis 1995; 20: 542-8.
17. Veraldi S, Camozzi S, Scarabelli G. Tungiasis presenting with sterile
pustular lesions on the hand. Acta Derm Venereol (Stockh) 1996;
76: 495.
REFERENCES
1. Borelli S, Müller E. Tungiasis in der poliklinischen Sprechstunde
in München. Hautartz 1962; 13: 23-5.
2. Bazex A, Salvador R, Dupré A, Vitas P, Balas D. Sarcopsyllose
(Tungiasis) ou puce chique d'origine péruvienne. Bull Soc Fr
Dermatol Syphil 1968; 75: 143-6.
3. Tan-Lim KN, Pluis AHG. Tungiasis. Dermatologica 1971; 143:
245-6.
4. Lèques B, Comby F, Seurat P, Bullier R, Josseran R. Présentation
de photos cliniques et parasitologiques d'un cas bordelais importé
de Tungose. Bull Soc Fr Dermatol Syphil 1973; 80: 152-3.
5. Laugier P. Tungose africaine. Bull Soc Fr Dermatol Syphil
1974; 81: 597-8.
6. Laugier P, Hunziker N, Orusco M, Brun R, Reiffers J, Posternak F.
Tungose africaine. Dermatologica 1975; 150: 222.
7. Bäurle G, Stroothenke M. Tungiasis eine "Urlaubsdermatose".
Hautarzt 1981; 32: 372-3.
8. Peschlow I, Schlenzka K, Merk G, Neumann HJ. Tropendermatosen aktuell
Tungiasis, Ulcus tropicum, Leishmaniase Beobachtungen aus der Praxis.
Dermatol Monatsschr 1983; 169: 120-4.
9. Schuller-Petrovic S, Mainitz M, Böhler-Sommeregger K. Tungiasis
eine immer häufigere Urlaubsdermatose. Hautarzt 1987;
38: 162-4.
10. Fimiani M, Reimann R, Alessandrini C, Miracco C. Ultrastructural
findings in tungiasis. Int J Dermatol 1990; 29: 220-2.
11. Trevisan G, Pauluzzi P, Kokelj F. Tungiasis: report of a case. J
Eur Acad Dermatol Venereol 1992; 1: 73-5.
12. Carabelli A, Di Vincenzo R, Vanotti P, Bertani E. La tungose. Nouv
Dermatol 1992; 11: 826.
13. Bolzinger T, Beylot-Barry M, Babin B, Beylot C. Cas pour diagnostic.
Ann Dermatol Venereol 1994; 121: 55-6.
14. Wardhaugh AD, Norris JF. A case of imported tungiasis in Scotland
initially mimicking verrucae vulgaris. Scott Med J 1994; 39: 146-7.
15. Douglas-Jones AG, Llewelyn MB, Mills CM. Cutaneous infection with
Tunga penetrans. Br J Dermatol 1995; 133: 125-7.
16. Caumes E, Carriere J, Guermonprez G, Bricaire F, Danis M, Gentilini
M. Dermatoses associated with travel to tropical countries: a prospective
study of the diagnosis and management of 269 patients presenting to a
tropical disease unit. Clin Infect Dis 1995; 20: 542-8.
17. Veraldi S, Camozzi S, Scarabelli G. Tungiasis presenting with sterile
pustular lesions on the hand. Acta Derm Venereol (Stockh) 1996;
76: 495.
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