ARTICLE
A 25-year-old German female presented with an indurated, 1.1 x 2.0 cm
nodule on the left cheek (Fig.
1). The lesion was ulcerated and covered with a thick yellowish
crust. Multiple additional nodules were seen in a sporotrichoid distribution
on the right arm. The lesions arose 2 weeks before the initial appointment.
Interestingly, the patient, who had just returned from an archeological
expedition in Syria (Aleppo province), reported that similar lesions had
arisen in several other participants of the expedition.
Histologic findings
In Giemsa-stained tissue smears taken from the edge of the cheek ulcer
as well as in a biopsy taken from a nodule on the arm, typical Leishman-Donovan
bodies were seen in the cytoplasm of macrophages (Fig.
2).
Treatment and course
The patient was treated topically with 15% paromomycin sulfate (Humatin®)
in petrolatum, which was applied twice daily under occlusion. Although
the patient developed contact dermatitis caused by the wound dressing
(colophony resin), the lesions became less infiltrated and smaller in
size within the first week of treatment. Open application of the paromomycin
ointment was continued for another 3 weeks and then stopped, since the
lesions were flat and without any signs of activity (Fig.
3). Follow up examinations confirmed the healing of the infection.
Discussion
Leishmaniasis is caused by an intracellular protozoan parasite, which
is transmitted by bites of sandflies of the genus Phlebotomus.
Clinical features of the disease are determined by the species of Leishmania
as well as the immune response of the patients. Leishmaniasis may affect
skin, mucous membranes or even visceral organs.
Old World cutaneous leishmaniasis, also known as oriental sore, Aleppo
boil, Baghdad or Lahore sore is a chronic but usually self-limiting skin
infection. As indicated by the designations, the disease is endemic in
countries of the middle east. The morphologically identical species L.
tropica and L. major are the infectious agents in this geographical
region. New World cutaneous leishmaniasis, found in Latin America, has
similar clinical features, but is caused by different Leishmania
species.
Following an incubation period of a few weeks (infrequently up to 2
years), furuncle-like nodules arise at inoculation sites. Induration of
the flat ulcerated lesions is a characteristic feature. In immunocompetent
hosts, the disease is self-limiting. After 2-6 months the lesions heal
spontaneously and leave lifelong immunity [1]. Clinical diagnosis can
be confirmed by tissue smears or biopsies with the microscopic demonstration
of Leishman Donovan bodies in histiocytes. Although CL is a self-limiting
disease which does not necessarily require specific therapy, facial lesions
should be treated to avoid or to minimize possible scarring.
A wide range of treatment modalities for CL have been recommended including
indigenous plants, hyperthermia or cryotherapy, topical petroleum by-products,
antibiotics or antimalarials, topical or systemic ketoconazole or itraconazole,
systemic allopurinol, meglumine antimonate and gamma interferon [2-9].
Intralesional injection of sodium stibogluconate antimony has been recommended
as therapy of choice because of its efficacy, although this procedure
is often painful [10].
Recently, the therapeutic efficacy of a new
treatment modality for Old World CL, topical application of an ointment
containing paromomycin sulfate and methylbenzethonium chloride has been
confirmed in a double blind study [11, 12]. This combination seems to
be also effective in the treatment of New World CL [13-15], although in
mice infected with L. mexicana or L. panamensis this combination
failed to cure the lesions [16]. In some areas infested with Old World
leishmaniasis a preparation containing 15% paromomycin sulfate and 5%
methylbenzethonium chloride is commercially available.
Paromomycin (Humatin®) is an aminogylcoside antibiotic,
which is commonly used for reduction of normal and pathogenic microorganisms
of the gastrointestinal tract. Additionally, the substance is effective
in the treatment of intestinal amebiasis and various tapeworms. Methylbenzethonium
chloride is a quaternary ammonium compound which acts as a detergent as
well as an antiseptic and desinfectant.
Since we could not obtain this preparation quickly, we administered
15% paromomycin sulfate in petrolatum, which was readily available. The
impressive improvement of the lesions within 1 week and cure after 4 weeks
of treatment suggests that this monotherapy was effective. Therefore,
topical paramomycin monotherapy or combined with urea [11] may be recommended
as an inexpensive and effective treatment with minimum or no side effects
for cases in which a commercial preparation is not available. It should
be noted that, local treatment with paromomycin should be carried out
for at least 4 weeks or until the lesions clear, since a recent study
[17] failed to detect a benefit after 2 weeks of treatment.
REFERENCES
1. Canizares O, Harman R. Old World cutaneous leishmaniasis. In: Canizares
O, Harman RRM, eds. Clinical Tropical Dermatology. 2nd ed. Boston:
Blackwell Scientific Publ., 1992: 293-300.
2. Arana B, Navin T, Arana F, Berman J. Efficacy of a short course (10
days) of high dose meglumine antimonate with or without interferon gamma
in treating cutaneous leishmaniasis in Guatemala. Clin Infect Dis
1994; 18: 381-4.
3. Bassiouny A, Elmeshad M, Talaat M, Metawaa B. Cryosurgery in cutaneous
leishmaniasis. Brit J Dermatol 1982; 107: 467-74.
4. Brazilai A, Friedman J. Treatment of cutaneous leishmaniasis with
allopurinol. J Am Acad Dermatol 1995; 32: 518.
5. Momeni AZ, Aminjavaheri M. Treatment of recurrent cutaneous leishmaniasis.
Int J Dermatol 1995; 34: 129-33.
6. Memisoglu H, Kotogyan A, Alpaslan M. Ergotherapy in cases with leishmaniasis
cutis. J Europ Acad Dermatol Venerol 1995; 4: 9-13.
7. Norman L. Cutaneous leishmaniasis treated with controlled localized
heating. Arch Dermatol 1992; 128: 759-61.
8. Weigel MM, Armijos RX, Rucines RJ. Cutaneous leishmaniasis in subtropical
Equador: popular perception knowledge and treatment. Bull Pan Am Health
Organ 1994; 28: 142-55.
9. Van den Enden E, van Gompel A, Stevens A, Vandeghinste N, Le Ray
D, Gigase P, de Beule K, van den Ende J. Treatment of cutaneous leishmaniasis
with oral itraconazole. Int J Dermatol 1994; 33: 285-6.
10. Faris RM, Jarallah JS, Khoja TA, Al-Yamani MJ. Intralesional treatment
of cutaneous leishmaniasis with sodium stibogluconate antimony. Int
J Dermatol 1993; 32: 610-2.
11. Bryceson AD, Murphy A, Moody AH. Treatment of "Old World" cutaneous
leishmaniasis with aminosidine ointment: results of an open study in London.
Trans R Soc Trop Med Hyg 1994; 88: 226-8.
12. El-On J, Halevy S, Grunwald MH, Weinrauch L. Topical treatment of
Old World cutaneous leishmaniasis caused by Leishmania major: a
double blind control study. J Am Acad Dermatol 1992; 27: 227-31.
13. El Safi SH, Murphy AG, Bryceson A, Neal R. A double blind clinical
trial of the treatment of cutaneous leishmaniasis with paromomycin ointment.
Trans R Soc Trop Med Hyg 1990; 84: 690-1.
14. Krause G, Kroeger A. Topical treatment of American cutaneous leishmaniasis
with paromomycin and methylbenzethoniumchloride. Trans R Soc Trop Med
Hyg 1994; 88: 92-4.
15. Weinrauch L, Cawich F, Craig P, Sosa SJX, El-On J. Topical treatment
of New World cutaneous leishmaniasis in Belize: a clinical study. J
Am Acad Dermatol 1993; 29: 443-6.
16. Neal RA, Murphy AG, Olliaro P, Croft SL. Aminosidine ointment for
the treatment of experimental cutaneous leishmaniasis. Trans R Soc
Trop Med Hyg 1994; 88: 223-5.
17. Ben Salah A, Zakraoui H, Zaatour A, Ftaiti A, Zaafouri B, Garraoui
A, Olliaro PL, Dellagi K, Ben Ismail R. A randomized, placebo-controlled
trial in Tunisia treating cutaneous leishmaniasis with paromomycin ointment.
Am J Trop Med Hyg 1995; 53: 162-6.
|