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Mastocytosis-like Cutaneous Leishmaniasis:Unusual Presentation of Cutaneous Leishmaniasis

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Mastocytosis-like Cutaneous Leishmaniasis:

Unusual Presentation of Cutaneous Leishmaniasis

Letter To The Editor DOI: 10.6003/jtad.1481l1

Published: J Turk Acad Dermatol 2014; 8 (1): 1481l1. This article is available from: http://www.jtad.org/2014/1/jtad1481l1.pdf Key Words: Mastocytosis, Cutaneous leishmaniasis

To the Editor.- A 6-month-old male infant patient presented to our outpatient clinic due to red swel- lings in his abdomen, forehead and chin. Following the complaint that started in the form of a small swelling in the abdomen 2 months ago, similar swellings occurred beneath the chin and behind the right ear. The patient's medical history showed that the patient did not have people with similar complaints around him and he did not have any other known diseases. The dermatological exami- nation showed brown-reddish plaques at varying diameters with prominent delineations and in a neat layout on the front part of the abdomen, be- hind the left ear, on the forehead and beneath the chin (Figure 1). The systemic examination result was normal.

Our patient's routine laboratory examinations sho- wed normal results for the whole blood analysis, full urinalysis, hepatic and renal function tests.

The results of gram stain, ARB stain, acid fast stain and PPD tests conducted were negative.

Novy-Mac Neal-Nicole (NNN) medium and Sabou- raud's dextrose agar cultivation as well as tuber- culosis culture tests were performed. Pulmonary x-ray and abdomen ultrasonography were normal.

Amastigotes were observed on the Giemsa stain of the smear preparation collected from the lesion.

Preliminary diagnoses for deep fungal infections, cutaneous tuberculosis, cutaneous leishmaniasis (CL), sarcoidosis, mastocytosis, Langerhans cell hystosis and xantomas as well as skin biopsy were conducted on a sample collected from the perip- hery of the ulcerated lesion on the left forearm of the patient. Amastigotes were observed on the mic- roscopic examination of the biopsy material (Figu- res 2 and 3).

As a result of clinical and laboratory assessments, CL diagnosis was made and intralesionary antimo- niate (Glucantime) treatment was initiated. Post- treatment, brown postinflammatory hyperpigmen- tation recovered.

Leishmaniasis is a parasitic disease and a public health problem, which is caused by protozoa of the genus Leishmania. It is estimated that leishmania- sis affects approximately 12 million people in 88 countries [1]. Şanlıurfa Province, in southeastern Anatolia, Turkey, is highly endemic for CL and has drawn considerable attention. In Turkey, CL agents are Leishmania tropica and Leishmania in- fantum [2].

CL emerges on the exposed parts of the body such as face and hands in the form of asymptomatic, erythematous papulae, it becomes ulcerated after reaching the sizes of 1-2 cm by growing in 4-6 months on average and a crust that is securely at- tached to the bottom develops on it over time. In the absence of treatment, healed lesions cause scarring [2].

Page 1 of 2

(page number not for citation purposes) Figure 1.Brown-reddish plaques

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CL often appears in the forms of papulae, nodules, nodulo-ulcerative plaques and ulcerative plaques [2]. In addition to these classical clinical types, CL may also present in atypical forms such as psoria- siform, mycetomatous, DLE-like, squamous cell carcinoma-like, erysipeloid, zosteriform, eczema- tous, sporotrichoid, hiperkeratosic forms [3].

As seen in our case, we may also encounter other atypical forms of CL that mimic cutaneous mas- tocytosis differently from what has been reported in the literature.

As a result, CL may mimic many forms of derma- tosis and cause misleading results in diagnosis, which may lead to unnecessary treatments due to the morphological variety as was the case with our patient.

Yavuz Yeşilova,1MD Enver Turan,1MD Hacer Altun Sürücü,1MD Sezen Kocarslan,2MD Osman Tanrıkulu,1MD

1Harran University School of Medicine, Dermatology,

2Harran University School of Medicine, Pathology, Şanlıurfa, Turkey.

E-mail: yavuzyesilova@gmail.com

References

1. Shirbazou Sh, Jafari M. The Multiple Forms of Leish- mania major in BALB/C Mice Lung in Iran. Iran J Parasitol 2012; 7: 99–102. PMID: 23109953 2. Gurel MS, Ulukanligil M, Ozbilge H. Cutaneous leish-

maniasis in Sanliurfa: epidemiologic and clinical fea- tures of the last four years (1997–2000). Int J Dermatol 2002; 41: 32-37. PMID: 11895511 3. Bari AU, Rahman SB. Indian J Dermatol Venereol

Leprol 2008; 74: 23-27. PMID: 18187818

J Turk Acad Dermatol 2014; 8 (1): 1481l1. http://www.jtad.org/2014/1/jtad1481l1.pdf

Page 2 of 2

(page number not for citation purposes) Figure 2. Amastigotes seen with microscopic

examination of the biopsy material

Figure 3. Amastigotes seen with microscopic examination of the biopsy material

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