- Case Report
- Open access
- Published:
Misdiagnosis and inappropriate treatment of cutaneous leishmaniasis: a case report
Tropical Diseases, Travel Medicine and Vaccines volume 8, Article number: 18 (2022)
Abstract
Background
Leishmaniasis is a widespread disease in tropical and subtropical countries, except for Australia and Oceania. In Poland, tourists, migrants and travellers from leishmaniasis-endemic countries may carry Leishmania.
Case presentation
We present a case of undiagnosed cutaneous leishmaniasis in a patient who received many weeks of inadequate antibiotic treatment. Ulceration in the right submandibular region was thought to be a purulent complication after laser surgery. Six weeks before the ulcer developed, the patient had visited the jungle (Guatemala). Cutaneous leishmaniasis was finally diagnosed after nine months based on a proper history and a polymerase chain reaction (PCR) assay. Treatment with antimony derivatives was administered. After three months, the ulcer healed but left a scar.
Conclusion
A lack of knowledge about tropical diseases among doctors and an incomplete medical history were the reasons for many weeks of erroneous treatment of cutaneous leishmaniasis with antibiotics. This is the first reported case of cutaneous leishmaniasis misdiagnosed as a complication after an aesthetic medical procedure.
Background
Cutaneous leishmaniasis is a tropical disease caused by a protozoan in the genus Leishmania. It is a transmissible disease and is carried by sand flies of the genera Phlebotomus (Mediterranean, Middle East) and Lutzomyia (Central and South America). The disease has been reported in 98 countries, and more than 350 million people are at risk of infection [1]. Approximately 2 million people worldwide are infected with leishmaniasis each year [2]. Leishmaniasis accounts for 5 to 10% of illnesses in tourists returning from the tropics [3].
Domestic (mainly dogs, rarely cats) and wild mammals, mainly foxes, are the reservoirs of leishmaniasis. Leishmania is an intracellular parasite of macrophages.
Cutaneous leishmaniasis is characterized by a long incubation period. A nonitchy papule appears after several weeks at the site of a bite from a Leishmania-infected sand fly, usually on an exposed part of the body. It then transforms into a nodule, from which asymptomatic ulceration develops, which enlarges without proper treatment. Usually, the adjacent lymph nodes are not enlarged.
There are three clinical forms of leishmaniasis: cutaneous, dermal-mucosal and visceral. Clinical forms are restricted to their area. There are several species of Leishmania that cause cutaneous leishmaniasis in humans, including L. major, L. tropica, L. infantum, L. mexicana, L. amazonensis, L. braziliensis, L. guyanensis, and L. panamensis [4].
Case presentation
A 52-year-old woman spent two weeks in Guatemala on a two-day jungle hike during which she was bit by insects. Five weeks after her visit to the jungle, she underwent advanced pulsed light (APL) laser hair removal in the neck area. One week after laser treatment, a nonitchy papule that was not associated with any other symptoms appeared in the right submandibular region; the nodule gradually enlarged and developed into a hard, dark red nodule with a soft edge. Over time, the nodule ulcerated and increased to 2 × 1 cm in size after five months (Fig. 1).
Initially, bacterial infection was diagnosed by swabbing the ulcer and subjecting the swabs to fungal and bacterial culture, but the culture results were negative. Despite the negative result, the doctor recommended antibacterial treatment, including orally Augmentin 1.0 g (Amoxicillinum + Acidum Clavulanicum) for two weeks. Topical Mupirox 20 mg/g ointment was also applied. There was no improvement, and the patient visited a dermatologist and an ear, nose, and throat (ENT) specialist; these visits were followed by two hospital stays in the departments of infectious diseases and dermatology. A diagnosis of purulent dermatitis was made and topical and general antibiotics were continued (2% Argosulfan cream, 2% Detreomycin ointment), and general were continued (intravenously Taromentin were recommended for 2 weeks). The laboratory results were normal. Eight months after the onset of symptoms, the ulceration had enlarged (10× 5 cm); it had an erythematous base and was covered with fibropurulent exudate and a thick scab on the periphery (Fig. 2). The surrounding lymph nodes were not enlarged. The ulcer was swabbed for fungal and bacterial culture, which were both negative. Local and systemic antibiotic therapy consisting of 2% Detreomycin ointment and orally Ciprofloxacinum 0.5 g 2x/day was continued in the hospital setting for 7 days.
Nine months after the onset of symptoms, the patient was hospitalized in the Department of Tropical and Parasitic Diseases at the University Centre for Maritime and Tropical Medicine in Gdynia. Nine months after symptom onset, the ulcer was large (10× 5 cm); it had an erythematous base and was covered with fibropurulent exudate and a thick scab on the periphery (Fig. 3).
On the basis of the patient’s travel history and the PCR findings, cutaneous leishmaniasis was diagnosed. Treatment with antimony derivatives intramuscularly (Glucantime 30 ampoules), local cryotherapy and 2% Argosulfan cream was administered. During treatment, there was gradual improvement (Figs. 4 and 5). After three months of treatment with antimony, the lesions healed but left an unsightly scar (Fig. 6).
Discussion
The case presented herein is unique because the symptoms of cutaneous leishmaniasis were misdiagnosed as a complication after an aesthetic medicine procedure.
Failure to diagnose cutaneous leishmaniasis and an incomplete patient history led to many weeks of inadequate antibiotic treatment. Many researchers note the importance of collection of a thorough medical history in medical practice [5,6,7,8].
In the present case, the doctors initially diagnosed the ulcer as a complication of laser treatment, and for this reason, the patient was treated for several weeks with general and topical antibiotics. It was not until nine months later that she was referred to the Department of Tropical and Parasitic Diseases at the University Centre for Maritime and Tropical Medicine in Gdynia, where leishmaniasis was diagnosed by PCR with the following primers: LGITSF2 and LGITSR2 [9]. The composition of the reaction mixture was as follows: 12.5 μl of PCR Master MixPlus High GC (ready-to-use PCR mixture containing Taq DNA polymerase, PCR buffer, MgCl2 and dNTPs; A&A Biotechnology), 1 μl of each primer (concentration 10 μM) and 4 μl of DNA template, supplemented with deionized water up to 25 μl [10].
Proper diagnosis and treatment with antimony derivatives and cryotherapy resulted in a substantial improvement, and cure was achieved within three months. In the initial stage of cutaneous leishmaniasis, cryotherapy is very effective and safe [11, 12].
Approximately 1-10% of cases of cutaneous leishmaniasis caused by L. braziliensis in Southern and Central America may develop into the dermal-mucosal form [13,14,15]. The diagnosis of leishmaniasis is sometimes a difficult task, even for infectious disease physicians and dermatologists [16]. The problem of incorrect diagnosis and, consequently, incorrect treatment of cutaneous leishmaniasis has been described in Poland and other European countries [16,17,18,19,20].
Because of the various clinical manifestations, physicians in the Middle East and Central and South America, where leishmaniasis is endemic, also face challenges in making a correct diagnosis and thus administering appropriate treatment. Leishmaniasis cases have been misdiagnosed as skin cancer, lupus erythematosus, mycosis fungoides and tuberculosis [1, 15, 21]. As a result of travel and migration, leishmaniasis has been reported in countries that were previously nonendemic, e.g., Thailand [22].
Conclusions
In this case, the patient first presented to the hospital four months after the appearance of a nonhealing ulceration in the right submandibular region. Laser treatment (APL) of the right submandibular region had no effect on the development of cutaneous leishmaniasis.
An incomplete history and the inexperience of the doctors in diagnosing tropical diseases were the reasons for inadequate treatment with antibiotics in this patient. Cutaneous leishmaniasis was finally diagnosed and treated with antimony derivatives after nine months based on a detailed medical history and PCR results.
This case is presented herein to disseminate knowledge about leishmaniasis and inform the medical community of the discussed issue. Specialist knowledge about tropical diseases and collection of a thorough medical history will contribute to the correct diagnosis and treatment of patients in medical practice [23].
Strengths of the presented case
A case of a large ulcer in the submandibular region was presented. The presented case can increase awareness among the medical community regarding the diagnosis of leishmaniasis and the importance of collecting a thorough medical history.
Limitations of the presented case
The patient was treated with long-term and ineffective antibiotics due to an incorrect diagnosis.
Availability of data and materials
Data supporting the findings are available upon request. Please contact the corresponding author, Katarzyna Van Damme-Ostapowicz (katarzyna.van.damme-ostapowicz@hvl.no), for data access.
Abbreviations
- APL:
-
Advanced pulsed light
- PCR:
-
Polymerase chain reaction
References
Bastolaa A, Shrestha M, Lamsal M, Shrestha S, Prajapati S, Adhikari A, et al. A case of high altitude cutaneous leishmaniasis in a non-endemic region in Nepal. Parasitol. Int. 2020;74(101991). https://doi.org/10.1016/j.parint.2019.101991.
Machado GU, Prates FV, Machado PRL. Disseminated leishmaniasis clinical pathogenic and therapeutic aspects. An Bras Dermatol. 2019;94(1):9–16. https://doi.org/10.1590/abd1806-4841.20198775.
Gregorio AW, Vasconcellos MRA, Enokihara MMSS, Guerra JM, Nonogaki S, Tomimori J. Cutaneous schistosomiasis and leishmaniasis coinfection: a case report. J Eur Acad Dermatol Venereol. 2019;33(9):1781–3. https://doi.org/10.1111/jdv.15521.
Mhadhbi M, Sassi A. Infection of the equine population by Leishmania parasites. Equine Vet. I. 2020;52(1):28–33. https://doi.org/10.1111/evj.13178.
Brummaier T, Bertschy S, Arn K, Treumann T, Ruf MT, Nickel B, et al. A blind passenger: a rare case of documented seroconversion in an Angiostrongylus cantonensis induced eosinophilic meningitis in a traveler visiting friends and relatives. Trop Dis Travel Med Vaccines. 2019;5:6. https://doi.org/10.1186/s40794-019-0084-x.
Fidler BD. Use of a virtual patient simulation program to enhance the physical assessment and medical history taking skills of doctor of pharmacy students. Curr Pharm Teach Learn. 2020;7:810–6. https://doi.org/10.1016/j.cptl.2020.02.008.
Takemura Y, Atsumi R, Tsuda T. Identifying medical interview behaviors that best elicit information from patients in clinical practice. Tohoku J Exp Med. 2007;213(2):121–7. https://doi.org/10.1620/tjem.213.121 PMID: 17917405.
Takemura Y, Sakurai Y, Yokoya S, Otaki J, Matsuoka T, Ban N, et al. Open-ended questions: are they really beneficial for gathering medical information from patients? Tohoku J Exp Med. 2005;206(2):151–4. https://doi.org/10.1620/tjem.206.151 PMID: 15888971.
de Almeida ME, Steurer FJ, Koru O, Herwaldt BL, Pieniazek NJ, da Silva AJ. Identification of Leishmania spp. by Molecular Amplification and DNA Sequencing Analysis of a Fragment of rRNA Internal Transcribed Spacer 2. J Clin Microbiol. 2011;49(9):3143–9. https://doi.org/10.1128/JCM.01177-11.
Myjak P, Szostakowska B, Lass A, Pietkiewicz H, Szulta J, Nahorski WL, et al. Diagnostyka leiszmaniozy z uwzglednieniem genotypowania. Diagnosta laboratoryjny. 2012;3(28):6–10.
Mohammadzadeh M, Behnaz F, Golshan Z. Efficacy of glucantime for treatment of cutaneous leishmaniasis in Central Iran. J. Infect Public Health. 2013;6(2):120–4.
Negera E, Gadisa E, Hussein J, Engers H, Kuru T, Gedamu L, et al. Treatment response of cutaneous leishmaniasis due to Leishmania aethiopica to cryotherapy and generic sodium stibogluconate from patients in Silti, Ethiopia. Trans R Soc Trop Med Hyg. 2012;106(8):496–503.
Bashir U, Tahir M, Anwar MI, Manzoor F. Comparison of Intralesional Meglumine Antimonite along with oral Itraconazole to Intralesional Meglumine Antimonite in the treatment of Cutaneous. Pak J Med Sci. 2019;35(6):1669–73.
Kosaka A, Sakamoto N, Hikone M, Imai K, Washino MT, Maeda T, et al. Failure of Liposomal-amphotericin B Treatment for New World Cutaneous Leishmaniasis due to Leishmania braziliensis. Intern Med. 2020;59(9):1227–30. https://doi.org/10.2169/internalmedicine.4096-19.
Saab J, Fedda F, Khattab R, Yahya L, Loya A, Satti M, et al. Cutaneous leishmaniasis mimicking inflammatory and neoplastic processes: a clinical, histopathological and molecular study of 57 cases. J Cutan Pathol. 2012;39(2):251–62.
Kuna A, Gajewski M, Bykowska M, Pietkiewicz H, Olszański R, Myjak P. Imported cutaneous leishmaniasis: a 13-year experience of a Polish tertiary center. Postepy Dermatol Alergol. 2019;36(1):104–11. https://doi.org/10.5114/ada.2019.82830.
Bart A, van Thiel P, de Vries H, Hodiamont C, Van Gool T. Imported leishmaniasis in the Netherlands from 2005 to 2012: epidemiology, diagnostic techniques and sequence-based species review from 195 patients. Euro Surveill. 2013;18(30):1–8.
Stebut E, Schleicher U, Bogdan C. Cutaneous leishmaniasis as travelers' disease. Clinical presentation, diagnostics and therapy. Hautarzt. 2012;63(3):233–46.
Poeppl W, Oeser C, Grabmeier-Pfistershammer K, Walochnik J, Burgmann H. Clinical findings and management of imported cutaneous leishmaniasis: report of 14 cases from Austria. Travel Med Infect Dis. 2013;11:90–4.
Kelly P, Baudry T, Peyron F. Imported cutaneous leishmaniasis in a short-term traveller returning from Central Mali - The role of PCR. Travel Med Infect Dis. 2012;10(2):97–100.
Vernal S, Yl C, Vieira LT, Amato VS, Duarte MIS, Nastri ACSS. Tegumentary leishmaniasis mimicking visceralization in a cirrhotic patient: atypical cutaneous lesions and local immunological features. Rev Soc Bras Med Trop. 2020;53:e20190380. https://doi.org/10.1590/0037-8682-0380-2019.
Kattipathanapong P, Akaraphanth R, Krudsood S, Riganti M, Viriyavejakul P. The first reported case of autochthonous cutaneous leishmaniasis in Thailand. Southeast Asian J Trop Med Public Health. 2012;43(1):17–20.
Kitano H, Sanjoba C, Goto Y, et al. Complicated cutaneous leishmaniasis caused by an imported case of Leishmania tropica in Japan: a case report. Trop Med Health. 2021;49:20. https://doi.org/10.1186/s41182-021-00312-4.
Acknowledgements
Not applicable.
Funding
This research received no external funding.
Author information
Authors and Affiliations
Contributions
All authors were involved in the study conception and design. All authors were involved in data collection, and RO was involved in data supervision. The literature search and the first draft of the manuscript were performed and written by RO and KVDO. All other authors contributed to data interpretation and critical review of the manuscript. All authors have read and approved the submitted version of the manuscript.
Corresponding author
Ethics declarations
Ethics approval and consent to participate
The patient provided consent for use of her clinical and imaging data for publication and education purposes.
Consent for publication
The patient provided written informed consent for the publication of this case report and the accompanying images.
Competing interests
The authors declare that they have no competing interests.
Additional information
Publisher’s Note
Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
Rights and permissions
Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
About this article
Cite this article
Sikorska, K., Gesing, M., Olszański, R. et al. Misdiagnosis and inappropriate treatment of cutaneous leishmaniasis: a case report. Trop Dis Travel Med Vaccines 8, 18 (2022). https://doi.org/10.1186/s40794-022-00175-5
Received:
Accepted:
Published:
DOI: https://doi.org/10.1186/s40794-022-00175-5