10.17843/rpmesp.2020.372.4799
BRIEF REPORT
Manipulation of cutaneous leishmaniasis lesions: case series in a peruvian hospital
Juan Pineda-Reyes
1, Physician
Ricardo Marín
1, Physician
Andrea Tinageros-Zevallos
1, Physician
Ana P. Ramos
2, Physician
Fiorela Alvarez 2, Specialist in Infectious and Tropical Diseases;
Alejandro Llanos-Cuentas
2, Specialist in Infectious and Tropical Diseases, Doctor of Medicine and Epidemiology
1 Facultad de
Medicina Alberto Hurtado, U4niversidad Peruana Cayetano Heredia, Lima, Perú.
2 Instituto de Medicina Tropical Alexander von Humboldt,
Universidad Peruana Cayetano Heredia, Lima, Perú.
This study is part of the thesis: Pineda-Reyes J, Marín R, Tinageros-Zevallos A. The effect of lesion manipulation in patients with cutaneous leishmaniasis in a hospital series of a national referral center during the period June 2017 - December 2017 [bachelor thesis]. Lima: Alberto Hurtado School of Medicine, Universidad Peruana Cayetano Heredia; 2019.
ABSTRACT
In cutaneous leishmaniasis endemic areas it is a common practice for patients to manipulate their lesions with traditional treatments as a first therapeutic option. A case series study was conducted in order to describe the frequency and the variations of the patient manipulation of cutaneous leishmaniasis lesions at the Cayetano Heredia Hospital. The study included 124 patients with cutaneous leishmaniasis. From the patient population it was found that 54% (67/124) manipulated their lesions. Of this, 92.5% (62/67) did so with chemicals, and 43.3% (29/67) with plants. The most frequent local changes reported by patients were increased lesion size in 35.8% (24/67) and increased inflammation in 28.4% (19/67). Manipulation by patients decreased the positivity of the parasitological diagnosis in those patients with ulcerative lesions.
Keywords: Leishmaniasis, Cutaneous; Medicine, Traditional; Diagnosis (source: MeSH NLM).
INTRODUCTION
Leishmaniasis is a neglected disease caused by protozoa of the genus Leishmania, which are transmitted by insects of
the genus Lutzomyia (1). Cutaneous leishmaniasis (CL) is the most common clinical form and
approximately 7,000 cases are reported each year in Peru (1-4).
In endemic
areas, particularly in rural areas, the use of traditional medicine is usually
a first option, due to the lack of access to health services, mistrust of
Western medicine, unavailability of standardized treatment, fear of side
effects, among others (3, 5). Traditional treatments include topical
application of plants, chemical or thermal substances, antibiotics, etc. (3,5-7) The use of these products could alter the lesion
morphology and decrease its parasitic load; but also alter the histopathology
and, consequently, the diagnosis of the disease. Therefore, the use of such
products is relevant in Peru, where observation of the parasite is a
requirement for the initiation of free standardized treatment (8).
It should be noted that currently there are other methods for the diagnosis of
CL, such as culture, histopathology and molecular methods, which are less
accessible in our context.
To date, the prevalence of lesion manipulation in referral hospitals, how it would affect light microscopy diagnosis and the appearance of the lesion are unknown. This study describes the frequency and types of manipulation, as well as the results from light microscopy (smear) and the clinical characteristics of CL lesions.
KEY MESSAGES |
Motivation for the study: Currently, the frequency of manipulation of cutaneous leishmaniasis (CL) lesions in hospitals and its impact on microscopy diagnosis are unknown. Main findings: More than half of patients with CL manipulated their wounds, most of them with chemicals. There was an increase in the size of lesions after manipulation. In patients with ulcers, manipulation was found to be negative on light microscopy. Implications: The diagnosis of leishmaniasis by microscopy is widely used in the first level of healthcare, so patients must be educated to avoid the manipulation of lesions; this will help achieving early diagnosis and getting timely treatment. |
THE
STUDY
A
descriptive, case series type, observational study was conducted by using
information obtained from clinical records of the Leishmaniasis
Program of the Alexander von Humboldt Institute of Tropical Medicine from the
Universidad Peruana Cayetano Heredia, a referral hospital
in Lima. Leishmaniasis was diagnosed and treated in
patients who attended the afore4mentioned hospital, from June to December 2017.
Physicians of
the Leishmaniasis Program considered as study cases the
medical records from patients of all ages, with established diagnosis of
uncomplicated CL (without mucosal involvement and in immunocompetent host).
Epidemiological, clinical, parasitological and/or immunological criteria were
evaluated. The clinical diagnosis was based on the presence of ulcers with
regular, well-defined, indurated, purplish, raised edges, with granulomatous
and thick background (9). We included medical records that had smear
test and leishmanin skin test (LST) results when at
least one of these was positive, and excluded records with incomplete data.
Lesion
manipulation was defined as the topical application of plants on at least two
occasions (direct placement, plasters, infusion),
chemicals (battery acid, blue stone or pharmaceutical chemicals, such as
antibiotic, antifungal or corticoid creams) or heat. It was the patients
themselves, with the exception of underage patients, who handled the lesions. The
changes made by lesion manipulation were described in this research as what was
reported in the clinical records by the patients themselves. Changes were
classified as increase/decrease in size of the lesion (diameter),
increase/decrease in inflammation (erythema, pain, edema, secretions) or none.
The information
was entered into an Excel® database, and the data was analyzed in Stata 15 (StataCorp, College Station, Texas, USA) and StatCalc at EpiInfo™.
Frequencies, proportions, central tendency measures, and dispersion were
calculated. The qualitative variables of microscopy, gender, time of illness,
age group, and lesion type were crossed with the presence of manipulation and
the smear result. Their statistical significance was determined with chi‑square
and Fisher’s exact tests.
The project
was approved by the ethics committees of the Universidad Peruana Cayetano Heredia and the Cayetano
Heredia Hospital (Certificate No. 0670519).
FINDINGS
From June to December 2017, 150 patients with CL were identified and 26 were excluded due to incomplete information; thus, the total number of patients enrolled was 124. The male/female ratio was 2.64. The median age was 38 years old (interquartile range 22-50) and the predominant age group was constituted by adults in 71.8% (89/124) of the study population (Table 1). 68.6% (85/124) of patients were from the department of Lima. The city of Lima, Madre de Dios and Cusco were the main places of contagion.
Table 1. Clinical and laboratory characteristics of 124 patients with cutaneous leishmaniasis and manipulation of lesions who were treated at the Institute of Tropical Medicine of Universidad Peruana Cayetano Heredia.
Characteristic |
Manipulated |
Non-manipulated |
p-value b |
Gender |
|
|
0.800 |
Male |
48 (53.7) |
42 (46.7) |
|
Female |
19 (55.9) |
15 (44.1) |
|
Place of origin |
|
|
0.678 |
Lima |
47 (55.3) |
38 (44.7) |
|
Province |
20 (51.3) |
19 (48.7) |
|
Smear test |
|
|
0.198 |
Positive |
46 (50.5) |
45 (49.5) |
|
Negative |
21 (63.6) |
12 (36.4) |
|
Smear test from ulcer patients (n=100) |
|
|
0.029 |
Positive |
35 (46.7) |
40 (53.3) |
|
Negative |
18 (72.0) |
7 (28.0) |
|
Time of illness a |
|
|
0.111 |
≤3 months |
28 (46.7) |
32 (53.3) |
|
>3 months |
39 (60.9) |
25 (39.1) |
|
Age group a |
|
|
|
Infant |
8 (53.3) |
7 (46.7) |
0.954 |
Adolescent |
5 (62.5) |
3 (37.5) |
0.725 c |
Adult |
49 (55.1) |
40 (44.9) |
0.716 |
Older adult |
5 (41.7) |
7 (58.3) |
0.382 |
Type of lesion (n=205) a |
|||
Ulcerative |
71 (47.7) |
78 (52.3) |
0,059 |
Nodular |
18 (62.1) |
11 (37.9) |
0,229 |
Infiltrative |
6 (54.5) |
5 (45.5) |
1,000 |
Verrucose |
2 (100) |
0 (0.0) |
0,498 c |
Scabbed |
0 (0.0) |
2 (100) |
0,232 c |
Polymorphic |
9 (75.0) |
3 (25.0) |
0,137 c |
a p-value calculated by comparing the proportion with the category complement
b Chi-square test
c Fisher’s exact test
The
majority of patients, 59.7% (74/124), had only one lesion, and 16.9%, three or
more. A total of 205 lesions were registered. Ulcers were the most common
lesion in 72.7% (149/205) of the total registered lesions (Table 1), followed
by nodular and infiltrative lesions. The most frequent lesion locations were
upper limb, 32.7% (67/205), head and lower limb, both 27.8% (57/205).
The smear
test was positive in 73.4% (91/124) of the patients and the LST in 91.9%
(114/124) (Table 1). Analyzing all types of lesions, no statistical difference
(p = 0.198) was observed in the smear positivity between manipulated
(50.5%) and non-manipulated (49.5%) lesions. However, considering only
ulcerative lesions, manipulation significantly reduced smear positivity (p = 0.029).
From the total of patients, 67 (54.0%) manipulated their lesions, both adults
and children, 65.7% (44/67) and 16.4% (11/67), respectively. The patients who
manipulated their lesions were mainly from Lima (Table 1).
In lesions with a longer time of illness (more than three months), parasitological demonstration was significantly lower regardless of the occurrence of manipulation (Table 2). The most used products were chemicals in 92.5% (62/67) of cases, and plants in 43.3% (29/67). 49.3% (33/67) of the patients used only chemicals and 6.0% (4/67) used only plants, while 34.3% (23/67) reported using both products.
Table 2. Smear results according to manipulation and time of disease in patients with cutaneous leishmaniasis who were treated at the Institute of Tropical Medicine of the Universidad Peruana Cayetano Heredia.
Manipulation |
Time of illness |
p-value |
|
≤3 months |
>3 months |
|
|
Manipulated |
|
|
0.003 a |
Positive smear test |
25 |
21 |
|
Negative smear test |
3 |
18 |
|
Non-manipulated |
|
|
0.003 a |
Positive smear test |
30 |
15 |
|
Negative smear test |
2 |
10 |
|
a Fisher’s exact test
62 patients used chemicals to manipulate their lesions; the most commonly used were antibiotic or antifungal creams and hydrogen peroxide (Table 3). Patients also reported having used the following plants: Plantago major (llantén), Piper aduncum (matico), Chamaemelum nobile (chamomile), Oenothera rosea (chupasangre), among others. 29 patients manipulated their lesions with plants, llantén was the most used, followed by matico and chamomile. Only 6 patients used thermal burns and another 6 used products such as beef liver, pig fat, honey, urine and excreta.
Table 3. Products used in cutaneous leishmaniasis lesions by patients treated at the Institute of Tropical Medicine of the Universidad Peruana Cayetano Heredia (n=67)
Product |
n (%) |
Chemicals |
62 (92.5) |
Antibiotic cream |
16 (23.9) |
Hydrogen peroxide |
14 (20.9) |
Antimycotic cream |
9 (13.4) |
Antibiotic tablet |
7 (10.5) |
Topical corticoid |
5 (7.5) |
Lemon |
4 (6.0) |
Salt |
4 (6.0) |
“Blue stone” |
3 (4.5) |
Battery acid |
3 (4.5) |
Gentian violet |
3 (4.5) |
Others |
37 (55.2) |
Plants |
29 (43.3) |
Plantago major (llantén) |
13 (19.4) |
Piper aduncum (matico) |
8 (11.9) |
Chamaemelum nobile (manzanilla) |
5 (7.5) |
Oenothera rosea (chupasangre) |
3 (4.5) |
Croton lechleri (sangre de grado) |
3 (4.5) |
Others |
12 (17.9) |
Finally, the most reported change was increased size with 35.8% (24/67), followed by increased inflammation with 28.4% (19/67). No change in lesions was reported by 31.3% (21/67) (Table 4).
Table 4. Changes observed in manipulated lesions of cutaneous leishmaniasis by patients treated at the Institute of Tropical Medicine of the Universidad Peruana Cayetano Heredia (n=67)
Characteristic |
n (%) |
Type of change |
|
Increased size |
24 (35.8) |
Increased inflammation |
19 (28.4) |
Decreased inflammation |
7 (10.5) |
Decreased size |
2 (3.0) |
No change |
21 (31.3) |
Most frequent changes |
|
Only plants |
|
No change |
2 (3.0) |
Increased size |
1 (1.5) |
Increased inflammation |
1 (1.5) |
Only chemical substances |
|
Increased size |
15 (22.4) |
Increased inflammation |
10 (14.9) |
No change |
9 (13.4) |
Decreased inflammation |
2 (3.0) |
Decreased size |
1 (1.5) |
Only thermal |
|
Increased size |
1 (1.5) |
Plants and chemical substances |
|
No change |
10 (14.9) |
Increased inflammation |
6 (9.0) |
Increased size |
5 (7.5) |
Decreased inflammation |
3 (4.5) |
Chemical and thermal |
|
Decreased inflammation |
1 (1.5) |
DISCUSSION
In this case series, manipulation of CL ulcerative lesions with
traditional treatments significantly reduced parasite observation effectiveness. This practice prevents definitive
diagnosis, which is necessary for a patient with CL to receive free treatment,
as specified by the Ministry of Health’s national standard for the treatment of
leishmaniasis (8).
More than
half of the patients with CL (54.0%) came to consultation with history of having
handled their lesions; most of them with multiple products, usually chemicals
(92%). However, literature shows higher frequencies of manipulation (71.2%) in
populations from long-standing leishmaniasis endemic
areas (3) and in studies from Latin American countries (10-12).
In rural populations located in CL-endemic areas it is common to use
traditional medicine, even in communities with health services (3).
The origin of this cultural habit is attributed to the lack of information or
distorted perceptions about the disease, the desire to prevent its progression,
or the lack of an adequate diagnosis (10,12).
Most
patients in the study were male, probably because they have a higher risk of
transmission (13,14). Similar findings have
been reported in Guatemala and Ecuador (10,12),
where infection is associated with occupational risks (agriculture, livestock).
However, there are areas where children under 15 are the most vulnerable,
especially when transmission occurs within the household (13).
Lesion manipulation
often occurs before seeking health care (3,12),
which affects diagnosis negatively. Not only does it decrease the probability
of detecting the parasite with the smear test, but it alters the morphology of
the lesions, making clinical diagnosis by health personnel with limited
training difficult. Based on the experience of the Cayetano
Heredia Hospital, it is relatively common for any chronic ulcer in patients
from rural areas to be classified as leishmaniasis, corresponding
in many cases to other diseases such as sporotrichosis,
pyogenic infections, insect bites, skin cancer, and skin tuberculosis, among
others. Likewise, the handling of lesions delays and makes the diagnosis of CL
more expensive. The usual procedure at the Cayetano
Heredia Hospital is to obtain the result of the smear test within a few hours
for non-manipulated lesions and to begin treatment the following day. However,
in patients with manipulated lesions, the diagnosis exceeds one week and additional
tests are required, such as cultures, pathological anatomy or polymerase chain
reaction (PCR). This implies increased costs for patients (prolonging their
stay in Lima) and for the health system.
The time of
illness is known to affect parasitological diagnosis, especially the classic
diagnostic methods (15,16). In this study,
it was found that the lesions with the longest time of illness (three months or
more), independently of the presence of manipulation, had a lower proportion of
positive smears, due to reduction of the parasitic load as a result of the
immune response (15).
Inhabitants
of endemic communities manipulate their lesions mainly with caustic products; most
of them used chemicals (92%) and less than half (43%) used plants. At least a
third of those who manipulated their lesions recognized that there was an
increase in the size of the lesion or inflammation. Lesion manipulation
frequently results in inflammation, superinfection, necrosis (3) and
first- to third-degree burns (12). Damage magnitude depends on the
product used; the use of sulfur or acids generates more damage, which causes extensive
subcutaneous tissue infection. The plants used caused less adverse effects on
the lesions. In Colombia, it was found that people initially used “strong”
treatments (burns, caustics) followed by “soft” treatments (plants) to heal (11).
Patients
who come to the Cayetano Heredia Hospital recognize
that handling their lesions with these substances causes pain and burns, but
they hope the injury will heal. In some cases, they succeed; but most fail,
because the burn is not regulated and causes many damaged tissues (dermal and
lymphatic) to remain with parasites that later help lesion growth.
Thermotherapy has used this knowledge to produce a regulated second-degree burn
at a temperature below 52 °C with a time limit of 30 seconds (17).
As for study
limitations, the time between the last manipulation and the first contact with
the referral center was not considered, which generates a confusing bias due to
the chronicity of the injury. In addition, there could be a bias from the
interviewer to adequately obtain the information since the population initially
tends to deny the manipulation, underestimating its prevalence. The Leishmania species was not typified,
therefore it could not be assessed whether it constitutes a confounding
variable. Future studies with a prospective design and access to molecular
methods could evaluate the effect of manipulation of CL lesions on parasite
load, PCR results and Leishmania species
identification.
In
conclusion, manipulation of cutaneous leishmaniasis
lesions could determine a negative effect in the smear result of ulcerative
lesions and also distort their morphology, which makes the clinical diagnosis
difficult. This would prevent timely and free treatment provided by the
Ministry of Health, which requires parasitological demonstration. First-level healthcare
usually lack the clinical experience found in referral hospitals. Therefore,
the greatest impact would be felt at first-level health care, where the main
diagnostic method is light microscopy. This is why it is necessary to implement
educational programs in endemic areas to reduce leishmaniasis
lesions manipulation.
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Citation: Pineda-Reyes J, Marín R, Tinageros-Zevallos A, Ramos AP, Alvarez F, Llanos-Cuentas A. Manipulation of cutaneous leishmaniasis lesions: case series in a peruvian hospital. Rev Peru Med Exp Salud Publica. 2020;37(2):265-9. doi: https://doi.org/10.17843/ rpmesp.2020.372.4799
Correspondence to: Alejandro Llanos Cuentas; Av. Honorio Delgado 262, San Martín de Porres, Lima, Perú; alejandro.llanos.c@upch.pe
Authorship
contributions: JPR,
RM, ATZ and ALlC participated in the article
conception, in the analysis and interpretation of data and, in the writing and
critical review of the manuscript. JPR, RM and ATZ collected the data. APR and
FA were involved in patient assessment, data recording, and manuscript writing.
All authors approved the final version and assume responsibility for the
contents of the manuscript.
Funding
sources:
Self-funded.
Conflicts of interest: Authors have no conflict of interest to declare.
Received: 12/09/2019
Approved: 13/04/2020
Online: 10/06/2020