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Vol. 96. Núm. 5.
Páginas 617-619 (1 setembro 2021)
Research Letter
Open Access
Clinical and epidemiological profile of mycetoma patients from a tertiary care center in Karachi, Pakistan
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Yousuf Abd Mallick
Autor para correspondência
youmay2006@gmail.com

Corresponding author.
, Nausheen Yaqoob
The Indus Hospital, Karachi, Pakistan
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Table 1. Socio-demographic details of mycetoma cases.
Table 2. Histopathological and microbiological details of mycetoma cases.
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Dear Editor,

Mycetoma is a chronic, suppurative and granulomatous infection of soft tissues and bones, which can involve any body part, but feet are the site of predilection. The famous triad consists of the formation of multiple draining sinuses, the presence of colored grains and painless subcutaneous swellings.1 Bacteria and fungi both are responsible for this condition, causing “actinomycetoma” and “eumycetoma” respectively. Mycetoma is predominantly reported from a typical geographical zone, known as “mycetoma belt”, which exists between 15° South and 30° North over the globe and has an abundance of different plant species, especially Acacia, with long, sharp, and firm thorns. These thorns, in turn, promote the deposition of spores deep into the tissues upon penetrating injuries.2,3

Mycetoma has no documented zoonotic transmission, neither vector nor any animal reservoir.4 Rural areas are most affected and those who work barefoot are predominant victims like farmers, shepherds, dairy farm workers, gardeners, livestock workers, and daily laborers. No age is immune to mycetoma but it has been seen more often in young males between 20 to 40 years of age with a male to female ratio of 3:1.4,5

This was a retrospective, descriptive study conducted at a tertiary care center in Karachi, a city in southern Pakistan. Untreated or inadequately treated mycetoma cases of all age groups and gender, visited the institution’s dermatology outpatient department between October 2017 to March 2020 were selected. Patients who had completed treatment from other hospitals, amputated cases, and those having concomitant tuberculosis, Human Immunodeficiency Virus and Acquired Immunodeficiency Syndrome were excluded.

Two or more biopsies were done in each patient and sent for histopathology and tissue culture. Extraction of grains, followed by potassium hydroxide mount, Gram’s staining, acid-fast staining, and extensive microbiological cultures were performed in all cases.

X-rays and Magnetic Resonance Imaging (MRI) with contrast was done as a baseline investigations to detect the extent of disease and bone involvement. Bone involvement on MRI was labeled as none, minimal (1 to 3 bones involved) and extensive (more than 3 bones involved).

Permission from the institutional ethical review committee was taken. Study IRB Number: IRD_IRB_2020_04_004.

In this study, out of 12 selected patients; 7 were male and 5 were female with M:F ratio of 1.4:1. Only one patient was a child, mean age of adults was 43.54 ± 11.76 years. Nine patients belonged to rural areas with a Rural to Urban ratio of 3:1. The most common profession of affected patients was farmers (5 patients), followed by daily laborers (2 patients), housewives (2 patients), shopkeepers (1 patient), and student (1 patient). The foot was affected in 10 patients while the hand and knee were affected in 1 patient each. The mean duration of delay in diagnosis was 7 years (Table 1).

Table 1.

Socio-demographic details of mycetoma cases.

Case nº  Age (years)  Sex  Residence  Occupation  Body region  Delay in diagnosis 
44  Urban  Housewife  Right foot  14 years 
60  Rural  Shopkeeper  Right foot  3 months 
45  Rural  Fisherman  Right hand  12 years 
48  Rural  Farmer  Right foot  8 years 
64  Rural  Farmer  Right foot  10 years 
41  Rural  Farmer  Left foot  12 years 
49  Rural  Farmer  Left foot  7 years 
9.3  Rural  Student  Left foot  3.5 years 
32  Urban  Housewife  Right foot  3 years 
10  40  Rural  Daily laborer  Left foot  7 years 
11  26  Urban  Daily laborer  Left foot  3 years 
12  30  Rural  Farmer  Right knee  6 years 

Histopathology helped in 9 cases to establish a diagnosis. Six and 2 biopsies were in favor of eumycetoma and actinomycetoma respectively, while 1 showed features of both organisms i.e., a mixed infection with actinomycetes and fungi which was later confirmed by cultures (Fig. 1).

Figure 1.

Histopathology showing two different types of colonies (Hematoxylin & eosin, ×10).

(0.57MB).

The culture was positive in 9 cases and reported fungal, bacterial, and mixed organisms in 5, 3, and 1 case, respectively. Cultures remained negative in 3 cases despite every effort to grow on different aerobic, anaerobic, microaerophilic, and Modified Sabouraud agar media. Aspergillus was reported as the most common species in 5 patients. The rest of the reported organisms and the color of grains are mentioned in Table 2.

Table 2.

Histopathological and microbiological details of mycetoma cases.

Case nº  Colour of grains  Biopsy findings  Culture  Type of species  Name of species  Final diagnosis  Bone involvement 
White  M.M.  Positive  Both  Actinomadura madurae & Aspergillus fumigatus  Mixed mycetoma  Minimal 
White  I.C.  Positive  Bacteria  Streptomyces species  Actinomycetoma  None 
Black  F.M.  Positive  Fungi  Madurella mycetomatis  Eumycetoma  Extensive 
Black  F.M.  Positive  Fungi  Aspergillus niger  Eumycetoma  Minimal 
White  B.M.  Positive  Bacteria  Actinomadura madurae  Actinomycetoma  Extensive 
Black  F.M.  Positive  Fungi  Aspergillus niger  Eumycetoma  None 
White  F.M.  Positive  Fungi  Aspergillus flavus  Eumycetoma  Minimal 
Red  B.M.  Positive  Bacteria  Actinomadura pelletieri  Actinomycetoma  Extensive 
Black  F.M.  Negative  None  None  Eumycetoma  Extensive 
10  Yellow  F.M.  Negative  None  None  Eumycetoma  Extensive 
11  Yellow  I.C.  Negative  None  None  None  Extensive 
12  White  I.C.  Positive  Fungi  Aspergillus flavus  Eumycetoma  None 

B.M., Bacterial Mycetoma; F.M., Fungal Mycetoma; I.C., Inconclusive; M.M., Mixed Mycetoma.

The most striking feature reported in this study was the detection of Aspergillus niger in 2 patients, which is a novel fungal species associated with mycetoma (Fig. 2). Both patients were residents of the Eastern part of province Sindh, a farmer in wheat fields, and lived in similar environmental conditions. Despite being a late diagnosis, years after acquiring the infection, there was none to minimal bone involvement in them.

Figure 2.

Septate fungal hyphae with hyaline budding surrounded by multinucleated giant cells, neutrophils, eosinophils, and lymphocytes (Hematoxylin & eosin, ×40).

(0.4MB).

A final diagnosis was established in 11 patients (91.67%). Out of these, 7 were eumycetoma, 3 were actinomycetoma and 1 was mixed infection while 1 patient still remains undiagnosed. The ratio of eumycetoma to actinomycetoma was 2.3:1 (7 vs. 3).

Bone involvement was variable and did not correlate with the species involved or final diagnosis (Table 2). Only one patient (case # 12) had metastatic deposit in the right inguinal region from the primary locus at the right knee. The culture showed Aspergillus flavus species from both sites.

Voriconazole 400 mg/day and terbinafine 500 mg/day were given in 6 and 1 patients of eumycetoma respectively for at least 6 months. Response to therapy was poor and amputation was planned in 3 patients. Others responded variably on voriconazole and surgical debulking was required in the majority.

Both patients with Aspergillus niger eumycetoma received voriconazole for 1 year and achieved complete clinical and microbiological cure, one with voriconazole alone and the other with associated surgical management, with no relapse of disease on MRI on follow-ups.

Among actinomycetoma cases, 1 case with Streptomyces species mycetoma was treated with a combination of co-trimoxazole and rifampicin with excellent response and disease clearance after 6 months. The other 2 cases with Actinomadura species were treated with Welsh regimen (Amikacin and Co-trimoxazole combination) with partial response and needed surgical debulking later on.

A mixed mycetoma case was treated with antibiotics (amoxycillin 1000 mg/day for 18 months along with linezolid 1200 mg/day for 6 months) and antifungals (itraconazole 400 mg/day for 6 months followed by voriconazole 400 mg/day for 15 months). Sequestrectomy was done once. MRI scans on follow-up did not reveal any signs of disease.

In conclusion, mycetoma is a potentially preventable disease. Protective measures, patient education with early diagnosis and treatment can save many patients from permanent disabilities and amputations. This study showed eumycetoma is more common in the southern part of Pakistan and Aspergillus is the predominant species responsible for this. A novel fungal agent Aspergillus niger is also prevalent in this part of the World and responsible for causing mycetoma in immunocompetent individuals.

Financial support

None declared.

Authors’ contributions

Yousuf Abd Mallick: Conception and design of the study; critical review of the literature; elaboration and writing of the manuscript; approval of the final version of the manuscript.

Nausheen Yaqoob: Conception and design of the study; collection and analysis of data; drafting of the article; critical review of the manuscript; approval of the final version of the manuscript.

Conflicts of interest

None declared.

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[2]
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How to cite this article: Mallick YA, Yaqoob N. Clinical and epidemiological profile of mycetoma patients from a tertiary care center in Karachi, Pakistan. An Bras Dermatol. 2021;96:617–9.

Study conducted at the The Indus Hospital, Karachi, Pakistan.

Copyright © 2021. Sociedade Brasileira de Dermatologia
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