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2015, Volume 31, Number 3, Page(s) 223-225
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DOI: 10.5146/tjpath.2013.01197
Cutaneous Chromoblastomycosis Mimicking Tuberculosis Verrucosa Cutis: Look for Copper Pennies!
Arghya BANDYOPADHYAY1, Kaushik MAJUMDAR2, Mimi GANGOPADHYAY1, Sabyasachi BANERJEE3
1Department of Pathology, North Bengal Medical College, WEST BENGAL, INDIA
2Department of Pathology, G B Pant Hospital, NEW DELHI, INDIA
3Department of Dermatology, North Bengal Medical College, WEST BENGAL, INDIA
Keywords: Chromoblastomycosis, Dermatomycoses, Infectious skin diseases
Abstract
Chromoblastomycosis is a rare chronic fungal infection of skin and subcutaneous tissue. It is primarily a disease of tropical and subtropical regions and affects mainly the agricultural workers following trauma with vegetable matter. Cutaneous Chromoblastomycosis may clinically mimic cutaneous tuberculosis as both the condition usually presents with hyper pigmented verrucous lesion of skin.

Here in we report a case of chronic cutaneous Chromoblastomycosis in a middle aged woman from north eastern part of India, who was initially misdiagnosed as Tuberculosis verrucosa cutis. In histopathology characteristic brown colored spores of the fungus (also known as copper pennies) were seen within dermal abscess. The organism isolated from culture of the biopsy material was Fonsecaea pedrosoi thus confirming our diagnosis of cutaneous chromoblastomycosis. The patient responded well to oral Itraconazole.

The dermatologists and pathologists should be aware of this condition especially when dealing with verrucous lesion of the skin. The pathologists should search for fungal spores in cutaneous lesion with pseudoepitheliomatous hyperplasia and dermal abscess.

Introduction
Chromoblastomycosis is a localized chronic infection of skin and subcutaneous tissue caused by any of the several related dematiaceous (pigmented) fungi1. Cases have been documented from several states of India1-5. The characteristic lesions are warty papules, verrucous plaques or solid nodules developing in the skin at the site of traumatic implantation of the fungus, usually at an extremity6. Diagnosis depends on demonstration of the fungus in histopathological section or in culture1. The condition is often misdiagnosed as it is clinically indistinguishable from cutaneous tuberculosis1,3. Here in we report a case of cutaneous Chromoblastomycosis from sub-Himalayan region of West Bengal, India, presenting with multiple hyperpigmented verrucous plaques and was initially misdiagnosed as tuberculosis verrucosa cutis and offered treatment for the same.
  • Top
  • Abstract
  • Introduction
  • Case Presentation
  • Disscussion
  • References
  • Case Presentation
    A 50-year-old lady who was an agricultural worker presented to the dermatology outpatient department of North Bengal Medical College hospital with multiple hyperpigmented verrucous plaques in her right arm (Figure 1). The lesions initially appeared erythematous, and gradually became verrucous during a period of one and half years. She had no regional lymphadenopathy. Cutaneous tuberculosis was diagnosed in a rural health centre and subsequently treated with anti-tubercular drugs for 6 months, without any response. Her routine hematological and biochemical parameters were within normal limits. Direct KOH mount for fungus were negative. Histopathology (HP) section of the skin lesion revealed marked acanthosis with pseudoepitheliomatous hyperplasia. Dermis showed inflammatory infiltrate comprising of neutrophils, lymphocytes, histiocytes and foreign body giant cells. At places, microabcess formation along with multiple round thick walled dark brown sclerotic bodies resembling “copper pennies”, in accordance with the morphology of chromoblastomycosis were seen (Figure 2). These fungal spores were 5-12 μm in diameter, present in singles, small chains and small clusters (Figure 3). The spores also showed intracellular wall formation, that indicates reproduction. Ziehl-Neelsen (ZN) stain for acid fast bacilli (AFB) was negative. The organism isolated from culture of the biopsy material was Fonsecaea pedrosoi thus confirming our diagnosis of cutaneous chromoblastomycosis. The patient responded well to Itraconazole 100 mg twice daily and she was on monthly follow up. The lesion gradually subsided by 6 months.


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    Figure 1: Hyperpigmented verrucous lesion in the arm.


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    Figure 2: Scanner view of the histopathology section showing pseudoepitheliomatous hyperplasia, dermal abscess formation, collection of multinucleated giant cells (arrow) and barely visible fungal profiles (encircled) in this magnification (H&E stain, x40) Inset: Brown-colored spores of Chromoblastomycosis (copper pennies) (H&E stain, x400).


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    Figure 3: Higher magnification showing brown-colored spores of Chromoblastomycosis (copper pennies) within dermal microabscess (H&E stain, x400x).

  • Top
  • Abstract
  • Introduction
  • Case Presentation
  • Disscussion
  • References
  • Discussion
    Chromoblastomycosis was first described in 1914 by Max Rudolph in Brazil2. Subsequently Medlar described the characteristic histological appearance of sclerotic bodies, which thereafter were named as ‘Medlar bodies’. Other synonyms are “copper-pennies” or “mauriform” cells2. Chromoblastomycosis is belong to phaeohypomycosis group and caused by dematiaceous (naturally pigmented) fungi such as Fonsecaea pedrosoi, Phialophora verrucosa, Fonsecaea compactum, Cladophialophora carrionii, Exophiala jeanselmei, E. castellanii and Rhinocladiella aquaspersa. Fonsecaea pedrosoi is the most common causative agent of this condition1,7.

    Chromoblastomycosis is an indolent cutaneous infection, which can present as nodular, plaque like, verrucous, or cicatrical lesions6. The disease is cosmopolitan in distribution but most cases are encountered in tropical or sub-tropical regions. Mode of transmission is inoculation of soil or vegetable matter contaminated by the pigmented fungi though minor trauma8. Our patient being an agricultural worker, may have encountered a similar trivial injury which she could not recollect.

    Primary lesions develop at the site of injury and remain localized for many years8. New lesions develop by autoinoculation or through propagation by lymphatic vessels causing elephantiasis; hematogenous spread can also occur rarely. Development of squamous cell carcinoma had also been reported in the long standing cases9. The HP of cutaneous Chromoblastomycosis reveals pseudoepitheliomatous hyperplasia, dermal abscess formation, chronic granulomatous inflammation with multinucleated giant cells and diagnostic ‘copper penny’ bodies1,2,10. In this case though well defined granuloma was not observed, histiocytes and foreign body giant cells were noted. As the spores are naturally pigmented with melanin, diagnosis can be made on morphology alone; no special stains are required to demonstrate the fungi10. The brown colored sclerotic bodies are best demonstrated in H&E sections and easily identified in colorless background of unstained or de stained sections10. Thus examination of unstained or de stained sections for spores after their detection in H&E section provides confirmation of diagnosis without the use of unnecessary special stains10. Causative agents of chromoblastomycosis can be distinguished in culture but their tissue forms are identical. Culture of the organism show slow growing green to black colonies, and microscopic appearance of the conidia formation identifies the species1,4.

    Clinically the condition may simulate tuberculosis verrucosa cutis, squamous cell carcinoma, plamoplantar psoriasis and sporotrichosis1,2,3. This case was misdiagnosed as tuberculosis verrucosa cutis clinically and undergone treatment for the same, with no response. Pradeepkumar et al.1 and De et al.3 also reported cases of Chromoblastomycosis mimicking cutaneous tuberculosis.

    Treatment of Chromoblastomycosis is not well established3. Previously radical, often mutilating surgery was considered as the optimal approach4. Recently itraconazole (200-400mg/ day) has been effectively used with 80-90% success rate3. This patient also responded well to itraconazole, with resolution of lesion within 6 months.

    In conclusion, physicians, dermatologists and pathologists should consider chromoblastomycosis as one of the differentials during work up of verrucous lesions of the skin. The pathologists should purposefully search for the fungal profiles and ‘copper pennies’ in verrucous cutaneous lesions with pseudoepitheliomatous hyperplasia and dermal abscess.

    ACKNO WLEDGEMENTS
    We wish to thank Prof. Mamata Guha Mallik, Professor, Department of Pathology, North Bengal Medical College for her help and support.

  • Top
  • Abstract
  • Introduction
  • Case Presentation
  • Discussion
  • References
  • References

    1) Pradeepkumar NS, Joseph NM. Chromoblastomycosis caused by Cladophialophora carrionii in a child from India. J Infect Dev Ctries. 2011;5:556-60.

    2) Pradhan SV, Talwar OP, Ghosh A, Swami RM, Shiva Raj KC, Gupta S. Chromoblastomycosis in Nepal: A study of 13 cases. Indian J Dermatol Venereol Leprol. 2007;3:176-8.

    3) De A, Gharami RC, Datta PK. Verrucous plaque on the face: What is your diagnosis? Dermato Online J. 2010;16:6.

    4) S ayal SK, Prasad GK, Jawed KZ, Sanghi S, Satyanarayana S. Chromoblastomycosis. Indian J Dermatol Venereol Leprol. 2002;68:233-4.

    5) Rajendran C, Ramesh V, Misra RS, Kandhari S, Upreti HB, Datta KK. Chromoblastomycosis in India. Int J Dermatol. 1997;36:29-33.

    6) Carrión AL. Chromoblastomycosis and related infections: New concepts, differential diagnosis, and nomenclatorial implications. Int J Dermatol. 1975;14:27-32.

    7) Sharma NL, Sharma RC, Grover PS, Gupta ML, Sharma AK, Mahajan VK. Chromoblastomycosis in India. Int J Dermatol. 1999;38:846-51.

    8) Tschen JA, Knox JM, McGavran MH, Duncan WC. Chromomycosis. The association of fungal elements and wood splinters. Arch Dermatol. 1984;120:107-8.

    9) Caplan RM. Epidermoid carcinoma arising in extensive chromoblastomycosis. Arch Dermatol. 1968;97:38-41.

    10) Chavan SS, Kulkarni MH, Makannavar JH. ‘Unstained’ and ‘de stained’ sections in the diagnosis of chromoblastomycosis: A clinico-pathological study. Indian J Pathol Microbiol. 2010;53:666-71.

  • Top
  • Abstract
  • Introduction
  • Case Presentation
  • Discussion
  • References
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