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Case Reports in Infectious Diseases
Volume 2013 (2013), Article ID 450153, 3 pages
Case Report

Hidden under a Cauliflower-Like Skin Tumor: Chromoblastomycosis

1Division of Infectious Diseases and Hospital Epidemiology, University Hospital Basel, Petersgraben 4, 4031 Basel, Switzerland
2Division of Infectious Diseases and Hospital Epidemiology, Kantonsspital Aarau, Tellstraße, 5000 Aarau, Switzerland
3Department of Pathology, Kantonsspital Aarau, Tellstraße, 5000 Aarau, Switzerland
4Department of Plastic, Reconstructive and Aesthetic Surgery, Kantonsspital Aarau, Tellstraße, 5000 Aarau, Switzerland

Received 6 May 2013; Accepted 11 June 2013

Academic Editors: P. Horrocks, C. G. Meyer, P. O. Sumba, and S. Talhari

Copyright © 2013 B. Jakopp et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.


We present the case of an 80-year-old patient with a recurrent hyperpigmented and cauliflower-like skin tumor on the stump of his left index finger. Despite suggestive clinical appearance for chromoblastomycosis the tumor was initially clinically and also histopathologically misdiagnosed as recurrent squamous cell carcinoma. Due to a cardiogenic shock, the patient died shortly after the diagnosis of chromoblastomycosis, before adequate treatment could be introduced. In non-tropical regions chromoblastomycosis is an uncommon chronic fungal infection with Fonsecaea pedrosoi being the most prevalent etiological agent. Mostly lower extremities are involved. It is not unusual that, clinically, in the absence of pigmentation, and, histopathologically, because of pseudoepitheliomatous hyperplasia of the epidermis, chromoblastomycosis is confounded with squamous cell cancer, and delays in diagnosis of one to 3 years are common. Therefore, a high grade of clinical suspicion and inclusion of chromoblastomycosis in the differential diagnosis of pigmented skin tumors are important to initiate adequate therapy. Our case is remarkable in many aspects. The localization on an upper extremity and the grade of invasiveness with involvement of bone are unusual; furthermore the lack of a tropical travel history emphasizes that the infection almost surely occurred in Switzerland.