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Cutaneous Fusarium infection in a renal transplant recipient: a case report

Journal of Medical Case Reports20115:205

https://doi.org/10.1186/1752-1947-5-205

Received: 19 May 2010

Accepted: 25 May 2011

Published: 25 May 2011

Abstract

Introduction

Fungal infections in the immunocompromised host are fairly common. Of the mycoses, Fusarium species are an emerging threat. Fusarium infections have been reported in solid organ transplants, with three reports of the infection in patients who had received renal transplants. To the best of our knowledge, this is the first case of an isolated cutaneous lesion as the only form of infection.

Case presentation

We report the case of a 45-year-old South Indian man who presented with localized cutaneous Fusarium infection following a renal transplant.

Conclusion

In an immunocompromised patient, even an innocuous lesion needs to be addressed with the initiation of prompt treatment.

Introduction

Fusarium species are common soil saprophytes and plant pathogens. Young and Meyers [1] first reported Fusarium infection in the late 1970s. Since then, several species have been recognized to be agents of superficial infections (keratitis, cutaneous infections, onychomycosis and infection of wounds or burns) in humans [2]. More recently, deep-seated, disseminated infections have been increasingly described in immunocompromised patients, especially in neutropenic patients [3, 4]. The prognosis is very poor, and death occurs in up to 70% of the cases despite antifungal therapy [4]. The Fusarium species most frequently involved in human infections are Fusarium solani, F. oxysporum and F. moniliforme.

Case report

A 45-year-old South Indian man underwent a renal allograft transplant for end-stage renal disease. He was administered tacrolimus, mycophenolate and prednisolone as immunosuppressive therapy. On follow-up at six months, he complained of a small, painless nodule on his right calf. He had no fever, redness or pruritus. He had no other opportunistic infection. Clinical examination revealed a subcutaneous, 2 × 2-cm, firm, violaceous nodule with normal surrounding skin (Figure 1). He had no other similar lesions. There was no regional lymphadenopathy. The rest of the physical examination was normal. His hemogram was normal, as were his computed tomographic chest and abdominal ultrasound scans. He underwent fine-needle aspiration of the nodule, which was reported to have inflammatory cells and a few fungal hyphae. He subsequently underwent excision of the nodule, which was sent for microbiological evaluation. The finding was reported to be Fusarium solani.
Figure 1

Nodule on the patient's right calf.

A biopsy sample was cultured for fungi on Sabouraud dextrose agar without cycloheximide and was incubated at 25°C in air for four days. It grew whitish-gray cottony colonies suggestive of Fusarium spp. Successive subcultures performed on potato dextrose agar in the dark stained with periodic acid-Schiff showed sickle-shaped, multiseptated macroconidia, and one- to two-celled microconidia had formed from unbranched phialides, conidiophores and chlamydospores typical of Fusarium solani (Figure 2).
Figure 2

Periodic acid-Schiff stain-positive spores of Fusarium solani.

Subsequently, species identification was further performed using immunohistochemistry (Figure 3). The patient was successfully treated with surgical excision of the lesion followed by four weeks of oral voriconazole treatment.
Figure 3

Fusarium solani identified by immunohistochemical staining.

Discussion

Fusarium species are ubiquitous and may be found in the soil and air and on plants. In humans, Fusarium species cause disease that is localized, focally invasive or disseminated. The pathogen generally affects immunocompromised individuals, with infection of immunocompetent persons being rarely reported. Localized infection includes septic arthritis, endophthalmitis, osteomyelitis, cystitis and brain abscess. In these situations, a relatively good response may be expected following appropriate surgery and oral antifungal therapy. Disseminated infection occurs when two or more noncontiguous sites are involved [5]. The skin can be an important and early clue to diagnosis, since cutaneous lesions may be observed at an early stage of the disease. Typical skin lesions may be painful red or violaceous nodules, the center of which often becomes ulcerated and covered by a black eschar. The multiple necrotizing lesions are often observed on the trunk and the extremities [6].

Our patient had a single, localized nodule that was treated successfully with surgical excision and antifungal therapy. He did not have any signs of disseminated infection. At the last follow-up appointment, he had no symptoms of any disseminated fungemia. Amphotericin has been the drug of choice to treat most fungal infections. The use of azoles, namely, voriconazole, posaconazole and ravuconazole, has also been found to be promising [7]. As the patient was a renal transplant recipient, we chose to use voriconazole to treat him as it has shown good response in most zygomycoses.

Conclusion

Opportunistic infections in transplant recipients can be life-threatening. Fusarium infections are recognized more often, and unless they are diagnosed and treated early, they can be a cause of significant morbidity and mortality.

Consent

Written, informed consent was obtained from the patient for publication of this case report and accompanying images. A copy of the written consent is available for review by the Editor-in-Chief of this journal.

Declarations

Acknowledgements

We acknowledge the contribution of Dr. Sanjeev Shah from the Department of Pathology.

Authors’ Affiliations

(1)
Department of Urology, Unit 1, Christian Medical College

References

  1. Young CN, Meyers AM: Opportunistic fungal infection by Fusarium oxysporum in a renal transplant patient. Sabouraudia. 1979, 17: 219-223. 10.1080/00362177985380331.View ArticlePubMedGoogle Scholar
  2. Guarro J, Gené J: Opportunistic fusarial infections in humans. Eur J Clin Microbiol Infect Dis. 1995, 14: 741-754. 10.1007/BF01690988. 1995View ArticlePubMedGoogle Scholar
  3. Boutati EI, Anaissie EJ: Fusarium, a significant emerging pathogen in patients with hematologic malignancy: ten years' experience at a cancer center and implications for management. Blood. 1997, 90: 999-1008.PubMedGoogle Scholar
  4. Rabodonirina M, Piens MA, Monier MF, Guého E, Fière D, Mojon M: Fusarium infections in immunocompromised patients: case reports and literature review. Eur J Clin Microbiol Infect Dis. 1994, 13: 152-161. 10.1007/BF01982190.View ArticlePubMedGoogle Scholar
  5. Blazar BR, Hurd DD, Snover DC, Alexander JW, McGlave PB: Invasive Fusarium infections in bone marrow transplant recipients. Am J Med. 1984, 77: 645-551. 10.1016/0002-9343(84)90355-3.View ArticlePubMedGoogle Scholar
  6. Girardi M, Glusac EJ, Imaeda S: Subcutaneous Fusarium foot abscess in a renal transplant patient. Cutis. 1999, 63: 267-270.PubMedGoogle Scholar
  7. Walsh TJ, Groll AH: Emerging fungal pathogens: evolving challenges to immunocompromised patients for the twenty-first century. Transpl Infect Dis. 1999, 1: 247-261. 10.1034/j.1399-3062.1999.010404.x.View ArticlePubMedGoogle Scholar

Copyright

© Banerji and Singh J; licensee BioMed Central Ltd. 2011

This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.