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Inicio Enfermedades Infecciosas y Microbiología Clínica (English Edition) Ringworm by Nannizzia nana: Clinical case and literature review
Información de la revista
Vol. 41. Núm. 8.
Páginas 501-504 (octubre 2023)
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246
Vol. 41. Núm. 8.
Páginas 501-504 (octubre 2023)
Brief report
Acceso a texto completo
Ringworm by Nannizzia nana: Clinical case and literature review
Tiña por Nannizzia nana: caso clínico y revisión bibliográfica
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246
Josué Pendones-Ulerioa,
Autor para correspondencia
josuependones@gmail.com

Corresponding author.
, Monica Martins-Lopesb, Fernando García-Garrotea, Paula Hernández-Calvoa, Manuela Yuste-Chavesb, María Nieves Gutiérrez-Zufiaurrea
a Servicio de Microbiología, Complejo Asistencial Universitario de Salamanca, Salamanca, Spain
b Servicio de Dermatología, Complejo Asistencial Universitario de Salamanca, Salamanca, Spain
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Table 1. Sociodemographic and clinical characteristics, treatment and outcomes of infections by N. nana.
Abstract
Introduction

Human dermatophytoses are the most widespread infections caused by fungi. These are capable of invading the keratin-containing tissues of animals. Nannizzia nana (N. nana) can cause ringworm in pigs and rarely cause infections in humans.

Methods

We conducted a search using PUBMED for articles published from January 1, 1990 to March 31, 2022 to identify additional cases. The search terms used were “Microsporum nanum” and “Nannizzia nana”.

Results

After reviewing the literature, we identified a total of 16 cases of dermatophytosis due to N. nana since 1990. In most of the patients, the clinical diagnosis was tinea corporis and the most widely used antifungals were: terbinafine and griseofulvin.

Conclusion

N. nana is a dermatophyte species isolated infrequently in humans, but it represents a potential source of dermatophytosis in people who come into direct or indirect contact with animals and soil.

Keywords:
Nannizzia nana
Microsporum nanum
Ringworm
Dermatophyte
Resumen
Introducción

Las dermatofitosis humanas son el grupo más extendido de infecciones causadas por hongos. Estos son capaces de invadir los tejidos que contienen queratina de los animales. Nannizzia nana (N. nana) puede causar tiña en cerdos y que de manera excepcional puede producir infecciones en humanos.

Métodos

Realizamos una búsqueda en PubMed de artículos publicados desde el 1 de enero de 1990 hasta el 31 de marzo de 2022 para identificar casos adicionales. Los términos de búsqueda empleados fueron «Microsporum nanum» y «Nannizzia nana».

Resultados

Tras la revisión bibliográfica identificamos un total 16 casos de dermatofitosis por N. nana desde 1990. En la mayoría de los pacientes, el diagnóstico clínico fue tinea corporis y los antifúngicos más utlilizados fueron: terbinafina y griseofulvina.

Conclusión

N. nana es una especie de dermatofito aislada infrecuentemente en humanos, pero que representa una fuente potencial de dermatofitosis en personas que entran en contacto directo o indirecto con animales y con el suelo.

Palabras clave:
Nannizzia nana
Microsporum nanum
Tiña corporal
Dermatofito
Texto completo
Introduction

Dermatophytes are keratinophilic fungi capable of invading keratin-containing tissues (skin, nails and hair) in animals and humans and causing infection.1Nannizzia nana (formerly Microsporum nanum) is a geophilic and zoophilic fungus that can cause ringworm in pigs and occasionally causes infections in humans. Just over 40 cases have been described in humans worldwide, with tinea corporis being the most common form of presentation.1–3 In Spain, the first case in humans was published in 2007.4 In this article we present a case report and review all the cases published in humans in the last 30 years.

Case report

This was a 48-year-old Spanish woman with no relevant medical history who attended the Dermatology clinic with a three-month history of a pruritic skin lesion on the flexure of the right arm, which had been treated topically with corticosteroids, antibiotics and ciclopirox, with no clinical improvement. She reported no trips abroad in the previous 12 months. Four years earlier, she had onychomycosis which was treated with oral itraconazole with clinical improvement. She did not live in a rural environment and nor did she have any direct contact with animals. However, she worked in a textile company handling virgin wool from sheep, wearing gloves as personal protective equipment.

The patient had a ring-like lesion of approximately 7cm in diameter on physical examination cm in diameter with a scaly, erythematous border. Based on the above data, a clinical diagnosis was made of probable tinea corporis. Mycology culture was carried out by scraping scales from the active edge of the lesion which were then inoculated on Sabouraud glucose agar plates (bioMérieux SA 376, Chemin de l'Orme, 69,280 Marcy-l'Etoile, France) and Dermasel dermatophyte selective medium (Thermo Fisher Diagnostics S.L.U. via de los Poblados, No 17, Nave 3–13, 20833 Madrid, Spain) and incubated at 30°C. After one week of incubation, colonies with a velvety texture, beige-coloured on the surface, and red/brown on the reverse, grew in the culture media (Fig. 1). Microscopic examination of the colony with lactophenol cotton blue revealed short, thick-walled, pyriform macroconidia of one to three cells (mostly two), identified as N. nana. The identification was confirmed by culture and microscopy at the Mycology Unit of the Instituto de Salud Carlos III National Microbiology Centre in Majadahonda, Spain.

Figure 1.

Figure 1 A-B) Reverse-front aspect of the colony on Sabouraud agar. C) Two-cell macroconidia with lactophenol cotton blue (40⋅) at 14 days (potato agar). D) Skin lesion on the arm and ulnar fold.

(0.38MB).

The patient was treated with topical terbinafine 10mg/g every 12h and topical methylprednisolone 1mg/g every 24h for one month. At the patient's follow-up one month after starting the treatment, there was complete remission of the lesion.

Methods

We have reported a case and performed a PubMed search for articles published from 1 January 1990 to 31 March 2022 to identify additional cases. The search terms used were "Microsporum nanum" and "Nannizzia nana". Secondary sources cited in the articles found were also reviewed. We only considered publications in English, French, Portuguese and Spanish. In all the cases found, the following information was reviewed: country of origin, age; gender; type of infection; site of the infection; contact with animals; treatment; and cure.

Results

After reviewing the literature, we identified 16 cases of dermatophytosis due to N. nana since 1990 (Table 1). These cases are distributed across nine countries: Guatemala, Mexico, Brazil, Poland, Spain, Morocco, Malawi, India and Thailand.1–10 The median age of the patients was 35 (range: 0.9–75 years) with an equivalent proportion of males and females. Half of the cases had had contact with animals, pigs being the most common.

Table 1.

Sociodemographic and clinical characteristics, treatment and outcomes of infections by N. nana.

  Year  Country  Age  Gender  Contact with animals  Site  Treatment  Duration  Clinical course  Infection  Reference  Molecular identification 
1997  India  16  Pigs  Back, leg and chest  Griseofulvin 750mg PO  1 month  Cured  Ringworm  Ranganathan et al.  No 
1995  Malawi  17  Pigs  Popliteal fossa  Benzoic acid and salicylic acid 5%a  ND  Cured  Ringworm  Ponnighaus et al.  No 
1992  Brazil  9 months  ND  Pigs  Back  ND  ND  Cured  Ringworm  De Camargo et al.  No 
2007  Spain  35  Pigs  Forearm  Terbinafine 250mg PO  1 month  Cured  Tinea corporis  Lamilla Yerga et al.  No 
2007  Morocco  50  No  Scalp  Griseofulvin 500mg PO  6 weeks  Cured  Tinea capitis  Moutaj et al.  No 
2020  Poland  28  No  Neck  Terbinafine 250mg PO and ketoconazole 2%  20 days  Cured  Tinea corporis  Gnat et al.  Yes 
2020  Poland  41  Cows and dogs  Feet  Terbinafine 250mg PO and ketoconazole 2%  40 days  Cured  Tinea pedis  Gnat et al.  Yes 
2020  Poland  75  Cats  Nail  Terbinafine 250mg PO and ketoconazole 2%  6 weeks and resection  Cured  Tinea unguium  Gnat et al.  Yes 
2021  Guatemala  32  No  Groin  Terbinafine 250mg PO  2 weeks  Cured  Tinea cruris  Porras-López et al.  Yes 
10  2021  Guatemala  48  No  Feet  Terbinafine 250mg PO  2 weeks  Cured  Tinea pedis  Porras-López et al.  Yes 
11  2021  Guatemala  35  No  Nail  Terbinafine 250mg PO  3 months  Cured  Tinea unguium  Porras-López et al.  Yes 
12  2014  Brazil  35  ND  Nail  Itraconazolea  ND  Cured  Tinea unguium  Martínez Herrera et al.  No 
13  2020  Thailand  59  No  Ankle  Itraconazole 100mg PO and ciclopirox 1%  1 month  Cured  Tinea pedis  Ramon-Torrell et al.  No 
14  2019  Mexico  Yes  Scalp  Griseofulvin 15mg/kg/day PO and prednisone 0.5mg/kg/day PO  40 days  Cured  Tinea capitis  Bonifaz et al.  No 
15  2019  Mexico  Yes  Face, chest and arms  Griseofulvin 15mg/kg/day PO and ketoconazole 2%  20 days  Cured  Tinea corporis  Bonifaz et al.  No 
16  2022  Spain  48  No  Arm  Terbinafine 10mg/g and methylprednisolone  1 month  Cured  Tinea corporis  This article  No 

ND: not determined; M: male; F: female; PO: per oral.

a

Dose not specified.

In most of the patients, the clinical diagnosis was tinea corporis (50%), followed by tinea unguium (18.7%) and tinea pedis (18,7%), and less often tinea capitis (12.5%).

The treatment used was specified in all but one of the patients. The most used antifungals were: terbinafine (8 cases) and griseofulvin (4 cases). Topical ketoconazole was added in four patients and topical prednisone in two. A different antifungal, such as itraconazole, was used in two patients. The mean duration of therapy was 34.5 days (range: 14–90 days). All the patients were cured.

Discussion

We have reported on a new case of tinea corporis due to N. nana and reviewed the cases published over the last 30 years. This is a zoophilic and geophilic fungus which causes ringworm in pigs and other animals and, very occasionally, can cause infection in humans.1,3 Since 1990, 15 infections related to this dermatophyte have been published in South America, Europe, Asia and Africa, indicating its wide geographic distribution and low incidence.1–10

In Spain, two cases have been reported in humans. The first, published in 2007, was in a pig farmer, and the second was an imported case after a trip to Thailand.2,4 In Spain, a ringworm outbreak was reported on a pig farm that only affected animals.11

Infections by N. nana are associated with animals and mostly with exposure to pigs, so people in contact with pigs have a higher risk of contracting the infection.1,4,5 Despite the country's large pig population, its low incidence in Spain is surprising. It may be because the cases are treated empirically, and the samples do not reach the microbiology laboratories due to their low virulence or diagnostic errors.3

Infections in humans by zoophilic dermatophytes occur directly through contact with colonised or infected animals or indirectly through materials contaminated with the fungus which have been in contact with the animals.6 About half of the infections in this review affected people who had no contact with animals, highlighting the importance of the geophilic nature of this dermatophyte. N. nana has been isolated from the soil, where it can multiply as a saprophyte. Therefore, in patients who have had no contact with animals, a possible telluric or environmental origin should be investigated as the source of infection.3,5

Our patient had no contact with animals and lived in an urban area. Her only contact with animals was indirect, as she worked with wool in a textile factory, which may have been the source of her infection. Sheep are important in the transmission and persistence of some dermatophytes. In one study, N. nana was the third most common dermatophyte species isolated from sheep hair after Trichophyton verrucosum and T. mentagrophytes.12 We, therefore, think that the most likely route of infection was through the wool that she handled as part of her job. However, it was impossible to analyse wool samples, so this source could not be proven microbiologically. We would also need to rule out a possible route of infection through the soil or the environment, but that could be clearer in our case too.

There is not a well-established treatment for infections by N. nana, and therapy is based on that used in other dermatomycoses caused by other species of the genus Microsporum.1,3 There are few data on the sensitivity of N. nana to antifungals, but it has been documented to be sensitive in vitro to miconazole, clotrimazole, ketoconazole, itraconazole, voriconazole, terbinafine and griseofulvin.1,3,5,13,14 In the studies analysed, the most used antifungals were terbinafine and griseofulvin. All the patients treated with these antifungals made good progress with a resolution of the lesions. Steroids are also often added to the treatment to reduce the inflammatory reaction that can appear in some cases.1

It is important to characterise the fungus at the species level to avoid inappropriate treatment and to determine its epidemiology.5 In the articles we reviewed, the fungus was correctly identified by microscopic examination of the culture. In some studies, this identification is complemented with molecular methods by amplifying and sequencing the ITS1-5.8S-ITS2 fragment.1,5 Microscopy enables a fast and reliable diagnosis thanks to this dermatophyte has distinctive morphological characteristics.15,16 Other fungi that produce similar fungal elements have to be considered, such as Trichothecium spp.,7 which produces bicellular conidia similar to those of N. nana, although the mode of fruiting is different, as the macroconidia of N. nana are isolated while those of Trichothecium spp. are arranged in clusters.8,15,16

This study has limitations inherent to a literature review based on case reports in which publication bias cannot be ruled out. However, the information from the literature review updates the knowledge on this dermatophyte, its epidemiology and associated infections.

In conclusion, N. nana is a dermatophyte species isolated only occasionally in humans. Still, it represents a potential dermatophytosis source in people with direct or indirect contact with animals and the soil. Clinically it mainly presents as tinea corporis, although there are other clinical forms. The prognosis is good if adequate antifungal treatment is provided.

Conflicts of interest

None.

References
[1]
A. Bonifaz, B. Córdoba-García, T. Simancas-Llanos, A. Marco, M.A. Hernández, E. Martínez-Herrera, A. Tirado-Sánchez.
Dermatophytosis caused by Nannizzia nana in two siblings.
Rev Iberoam Micol, 36 (2019), pp. 30-33
[2]
J.M. Ramon-Torrell, P. Ferrara, C. Masuet-Aumatell, O. Servitje.
Microsporum nanum cutaneous infection in a traveller returning from Thailand: a diagnostic challenge.
Travel Med Infect Dis, 38 (2020),
[3]
S. Gnat, D. Łagowski, A. Nowakiewicz, M. Dyląg.
Unusual dermatomycoses caused by Nannizzia nana: the geophilic origin of human infections.
Infection, 48 (2020), pp. 429-434
[4]
A.M. Lamilla Yerga, I.M. Rodríguez-Nevado, J.M. Fernández-Recio, A.J. Chaves-Álvarez, G.A. Fernández-Durán, E. Garduño-Echevarri.
Infección cutánea por Microsporum nanum.
Semergen, 33 (2007), pp. 159-160
[5]
C. Porras-López, E. Martínez-Herrera, M.G. Frías-De-León, G. Moreno-Coutiño, M.R. Reyes-Montes, R. Arenas, et al.
Dermatophytosis caused by Nannizzia nana.
J Mycol Med, 31 (2021),
[6]
R. Moutaj, N. Soraa, K. Laissaoui, M. Jana.
Une teigne humaine rare à Microsporum nanum: à propos d’une observation marocaine.
J Mycol Med, 17 (2007), pp. 65-69
[7]
R.M. De Camargo, M.R. Silvares, C.R. Carvalho, N.L. Dillon, S.A. Marques.
Microsporum nanum. A fourth report of human infection in Brazil.
Rev Inst Med Trop Sao Paulo, 34 (1992), pp. 581-585
[8]
J.M. Ponnighaus, D. Warndorff, G. Port.
Microsporum nanum — a report from Malawi (Africa).
[9]
S. Ranganathan, T. Menon, S.A. Balajee.
Isolation of Microsporum nanum from a patient with tinea corporis in Madras, India.
[10]
E. Martínez Herrera, M. Ameen, D. Tejada, R. Arenas.
Microsporum spp. onychomycosis: disease presentation, risk factors and treatment responses in an urban population.
Brazil J Infect Dis, 18 (2014), pp. 181-186
[11]
A. García-Sánchez, J. Bazán, J.H. de Mendoza, R. Martínez, S. Sánchez, M.H. de Mendoza.
Outbreak of ringworm in a traditional Iberian pig farm in Spain.
Mycoses, 54 (2011), pp. 179-181
[12]
M.S. Ali-Shtayeh, H.M. Arda, M. Hassouna, S.F. Shaheen.
Keratinophilic fungi on sheep hairs from the West Bank of Jordan.
Mycopathologia, 106 (1989), pp. 95-101
[13]
J.A. Roller, T.U. Westblom.
Microsporum nanum infection in hog farmers.
J Am Acad Dermatol, 15 (1986), pp. 93-99
[14]
A. Wildfeuer, H.P. Seidl, I. Paule, A. Haberreiter.
In vitro evaluation of voriconazole against clinical isolates of yeasts, moulds and dermatophytes in comparison with itraconazole, ketoconazole, amphotericin B and griseofulvin.
[15]
D.H. Larone.
Medically important fungi: a guide to identification.
4th ed., ASM press, (2002),
[16]
G.S. De Hoog, J. Guarro, J. Gené, M.J. Figueras.
Atlas of clinical fungi.
2nd ed., Centraalbureau voor Schimmelcultures/Universitat Rovira i Virgili, (2000),
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