Buscar en
Enfermedades Infecciosas y Microbiología Clínica
Toda la web
Inicio Enfermedades Infecciosas y Microbiología Clínica Infectious pubic plaque
Información de la revista
Vol. 37. Núm. 10.
Páginas 673-674 (Diciembre 2019)
Compartir
Compartir
Descargar PDF
Más opciones de artículo
Visitas
3076
Vol. 37. Núm. 10.
Páginas 673-674 (Diciembre 2019)
Diagnosis at first sight
Acceso a texto completo
Infectious pubic plaque
Placa infecciosa púbica
Visitas
3076
Ignacio Torres-Navarroa,
Autor para correspondencia
ignaciotorresnavarro@gmail.com

Corresponding author.
, María Jesús Castaño-Arocab, Miguel Ángel Navarro-Miraa, Rafael Botella-Estradaa,c
a Dermatology Department, Hospital Universitario y Politécnico la Fe, Valencia, Spain
b Microbiology Department, Hospital Universitario y Politécnico la Fe, Valencia, Spain
c Universitat de València, Valencia, Spain
Este artículo ha recibido
Información del artículo
Texto completo
Bibliografía
Descargar PDF
Estadísticas
Figuras (3)
Mostrar másMostrar menos
Texto completo
Clinical description

A Ukrainian woman of 35 years, with no relevant medical history, consulted for a skin lesion, located in the pubis, of one and a half months of evolution, treated with oral and topical antibiotics, and topical antifungals, without having obtained any improvement. The skin lesion was very painful, especially when walking. The patient had no fever or systemic symptoms. No other skin lesions were observed in the clinical examination. The patient worked in a chicken farm.

Physical examination revealed an erythemato-edematous plaque on the pubis and the inguinal region, with follicular and non-follicular pustules, yellowish crusts and edema of the labia majora (Fig. 1). No adenopathies were detected on palpation. There were no alterations in the blood count, biochemistry or coagulation. The serology of HIV was negative.

Fig. 1.

Pubic Majocchi's granuloma.

(0,1MB).

A dermatophytosis was suspected, and a scraping of the lesion was performed to carry out a microbiological culture, as well as direct examination with 40% potassium hydroxide, which allowed the visualization of fungal structures (Fig. 2). After 5 days of incubation at 30°C on Sabouraud agar, the growth of a filamentous fungus with a powdery texture and a high central button was observed. It had irregular edges, cream white colored on the surface, with an ocher reverse and a yellowish pigment that diffused to the medium. Microscopic examination of the colony revealed hyaline, septate hyphae, some of them spirally branched conidiophores, bearing numerous spherical conidia arranged in grape-like clusters (Fig. 3). The macro and microscopic identification of the fungus was completed with the urea hydrolysis test, which was positive at 3 days, identifying the fungus as Trichophyton mentagrophytes complex.

Fig. 2.

Skin scraping direct microscopic examination showing hyphae and thick-walled arthroconidia in formation (KOH mount, 60×).

(0,11MB).
Fig. 3.

KOH mount from the colony of T. mentagrophytes complex (40×) showing septate hyphae, some of them spiraling, and branched conidiophores bearing numerous spherical conidia arranged in grape like clusters.

(0,2MB).
Clinical evolution

Majocchi granuloma (MG) was diagnosed. Treatment was started with oral fluconazole of 100mg/day and topical terbinafine for 8 weeks, achieving resolution of the lesions without alopecia or residual scars.

Final comment

Majocchi described the “trichophytic granuloma” in 1883 as an intracutaneous or subcutaneous granulomatous inflammation resulting from the invasion of Trichophyton tonsurans.1

Two forms of MG have been defined. A follicular form due to the occlusion of the follicle after a previous cutaneous trauma, which causes the passive transfer of the dermatophyte to the dermis together with keratin or necrotic material. It usually occurs in immunocompetent patients, more frequently in women after shaving her legs. In this form, hair infection is endothrix and granuloma formation is favored by the use of corticosteroids.2 The subcutaneous form is typical of immunocompromised patients, and it is characterized by the appearance of subcutaneous nodules on the scalp, face or forearms.3

Deep pubic dermatophytosis is very rare.2,4,5 Frequently, the direct examination of the scraping of the lesion is negative because the dermatophyte is found in the deeper layers of the stratum corneum. Therefore, in case of suspicion, it is important to carry out a culture, and in case of doubt, a biopsy.3 The differential diagnosis should be made with cellulitis of bacterial or fungal origin, eosinophilic cellulitis, bacterial folliculitis, actinomycosis, and hidradenitis suppurativa.2–5

The pathogenic species that most frequently cause MG are Trichophyton rubrum, T. mentagrophytes, Trichophyton violaceum and Epidermophyton floccosum.6

T. mentagrophytes complex7 is an anthropophilic and zoophilic dermatophyte fungus of worldwide distribution that affects the human species and a wide variety of animals. Transmission of the pathogen can occur through contact with other people or infected animals, autoinoculation or through the soil.8 When human beings are infected by this type of fungus, especially when it is due to zoophilic dermatophytes, a great immune response occurs, with formation of microabscesses and pustules,9 which could explain the severe inflammation in our patient.

MG treatment should include systemic antifungals. Topical antifungals in monotherapy are ineffective, as occurred initially in our patient, due to their inability to penetrate through the dermis. The best result is obtained with the combination of topical and systemic antifungals.2–5

Deep dermatophyte infections can spread, affecting both the lymph nodes and other organs, such as the liver or brain, so they can become lethal.6

Authorship

All authors had access to the data and played a role in writing this manuscript.

Conflict of interests

The authors declare that they have no conflicts of interest.

Acknowledgments

The authors thank Javier Pemán for his assessment.

References
[1]
D. Majocchi.
Sopra una nuova tricozia (Granuloma tricotico) Studi clinici e micologici.
Bull R Acad Med Roma, 266 (1883), pp. 220-223
[2]
M. Ilkit, M. Durdu, M. Karakaş.
Majocchi's granuloma: a symptom complex caused by fungal pathogens.
Med Mycol, 50 (2012), pp. 449-457
[3]
R. Del Río Reyes, M. Rodríguez Vázquez, A. Comunión Artieda, Á. Santos-Briz Terrón, A. Guerra Tapia, L. Iglesias Díez.
Folliculitis caused by Tricophyton rubrum (Majocchi's granuloma).
Actas Dermosifiliogr, 92 (2001), pp. 379-429
[4]
E. Rallis, A. Katoulis, D. Rigopoulos.
Pubic Majocchi's granuloma unresponsive to itraconazole successfully treated with oral terbinafine.
Ski Appendage Disord, 1 (2016), pp. 111-113
[5]
T. Gracia-Cazaña, A. Milagro, A. Rezusta, Y. Gilaberte.
Querion de Celso de la vulva: una enfermedad común en una localización infrecuente.
Rev Iberoam Micol, 34 (2017), pp. 123-125
[6]
R.J. Hay.
Dermatofitosis (tiñas) y otras micosis superficiales.
Mandell, Douglas y Bennett. Enfermedades infecciosas. Principios y práctica, 8.ª ed., pp. 3155-3161
[7]
P. Nenoff.
A clarion call for preventing taxonomical errors of dermatophytes using the example of the novel Trichophyton mentagrophytes genotype VIII uniformly isolated in the Indian epidemic of superficial dermatophytosis.
Mycoses, (2019), pp. 6-10
[8]
I. Trocoli Drakensjö, I. Vassilaki, M. Bradley.
Majocchis granuloma caused by Trichophyton mentagrophytes in 2 immunocompetent patients.
Actas Dermosifiliogr, 108 (2017), pp. e6-e8
[9]
J.A. Jacobs, D.N. Kolbach, A.H. Vermeulen, M.H. Smeets, H.A. Neuman.
Tinea incognito due to Trichophytom rubrum after local steroid therapy.
Clin Infect Dis, 33 (2001), pp. E142-E144
Copyright © 2019. Elsevier España, S.L.U. and Sociedad Española de Enfermedades Infecciosas y Microbiología Clínica
Opciones de artículo
Herramientas
es en pt

¿Es usted profesional sanitario apto para prescribir o dispensar medicamentos?

Are you a health professional able to prescribe or dispense drugs?

Você é um profissional de saúde habilitado a prescrever ou dispensar medicamentos

Quizás le interese:
10.1016/j.eimc.2023.09.005
No mostrar más