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C

ASE

R

EPORT

Primary cutaneous histoplasmosis developed in the penis of

an immunocompetent patient

*

Mauricio Paixão

1

Hélio Amante Miot

2

João Avancini

3

Walter Belda Júnior

3

DOI: http://dx.doi.org/10.1590/abd1806-4841.20153224

Abstract:A 70-year-old male presenting a 3-month history of genital painless erythematous nodules in the bal-anopreputial sulcus was referred to our service. Histopathological exam presented a chronic dermatitis with epithelioid granulomas and Grocott staining revealed numerous fungal structures with a suggestive morpholo-gy of Histoplasma sp. Cultures evidenced Histoplasma capsulatum var. capsulatum. Treatment with oral itra-conazole led to complete remission of lesions.

Keywords:Bacterial infections and mycoses; Genital diseases, male; Genitalia, male; Histoplasmosis; Infection; Mycoses

Received on 25.10.2013.

Approved by the Advisory Board and accepted for publication on 12.11.2013.

* Work performed at the Teaching Hospital (Hospital das Clínicas), Universidade de São Paulo (HC-FMUSP) – São Paulo (SP), Brazil. Financial Support: none

Conflict of Interests: none

1 Private clinic – São Paulo (SP), Brazil.

2 Universidade Estadual Paulista "Júlio de Mesquita Filho" (UNESP) – Botucatu (SP), Brazil. 3 Universidade de São Paulo (USP) – São Paulo (SP), Brazil.

©2015 by Anais Brasileiros de Dermatologia INTRODUCTION

Histoplasma capsulatum is commonly found in soil contaminated by feces of birds and bats. Most human infections are subclinical. Symptomatic cases are usually manifested as self-limiting respiratory tract infections and disseminated infections are pri-marily associated with immunosuppression.1 Skin

lesions occur in 4-11% of patients and result from sec-ondary invasion of the skin in patients with dissemi-nated infection. Primary cutaneous histoplasmosis is an extremely rare clinical entity and previously reported cases were mostly related to traumatic inoc-ulation.2,3

CASE REPORT

We report the case of a 70-year-old male patient, white, from the urban area of Sao Paulo (Brazil), pre-senting a 3-month history of genital painless erythe-matous nodules in the balanopreputial sulcus, meas-uring 2.0 cm and 0.7 cm in diameter (Figures 1-3). Adenopathy and systemic symptom were absent. Type II Diabetes mellitus was diagnosed 15 years ago (using Metformin and Glimepiride), hypertension (using Captopril and Atenolol) and cigarette smoking

for 50 years. He denied previous local trauma, but fre-quently traveled to a farm (countryside of the state of Sao Paulo), where he usually spent time cleaning one of the rooms where he often found bats. Patient also bred birds at home. Histopathological exam present-ed chronic dermatitis with epithelioid granulomas characterized by the presence of epithelioid or vacuo-lated histiocytes, some of which were grouped into giant cells, often phagocytizing the etiologic agent.

255 FIGURE1: C l i n i c a l Picture An Bras Dermatol. 2015;90(2):255-7. Revista2Vol90ingles_Layout 1 25/02/15 15:05 Página 255

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Primary cutaneous histoplasmosis developed in the penis of an immunocompetent patient 256

An Bras Dermatol. 2015;90(2):255-7.

DISCUSSION

Systemic mycoses with cutaneous involvement such as histoplasmosis, coccidioidomycosis and para-coccidioidomycosis are usually acquired by pul-monary inoculation through inhalation, and later dis-seminated to other organs such as the skin. The emer-gence of isolated skin lesions leads to the possibility of primary cutaneous inoculation, which is difficult to prove.4Reports of genital ulcers caused by Histoplasma

capsulatum are rare and most reports of cutaneous histoplasmosis occurred in immunosuppressed patients.5The inoculation process in this report is not

clear, since the patient doesn’t refer previous genital trauma. Dust rich in spores that might be held in clothes after cleaning contaminated sites is a hypothe-Grocott staining revealed numerous fungal structures

with a suggestive morphology of  Histoplasma sp. Sabouraud-agar with chloramphenicol and later Mycosel-agar cultures evidenced Histoplasma

capsula-tum var. capsulacapsula-tum (Figure 4). Blood tests resulted negative for HIV 1/2, HCV, HBV, VDRL and ANA; C3, C4, ESR, total protein fractions, protein elec-trophoresis, electrolytes, fasting glucose, renal func-tion test and CBC were all within normal values. Serological tests (immunodiffusion and counterim-munoelectrophoresis) directed to Histoplasma

capsula-tumwere negative. Chest radiography and computed tomography were performed and no changes were observed in the lung parenchyma. Treatment with Itraconazole 200mg-day was prescribed and

impor-tant regression of cutaneous lesions was noted after 1 month. A new biopsy with specimen culture was per-formed in the sixth month of treatment, presenting caseous necrosis. No fungal structures were visual-ized and the new cultures were negative. After nine months, treatment was discontinued and the patient now has a 1-year clinical follow-up, sustaining com-plete remission of lesions (Figures 5-6).

FIGURE2: C l i n i c a l Picture FIGURE3: C l i n i c a l Picture FIGURE5: C o m p l e t e r e m i s s i o n after treat-ment with oral itraco-nazole FIGURE6: C o m p l e t e r e m i s s i o n after treat-ment with oral itraco-nazole FIGURE4: Microculture p r e s e n t i n g Histoplasma capsulatum Revista2Vol90ingles_Layout 1 25/02/15 15:05 Página 256

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sis that should be explored.

Despite the absence of immunosuppression signs, the elderly are associated with lower function of cellular immune response as well as worse vigilance against cancer and infectious diseases.6

Genital dermatoses comprise several diseases whose clinical manifestations can differ from their else-where presentations. Sexually transmitted diseases

such as syphilis, chancroid and genital herpes may present as ulcerous lesions with adenopathy; neo-plasms, inflammatory such as Behçet disease, trauma-tic and infectious diseases can have genital manifesta-tions which dermatologists must be aware of.

We report the present case due to its very rare presentation of primary cutaneous histoplasmosis affecting a patient without evidence of immunosup-pression or trauma.❑

257 Paixão M, Miot HA, Avancini J, Belda Júnior W

An Bras Dermatol. 2015;90(2):255-7.

REFERENCES

Ferreira MS, Borges AS. Histoplasmosis. Rev Soc Bras Med Trop. 2009;42:192-8. 1.

Krunic AL, Carag H, Medenica MM, Lorincz AL. A Case of Cutaneous 2.

Histoplasmosis in a Patient with Diabetes and Multi-Infarct Dementia. J Dermatol. 2002;29:797-802.

Saheki MN, Schubach AO, Salgueiro MM, Conceição-Silva F, Wanke B, Lazera M. 3.

Primary cutaneous histoplasmosis: case report on an immunocompetent patient and review of the literature. Rev Soc Bras Med Trop. 2008;41:680-2. Tesh RB, Schneidau Jr JD. Primary cutaneous histoplasmosis. N Engl J Med. 1966 4.

Sep 15;275:597-9.

de Oliveira EV, Miduati FB, Antonio JR, de Negreiros Moraes R, de Almeida MT, 5.

D'Avilla SC, et al. Histoplasmosis as cause of penile ulcer in acquired immune defi-ciency syndrome (AIDS): three case reports. Mycopathologia. 2007;164:295-9. Butcher SK, Killampalli V, Chahal H, Kaya Alpar E, Lord JM. Effect of age on sus-6.

ceptibility to post-traumatic infection in the elderly. Biochem Soc Trans. 2003;31:449-51.

MAILINGADDRESS:

João de Magalhães Avancini Ferreira Alves Av. Dr. Enéas de Carvalho Aguiar, 255, sala 3068 05403-900 - Sao Paulo - SP

Brazil

E-mail: joao.avancini@hc.fm.usp.br

How to cite this article: Paixão M, Miot HA, Avancini J, Belda Junior W. Primary cutaneous histoplasmosis deve-loped in the penis of an immunocompetent patient. An Bras Dermatol. 2015;90(2):255-7.

Referências

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