alexa Blastomycosis-Like Pyoderma in a Patient with Syphilis and HIV Resolving with Antibiotic Therapy | Open Access Journals
ISSN: 2165-7920
Journal of Clinical Case Reports
Make the best use of Scientific Research and information from our 700+ peer reviewed, Open Access Journals that operates with the help of 50,000+ Editorial Board Members and esteemed reviewers and 1000+ Scientific associations in Medical, Clinical, Pharmaceutical, Engineering, Technology and Management Fields.
Meet Inspiring Speakers and Experts at our 3000+ Global Conferenceseries Events with over 600+ Conferences, 1200+ Symposiums and 1200+ Workshops on
Medical, Pharma, Engineering, Science, Technology and Business

Blastomycosis-Like Pyoderma in a Patient with Syphilis and HIV Resolving with Antibiotic Therapy

Nathan Jetter*, Mark Juhl and Maria Tsoukas*

Department of Dermatology, University of Illinois, College of Medicine East Building, USA

*Corresponding Author:
Nathan Jetter
Department of Dermatology, University of Illinois
College of Medicine East Building, USA
Tel: (312)9966966
Fax: (312)9961188
E-mail: njette2@uic.edu
Maria M Tsoukas
Department of Dermatology, University of Illinois
College of Medicine East Building, USA
Tel: (312)9966966
Fax: (312)9961188
E-mail: tsoukasm@UIC.edu

Received date: May 03, 2017; Accepted date: May 22, 2017; Published date: May 27, 2017

Citation: Jetter N, Juhl M, Tsoukas M (2017) Blastomycosis-Like Pyoderma in a Patient with Syphilis and HIV Resolving with Antibiotic Therapy. J Clin Case Rep 7:965. doi: 10.4172/2165-7920.1000965

Copyright: © 2017 Jetter N, et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.

Visit for more related articles at Journal of Clinical Case Reports

Abstract

Blastomycosis-like pyoderma (BLP) is a rare, exaggerated, vegetative tissue reaction that occurs in patients with local or systemic immune dysregulation. Reported causes of immune compromise include human immunodeficiency virus, malnutrition, alcoholism, leukemia, immunosuppressant use, radiation therapy, and others. Nearly all cases involve an underlying, prolonged pyogenic bacterial infection. Historically monotherapy with systemic antibiotics requires long-term treatment and often fails. We describe a case of a male patient with BLP of the face and scalp, which cultured positive for methicillin-resistant Staphylococcus aureus (MRSA). Subsequent evaluation uncovered a concurrent Treponema pallidum and HIV infections. Treatment of the MRSA with a short course of doxycycline and the syphilis with penicillin, resulted in complete resolution of the skin lesions. Highly Active Anti-Retroviral Therapy for HIV was initiated after the skin lesions had cleared. Resolution of BLP by antibiotic therapy alone in the context of untreated HIV leads the authors to postulate that syphilis may have been the relevant factor contributing to his immune dysregulation.

Keywords

Blastomycosis-like pyoderma; BLP; Syphilis; HIV; Psudoepitheliomatous hyperplasia; Doxycycline

Introduction

Blastomycosis-like pyoderma (BLP) is a rare chronic form of pyoderma that presents with one or more large, indurated, verrucous plaques studded with pustules and draining sinuses [1,2]. This slowgrowing, vegetative infection typically presents similarly to the cutaneous manifestations of blastomycosis, a dimorphic fungi prevalent in the Ohio and Mississippi river valleys of North America. The fungus most commonly affects the lungs (91%), followed by the skin (18%) and bones (4%). Cutaneous lesions due to blastomycosis have been described variously as nodular, papular, and verrucous, grow slowly, and often ulcerate. While blastomycosis can infect both immunocompetent and immunocompromised patients, Blastomycosis-like pyoderma itself rarely occurs outside the setting of immune dysregulation [3]. It has been postulated previously that BLP’s pathogenesis includes an exaggerated tissue reaction due to the host’s inability to clear a bacterial colonization [3,4].

In 1979, various diagnostic criteria have been put forward with recent literature generally agreeing on: (1) large verrucous plaques with multiple pustules and an elevated border, (2) typical histologic findings of psudoepitheliomatous hyperplasia with abscesses on biopsy, (3) growth of one or more pathogenic bacteria, and (4) negative cultures for other infectious etiologies, particularly fungi or mycobacteria. In their original publication Su et al. included two additional criteria: (5) negative fungal serology, and (6) normal bromide and iodide blood levels [5]. However, modern case reports of BLP tend to make the diagnosis with fewer criteria. Of the fourteen case reports published in Englishlanguage journals since 1995, only one tested for fungal serology [6]. Similarly, only two reports tested for halogen toxicity with the majority of papers stating that halogenoderma could be satisfactorily ruled out by a lack of halogen medication or ingestion in the patient’s history [4,6].

Many systemic immune dysregulatory states have been described in patients diagnosed with BLP including leukemia, chemotherapy, malnourishment, and alcoholism [3,7]. There are cases of BLP arising at areas of local disturbance such as sun exposure, trauma and tattoo in immunocompetent persons [2,3,7].

Multiple treatments modalities with varying results have been reported in the literature, including: curettage, surgical excision, carbon dioxide laser, potassium iodide, permanganate soaks, radiotherapy, disodium chromoglycate, and acitretin [4,8,9]. Effective treatment with systemic retinoids has also been reported [7].

We present a case of BLP with positive cultures for S. aureus and C. koseri in a patient with syphilis and HIV who responded to antibiotic therapy with doxycycline and penicillin G.

Case Report

A 35-year-old male presented for a facial rash of six months duration. He described several small papules, initially on the left chin, which progressively enlarged. Subsequently, he developed similar boggy lesions on the scalp and cheek. The lesions were mildly pruritic but otherwise asymptomatic. He endorsed shaving, but denied other forms of trauma, sick contacts, or recent travel.

On examination, the mentum and submentum had a large, crusted, eroded, and indurated verrucous plaque w/a raised border and draining purulent material (Figure 1). Similar boggy plaques were noted on the left cheek and left scalp (Figure 2). There was no regional lymphadenopathy.

clinical-case-reports-Mentum-submentum

Figure 1: Mentum and submentum with large, crusted, eroded, and indurated verrucous plaque w/a raised border in a patient with Blastomycosis-like Pyoderma.

clinical-case-reports-Boggy-plaques

Figure 2: Boggy plaques on the left cheek (a) and scalp (b) of a patient with Blastomycosis-like Pyoderma.

The patient underwent biopsy for tissue culture and H&E. Tissue culture revealed methicillin-resistant Staphylococcus aureus (MRSA) and Citrobacter koseri. HIV antibody screen and HIV-1 multispot were positive. Follow-up quantitative testing revealed a CD4 count of 607 cells/μl and a viral load of 910 copies/ml. Additionally, syphilis serology was positive with a titer of 128. Anaerobic bacteria, fungal, and atypical mycobacterium tissue cultures were negative. Hepatitis A antibody was positive. Hep B surface antigen and hepatitis C antibody were negative. Quantiferon gold was also negative.

Histopathologic examination on H&E showed pseudoepitheliomatous hyperplasia with dense dermal inflammation, composed of neutrophils, lymphocytes, and plasma cells (Figure 3). Direct microscopy with GMS and Fite stains were negative. Treponemal immunostaining was also negative. A gram stain showed gram-positive cocci in clusters.

clinical-case-reports-Histopathologic-examination

Figure 3: Histopathologic examination on H&E showing pseudoepitheliomatous hyperplasia with dense dermal inflammation, composed of neutrophils, lymphocytes, and plasma cells in a patient with Blastomycosis-like Pyoderma.

Based on these findings a diagnosis of blastomycosis-like pyoderma was made. A 14-day course of doxycycline was initiated based on sensitivities. Simultaneously, he was referred to infectious disease for treatment of concurrent syphilis with benzathine penicillin G, to which both cultured bacteria were resistant. Skin lesions resolved after five weeks (Figure 4). After undergoing HIV genotyping, the patient started antiretroviral therapy five weeks after resolution of the skin lesions. Two months after penicillin G treatment, follow up syphilis titer was 8 and viral load was not detectable.

clinical-case-reports-Skin-lesions-resolved

Figure 4: Skin lesions resolved after five weeks in a patient with Blastomycosislike Pyoderma after a 14-day course of doxycycline concurrent treatment for syphilis with benzathine Penicillin G.

Discussion

First described in 1903 as “pseudoepiteliomas cutanés,” blastomycosis-like pyoderma (BLP) is a chronic pyoderma that presents similarly to vegetating deep fungal infections [3,7]. It typically presents as one or multiple vegetating nodules and/or plaques on the extremities of middle aged to elderly adults [10]. Necrosis, pustules, fistulae, and abscesses may also be present [10]. The differential diagnosis includes blastomycosis and other deep fungal infections, halogenoderma, pemphigus vegetans, tuberculosis verrucosa cutis, pyoderma gangrenosum, mycobacterial infections, giant keratoacanthoma, and squamous cell carcinoma [2,4,7-12]. Our patient had four of the six criteria for BLP established by Su et al. In accordance with the pertinent literature, we refrained from preforming fungal serology and blood halogen level testing.

Minor trauma, such as shaving, and chronic sun-damage are thought to increase the likelihood of BLP [8-12]. The most commonly reported pathogen is Staphylococcus aureus [2]. Additionally, β-hemolytic streptococci, Pseudomonas aeruginosa, and citrobacter species have been reported [1].

Monotherapy with systemic antibiotics usually requires longterm treatment and often fails [7,9]. Our patient’s immune status was compromised by an untreated HIV infection, as well as a concurrent syphilitic infection. Syphilis has been reported to cause immune dysregulation including altered cell surface markers and increased likelihood of HIV co-infection [13]. Further, the probability of HIV transmission is higher when syphilis is present in either individual in a sexual partnership involving discordant HIV infection status [13,14]. It has been shown that secondary syphilis markedly decreases total circulating NK-cell numbers and is associated with the emergence of an atypical circulating CD56-negative CD16-positive NK-cell population which is poorly cytolytic and has impaired capacity to produce IFN gamma and other cytokines [15]. Interestingly, these NK-cell line changes are also observed in uncontrolled HIV patients. The mechanism for syphilis-driven immune dysregulation is not fully elucidated. The spread of syphilis into the bone marrow may alter the proper development of the myeloid and lymphoid progenitors of NKcells along with macrophages and dendritic cells [15,16].

Our patient’s rapid and complete response to a short course of doxycycline is unusual for BLP. Resolution of the skin lesions in the context of untreated HIV raises the hypothesis that the concurrent syphilitic infection may have contributed to immune evasion by these bacteria.

Although our patient underwent treatment of syphilis with penicillin, both cultured bacteria were resistant. This leads the authors to postulate that treatment of syphilis may have hastened the resolution of his BLP lesions. Patients presenting with vegetating skin lesions should be evaluated for treatable causes of immunocompromise including syphilis and HIV. Our patient represents a unique case of MRSA-induced BLP in a patient with syphilis and untreated HIV that resolved with antibiotic therapy.

References

Select your language of interest to view the total content in your interested language
Post your comment

Share This Article

Relevant Topics

Recommended Conferences

  • Global Experts meeting on Oncology Case Reports
    Aug 29-31, 2017 London, UK
  • Global Experts Meeting on Case Reports
    Osaka, Japan October 09-11, 2017
  • 6th Global Experts Meeting on Medical Case Reports
    October 16-18, 2017 San Francisco, California, USA

Article Usage

  • Total views: 104
  • [From(publication date):
    May-2017 - Jun 26, 2017]
  • Breakdown by view type
  • HTML page views : 83
  • PDF downloads :21
 
 

Post your comment

captcha   Reload  Can't read the image? click here to refresh

Peer Reviewed Journals
 
Make the best use of Scientific Research and information from our 700 + peer reviewed, Open Access Journals
International Conferences 2017-18
 
Meet Inspiring Speakers and Experts at our 3000+ Global Annual Meetings

Contact Us

Agri, Food, Aqua and Veterinary Science Journals

Dr. Krish

agrifoodaquavet@omicsonline.com

1-702-714-7001 Extn: 9040

Clinical and Biochemistry Journals

Datta A

clinical_biochem@omicsonline.com

1-702-714-7001Extn: 9037

Business & Management Journals

Ronald

business@omicsonline.com

1-702-714-7001Extn: 9042

Chemical Engineering and Chemistry Journals

Gabriel Shaw

chemicaleng_chemistry@omicsonline.com

1-702-714-7001 Extn: 9040

Earth & Environmental Sciences

Katie Wilson

environmentalsci@omicsonline.com

1-702-714-7001Extn: 9042

Engineering Journals

James Franklin

engineering@omicsonline.com

1-702-714-7001Extn: 9042

General Science and Health care Journals

Andrea Jason

generalsci_healthcare@omicsonline.com

1-702-714-7001Extn: 9043

Genetics and Molecular Biology Journals

Anna Melissa

genetics_molbio@omicsonline.com

1-702-714-7001 Extn: 9006

Immunology & Microbiology Journals

David Gorantl

immuno_microbio@omicsonline.com

1-702-714-7001Extn: 9014

Informatics Journals

Stephanie Skinner

omics@omicsonline.com

1-702-714-7001Extn: 9039

Material Sciences Journals

Rachle Green

materialsci@omicsonline.com

1-702-714-7001Extn: 9039

Mathematics and Physics Journals

Jim Willison

mathematics_physics@omicsonline.com

1-702-714-7001 Extn: 9042

Medical Journals

Nimmi Anna

medical@omicsonline.com

1-702-714-7001 Extn: 9038

Neuroscience & Psychology Journals

Nathan T

neuro_psychology@omicsonline.com

1-702-714-7001Extn: 9041

Pharmaceutical Sciences Journals

John Behannon

pharma@omicsonline.com

1-702-714-7001Extn: 9007

Social & Political Science Journals

Steve Harry

social_politicalsci@omicsonline.com

1-702-714-7001 Extn: 9042

 
© 2008-2017 OMICS International - Open Access Publisher. Best viewed in Mozilla Firefox | Google Chrome | Above IE 7.0 version