Case Reports in Rheumatology

Case Reports in Rheumatology / 2016 / Article

Case Report | Open Access

Volume 2016 |Article ID 2019250 |

Carla F. Gamarra-Hilburn, Grissel Rios, Luis M. Vilá, "Olecranon Bursitis Caused by Candida parapsilosis in a Patient with Rheumatoid Arthritis", Case Reports in Rheumatology, vol. 2016, Article ID 2019250, 5 pages, 2016.

Olecranon Bursitis Caused by Candida parapsilosis in a Patient with Rheumatoid Arthritis

Academic Editor: George S. Habib
Received09 May 2016
Revised14 Jul 2016
Accepted17 Jul 2016
Published09 Aug 2016


Septic bursitis is usually caused by bacterial organisms. However, infectious bursitis caused by fungi is very rare. Herein, we present a 68-year-old woman with long-standing rheumatoid arthritis who developed pain, erythema, and swelling of the right olecranon bursa. Aspiration of the olecranon bursa showed a white blood cell count of (41% neutrophils, 30% lymphocytes, and 29% monocytes). Fluid culture was positive for Candida parapsilosis. She was treated with caspofungin 50 mg intravenously daily for 13 days followed by fluconazole 200 mg orally daily for one week. She responded well to this treatment but had recurrent swelling of the bursa. Bursectomy was recommended but she declined this option. This case, together with other reports, suggests that the awareness of uncommon pathogens, their presentation, and predisposing risk factors are important to establish an early diagnosis and prevent long-term complications.

1. Introduction

Septic bursitis occurs in the olecranon bursa very commonly [1]; this is due to its superficial location and vulnerability to trauma [1]. Among predisposing factors for septic bursitis are immunosuppression, surgical intervention, chronic diseases, and any occupation that can produce trauma to the area [1, 2]. Bacteria are the most frequent culprit, with Staphylococcus aureus producing the majority of the cases [1, 2]. Fungal infection is rare and there are only few cases published in the medical literature. Septic bursitis due to Candida (parapsilosis, albicans, tropicalis, and glabrata) species, Penicillium species, Anthopsis deltoidea, Aspergillus terreus, and Phialophora richardsiae has been reported [113]. Herein, we report a case of an elderly woman with long-standing rheumatoid arthritis (RA) who presented with septic olecranon bursitis secondary to Candida parapsilosis. We also present a literature review of bursitis caused by Candida species.

2. Case Presentation

A 68-year-old female was referred to our service for evaluation of erythema and swelling of the right elbow. She was admitted to the hospital 12 days before because of an infected left foot ulcer that required debridement and intravenous antibiotic therapy. Six weeks prior to admission she was seen by a pain management specialist for swelling of the right elbow and she was diagnosed with olecranon bursitis. She was treated with bursa aspiration and corticosteroid injection. Cultures were reportedly negative. One to two weeks after the procedure, she had worsening of swelling, as well as pain and erythema of the olecranon bursa. She did not report fever, weight loss, fatigue, or weakness.

Her past medical history was remarkable for RA diagnosed at 30 years of age, arterial hypertension, peripheral vascular disease, and asthma. Her surgical history included amputations of the first and second toes of the left foot and two tendon repairs (left hand and left shoulder). She received multiple therapies for RA including auranofin, methotrexate, leflunomide, and etanercept. Her last treatment was golimumab, which she used for 4 years. She did not have further follow-up with her rheumatologist and stopped this treatment about 2 years before onset of olecranon bursitis.

On initial evaluation, she had normal vital signs. Scleromalacia was noted bilaterally. Examination of the upper extremities showed ulnar deviation of the metacarpophalangeal joints and swan neck deformities bilaterally. The left wrist had marked limitation of flexion and extension. The right olecranon bursa was tender and swollen, and the overlying skin was erythematous (Figure 1). Range of motion of the right elbow was not limited. She had multiple subcutaneous nodules in the right leg and a stage IV ulcer on the medial aspect of the left foot. Generalized muscle atrophy was observed. The rest of the examination was unremarkable.

Laboratory tests showed a white blood cell count of , lymphocytic count of , hemoglobin of 9.6 g/dL, and platelet count of . Serum creatinine was 0.5 mg/dL and blood urea nitrogen was 17 mg/dL. Wound cultures were negative. Chest X-ray showed mild prominence of the pulmonary markings in the right infrahilar region.

The olecranon bursa was aspirated and 9 mL of hemorrhagic fluid was obtained. No crystals were observed under polarized microscopy. Fluid analysis showed a white blood cell count of (41% neutrophils, 30% lymphocytes, and 29% monocytes). Bacterial cultures were negative. Fungal culture was positive for Candida parapsilosis; this was sensitive to anidulafungin, micafungin, caspofungin, 5-flucytosine, voriconazole, itraconazole, and fluconazole. The VITEK 2 system (bioMérieux, Inc., Hazelwood, Missouri, USA) was used for fungus identification. The Sensititre YeastOne system (Trek Diagnostic Systems, Cleveland, Ohio, USA) was utilized to determine antifungal susceptibility.

She was treated with caspofungin 50 mg intravenously daily for 13 days. Four aspiration procedures were required (every 3–5 days) due to fluid reaccumulation. All samples were cultured but only the first two were positive for Candida parapsilosis. After intravenous therapy, fluconazole 200 mg orally daily was prescribed for one week. She responded well to this therapy but had recurrent swelling of the bursa. Bursectomy was recommended but she did not wish to proceed with the intervention or receive further treatment. After 3 months of follow-up, she continued to have fluid in the olecranon bursa and had some discomfort in the area.

3. Discussion

Symptoms and signs of septic bursitis, either bacterial or fungal, are similar. However, fungal bursitis seems to have a more indolent course which may cause a delay in diagnosis and treatment [2, 47]. Among all bursae, the olecranon and the prepatellar bursae are the most commonly involved; this is because they are superficial, and pathogens can migrate transcutaneously through minor trauma [2]. Although septic bursitis is almost always secondary to direct inoculation, hematogenous spread can also occur [8, 9].

Fungal septic bursitis is rare. Candida (parapsilosis, albicans, tropicalis, and glabrata), Penicillium species, Anthopsis deltoidea, Aspergillus terreus, and Phialophora richardsiae have been isolated [113]. Specifically, very few cases of olecranon bursitis secondary to Candida parapsilosis have been reported in the medical literature [3, 7, 10, 11]. Unlike Candida albicans and Candida tropicalis, Candida parapsilosis is not an obligate human pathogen [14]. The clinical spectrum of Candida parapsilosis infection is variable, ranging from vulvovaginitis to fungemia and endocarditis. It is also known to cause arthritis which can be secondary to fungemia, intra-articular injections, or catheterizations or related to prosthetic joints [8, 9, 11, 15].

To the best of our knowledge, 11 cases of septic bursitis due to Candida species, including ours, have been reported in the medical literature (Table 1) [1, 3, 4, 713]. Five cases, including our case, were secondary to Candida parapsilosis [3, 7, 10, 11]. Two cases were secondary to Candida tropicalis [8, 9], and the other three were due to Candida albicans [1], Candida lusitaniae [13], and Candida glabrata [12] (one each). The subclass identification of Candida species was not done in one patient with subacromial bursitis and the diagnosis was achieved histopathologically after bursectomy was performed [4]. Regarding the site involved, the olecranon bursa was affected in 7 of the 11 cases including our patient [3, 7, 8, 1113]; the subacromial bursa was affected in 3 patients [1, 4, 10]; and the popliteal bursa was affected in 1 case [9]. Six patients were immunosuppressed and 1 patient was receiving prednisone at low dose (10 mg daily) [1, 79, 1113]. Our patient had severe joint damage from RA, but she was not receiving immunosuppressive therapy at the time of septic bursitis.

Case numberCandida strain/culture siteAuthor/year of publicationAge/sexInfected bursaClinical presentation of bursitisComorbiditiesOther risk factors Probable source of infectionTreatmentOutcome

1C. albicans
Bursal fluid
Rosochmann and Bell/1987
73/MSubacromialAcute, 5 daysSLECorticosteroidsFungemiaAmphotericin BComplete resolution

2C. glabrata
Phlegmon-like material form olecranon bursae
Skedros et al./2013
63/FOlecranonAcute, 2 weeks after corticosteroid injectionCOPD
Arterial hypertension
Recurrent oropharyngeal candidiasis
Prednisone 10 mg dailyCorticosteroid injectionCaspofungin
Debridement, irrigation, and bursectomy
Complete resolution

3C. lusitaniae
Bursal fluid
Behar and Chertow/1998
59/FOlecranonChronic, 6 monthsSLE
Methotrexate 15 mg weekly
Prednisone 30 mg daily
Superficial traumaFluconazole 100 mg a day; 5-fluorocytosineRecurrence after several months

4C. parapsilosis
Bursal fluid
Schlesinger and Hoffman/1995
62/FOlecranonAcuteBreast cancer
Prednisone 40 mg dailyUndeterminedAmphotericin B IV over 9 days
Ketoconazole (400 mg/d for 2 months)
Complete resolution

5C. parapsilosis
Bursal fluid
Jiménez-Palop et al./2002
32/MOlecranonChronic, around 3 monthsNoneNoneCorticosteroid injectionFluconazole 400 mg for 7 days, followed by 200 mg a day
Complete resolution

6C. parapsilosis
Bursa tissue culture
Miyamoto et al./2012
60/F OlecranonDuration of the disease not mentioned. It presented 7 months after infliximab therapy was startedRAInfliximab
Methotrexate Prednisolone
UndeterminedBursectomyComplete resolution of bursitis. Later developed wrist arthritis

7C. parapsilosis
Shoulder synovial fluid 
Tissue culture
Jeong et al./2013
74/M Subacromial, subdeltoid, and subcoracoidChronic, >18 monthsNoneNoneUndeterminedFluconazole (neither dose nor length of therapy specified)
Surgical exploration with drainage, debridement, and bursectomy
Complete resolution

8C. parapsilosis
Bursal fluid
Current case68/FOlecranonAcute, 1-2 weeks after bursa aspiration and corticosteroid injectionRA
Infected ulcer
NoneCorticosteroid injectionCaspofungin 50 mg IV daily for 2 weeks, followed by fluconazole 200 mg a day for 1 weekPersistence

9C. tropicalis
Bursal fluid 
Murray et al./1976
77/MOlecranon ChronicBladder cancer
Urethral and venous catheters
FungemiaAmphotericin B IV for 9 weeks 
Complete resolution

10C. tropicalis
Fluid from ruptured bursae
Wall et al./1982
48/MFirst, knee septic arthritis; later, popliteal bursitisAcute, 2 weeks after chemotherapyLymphocytic lymphomaChemotherapy
FungemiaAmphotericin B IV for 5 months
Bursectomy and calf dissection
Complete resolution

11Candida species 
No cultures, diagnosis done by histopathology
Khazzam et al./2005
65/MSubacromialChronic, >4 months Myocardial infarctionNoneCorticosteroid injectionVoriconazole 200 mg twice daily for 6 weeks
Complete resolution

C: Candida; M: male; F: female; SLE: systemic lupus erythematosus; COPD: chronic obstructive pulmonary disease; IV: intravenous; RA: rheumatoid arthritis.

In the 11 cases reported with Candida bursitis, the probable source of infection was thought to be fungemia in 3 cases [1, 8, 9], one case was thought to be secondary to superficial trauma [13], and in 3 cases the source of infection was undetermined [7, 10, 11]. Four cases were likely related to corticosteroid injection, including our case [3, 4, 12]. In our patient, although her musculoskeletal deformities and her duties as an administrative assistant predisposed to continuous trauma to the area, her symptoms worsened after the intrabursal injection. This event suggests that the pathogen could have been inoculated during the aspiration and corticosteroid injection. She could have also acquired the infection through transient fungemia from the wound in her foot. However, wound cultures were negative.

The course of septic bursitis due to fungi can be chronic and this delays diagnosis and treatment. Six of the 10 reported cases had a chronic course ranging from 4 to 18 months [3, 4, 8, 10, 13]; the remaining cases had an acute onset [1, 7, 9, 12]. In one case, the duration of the disease was not described but it presented 7 months after infliximab therapy was started [11]. Regarding the age at presentation, more than 70% of the patients were older than sixty years of age, this including our patient.

Fungal bursitis is treated with oral or parenteral antifungals as well as drainage of infected bursal fluid; this is frequently done by needle aspiration. Bursectomy is indicated when there is no response to this treatment, when the bursal fluid cannot be drained with a needle, or when there is infection of the surrounding soft tissue [2]. All of the patients that we describe in Table 1 received antifungal therapy at some point, but 7 required bursectomy to achieve cure [3, 4, 812]. Two patients were cured with antifungal therapy alone [1, 7]. One of the patients, who had olecranon bursitis due to Candida lusitaniae, was severely immunosuppressed, had recurrent bursitis, and ultimately died of Pneumocystis jirovecii infection [13]. Our patient had reaccumulation of fluid and bursectomy was indicated but she declined this option.

In summary, fungal infection due to C. parapsilosis is rare and follows an indolent course. Immunosuppression and advanced age appear to be predisposing factors for bursitis caused by Candida species. Septic bursitis caused by bacterial organisms usually responds well to antimicrobial therapy and fluid aspiration. In contrast, this therapeutic approach is not entirely effective for fungal bursitis caused by Candida species as recurrent bursitis is quite common. Definite cure is attained with bursectomy for which this procedure should be highly considered early in the management of these cases.

Competing Interests

The authors have no competing interests to disclose.


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Copyright © 2016 Carla F. Gamarra-Hilburn et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

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