Case Reports in Cardiology
Volume 2017 (2017), Article ID 3626917, 5 pages
https://doi.org/10.1155/2017/3626917

Case Report

H. capsulatum: A Not-So-Benign Cause of Pericarditis

Paolo K. Soriano,¹ Muhammad Iqbal,¹ Shakthishri Kandaswamy,¹ Sami Akram,² Abhishek Kulkarni,³ and Tamer Hudali⁴

¹Department of Internal Medicine, Southern Illinois University, 751 N Rutledge, Springfield, IL 62702, USA
²Infectious Disease, Southern Illinois University, 751 N Rutledge, Springfield, IL 62702, USA
³Division of Cardiology, Southern Illinois University, 751 N Rutledge, Springfield, IL 62702, USA
⁴Clinical Internal Medicine, Southern Illinois University, 751 N Rutledge, Springfield, IL 62702, USA

Correspondence should be addressed to Paolo K. Soriano; psoriano27@siumed.edu

Received 17 May 2017; Accepted 24 July 2017; Published 7 September 2017

Academic Editor: Kuan-Rau Chiou

Copyright © 2017 Paolo K. Soriano 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.

Abstract.

The common causes of pericarditis and its course are benign in the majority of cases. Thus, further testing is usually not pursued and treatment for a presumptive viral etiology with nonsteroidal agents and steroids has been an accepted strategy. We present a patient with pericarditis who was unresponsive to first-line therapy and was subsequently found to have necrotizing granulomas of the pericardium with extensive adhesions and fungal elements seen on tissue biopsy. Serologic testing confirms active H. capsulatum infection, and he responded well to Itraconazole treatment. In patients with pericarditis who fail standard therapy with NSAIDs and steroids, it is suggested that they undergo thorough evaluation and that histoplasmosis be considered as an etiology, especially in endemic regions.

1. Case Introduction

We report an uncommon case of an adult male from the Midwestern United States presenting with as acute pericarditis due to Histoplasma capsulatum infection. We reviewed the literature on H. capsulatum pericarditis and discussed the diagnosis and management of necrotizing granulomatous pericarditis due to H. capsulatum. We recommend that histoplasmosis infection be on the differential diagnoses in patients having acute pericarditis in endemic regions.

2. Case History

A 56-year-old male with obesity, hypertension, diabetes mellitus type 2, and dyslipidemia presented with nonexertional chest pain that wakes him up at night exacerbated by coughing and laying supine. There were no associated fever, dizziness syncope, and palpitation. He recalls symptoms of an upper respiratory tract infection which have resolved a few weeks earlier. Our patient is an office worker with no additional risk factors as smoking, chest trauma, recent travel, significant outdoor exposure, and family history of malignancy.

On evaluation, blood pressure was 144/68 mmhg, HR was 101 bpm, RR was 24 cpm, and the patient was afebrile. Eye and oral examination showed no suspicious lesions. There was no skin rash and synovitis. Cardiovascular examination was negative for jugular venous distention and hepatojugular reflex. Precordium was mildly tender, point of maximal impulse was adynamic and nondisplaced, and there was no palpable ventricular heave. On auscultation, S1 and S2 sounds were muffled; a precordial rub was appreciated over the left sternal border and is heard throughout the cardiac cycle. The remainder of the physical examination was unremarkable.

Electrocardiography showed nonspecific ST-T wave changes and no PR abnormalities. Troponin values were normal. A transthoracic echocardiogram demonstrated a mildly thickened pericardium with no pericardial effusion. Global ventricular wall motion was normal. Results of the initial laboratory investigation are outlined in Table 1. This shows leukocytosis with lymphopenia and monocytosis, elevated ESR, and normal renal function. The patient was then started on a course of Ibuprofen and Prednisone for suspected viral pericarditis.

Table 1: Laboratory evaluation and serologic testing.

WBC
7.4 (3.4–9.4 K/mm³)

    Neut
64% (47–67%)

    Lymph
21% (25–45%)

    Mono
12% (1–9%)

    Eos
2% (0–6%)

ESR
25 (0–20 mm/hr)

Blood cultures
Negative

Serum calcium
9 (8.5–10.5 mg/dl)

BUN
14 (6–22 mg/dl)

Serum creatinine
0.9 (0.7–1.4 mg/dl)

Histoplasma yeast Ab
<1 : 8 (normal < 1 : 8)

Histoplasma mycelial Ab
<1 : 8 (normal < 1 : 8)

Histoplasma IF
Positive (M band)

Blastomyces Ab
<1 : 8 (normal < 1 : 8)

Blastomyces IF
Negative

Coccidioides Ab
<1 : 2 (<1 : 2)

Coccidioides IF
Negative

Aspergillus IF
Negative

Angiotensin-converting enzyme
12 (9–67)

HIV 1 & 2 Ab
Nonreactive

QuantiFERON-TB
Negative

ESR: erythrocyte sedimentation rate; BUN: blood urea nitrogen; Ab: antibody; IF: immunodiffusion.

During his 4-week follow-up, the patient reported some improvement of the chest discomfort but now endorses decreased exercise tolerance, exertional dyspnea, and worsening fatigue. D-Dimer was obtained and was slightly elevated, 0.47 (reference: 0.27–0.40 mcg/ml). Computed tomography of the chest demonstrated no pulmonary artery embolism. The pericardium was markedly thickened, along with a small amount of nonloculated pericardial effusion. Visualized were multiple enlarged mediastinal and subcarinal lymph nodes and a 1.2 cm pulmonary nodule in the left lower lobe (Figure 1). Taking his risk factors into account, his symptoms were now concerning for coronary ischemia. Myocardial Perfusion Scanning revealed a moderately intense area of reversible defect consistent with ischemia and infarction of the inferior wall. There were no features of hemodynamic collapse. Subsequent Coronary Angiography confirmed severe three-vessel coronary artery disease (mid-LAD 80%, 1st Diagonal 90% ostial lesion, 2nd Diagonal 80%, and RCA 100% with collaterals). Left ventriculogram showed hypokinesis of the basal inferior myocardium with an estimated EF of 50%.

Figure 1: Chest CT imaging. Coronal view of noncontrast chest CT scan showing hyperattenuated pericardium (arrows). Axial chest CT scan showing the same diffusely thickened pericardium. Enlarged mediastinal lymph node (arrowhead). Note the solitary nodule in the Left lower lobe (encircled).

The patient underwent urgent Coronary Artery Bypass Grafting (CABG). Intraoperatively, upon violating the pericardial sac, it was immediately evident that he had extensive nodular adhesions on the visceral and parietal pericardium. Gram stain and cultures for bacteria and acid fast bacilli were negative. Histopathology demonstrated a necrotizing granulomatous inflammation that stained positive for fungal elements within the central necrotic tissue. No malignant cells were identified (Figure 2). Screening for sarcoidosis, tuberculosis, and HIV infection was negative. Further serologic testing confirms H. capsulatum infection (Table 1). His postoperative course remained unremarkable. Treatment with Itraconazole was initiated with instructions to complete a 6-month course and a follow-up chest CT scan to monitor progression of the visualized solitary pulmonary nodule.

Figure 2: Histologic images. H&E stain of the atrial appendage showing epithelioid histiocytes (arrows), lymphocytes, and caseating granuloma (high power view of hematoxylin-eosin stain). Fungal elements (arrows) within central necrosis (Grocott methenamine silver stain, 400x magnification).

3. Discussion

Our index case fulfilled the clinical diagnostic criteria for acute pericarditis with typical chest pain, pericardial friction rub, and new pericardial effusion [1]. There were no diffuse ST-T wave changes on electrocardiogram and there was no pericardial effusion on echocardiography. The diagnosis is clinical and, in eighty percent of cases, the etiology is viral [2–4]. Therapy is empirically directed towards inflammation [3, 5].

Management of his condition included prednisone and nonsteroidal anti-inflammatory agents. Due to the benign course of the illness associated with the common causes of pericarditis, it is not necessary to search for the etiology in all patients [2–4], especially in areas with low rates of tuberculosis [6]. Hence, treatment for a presumptive viral etiology is an acceptable strategy. Even with extensive evaluation, a definite cause is established in only 16% of cases [7, 8]. Similarly, in a three case series that included a total of 784 unselected patients who underwent extensive testing, a specific diagnosis was only obtained in 130 cases (17%) [7, 9, 10].

H. capsulatum is a thermally dimorphic fungus endemic to North and Central America and is a common cause of fungal pericarditis in patients with an intact immune system [11–13]. Histoplasma pericarditis was first described in 1955 by Billings and Couch in a patient with pericardial calcification and positive histoplasmin skin test [14]. Three years later, Heiner (1958) reported a case of constrictive pericarditis in a pediatric patient. The etiologic agent was diagnosed as H. capsulatum by skin and serologic testing [15]. Perhaps the largest case series, with sixteen patients, by Picardi et al. (1976) concluded that this form of granulomatous pericarditis carries a good prognosis [16]. To date, we found approximately 35 reported cases of pericarditis caused by H. capsulatum.

The pathogenesis of pericarditis due to histoplasmosis is thought to be due to hypersensitivity to antigens from the yeast-phase cells of H. capsulatum within the mediastinal lymph nodes or adjacent pulmonary focus of the host [16, 17]. Pericardial involvement occurs as a complication of inflammation and represents an inflammatory condition rather than infection of the pericardium [18]. This explains why organisms are not recovered from pericardial fluid and cannot typically be isolated and cultured from biopsy specimens [19, 20].

In biopsy specimens, granulomas are common [13, 21]. Granulomas are a form of highly effective, nonspecific antifungal immune response mediated by macrophages infected with Histoplasma. This mechanism is essential to contain fungal growth, prevent systemic dissemination, and protect the organs from widespread inflammatory tissue damage [22]. The cytokines involved in this process are mainly TNF- and IFN- [22]. This places histoplasmosis in the differential diagnosis of sarcoidosis, tuberculosis, and malignancy. It is especially important that the distinction between sarcoidosis and histoplasmosis be made. Failure to exclude the diagnosis of histoplasmosis before treatment for a cardiac sarcoid may lead to marked disease exacerbation if immunosuppressive therapy is initiated in a patient who actually has acute histoplasmosis [23]. Ineffective cell-mediated immunity leads to the inability to control reticuloendothelial spread of histoplasmosis and disseminated disease [13, 24, 25]. In this case, the angiotensin-converting enzyme level and the QuantiFERON-TB test were notably negative. Suspicion for fungal etiology was triggered when fungal elements were visualized on GMS staining. The diagnosis of histoplasmosis was eventually made with serologic testing (Table 2).

Table 2: Etiology of acute pericarditis: data from 3 large case series.

Permanyer-Miralda et al. ( = 231)
Zayas et al. ( = 100)
Imazio et al. ( = 453)

Years
1977–1983
1991–1993
1996–2004

Location
Spain
Spain
Italy

Idiopathic
199
78
377

Specific etiology
32 (14%)
22 (22%)
76 (16.8%)

Neoplastic
12
7
23

Tuberculosis
9
4
17

Autoimmune
4
3
33

Purulent
2
1
3

Data from [7–9].

A variety of tests may be utilized for detecting histoplasmosis including histopathology stains for fungi, fluid, and tissue cultures and Ag-Ab detection. Complement fixation and immunodiffusion (IF) are both serologic tests utilized in H. capsulatum detection with similar sensitivities above 90% [26]. The immunodiffusion test is less sensitive compared to immunodiffusion but has specificity of almost 100% [27, 28] In immunodiffusion, test results are reported as M or H precipitins or bands. Most patients will develop an M band, while the H precipitin band is detectable in fewer than 20% of cases and is seen most often in patients with disseminated disease [29]. Antigen testing in our patient revealed comp-fix titers of 1 : 8 and a positive M band with IF. Although higher comp-fix titers are highly suggestive of an acute infection, lower titers as seen in this case are seen in one-third of active disease.

Management of Histoplasma pericarditis is based on the guideline released in 2007 by the Infectious Diseases Society of America. NSAIDs are the mainstay of therapy for mild disease [18]. In the event of hemodynamic compromise and in individuals who fail to improve on NSAIDs, prednisone may be used. Pericardiocentesis is also indicated in those with evidence of hemodynamic compromise. Although there is no active pericardial fungal infection, the use of Itraconazole is advocated in moderate-to-severe disease [18]. However, due to lack of clinical trials, it is unclear whether antifungal therapy alters the course of histoplasmosis pericarditis [30].

Once treatment is initiated, a quantitative antigen enzyme immunoassay may be used to monitor decreases in serum and urine H. capsulatum antigens [31]. This strategy was not employed for our patient, since he had very low antigen titers before treatment. In this situation, there is no test to document disease eradication. Improvement is assessed based solely on clinical findings.

Since the submission of this article, our patient presented for biopsy of the left lower lobe pulmonary nodule. Results reveal a benign tissue with necrotizing granuloma, negative for fungal and mycobacterial elements. No repeat antigen testing was performed and he remains asymptomatic to this day.

4. Conclusion

We present a rare case of histoplasmosis pericarditis that failed therapy with NSAIDs and steroids but responded to Itraconazole treatment. We recommend that, in endemic regions, clinicians should further evaluate patients with typical symptoms of pericarditis and consider histoplasmosis as an etiology, especially in patients that fail first-line therapy.

Conflicts of Interest

The authors declare that there are no conflicts of interest regarding the publication of this article.

Acknowledgments

Special thanks are due to Dr. Jeff F. Wang, Dr. Nasariah Nallamothu, Dr. Jeffrey Christy, Dr. Steven O’Marro, Dr. Logan Chastain, and Ms. Lydia Howes of the SIU School of Medicine Library.

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