Pulmonary histoplasmosis in a immunocompetent patient: A case report and literature review

Introduction

Primary pulmonary histoplasmosis is a lung disease caused by the dimorphic fungus Histoplasma capsulatum, with a worldwide incidence. It is endemic in certain areas of North America, and was first reported in China in 1958 (1). The severity of this mycosis is dependent upon the number of inhaled fungal particles and the immune status of the host (2). The morbidity and mortality rates of pulmonary histoplasmosis are low among immunocompetent patients. However, the morbidity and mortality rates of this mycosis are greater among immunocompromised individuals. In China, pulmonary histoplasmosis is sporadic. By 2015, only 76 cases with complete clinical data had been reported in the literature (3–20). Clinical presentations may include protean symptoms of fevers, chills, malaise, weight loss, cough and wheezing, symptoms. These are non-specific symptoms that may also occur with multiple other diseases. The majority of affected individuals present clinically silent manifestations and display no apparent symptoms (3). Therefore, misdiagnosis of pulmonary histoplasmosis as other pulmonary diseases, including tuberculosis, is highly likely. Misdiagnosis may delay the treatment, and the disease is fatal if left untreated (4).

Therefore, the present study reports the case of a patient diagnosed with pulmonary histoplasmosis. The study aimed to increase the understanding on the disease characteristics in order to facilitate the diagnosis and treatment of pulmonary histoplasmosis. The patient provided written informed consent for this case report.

Case report

A 54-year-old male patient was admitted to the Xiangya Hospital (Changsha, China) in June 2011 with a persistent cough that had appeared 1 week earlier due to contracting a cold. No signs of fever, sweating, chest pain, sputum, hemoptysis or other discomfort were noted. Pulmonary computed tomography (CT) scans conducted 2 days prior to admission detected a lump with enhanced intensity in the upper right lung and a large mass of high intensity in the right middle lobe with a pattern of air bronchogram observed in the mass (Fig. 1). Based on the characteristics observed in Fig. 1, the patient was suspected of having an infectious lung disease. Physical examination indicated the following: Body temperature, 36.5°C; heart rate, 76 beats/min; blood pressure, 140/80 mmHg. In addition, no superficial lymphadenopathy was noted, while bilateral symmetry was observed in thoracic cage. No abnormalities were identified in the bilateral lung on percussion. Laboratory examination was also performed and revealed the following results: White blood cell count, 9.4×109/l (normal range, 4–10×109/l); red blood cell count, 4.5×1012/l (normal range, 3.5–5.5×1012/l); hemoglobin level, 134 g/l (normal range, 110–150 g/l); blood platelet count, 237×109/l (normal range, 100–300×109/l); an elevated erythrocyte sedimentation rate, 70 mm/l (normal range, <20 mm/l); and negativity for tuberculosis antibody. In addition, the result of a G-test (for the detection of (1,3)-β-D-glucan, a fungal cell wall components) was abnormal at 57.0 pg/ml (normal range, <20 pg/ml). Bronchoscopy conducted 5 days after admission detected signs of inflammation of the bronchi, particularly the presence of severe inflammation in the right middle lobe. Negative acid-fast staining of the bronchus secretion was observed. Pathological examination under bronchoscopy revealed chronic mucosal inflammation in the branches of the right middle lobe. In combination with clinical data, the patient was preliminarily diagnosed with bacterial pneumonia. This diagnosis was made on the basis that lung infection is most commonly bacterial, whereas fungal infections often occur in immunodeficient patients and the present patient was an immunocompetent individual. Furthermore, G-tests may produce false positive results..

Figure 1. Computed tomography scans revealing bilateral pulmonary lesions 2 days before admission. (A) Pulmonary window and (B) mediastinal window.

The patient was treated with levofloxacin (0.6 g once daily, intravenously; Daiichi Sankyo, Tokyo, Japan) for 2 weeks, starting from day 1 after admission; however, the symptoms were not alleviated. Lung CT scans 12 days after admission revealed that the infectious lesions increased in number and in size, as shown in Fig. 2. CT-guided needle lung aspiration biopsy was then performed. Subsequent pathological examination revealed signs of granulomatous inflammation in the right middle lung, as shown in Fig. 3. Based on the findings of CT scans and hematoxylin-eosin staining, the patient was suspected with histoplasmosis. Subsequently, the patient was diagnosed with pulmonary histoplasmosis, which was confirmed by the aforementioned imaging and pathological findings.

Figure 2. Computed tomography scans revealing the changes in the lung lesions subsequent to misdiagnosis and inappropriate therapy (12 days after admission). (A) Pulmonary window and (B) mediastinal window.

Figure 3. Hematoxylin and eosin staining revealing the changes in the pulmonary lesions. (A) Magnification, ×200 and (B) magnification ×400.

Following diagnosis, the patient was treated with itraconazole (Janssen Pharmaceuticals, Inc., Titusville, NJ, USA) for 2 weeks, starting from 15 days after admission. The dosage was 200 mg, by intravenous infusion, twice daily for the first 2 days and 200 mg once daily thereafter. Subsequent lung CT scans conducted 4 weeks after admission revealed that the pulmonary infection was alleviated (Fig. 4), and the symptom of cough disappeared; thus, the patient was discharged from hospital. Subsequent to discharge, the treatment was altered to oral administration of itraconazole only (200 mg, twice daily, orally).

Figure 4. Computed tomography scans revealing the alleviation in the lung lesions subsequent to establishing the correct diagnosis and providing treatment (4 weeks after admission). (A) Pulmonary window and (B) mediastinal window.

A further three rounds of lung CT scans performed in September 2011, November 2011 and February 2012 demonstrated that the pulmonary lesions were gradually adsorbed, as illustrated in Fig. 5A-C, respectively. A second CT examination scan in February 2012, 10 days after the previous one, revealed that all the lesions in the lung had almost disappeared (Fig. 5D); therefore, oral use of itraconazole was discontinued.

Figure 5. Computed tomography scans revealing the disappearance of the lung lesions following discharge. These scans were obtained in (A) September 2011, (B) November 2011, (C) February 2012 and (D) 10 days after the previous scan (February 2012).

Discussion

Primary pulmonary histoplasmosFis is a primary lung disease caused by infection with fungus Histoplasma capsulatum. Histoplasma capsulatum is a thermally dimorphic fungus, found in soil, caves and abandoned constructions that are enriched in bat or bird excrement. .Infection with Histoplasma capsulatum occurs by the inhalation of microconidia or mycelial fragments, which then settle in the host's lungs and convert to yeast forms. The invasion of this fungus is intimately associated with the host immunity. If the patient has strong cellular immunity, then macrophages, epithelial cells and lymphocytes can eliminate the fungi. However, in immunocompromised individuals, Histoplasma capsulatum disseminates to a variety of organs, including the bones, spleen, liver, adrenal glands and mucocutaneous membranes, resulting in progressive disseminated histoplasmosis (21).

In the present study, ‘pulmonary histoplasmosis’ was selected as the keyword to search the literature for relevant studies published between 1990 and 2015. The CNKI, VIP and Wanfang databases were searched for relevant studies. In addition, the PubMed database was searched with ‘pulmonary histoplasmosis’ and ‘China’ as search terms. Exclusion criteria were as follows: i) Cases who were repeatedly reported; ii) cases with pulmonary histoplasmosis evolving into disseminated histoplasmosis; and iii) cases with incomplete clinical data. In total, 18 eligible studies reporting 76 cases were identified and included for systematic review (3–20). Complete clinical data, including age, gender, risk factors, primary disease, clinical manifestation, misdiagnosis, confirmed diagnosis, treatment and prognosis were pooled and evaluated. Exclusion criteria were as follows: i) Cases who were repeatedly reported; ii) cases with pulmonary histoplasmosis evolving into disseminated histoplasmosis; and iii) cases with incomplete clinical data. Subsequent to case screening, a total of 76 patients, including 40 male and 36 female aged 27–69 years, were eventually recruited for subsequent analysis.

Among these patients, 52 cases were found to present increased risk factors or primary diseases, 5 cases were treated with glucocorticoid therapy or chemotherapy, and 1 case was orally treated with immunosuppressive agents for an immunodeficiency disease. In total, 46 patients were complicated with alternative diseases or high risk factors, including diabetes mellitus, viral hepatitis, tuberculosis, history of surgery and contact with poultry. However, the case reported in the present study had seldom contacted with duck, swine, cattle and other poultry, and had no history of any systemic disorders or use of immunosuppressive drugs prior to onset. The environment in which the present patient worked was not likely to have caused infection with Histoplasma capsulatum spore, suggesting that not all cases of pulmonary histoplasmosis have contact with the fungal spore or exposure to high risk factors.

Previous studies demonstrated that the symptoms of pulmonary histoplasmosis greatly vary, and ~95% of patients diagnosed with pulmonary histoplasmosis present with atypical clinical manifestations (3–15). Common symptoms observed in the eligible studies mainly included fever in 11 cases, chest pain in 6 cases and other respiratory symptoms in 13 cases. However, in the current report, the patient solely presented with cough without apparent pulmonary infection.

The imaging manifestations of patients with pulmonary histoplasmosis are significantly diverse. Among the 77 cases, which included the 76 previous cases (3–20) and the patient in the present study, nodular or lump lesions were noted in 50 patients (64.9%), pneumonia-like exudative lesions were noted in 19 patients (24.7%) and different shapes of lung lesions were detected in 8 patients (10.4%) (22). Based on the findings of the present literature review, the following lung CT manifestations can be summarized for cases of pulmonary histoplasmosis: i) Cases with a short medical history of the disease are predominantly manifested as multiple sporadic exudative lesions of varying sizes and indistinct boundary. By contrast, cases with a long history of pulmonary histoplasmosis present with nodular lesions with an explicit boundary or Histoplasma capsulatum-infected tumors, or both; ii) sporadic or multiple lesions are frequently noted in the middle upper lobe of bilateral lungs; iii) pneumonia-like lesions, nodular lesions or both are observed; iv) exudates surround the pathological changes; v) the intensity enhancement is not evident; vi) pleural thickening is noted rather than pleural traction; and vii) the disease has a slow course. In the current study case report, the patient was found to have lump lesions in the right middle lung and exudates surrounding the lesions with insignificant enhancement. Initially, the present patient was misdiagnosed with bacterial pneumonia.

Lung tissue biopsy and fungal culture have been widely recognized as the gold standards for diagnosing pulmonary histoplasmosis (23,24). Among the 77 cases enrolled in the present study, 74 cases were diagnosed by lung tissue biopsy, while the remaining 3 cases were diagnosed by fungal culture. However, the fungal culture endured for at least 3 weeks and the positive rate was not adequately high; therefore, it has limited application in clinical practice (3–20). Similarly, the patient in the present case study was misdiagnosed with infectious pneumonia and showed no improvement following anti-infectious medication therapy. Subsequently, CT-guided percutaneous lung aspiration biopsy was conducted, which confirmed the diagnosis of pulmonary histoplasmosis. Consequently, bronchoscopy or CT-guided percutaneous lung aspiration biopsy is recommended to obtain histopathologic evidence and enhance the diagnostic accuracy when the diagnosis is ambiguous and undetermined.

According to the practice guidelines for histoplasmosis updated by the Infectious Diseases Society of America (25), different therapies should be delivered for acute or chronic pulmonary and disseminated histoplasmosis. Following literature analysis, 45 patients with histoplasmosis were surgically treated, 20 were treated with antifungal medication, 4 received itraconazole, 3 received triazole and 1 received with amphotericin B. In the present study, the patient fully recovered following the use of levofloxacin combined with itraconazole for 2 weeks during hospitalization and oral liquid of itraconazole for 10 months after discharge. Among the 77 cases, 38 patients were subject to follow-up for as long as >20 years. The majority of these patients were successfully treated or improved, whereas a minority of cases progressed into disseminated histoplasmosis or succumbed to the disease. In the current study, the patient was followed-up for >10 months and fully recovered following effective antifungal medication therapy.

In conclusion, the present study reported a case of pulmonary histoplasmosis that was initially misdiagnosed as bacterial pneumonia, and later successfully treated with antifungal therapy. For suspicious cases based on medical history and imaging manifestations, bronchoscopy or CT-guided lung needle aspiration biopsy should be actively performed to facilitate the differential diagnosis of pulmonary infection. After the diagnosis is confirmed, effective and proper antifungal treatment should be timely delivered upon the individual situations, aiming to enhance the clinical efficacy.

References