Characteristics of Sinus Fungus Ball: A Unique Form of Rhinosinusitis.

OBJECTIVE: The purpose of this study was to investigate the characteristics of this unique form of rhinosinusitis.
METHODS: Ninety-one patients with sinus fungus balls were evaluated for clinical characteristics. Nasal tissues obtained from 38 patients with sinus fungus ball, along with 26 controls were used for histopathological, cytokines/chemokines, western blotting, and genetic analyses.
RESULTS: Patients with fungus balls had significantly more females and their age was older. The presentation of fungus ball was predominantly unilateral (97.8%). Thirty-three patients (36.3%) had risk factors for fungal infection. Macrophage and neutrophil dominated cellular infiltration was found in nasal tissues of fungus ball patients. A tendency of reduced tight junction staining (e-cadherin) and protein expression was found. Interleukin 8 (IL8) and granulocyte colony stimulating factor (G-CSF) significantly increased in sinus fungus ball tissue homogenates when compared with those from controls. Higher prevalence of a single single nucleotide polymorphism (SNP) with E-cadherin was found in the patients with fungus ball.
CONCLUSIONS: We found that patients with sinus fungus ball had robust immune responses, allowing recruitment and activation of macrophages and neutrophils. However, patients with sinus fungus ball could have genetic or acquired weakness in immunity. The fungal hyphae were localized and accumulated within single sinus instead of being eradicated by host.

Introduction

The prevalence of fungal rhinosinusitis has been on the rise despite its rarity.[1-3] The disorder encompasses a variety of manifestations; from being innocuous to rapidly becoming fatal. Fungal rhinosinusitis is broadly divided into two forms: invasive and noninvasive. Its different types are the result of a variety of host-microbial interactions.[4] For example, fungus acting as an antigen can cause allergic fungal rhinosinusitis. Fungus can also play a role as an aggressive pathogen able to infect immunocompromised hosts, thus resulting in the invasive fungal rhinosinusitis. Fungus ball (mycetoma) is a noninvasive form of this disorder mostly presented through the accumulation of fungal hyphae in the maxillary sinus. Occasionally, the hyphae accumulation may appear in the sphenoid or other sinuses.[5] Sinus fungus balls usually affect immunocompetent hosts and the hyphae do not invade the sinus mucosa, bone or blood vessels. However, with host immunity deteriorating the fungus ball may progress to the invasive form.[6]

Sinus fungus ball could erode the sinus wall causing facial pain or obstruct the sinus ostium resulting in secondary bacterial infections. Symptomatic fungus ball is an indication that sinus surgery may be required.[7-9] Following the complete surgical removal of the fungus ball, anti-fungal medication is not usually indicated.[7-9] Patients with asymptomatic sinus fungus ball were occasionally diagnosed through the use of image studies which were performed for other purposes. There are no guidelines for treatment of asymptomatic sinus fungus ball. Nevertheless, removal of the fungus ball for pathologic diagnosis is proper procedure with a low morbidity.[1] Based on the low incidence of fungal rhinosinusitis, its detailed pathophysiology has not been fully explored; even though both the genetic background and immune status of the affected hosts have been proposed to be involved in the underlying etiology, along with involvement in anatomical obstruction, environmental exposure, and the toxicity of microbes.[10] The purpose of this study was to investigate the clinical presentation, histopathological, inflammatory pattern, and host genetic features of sinus fungus ball.

Methods

Study subjects

The retrospective chart review covered an 8-year period from January 2006 to January 2014. Patients enrolled included those who had undergone sinus surgery in our hospital for the treatment of sinus fungus balls. Their diagnosis was based on radiologic, endoscopic and pathological evidence of fungi contained in a sinus cavity.[4,11,12] In brief, radiologic studies showed sinus opacification or calcification. A cheesy or clay-like material was found by use of a sinus endoscopy. In addition, a histopathological examination confirmed the accumulation of dense hyphae in surgical specimens. Patients who demonstrated evidence of an invasive fungal infection, including pathological tissue invasion or associated neurologic or vascular deficits, were excluded. The clinical characteristics (age, gender, and co-morbidities) of the enrolled subjects were analyzed. All subjects with sinus fungus ball underwent computed tomography (CT) scans of the sinuses prior to undergoing surgery. Their CT scans were scored according to the Lund-Mackay system.[13]

Nasal tissues were obtained from patients who had donated their surgical specimens to the tissue bank of our hospital. Specifically, tissue samples were harvested from the osteomeatal complex from those patients who had maxillary fungus balls, or the sphenoid ostia from those who had sphenoid fungus balls. Control tissues were from the nasal cavity of patients who had undergone septoplasty and partial turbinectomy.

Histologic characteristics and immunohistochemistry of sinus fungus balls

Tissues were fixed overnight in a 10% neutral buffered formalin. Following fixation, tissues were embedded in paraffin, cut into 4-μm-thick sections, and stained with hematoxylin and eosin (H&E). Immunohistochemistry (IHC) was performed to determine tissue cellular infiltration, changes in tight junction, and mucus production. Paraffin sections were de-paraffinized and repeatedly rinsed before being incubated with primary antibodies for 20-80 minutes at 37°C. An UltraView Universal DAB Detection Kit (Ventana Medical Systems, Inc., Tucson, AZ, USA) was used for chromogenic detection. Some sections were further counterstained with haematoxyline (Sigma-Aldrich, Bornem, Belgium). CD68 (Agilent Technologies, Inc., Santa Clara, CA, USA; 1:200 dilution), and MPO (Agilent Technologies, Inc., Santa Clara, CA, USA; 1:10,000 dilution) were used as the primary antibodies for the evaluation of cellular infiltrations (macrophages and neutrophils). Zo-1 (Heidelberg Engineering Inc., Franklin, MA, USA; 1:200 dilution) and E-cadherin (Thermo Fisher Scientific Inc., Fremont, CA, USA; 1:100 dilution) were used as the primary antibodies for evaluating the epithelium inter-cellular junction. Periodic acid–Schiff (PAS) staining (Muto Pure Chemicals CO., LTD., Tokyo, Japan) was used to visualize fungal hyphae and to evaluate mucus production. Histological slides were ultimately examined using a bright-field microscope, with the digital images captured for analyses. Tissue cellular infiltration was determined by the amount of inflammatory cells (eosinophil, neutrophil, or macrophage) found in the sub-epithelial area. Loss of epithelial integrity was defined as epithelium staining of Zo-1 and E-cadherin. Slides were evaluated independently by two coauthors (KL Liang and WC Wang). For each slide, the quantity of staining was assessed using a semi-quantitative approach according to an arbitrary 5-point visual scale outlined as follows: 0 absent, 1 weak, 2 moderate, 3 intense, and 4 very intense.[14]

Western blotting

Nasal tissues were lysed with a T-per tissue protein extraction buffer (Thermo Scientific, Waltham, MA, USA). Protein concentrations were measured with BAC Protein Assay (Pierce Chemical Co., Rockford, IL, USA). Equal amounts of proteins from samples were subjected to electrophoretic separation in either 8% or 12% polyacrylamide gel prior to being transferred to a polyvinylidene difluoride membrane. They were then healed in blocking buffer for 1 hour at room temperature. The membrane was incubated with primary antibodies of Zo-1 (Thermo Scientific, Waltham, MA, USA), E-cadherin (BD Pharmingen, San Diego, CA, USA), Claudin-1, Catenin-β (both supplied by Elabscience Biotechnology, Houston, USA), and glyceraldehyde phosphate dehydrogenase (GAPDH; Proteintech, Rosemont, USA) overnight at 4°C. On the following day, the membranes were subsequently incubated with an horseradish peroxidase (HRP)-conjugated secondary antibody after repeated washing and reacted at room temperature for 1 hour, followed by electrochemiluminescent detection (Millipore Billerica, MA, USA). The density of each protein band was scanned using ImageJ Software, version 1.46r (National Institutes of Health, Bethesda, MD) and compared by densitometry.

Inflammatory cytokines/chemokines expression of nasal tissues

Cytokines/chemokines in nasal tissue homogenates were determined using Bio-Plex® (Bio-Rad, Hercules, CA, USA) including interferon-gamma (IFN-γ), tumor necrosis factor alpha (TNF-α), IL1β, IL4, IL6, IL8, IL10, IL13, IL17A, granulocyte colony stimulating factor (G-CSF), granulocyte-macrophage colony-stimulating factor (GM-CSF), Eotaxin and RANTES. The tests were performed according to the manufacturer’s recommendations.

Detecting clinically relevant single nucleotide polymorphisms in patients with sinus fungus ball

Human genomic DNA was isolated from both the nasal tissues of the fungus balls and controls using the QIAmp DNA miniKit (Qiagen Biosciences, Germantown, MD) according to standard procedures. Genotyping assays were performed using the commercially available Taqman® pre-developed assay reagents for allelic discrimination (Applied Biosystems, Foster City, CA, USA) in 20 μL reactions containing approximately 1 μL of DNA input (20 ng), nuclease free water, genotype Master Mix, and probe/primer assay mix. Reactions were run on the StepOnePlus Real-Time polymerase chain reaction (PCR) system according to standard procedures for 40 cycles. The names and details of single nucleotide polymorphism (SNP) used are listed in Table 1.

Table 1.

Selected single nucleotide polymorphisms in this study.

SNP name	Substitution	SNP ID	TaqMann® Assay ID (Applied Biosystems, Foster City, CA, USA)
IL8[15]	A/T	rs4073	C_11748116_10
IL10[16,17]	T/G	rs1800872	C_1747363_10
IL10[16,17]	T/C	rs1800896	C_1747360_10
IL15[18]	T/C	rs12508866	C_1752409_10
IL15[18]	G/T	rs6842735	C_29318124_10
IL15[18]	A/G	rs1519551	C_8865650_10
TNFα[15]	G/A	rs1800629	C_7514879_10
INFγ[19]	G/A	rs2069705	C_15944115_20
CR1[15]	A/G	rs17047660	C_25598593_10
CR1[15]	A/G	rs17047661	C_25473166_10
IL1RN[18]	C/T	rs4252041	C_27884744_10
TLR4[17,20]	A/G	rs4986790	C_11722238_20
TLR9[21]	A/G	rs5743836	C_32645383_10
CH1[22]	A/G	rs16948383	C_32810010_10
CH1[22]	C/T	rs2276330	C_15881320_10
CH1[22]	A/C	rs3785078	C_27481925_20
CH1[22]	C/G	rs7203904	C_29032982_30

Ethical consideration

Enrolled subjects had all signed informed consents prior to enrollment. The Institutional Review Board of the study hospital approved the study.

Statistical analyses

Clinical data were represented in terms of frequencies and means (with standard error, SD). Statistical comparisons were performed using GrapPad Prism software version 6 (GraphPad Software, Inc., La Jolla, California, USA). Both Mann–Whitney and Pearson chi-square tests were applied whenever appropriate.

Results

A total of 91 patients with sinus fungus ball were enrolled for the evaluation of their clinical data. Thirty-eight sinus tissues from fungus ball patients harvested during functional endoscopic sinus surgery (FESS) and 26 nasal tissues harvested during septoplasty and turbinectomy were used for histopathological, cytokines/chemokines, western blotting, and genetic analyses. Tissue samples were randomly assigned for the aforementioned studies.

Clinical characteristics of study subjects

The clinical characteristics of the 91 patients with sinus fungus ball are listed in Table 2. We discovered that the subjects with sinus fungus ball were more likely to be females and at an older age. A great majority of sinus fungus ball was presented unilaterally (97.8%). Only two patients had bilateral sinus mycetoma, with one experiencing post-irradiated nasopharyngeal carcinoma and the other chronic leukemia. Thirty-three patients (36.3%) had known risk factors in the etiology of fungal infections, including diabetes, liver cirrhosis, hematological malignancy, medical immune depressant, and had been receiving chemotherapy. Those who had known risk factors for fungal infections were found to be older than those who were without risk factors (P < .001). Except for that circumstance, all other clinical characteristics were similar.

Table 2.

Clinical characteristics of study subjects.

Group	Fungus ball (N = 91)
Mean age (range)	57.51 (23-82)
Female (N, %)	66 (72.5%)
Unilateral (N, %)	89 (97.8%)
Side (Right/left/bilateral)	(56/33/2)
Maxillary sinus (N, %)	79 (86.8%)
Sphenoid sinus (N, %)	12 (13.2%)
Smoker[a] (N, %)	11 (12.1%)
Allergic rhinitis (N, %)	9 (9.9%)
Asthma (N, %)	1 (1.1%)
Symptoms (N, %)
Nasal obstruction	36 (39.6%)
Rhinorrhea	33 (36.3%)
Nasal bleed	17 (18.7%)
Foul odor	10 (11%)
Post nasal drip	35 (38.5%)
Headache	11 (12.1%)
Facial pain	13 (14.3%)
Hyposmia	3 (3.3%)
Facial swelling	2 (2.2%)
Asymptomatic	3 (3.3%)
Pathogen (identified by morphology)
Aspergillus	86 (94.5%)
Undetermined	5 (5.5%)
Computed tomography findings
Mean Lund-Mackay CT score (SD)	4.74 (2.53)
Calcified density (N, %)	66 (72.5%)
Sclerotic changes (N, %)	57 (62.6%)
Bony erosion (N, %)	59 (64.8%)
Deviated nasal septum (N, %)	5 (5.5%)
Concha Bullosa (N, %)	8 (8.8%)
Risk factors of fungal infection (N, %)	33 (36.3%)
Diabetes	16 (17.6%)
Hematological malignancy	1 (1.1%)
Non-hematological malignancy[§]	6 (6.6%)
Medical immunosuppressant	7 (7.7%)
Liver cirrhosis	2 (2.2)
Chronic renal disease	1 (1.1%)

Current or ex-smoker.

Head neck cancers and a gastric cancer.

Histologic characteristics and IHC of sinus fungal balls

Ten nasal samples were obtained from the tissue bank (5 fungal balls and 5 controls) for the purpose of IHC studies. Representative photomicrographs are shown in Figure 1. The summary for abundance of staining regarding the H&E and IHC staining scores are shown in Figure 2. Mild eosinophils infiltration was identified in the H&E staining of sinus fungus ball tissues. Predominantly, macrophages and neutrophils infiltration were found in nasal tissues from patients with fungus ball. There was mildly decreased staining of tight junction staining (Zo-1 and E-cadherin). However, there were no significant changes in mucosal integrity between the controls and the patients with fungus ball in mucosal integrity.

Figure 1.

Representative microphotographs of H&E staining and immunohistochemistry (IHC) staining showing morphological and inflammatory changes of nasal mucosa in the controls and fungus ball. H&E staining 400X (A), eosinophils marked with red arrow head; CD68 200X (B); MPO 200X (C); PAS staining 100X (D); E-cadherin 100X (E); Zo-1 100X (F).

Figure 2.

Compare the abundance of immunohistochemistry staining between tissue sections of the controls and fungus ball. The abundance of staining was assessed with a semi-quantitative approach according to an arbitrary 5-point visual scale described as follows: 0 absent, 1 weak, 2 moderate, 3 intense, and 4 very intense.

Western blotting of nasal tissue

Nine nasal samples were used for analysis of tight/adherens junction protein expression. The results are summarized in Figure 3. There were no significant differences in tight junction protein expression between the nasal samples of the controls and fungus ball patients (P = .873, .381, .191, and .5 for zo-1, E-cadherin, claudin, and catenin-β, respectively). Nevertheless, there was a tendency for decreased E-cadherin protein expression in nasal tissues from fungus ball patients.

Figure 3.

Western blot analyses of tight junction protein expression obtained in 9 study subjects (A). The relative expressions to house keeping protein are shown in (B).

Inflammatory cytokines/chemokines concentration in nasal tissue

Twenty-six nasal samples were obtained for cytokines/chemokines analyses (14 fungus balls and 12 controls). The results of cytokine and chemokine levels are shown in Figures 4 and 5. IL1β and IL8 significantly increased in tissues from patients with fungus ball (P = .007 and 0.0008, respectively). There were no significant differences in TH2, Treg, and T17 cytokines including IL-4, IL-13, IL10, and IL17 between tissues from the controls and fungus ball patients (P = .163, 0.716, > 0.99, and 0.134, respectively). Among chemokines, only G-CSF significantly increased in tissues from fungus ball patients than those of the controls (P = .002).

Figure 4.

Comparison of cytokine level in tissue homogenates between sinus fungus ball and controls.

Figure 5.

Comparison of chemokine level in tissue homogenates between sinus fungus ball and controls.

Association of genotype with sinus fungal ball susceptibility

Nineteen nasal samples (5 controls and 14 fungus balls) were used for genotype analyses. The genotype and allele distribution associated with fungus infection in lungs are listed in Table 3. We found no differences in genotype and allele distribution among SNPs that are known to be associated with invasive pulmonary fungal infection and fungus ball in the lung. However, a significant difference in prevalence was found with a SNP (rs7203904) among patients with fungus balls (Table 4). This SNP has been reported to be associated with epithelial E-cadherin expression in the asthma patients.

Table 3.

Genotype and allele frequencies of the selected SNPs associated with fungal infection of the lung.

SNPs	Genotype	Fungus ball (N = 14)	Control (N = 5)	P [a]	P [b]
IL8	AA	1	1	.575
rs4073(A > T)	AT	9	2
	TT	4	2
	A allele	11	4		.968
	T allele	17	6
IL10	TT	6	2	.190
rs1800872 (T > G)	TG	7	1
	GG	1	2
	T allele	19	5		.315
	G allele	9	5
IL10	CC	14	5	-
rs100896 (T > C)					-
IL15	TT	9	3	.981
rs12508866 (T > C)	CT	5	2
	T allele	23	8		.986
	C allele	5	2
IL15	GG	9	3	.951
rs6842735 (G > T)	GT	5	2
	G allele	23	8		.963
	T allele	5	2
IL15	AG	1	1	.674
rs1519551 (G > A)	AA	13	4
	G allele	1	1		.687
	A allele	27	9
TNFα	GG	11	4	.814
rs1800629 (G > A)	AG	2	1
	AA	1	0
	G allele	24	9		.923
	A allele	4	1
IFNγ	GG	6	2	.577
rs2069705 (G > A)	AG	6	3
	AA	2	0
	G allele	18	7		.781
	A allele	10	3
CR1	AA	14	5	-
rs17047660 (A > G)					-
CR1	AA	14	5	-
rs17047661 (A > G)					-
IL1RN	CC	14	5	-
rs4252041 (C > T)					-
TLR4	AA	14	5	-
rs4986790 (A > G)					-
TLR9	AA	14	5	-
rs5743836 (A > G)					-

Chi square test for differences in frequency distribution of genotypes between cases and control.

Chi square test for differences in frequency distribution of alleles between cases and controls.

Table 4.

Genotype and allele frequencies of the selected SNPs associated with E-cadherin.

SNPs	Genotype	Fungus ball (N = 14)	Control (N = 5)	P [a]
CH1	AA	1	0	.209
rs16958383 (A > G)	AG	5	0
	GG	8	5
	A allele	7	0	.08
	G allele	21	10
CH1	CT	1[b]	0	.523
rs2276330 (C > T)	TT	12	5
	C allele	1[b]	0	.529
	T allele	25	10
CH1	AA	12	3	.226
rs3785078 (A > C)	AC	2	2
	A allele	26	8	.255
	C allele	2	2
CH1	CC	1	0	.085
rs7203904 (C > G)	CG	7	0
	GG	6	5
	C allele	9	0	.040[c]
	G allele	19	10

Chi square test for differences in frequency distribution of genotypes or alleles between cases and controls.

One sample failed to determine the genotype.

P < .05.

Discussion

Sinus fungus balls mostly occurring in females and older individuals with a predominantly unilateral presentation are findings that are consistent with previous studies.[23,24] Our results also demonstrated that fungus ball mostly occurs in the maxillary sinus. CT scans of sinus fungus ball were characterized with calcified density, sclerotic, or erosion changes in the sinus wall.[2] Otherwise, symptoms from sinus fungus ball were not specific and were difficult to differentiate from non-fungal rhinosinusitis. The etiology of fungus ball has not been well investigated. Tai et al[25] reported that fungus ball is not associated with osteomeatal complex obstruction but with another as-yet-unexplained mechanism. The host’s immunological status is presumably the main determinant for fungal rhinosinusitis. Fungus balls more often occur in immunocompetent hosts or persons with a very subtle immunodeficiency.[4,6,12] However, a substantial proportion (36.3%) of these types had known risk factors associated with fungal infection in our study. These included those with diabetes under treatment, those who had received chemotherapy or immunosuppressant regents, had a history of hematological malignancy, or experienced chronic renal diseases. It has been reported that those patients who developed an immunocompromised status could experience their fungus balls progressing into invasive fungal sinusitis.[6] It is therefore advisable to carefully follow-up on such patients with immunodeficiency in order to minimize their risk of developing invasive fungal rhinosinusitis.

The main diagnostic tool for detecting fungal infection is the histopathological examination of affected tissues. Previous studies have reported that only a minority of fungus balls (10%-30%) exhibited positive findings in their tissue cultures.[8,26,27] A possible explanation for this is that most fungi in fungus balls are localized outside the mucosa, while also being non-viable for culture. The procedure involving a fugal culture is typically time-consuming and carries a very low diagnostic sensitivity, whereas histopathology usually provides a rapid presumptive diagnosis. In certain circumstances, histopathology is the only means of locating evidence related to the absence of culture findings. Identifying the morphological characteristics of fungal elements can help toward the classification of the infecting fungus. Finally, the host’s reactions to fungal infection (e.g. inflammation, necrosis, or hemorrhage), and the extent of fungal infection revealed by histopathology provides valuable information for physicians.[28] PAS staining is the standard method for microscopic visualization of fungal hyphae.[29] All patients diagnosed with fungus balls in this study had visualized conglomerated fungal hyphae in their nasal specimens. In addition, PAS staining remains an important tool for the purpose of evaluating mucus production. Increased epithelial mucus production and granular hypertrophy were observed in patients with fungus balls.

IHC and inflammatory cytokines/chemokines analyses in this study provided important information on the disease mechanism of sinus fungus ball. Park et al[30] reported that mucosal cellular infiltration increases with sinus fungus ball. We discovered that there was mild eosinophils infiltration in patients with sinus fungus balls. Nevertheless, neutrophils and macrophages were the predominant inflammatory cells in the mucosa of fungus balls. Specific inflammatory cytokine/chemokine changes were found in the tissue homogenates of sinus fungus ball patients. IL-1β, which was produced by activated macrophage, significantly elevated in fungus ball. TH2, Treg, and T17 cytokines in nasal tissues from fungus ball patients were not significantly different to those of the controls. The IL-17A level of fungus ball tissue slightly increased compared to that of the controls. Werner et al[31] had reported that IL-17A provided clearance of Aspergillus fumigatus in their mice experiments. Chemotactic factors (IL8, Eotaxin, and G-CSF) elevated in sinus fungus ball tissues, indicating that there was activation and recruitment of macrophage, eosinophils and neutrophils. Immune responses to Aspergillus in humans involved both macrophages and neutrophils, which can ingest and kill the fungus.[16] Indeed, we did discover that cytokines associated with the function of macrophage and neutrophil were specifically high. The significant rise of chemokines and cytokines indicated a robust innate immunity with activation and recruitment of innate cells in patients with sinus fungus ball.

E-cadherin and Zo-1 are tight junction proteins important in both the control of tissue architecture and the maintenance of tissue integrity. Consistent with this, Man et al[32] found that manipulation of the E-cadherin function alters epithelial integrity, resulting in airway infections. Another study reported that E-cadherin CDH1 polymorphism was associated with airway remodeling and lung function in patients with asthma.[22] Our findings are in line with that study, as we too saw a decrease in epithelial tight junction protein expression in patients with fungus balls. These findings are consistent with the role of tight/adherens junction protein in structural abnormality of the airway, as related to the defective clearance of inhaled fungal spores that may subsequently develop into hyphae.[22]

It remains unclear why most individuals remain asymptomatic after inhalation of this fungus while only a small minority experience fungal infections. It is becoming apparent that Single Nucleotide Polymorphism (SNP) in key immunity genes can increase susceptibility to certain infections.[21,33] It is plausible that such genetic variations in the immune system may lead to an imbalance between the pro- and anti-inflammatory responses, resulting in a predisposition to fungal infections.[21] Several gene polymorphisms are candidates for prognostic biomarkers regarding invasive aspergillosis in the lung.[17,19-21] Few studies with small patient numbers have investigated the genetic association of pulmonary aspergilloma, a disorder similar to sinus fungus ball. These limited studies have shown that polymorphisms in several genes involved in innate immunity and cytokines predispose a patient’s susceptibility to mycetoma.[15,17,18,20,21] No studies have yet investigated the role of SNP in sinus fungus ball. In our study, no increased prevalence was found with the several SNPs known to be associated with fungal infections. One possible explanation for this discrepancy with other reports is the differences in geographical location and the ethnic population of patients. In addition, our case number was small. Furthermore, the lack of SNP variations associated with invasive Aspergillosis may partly explain our findings that those fungus ball patients with immunodeficiency did not progress to experiencing invasive fungal infections. Despite that, we found an increase in SNP variations was related to E-cadherin in our patients with fungal balls.

Conclusions

There are unique characteristics surrounding sinus fungus ball, including its occurrence in female patients, older individuals, patients with subtle immune deficiency, and with those with a predominantly unilateral presentation. We performed immunochemistry staining, western blotting, chemokines and cytokines analyses, and discovered the prevalence of several known SNPs associated with fungal infection or respiratory diseases. We found that patients with sinus fungus ball experienced robust immune responses, allowing for the recruitment and activation of both macrophages and neutrophils. However, patients with sinus fungus ball could possibly have a genetic or acquired weakness in their immunity or barrier function. The fungal hyphae were localized and accumulated within a single sinus, rather than being eradicated by its host.