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POLIP
POLIP
DOI: 10.21276/APALM.1173
ABSTRACT
Background: Nasal Polyp is commonly encountered in clinical practice and important from clinical and pathological perspectives as they
have varieties of histological patterns. The Polypoidal masses in nasal cavity form a complex group of lesions with wide spectrum of
histopathological features, mainly grouped under allergic and inflammatory. Histopathological examination shows a spectrum of lesions
ranging from the non-neoplastic ones to neoplastic tumors.
Methods: Present study included 153 polypoidal lesions of the nasal cavity during a period of one year. All the tissues were fixed in 10%
buffered formalin, processed, stained with H & E and studied for various histopathological patterns. Periodic acid Schiff’s and reticulin
stains were used wherever necessary.
Results: classifying the sinonasal lesions according to histo-pathological features into various types helps us to know the clinical
presentation, treatment, clinical outcome and prognosis of the disease. Although most of nasal polyps sent for histopathology are
inflammatory, secondary to infection or allergy, various benign and malignant lesions of nose may present as polypoidal masses,
Conclusion: The study recommends, all polyps need histo-pathological examination.
It has been established that patients with chronic rhinosinusitis with nasal polyps (CRSwNP) often have
co-existing asthma.
Objective
We aimed to test two hypotheses: (i) upper and lower airway inflammation in CRSwNP is uniform in
agreement with the united airways concept; and (ii) bronchial inflammation exists in all CRSwNP
patients irrespective of clinical asthma status.
Methods
We collected biopsies from nasal polyps, inferior turbinates and bronchi of 27 CRSwNP patients and 6
controls. All participants were evaluated for lower airway disease according to international guidelines.
Inflammatory cytokines were investigated using a Th1/Th2 assay including 14 chemokines and
cytokines; tissue concentrations were normalized according to tissue weight and total protein
concentration. Individual cytokines and multivariate inflammatory profiles were compared between
biopsy sites and between patients and controls.
Results
We found significantly higher concentrations of Th2 cytokines in nasal polyps compared to inferior
turbinate and bronchial biopsies. In addition, we showed that the inflammatory profile of nasal polyps
and bronchial biopsies correlated significantly (p<0.01). From the Th2 cytokines measured, IL-13 was
significantly increased in bronchial biopsies from CRSwNP patients with, but not without asthma.
Conclusion
Our findings support the united airways concept; however, we did not find evidence for subclinical
bronchial inflammation in CRSwNP patients without asthma. Finally, this study indicates for the first
time that nasal polyps potentially play an important role in the airway inflammation rather than being a
secondary phenomenon.
Abstract
Chronic rhinosinusitis with nasal polyps (CRSwNP) is characterized by both a chronic inflammation and
tissue remodelling; as indicated by extracellular matrix protein deposition, basement membrane
thickening, goblet cell hyperplasia and subepithelial edema, with reduced vessels and glands. Although
remodelling is generally considered to be consequence of persistent inflammation, the chronological
order and relationship between inflammation and remodelling in polyp development is still not clear.
The aim of our study was therefore to investigate the pathological features prevalent in the development
of nasal polyps and to elucidate the chronological order and relationship between inflammation and
remodelling, by comparing specific markers of inflammation and remodelling in early stage nasal polyps
confined to the middle turbinate (refer to as middle turbinate CRSwNP) obtained from 5 CRSwNP
patients with bilateral polyposis, mature ethmoidal polyps from 6 CRSwNP patients, and normal nasal
mucosal tissue from 6 control subjects. Middle turbinate CRSwNP demonstrated significantly more
severe epithelial loss compared to mature ethmoidal polyps and normal nasal mucosa. The epithelial cell
junction molecules E-cadherin, ZO-1 and occludin were also expressed in significantly lower amounts in
mature ethmoidal polyps compared to healthy mucosa. Middle turbinate CRSwNP were further
characterized by significantly increased numbers of subepithelial eosinophils and M2 type macrophages,
with a distinct lack of collagen and deposition of fibronectin in polyp part. In contrast, the turbinate area
of the middle turbinate CRSwNP was characterized by an increase in TGF-β activated myofibroblasts
expressing α-SMA and vimentin, an increase in the number of pSmad2 positive cells, as well as
increased deposition of collagen. These findings suggest a complex network of processes in the
formation of CRSwNP; including gross epithelial damage and repair reactions, eosinophil and
macrophage cell infiltration, and tissue remodelling. Furthermore, remodelling appears to occur in
parallel, rather than subsequent to inflammation.
Immune Imbalance in Nasal Polyps of
Caucasian Chronic Rhinosinusitis Patients Is
Associated with a Downregulation of E-
Selectin
Abstract
Chronic rhinosinusitis with nasal polyps (CRSwNP) in Caucasians is a chronic Th2 inflammatory disease of
the nasal and paranasal mucosa and the recruitment of leukocytes to the site of inflammation is poorly
understood. We studied mRNA and protein expression profiles of adhesion molecules in nasal polyp and
associated inferior turbinate tissues using molecular, biochemical, and immunohistological methods.
Analysis showed a strongly decreased E-selectin expression in nasal polyps with a significant difference
between eosinophil and neutrophil counts in nasal polyps and balanced counts in inferior turbinates. E-
selectin expression is known to be downregulated in a Th2 milieu and has an essential role in
immunosurveillance by locally activating neutrophil arrest and migratory function. A downregulation of E-
selectin may come along with an immune imbalance in Caucasian nasal polyps due to a significant
inhibition of neutrophil recruitment. Therefore, we suggest that an upregulation of E-selectin and the
associated influx of neutrophils may play a significant role in the resolution of inflammation as well as for
the pathophysiology of nasal polyps of Caucasian chronic rhinosinusitis patients.
inflammation.
treatment which may point to the mechanisms of
therapeutic benefit. In addition, these observations
illustrate the value of markers that indicate cell functional
activity rather than just cell numbers.
Effect of topical
nasal steroid.
Topical nasal corticosteroid therapy produces clinical
improvement in patients with nasal polyposis. To
examine the mechanisms of steroid effect, we quantified
the number of inflammatory cell types as well as the
expression of relevant cell markers in nasal polyps from
steroid treated patients (n = 11) and polyps from
untreated patients (n = 10) judged to require
polypectomy for symptomatic relief. We found that the
majority of eosinophils in these tissues were in the
stromal layers, and that the proportion of activated
eosinophils (EG2+ versus total eosinophil count) was
significantly lower in polyps from patients treated with
the topical nasal steroid budesonide, 200 to 400
micrograms/d for 1 mo, than in polyps from untreated
patients. We also found that in polyps from treated
patients, the superficial stromal layer (SSL) and deep
stromal layer (DSL) both contained a significantly lower
tissue density of lymphocytes of CD3, CD4, and CD8
subsets. Treatment was also associated with a lower,
albeit nonsignificant, expression of ICAM-1 and HLA-DR in
and dyspnea. It has been proved that
Omalizumab reduces the size of nasal polyps
The Use of Omalizumab and improves the quality of life. This finding
could be due to the local formation of IgE in
in Thetreatment of Nasal nose and lungs.