Pathology of the Head and Neck
Pathology of the Head and Neck
Pathology of the Head and Neck
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Nasal Cavity <strong>and</strong> Paranasal Sinuses Chapter 2 43This lesion is differentiated from <strong>the</strong> very rare sinonasalteratoma by <strong>the</strong> limited variety <strong>of</strong> tissue types <strong>and</strong><strong>the</strong> absence <strong>of</strong> endodermal components [100]. Epidermalinclusion cysts do not contain adnexa. Dermoidcysts <strong>of</strong> <strong>the</strong> nose should also be distinguished from encephalocele.We are unaware <strong>of</strong> hairy polyps occurringin <strong>the</strong> nose.2.5 Pseudotumours2.5.1 MucoceleMucocele is a cyst filled with mucus that develops withina sinus cavity as <strong>the</strong> result <strong>of</strong> occlusion <strong>of</strong> <strong>the</strong> ostium.Most commonly it is due to infection, but may also resultfrom trauma or be congenital [109]. Retained secretionscause expansion <strong>of</strong> <strong>the</strong> sinus <strong>and</strong> bone erosion. Themost common sites <strong>of</strong> occurrence are <strong>the</strong> frontal <strong>and</strong> <strong>the</strong>sphenoidal sinuses. The cyst is lined by respiratory epi<strong>the</strong>liumthat shows prominent goblet-cell hyperplasia[158, 184]. Expansion <strong>of</strong> <strong>the</strong> cyst may cause atrophy <strong>and</strong>metaplasia <strong>of</strong> <strong>the</strong> epi<strong>the</strong>lium.2.5.2 Organising HaematomaOrganising haematoma, also known as “ cholesterolgranuloma” or “rhinitis caseosa”, is in most cases <strong>the</strong> result<strong>of</strong> occult submucosal haemorrhage in <strong>the</strong> maxillarysinus due to external trauma or tooth extraction [147].Resolution <strong>of</strong> <strong>the</strong> haematoma produces <strong>the</strong> formation <strong>of</strong>cholesterol granulomas <strong>and</strong> fibrosis, simulating a foreignbody reaction.2.5.4 MyospherulosisMyospherulosis is characterised by <strong>the</strong> presence <strong>of</strong> cystlikespaces lined by flattened histiocytes <strong>and</strong> containingclusters <strong>of</strong> brownish spherules resembling fungi [198,217, 230]. They lie loosely or within sacs formed by thinrefractile membranes. The brownish spherules do notstain with PAS or Gomori methanamine silver <strong>and</strong> <strong>the</strong>irmorphology does not correspond to any known fungus[228]. They are found within fibrous granulation tissue,which may show a foreign body reaction. The lesion isusually found in patients who have had previous operations[145]. It is now recognised that <strong>the</strong> spherules areextravasated red cells that have been altered by interactionwith traumatised fat or petrolatum-based ointments<strong>and</strong> gauzes used in surgical procedures.2.5.5 Eosinophilic Angiocentric FibrosisEosinophilic angiocentric fibrosis is a rare, chronic, benign,idiopathic condition <strong>of</strong> <strong>the</strong> upper respiratory tractoccurring predominantly in adult women [214, 248].Initially, <strong>the</strong> histologic picture is characterised by nonnecrotisingeosinophilic vasculitis involving capillaries<strong>and</strong> venules <strong>of</strong> <strong>the</strong> sinonasal mucosa, accompanied by aninflammatory infiltrate with lymphocytes, plasma cells,histiocytes <strong>and</strong> occasional neutrophils [214]. In late lesions<strong>the</strong>re is a characteristic obliterative perivascularonion-skin fibrosis, while <strong>the</strong> inflammatory infiltrate isless dense <strong>and</strong> eosinophils predominate [214]. The differentialdiagnosis includes reactive processes <strong>of</strong> <strong>the</strong> sinonasalmucosa, like Wegener’s granulomatosis, Churg-Strauss syndrome, Kimura disease, <strong>and</strong> angiolymphoidhyperplasia with eosinophilia.2.5.3 AmyloidosisIsolated amyloid deposition in <strong>the</strong> sinonasal mucosa isa rare event, with about 20 cases reported in <strong>the</strong> English-languageliterature [180, 258]. Grossly, <strong>the</strong> lesionappears as a friable tumour-like mass, with a tendencyto bleed. Histologically, <strong>the</strong>re is a deposition <strong>of</strong> intenselyeosinophilic material in <strong>the</strong> stroma, around blood vessels<strong>and</strong> around ducts <strong>of</strong> <strong>the</strong> mucoserous gl<strong>and</strong>s, whichis <strong>of</strong>ten associated with diffuse chronic inflammation<strong>and</strong> foreign body granulomatous reaction. Amyloidstains orange with Congo red, <strong>and</strong> showed apple greenbirefringence under polarised light examination. Immunohistochemistrymay help to identify <strong>the</strong> type <strong>of</strong>amyloid deposition.2.5.6 Heterotopic Brain TissueThis lesion mostly occurs in young children, usually <strong>the</strong>result <strong>of</strong> a congenital abnormality related to a variant <strong>of</strong>meningoencephalocele [136, 196]. Commonly used synonymsare glial heterotopia <strong>and</strong> nasal glioma, although<strong>the</strong> latter is a misnomer. The lesion mainly arises at <strong>the</strong>base <strong>of</strong> <strong>the</strong> nose or in <strong>the</strong> upper part <strong>of</strong> <strong>the</strong> nasal cavity,<strong>and</strong> grossly may be polypoid. Histologically, it is mostlycomposed <strong>of</strong> a mixture <strong>of</strong> astrocytes, glial fibres <strong>and</strong>fibrous connective tissue. Multinucleated glial cells arefrequently found. Some glial cells can have large nucleiresembling nerve cells. Immunostaining for glial fibrillaryacidic protein is a helpful diagnostic adjunct. A fewtrue nerve cells or even ependymal elements can rarelybe identified. Mitoses are not found.