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Pathology of the Head and Neck

Pathology of the Head and Neck

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Ear <strong>and</strong> Temporal Bone Chapter 8 2478.3.1.3 Unusual Inflammatory LesionsTuberculous otitis media is an unusual form <strong>of</strong> chronicotitis media, which is generally associated with activepulmonary tuberculosis. In <strong>the</strong> initial stages multipleperforations <strong>of</strong> <strong>the</strong> tympanic membrane develop.Granulations in <strong>the</strong> middle ear may appear pale <strong>and</strong>are <strong>of</strong>ten pr<strong>of</strong>use. Complications, especially involvement<strong>of</strong> <strong>the</strong> facial nerve, are more frequent than in <strong>the</strong>commoner form <strong>of</strong> chronic otitis media. The diagnosisis usually made by histopathological examination <strong>of</strong>biopsy material from middle ear contents. This is <strong>of</strong>tendelayed because surgeons are reluctant to take biopsiesfrom cases <strong>of</strong> chronic otitis media that seem fairly typical.Culture <strong>of</strong> middle ear inflammatory tissue may producetubercle bacilli. Histological examination showstuberculoid granulation tissue composed <strong>of</strong> epi<strong>the</strong>lioidcells, Langerhans giant cells <strong>and</strong> areas <strong>of</strong> caseation situatedin <strong>the</strong> middle ear mucosa. There is much bone destruction.Acid-fast bacilli are found with difficulty in<strong>the</strong> granulomatous material.8.3.2 Neoplasms<strong>and</strong> Lesions ResemblingNeoplasms8.3.2.1 Choristoma(Salivary Gl<strong>and</strong>, Glial<strong>and</strong> Sebaceous Types)A hamartoma is a focal overgrowth, in improper proportions,<strong>of</strong> tissues normally present in that part <strong>of</strong> <strong>the</strong>body. A choristoma is similar to hamartoma, exceptthat <strong>the</strong> tissues <strong>of</strong> which it is composed are not normallypresent in <strong>the</strong> part <strong>of</strong> <strong>the</strong> body where it is found.Choristomas are occasionally seen in <strong>the</strong> middle ear.They are composed <strong>of</strong> one or o<strong>the</strong>r <strong>of</strong> three types <strong>of</strong>tissue: salivary gl<strong>and</strong>, glial or sebaceous gl<strong>and</strong>ular tissue.Salivary gl<strong>and</strong> choristomas consist as a rule <strong>of</strong> mixedmucous <strong>and</strong> serous elements like <strong>the</strong> normal subm<strong>and</strong>ibularor sublingual gl<strong>and</strong>, but unlike <strong>the</strong> parotidgl<strong>and</strong>. The lesion typically consists <strong>of</strong> a lobulated mass<strong>of</strong> histologically normal salivary gl<strong>and</strong> tissue in <strong>the</strong> middleear attached posteriorly in <strong>the</strong> region <strong>of</strong> <strong>the</strong> oval window.Frequently, <strong>the</strong> mass is intimately associated with<strong>the</strong> facial nerve. There are usually absent or malformedossicles [44].Glial choristomas are composed largely <strong>of</strong> astrocyticcells with large amounts <strong>of</strong> glial fibrils, <strong>the</strong> identity<strong>of</strong> which may be confirmed by immunohistochemicalstaining for glial acidic fibrillary protein. When suchmasses are identified in biopsy material from <strong>the</strong> middleFig. 8.13. Adenoma <strong>of</strong> <strong>the</strong> middle ear. Reproduced from Michaels<strong>and</strong> Hellquist [68]ear a bony deficit with consequent herniation <strong>of</strong> braintissue into <strong>the</strong> middle ear should be ruled out [53]. Threecases <strong>of</strong> heterotopic brain tissue in <strong>the</strong> middle ear associatedwith cholesteatoma have been reported [62]. It ispossible that in all three, brain herniation occurred as aresult <strong>of</strong> inflammatory damage to <strong>the</strong> tegmen tympani.Spontaneous herniations <strong>of</strong> brain (encephaloceles) mayoccur into <strong>the</strong> middle ear through a congenital deficiency<strong>of</strong> <strong>the</strong> tegmen or o<strong>the</strong>r sites [47].A case <strong>of</strong> sebaceous choristoma <strong>of</strong> <strong>the</strong> middle ear hasbeen described [82].8.3.2.2 AdenomaICD-O:8140/0Adenoma is <strong>the</strong> commonest neoplasm <strong>of</strong> <strong>the</strong> middle ear.The epi<strong>the</strong>lium <strong>of</strong> <strong>the</strong> middle ear has a propensity towardsgl<strong>and</strong> formation in otitis media (see above) <strong>and</strong>adenoma would seem to represent a benign neoplastictransformation <strong>of</strong> <strong>the</strong> epi<strong>the</strong>lium along <strong>the</strong> same lines.The neoplasm has been described as being white, yellow,grey or reddish brown at operation <strong>and</strong> unlike paragangliomais usually not vascular. It is usually situatedin <strong>the</strong> middle ear cavity, sometimes extending into <strong>the</strong>mastoid. It seems to peel away from <strong>the</strong> walls <strong>of</strong> <strong>the</strong> surroundingmiddle ear with ease, although ossicles maysometimes be entrapped in <strong>the</strong> tumour mass <strong>and</strong> mayeven show destruction.Adenoma is formed by closely apposed small gl<strong>and</strong>swith a “back to back” appearance (Fig. 8.13). In someplaces a solid or trabecular arrangement is present.Sheet-like, disorganised areas are seen in which <strong>the</strong>gl<strong>and</strong>ular pattern appears to be lost. This may be artefactual<strong>and</strong> related to <strong>the</strong> effects <strong>of</strong> trauma used intaking <strong>the</strong> biopsy specimen on <strong>the</strong> delicate structure <strong>of</strong><strong>the</strong> cells, but <strong>the</strong> appearance may erroneously lead oneto suspect malignancy. The cells are regular, cuboidalor columnar <strong>and</strong> may enclose luminal secretion. A dis-

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