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  Squamous Cell Carcinoma

       of Middle/Inner Ear


 

               

Visit:  Squamous Cell Carcinoma Cutaneous Squamous Cell Carcinoma (Image &abstracts) ; Basal Cell Carcinoma .

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Squamous cell carcinoma of the middle ear is a rare tumour.

The patient may have a history of chronic otitis media. Clinically the patient may complain of aural discharge, conductive hearing loss, pain in the ear, bleeding and facial palsy.

Microscopic features:  Histologically, the tumour is similar in its range of keratinization and epithelial differentiation to tumours of the same histologic type elsewhere in the upper respiratory tract. Carcinoma in-situ may be present focally adjacent to the invasive carcinoma. Middle ear corpuscles may be confused with keratinized pearls of squamous carcinoma specially during frozen section. 

Spread:  There is penetration by tumour of the bony wall on the medial wall of the middle ear to infiltrate the carotid canal.

The tumour penetrates the thin layer of bone between the posterior mastoid air cells and the dura with subsequent invasion along the dura and into the internal auditory meatus. In some cases the cochlea may be infiltrated.

There may be extensive involvement of the inner ear by cancer destroying the lower part of the otic capsule. In such cases it is assumed that squamous cell carcinoma overcame the biological resistance to neoplastic infiltration which probably exists in the otic capsule and the membranous labyrinth.

                  

Squamous cell carcinoma of the temporal bone: a radiographic -pathologic correlation. Arch Otolaryngol Head Neck Surg.2001 Jul;127(7):803-7.

OBJECTIVE: To assess the utility of a previously proposed staging system for patients with primary squamous cell carcinoma of the temporal bone. METHODS: Retrospective chart review of 15 patients treated for squamous cell carcinoma of the temporal bone over a 13-year period at an academic tertiary referral center. A review of the medical and surgical records, radiographic studies, and surgical pathology reports allowed for an evaluation of the University of Pittsburgh staging system. Outcome analysis was performed on 13 patients with more than 24 months of follow-up. RESULTS: Radiographic and surgical pathology staging according to the University of Pittsburgh staging system correlated in 11 (73%) of 15 cases. The radiographic staging system was more accurate for larger (T3/T4) tumors than for smaller (T1/T2) tumors (83% vs 67%). When compared with patients with no evidence of disease, nonsurvivors were more likely to present with otalgia (67% vs 43%), facial nerve paralysis (33% vs 0%), and T3/T4 tumors (100% vs 14%). CONCLUSIONS: Pathologic staging by the University of Pittsburgh staging system closely correlates with patient outcome and is more sensitive than preoperative radiographic staging. Prognosis in squamous cell carcinoma of the temporal bone is largely determined by the extent of local disease at the time of presentation.

Squamous cell carcinoma of the temporal bone arising 43 years after fenestration procedure. Am J Otol.1993 Sep;14(5):512-4.

Squamous cell carcinoma originating in the middle ear cleft is a rare tumor that tends to be diagnosed late in its course. The presenting symptoms mimic inflammatory disease of the middle ear space, and hence biopsy is often delayed. Herein we present a case of squamous cell carcinoma of the temporal bone arising 43 years after fenestration procedure. Operative findings were significant for complete dissolution of the tegmen tympani, tegmen mastoideum, and posterior fossa dura plate with dural exposure and sigmoid sinus exposure. Tumor was noted to invade the labyrinth at the horizontal semicircular canal. This case report highlights the aggressiveness of this particular tumor in a previously exenterated mastoid cavity and its proclivity to penetrate the otic capsule via pre-formed pathways. The treatment of choice is aggressive surgical resection followed by radiotherapy.

Squamous cell carcinoma of the middle ear. A 25-year retrospective study. Ann Otol Rhinol Laryngol.1985 May-Jun;94(3):273-7.

Squamous cell carcinomas of the middle ear cleft are highly unpleasant tumors which pose many problems for the otologist. We have retrospectively reviewed the hospital notes of 21 patients (22 ears) who presented with this disease in order to try to clarify those features which are of prognostic significance. We confirmed that a history of chronic suppuration with or without cholesteatoma predisposes the patient to tumor development and that, in the presence of continuing otorrhea, patients are not protected by mastoid surgery. These patients have been treated with conservative surgery and radiotherapy without en bloc resection of the temporal bone and, in these circumstances, the histological grade of the tumor at presentation appears to bear a direct relationship to survival.

Primary squamous cell carcinoma of the middle ear invading the cochlea. A histopathological case report. Ann Otol Rhinol Laryngol.1983 May-Jun;92(3 Pt 1):290-4.

This report describes the histopathological changes in the temporal bone of a 71-year-old man who died of meningitis and epidural abscess complicated by primary squamous cell carcinoma of the middle ear. The present case is unusual and differs somewhat from previously reported cases of the primary squamous cell carcinoma of the middle ear in three respects: 1) an extensive invasion of the cancer into the membranous labyrinth, 2) cholesterol deposits in the cochlear spiral canal, and 3) presence of ossifying labyrinthitis. Among these findings, extensive involvement of the inner ear by cancer destroying the lower part of the otic capsule is particularly unusual. It is assumed that squamous cell carcinoma overcame the biological resistance to neoplastic infiltration which probably exists in the otic capsule and the membranous labyrinth.

Squamous cell carcinoma of the middle ear. Clin Otolaryngol Allied Sci.1980 Aug;5(4):235-48.

The clinic features of 28 cases of squamous cell carcinoma of the middle ear are reviewed. Only one patient developed cervical lymph node metastasis and one radiological evidence of pulmonary metastasis. Fourteen of 23 patients (61%) died within 5 years after treatment from intracranial extension of the neoplasm. The pathological findings in three cases in which serially sectioned temporal bones were available are described. An important feature in each case was a penetration by tumour of the bony wall on the medial wall of the middle ear to infiltrate the carotid canal and b penetration by tumour of the thin layer of bone between the posterior mastoid air cells and the dura with subsequent invasion along the dura and into the internal auditory meatus. In one case the cochlea was infiltrated from the latter situation, but direct invasion of the cochlea from the middle ear was not observed. In view of the extensive infiltration that is probably already present at the time of diagnosis, radical surgical procedures are contraindicated.


December 2007

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Accessory Tragus

First Branchial Cleft Anomalies

Salivary Gland Choristoma

Gout of Ear

Malakoplakia of Ear

Granuloma Inguinale

Idiopathic Auricular Ossificans

Idiopathic Cystic Chondromalacia of Auricular Cartilage

Inflammatory Aural Polyp

Angiolymphoid Hyperplasia with Eosinophilia of Ear

Kimura's Disease of Ear

Labyrinthitis

Meniere's Disease

Chondrodermatitis Nodularis Chronica Helicis

Necrotizing "Malignant" External Otitis

Relapsing Polychondritis

Paget's Disease of Temporal Bone

Otosclerosis

Wegener's Granulomatosis of Ear

Myospherulosis of Ear

Pneumocystiis Carnii Of Ear

Presbycusis

Acquired Cholesteatoma

Congenital Cholesteatoma

Histopathology Image of Cholesteatoma

Neoplasms of the External Ear