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                   Lipoma of 

       Internal Auditory Canal


 

                
Lipomas of the internal auditory canal are extremely rare. The origin of lipomas in this location is uncertain, but they are believed to be a malformation rather than a neoplasm.

 Visit: Lipoma and variants

The lesion occurs in only 0.08% of general autopsies.

The tumour occurs in the third to fifth decade of life. There is a male predominance of 2–5:1.

Lipomas of the internal auditory canal may involve cranial nerves VII and VIII, whereas cerebellopontine angle lipomas may involve cranial nerves V through XII.

Symptoms show unilateral hearing loss, tinnitus, and vertigo and are clinically and audiologically indistinguishable from those of eighth cranial nerve schwannomas. Vestibular Schwannoma of the Ear

Grossly, these lesions are composed of soft, lobulated, yellow, fatty-appearing tissue that is difficult to dissect from the adjacent nerves because the growth pattern is infiltrative rather than expansile.

Histologically, lipomas are composed of nerve fascicles, ganglion cells, and mature adipose tissue, which infiltrate and separate the nerve fibers. Cartilaginous elements have been described on rare occasion.

Differential diagnosis: - The primary histologic differential diagnosis is lipoblastic meningioma. Meningiomas, however, are typically much larger than lipomas, and only rarely are confined to the internal auditory canal.

- When adipose tissue is present along with thick-walled blood vessels, smooth muscle, and skeletal muscle, the finding is termed lipochoristoma.

Visit:  Meningioma of the Middle Ear ; Lipochoristoma of middle/ inner ear or temporal bone .

                  

Lipomas of the internal auditory canal--report of two cases and review of the literature. Zentralbl Neurochir.2004 May;65(2):88-94.

OBJECTIVE: Lipomas of the internal auditory canal are extremely rare. So far, only 21 cases have been described in the literature. We present here two of our own cases and review the literature to date with special emphasis on the diagnostic and therapeutic options. METHOD: During the last seven years two lipomas of the internal auditory canal were surgically treated in our department. Despite native and gadolinium-enhanced MRI and a thin-sliced temporal bone CT scan they were misdiagnosed as intracanalicular acoustic neurinomas. RESULTS: Total tumour removal could be achieved, the facial nerve function was conserved, but both patients were rendered functionally deaf after surgery. CONCLUSION: Lipomas' radiological behaviour may mimic acoustic neurinomas; without fat-suppressed T(1)-weighted images they are often preoperatively misdiagnosed as acoustic neurinomas. Although the postoperative morbidity with respect to cochlear and facial nerve function is much higher than in small acoustic schwannomas, early surgery may be justified, because complete removal is only possible in this stage. No reliable data are available concerning the natural history of this kind of lesion.

Internal auditory canal mass in a 46-year-old woman. Arch Pathol. Lab Med.2005 Nov;129(11):1491-2.

Diagnosis and treatment of lipomas of the internal auditory canal. Ear Nose Throat J.2001 May;80(5):340-2, 345.

A Chinese woman came to the otolaryngology department with a complaint of a longstanding progressive left hearing loss and intractable tinnitus. A finding of asymmetry on sensorineural hearing loss and auditory brainstem response testing provided evidence of a retrocochlear lesion on the left side. Computed tomography and magnetic resonance imaging detected a tumor in the left internal auditory canal (IAC). In addition to these radiologic features, our suspicion of the possibility of an IAC lipoma was raised by the observation of multiple lipomas over the patient's trunk and limbs. The patient underwent a complete tumor resection via the translabyrinthine approach, Pathology confirmed the diagnosis of an IAC lipoma. Although we were not able to preserve the hearing in her left ear, the patient was satisfied that we had relieved her constant tinnitus. In this article, we review the particulars of this case and discuss the clinical, radiologic, and pathologic features of IAC lipomas.

Lipomas of the internal auditory canal and cerebellopontine angle. Laryngoscope.1998 Oct;108(10):1459-69.

OBJECTIVE: To evaluate lipomas of the internal auditory canal (IAC) and cerebellopontine angle (CPA). STUDY DESIGN: Retrospective review. METHODS: Review of a multi-institutional series of 17 lipomas of the IAC/CPA, combined with a Medline review of the 67 cases reported in the world literature. RESULTS: This series of 17 IAC/CPA lipomas is the largest reported series to date, bringing the total number of documented cases to 84. There appears to be a nearly 2:1 male to female predominance. Sixty percent were left-sided lesions, and three were bilateral. Hearing loss, dizziness, and tinnitus were the most common presenting symptoms. Surgical resection was performed in 52 (62%) of these lesions; however, total tumor removal was accomplished in only 17 (33%), which is most likely because of the fact that these tumors tend to have a poorly defined matrix and a dense adherence to neurovascular structures. Sixty-eight percent of patients experienced a new deficit postoperatively, 11% were unchanged, and only 19% improved with no new deficit. Only one documented case of tumor growth was identified; however, the reported follow-up was short (average, less than 3 years). CONCLUSION: With the magnetic resonance imaging techniques now available, lipomas can be reliably differentiated from other masses within the CPA and IAC, so histopathologic diagnosis is rarely necessary. Because of the potential for significant morbidity with resection of these lesions, we believe that conservative follow-up is the best treatment option for patients with these rare lesions. Surgery is indicated only when significant progressive or disabling symptoms are present.

Lipoma of the internal auditory canal. Report of two cases simulating acoustic neuroma. Ann Pathol.1998 Feb;18(1):52-4.

We report two cases of intra-auditory canal lipoma, presenting as acoustic neuroma, observed in respectively 45 and 53 year old patients. Cerebellopontine angle lipomas are unusual lesions, more exceptional than their intracranial counter-parts. The knowledge of these tumoral lesions and of their close relationships with cranial nerves incite to perform a frozen section when imagery is evocative, to limit functional postoperative sequelae.

Lipomas of the internal auditory canal. Laryngoscope.1997 Mar;107(3): 364-8.

Lipomas of the internal auditory canal (IAC) are rare, benign neoplasms occurring in the third to fifth decade of life predominately in Caucasian males. Eleven cases of IAC lesions have been previously reported; we report four more. Two of four cases showed atypical findings on preoperative radiographic evaluation. These two patients had surgery. Two patients with small tumors elected for observation with close follow-up. Fat suppression of T1-weighted images on magnetic resonance imaging (MRI) offers the most precise preoperative diagnostic tool of IAC lipomas. Because of the infiltrative nature of these tumors, hearing conservation surgery is unlikely to succeed. We recommend observation for those patients with small tumors and serviceable hearing.

Lipomas of the internal auditory canal. Arch Pathol Lab Med.1996 Jul;120(7):681-3.

Lipoma of the internal auditory canal is a rare tumor that may be confused clinically with the much more common vestibular schwannoma. We present two cases of lipoma of the internal auditory canal. The clinical presentation is indistinguishable from that of vestibular schwannomas. The high signal intensity on T1-weighted magnetic resonance imaging, both with and without contrast, is consistent with other reports of lipoma. Review of the literature shows that lipomas of the internal auditory canal are histopathologically similar to lipomas of the cerebellopontine angle. The symptoms, erosive effect on the auditory canal, and gross appearance of this uncommon tumor are sometimes difficult to differentiate from those of a vestibular schwannoma. The diagnosis can be established by intraoperative examination of frozen sections.

Lipoma of internal auditory canal. Otolaryngol head Neck Surg.1992 Sep;107(3):374-6.

Lipoma of the internal auditory canal is a rare tumor. Clinically, it presents like an acoustic tumor. The diagnosis can be made with the use of a magnetic resonance imaging showing a high intensity on T1- and low intensity on T2-weighted image with no enhancement. Pathologically, this is a soft, smooth, yellow tumor with some fat in it that can resemble grossly any acoustic tumor. The lipoma is intermixed with the eighth nerve and can be adherent to adjacent structures. The growth of a lipoma can be slower than an acoustic tumor. A patient diagnosed with lipoma of the internal auditory canal can often have quite good hearing. As an alternative to surgical removal, another therapeutic option is to watch the growth of the lipoma with periodic magnetic resonance imaging, probably on a yearly basis initially.

Lipomas of the internal auditory canal. Laryngoscope.1991 Oct;101 (10):1031-7.

Intracranial lipomas are rare tumors which may occur in the cerebellopontine angle (CPA) or internal auditory canal (IAC). Although seemingly innocuous in other parts of the body, lipomas within the CPA and IAC often involve the surrounding cranial nerves, making attempts at hearing conservation largely unsuccessful. In an attempt to differentiate the IAC lipoma from the more commonly found acoustic schwannoma, the preoperative imaging studies (magnetic resonance and computerized tomography) on five previously unreported cases of IAC lipomas were evaluated. Based on these studies, features were determined that may allow the surgeon to diagnose IAC lipomas preoperatively. These features will be discussed, as well as the surgical and pathological findings.

Lipoma of the internal auditory canal. An anatomo-clinical case study and review of the literature about cranial nerve lipomas. Arch Anat Cytol Pathol.1991;39(4):147-50.

A 36-year-old female presented with vertigo and worsening of a right hearing loss with tinnitus. Clinical and radiologic investigations revealed a tumor of the right internal acoustic meatus, first diagnosed as a neuroma. Histologic study of surgical samples led to a final diagnosis of lipoma. Cranial nerve lipomas are rare and usually located in the cerebellopontine angle. Lipomas confined to the internal acoustic meatus are much rarer. The review of the literature however, shows that their histologic characteristics and their behavior are identical to those of cerebellopontine angle lipomas, and that a minimal surgical resection is therefore advised.

Lipomas of the internal auditory canal. Arch Otolaryngol.1978 Aug;104 (8):431-6.

We present two cases of lipoma of the cerebellopontine angle (CPA), which brings, to our knowledge, the total reported in the literature to six. These cases had a clinical, surgical, and postoperative course that was similar to a small acoustic neuroma. The roentgenographic aspects were in keeping with small, CPA tumors. A review of the literature of CPA tumors and lipomas of the CNS is presented. We discuss the controversy surrounding the origin of lipomas of the CNS.


December 2007

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Accessory Tragus

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Idiopathic Cystic Chondromalacia of Auricular Cartilage

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Histopathology Images of Ceruminous Adenoma

Pleomorphic Adenoma of the External Ear 

Syringocystadenoma Papilliferum of External Ear

Cylindroma of External Ear

Myxoma of External Ear

Myofibromatosis of External Auditory Canal

Benign Fibro-Osseous Lesion of External Ear

Exostosis of  External Ear

Osteoma of Ear (external auditory canal and middle ear)

Solitary Fibrous Tumour of External Ear

Keloid of Ear

Keratoacanthoma of External Ear

Squamous Cell Carcinoma of the External Ear 

Verrucous Carcinoma of the External Ear

Basal cell carcinoma of the External Ear

Ceruminous Adenocarcinoma

Adenoid Cystic Carcinoma of the External Ear 

Melanocytic Tumours of the External Ear

Rhabdomyosarcoma of the External Ear

Langerhans Cell Histiocytosis of the Ear

Primary Lymphoma of the Ear

Middle Ear Adenoma

Melanocyoma