- Case report
- Open Access
- Open Peer Review
Inflammatory myofibroblastic tumor of the temporal bone presenting with pulsatile tinnitus: a case report
© Zhou et al.; licensee BioMed Central Ltd. 2013
- Received: 26 December 2012
- Accepted: 15 May 2013
- Published: 20 June 2013
Inflammatory myofibroblastic tumor of the temporal bone is an unusual but distinct disease entity. The most common presenting symptoms are otalgia, otorrhea, hearing loss, facial palsy, and vertigo. We describe here what we believe to be the first reported case of a patient presenting with persistent pulsatile tinnitus. The clinical features, radiological and histopathologic findings, and treatment outcomes of the patient are presented.
A 59-year-old woman of Chinese Han origin presented with complaints of left-sided pulsatile tinnitus and progressive hearing loss for several years. Clinical evaluations revealed a reddish mass behind the intact tympanic membrane, and a moderately severe conductive hearing loss in the left ear. The computed tomographic imaging of the temporal bone demonstrated a slightly ill-defined left middle ear soft tissue mass involving the posterior portion of the mesotympanum and epitympanum, and the mastoid antrum. The patient underwent surgical excision of the lesion which subsequently resolved her symptoms. Postoperative pathology was consistent with an inflammatory myofibroblastic tumor.
An inflammatory myofibroblastic tumor of the temporal bone can present clinically with pulsatile tinnitus and masquerade as venous hum or vascular tumors of the middle ear; therefore, it should be included in the differential diagnosis of pulsatile tinnitus.
- Inflammatory Myofibroblastic Tumor
- Middle Ear
- Pulsatile Tinnitus
- Temporal Bone
Inflammatory myofibroblastic tumors (IMFT), also known as inflammatory pseudotumors, include a diverse group of lesions characterized by inflammatory cell infiltration and variable fibrotic responses . It is an unusual histologically benign yet clinically invasive mass lesion of unknown etiology that most frequently involves the lung, but it has been described in almost any location, in both genders, at all ages [2, 3]. IMFT of the head and neck are uncommon, accounting for fewer than 5% of all extrapulmonary cases. In the head and neck, the most common location is the orbit, followed by the meninges, paranasal sinuses, infratemporal fossa, and soft tissues. The temporal bone, skull base, and facial nerve are very rarely involved [3, 4]. A recent review of the literature by Ajibade et al. identified only 35 such cases . However, IMFT of the temporal bone appears to have a more aggressive and unpredictable course than those in other body sites. IMFT occurring in the middle ear and mastoid may erode into the surrounding dura, sigmoid sinus, tentorium, and even brain parenchyma [3, 5–8]. Intratemporal extensions to the otic capsule, facial nerve, petrous apex, and internal auditory canal are also common [3, 8–10]. This makes the clinical manifestations of this rare disease entity more variable, and the diagnosis and the treatment more challenging than IMFT of the lung.
In this article we describe what we believe is the first reported case with an IMFT in a 59-year-old woman presenting with persistent pulsatile tinnitus. The clinical features, radiological and histopathologic findings, and treatment outcomes are presented.
A 59-year-old woman of Chinese Han origin presented with a complaint of a left pulsatile tinnitus. She had been extremely depressed for 10 years because this tinnitus was constant and prevented her from sleeping. She had visited the otological clinics at different hospitals several times. At each presentation, the tympanic membrane was carefully examined otoscopically and was found to be normal. A computed tomographic (CT) scan of the temporal bone was also performed 9 years prior to her presentation to our hospital with a negative finding. With the initial diagnosis of venous hum, she received no effective treatment.
With the suspicion of a neoplastic lesion, the patient underwent an exploration surgery through a postauricular approach. During this procedure, the lesion was noted to center in the fossa incudis which apparently encased the incus and eroded through the second genu of the fallopian canal, but the lateral semicircular canal and facial nerve were not involved. There was extension of the mass into the posterior mesotympanum. Intraoperative frozen sections were obtained and documented a chronic inflammation. The patient then underwent complete removal of the lesion followed by stage I ossicular reconstruction. The facial nerve was carefully decompressed meanwhile without incision of the neural sheath.
The postoperative course was uneventful, and the patient’s pulsatile tinnitus disappeared immediately after surgery. She was discharged home at the third postoperative day. During a 5-year follow-up period, no signs of recurrence were noted.
The causes of pulsatile tinnitus are numerous. An IMFT of the temporal bone presenting with pulsatile tinnitus represents a diagnostic and therapeutic dilemma because of its rarity. Clinical history and physical examination are of the utmost importance in establishing the correct diagnosis. For patients with an otoscopically visible retrotympanic lesion, a CT scan of the temporal bone should be ordered to detect underlying causes, these include [11–14]: (1) vascular tumors of the middle ear, such as glomus tympanicus, glomus jugulare tumor, and hemangioma; (2) vascular abnormalities, such as high jugular bulb, an aberrant carotid artery or persistent stapedial artery; and (3) inflammatory or other neoplastic lesions, such as cholesterol granuloma, aural polyp, meningioma, and occasionally middle ear adenoma.
The patient we present here was a 59-year-old woman. She had a complaint of left-sided pulsatile tinnitus for 10 years, and recently a progressive hearing loss in the same ear for 2 years. Otoscopic examination revealed a reddish middle ear mass behind her left tympanic membrane. CT scans of the temporal bone demonstrated a soft tissue mass around the incus with extension into the posterior portion of the mesotympanum and epitympanum. For that reason, the clinical suggestion was a possible neoplastic or inflammatory lesion, especially a vascular tumor. Histologically, diagnosis of IMFT was a surprise.
IMFT or inflammatory pseudotumor is an unusual disease entity. The World Health Organization classification recognizes this disease, but very few cases in the temporal bone area have been published [3, 4, 15]. The common presenting symptoms of the disease are otalgia, otorrhea, hearing impairment, facial palsy, and vertigo [4, 8]. Other symptoms include tinnitus, ear fullness, headache, retrobulbar pain, diplopia, facial pain, and visual dimness. However, an IMFT presenting with pulsatile tinnitus has not been reported previously (as researched by an Ovid Medline search using the medical subject headings ‘Pulsatile tinnitus/’ and ‘Inflammatory myofibroblastic tumor/Inflammatory pseudotumor’). To the best of our knowledge, this is the first such reported case.
A review of the literature suggests that the IMFT of the temporal bone has no distinctive characteristics, both clinically and radiologically. Thus, a diagnosis can only be made with histopathologic appearances and is confirmed by immunohistochemical studies . The differential diagnoses include: Wegener’s granulomatosis, chronic osteomyelitis, sarcoidosis, cholesterol granuloma, cholesteatoma, histiocytosis X, eosinophilic granuloma, lymphoproliferative disorders, and other malignancies . Treatment remains controversial. Surgical excision, steroid therapy, and radiation therapy have been employed, with the decision on treatment modality based on tumor location, size, and behavior . As far as our patient is concerned, the diagnostic process is meandering. She had presented several times to different hospitals during a period of 10 years. Comprehensive medical evaluations including an earlier CT scan of the temporal bone had been carried out but failed to identity the underlying cause of her left pulsatile tinnitus, until a retrotympanic lesion was suspected and a second CT scan was performed in our hospital. This ultimately led to the exploration surgery and the final diagnosis of an IMFT. Fortunately, her pulsatile tinnitus was completely eliminated with radical excision of the lesion.
IMFT of the temporal bone is an unusual but distinct disease entity. The most common presenting symptoms are otalgia, otorrhea, hearing loss, facial palsy, and vertigo. An IMFT can also present clinically with pulsatile tinnitus and masquerade as venous hum or vascular tumors of the middle ear, as in our case report. Therefore, an IMFT should be included in the differential diagnosis of pulsatile tinnitus, especially for those cases with a visible retrotympanic mass lesion.
Written informed consent was obtained from the patient for publication of this case report and accompanying images. A copy of the written consent is available for review by the Editor-in-Chief of this journal.
This work was supported by a grant from Jiangsu Health Administration of China to G. Xing (grant number: LJ201120).
- Cho KJ, Lee DH, Jung SH, Kim JH: A case of an inflammatory myofibroblastic tumor of the mastoid presenting with chronic suppurative otitis media. Auris Nasus Larynx. 2007, 34: 523-526. 10.1016/j.anl.2007.03.005.View ArticlePubMedGoogle Scholar
- Santaolalla-Montoya F, Ereño C, Zabala A, Carrasco A, Martínez-Ibargüen A, Sánchez-Fernández JM: Inflammatory myofibroblastic tumor of the temporal bone: A histologically nonmalignant lesion with fatal outcome. Skull Base. 2008, 18: 339-343. 10.1055/s-0028-1086060.View ArticlePubMedPubMed CentralGoogle Scholar
- Williamson RA, Paueksakon P, Coker NJ: Inflammatory pseudotumor of the temporal bone. Otol Neurotol. 2003, 24: 818-822. 10.1097/00129492-200309000-00021.View ArticlePubMedGoogle Scholar
- Ajibade DV, Tanaka IK, Paghdal KV, Mirani N, Lee HJ, Jyung RW: Inflammatory pseudotumor (plasma cell granuloma) of the temporal bone. Ear Nose Throat J. 2010, 89: E1-E13.PubMedGoogle Scholar
- Gasparotti R, Zanetti D, Bolzoni A, Gamba P, Morassi ML, Ungari M: Inflammatory myofibroblastic tumor of the temporal bone. Am J Neuroradiol. 2003, 24: 2092-2096.PubMedGoogle Scholar
- Cho AH, Lee BH, Kwak KW, Kang JK: Inflammatory pseudotumor of temporal bone with pachymeningitis, cranial neuropathies and uveitis. Eur Neurol. 2004, 51: 238-240. 10.1159/000078550.View ArticlePubMedGoogle Scholar
- Strasnick B, Vaughan A: Inflammatory pseudotumor of the temporal bone: A case series. Skull Base. 2008, 18: 49-52. 10.1055/s-2007-993047.View ArticlePubMedPubMed CentralGoogle Scholar
- Coulson C, George A, Biswas A, Phelan C, De R: Pseudotumour of the temporal bone: an unusual [corrected] cause of otorrhoea and facial palsy. Eur Arch Otorhinolaryngol. 2008, 265: 713-715. 10.1007/s00405-007-0500-0.View ArticlePubMedGoogle Scholar
- Mulder JJ, Cremers WR, Joosten F, Wiersma A, van den Broek P: Fibroinflammatory pseudotumor of the ear. A locally destructive benign lesion. Arch Otolaryngol Head Neck Surg. 1995, 121: 930-933. 10.1001/archotol.1995.01890080096019.View ArticlePubMedGoogle Scholar
- Schönermark MP, Issing P, Stöver T, Ruh S, Lenarz T: Fibroinflammatory pseudotumor of the temporal bone. Skull base Surg. 1998, 8: 45-50. 10.1055/s-2008-1058590.View ArticlePubMedPubMed CentralGoogle Scholar
- Sismanis A: Pulsatile tinnitus: A 15-year experience. Am J Otol. 1998, 19: 472-477.PubMedGoogle Scholar
- Mattox DE, Hudgins P: Algorithm for evaluation of pulsatile tinnitus. Acta Oto-Laryngologica. 2008, 128: 427-431. 10.1080/00016480701840106.View ArticlePubMedGoogle Scholar
- Tokyol C, Yilmaz MD: Middle ear hemangioma: A case report. Am J Otolaryngol. 2003, 24: 405-407. 10.1016/S0196-0709(03)00086-3.View ArticlePubMedGoogle Scholar
- Liyanage SH, Singh A, Savundra P, Kalan A: Pulsatile tinnitus. J Laryngol Otol. 2006, 120: 93-97.PubMedGoogle Scholar
- Yanagihara N, Segoe M, Gyo K, Ueda N: Inflammatory pseudotumor of the facial nerve as a cause of recurrent facial palsy: case report. Am J Otol. 1991, 12: 199-202.PubMedGoogle Scholar
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