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2.
Otol Neurotol ; 41(2): 202-207, 2020 Feb.
Article in English | MEDLINE | ID: mdl-31663997

ABSTRACT

OBJECTIVE: Cochlear obliteration after vestibular schwannoma excision has been noted, with implications on cochlear implantation. Early postoperative cochlear enhancement with gadolinium on magnetic resonance imaging (MRI) has also been observed. Timing of enhancement and association with obliteration is described here. STUDY DESIGN: Retrospective case review. SETTING: Tertiary referral center, ambulatory. PATIENTS: Patients receiving vestibular schwannoma excision surgery by the senior author performed at one institution between January 2015 and July 2017 with postoperative MRIs INTERVENTION:: Diagnostic. MAIN OUTCOME MEASURE(S): The imaging characteristics on postoperative MRIs examined were loss of fluid signal on postoperative T2 images and cochlear enhancement on gadolinium enhanced T1 images. In the patients receiving labyrinthine sparing procedures, presence of postoperative hearing was evaluated. RESULTS: Of the 42 patients evaluated, 24 received the translabyrinthine approach and 18 received a labyrinth sparing surgery. Twenty-nine had evidence of cochlear enhancement on T1 with gadolinium contrast, and 27 had evidence of cochlear obliteration on T2 images. The odds ratio of patients with cochlear enhancement having obliteration was 30.0:1 (p < 0.0001). Intense cochlear enhancement (n = 21) appeared a median of 163 days after surgery, and complete or near complete obliteration (n = 18) appeared a median of 480 days after surgery, a statistically significant difference (p < 0.001). Within the labyrinth sparing group, there was no statistically significant association between hearing loss and cochlear obliteration or enhancement. CONCLUSIONS: Cochlear enhancement is correlated with cochlear obliteration and may precede it.


Subject(s)
Cochlear Implantation , Ear, Inner , Neuroma, Acoustic , Cochlea/diagnostic imaging , Ear, Inner/surgery , Humans , Magnetic Resonance Imaging , Neuroma, Acoustic/diagnostic imaging , Neuroma, Acoustic/surgery , Retrospective Studies
3.
Otol Neurotol ; 37(2): 167-70, 2016 Feb.
Article in English | MEDLINE | ID: mdl-26719960

ABSTRACT

OBJECTIVE: Can magnetic resonance imaging (MRI) diagnose abnormally thin and dehiscent superior semicircular canals (SSCs) that traditionally rely on evaluation by computed tomography (CT) imaging? STUDY DESIGN: Retrospective clinical study. SETTING: Tertiary referral center. PATIENTS: Adults who underwent both MRI and CT of the temporal bones over the past 3 years. INTERVENTIONS: CT and MR images of SSCs were separately reviewed, in a blinded fashion by three neuroradiologists at our institution. CT diagnosis of abnormally thin or dehiscent SSC was used as the "gold" standard. MAIN OUTCOME MEASURES: 1) Dehiscent SSC. 2) Abnormally thin SSC. 3) Normal SSC. RESULTS: One hundred temporal bones with evaluable superior semicircular canals from 51 patients were eligible for review on CT and MR imaging. There were 26 patients of thin SSC and 17 patients of SSC dehiscence on CT imaging, of which 13 and 15 respectively were also found on MRI. There were nine false-positive dehiscent SSC patients and four thin SSC patients observed on MR imaging while not observed on CT. For thin SSCs, MRI sensitivity was 61.9% and specificity of 94.3% with a positive predictive value of 81.3% and a negative predictive value of 86.2%. For dehiscent SSCs, sensitivity was 88.2% and specificity of 89.2% with a positive predictive value of 62.5% and a negative predictive value of 97.4%. CONCLUSION: In this series, MRI in the axial and coronal plane had a high negative predicative value for thin SSC (86%) and dehiscent SSC (97%). However, MRI cannot conclusively diagnose thin or dehiscent SSCs.


Subject(s)
Labyrinth Diseases/diagnosis , Magnetic Resonance Imaging , Semicircular Canals/pathology , Tomography, X-Ray Computed , Adult , Aged , Female , Humans , Male , Middle Aged , Retrospective Studies , Sensitivity and Specificity , Temporal Bone/pathology , Young Adult
4.
Head Neck ; 35(3): E74-6, 2013 Mar.
Article in English | MEDLINE | ID: mdl-22076703

ABSTRACT

Sialadenoma papilliferum is a rare benign salivary gland tumor. We present an unusual case of sialadenoma papilliferum of the parotid gland, discuss clinical presentation, diagnostic challenges, and review of the literature. A 65-year-old male smoker presented with a large, exophytic, fungating, painless mass in the tail parotid for 8 years. The tumor developed an exophytic component 2 years before presentation. The patient subsequently underwent superficial parotidectomy with facial nerve preservation. Initial pathological analysis suggested a variant of Warthin's tumor. The pathology underwent extensive internal and external review. Final diagnosis was consistent with sialadenoma papilliferum. We present the fourth reported case of sialadenoma papilliferum within the parotid gland and only the second that has presented with breach of the overlying skin. The clinical presentation may mimic an advanced parotid malignancy. However, facial nerve preservation and good surgical outcomes can be obtained.


Subject(s)
Adenolymphoma/pathology , Parotid Gland/pathology , Parotid Neoplasms/pathology , Salivary Glands, Minor/pathology , Adenolymphoma/diagnosis , Aged , Diagnosis, Differential , Humans , Male , Parotid Neoplasms/diagnosis , Parotid Neoplasms/surgery
5.
World J Surg Oncol ; 9: 78, 2011 Jul 18.
Article in English | MEDLINE | ID: mdl-21767364

ABSTRACT

OBJECTIVE: To describe the management of bilateral oral ranulas with the use of the da Vinci Si Surgical System and discuss advantages and disadvantages over traditional transoral resection. STUDY DESIGN: Case Report and Review of Literature. RESULTS: A 47 year old woman presented to our service with an obvious right floor of mouth swelling. Clinical evaluation and computerized tomography scan confirmed a large floor of mouth ranula on the right and an incidental asymptomatic early ranula of the left sublingual gland. After obtaining an informed consent, the patient underwent a right transoral robotic-assisted transoral excision of the ranula and sublingual gland with identification and dissection of the submandibular duct and lingual nerve. The patient had an excellent outcome with no evidence of lingual nerve paresis and a return to oral intake on the first postoperative day. Subsequently, the patient underwent an elective transoral robotic-assisted excision of the incidental ranula on the left sublingual gland. CONCLUSION: We describe the first robotic-assisted excision of bilateral oral ranulas in current literature. The use of the da Vinci system provides excellent visualization, magnification, and dexterity for transoral surgical management of ranulas with preservation of the lingual nerve and Wharton's duct with good functional outcomes. However, the use of the robotic system for anterior floor of mouth surgery in terms of improved surgical outcomes as compared to traditional transoral surgery, long-term recurrence rates, and cost effectiveness needs further validation.


Subject(s)
Oral Surgical Procedures/methods , Ranula/surgery , Robotics , Sublingual Gland Neoplasms/surgery , Sublingual Gland/surgery , Biopsy , Diagnosis, Differential , Female , Follow-Up Studies , Humans , Middle Aged , Ranula/diagnosis , Sublingual Gland/pathology , Sublingual Gland Neoplasms/diagnosis , Tomography, X-Ray Computed
6.
Skull Base Rep ; 1(2): 139-44, 2011 Nov.
Article in English | MEDLINE | ID: mdl-23984217

ABSTRACT

This study was conducted to describe a retropharyngeal myxoma and discuss clinical concerns regarding this pathology and a retropharyngeal site of occurrence. We present a case report and review of literature. A 71-year-old woman presented with mild right neck pressure for 3 weeks. Imaging studies and head neck examination confirmed a 5.3 × 3.1 × 1.0 cm retropharyngeal mass with no communication to the vertebral column but was intimately involved with the pharyngeal mucosa. A transoral fine needle aspiration biopsy suggested a possible spindle cell neoplasm. A presurgical swallowing consultation was obtained. A transoral excision of the tumor was possible with no intraoperative complications. Histopathology was a cellular myxoma. Postoperative dysphagia required swallowing therapy and nasogastric tube feeding for 2 weeks before oral intake was possible. The patient has no evidence of clinical or radiological recurrence more than 1 year after surgical intervention. We present the second case of a myxoma in the retropharynx reported in English literature. Transoral excision was safe, feasible, and cosmetically appealing option in our patient. Additional clinical data are required to valid its safety and utility as an approach to tumors in the retropharynx. Postoperative dysphagia can be significant and consequently we recommend preoperative swallowing evaluation and counseling.

7.
Neurosurgery ; 65(4): 733-40; discussion 740, 2009 Oct.
Article in English | MEDLINE | ID: mdl-19834379

ABSTRACT

OBJECTIVE: We report a rare case of internal carotid artery pseudoaneurysm owing to rhinocerebral mucormycosis and review 40 reported cases from 1980 to present. CLINICAL PRESENTATION: A 38-year-old Caucasian man presented with a 3-day history of headache, diplopia, and numbness in the distribution of the left ophthalmic and maxillary branches of the trigeminal nerve. A complete left cavernous syndrome was discovered upon neurological examination. Magnetic resonance imaging scans revealed an inflammatory process involving the paranasal sinuses with extension into the left cavernous sinus, temporal fossa, and petrous bone. INTERVENTION: The patient was immediately treated with amphotericin B, atorvastatin, and daily hyperbaric oxygen sessions before surgical intervention. The patient underwent endovascular treatment of the associated mycotic pseudoaneurysm after carotid test occlusion in addition to a radical bilateral debridement of the paranasal sinuses and infratemporal and temporal fossa. CONCLUSION: Aggressive multimodal therapy is imperative for late-stage rhinocerebral mucormycosis. Extensive resection of infected tissue combined with amphotericin B, atorvastatin, and hyperbaric oxygen seems to be the best course of management. If the internal carotid artery is involved, endovascular intervention is clearly an option to attain this goal. Further research and longer follow-up periods are required to better understand the long-term implications of endovascular coiling and hyperbaric oxygen therapy for rhinocerebral mucormycosis.


Subject(s)
Carotid Artery Injuries/surgery , Mucormycosis/complications , Mucormycosis/surgery , Neurosurgical Procedures/methods , Paranasal Sinus Diseases/complications , Skull Base/surgery , Adult , Antifungal Agents/therapeutic use , Carotid Artery Injuries/microbiology , Carotid Artery Injuries/pathology , Cavernous Sinus/microbiology , Cavernous Sinus/pathology , Cavernous Sinus/surgery , Cranial Fossa, Middle/microbiology , Cranial Fossa, Middle/pathology , Cranial Fossa, Middle/surgery , Debridement/methods , Humans , Hyperbaric Oxygenation , Magnetic Resonance Imaging , Male , Mucormycosis/pathology , Paranasal Sinus Diseases/microbiology , Paranasal Sinus Diseases/pathology , Paranasal Sinuses/microbiology , Paranasal Sinuses/pathology , Skull Base/microbiology , Skull Base/pathology , Temporal Bone/microbiology , Temporal Bone/pathology , Temporal Bone/surgery , Treatment Outcome , Trigeminal Nerve Diseases/microbiology , Trigeminal Nerve Diseases/physiopathology , Vascular Surgical Procedures/methods
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