Olfactory Neuroblastoma: A Rare Cause of External Ophthalmoplegia, Proptosis and Compressive Optic Neuropathy.
Olfactory neuroblastoma (ONB), also referred to as esthesioneuroblastoma, was first described by Berger in 1924. It is a rare neuroectodermal malignant tumor of the nasal cavity originating from the olfactory neuroepithelium. (1) ONB constitutes 2-6% of all malignancies of the nasal cavity and paranasal sinuses. The incidence is highest in the second and sixth decades of life. (2,3,4) This fast-growing tumor can be asymptomatic until it fills the nasal cavity and causes obstruction and/or epistaxis. It may spread into the cranium, orbit, and paranasal sinuses. Orbital invasion can lead to vision loss, ophthalmoplegia, and proptosis. In this study, we present the clinical features of a 62-year-old female patient with olfactory neuroblastoma showing orbital invasion.
A 62-year-old female patient presented to our unit with complaints of double vision. She stated that her double vision had started approximately one month earlier. Neuroophthalmologic examination revealed bilateral light responses with no afferent pupil defect. Color vision test with Ishihara (14 card print) was 14/14 in both eyes. The patient exhibited abnormal head posture (face turn to right) and hypertropia of the left eye (10 prism diopters). Slight restriction of left eye movement was noted in down/right gaze. There were no obvious limitations in the other positions of gaze. In the Bielschowsky head tilt test, hypertropia increased when the head was tilted to the left. Best corrected visual acuity on Snellen chart was 10/10 in both eyes. Anterior segment and fundus examinations were normal in both eyes. The patient was diagnosed with left fourth cranial nerve palsy and cranial imaging was requested to establish etiology; however, the patient did not return for follow-up. Approximately 2 months later, our unit was consulted again regarding the patient due to complaints of reduced vision and pain in the left eye. She also had complaints of progressive swelling in the left half of her face and enlargement of her left eye for about one month. On neuroophthalmologic examination, light response was normal in the right eye and weak in the left eye. Relative afferent pupil defect was noted in the left eye. Right eye movements were unrestricted in all directions, while left eye movements were restricted in all directions with minimal upward gaze (Figure 1). Proptosis was noted in the left eye, and Hertel exophthalmometer measurements were 18 mm for the right eye and 24 mm for the left eye. Best corrected visual acuity on Snellen chart was 9/10 in the right eye and counting fingers from 2 m in the left eye. Color vision score was 14/14 in the right and 0/14 in the left eye. Chemosis and upper lid edema were observed in the left eye on slit-lamp examination. The anterior segment appeared normal. Intraocular pressure measured by Goldmann applanation tonometry was 15 mmHg in both eyes. Fundus examination was normal in the right eye, while optic disc hyperemia and increased tortuosity and caliber of the retinal vessels were observed in the left eye (Figure 2). Reliable results could not be obtained in visual field and visual evoked potential tests. Computed tomography scans revealed a mass filling the left nasal cavity and anterior/posterior ethmoid sinuses, extending beyond the medial rectus muscle into the cone and compressing the optic nerve. Orbital magnetic resonance imaging revealed a soft tissue mass with homogeneous enhancement, hypointense in T1-weighted sequences and hyperintense in T2-weighted sequences, which appeared to be displacing the optic nerve inferiorly (Figure 3). Based on the results of histopathological examination of a punch biopsy obtained from the nasal passage, the patient was diagnosed with olfactory neuroblastoma (Hyams grade III). Immunohistochemical staining for differential diagnosis of the round cell tumor was negative for CD2, CD3, CD20, CD38, cytokeratin, CD99, HMB45 and GFAP. A small number of cells were positive for CD56, chromogranin, and synaptophysin, while very few cells were positive for BCL2, NF, and S100. Ki-67 labeling index was 25% (Figure 4).
The most common symptom of ONB was reported by Dulguerov and Calcaterra (5) as unilateral nasal obstruction, which they observed in 71% of 26 patients. Other common symptoms are anosmia, headache, lacrimation, proptosis, and reduced vision. In rare cases, ONB secretes antidiuretic hormone (ADH) and causes syndrome of inappropriate ADH secretion, or produces ectopic adrenocorticotropic hormone and leads to Cushing's syndrome. (6) In a large series including 38 cases of ONB, Rakes et al. (7) reported that 53% of patients had orbital or ocular symptoms and that the most common symptoms were periorbital pain and lacrimation. In addition, they determined that diplopia was the initial ocular symptoms in 8% of the patients. (7) Most patients develop diplopia secondary to tumor invasion of the orbit. On the other hand, ONB can cause cranial nerve palsy without orbital invasion. Rakes et al. (7) reported cranial nerve palsy in a patient without orbital involvement in their series. Lee and Tang (8) also reported third cranial nerve palsy with pupil involvement due to mass extension to the cavernous sinus, without orbital involvement. Fourth cranial nerve palsy was the first clinical finding in our case; however, as the patient did not attend follow-up, the diagnosis was established after she presented a second time with ophthalmoplegia and proptosis, likely due to expansion of the tumor tissue within the orbit. ONB-associated optic neuropathy may develop due to compressive and/or infiltrative causes. (9) In our case, we observed that the tumor inferiorly displaced the optic nerve in orbital imaging and thus believed neuropathy was a result of compression. However, it should be noted that tumor infiltration cannot be excluded without histopathological evaluation.
Hyams et al. (10) divided ONB into four histological grades. The grading system is based on evaluations of mitotic index, necrosis, rosette formation, calcification, pleomorphism, lobular structure, and the neurofibrillary matrix. Grade III and IV have been associated with poor prognosis. (10) Currently, standard treatment of ONB consists of total surgical excision (open or endoscopic craniofacial resection) and adjuvant radiotherapy. (11,12) The most common site of metastasis in ONB patients is the cervical lymph nodes, seen in 20-25% of patients. Neck metastases are detected in 5-8% of patients at time of diagnosis.
In brief, ONB is a rare endonasal tumor. It may manifest with initial findings of cranial nerve palsy, proptosis, and/or compressive optic neuropathy. Therefore, this rare etiology must be considered in the differential diagnosis of cranial nerve palsy, external ophthalmoplegia, and proptosis.
Informed Consent: Patient's written consent was obtained.
Peer-review: Externally peer-reviewed.
Surgical and Medical Practices: Tagkin Tokat, Concept: Omer Karti, Mehmet Ozgur Zengin, Design: Omer Karti, Mehmet Ozgir Zengin, Data Collection or Processing: Ozan Celik, Omer Karti, Analysis or Interpretation: Tuncay Kisbeci, Omer Karti, Mehmet Ozgir Zengin, Literature Search: Tuncay Kusbeci, Omer Karti, Mehmet Ozgur Zengin, Tagkin Tokat, Ozan Celik, Writing: Omer Karti.
Conflict of Interest: No conflict of interest was declared by the authors.
Financial Disclosure: The authors declared that this study received no financial support.
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[??] Omer Karti (*), [??] Mehmet Ozgur Zengin (*), [??] Ozan Celik (*), [??] Taskin Tokat (**), [??] Tuncay Kusbeci (*)
(*) University of Health Sciences, Izmir Bozyaka Training and Research Hospital, Ophthalmology Clinic, Izmir, Turkey (**) University of Health Sciences, Izmir Bozyaka Training and Research Hospital, Otolaryngology Clinic, Izmir, Turkey
Address for Correspondence: Omer Karti MD, University of Health Sciences, Izmir Bozyaka Training and Research Hospital, Ophthalmology Clinic, Izmir, Turkey
Phone: +90 505 598 56 85 E-mail: firstname.lastname@example.org ORCID-ID: orcid.org/0000-0001-5085-0079
Received: 27.06.2017 Accepted: 03.10.2017
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|Title Annotation:||Case Report|
|Author:||Karti, Omer; Zengin, Mehmet Ozgur; Celik, Ozan; Tokat, Taskin; Kusbeci, Tuncay|
|Publication:||Turkish Journal of Ophthalmology|
|Article Type:||Case study|
|Date:||Mar 1, 2018|
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