|Year : 2021 | Volume
| Issue : 3 | Page : 605-607
Paraneoplastic orbital myositis in a patient with natural killer/T-cell lymphoma
Areum Jeong1, Min Kyoung Kim2, Joon Hyuk Choi3, Won Jae Kim1
1 Department of Ophthalmology, Yeungnam University College of Medicine, Daegu, South Korea
2 Department of Internal Medicine, Yeungnam University College of Medicine, Daegu, South Korea
3 Department of Pathology, Yeungnam University College of Medicine, Daegu, South Korea
|Date of Submission||02-Sep-2020|
|Date of Acceptance||02-Mar-2021|
|Date of Web Publication||02-Jul-2021|
Prof. Won Jae Kim
170, Hyeonchung-ro, Nam-gu, Daegu, 42415
Source of Support: None, Conflict of Interest: None
Paraneoplastic orbital myositis can occur in patients with natural killer/T-cell lymphoma (NKTL). A discrepancy between ocular motility examinations and imaging findings may suggest paraneoplastic orbital myositis in patients with malignancy. Extraocular muscle biopsy should be performed for definite diagnosis and appropriate treatment, especially in patients with atypical clinical manifestations.
Keywords: Diplopia, paraneoplastic syndromes, orbital myositis
|How to cite this article:|
Jeong A, Kim MK, Choi JH, Kim WJ. Paraneoplastic orbital myositis in a patient with natural killer/T-cell lymphoma. Indian J Ophthalmol Case Rep 2021;1:605-7
|How to cite this URL:|
Jeong A, Kim MK, Choi JH, Kim WJ. Paraneoplastic orbital myositis in a patient with natural killer/T-cell lymphoma. Indian J Ophthalmol Case Rep [serial online] 2021 [cited 2021 Jul 26];1:605-7. Available from: https://www.ijoreports.in/text.asp?2021/1/3/605/320017
The extraocular muscle enlargement is usually associated with thyroid eye disease., However, it can also be caused by other conditions including inflammatory, vascular, neoplastic, infectious, and metabolic disorders., The neoplastic causes include primary tumor, metastasis, and paraneoplastic syndrome.,, When patients with a history of lymphoma show enlargement of the extraocular muscles in neuroimages, direct involvement of lymphoma may be the first consideration., The orbital myositis caused by paraneoplastic syndrome has rarely been reported throughout the literatures.,,, We report a case of paraneoplastic orbital myositis in a patient with natural killer/T-cell lymphoma (NKTL).
| Case Report|| |
A 57-year-old man visited our department presenting with an insidious onset of vertical diplopia 4 months ago. He was diagnosed with NKTL 4 years ago and treated with VIDL (etoposide, ifosfamide, dexamethasone, and L-asparaginase) and radiotherapy. The cancer recurred 1 year after complete remission and was treated with SMILE (dexamethasone, methotrexate, ifosfamide, L-asparaginase, and etoposide). The lymphoma involved nasal cavity, nasopharynx, and neck. No other systemic disease was noted. The symptoms did not have a diurnal variation or any relationship with fatigue. There was mild chemosis and injection of the left eye without ocular pain. The best-corrected visual acuity was 20/20 in both eyes. The pupils showed a normal response to both light and near stimulation. There was no proptosis or abnormal lid problem in both eyes. Extraocular examination revealed 14 prism diopters (PD) left hypertropia in a primary gaze with moderate elevation limitation of the left eye [Figure 1]. Serologic examinations, including a thyroid function and anti-acetylcholine receptor antibody tests, revealed normal results. Magnetic resonance imaging (MRI) of the brain and orbit revealed enlargement and contrast enhancement of the medial rectus muscle (MR), inferior rectus muscle (IR), and superior oblique muscle (SO) of the left eye [Figure 2]a and [Figure 2]b. The lesion of the nasal cavity and nasopharynx were improved compared with the previous study. Position-emission tomography (PET) showed increased FDG (2-(F-18) fluoro-2deoxy-d-glucose) uptake by the MR and IR of the left eye. The whole-body PET-computed tomography (CT) did not show any abnormal uptake in other sites of body.
|Figure 1: A 57-year-old man was consulted in our department with a complaint of binocular vertical diplopia. There was no proptosis or lid retraction in both eyes. Extraocular examination revealed the 14 prism diopters of hypertropia with moderate elevation limitation of the left eye|
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|Figure 2: (a and b). Initial magnetic resonance imaging (MRI) of the brain and the orbit in our patient who had a history of NKTL and presented with binocular vertical diplopia. The MRI showed enlargement and contrast enhancement of medial rectus muscle (MR), inferior rectus muscle (IR), and superior oblique muscle (SO) of the left eye ((a) Coronal view, (b) Sagittal view, arrow). (c and d). The follow-up MRI showed that the enlargement of MR, IR, and SO was improved after steroid treatment compared with initial examination (C: Coronal view, D: Sagittal view, arrowhead)|
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The extraocular muscle biopsy was performed to make a definitive diagnosis and confirm effectiveness of chemotherapy. The forced duction test was performed under general anesthesia and revealed a mild tightness of the MR and IR. The biopsy of both MR and IR was performed throughout the limbal approach. The muscle was divided into longitudinal thirds using the Stevens hook parallel to the fibers of the muscle. The central segment of muscle was biopsied. The specimen shows focally mild infiltration of mature lymphocytes in the muscle fiber without malignant cells. The pathologic report confirmed myositis of the extraocular muscles [Figure 3]a and [Figure 3]b. He was diagnosed with orbital myositis caused by paraneoplastic syndrome, and steroid treatment was initiated (Dexamethasone 40 mg/D, IV) for 4 days. The additional oral steroids were prescribed. One month later, the follow-up MRI showed that the enlargement of the extraocular muscle had improved compared with that at the initial examination [Figure 2]c and [Figure 2]d. Extraocular examination showed 2 PD left hypertropia in the primary gaze without ocular movement limitation. However, hypertropia and diplopia relapsed after discontinuation of steroids. At 8 months after the biopsy, the ocular motility findings deteriorated to 35 PD left hypertropia and 20 PD exotropia in a primary gaze with moderate elevation and adduction limitation of the left eye. The follow-up MRI demonstrated the enlargement of MR, IR, and SO without other orbital involvement. He is being followed-up with monocular occlusion for diplopia and currently tolerating chemotherapy (GDP, Gemcitabine, Dexamethasone, and Cisplatin). The surgical treatment for strabismus is considering.
|Figure 3: (a and b) Histologic findings. (a) Infiltrated lymphocytes in the orbital muscle fibers (hematoxylin and eosin stain, original magnification 200×). (b) CD3-positive T lymphocytes are present (CD3 immunohistochemical stain, original magnification 200×)|
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| Discussion|| |
Paraneoplastic myositis is considered to involve autoantibodies directed against the tumor that cross-react with extraocular muscle antigens and induced autoimmune inflammation.,, In Shafi et al.'s study of 16 patients with non-thyroid-related extraocular muscle enlargement, 4 patients were paraneoplastic myositis. Paraneoplastic myositis has been reported to associate with breast cancer, thyroid cancer, lymphoma, and seminoma.,,,
In this case, the patient had an insidious onset of diplopia without definitive ocular pain, which is different from the typical clinical features of orbital myositis., Orbital myositis is usually idiopathic with an acute onset, presents with painful diplopia, and responds dramatically to corticosteroid therapy.,,, However, previous studies showed that the clinical manifestations of paraneoplastic myositis are not associated with acute painful diplopia.,, There are many atypical cases occurring in the setting of systemic inflammatory or infective conditions.
Because this patient had a history of lymphoma, direct involvement to the extraocular muscles was considered. Clinical findings of our patients were different from previous reports with patients with orbital involvement of NKTL. Orbital involvement usually rapidly progressive and occur in multiple orbital structures in patient with NKTL., The inferior oblique muscles were most commonly affected extraocular muscles in orbital involvement of NKTL. Our patient showed the enlargement of MR, IR, and SO without other orbital involvement. The pre-existing lesions including nasal cavity and nasopharynx improved during the follow-ups. The pathologic examination did not show any direct involvement of NKTL. It is therefore likely that the extraocular enlargement in our patient was caused by a paraneoplastic myositis.
In the present case, the extraocular motility findings did not correlate with those of MRI. The MRI showed the enlargement of MR, IR, and SO of the left eye. The forced duction test confirmed mild mechanical restriction of MR and IR. These findings may suggest left hypotropia or esotropia in primary gaze with an up-gaze limitation. However, he showed left hypertropia in primary gaze with an up-gaze limitation of the left eye. This orbital myositis probably affected multiple extraocular muscles and was in a combined paretic and restrictive clinical phase. Ocular motility findings of myositis vary according to the clinical course. Orbital myositis may exhibit the following clinical course over time: normal motility for several days, followed by a paretic phase, then combined paretic and restrictive phase, and finally a restrictive phase. Another study showed that idiopathic orbital myositis showed variable degrees of ocular motility limitation, and limitations in the same direction as that of the action of the affected muscle were more frequent. Therefore, the discrepancy between ocular motility findings and neuroimaging results may indicate orbital myositis.
In addition, orbital imaging alone is not diagnostic, and extraocular muscle measurement can vary between modalities. Extraocular muscle biopsy may be necessary for patients with atypical clinical features accompanying extraocular muscle enlargement.
| Conclusion|| |
The orbital myositis can occur due to paraneoplastic syndrome, and extraocular muscle biopsy can be considered for definite diagnosis and appropriate treatment when the findings of imaging are not correlated with ocular movement in patients with tumors.
Declaration of patient consent
The authors certify that they have obtained all appropriate patient consent forms. In the form the patient(s) has/have given his/her/their consent for his/her/their images and other clinical information to be reported in the journal. The patients understand that their names and initials will not be published and due efforts will be made to conceal their identity, but anonymity cannot be guaranteed.
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Conflicts of interest
There are no conflicts of interest.
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[Figure 1], [Figure 2], [Figure 3]