Unusual orbital lymphoma undetectable by magnetic resonance imaging: a case report
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We report the case of a patient with orbital malignant lymphoma that was not detected by imaging studies when she presented with impaired vision, which lead to her eventual loss of sight.
A 71-year-old Japanese woman complained of deteriorating vision in her left eye. On examination, papilledema was detected, but magnetic resonance imaging only showed slight thickening and enhancement of the left optic nerve. A diagnosis of idiopathic optic neuritis was made and corticosteroid pulse therapy was administered. During the next four months, the patient received a total of four courses of corticosteroid pulse therapy, but she still suffered from bilateral loss of vision. A second magnetic resonance imaging procedure revealed tumors in both orbits and a biopsy showed diffuse large B-cell malignant lymphoma.
The possibility of malignant lymphoma should be considered in patients with recurrent optic neuropathy despite administration of corticosteroid pulse therapy, even when there are no abnormalities on cerebrospinal fluid examination or magnetic resonance imaging.
KeywordsOptic Nerve Optic Neuritis Optic Neuropathy Papilledema Orbital Tumor
magnetic resonance imaging
oculus sinister (Latin for "left eye")
relative afferent pupil defect.
Primary malignant lymphoma is relatively frequent among orbital tumors  and is usually not difficult to detect because it forms a mass lesion that causes changes such as proptosis . Primary malignant lymphoma of the orbit can present with palpebral swelling, proptosis, tumor formation, diplopia, blepharoptosis, and ocular displacement , but few authors have reported orbital lymphoma presenting with optic neuropathy . In patients with visual disorders, imaging generally reveals compression of the optic nerve by the tumor.
Here we report the case of a patient with orbital lymphoma that was not detected by imaging studies at the time when she developed the initial symptom of visual impairment, and which eventually lead to loss of sight. It is very rare for imaging studies to only show optic nerve swelling despite marked bilateral loss of vision, as occurred in this case.
A diagnosis of idiopathic optic neuritis was made and corticosteroid pulse therapy was started on February 3rd. After four days, her visual acuity was 20/20 oculus sinister (OS) and the swelling of the left optic disk had already resolved. The patient's response to corticosteroid therapy and her age suggested a diagnosis of autoimmune optic neuritis. On March 14th and April 12th, visual acuity was reduced to 20/200 OS. There was neither RAPD nor any abnormal ocular findings. Corticosteroid pulse therapy was started again because her vision had deteriorated after reduction of the steroid dose. However, visual acuity on the left side declined to no light perception by May 10th.
On May 20th, the right eye showed a decrease of acuity to 20/600 despite the absence of abnormal ocular findings. On May 24th, the patient was again started on corticosteroid pulse therapy. An MRI of the head and orbits revealed swelling of the left optic nerve (Figure 1c, d). Cerebrospinal fluid (CSF) examination did not show any increase in cell count, abnormal cells or any other findings. On June 3rd, hemorrhage was detected around the left optic disk. On June 10th, slight papilledema was observed on the patient's right eye. Visual acuity declined to no light perception on the right side by June 21st. On July 4th, she complained of left eye pain, and proptosis and subcutaneous hemorrhage were noted around the eyes which suggested thrombosis of tumor pressure.
Immunohistochemical studies showed that the tumor cells were negative for expression of T cell markers (CD3 and CD56) and for Ki-1 (CD30), which is a marker of Hodgkin's and Reed-Sternberg cells. The cells were also negative for cell marker p53 and Epstein-Barr virus-encoded small RNA. Instead, the atypical lymphocytes expressed the B cell markers CD20 and CD79a (data not shown).
On July 28th, the patient was referred to another hospital for chemotherapy and radiotherapy. The succeeding 42 months showed no evidence of local recurrence or systemic metastasis of the lymphoma.
The tumor found in our patient may have developed around her optic nerves and caused compression until the second course of corticosteroid pulse therapy was administered. Although visual acuity recovered during corticosteroid pulse therapy, it deteriorated again after the dose was decreased. These dose-dependent changes of the visual symptoms suggest that circulatory impairment related to the perivascular infiltration of tumor cells led to rapid loss of vision during the period before the tumor could be detected by MRI.
Almost all orbital lymphomas can be diagnosed from swelling of the optic nerve on imaging studies and from abnormal findings upon examination of the CSF [3, 4, 5]. However, there was no optic nerve swelling in our patient until after the third course of corticosteroid pulse therapy was administered. Therefore, orbital lymphoma can sometimes cause loss of sight without being detected by imaging.
The possibility of orbital lymphoma should be considered in patients with an early recurrence of optic neuropathy after corticosteroid pulse therapy, even when there are no abnormal findings on CSF examination or MRI.
Written informed consent was obtained from the patient for publication of this case report and any accompanying images. A copy of the written consent is available for review by the Editor-in-Chief of this journal.