1.Multiple Myeloma Manifesting as a Fluctuating Sixth Nerve Palsy.
Jung Hwa NA ; Shin Hae PARK ; Sun Young SHIN
Korean Journal of Ophthalmology 2009;23(3):232-233
We report a case of multiple myeloma that presented as a fluctuating sixth cranial nerve palsy in the absence of widespread signs of systemic disease. A 63-year-old woman presented with horizontal diplopia of two weeks duration that subjectively changed over time. Ocular examination showed a fluctuating sixth nerve palsy. A computed tomography (CT) scan of the brain showed multiple, enhancing, soft tissue, mass-like lesions involving the left cavernous sinus and the apex of both petrous bones. Based on bone marrow biopsy and hematologic findings, she was diagnosed with multiple myeloma. Multiple myeloma may be included in the differential diagnosis of a fluctuating sixth nerve palsy, and although ophthalmic signs are rare and generally occur late in the course of multiple myeloma, they can still be its first signs.
Abducens Nerve Diseases/diagnosis/*etiology
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Brain/pathology/radiography
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Diagnosis, Differential
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Diplopia/etiology
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Esotropia/etiology/physiopathology
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Female
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Humans
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Magnetic Resonance Imaging
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Middle Aged
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Multiple Myeloma/*complications/diagnosis
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Tomography, X-Ray Computed
2.A Case of Pediatric Idiopathic Intracranial Hypertension Presenting with Divergence Insufficiency.
Korean Journal of Ophthalmology 2011;25(4):289-293
An 11-year-old female presenting diplopia only at distance was found to have comitant esotropia of 20 prism diopters (PD) at distance and normal alignment at nearer proximity. Other ocular movement, including abduction, was normal and a thorough neurologic examination was also normal. The deviation angle of esotropia was increased to 35 PD in 6 months, and a brain magnetic resonance imaging with venogram at that time demonstrated no intracranial lesion. A lumbar puncture showed increased opening pressure but the cerebrospinal fluid composition was normal. The patient was diagnosed as having idiopathic intracranial hypertension and treated with oral acetazolamide. Three months after treatment, the deviation angle decreased to 10 PD. This is a case report of divergence insufficiency in pediatric idiopathic intracranial hypertension, with an increasing deviation angle of esotropia. Although sixth cranial nerve palsy is a common neurologic manifestation in intracranial hypertension, clinicians should be aware of the possibility of divergence insufficiency. Also, ophthalmoparesis may not be apparent and typical at first presentation, as seen in this case, and therefore ophthalmologists should be aware of this fact, while conducting careful and proper evaluation, follow-up, and intervention.
Acetazolamide/administration & dosage
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Administration, Oral
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Child
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Diagnosis, Differential
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Diuretics/administration & dosage
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Esotropia/diagnosis/*etiology/physiopathology
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Exotropia/diagnosis/*etiology/physiopathology
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Eye Movements
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Female
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Follow-Up Studies
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Humans
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Intracranial Pressure
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Magnetic Resonance Imaging
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Pseudotumor Cerebri/*complications/diagnosis/drug therapy
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Spinal Puncture/methods
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Vision, Binocular
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Visual Acuity
3.Acute Comitant Esotropia in a Child With a Cerebellar Tumor.
Jong Min LEE ; Sin Hoo KIM ; Jeong Il LEE ; Ji Yong RYOU ; Sook Young KIM
Korean Journal of Ophthalmology 2009;23(3):228-231
We report a case of acute comitant esotropia in a child with a cerebellar tumor. A 3-year-old boy was referred for management of a 9 month history of acute acquired comitant esotropia. On first presentation, the patient's angle of esodeviation was 50 prism-diopters (PD) at distance and near fixation without any lateral incomitance. The cycloplegic refraction revealed +0.75 diopters in both eyes. Very mild bilateral papilledema was found on the fundus examination, but the neurological examination did not reveal any other pathological findings. Brain MRI showed a 5 cm mass located in the midline of the cerebellum as well as hydrocephalus. The mass was completely excised and histological examination confirmed the diagnosis of pilocytic astrocytoma. Despite neurosurgery, the patient's strabismus remained unresolved. One year after neurosurgery, both medial rectus muscles were surgically recessed by 6 mm, resulting in esotropia of 8PD at distant and near fixation without restoration of bifoveal fusion at follow-up 2 years after the eye muscle surgery. Therefore, acute onset comitant esotropia in a child can be the first sign of a cerebellar tumor, even without any other neurological signs and symptoms.
Acute Disease
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Astrocytoma/*complications/surgery
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Brain/pathology
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Cerebellar Neoplasms/*complications/diagnosis/surgery
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Child, Preschool
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Esotropia/*etiology/pathology/physiopathology/surgery
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Humans
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Magnetic Resonance Imaging
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Male
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Neurosurgical Procedures
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Oculomotor Muscles/surgery
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Refraction, Ocular
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Time Factors