Abstract
Introduction: Recurrent oculomotor nerve palsies are extremely rare clinical conditions.
Case report: Here, we report on a unique case of a short-lasting recurrent unilateral incomplete external and complete internal oculomotor nerve palsy. The episodic palsies were probably caused by an ipsilateral mesencephalic metastasis of a breast carcinoma and occurred after successful brain radiation therapy.
Discussion: While the pathogenic mechanism remains unclear, the recurrent sudden onset and disappearance of the palsies and their decreasing frequency after antiepileptic treatment suggest the occurrence of epilepsy-like brainstem seizures. A review of case reports of spontaneous reversible oculomotor nerve palsies is presented.
Introduction
A recurrent isolated oculomotor nerve palsy is an extremely rare clinical condition that to date has been described in ophthalmoplegic migraine, possible nerve compressive conditions (ethmoidal mucocele, neurofibromatosis type 2, recurrent hemorrhage in pituitary adenoma, pseudotumor cerebri, carotid basilar anastomosis, a Reye-like syndrome), essential mixed cryoglobulinemia, diabetes mellitus, and postvaccinal. The attacks last from 24 h to 6 months (Table 1). In Tolosa–Hunt syndrome, recurrent oculomotor nerve palsies also may occur; however, they are usually accompanied by other cranial nerve palsies ().
Table 1
| Reference | Etiology | Number and duration of the episodes | Suspected or possible mechanisms |
|---|---|---|---|
| Barrett et al. () | Neurofibromatosis type 2 | 3: 3 months – 1 week – 6 months | Acute conduction block |
| Bek et al. () | Ophthalmoplegic migraine | Several episodes: about 3 months | Inflammatory process |
| Doh-ura et al. () | Posterior ethmoidal mucocele | 6: Duration not presented | Compression or inflammatory infiltration from the mucocele |
| Kotwica et al. () | Diabetes mellitus | 5: 1–3 months – several days – 8 weeks – 3 months | Not discussed |
| Lance and Zagami () | Ophthalmoplegic migraine | Case # 1: several attacks 2 days – 2 months; case # 2: not presented; case # 3: 20 days; case # 4: 3 weeks | Demyelinization or inflammation of the oculomotor nerve |
| Madonick and Ruskin () | Carotid basilar anastomosis | 2: 1–2 days – 6 weeks | Pressure on the oculomotor nerve |
| Manzotti et al. () | Measles mumps rubella vaccination | 2: 24–48 h – 1 week | Not presented |
| Mattigk and Gaida () | Reye-like syndrome | 2: 4–8 weeks | Transient increased intracranial hypertension |
| McCammon et al. () | Pseudotumor cerebri | 2: Several hours – 14 days | Raised intracranial pressure |
| McMillan et al. () | Ophthalmoplegic migraine | Case # 1: 2 months – 10 weeks; case # 2: 2–3 days – 2–3 weeks (two additional episodes; duration not presented) | Inflammatory cranial neuropathy |
| Messier et al. () | Essential mixed cryoglobulinaemia | 2: 24 h – not presented | Vasculitis of the vasa nervorum |
| Mohanty () | Hemorrhage in pituitary adenoma | 2: 4 days – 8 months | Reversible compression of the oculomotor nerve |
| Mokta et al. () | Neurocysticercosis at the tegmentum of the left midbrain | 2: 1–4 days | Not discussed |
| Ramelli et al. () | Ophthalmoplegic migraine | 2: 2 weeks – not presented | Swelling of the oculomotor nerve |
| Schmal and Schulz () | Ophthalmoplegic migraine | 2: a few days – 2 weeks | Not discussed |
| Present case | Meningeosis carcinomatosa, mesencephalic metastasis | Several: minutes | Epilepsy-like discharges |
Spontaneously recovering recurrent oculomotor nerve palsies.
Here, we report on the case of a 57-year-old woman presenting with repeated unilateral internal and external short-lasting oculomotor nerve palsies caused by a neoplastic brain stem process that lasted only several minutes.
Case History
The female patient suffered from advanced stage breast carcinoma pT1cG3pN1, initially diagnosed 15 years ago, with metastases of the liver, soft tissues, and bone that had been treated with the administration of numerous chemotherapeutics, radiation, and chemoembolization. Finally, she developed cerebral metastases and meningeal carcinomatosis diagnosed by lumbar puncture presenting 115 leukocytes/μl (normal: ≤4/μl), increased protein content of 850 mg/l (normal: 150–450 mg/l), reduced glucose concentration of 1.8 mmol/l (normal: 2.2–4.4 mmol/l), high lactate concentration of 9.4 mmol/l (normal: 1.2–2.1 mmol/l), as well as tumor cells (Papanicolaou group V). Several supratentorial intra-cerebral contrast-enhancing lesions, which were most prominent left-sided in the mesencephalon with a diameter of 8 mm and in the left thalamus (Figure 1), were present on magnetic resonance images (MRI). Assuming the presence of cerebral metastases, a palliative radiation of the brain with 30.0 gray was performed. In addition, three cycles of 15 mg methotrexate were administered intrathecally through a Rickham reservoir.
Figure 1
The patient was hospitalized into the neurological department because of newly occurring headaches and temporarily reduced alertness. The initial neurological examination revealed diminished consciousness, slight neck stiffness, only small pupillary reaction of the right pupil and a large, unreactive, and maximally enlarged left pupil, a quadriparesis with only weak movements of the right arm, loss of tendon reflexes of the lower extremities, and a left-sided positive Babinski sign. During her stay, an episode of sudden complete loss of consciousness accompanied by left-sided blepharoptosis and mydriasis, and bradycardia occurred. Before and after it no weakness of the extraocular muscles, ptosis, unreactivity of the left pupil, or anisocoria were present (Figure 2). While native and gadolinium-enhanced MRI performed on the same day demonstrated an acute ischemia in the right frontal lobe, the cerebral metastases were considerably less obvious after interim brain radiation therapy (Figure 1). Assuming an atypical epilepsy-like brainstem seizure, she was treated with levetiracetam 1.5 g b.i.d. During the subsequent days, several episodes of sudden maximal mydriasis of the left pupil were observed that were occasionally accompanied by complete blepharoptosis that spontaneously disappeared after several minutes (Figure 2). During these episodes, her consciousness occasionally diminished further. Due to diminished consciousness, the oculomotor motility could not be examined properly during the attacks. In the intervals, no weakness of the extra- and intraocular muscles on either side was evident. Three electroencephalograms showed slight to pronounced general slowing down with or without few focal epileptic discharges. Lacosamide 200 mg b.i.d. was added resulting in a lower frequency of these ophthalmoplegic episodes. Furthermore, the patient became alert and orientated. However, she died 20 days after admission. An autopsy was not performed.
Figure 2
Discussion
The nucleus n. oculomotorii, which innervates the lid elevators and other extraocular muscles, and the parasympathetic fibers in the Edinger–Westphal nucleus, which are responsible for the mydriasis, are located in the mesencephalon () where a metastasis was shown in MRI before radiation. Rarely, patients with isolated persistent oculomotor nerve palsy that was secondary to a single mesencephalic metastasis have been described, e.g., by Modi et al. (). In another case described by Rotondo et al. (), the oculomotor nerve palsy disappeared after microsurgical excision of the metastasis of a breast cancer. In our case, sudden onset and reversibility of the palsy due to injury of the extracerebral course of the oculomotor nerve, e.g., due to increased intracranial pressure, seems to be very unlikely. Thus, the transient malfunction of the oculomotor nerve probably must also be attributed to the mesencephalic lesion. Usually, the degree of external ophthalomoplegia is more severe than the internal weakness. In our case, obviously the Edinger–Westphal nucleus or parasympathetic fibers are more affected than the motor nucleus n. oculomotorii. To the best of our knowledge, to date, no case of recurrent oculomotor nerve palsy with sudden onset and disappearance has been published.
Neither increased intracranial pressure due to meningeal carcinomatosis, meningeal carcinomatosis itself, low intracranial pressure, which rarely induces isolated third nerve palsy () due to the Rickham reservoir, toxic effects of intrathecally applied methotrexate, intracranial infections such as aspergillosis (), vasculopathy induced by brain radiation therapy or a possible aneurysma of the posterior cerebral nor a posterior communicating artery can explain the sudden occurrence and disappearance of an oculomotor nerve palsy. The unilateral affection argues against a pharmacological effect. Transient migraine-like headaches accompanied by transient focal neurological deficits (SMART syndrome) only occur several years after brain radiation therapy. Moreover, these deficits are linked to a unilateral cortical region. However, epileptic seizures, for instance, originating from the frontal lobe, may explain transient bilateral but not unilateral enlarging of the pupils. The levator palpebralis nucleus projects bilaterally and the rectus superior nucleus contralaterally. Thus, unilateral ptosis indicates that only the brainstem fascicles were affected.
The sudden onset and disappearance of the oculomotor nerve palsy as well as the observed improvement with antiepileptic drugs suggest the presence of epilepsy-like seizures that were possibly triggered by ephapses due to post-radiation scars between the mesencephalic focus and fibers of the oculomotor nerve. Possible rostral spreading of these discharges, spreading of these discharges to the formatio reticularis or additional epileptic discharges deriving from the thalamic focus may have resulted in the observed diminished consciousness.
In conclusion, the observations presented in this case report raise the question whether short-lasting cranial nerve palsies may be caused by abnormal electrophysiological discharges such as a hitherto undescribed type of brainstem seizures.
Statements
Acknowledgments
T. Bienz, Bergen, Norway, and B. Gulcz, Bad Berka, Germany, kindly translated the Japanese and Polish articles.
Conflict of interest
The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.
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Summary
Keywords
recurrent oculomotor nerve palsy, mesencephalic metastasis, radiation, breast carcinoma, meningeal carcinomatosis
Citation
Grabau O, Leonhardi J and Reimers CD (2014) Recurrent Isolated Oculomotor Nerve Palsy after Radiation of a Mesencephalic Metastasis. Case Report and Mini Review. Front. Neurol. 5:123. doi: 10.3389/fneur.2014.00123
Received
08 April 2014
Accepted
26 June 2014
Published
24 July 2014
Volume
5 - 2014
Edited by
Valerie Purvin, Midwest Eye Institute, USA
Reviewed by
An-Guor Wang, Taipei Veterans General Hospital, Taiwan; Wanicha Chuenkongkaew, Mahidol University, Thailand
Copyright
© 2014 Grabau, Leonhardi and Reimers.
This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
*Correspondence: Carl D. Reimers, Neuer Wall 19, Hamburg D-20354, Germany e-mail: c.d.reimers@t-online.de
This article was submitted to Neuro-Ophthalmology, a section of the journal Frontiers in Neurology.
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