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      Journal of Neurosciences in Rural Practice
      Medknow Publications & Media Pvt Ltd

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          Abstract

          Cysticercosis is an important cestode infection. It can be seen in tropical world and becomes a concern in tropical medicine. This infection is a tissue-embedded parasitosis. The infection can be seen at any organs in human body including neurological system. Neurocysticercosis is considered a serious form of cysticercosis. Neurocysticercosis can induce the neurological manifestations and can be deadly. Due to the nature of tissue invasiveness, the parasitic cyst can be seen anywhere in central nervous system. It is suggested that neurocysticercosis should be included in differential diagnosis of any patients from tropical areas who present with neurological problems.[1] The main part of central nervous system that is usually affected is the cerebral cortex. However, the involvement of other locations can be expected. The pontine involvement in neurocysticercosis is uncommon. This can be difficult for diagnosis. In the recent publication in the journal, an interesting case presenting with Millard Gubler syndrome was reported.[2] Indeed, the ventral pontine syndrome is a rare syndrome, and it is usually due to the infarction.[3] The infectious etiology has not been clearly mentioned. Focusing on pontineneurocysticercosis, the neurological signs, and symptoms are usually due to the mass effect. Cranial nerve deterioration can be expected. There are some previous case reports on pontineneurocysticercosis-induced cranial nerve palsy.[4 5] However, there is no complete report on Millard Gubler syndrome. Indeed, the diagnosis of Millard Gubler syndrome is usually based on neurological imaging. Magnetic resonance angiography findings usually show infarction.[6] However, the unexpected lesion as parasitic cyst might be seen as in the present case. Indeed, imaging studies are recommended in all patients with cranial nerve neuralgia before starting any treatment.[4] The exact final diagnosis has to be derived before any treatment since there are large difference in clinical therapeutic guidelines. Finally, there are some facts to be noted: Neurocysticercosis is an important tropical neurological infection that is reported sporadically. Hence, it should be in differential diagnosis of any cases with neurological problems in the tropical. Neurocysticercosis can be silent and chronic progressive. The clinical manifestations might be delayed. The unusual clinical manifestation of neurocysticercosis can be expected. The cranial nerve palsy is a good example. Not only the Millard Gubler syndrome, but also other neurological syndrome, such as Claude's syndrome,[7] can be the first clinical presentation. Although parasitic cyst is detected, it does not mean that it is the cause of neurological problem but accidental finding. Before making final decision that neurological manifestation is due to the neurocysticercosis, the other causes must be found out. Also, it can be said that the concomitant occurrence can be expected.

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          Most cited references7

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          Neurocysticercosis: A Review

          Neuroysticercosis is the most common helminthic infection of the nervous system, and a leading cause of acquired epilepsy worldwide. The disease occurs when humans become intermediate hosts of Taenia solium by ingesting its eggs from contaminated food or, most often, directly from a taenia carrier by the fecal-to-oral route. Cysticerci may be located in brain parenchyma, subarachnoid space, ventricular system, or spinal cord, causing pathological changes that are responsible for the pleomorphism of neurocysticercosis. Seizures are the most common clinical manifestation, but many patients present with focal deficits, intracranial hypertension, or cognitive decline. Accurate diagnosis of neurocysticercosis is possible after interpretation of clinical data together with findings of neuroimaging studies and results of immunological tests. The introduction of cysticidal drugs have changed the prognosis of most patients with neurocysticercosis. These drugs have shown to reduce the burden of infection in the brain and to improve the clinical course of the disease in most patients. Further efforts should be directed to eradicate the disease through the implementation of control programs against all the interrelated steps in the life cycle of T. solium, including human carriers of the adult tapeworm, infected pigs, and eggs in the environment.
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            Millard-Gubler syndrome: MR findings.

            We present magnetic resonance imaging findings in Millard-Gubler syndrome. In our case, Millard-Gubler syndrome was described first by magnetic resonance angiography findings. MR imaging revealed an infarct in the left side of the ventral pons. Clinical examination and MR imaging revealed Millard-Gubler syndrome.
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              Contralateral trigeminal neuralgia: a new clinical manifestation of neurocysticercosis: case report.

              In cysticercosis, the central nervous system is one of the most commonly affected sites; the clinical manifestations of this disease in the central nervous system can be very severe. The nature and intensity of the signs and symptoms depend on the location of the parasite; cysticeric situated in the cysternae may cause arachnoiditis and vasculitis, but the manifestations are rarely the result of their mass effect. We report the case of a 52-year-old woman with a racemose cysticercus in the left cerebellopontine angle, who presented with contralateral trigeminal neuralgia. The parasite was completely removed via a left suboccipital craniotomy. On the first postoperative day, the patient indicated that the pain had disappeared. The neuralgia was possibly caused by the distortion of the brain stem and the compression of the nerve against an arterial loop at the entry zone. This case demonstrates the advisability of obtaining imaging studies in all patients with trigeminal neuralgia before starting any treatment.
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                Author and article information

                Journal
                J Neurosci Rural Pract
                J Neurosci Rural Pract
                JNRP
                Journal of Neurosciences in Rural Practice
                Medknow Publications & Media Pvt Ltd (India )
                0976-3147
                0976-3155
                Sep-Dec 2012
                : 3
                : 3
                : 377-378
                Affiliations
                [1 ] Wiwanitkit House, Bangkhae, Bangkok, Thailand
                [2 ] Hainan Medical University, China
                [3 ] Joseph Ayobabalola University, Nigeria
                Author notes
                Address for correspondence: Prof. Viroj Wiwanitkit, Wiwanitkit House, Bangkhae, Bangkok, Thailand. E-mail: wviroj@ 123456yahoo.com
                Article
                JNRP-3-377
                3505346
                23189007
                d66ed27d-9c04-4836-8c5d-5cf77834ecd2
                Copyright: © Journal of Neurosciences in Rural Practice

                This is an open-access article distributed under the terms of the Creative Commons Attribution-Noncommercial-Share Alike 3.0 Unported, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

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