1.Immunocytochemical and ultrastructural study of localization of the putrescine in rat medulla oblongata.
Jong Eun LEE ; Kyung Ah PARK ; Seung Gwan LEE ; Young Dong CHO
Korean Journal of Anatomy 1991;24(4):409-421
No abstract available.
Animals
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Medulla Oblongata*
;
Putrescine*
;
Rats*
2.Isolated Tongue Paralysis as Presentation of Seropositive Neuromyelitis Optica Spectrum Disorder.
Hye Seon JEONG ; Ju Heon LEE ; Yong Soo KIM ; Ae Young LEE ; Jae Moon KIM ; Eun Hee SOHN
Journal of the Korean Neurological Association 2016;34(5):367-370
Neuromyelitis optica spectrum disorder (NMOSD) is characterized by a characteristic clinical presentation or positivity for the anti-aquaporin-4 antibody. Lesions involving the dorsal medulla are typical of NMOSD, but isolated tongue paralysis has not been reported previously. We report a rare case of NMOSD presenting with isolated tongue paralysis and swelling due to intrinsic tongue muscle paralysis, which was caused by bilateral involvement of the hypoglossal nuclei in the lower dorsal medulla oblongata.
Medulla Oblongata
;
Neuromyelitis Optica*
;
Paralysis*
;
Tongue*
3.Restricted Spinothalamic Sensory Loss Below Thoracic Dermatomal Level Caused by Pontine Infarction.
Kwangsub LEE ; Heeyoung KANG ; Eunjeong JOO ; Nack Cheon CHOI ; Kyusik KANG ; Oh Young KWON ; Ki Jong PARK ; Byeong Hoon LIM
Journal of the Korean Neurological Association 2009;27(3):279-281
Cerebral lesions can cause dermatomal sensory deficit. The most commonly reported site is the medulla oblongata due to its well-separated sensory systems. Dermatomal sensory deficit that has developed after pontine infarctions have been reported in several cases, the majority of which involved the medial lemniscus. However, restricted spinothalamic sensory loss has rarely been reported in pontine infarctions. We report herein a patient who presented with dermatomal spinothalamic sensory deficits below the tenth thoracic level after pontine infarction.
Humans
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Infarction
;
Medulla Oblongata
;
Spinothalamic Tracts
4.One case of Medial Medullary Syndrome.
Se Hee CHANG ; Doo Yong KIM ; Oh Sang KWON
Journal of the Korean Neurological Association 1993;11(3):459-461
Medial medullary syndrome is a clinical disorder charactenzed by ipsilateral paralysis of tongue and contralateral hemiparalysis and contralateral hemisensory disturbance of vibration or position but face sparing. The syndrome is ususlly due to lesion of medial medulla oblongata. Involved structures are pyramid, hypoglossal nucleus, medial lemniscus and/or medial longitudinal fasciculus. We present 1 case of medial medullary syndrome with MRI finding, which showed infarction of left medial medulla oblongata.
Infarction
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Magnetic Resonance Imaging
;
Medulla Oblongata
;
Paralysis
;
Tongue
;
Vibration
5.Successful Removal of Hemangioblastoma Originating in the Medulla Oblongata: Report of 1 Case.
Gi Han BAE ; Jin Hwa EUM ; Dae Jo KIM ; Kwan Hee PARK
Journal of Korean Neurosurgical Society 1995;24(3):331-337
Solid hemangioblastomas of the medulla oblongata are benign vascular neoplasms located in a critical area. We experienced a case of solid hemangioblastoma originated in the medulla oblongata with the syrinx in the cervical spinal cord. Preoperative magnetic resonance imaging provided precise anatomical location and radiologic features of the tumor, which facilitated its total removal. Cardiovascular and pulmonary disorders often complicate this type of surgery, and postoperative dysphagia is a frequent sequelae.
Deglutition Disorders
;
Hemangioblastoma*
;
Magnetic Resonance Imaging
;
Medulla Oblongata*
;
Spinal Cord
;
Vascular Neoplasms
7.Two Cases of Avellis Syndrome.
Se Hee JANG ; Dong Suk HAM ; Woo Jung KIM ; Doo Young KIM ; Oh Sang KWON
Journal of the Korean Neurological Association 1992;10(3):362-365
Avellis syndrome is a clinical disorder characterized by ipsilateral paralysis of palate, larynx, and vocal cord paralysis and contralateral hemianesthesia. The syndrome is usually due to lesion of medulla oblongata. Involeved structures are nucleus ambiguus, lateral spinothalamic tract, and descending sympathetic fibers. We present 2 cases of Avellis syndrome with MRI findings, which showed infarction of right-sided upper medulla oblongata.
Adrenergic Fibers
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Infarction
;
Larynx
;
Magnetic Resonance Imaging
;
Medulla Oblongata
;
Palate
;
Paralysis
;
Spinothalamic Tracts
;
Vocal Cord Paralysis
8.A Case of Rhombencephalitis Presented with Intractable Hiccup.
Journal of the Korean Child Neurology Society 2012;20(2):108-111
The term 'rhombencephalitis' refers to inflammatory diseases affecting the hindbrain. We experienced a case of rhombencephalitis in a 14 years old girl, who presented with fever, headache, and intractable hiccup for one week prior to admission. Brain MRI on admission showed bilateral high signal intensities in the dorsal portion of the medulla oblongata on T2WI and FLAIR. Examination of cerebrospinal fluid showed increased WBC count (33/mm3, Lymphocyte 81%), normal protein and glucose level. Immunoserologic study showed decreased C3, C4 level and increased Anti-ds DNA level. However, FANA was negative. The hiccup was controlled by administration of IVIG (1 g/kg/day for 2 days) and steroid (30 mg/kg/day for 3days) without any neurologic symptoms. We report a case with the brief review of related literatures.
Brain
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DNA
;
Encephalitis
;
Fever
;
Glucose
;
Headache
;
Hiccup
;
Immunoglobulins, Intravenous
;
Lymphocytes
;
Medulla Oblongata
;
Neurologic Manifestations
;
Rhombencephalon
9.Intracranial Lipoma in Medulla Oblongata.
Ji Kwang YUN ; Dae Won KIM ; Tae Young KIM ; Jong Moon KIM
Journal of Korean Neurosurgical Society 2007;41(5):330-332
Intracranial lipomas are rare, and most of these tumors are found in the region of the corpus callosum, followed by cerebellopontine angle. We present a case of a intracranial lipoma in 30-year-old man. Brain computed tomography (CT) scan and magnetic resonance images (MRI) showed a mass in the medulla oblongata extending to foramen magnum. The histopathologically, diagnosis of lipoma was confirmed. Although there were several cases of cervical intraspinal lipoma extending into posterior cranial fossa, there have been no previous reports of a lipoma arising from the medulla oblongata that extended into the foramen magnum. We describe a rare case of intradural subpial lipoma in the medulla oblongata with a review of the literature.
Adult
;
Brain
;
Cerebellopontine Angle
;
Corpus Callosum
;
Cranial Fossa, Posterior
;
Diagnosis
;
Foramen Magnum
;
Humans
;
Lipoma*
;
Medulla Oblongata*
10.Intractable Hiccup as the Presenting Symptom of Cavernous Hemangioma in the Medulla Oblongata: A Case Report and Literature Review.
Kyung Hwa LEE ; Kyung Sub MOON ; Min Young JUNG ; Shin JUNG
Journal of Korean Neurosurgical Society 2014;55(6):379-382
A case of intractable hiccup developed by cavernous hemangioma in the medulla oblongata is reported. There have been only five previously reported cases of medullary cavernoma that triggered intractable hiccup. The patient was a 28-year-old man who was presented with intractable hiccup for 15 days. It developed suddenly, then aggravated progressively and did not respond to any types of medication. On magnetic resonance images, a well-demarcated and non-enhancing mass with hemorrhagic changes was noted in the left medulla oblongata. Intraoperative findings showed that the lesion was fully embedded within the brain stem and pathology confirmed the diagnosis of cavernous hemangioma. The hiccup resolved completely after the operation. Based on the presumption that the medullary cavernoma may trigger intractable hiccup by displacing or compression the hiccup arc of the dorsolateral medulla, surgical excision can eliminate the symptoms, even in the case totally buried in brainstem.
Adult
;
Brain Stem
;
Diagnosis
;
Hemangioma, Cavernous*
;
Hiccup*
;
Humans
;
Medulla Oblongata*
;
Pathology