Area postrema syndrome as the only sign of medullary infarction adjacent to area postrema [PDF]
Area postrema syndrome (APS) is characterized by acute or subacute intractable nausea, vomiting, and/or hiccups lasting for at least 48 h. These symptoms can occur individually or in combination and are typically linked to periventricular brainstem ...
Patrick Stancu +5 more
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Neurenteric Cyst of the Area Postrema [PDF]
Neurenteric cysts are CNS lesions most frequently occurring in the spinal cord. Intracranial neurenteric cysts are rarer, typically presenting with headache, mass effect, or location-specific symptoms.
Claire M. Miller +4 more
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Seronegative Autoimmune Encephalomyelitis with Area Postrema Symptoms [PDF]
Introduction: Patients presenting with encephalopathy and longitudinally extensive myelitis pose a significant diagnostic challenge. Area postrema-related symptoms, such as intractable hiccoughs, can aid in narrowing the differential diagnosis.
David Andrew Prentice +4 more
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Neural stem cell self-renewal stimulation by store-operated calcium entries in adult mouse area postrema: influence of leptin [PDF]
Neural stem cells (NSCs) persist in specific brain germinative niches and sustain neurogenesis throughout life in adult mammals. In addition to the two major stem cell niches in the subventricular zone and the hippocampal dentate gyrus, the area postrema
Cyrine Ben Dhaou +8 more
doaj +3 more sources
Neuromyelitis optica spectrum disorder with AQP4‐IgG presenting as area postrema syndrome and progressing to myelitis: A rare case report [PDF]
Key Clinical Message Neuromyelitis optica spectrum disorders can less commonly present with area postrema syndrome progressing to myelitis. Management involves intravenous glucocorticoids, plasma exchange, and preventive immunotherapy.
Preethi Jagannath +6 more
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The distinction of area postrema syndrome between MOGAD and NMOSD [PDF]
Background and objectives: Both myelin oligodendrocyte glycoprotein-IgG associated disorders (MOGAD) and neuromyelitis optica spectrum disorder (NMOSD) are demyelinating diseases of the central nervous system. They present similar clinical manifestations
Ying Chen +5 more
doaj +2 more sources
Autoimmune glial fibrillary acidic protein astrocytopathy presented as isolated area postrema symdrome: a case report [PDF]
Background Area postrema syndrome (APS) as the isolated manifestation in autoimmune glial fibrillary acidic protein (GFAP) astrocytopathy has been rarely reported. Case presentation A 61-year-old male patient presented with intractable hiccup.
Jing Dang, Shengsuo Lei, Jihua Chen
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Area postrema syndrome with linear enhancement along the surface of the brainstem and fourth ventricle in autoimmune GFAP astrocytopathy [PDF]
Background Glial fibrillary acidic protein (GFAP) astrocytopathy, a novel autoimmune disease of the nervous system, was first defined in 2016. To our knowledge, area postrema syndrome (APS) with linear enhancement along the surface of the brainstem and ...
Xinming Liang, Yaoyao Shen
doaj +2 more sources
Sustained microglial activation in the area postrema of collagen-induced arthritis mice [PDF]
Background Central nervous system (CNS)-mediated symptoms, such as fatigue, depression, and hyperalgesia, are common complications among patients with rheumatoid arthritis (RA).
Takayuki Matsushita +5 more
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Area postrema neurons mediate interleukin-6 function in cancer cachexia [PDF]
Interleukin-6 (IL-6) has been long considered a key player in cancer cachexia. It is believed that sustained elevation of IL-6 production during cancer progression causes brain dysfunctions, which ultimately result in cachexia. However, how peripheral IL-
Qingtao Sun +9 more
doaj +2 more sources

