Abstract
Autoimmune autonomic ganglionopathy (AAG) is a disorder defined by antibodies to the nicotinic acetylcholine receptor of the autonomic ganglia. We report two patients with chronically progressing dysautonomia with Sjögren's syndrome (SS). The first case showed elevated titer of ganglionic acetylcholine receptor (AChR) antibody and improved with oral intake of prednisolone. In contrast, the second case showed no elevation of ganglionic AChR antibody titer and had poor response to immunomodulatory therapy. These two cases indicate that chronic AAG may be treatable by immunomodulatory therapy, and have relevance to SS.
MeSH terms
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Aged
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Antibodies, Antinuclear / blood
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Antibodies, Antinuclear / immunology
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Autoantibodies / blood
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Autoantibodies / immunology*
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Autoantigens / immunology*
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Autoimmune Diseases of the Nervous System / diagnosis
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Autoimmune Diseases of the Nervous System / etiology
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Autoimmune Diseases of the Nervous System / immunology*
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Autoimmune Diseases of the Nervous System / therapy
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Diagnosis, Differential
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Female
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Ganglia, Autonomic / immunology*
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Humans
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Immunosuppressive Agents / therapeutic use
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Male
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Prednisolone / therapeutic use
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Primary Dysautonomias / diagnosis
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Primary Dysautonomias / etiology
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Primary Dysautonomias / immunology*
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Primary Dysautonomias / therapy
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Pupil Disorders / etiology
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Pure Autonomic Failure / diagnosis
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Receptors, Nicotinic / immunology*
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Ribonucleoproteins / immunology
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SS-B Antigen
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Shy-Drager Syndrome / etiology
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Sjogren's Syndrome / complications*
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Sjogren's Syndrome / diagnosis
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Sjogren's Syndrome / immunology
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Urination Disorders / etiology
Substances
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Antibodies, Antinuclear
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Autoantibodies
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Autoantigens
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Immunosuppressive Agents
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Receptors, Nicotinic
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Ribonucleoproteins
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SS-A antibodies
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SS-A antigen
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SS-B antibodies
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nicotinic receptor subunit alpha3
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Prednisolone