Autonomic and sensory ganglionopathy occurring in a patient with fulminant type 1 diabetes mellitus |
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| Authors: | Mutsuki Makino Dai Hiwatashi Kesami Minemura Kenji Kawaguchi |
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| Affiliation: | 1. Department of Diagnostic Pathology, Shinonoi General Hospital, Nagano, Japan;2. Department of Endocrinology, Shinonoi General Hospital, Nagano, Japan |
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| Abstract: | A 63‐year‐old male with a previous infection was admitted to our hospital because of acute pancreatitis. Although he had no history of diabetes mellitus, laboratory examinations revealed marked hyperglycemia on admission, and intensive insulin treatment was required. After 2 weeks, he developed severe pandysautonomia and sensory impairment, and eventually died from colonic perforation caused by paralytic ileus at 1 year after onset. Autopsy findings showed a complete loss of pancreatic islet beta cells with mild fibrosis of the exocrine pancreas. Neuropathological examination showed myelin loss of the dorsal fasciculus at all levels of the spinal cord and ganglionopathy of the dorsal root and sympathetic truncus, revealing degeneration of ganglion cells and a decrease in their number with the formation of Nageotte nodules. On the basis of this clinicopathological evidence, fulminant type 1 diabetes mellitus (T1DM) and idiopathic immune‐mediated autonomic neuropathy were suspected. Here, we suggest a close etiological relationship between both diseases. |
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| Keywords: | fulminant type 1 diabetes mellitus ganglionopathy immune‐mediated autonomic neuropathy pandysautonomia |
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