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著者: Parker CM, Hanke CW, Madura JA, Liss EC.
雑誌名: J Dermatol Surg Oncol. 1984 Nov;10(11):884-9. doi: 10.1111/j.1524-4725.1984.tb01341.x.
Abstract/Text
The glucagonoma syndrome is characterized by dermatitis, glucose intolerance, hypoaminoacidemia, and hyperglucagonemia secondary to an alpha-cell tumor of the pancreas. Other clinical features include anemia, glossitis, and weight loss. A 62-year-old woman with the syndrome sought medical attention for a chronic dermatitis. A skin biopsy was suggestive of necrolytic migratory erythema. A glucagonoma was surgically removed from the tail of the pancreas. Review of the literature indicates that 56 proven and 33 probable cases of glucagonoma syndrome have been reported.
PMID 6092443 J Dermatol Surg Oncol. 1984 Nov;10(11):884-9. doi: 10.1111/j.1524-4725.1984.tb01341.x.
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