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Pseudoglucagonoma syndrome: Description of an 'Idiopatic' case
Gerardo Ferrara1, Irene Ingordo2, Vito Ingordo3
1Anatomic Pathology Unit, Hospital of Macerata, Macerata, Italy.
Abstract:
A case of pseudoglucagonoma syndrome, that is necrolytic migratory erythema, in a patient with no coexistent glucagonoma, is described. The patient was a 59-year-old man with waxing and waning dermatitis of the buttocks, characterised by arciform erythematous papulo-squamous lesions with micro-pustulation. Histopathology was characteristic for necrolytic migratory erythema, but no other underlying disease was detected. Other cases of pseudoglucagonoma syndrome described in literature are briefly reviewed.
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