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Pseudoglucagonoma syndrome: Description of an ‘Idiopatic’ case
Author(s) -
Ferrara Gerardo,
Ingordo Irene,
Ingordo Vito
Publication year - 2020
Publication title -
australasian journal of dermatology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.67
H-Index - 53
eISSN - 1440-0960
pISSN - 0004-8380
DOI - 10.1111/ajd.13323
Subject(s) - medicine , buttocks , erythema , histopathology , dermatology , pathology , surgery
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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