Anatomic Pathology Unit, Hospital of Macerata, Macerata, Italy.
Private practice, Milan, Italy.
Australas J Dermatol. 2020 Nov;61(4):e403-e405. doi: 10.1111/ajd.13323. Epub 2020 May 8.
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.
本文描述了一例无共存胰高血糖素瘤的假性胰高血糖素瘤综合征病例，即坏死性游走性红斑。患者为 59 岁男性，臀部的皮炎时好时坏，表现为弧形红斑性丘疹鳞屑性病变，伴有微脓疱。组织病理学特征为坏死性游走性红斑，但未发现其他潜在疾病。简要回顾了文献中描述的其他假性胰高血糖素瘤综合征病例。
