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A case of delayed diagnosis of Necrolytic Migratory Erythema
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  • wissal abdelli,
  • Fatima Alaoui,
  • Asmahene Souissi,
  • Wiem Sassi,
  • Ines Chelly,
  • Slim Haouet,
  • Mourad Mokni
wissal abdelli
Rabta Hospital

Corresponding Author:[email protected]

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Fatima Alaoui
Rabta Hospital
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Asmahene Souissi
Rabta Hospital
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Wiem Sassi
Rabta Hospital
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Ines Chelly
Rabta Hospital
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Slim Haouet
Rabta Hospital
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Mourad Mokni
Rabta Hospital
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Abstract

Necrolytic Migratory Erythema (NME) is a rare cutaneous paraneoplastic manifestation of glucagonoma. We report a case of a woman with a 6-year history of delayed diagnosis of Glucagonoma. This case highlights the atypical clinical features of NME which makes the diagnosis difficult.

Peer review status:Published

28 Jun 2021Submitted to Clinical Case Reports
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23 Jul 2021Submission Checks Completed
23 Jul 2021Assigned to Editor
04 Aug 2021Reviewer(s) Assigned
15 Sep 2021Review(s) Completed, Editorial Evaluation Pending
24 Sep 2021Editorial Decision: Revise Minor
14 Nov 20211st Revision Received
20 Nov 2021Submission Checks Completed
20 Nov 2021Assigned to Editor
20 Nov 2021Review(s) Completed, Editorial Evaluation Pending
23 Nov 2021Editorial Decision: Accept
Dec 2021Published in Clinical Case Reports volume 9 issue 12. 10.1002/ccr3.5179