Cargando…

First Report of Symmetrical Drug-related Intertriginous and Flexural Exanthema (SDRIFE or Baboon Syndrome) After Erenumab Application for Migraine Prevention

INTRODUCTION: Symmetrical drug-related intertriginous and flexural exanthema (SDRIFE), formerly also called baboon syndrome, is characterized by symmetrical erythematous rash with typical localization in the gluteal and intertriginous areas. A type IV delayed hypersensitivity immune response is thou...

Descripción completa

Detalles Bibliográficos
Autores principales: Göbel, Carl H., Heinze, Axel, Karstedt, Sarah, Cirkel, Anna, Münte, Thomas F., Göbel, Hartmut
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Healthcare 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9633906/
https://www.ncbi.nlm.nih.gov/pubmed/35908264
http://dx.doi.org/10.1007/s40122-022-00417-6
_version_ 1784824345886982144
author Göbel, Carl H.
Heinze, Axel
Karstedt, Sarah
Cirkel, Anna
Münte, Thomas F.
Göbel, Hartmut
author_facet Göbel, Carl H.
Heinze, Axel
Karstedt, Sarah
Cirkel, Anna
Münte, Thomas F.
Göbel, Hartmut
author_sort Göbel, Carl H.
collection PubMed
description INTRODUCTION: Symmetrical drug-related intertriginous and flexural exanthema (SDRIFE), formerly also called baboon syndrome, is characterized by symmetrical erythematous rash with typical localization in the gluteal and intertriginous areas. A type IV delayed hypersensitivity immune response is thought to be responsible for its development. CGRP monoclonal antibodies (CGRP mAbs) are a new class of drugs for the prevention of migraine. We present the first case of SDRIFE occurring in temporal relation to the use of erenumab for migraine prevention. CASE: A 48-year-old female patient with migraine received erenumab 140 mg subcutaneously in the thigh area for the prevention of migraine in repetitive cycles, each 1 month apart. Initially, the patient experienced no side effects. After the third cycle, a masseuse incidentally noticed a reddish, circular rash in the buttock area during a back massage. There were no other symptoms. The skin changes resolved spontaneously. Two years later, approximately 40 h after reapplication of erenumab 140 mg, the patient experienced a severe pain in the buttock area centered over the anal crease. The area of pain extended in a circular pattern with approximately 20 cm in diameter. The pain started abruptly and reached a severe intensity within about 30 min. Sitting on the buttocks was no longer possible for the patient. There was marked allodynia and hyperpathia in the entire buttocks region. A flat, broad-based blister-like skin swelling developed in this region. The blisters began opening up on the fourth day after the onset of the skin reaction. In addition, there was a pronounced redness in the entire buttock area. Here, the patient felt a strong burning pain, similar to a scald. RESULTS: The symptoms lasted for a period of 10 days. From this point on, they fully subsided under concomitant therapy with prednisolone. CONCLUSION: SDRIFE as a rare dermatological side effect should be considered in the monitoring of skin lesions during migraine prophylaxis. In view of the high migraine prevalence, knowledge of this uncommon syndrome is important. It is crucial to recognize the relationship between the medication and the circumscribed exanthema occurring distant from the injection site.
format Online
Article
Text
id pubmed-9633906
institution National Center for Biotechnology Information
language English
publishDate 2022
publisher Springer Healthcare
record_format MEDLINE/PubMed
spelling pubmed-96339062022-12-07 First Report of Symmetrical Drug-related Intertriginous and Flexural Exanthema (SDRIFE or Baboon Syndrome) After Erenumab Application for Migraine Prevention Göbel, Carl H. Heinze, Axel Karstedt, Sarah Cirkel, Anna Münte, Thomas F. Göbel, Hartmut Pain Ther Case Report INTRODUCTION: Symmetrical drug-related intertriginous and flexural exanthema (SDRIFE), formerly also called baboon syndrome, is characterized by symmetrical erythematous rash with typical localization in the gluteal and intertriginous areas. A type IV delayed hypersensitivity immune response is thought to be responsible for its development. CGRP monoclonal antibodies (CGRP mAbs) are a new class of drugs for the prevention of migraine. We present the first case of SDRIFE occurring in temporal relation to the use of erenumab for migraine prevention. CASE: A 48-year-old female patient with migraine received erenumab 140 mg subcutaneously in the thigh area for the prevention of migraine in repetitive cycles, each 1 month apart. Initially, the patient experienced no side effects. After the third cycle, a masseuse incidentally noticed a reddish, circular rash in the buttock area during a back massage. There were no other symptoms. The skin changes resolved spontaneously. Two years later, approximately 40 h after reapplication of erenumab 140 mg, the patient experienced a severe pain in the buttock area centered over the anal crease. The area of pain extended in a circular pattern with approximately 20 cm in diameter. The pain started abruptly and reached a severe intensity within about 30 min. Sitting on the buttocks was no longer possible for the patient. There was marked allodynia and hyperpathia in the entire buttocks region. A flat, broad-based blister-like skin swelling developed in this region. The blisters began opening up on the fourth day after the onset of the skin reaction. In addition, there was a pronounced redness in the entire buttock area. Here, the patient felt a strong burning pain, similar to a scald. RESULTS: The symptoms lasted for a period of 10 days. From this point on, they fully subsided under concomitant therapy with prednisolone. CONCLUSION: SDRIFE as a rare dermatological side effect should be considered in the monitoring of skin lesions during migraine prophylaxis. In view of the high migraine prevalence, knowledge of this uncommon syndrome is important. It is crucial to recognize the relationship between the medication and the circumscribed exanthema occurring distant from the injection site. Springer Healthcare 2022-07-31 2022-12 /pmc/articles/PMC9633906/ /pubmed/35908264 http://dx.doi.org/10.1007/s40122-022-00417-6 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by-nc/4.0/Open AccessThis article is licensed under a Creative Commons Attribution-NonCommercial 4.0 International License, which permits any non-commercial use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) .
spellingShingle Case Report
Göbel, Carl H.
Heinze, Axel
Karstedt, Sarah
Cirkel, Anna
Münte, Thomas F.
Göbel, Hartmut
First Report of Symmetrical Drug-related Intertriginous and Flexural Exanthema (SDRIFE or Baboon Syndrome) After Erenumab Application for Migraine Prevention
title First Report of Symmetrical Drug-related Intertriginous and Flexural Exanthema (SDRIFE or Baboon Syndrome) After Erenumab Application for Migraine Prevention
title_full First Report of Symmetrical Drug-related Intertriginous and Flexural Exanthema (SDRIFE or Baboon Syndrome) After Erenumab Application for Migraine Prevention
title_fullStr First Report of Symmetrical Drug-related Intertriginous and Flexural Exanthema (SDRIFE or Baboon Syndrome) After Erenumab Application for Migraine Prevention
title_full_unstemmed First Report of Symmetrical Drug-related Intertriginous and Flexural Exanthema (SDRIFE or Baboon Syndrome) After Erenumab Application for Migraine Prevention
title_short First Report of Symmetrical Drug-related Intertriginous and Flexural Exanthema (SDRIFE or Baboon Syndrome) After Erenumab Application for Migraine Prevention
title_sort first report of symmetrical drug-related intertriginous and flexural exanthema (sdrife or baboon syndrome) after erenumab application for migraine prevention
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9633906/
https://www.ncbi.nlm.nih.gov/pubmed/35908264
http://dx.doi.org/10.1007/s40122-022-00417-6
work_keys_str_mv AT gobelcarlh firstreportofsymmetricaldrugrelatedintertriginousandflexuralexanthemasdrifeorbaboonsyndromeaftererenumabapplicationformigraineprevention
AT heinzeaxel firstreportofsymmetricaldrugrelatedintertriginousandflexuralexanthemasdrifeorbaboonsyndromeaftererenumabapplicationformigraineprevention
AT karstedtsarah firstreportofsymmetricaldrugrelatedintertriginousandflexuralexanthemasdrifeorbaboonsyndromeaftererenumabapplicationformigraineprevention
AT cirkelanna firstreportofsymmetricaldrugrelatedintertriginousandflexuralexanthemasdrifeorbaboonsyndromeaftererenumabapplicationformigraineprevention
AT muntethomasf firstreportofsymmetricaldrugrelatedintertriginousandflexuralexanthemasdrifeorbaboonsyndromeaftererenumabapplicationformigraineprevention
AT gobelhartmut firstreportofsymmetricaldrugrelatedintertriginousandflexuralexanthemasdrifeorbaboonsyndromeaftererenumabapplicationformigraineprevention