Cargando…

Drug-Associated Eosinophilic Fasciitis: A Case of Eosinophilic Fasciitis Secondary to Cemiplimab Therapy

Patient: Female, 72-year-old Final Diagnosis: Drug induced eosinophilic fasciitis Symptoms: Joint pain • skin discoloration and induration Medication: — Clinical Procedure: Skin biopsy Specialty: Rheumatology OBJECTIVE: Rare disease BACKGROUND: Eosinophilic fasciitis, also known as Shulman syndrome,...

Descripción completa

Detalles Bibliográficos
Autores principales: Boppana, Sri Harsha, Dulla, Nageswara Rao, Beutler, Bryce D., Gullapalli, Nageshwara, Kaur, Ratinder
Formato: Online Artículo Texto
Lenguaje:English
Publicado: International Scientific Literature, Inc. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8380854/
https://www.ncbi.nlm.nih.gov/pubmed/34403405
http://dx.doi.org/10.12659/AJCR.932888
_version_ 1783741255575928832
author Boppana, Sri Harsha
Dulla, Nageswara Rao
Beutler, Bryce D.
Gullapalli, Nageshwara
Kaur, Ratinder
author_facet Boppana, Sri Harsha
Dulla, Nageswara Rao
Beutler, Bryce D.
Gullapalli, Nageshwara
Kaur, Ratinder
author_sort Boppana, Sri Harsha
collection PubMed
description Patient: Female, 72-year-old Final Diagnosis: Drug induced eosinophilic fasciitis Symptoms: Joint pain • skin discoloration and induration Medication: — Clinical Procedure: Skin biopsy Specialty: Rheumatology OBJECTIVE: Rare disease BACKGROUND: Eosinophilic fasciitis, also known as Shulman syndrome, is a rare inflammatory condition characterized by diffuse erythema and progressive collagenous thickening of the subcutaneous fascia. The underlying cause remains to be definitively established; however, several drugs have been linked to this uncommon clinical entity. We present a rare case of eosinophilic fasciitis secondary to immune checkpoint inhibitor therapy. CASE REPORT: A 72-year-old woman with metastatic cutaneous squamous cell carcinoma presented to the rheumatology clinic for evaluation of joint pain that developed 3 weeks after beginning treatment with cemiplimab. The correlation of clinical history and physical examination was most consistent with osteoarthritis. Symptoms improved after a short course of low-dose prednisone. The patient continued cemiplimab therapy for approximately 1 year and was subsequently transitioned to carboplatin and radiation therapy. However, relapse occurred shortly thereafter, and cemiplimab was restarted. Two weeks later, the patient developed severe joint pain, morning stiffness, and extensive cutaneous discoloration and induration. A skin biopsy was performed. Microscopic examination of a tissue sample showed a mononuclear infiltrate with plasma cells and eosinophils. A diagnosis of eosinophilic fasciitis was established. Cemiplimab was held and the patient was treated with hydroxychloroquine, prednisone, and sulfasalazine. Symptoms improved within 1 week. CONCLUSIONS: Eosinophilic fasciitis is a rare but important adverse effect of immune checkpoint inhibitors. Individuals receiving immunotherapy should be monitored closely for symptoms of eosinophilic fasciitis, as prompt treatment is essential to prevent long-term complications.
format Online
Article
Text
id pubmed-8380854
institution National Center for Biotechnology Information
language English
publishDate 2021
publisher International Scientific Literature, Inc.
record_format MEDLINE/PubMed
spelling pubmed-83808542021-09-01 Drug-Associated Eosinophilic Fasciitis: A Case of Eosinophilic Fasciitis Secondary to Cemiplimab Therapy Boppana, Sri Harsha Dulla, Nageswara Rao Beutler, Bryce D. Gullapalli, Nageshwara Kaur, Ratinder Am J Case Rep Articles Patient: Female, 72-year-old Final Diagnosis: Drug induced eosinophilic fasciitis Symptoms: Joint pain • skin discoloration and induration Medication: — Clinical Procedure: Skin biopsy Specialty: Rheumatology OBJECTIVE: Rare disease BACKGROUND: Eosinophilic fasciitis, also known as Shulman syndrome, is a rare inflammatory condition characterized by diffuse erythema and progressive collagenous thickening of the subcutaneous fascia. The underlying cause remains to be definitively established; however, several drugs have been linked to this uncommon clinical entity. We present a rare case of eosinophilic fasciitis secondary to immune checkpoint inhibitor therapy. CASE REPORT: A 72-year-old woman with metastatic cutaneous squamous cell carcinoma presented to the rheumatology clinic for evaluation of joint pain that developed 3 weeks after beginning treatment with cemiplimab. The correlation of clinical history and physical examination was most consistent with osteoarthritis. Symptoms improved after a short course of low-dose prednisone. The patient continued cemiplimab therapy for approximately 1 year and was subsequently transitioned to carboplatin and radiation therapy. However, relapse occurred shortly thereafter, and cemiplimab was restarted. Two weeks later, the patient developed severe joint pain, morning stiffness, and extensive cutaneous discoloration and induration. A skin biopsy was performed. Microscopic examination of a tissue sample showed a mononuclear infiltrate with plasma cells and eosinophils. A diagnosis of eosinophilic fasciitis was established. Cemiplimab was held and the patient was treated with hydroxychloroquine, prednisone, and sulfasalazine. Symptoms improved within 1 week. CONCLUSIONS: Eosinophilic fasciitis is a rare but important adverse effect of immune checkpoint inhibitors. Individuals receiving immunotherapy should be monitored closely for symptoms of eosinophilic fasciitis, as prompt treatment is essential to prevent long-term complications. International Scientific Literature, Inc. 2021-08-17 /pmc/articles/PMC8380854/ /pubmed/34403405 http://dx.doi.org/10.12659/AJCR.932888 Text en © Am J Case Rep, 2021 https://creativecommons.org/licenses/by-nc-nd/4.0/This work is licensed under Creative Common Attribution-NonCommercial-NoDerivatives 4.0 International (CC BY-NC-ND 4.0 (https://creativecommons.org/licenses/by-nc-nd/4.0/) )
spellingShingle Articles
Boppana, Sri Harsha
Dulla, Nageswara Rao
Beutler, Bryce D.
Gullapalli, Nageshwara
Kaur, Ratinder
Drug-Associated Eosinophilic Fasciitis: A Case of Eosinophilic Fasciitis Secondary to Cemiplimab Therapy
title Drug-Associated Eosinophilic Fasciitis: A Case of Eosinophilic Fasciitis Secondary to Cemiplimab Therapy
title_full Drug-Associated Eosinophilic Fasciitis: A Case of Eosinophilic Fasciitis Secondary to Cemiplimab Therapy
title_fullStr Drug-Associated Eosinophilic Fasciitis: A Case of Eosinophilic Fasciitis Secondary to Cemiplimab Therapy
title_full_unstemmed Drug-Associated Eosinophilic Fasciitis: A Case of Eosinophilic Fasciitis Secondary to Cemiplimab Therapy
title_short Drug-Associated Eosinophilic Fasciitis: A Case of Eosinophilic Fasciitis Secondary to Cemiplimab Therapy
title_sort drug-associated eosinophilic fasciitis: a case of eosinophilic fasciitis secondary to cemiplimab therapy
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8380854/
https://www.ncbi.nlm.nih.gov/pubmed/34403405
http://dx.doi.org/10.12659/AJCR.932888
work_keys_str_mv AT boppanasriharsha drugassociatedeosinophilicfasciitisacaseofeosinophilicfasciitissecondarytocemiplimabtherapy
AT dullanageswararao drugassociatedeosinophilicfasciitisacaseofeosinophilicfasciitissecondarytocemiplimabtherapy
AT beutlerbryced drugassociatedeosinophilicfasciitisacaseofeosinophilicfasciitissecondarytocemiplimabtherapy
AT gullapallinageshwara drugassociatedeosinophilicfasciitisacaseofeosinophilicfasciitissecondarytocemiplimabtherapy
AT kaurratinder drugassociatedeosinophilicfasciitisacaseofeosinophilicfasciitissecondarytocemiplimabtherapy