Aseptic abscess syndrome: a case report of a patient achieving remission with both infliximab originator and biosimilar administered at varied intervals

Aseptic abscesses syndrome is a rare but increasingly recognized disease that falls within the spectrum of autoinflammatory disorders. Here, we describe the case of a patient who presented with abdominal pain and fever, along with multiple abdominal and extra-abdominal abscesses, in the absence of underlying hematologic, autoimmune, infectious, or neoplastic conditions. Initially, the patient responded to glucocorticoids, but experienced several flares upon discontinuation, leading to the initiation of treatment with a TNFα inhibitor. After 5 years, an attempt to discontinue treatment resulted in a new flare of the disease. Remission was eventually achieved with a biosimilar TNFα inhibitor, albeit requiring shortened infusion intervals.

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Publication Details

Journal
Frontiers in Immunology
Published
2024-12-03
DOI
https://doi.org/10.3389/fimmu.2024.1454813
Citations
2
Primary Topic
Autoimmune and Inflammatory Disorders
Type
article
Field-Weighted Citation Impact
0.77
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article

Aseptic abscess syndrome: a case report of a patient achieving remission with both infliximab originator and biosimilar administered at varied intervals

Cristiano Alessandri, Fabrizio Conti, Rossana Scrivo, F. M. Ucci et al.
2 citations
Frontiers in Immunology
Autoimmune and Inflammatory Disorders
0.77
article

Aseptic abscess syndrome: a case report of a patient achieving remission with both infliximab originator and biosimilar administered at varied intervals

Cristiano Alessandri, Fabrizio Conti, Rossana Scrivo, F. M. Ucci, Roberta Priori
article en
2 citations

Abstract

Aseptic abscesses syndrome is a rare but increasingly recognized disease that falls within the spectrum of autoinflammatory disorders. Here, we describe the case of a patient who presented with abdominal pain and fever, along with multiple abdominal and extra-abdominal abscesses, in the absence of underlying hematologic, autoimmune, infectious, or neoplastic conditions. Initially, the patient responded to glucocorticoids, but experienced several flares upon discontinuation, leading to the initiation of treatment with a TNFα inhibitor. After 5 years, an attempt to discontinue treatment resulted in a new flare of the disease. Remission was eventually achieved with a biosimilar TNFα inhibitor, albeit requiring shortened infusion intervals.

Frontiers in ImmunologyVol. 15
Saint Camillus International University of Health and Medical Sciences (IT), Sapienza University of Rome (IT)
Good health and well-being
Openalex Percentile: Top 24%
Autoimmune and Inflammatory Disorders
0.77
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