CASE REPORT article

Front. Immunol.

Sec. Autoimmune and Autoinflammatory Disorders : Autoimmune Disorders

Volume 16 - 2025 | doi: 10.3389/fimmu.2025.1550551

Multiple aseptic abscesses and pulmonary involvement in a child with Behcet's disease phenotype: a case report

Provisionally accepted
  • 1Children’s Hospital of Nanjing Medical University, Nanjing, China
  • 2Department of Gastroenterology, Children’s Hospital of Nanjing Medical University, nanjing, China

The final, formatted version of the article will be published soon.

Background: Behcet's disease (BD) is a lifelong multi-systemic vasculitis disorder that can affect almost any organ. The frequency of involvement of each organ varies depending on demographic and geographical factors. The commonly affected systems include mucosal, articular, ocular, vascular, neurological, and gastrointestinal. Common gastrointestinal manifestations include mucosal ulcers, hemorrhage, and perforation while other phenotypes are very rare.We describe the case of a 3-year-old boy suffering from BD phenotype with multiple aseptic abscesses (AAs) and interstitial lung disease. Over the past four years since onset, the boy has presented a series of symptoms, including fever, skin necrosis, multiple ulcers in the intestines, multiple aseptic abscesses in the spleen, interstitial lung disease and an isolated abscess in the gastric wall. Through a regimen involving steroids, mercaptopurine, thalidomide endoscopic drainage of the gastric wall abscess, the child's condition has been effectively managed and improved.To our knowledge, this is the first reported case of BD phenotype with a gastric wall abscess treated with endoscopic drainage and steroids. Multiple AAs and interstitial lung disease may be the early signs of a BD phenotype in childhood which can respond effectively to glucocorticoids.

Keywords: Behcet's disease phenotype, Aseptic abscesses, Interstitial Lung Disease, case report, autoimme diseases

Received: 23 Dec 2024; Accepted: 26 May 2025.

Copyright: © 2025 Yan, Zheng, Kong, Guo and Liu. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

* Correspondence: Kunlong Yan, Children’s Hospital of Nanjing Medical University, Nanjing, China

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