Iliadis Alexandros S, Koletsa Triantafyllia, Vounotrypidis Periklis, Fassas Athanasios, Apostolidis Athanasios, Apostolidis Stylianos, Fotiadou Anastasia, Hytiroglou Prodromos
Department of Pathology (Laboratory of General Pathology & Pathological Anatomy), Aristotle University of Thessaloniki, Thessaloniki, GRC.
Department of Pathology, Laboratory of Diagnostic Histopathology, Thessaloniki, GRC.
Cureus. 2024 Nov 6;16(11):e73121. doi: 10.7759/cureus.73121. eCollection 2024 Nov.
The baseline inflammatory microenvironment in various organs of patients, which is shaped by pre-existing conditions and circulating drugs at the time before viral antigen exposure, may affect the severity of coronavirus disease-19 (COVID-19) infection and the nature of its complications. Inflammatory pseudotumor (IPT) of the spleen may represent one such complication that merits further investigation. We describe the case of a patient, who was under long-term treatment with a tumor necrosis factor inhibitor (TNFi), for psoriatic arthritis (PsA) and developed an inflammatory mass in the spleen, accompanied by systemic manifestations. This occurred with a history of four doses of nucleoside-modified messenger RNA (modRNA) vaccination for COVID-19 and shortly after a SARS coronavirus-2 (SARS-CoV-2) infection. Histologic examination of the splenectomy specimen supported by a large array of immunohistochemical stains and subsequent clinicopathological correlation indicated the diagnosis of splenic IPT in an immunologically altered background, due to modifying medication, immunization, and infection. Our case speculates that IPT may represent an adverse event related to immunogenicity of SARS-CoV-2, following antigen exposure (at first by sequential modRNA COVID-19 vaccinations and additionally by natural infection), despite the potentially protective effect of treatment with a TNFi.
患者各器官的基线炎症微环境由病毒抗原暴露前的既有病症和循环中的药物所塑造,可能会影响冠状病毒病19(COVID-19)感染的严重程度及其并发症的性质。脾脏炎性假瘤(IPT)可能就是这样一种值得进一步研究的并发症。我们描述了一例患者,该患者因银屑病关节炎(PsA)长期接受肿瘤坏死因子抑制剂(TNFi)治疗,脾脏出现炎性肿块,并伴有全身症状。这发生在该患者接种四剂用于COVID-19的核苷修饰信使核糖核酸(modRNA)疫苗后,且在感染严重急性呼吸综合征冠状病毒2(SARS-CoV-2)后不久。通过大量免疫组织化学染色支持的脾切除标本组织学检查以及随后的临床病理相关性分析表明,在免疫改变的背景下,由于药物调整、免疫接种和感染,诊断为脾脏IPT。我们的病例推测,尽管TNFi治疗可能具有保护作用,但IPT可能是抗原暴露(首先是通过连续的modRNA COVID-19疫苗接种,其次是通过自然感染)后与SARS-CoV-2免疫原性相关的不良事件。