Immune Reconstitution Inflammatory Syndrome Associated with Hepatosplenic Candidiasis in a Patient with Acute Myeloblastic Leukemia: Possible Pathogenesis and Treatment in the Light of Current Knowledge

Z. Bıçakcı, D. Koca, G Bozbeyoglu
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Abstract

Acquired immune deficiencies caused by different etiologies, promote invasive fungal infections. When this immunity begins to improve, it can induce an excessive inflammatory response defined as Immune Reconstitution Inflammatory Syndrome (IRIS). Hepatosplenic Candidiasis (HSC) can be considered a form of IRIS syndrome as it occurs following neutrophil recovery in patients treated for acute leukemia. Differentiating IRIS from a single fungal infection or treatment failure due to a similar clinical picture is a real diagnostic problem. Misdiagnosis and subsequently ineffective treatment with antifungal therapy instead of anti-inflammatory drugs, may lead fatal course of the disease. A deep and prolonged neutropenia developed after the first induction chemotherapy in our two and a half-year-old male patient who was followed up in our clinic with the diagnosis of Acute Myeloblastic Leukemia (AML). Our patient had fever, abdominal pain as well as his Gamma Glutamyl Transferase (GGT) and Alkaline Phosphatase (ALP) levels increased during neutropenia recovery. He was diagnosed with hepatosplenic candidiasis, by observing ‘target like abscesses’ on dynamic Magnetic Resonance Imaging (MRI) taken for his newly developing symptoms and laboratory findings while recovering neutropenia. After his first and third induction chemotherapy courses, his fever persisted although antifungal therapy, steroid treatment was initiated considering IRIS. After his re-intensification course, because of the same flare-up symptoms, we started immunglobulin in addition to steroid. With methylprednisolone and intravenous immunoglobulin, his symptoms improved and significant regression was observed in the lesions ‘target-like abscesses’ on MRI and in the laboratory values. Result: IRIS should be considered for patients with hepatic candidiasis whose have persistent fever despite appropriate antifungal therapy. Glucocorticoid should be started first for an anti-inflammatory effect.
急性髓母细胞白血病患者肝脾念珠菌病相关的免疫重建炎症综合征:根据目前的知识,可能的发病机制和治疗
不同病因引起的获得性免疫缺陷,促进侵袭性真菌感染。当这种免疫开始改善时,它可以诱导过度的炎症反应,定义为免疫重建炎症综合征(IRIS)。肝脾念珠菌病(HSC)可被认为是IRIS综合征的一种形式,因为它发生在急性白血病治疗患者中性粒细胞恢复后。鉴别IRIS与单一真菌感染或治疗失败,由于类似的临床表现是一个真正的诊断问题。误诊和随后用抗真菌治疗代替抗炎药物治疗无效,可能导致疾病的致命过程。我们的两岁半的男性患者在第一次诱导化疗后出现了深度和长期的中性粒细胞减少症,他被诊断为急性髓母细胞白血病(AML)。我们的病人有发烧,腹痛,并且他的γ -谷氨酰转移酶(GGT)和碱性磷酸酶(ALP)水平在中性粒细胞减少恢复期间升高。他被诊断为肝脾念珠菌病,在动态磁共振成像(MRI)上观察到“靶样脓肿”,这是他在恢复中性粒细胞减少症时新出现的症状和实验室结果。在他的第一次和第三次诱导化疗疗程后,他的发烧持续,尽管抗真菌治疗,类固醇治疗考虑IRIS开始。在他的再次强化治疗后,由于同样的突发症状,我们开始使用免疫球蛋白和类固醇。使用甲基强的松龙和静脉注射免疫球蛋白后,他的症状得到改善,MRI和实验室值显示病灶“靶样脓肿”明显消退。结果:肝念珠菌病患者经适当抗真菌治疗后仍持续发热,应考虑IRIS。首先应使用糖皮质激素,以发挥抗炎作用。
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