From the College of Medicine (Al Saud, AlRomaizan), Alfaisal University, and from the Department of Family Medicine and Polyclinic (Alkhunizan), King Faisal Specialist Hospital and Research Centre, Riyadh, Kingdom of Saudi Arabia.
Saudi Med J. 2024 Aug;45(8):848-850. doi: 10.15537/smj.2024.45.8.20231003.
Immune thrombocytopenia (ITP) is an autoimmune disorder marked by low platelet counts that puts patients at risk for spontaneous bleeding. A rare trigger for ITP is iron repletion, which has only been reported in a few cases. In this article, we present a unique case of a 54-year-old male with a history of recurrent ITP who experienced rapid thrombocytopenia following iron repletion with ferrous gluconate. Discontinuation of ferrous medications resulted in platelet counts returning to the normal baseline. Following more than 30 years of the patient's clinical timeline, this case demonstrates the chronic nature of ITP and the complexity of its causes. Further studies are needed to determine the prevalence of iron repletion-induced thrombocytopenia and its underlying mechanisms.
免疫性血小板减少症 (ITP) 是一种自身免疫性疾病,其特征是血小板计数低,使患者有自发性出血的风险。ITP 的一个罕见诱因是铁补充,这种情况仅在少数情况下有报道。本文介绍了一例独特的病例,一名 54 岁男性,既往有反复发作的 ITP 病史,在服用葡萄糖酸亚铁补充铁后迅速出现血小板减少。停用铁剂后,血小板计数恢复到正常基线。在患者的临床病程超过 30 年后,该病例表明了 ITP 的慢性性质及其病因的复杂性。需要进一步研究来确定铁补充诱导的血小板减少症的患病率及其潜在机制。