Jaradat Jaber H, Walid Wadi, Obeidat Aram F, Amro Raghad, Nashwan Abdulqadir J
Faculty of Medicine Mutah University Al Karak Jordan.
Department of Internal Medicine Al-Karak Governorate Hospital Al-Karak Jordan.
Clin Case Rep. 2025 Jan 30;13(2):e70107. doi: 10.1002/ccr3.70107. eCollection 2025 Feb.
Idiopathic digital infarction (IDI), a rare subset of digital infarction, is characterized by ischemic changes in the absence of identifiable underlying etiology. We present the first documented case of IDI in a 47-year-old female with insignificant medical history. Clinical evaluation revealed bluish discoloration of the left lateral three fingers. Negative findings on autoimmune serologies, echocardiogram, and coagulation profiles excluded common causes, such as vasculitis, cardiac embolism, and hypercoagulable states. Imaging studies demonstrated ischemic changes in the left cerebellar hemisphere and proximal left subclavian artery, which supported the diagnosis of acute infarction. The patient was managed conservatively and was discharged. This case underscores the diagnostic complexities of IDI and highlights the importance of thorough evaluation and management.
特发性指端梗死(IDI)是指端梗死的一种罕见类型,其特征是在没有可识别的潜在病因的情况下出现缺血性改变。我们报告首例有记录的IDI病例,患者为一名47岁女性,既往病史无特殊。临床评估发现左侧外侧三个手指呈蓝色变色。自身免疫血清学、超声心动图和凝血指标检查结果均为阴性,排除了血管炎、心脏栓塞和高凝状态等常见病因。影像学检查显示左侧小脑半球和左锁骨下动脉近端有缺血性改变,支持急性梗死的诊断。患者接受保守治疗后出院。该病例强调了IDI的诊断复杂性,并突出了全面评估和管理的重要性。