Fujishima Yuko, Hataya Yuji, Fujimoto Kanta, Iwakura Toshio, Matsuoka Naoki
Department of Diabetes and Endocrinology, Kobe City Medical Center General Hospital, Kobe 650-0047, Japan.
Oxf Med Case Reports. 2025 Aug 11;2025(8):omaf129. doi: 10.1093/omcr/omaf129. eCollection 2025 Aug.
Adrenal infarction (AI) is rare condition caused by inadequate blood supply to the adrenal glands, with few reports of its association with essential thrombocythemia (ET). Here, we report a case of bilateral AI as an initial thrombotic complication in a patient with ET. A 69-year-old man presented with right abdominal pain. Abdominal computed tomography (CT) showed diffuse enlargement and poor enhancement of bilateral adrenal glands. He was diagnosed with bilateral AI. Based on positive screening for thrombocytosis and the Janus kinase 2 V617F mutation, he was diagnosed with ET. After low-dose aspirin therapy, he showed no symptom recurrence. The cortisol response in the adrenocorticotropic hormone stimulation test decreased at onset but improved after three months. Furthermore, abdominal CT revealed improvement in bilateral adrenal enlargement and enhancement. In patients presenting with AI, ET should be considered as a potential underlying disease, and early diagnosis and treatment is important to prevent recurrence.
肾上腺梗死(AI)是一种因肾上腺血液供应不足引起的罕见病症,关于其与原发性血小板增多症(ET)关联的报道较少。在此,我们报告一例双侧AI作为ET患者初始血栓形成并发症的病例。一名69岁男性因右腹痛就诊。腹部计算机断层扫描(CT)显示双侧肾上腺弥漫性肿大且强化不佳。他被诊断为双侧AI。基于血小板增多症筛查阳性及Janus激酶2 V617F突变,他被诊断为ET。低剂量阿司匹林治疗后,他未再出现症状复发。促肾上腺皮质激素刺激试验中的皮质醇反应在发病时降低,但三个月后有所改善。此外,腹部CT显示双侧肾上腺肿大及强化情况有所改善。对于出现AI的患者,应考虑ET作为潜在的基础疾病,早期诊断和治疗对于预防复发很重要。