Toda Kazuya, Kuroda Kaku, Kuroda Moe, Kawai Kota, Sato Yukihiro
Kamiichi Community Medical Support Unit Toyama University Toyama Japan.
Division of Geriatrics & Aging, Department of Medicine University of Rochester Rochester New York USA.
J Gen Fam Med. 2025 Apr 29;26(5):479-484. doi: 10.1002/jgf2.70027. eCollection 2025 Sep.
Idiosyncratic drug-induced agranulocytosis is a rare but life-threatening condition that requires immediate medical intervention. Although sulbactam/ampicillin (SBT/ABPC) is a widely used antibiotic, no prior case reports of its associated agranulocytosis were identified in our narrative literature review. We present a case of an 85-year-old man who developed agranulocytosis following SBT/ABPC treatment for pressure ulcer infection and aspiration pneumonia, accompanied by a narrative literature review. Awareness of this condition, prompt discontinuation of the suspected agent, and close monitoring of total white blood cell counts are essential for early detection and management of this life-threatening complication.
特异质性药物性粒细胞缺乏症是一种罕见但危及生命的疾病,需要立即进行医学干预。虽然舒巴坦/氨苄西林(SBT/ABPC)是一种广泛使用的抗生素,但在我们的叙述性文献综述中未发现先前有其相关粒细胞缺乏症的病例报告。我们报告一例85岁男性病例,该患者在接受SBT/ABPC治疗压疮感染和吸入性肺炎后发生粒细胞缺乏症,并伴有叙述性文献综述。认识到这种情况、及时停用可疑药物以及密切监测白细胞总数对于早期发现和处理这种危及生命的并发症至关重要。