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甲氧苄啶-磺胺甲恶唑继发的突发严重血小板减少症

Sudden-Onset Severe Thrombocytopenia Secondary to Trimethoprim-Sulfamethoxazole.

作者信息

Spadafora Jonathan, Spadafora Philip, Spadafora James, Starcke Jonathan, Spadafora Philip F

机构信息

College of Osteopathic Medicine, New York Institute of Technology, Old Westbury, USA.

Internal Medicine, NYU Langone Hospital - Long Island, Mineola, USA.

出版信息

Cureus. 2025 Sep 8;17(9):e91830. doi: 10.7759/cureus.91830. eCollection 2025 Sep.

Abstract

Drug-induced immune thrombocytopenia (DITP) is a rare but life-threatening condition characterized by a sudden and serious drop in the number of platelets from drug-dependent antibodies against platelet glycoproteins. We report the case of a 57-year-old man who developed severe thrombocytopenia and mucocutaneous bleeding following a short course of trimethoprim-sulfamethoxazole (TMP-SMX) for presumed tick-borne disease. The patient experienced bleeding gums, pinpoint rashes, bruising, and extreme fatigue. The laboratory tests indicated a severely low platelet count of 1 × 1.0 × 10³/µL combined with a high immature platelet fraction (IPF). Workup for both infection and autoimmune disorders would be negative, along with the absence of intracranial hemorrhage demonstrated on imaging. The timeline and clinical picture suggested that TMP-SMX was the most likely culprit. The patient was placed on supportive care, including platelet transfusion and re-start of doxycycline after discontinuation of the drug. His platelet count began to rise, and his symptoms improved; he was discharged without issues. By presenting this instance, we place high importance on early recognition and immediate withdrawal of the offending agent to prevent life-threatening bleeding. Though confirmatory testing of antibodies is available, clinical diagnosis remains the gold standard due to delays in testing and availability.

摘要

药物性免疫性血小板减少症(DITP)是一种罕见但危及生命的疾病,其特征是针对血小板糖蛋白的药物依赖性抗体导致血小板数量突然严重下降。我们报告了一例57岁男性的病例,该患者因假定的蜱传疾病接受了短疗程的甲氧苄啶-磺胺甲恶唑(TMP-SMX)治疗后,出现了严重的血小板减少和皮肤黏膜出血。患者出现牙龈出血、瘀点皮疹、瘀伤和极度疲劳。实验室检查显示血小板计数严重偏低,为1×1.0×1³/µL,同时未成熟血小板分数(IPF)升高。感染和自身免疫性疾病的检查结果均为阴性,影像学检查也未发现颅内出血。时间线和临床表现表明,TMP-SMX最有可能是罪魁祸首。患者接受了支持性治疗,包括血小板输注,并在停药后重新开始使用强力霉素。他的血小板计数开始上升,症状也有所改善;他顺利出院。通过展示这个病例,我们高度重视早期识别和立即停用致病药物,以防止危及生命的出血。尽管可以进行抗体的确诊检测,但由于检测延迟和可及性问题,临床诊断仍然是金标准。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f943/12416223/b807f9369835/cureus-0017-00000091830-i01.jpg

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