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Case Report: Non-haemorrhagic bilateral adrenal infarction in a patient with antiphospholipid syndrome along with lupus myocarditis

机译:病例报告:抗磷脂综合征伴狼疮性心肌炎的患者非出血性双侧肾上腺梗死

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摘要

A 40-year-old woman with antiphospholipid syndrome presented with a 5-day history of right upper quadrant (RUQ) pain, radiating posteriorly, associated with fever and vomiting. She was admitted 1-week prior with an upper respiratory infection and erythema multiforme. Clinical assessment revealed sepsis with RUQ tenderness and positive Murphy's sign. Laboratory results showed raised inflammatory markers, along with renal and liver impairment. CT showed bilateral adrenal infarction and inferior vena cava thrombus. The patient was managed for sepsis and started on heparin. Further immunological investigations revealed a diagnosis of systemic lupus erythematous, an exacerbation of which culminated in lupus myocarditis. This case illustrates the importance of promptly recognising adrenal insufficiency in patients with antiphospholipid syndrome and the possible causative agents, which require careful consideration and exclusion to prevent further thrombotic events. It also highlights the importance of undertaking imaging, namely CT, in patients with antiphospholipid syndrome presenting with abdominal pain as well as considering concomitant autoimmune conditions.
机译:一名患有抗磷脂综合征的40岁女性,有右上腹(RUQ)疼痛的5天病史,向后放射,伴有发烧和呕吐。她在上呼吸道感染和多形性红斑发作前1周入院。临床评估显示败血症伴RUQ压痛和墨菲征阳性。实验室结果显示,炎性标志物升高,同时肾和肝功能受损。 CT显示双侧肾上腺梗塞和下腔静脉血栓。该患者接受了败血症治疗并开始使用肝素。进一步的免疫学调查显示,诊断为系统性红斑狼疮,其恶化最终导致狼疮心肌炎。该病例说明了迅速认识抗磷脂综合征患者肾上腺功能不全的重要性以及可能的病原体,这需要仔细考虑并排除以防止进一步的血栓形成事件。它还强调了在出现腹部疼痛的抗磷脂综合症患者中进行成像(即CT)的重要性,并考虑了伴随的自身免疫性疾病。

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