一种罕见的腹痛原因。

E M Dauchy, M Modica, N Masri
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引用次数: 0

摘要

病例:一名54岁女性甲状腺功能减退,在就诊前一周开始出现急性右侧疼痛。她最初被告知她患有尿路感染,治疗导致症状轻微改善。疼痛又回来了,她去了另一家急诊室;医生告诉他疼痛是由于便秘。第二天疼痛加重,患者再次去急诊科检查,WBC 19000 /uL, BUN/Cr 28/0.75 mg/dL, AST 31 U/L, ALT 92 U/L,总胆红素0.6 mg/dL。RUQ超声显示胆总管扩张明显。考虑到胆总管结石,她开始服用头孢吡肟和甲硝唑。MRCP显示胆囊扩张,无结石及少量囊周积液。同时注意到右肾的两个信号增强区域,与肿瘤或梗死有关。腹部计算机断层扫描显示中等大小的低密度区,符合肾梗死。梗塞的栓塞源检查未发现。肾动脉血管造影显示右肾动脉上支自发性剥离。由于有危及其他血管的风险,没有进行PCI,因此她在医学上使用利伐沙班、氢氯噻嗪和琥珀酸美托洛尔来保持她的收缩压在140毫米汞柱以下。手术后的第二天早上,病人告诉治疗小组,她的孙子喜欢从高处跳下来,她会抓住他的右边。我们认为这可能是她自发性夹层的病因。出院时,她的疼痛有所改善,8周后复查血管造影发现夹层愈合。讨论:自发性肾动脉夹层是一种罕见的腹痛的原因,往往提出了诊断和治疗的挑战。本病例强调了当排除其他常见病理时,考虑局部腹痛的其他病因的重要性。
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A Rare Cause of Abdominal Pain.

Case: A 54 year old woman with hypothyroidism presented with right flank pain that began acutely one week prior to presentation. She was told initially she had a urinary tract infection and treatment resulted in mild symptomatic improvement. The pain returned and she presented to another Emergency Department (ED); and was told the pain was due to constipation. She returned to the ED the next day when her pain worsened and her labs were notable for WBC of 19,000/uL, BUN/Cr of 28/0.75 mg/dL, AST of 31 U/L, ALT of 92 U/L and total bilirubin of 0.6 mg/dL. RUQ ultrasound was notable for dilation of the common bile duct. Given concern for choledocholithiasis, she was started on cefepime and metronidazole. MRCP demonstrated a distended gallbladder without stones and a small amount of pericholecystic fluid. Also noted were two areas of increased signal in the right kidney, concerning for neoplasia or infarction. Contrasted abdominal Computed tomography showed a moderate size area of hypodensity, consistent with renal infarct. Workup for embolic source of the infarction was unrevealing. Renal artery angiogram demonstrated a spontaneous dissection of the superior branch of the right renal artery. PCI was not performed due to risk of jeopardizing the other vessels and so she was managed medically with rivaroxaban along with hydrochlorothiazide and metoprolol succinate to keep her systolic blood pressure below 140 mmHg. The morning after the procedure, the patient told the treatment team that her grandson liked to jump from a height and she would catch him on her right side. This was felt to be a likely etiology of her spontaneous dissection. At the time of discharge, her pain was improved and repeat angiogram performed eight weeks later noted healing of the dissection.

Discussion: Spontaneous renal artery dissection is a rare cause of abdominal pain and often presents a diagnostic and therapeutic challenge. This case highlights the importance of considering alternate etiologies of localized abdominal pain when other common pathologies have been excluded.

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Where are we going? Refractory anemia. Urinary diversion. Schneiderian papilloma. Recurrent respiratory papillomatosis.
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