Subtil Joana, Carvalho Rui, Rebelo Ana Filipa, Guimarães Fernando
Internal Medicine, Centro Hospitalar de Trás-os-Montes e Alto Douro, Vila Real, PRT.
Internal Medicine, Centro Hospitalar de Trás-Os-Montes e Alto Douro, Vila Real, PRT.
Cureus. 2024 Nov 16;16(11):e73825. doi: 10.7759/cureus.73825. eCollection 2024 Nov.
Spontaneous subcapsular renal hematoma is a rare condition defined as spontaneous hemorrhage confined to the subcapsular and/or perirenal space. Its etiology can vary, ranging from renal tumors to vascular diseases, renal cysts, or infections. Here, we report the case of a 54-year-old male who presented to the emergency department with a two-day history of abdominal pain and fever. He was hemodynamically stable, with no abnormalities on physical examination except for mild pain on deep palpation of the left upper quadrant. Laboratory tests showed leukocytosis (24,200/μL), creatinine 1 mg/dL, C-reactive protein 20.77 mg/dL, and lactate 0.6 mmol/L. Urinalysis revealed leukocytes 10-25/HPF. An abdominal CT showed a hypodense area on the left kidney, suggesting focal pyelonephritis. He was admitted for acute pyelonephritis (APN), and empirical antibiotic therapy with ceftriaxone 2 g once daily was started. During hospitalization, Klebsiella pneumoniae was isolated from both blood and urine cultures, and antibiotic therapy was switched to cefotaxime according to susceptibility testing. Despite undergoing targeted antibiotic therapy, the patient maintained a fever, so another abdominal CT was performed, showing an external subcapsular collection of 9.1 cm × 7.9 cm × 2.8 cm, consistent with a subcapsular hematoma. Despite a drop in hemoglobin from 14 to 10 g/dL, the patient remained hemodynamically stable, so it was decided to continue conservative medical management. Spontaneous subcapsular renal hematoma, though rare in acute pyelonephritis, should be considered if symptoms persist despite antibiotics. Treatment may range from conservative monitoring to surgical intervention, depending on stability and the underlying cause.
自发性肾包膜下血肿是一种罕见病症,定义为局限于肾包膜下和/或肾周间隙的自发性出血。其病因多种多样,从肾肿瘤到血管疾病、肾囊肿或感染等。在此,我们报告一例54岁男性病例,该患者因腹痛和发热两天就诊于急诊科。他血流动力学稳定,体格检查无异常,仅左上腹深触诊时有轻度疼痛。实验室检查显示白细胞增多(24,200/μL)、肌酐1 mg/dL、C反应蛋白20.77 mg/dL以及乳酸0.6 mmol/L。尿液分析显示白细胞10 - 25/HPF。腹部CT显示左肾有一个低密度区,提示局灶性肾盂肾炎。他因急性肾盂肾炎(APN)入院,并开始经验性使用头孢曲松2 g每日一次进行抗生素治疗。住院期间,血培养和尿培养均分离出肺炎克雷伯菌,根据药敏试验将抗生素治疗改为头孢噻肟。尽管接受了针对性抗生素治疗,患者仍持续发热,因此再次进行腹部CT检查,显示一个9.1 cm×7.9 cm×2.8 cm的包膜下积液,符合包膜下血肿表现。尽管血红蛋白从14降至10 g/dL,但患者血流动力学仍保持稳定,所以决定继续采取保守治疗。自发性肾包膜下血肿在急性肾盂肾炎中虽罕见,但如果在使用抗生素后症状仍持续,应予以考虑。治疗方法可能从保守监测到手术干预不等,具体取决于稳定性和潜在病因。