绝经后患者一例罕见的无乳链球菌性子宫肌瘤。

HCA healthcare journal of medicine Pub Date : 2025-04-01 eCollection Date: 2025-01-01 DOI:10.36518/2689-0216.1489
Mariah Piazza, Sai V Nagula, Madeleine Salzberg, Darren Preuninger
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引用次数: 0

摘要

背景:子宫平滑肌瘤是一种罕见但可能致命的并发症。大多数病例发生在产后或绝经后的血管疾病患者,由于已有肌瘤的梗死和感染而发生。提出的诊断子宫肌瘤的三要素包括:1)败血症或菌血症;2)子宫平滑肌瘤;3)无其他明显的传染源。我们提出一个绝经后的病人谁提出了上述三位一体,并被发现有一个子宫肌瘤,阳性的无乳链球菌。病例介绍:一名67岁女性,既往无病史,因精神状态改变到急诊科就诊。虽然不发烧,但她有心动过速和高血压,初步评估时伴有严重的高血糖和白细胞增多。影像学显示多发性栓塞性脑梗死,但检查结果为心脏或血管源阴性。她的感染检查最终值得注意的是无乳杆菌血症和子宫肌瘤,腹部和骨盆计算机断层扫描(CT)上可见边缘增强积液。给予广谱抗生素治疗,ct引导下脓肿引流,无乳链球菌阳性。由于持续发烧和白细胞计数升高,患者接受了全腹部子宫切除术,双侧输卵管-卵巢切除术和盆腔冲洗。术中发现有带蒂的坏死子宫肌瘤,肌瘤内有化脓性物质,没有其他明显的胃肠道来源。最终病理是良性的,患者最终出院到住院康复机构。结论:子宫肌瘤虽然罕见,但对于任何产后或绝经后有血管疾病危险因素或已知血管疾病的患者,均应考虑患子宫肌瘤。与子宫肌瘤相关的高死亡率通常是由于患者屈服于压倒性的败血症,可能与诊断延误有关。因此,应在适当的情况下考虑子宫肌瘤,并保证及时诊断和治疗。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
A Rare Instance of Streptococcus agalactiae Pyomyoma in a Postmenopausal Patient: A Case Report.

Background: Pyomyoma is a rare, but potentially fatal, complication of uterine leiomyoma. Most cases occur in postpartum or postmenopausal patients with vascular disease and arise due to infarction and infection of existing fibroids. The proposed diagnostic triad for pyomyoma includes 1) sepsis or bacteremia; 2) uterine leiomyomata; and 3) no other apparent source of infection. We present a case of a postmenopausal patient who presented with the aforementioned triad and was found to have a pyomyoma, positive for Streptococcus agalactiae.

Case presentation: A 67-year-old woman with no known past medical history presented to the emergency department for altered mental status. Although afebrile, she was tachycardic and hypertensive, with severe hyperglycemia and leukocytosis on initial assessment. Multiple embolic cerebral infarcts were noted on imaging, but workup was negative for a cardiac or vascular source. Her infectious workup was ultimately notable for S agalactiae bacteremia and a fibroid uterus with a rim enhancing fluid collection seen on a computed tomography (CT) abdomen and pelvis scan. Broad spectrum antibiotics were initiated, and she underwent CT-guided drainage of the abscess, which was also positive for S agalactiae. Given continued fevers and elevated white blood cell counts, the patient underwent a total abdominal hysterectomy with bilateral salpingo-oophorectomy and pelvic washout. Intraoperative findings were notable for a pedunculated, necrotic uterine fibroid with purulent material within, and no other apparent gastrointestinal source. The final pathology was benign, and the patient was ultimately discharged to an inpatient rehabilitation facility.

Conclusion: While rare, pyomyoma should be considered for any postpartum or postmenopausal patient with risk factors for, or known, vascular disease, presenting with the triad noted above. The high mortality rate associated with pyomyoma is often due to patients succumbing to overwhelming sepsis, likely related to delays in diagnosis. As such, pyomyoma should be considered in the appropriate context and warrants prompt diagnosis and treatment.

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