一名青春期前健康女性患者的原发性腹膜炎。

IF 6.7 2区 医学 Q1 MEDICINE, GENERAL & INTERNAL
Danjel Miladinovic, Warren Hargreaves
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引用次数: 0

摘要

一名九岁的女性患者前来就诊,两周前出现呕吐、腹泻和腹痛,一周前出现排尿困难并伴有大面积血尿。近期没有咽炎或皮肤感染病史。她的既往病史包括服用治疗注意力缺陷多动障碍的药物,但没有其他重要病症。在急诊科检查时,患者心动过速,心率为155次/分(参考区间[RI]为70-130次/分),发热,体温为38.8°C(参考区间[RI]为36.4-37.4°C),腹部柔软,有全身压痛。没有高血压,也没有水肿迹象。血液结果显示白细胞增多,白细胞计数为 15.7 × 109/L(相关指数为 4.5-13.5 × 109/L),C 反应蛋白水平为 110 毫克/升(相关指数为 3 毫克/升)。没有中毒性休克综合征的相关证据。抗生素治疗前的床边尿液分析显示有白细胞、血液和蛋白质。尿液样本以及血液和粪便样本被送去做显微镜检查和培养。肾脏、输尿管和膀胱的超声波扫描结果无异常。鉴于几乎没有肾小球肾炎的临床证据,患者被推测为膀胱炎而入院,并开始静脉注射750毫克头孢唑啉。腹部检查发现了全身腹膜炎。腹部超声波扫描报告为 "提示急性阑尾炎"。患者接受了诊断性腹腔镜检查和阑尾切除术。术中,阑尾看起来正常,但整个腹部有浑浊液体和多处纤维蛋白沉积。输卵管和卵巢呈红斑状(方框),但术中妇科检查未发现盆腔炎。术前进行的出入导尿排出了带有沉淀物、脓液和血液的尿液,并再次送去进行显微镜检查和培养。患者在手术治疗前静脉注射了两剂 750 毫克的头孢唑啉。术后,抗菌治疗升级为静脉注射 4 克哌拉西林/0.5 克他唑巴坦,每 8 小时一次。术后过程顺利,患者接受了为期五天的静脉抗生素治疗,第5天出院,没有再接受抗菌治疗。出院两周后复查时,患者一切正常。复查时,手术组织病理学报告为 "阑尾周围炎,粘膜正常,中度急性浆膜炎,中性粒细胞浸润,仅轻度累及阑尾前膜和固有肌"。聚合酶链反应和 16-S 分子检测没有完成,但对诊断很有用。然而,血清抗 DNase B 和抗链球菌溶解素 O 滴度升高,支持 A 组链球菌(GAS)原发性腹膜炎的诊断。20 世纪中期,原发性腹膜炎的发病率占所有急腹症的 10%,死亡率为 40%-50%、5 2023 年,新南威尔士州卫生部发布警报,通知医疗从业人员和社区注意伽马菌感染的数量不断上升,以及随后到医院就诊的侵袭性 A 组链球菌感染(iGAS)的增加。原发性腹膜炎最常见的致病菌是肺炎链球菌、葡萄球菌和革兰氏阴性菌,但也有其他致病菌的报道。7, 8 发病机制被认为是通过呼吸道、皮肤或泌尿生殖道的血源性传播。腹腔镜检查和腹膜冲洗,并辅以适当的抗菌治疗,仍然是治疗原发性腹膜炎的推荐方法、据我们所知,这是自 1994 年以来文献报道的首例澳大利亚儿童(6 个月至 16 岁年龄组)GAS 原发性腹膜炎病例。本报告旨在提醒临床医生注意这一被遗忘的诊断,尤其是在GAS感染发病率不断上升的背景下。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Primary peritonitis in a previously healthy prepubertal female patient

A nine-year-old female patient presented with a two-week history of vomiting, diarrhoea, abdominal pain, and a one-week history of dysuria with macroscopic haematuria. There was no recent history of pharyngitis or a skin infection. Her past medical history included medication for attention deficit hyperactivity disorder, but no other significant conditions. On examination in the emergency department, the patient was tachycardic with heart rate 155 beats/minute (reference interval [RI], 70–130 beats/minute), febrile with temperature 38.8°C (RI, 36.4–37.4°C) and her abdomen was soft with generalised tenderness. There was no hypertension or evidence of oedema. Blood results showed leucocytosis with a white cell count of 15.7 × 109/L (RI, 4.5–13.5 × 109/L) and C-reactive protein level of 110 mg/L (RI, < 3 mg/L). There was no associated evidence of toxic shock syndrome. Bedside urine analysis before antibiotic therapy showed leucocytes, blood and protein. The urine sample, as well as a blood and faecal samples were sent for microscopy and culture. Ultrasound scan of the kidneys, ureters and urinary bladder was unremarkable. The patient was admitted for presumed cystitis given little clinical evidence of glomerular nephritis and started on 750 mg intravenous cefazolin.

Overnight, the patient developed worsening abdominal pain, further vomiting and had ongoing fever. Abdominal examination revealed generalised peritonitis.

An abdominal ultrasound scan was reported as “suggestive for acute appendicitis”. The patient underwent diagnostic laparoscopy and appendicectomy. Intra-operatively, the appendix appeared normal; however, throughout the abdomen there was turbid fluid and multiple fibrin deposits. The fallopian tubes and ovaries were erythematous (Box) but an intra-operative gynaecological review yielded no concern for pelvic inflammatory disease. In/out catheterisation pre-operatively drained urine with sediment, pus and blood and was again sent for microscopy and culture.

Both pre- and post-antibiotic therapy urine microscopy and culture showed no significant bacterial growth. The patient had received two doses of 750 mg cefazolin intravenously before operative management. Post-operatively, antimicrobial therapy was escalated to intravenous 4 g piperacillin/0.5 g tazobactam every 8 hours. The post-operative course was uneventful; the patient received five days of intravenous antibiotics and was discharged on Day 5 with no further antimicrobial treatment.

The patient was well when reviewed two weeks after discharge. On review, the surgical histopathology reported “peri-appendicitis with normal mucosa, moderate acute serositis and underlying neutrophil infiltrate involving the adventitia and muscularis propria only mildly”. Polymerase chain reaction and 16-S molecular testing was not completed but would have been useful for the diagnosis. However, serum anti-DNase B and antistreptolysin O titres were elevated, supporting the diagnosis of group A Streptococcus (GAS) primary peritonitis.

In the mid-20th century, primary peritonitis had an incidence of 10% of all abdominal emergencies with a mortality rate of 40–50%.1 Today there is a reported incidence of less than 2%.2, 3 Interestingly, the global incidence of GAS infection has been increasing.4, 5 In 2023, New South Wales Health distributed alerts to notify health practitioners and the community of the rising number of GAS infections and the subsequent increase in invasive group A Streptococcus infections (iGAS) presenting to our hospitals.6

The most common causative pathogens for primary peritonitis are Streptococcus pneumoniae, Staphyloccocus species and gram-negative organisms; however, other causative agents have been reported.7, 8 The pathogenesis is thought to be via haematogenous spread from the respiratory tract, skin or genitourinary tract.2, 9, 10 In this case, the likely origin was the urinary tract.

Conflicting symptoms and signs on presentation, in the absence of radiological findings, present a diagnostic challenge. Laparoscopy with peritoneal washout accompanied by appropriate antimicrobial therapy remains the recommended management of primary peritonitis.7, 8, 10 Appendicectomy is often performed to rule out intra-abdominal causes of peritonitis (secondary peritonitis).

To our knowledge, this is the first Australian paediatric case (six-month to 16-year age group) of GAS primary peritonitis reported in the literature since 1994.10 The increased incidence of GAS infections may increase the incidence of GAS primary peritonitis.

Primary peritonitis is a rare disease that should remain a differential diagnosis in previously healthy children presenting with acute abdominal pain. This report aims to remind clinicians of this forgotten diagnosis, particularly in the context of an increasing incidence of GAS infections.

No relevant disclosures.

Not commissioned; externally peer reviewed.

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来源期刊
Medical Journal of Australia
Medical Journal of Australia 医学-医学:内科
CiteScore
9.40
自引率
5.30%
发文量
410
审稿时长
3-8 weeks
期刊介绍: The Medical Journal of Australia (MJA) stands as Australia's foremost general medical journal, leading the dissemination of high-quality research and commentary to shape health policy and influence medical practices within the country. Under the leadership of Professor Virginia Barbour, the expert editorial team at MJA is dedicated to providing authors with a constructive and collaborative peer-review and publication process. Established in 1914, the MJA has evolved into a modern journal that upholds its founding values, maintaining a commitment to supporting the medical profession by delivering high-quality and pertinent information essential to medical practice.
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