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脾破裂异位妊娠:考虑非输卵管部位的重要性。

Ruptured Splenic Ectopic Pregnancy: The Importance of Considering Nontubal Sites.

作者信息

Fahmy Yomna, Ross Claire, Kiss Nora, Gumaa Duaa, Ngeyu Ee Xuan, Mavridou Despina, Bajracharya Rasana

机构信息

Department of Obstetrics and Gynaecology, Maidstone and Tunbridge Wells NHS Trust, Tunbridge Wells, UK.

Department of Surgery, Maidstone and Tunbridge Wells NHS Trust, Tunbridge Wells, UK.

出版信息

Case Rep Obstet Gynecol. 2025 Aug 6;2025:8867392. doi: 10.1155/crog/8867392. eCollection 2025.

Abstract

Splenic ectopic pregnancy is an exceptionally rare and life-threatening form of abdominal ectopic pregnancy, often presenting significant diagnostic and management challenges. We report a case of ruptured splenic ectopic pregnancy initially suspected to be a tubal miscarriage. A 36-year-old woman presented with mild left-sided pelvic pain, no vaginal bleeding and a positive pregnancy test. This was an unplanned pregnancy, and she was not sure of her LMP. This presentation in early pregnancy requires ruling out an ectopic pregnancy through clinical assessment and laboratory investigations. Clinical examination showed normal observations and generalized abdominal tenderness with no signs of peritonism. Initial investigations revealed a significantly elevated -hCG of 24,076 IU/L, and transvaginal ultrasound showed an empty uterus. Given the findings, an ectopic pregnancy was suspected, and diagnostic laparoscopy was performed. During laparoscopy, no ectopic pregnancy was identified in the pelvis, both tubes looked normal, but a left fimbrial cyst was noted, and 300 mL of haemoperitoneum was observed, without active bleeding. A tubal miscarriage was presumed with the plan to follow up -hCG to confirm resolution of the pregnancy. Postoperatively, the patient developed worsening pain and a significant haemoglobin drop to 97 g/L, inconsistent with the amount of intraoperative blood loss which raised the suspicion of extrapelvic ectopic pregnancy with active bleeding. A contrast-enhanced CT scan identified free blood surrounding the spleen and a 25-mm peripherally enhancing lesion with venous drainage into the splenic vein, consistent with a ruptured splenic ectopic pregnancy. An urgent multidisciplinary team discussion led to surgical management via midline laparotomy and splenectomy. The postoperative course was complicated by ileus, which resolved with conservative management. The patient's -hCG levels progressively declined, confirming resolution. This case highlights the importance of considering splenic ectopic pregnancy when -hCG is markedly elevated, and no pelvic ectopic pregnancy is identified. Prompt imaging and diagnosis are crucial to prevent morbidity associated with delayed management.

摘要

脾异位妊娠是一种极其罕见且危及生命的腹腔异位妊娠形式,常常带来重大的诊断和管理挑战。我们报告一例脾异位妊娠破裂病例,最初怀疑是输卵管流产。一名36岁女性出现轻度左侧盆腔疼痛,无阴道出血,妊娠试验呈阳性。这是一次意外妊娠,她不确定末次月经时间。孕早期出现这种情况需要通过临床评估和实验室检查排除异位妊娠。临床检查显示各项指标正常,全腹压痛但无腹膜炎体征。初步检查发现β-hCG显著升高至24,076 IU/L,经阴道超声显示子宫内为空。鉴于这些发现,怀疑为异位妊娠,并进行了诊断性腹腔镜检查。腹腔镜检查时,盆腔未发现异位妊娠,双侧输卵管外观正常,但发现左侧输卵管伞端囊肿,观察到300 mL腹腔积血,无活动性出血。推测为输卵管流产,计划随访β-hCG以确认妊娠消退。术后,患者疼痛加剧,血红蛋白显著降至97 g/L,这与术中失血量不符,从而怀疑有盆腔外异位妊娠伴活动性出血。增强CT扫描显示脾脏周围有游离血液,以及一个25 mm周边强化的病灶,静脉血流入脾静脉,符合脾异位妊娠破裂表现。紧急的多学科团队讨论后决定通过正中剖腹术和脾切除术进行手术治疗。术后病程因肠梗阻而复杂化,经保守治疗后缓解。患者的β-hCG水平逐渐下降,确认妊娠消退。 该病例强调了当β-hCG显著升高且未发现盆腔异位妊娠时,考虑脾异位妊娠的重要性。及时的影像学检查和诊断对于预防因治疗延迟而导致的并发症至关重要。

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