{"title":"怀孕 12 周时出现异位妊娠","authors":"Wiwin Suhandri, Diki Riandi","doi":"10.18203/2349-2902.isj20241306","DOIUrl":null,"url":null,"abstract":"Heterotopic pregnancy (HP) represents a rare and complex condition where simultaneous pregnancies occur at different implantation sites, with only one located within the uterine cavity. Typically diagnosed in the first trimester, HP presents diagnostic challenges due to its rarity and varying clinical presentations. Here, we present a unique case of HP diagnosed at Bengkalis Hospital involving a 42-year-old multipara at 12 weeks of gestation. The patient's presentation included regular uterine contractions and upper abdominal pain, with a positive Plano test upon admission. Despite experiencing vaginal bleeding two days prior and an initial refusal of care, further examination revealed a 2.13 cm gestational sac in the intrauterine cavity, consistent with the gestational age. Additionally, free intra-abdominal fluid was observed in the Douglas cavity. Haematological examination indicated a low haemoglobin level of 7.2 g/dl and elevated leukocytes at 16,000. An emergency laparotomy revealed a ruptured right ovarian tube containing a gestational sac, which was managed with hemostasis and a subsequent salpingectomy. The left ovarian tube underwent a tubectomy as a preventive measure. The patient received multiple blood transfusions, leading to an improvement in haemoglobin levels to 10.2 g/dl postoperatively. Following a two-day hospitalisation, the patient was discharged in good general condition. HP cases often necessitate laparotomies for tubal pregnancies, and ultrasound plays a crucial role in diagnosis, especially given its prevalence of 1 in 7000 due to assisted reproduction. Treatment typically involves laparoscopic or laparotomic intervention, highlighting the multidisciplinary approach required for managing this rare condition.","PeriodicalId":14372,"journal":{"name":"International Surgery Journal","volume":"49 22","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2024-05-16","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"A heterotopic pregnancy at 12 weeks’ pregnancy\",\"authors\":\"Wiwin Suhandri, Diki Riandi\",\"doi\":\"10.18203/2349-2902.isj20241306\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Heterotopic pregnancy (HP) represents a rare and complex condition where simultaneous pregnancies occur at different implantation sites, with only one located within the uterine cavity. Typically diagnosed in the first trimester, HP presents diagnostic challenges due to its rarity and varying clinical presentations. Here, we present a unique case of HP diagnosed at Bengkalis Hospital involving a 42-year-old multipara at 12 weeks of gestation. The patient's presentation included regular uterine contractions and upper abdominal pain, with a positive Plano test upon admission. Despite experiencing vaginal bleeding two days prior and an initial refusal of care, further examination revealed a 2.13 cm gestational sac in the intrauterine cavity, consistent with the gestational age. Additionally, free intra-abdominal fluid was observed in the Douglas cavity. Haematological examination indicated a low haemoglobin level of 7.2 g/dl and elevated leukocytes at 16,000. An emergency laparotomy revealed a ruptured right ovarian tube containing a gestational sac, which was managed with hemostasis and a subsequent salpingectomy. The left ovarian tube underwent a tubectomy as a preventive measure. The patient received multiple blood transfusions, leading to an improvement in haemoglobin levels to 10.2 g/dl postoperatively. Following a two-day hospitalisation, the patient was discharged in good general condition. HP cases often necessitate laparotomies for tubal pregnancies, and ultrasound plays a crucial role in diagnosis, especially given its prevalence of 1 in 7000 due to assisted reproduction. 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引用次数: 0
摘要
异位妊娠(HP)是一种罕见而复杂的病症,即同时妊娠发生在不同的着床部位,只有一个着床部位位于子宫腔内。异位妊娠通常在妊娠头三个月被诊断出来,由于其罕见性和不同的临床表现,给诊断带来了挑战。在此,我们介绍一例在 Bengkalis 医院确诊的独特 HP 病例,患者 42 岁,多胎,妊娠 12 周。患者表现为规律性子宫收缩和上腹部疼痛,入院时普拉诺试验呈阳性。尽管患者两天前曾出现阴道出血,而且最初拒绝接受治疗,但进一步检查发现宫腔内有一个 2.13 厘米的妊娠囊,与孕龄相符。此外,在道格拉斯腔内还发现了游离的腹腔积液。血液检查显示血红蛋白水平低至 7.2 g/dl,白细胞升高至 16 000。紧急开腹手术显示右侧卵巢管破裂,内含一个妊娠囊,经止血处理后进行了输卵管切除术。作为预防措施,对左侧卵巢管进行了切除。患者接受了多次输血,术后血红蛋白水平提高到 10.2 g/dl。经过两天的住院治疗,患者出院时全身状况良好。输卵管妊娠 HP 病例通常需要开腹手术,超声波在诊断中起着至关重要的作用,特别是考虑到由于辅助生殖,其发病率高达 1/7000。治疗方法通常包括腹腔镜或腹腔镜干预,这突出说明了治疗这种罕见疾病所需的多学科方法。
Heterotopic pregnancy (HP) represents a rare and complex condition where simultaneous pregnancies occur at different implantation sites, with only one located within the uterine cavity. Typically diagnosed in the first trimester, HP presents diagnostic challenges due to its rarity and varying clinical presentations. Here, we present a unique case of HP diagnosed at Bengkalis Hospital involving a 42-year-old multipara at 12 weeks of gestation. The patient's presentation included regular uterine contractions and upper abdominal pain, with a positive Plano test upon admission. Despite experiencing vaginal bleeding two days prior and an initial refusal of care, further examination revealed a 2.13 cm gestational sac in the intrauterine cavity, consistent with the gestational age. Additionally, free intra-abdominal fluid was observed in the Douglas cavity. Haematological examination indicated a low haemoglobin level of 7.2 g/dl and elevated leukocytes at 16,000. An emergency laparotomy revealed a ruptured right ovarian tube containing a gestational sac, which was managed with hemostasis and a subsequent salpingectomy. The left ovarian tube underwent a tubectomy as a preventive measure. The patient received multiple blood transfusions, leading to an improvement in haemoglobin levels to 10.2 g/dl postoperatively. Following a two-day hospitalisation, the patient was discharged in good general condition. HP cases often necessitate laparotomies for tubal pregnancies, and ultrasound plays a crucial role in diagnosis, especially given its prevalence of 1 in 7000 due to assisted reproduction. Treatment typically involves laparoscopic or laparotomic intervention, highlighting the multidisciplinary approach required for managing this rare condition.