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Bradycardia in the setting of postpartum preeclampsia and influenza A: A case report 产后子痫前期和甲型流感的心动过缓1例报告
IF 0.6 Q4 OBSTETRICS & GYNECOLOGY Pub Date : 2026-01-15 DOI: 10.1016/j.crwh.2026.e00785
Dalia Rahmon, Kelly Dubay, Sarah Deighton-Collins
Postpartum bradycardia is a rare clinical finding, with limited guidance regarding its evaluation and management. Prior literature suggests that postpartum bradycardia is most commonly associated with preeclampsia, underlying cardiac disease, medication effects, or neuraxial anesthesia. In patients with preeclampsia, management may be particularly challenging, as magnesium sulfate—used for seizure prophylaxis—is theorized to exacerbate bradycardia.
This report concerns the case of a 33-year-old woman (G3P3003) with an otherwise uncomplicated pregnancy and cesarean delivery who was diagnosed with Influenza A on postpartum day 1 and treated with oseltamivir. She was readmitted on postpartum day 7 with epigastric pain and shortness of breath and was found to have severe sinus bradycardia (heart rate 32–42 beats per minute) and highly elevated blood pressure, consistent with new-onset postpartum preeclampsia with severe features. Cardiac evaluation, including electrocardiography and transthoracic echocardiography, revealed no structural or ischemic abnormalities. The patient was treated with magnesium sulfate for seizure prophylaxis and antihypertensive therapy. Despite persistent bradycardia, she remained hemodynamically stable, and her heart rate gradually normalized over three days without additional intervention. She was discharged in stable condition and remained asymptomatic at follow-up.
This case highlights postpartum bradycardia as a potential presenting sign of delayed-onset preeclampsia, even following a normotensive pregnancy. Although magnesium sulfate and recent influenza infection were considered as contributing factors, the clinical course supported preeclampsia as the primary etiology. Postpartum bradycardia is often benign and self-limited; however, thorough evaluation is essential to exclude cardiac pathology and guide appropriate management.
产后心动过缓是一种罕见的临床表现,对其评估和管理的指导有限。先前的文献表明,产后心动过缓最常与先兆子痫、潜在的心脏疾病、药物作用或神经轴麻醉有关。对于先兆子痫患者,管理可能特别具有挑战性,因为理论上用于预防癫痫发作的硫酸镁会加剧心动过缓。本报告涉及一名33岁妇女(G3P3003)的病例,她的妊娠和剖宫产没有并发症,在产后第1天被诊断患有甲型流感,并接受奥司他韦治疗。产后第7天因上腹痛、呼吸短促再次入院,发现严重窦性心动过缓(心率32-42次/分钟)、血压升高,符合新发产后子痫前期的严重特征。心脏评估,包括心电图和经胸超声心动图,未发现结构性或缺血性异常。患者给予硫酸镁预防癫痫发作和抗高血压治疗。尽管持续的心动过缓,她的血流动力学保持稳定,在没有额外干预的情况下,她的心率在三天内逐渐恢复正常。出院时病情稳定,随访时无症状。本病例强调产后心动过缓是迟发性先兆子痫的潜在表现,即使妊娠血压正常。虽然硫酸镁和最近的流感感染被认为是促成因素,但临床过程支持先兆子痫是主要病因。产后心动过缓往往是良性的、自限性的;然而,彻底的评估是必要的,以排除心脏病理和指导适当的管理。
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引用次数: 0
Sono-embryonic detection of monochorionic, diamniotic triplets with conjoined twins after in vitro fertilization: A case report and review of the literature 体外受精后单绒毛膜双羊膜三胞胎的超声胚胎检测:1例报告及文献复习
IF 0.6 Q4 OBSTETRICS & GYNECOLOGY Pub Date : 2026-01-06 DOI: 10.1016/j.crwh.2026.e00780
Ashley B. Zimmermann, Jamie A. Burns, Eran Bornstein
Monochorionic diamniotic triplets with a conjoined pair are exceedingly rare and arise from multiple splitting events of a single zygote. This report presents the earliest documented ultrasound diagnosis of MCDA triplets with a conjoined pair, at 8 weeks and 5 days of gestation, in a patient who underwent in-vitro fertilization with a single embryo transfer. High-resolution transvaginal ultrasound revealed a monochorionic diamniotic configuration with two amniotic sacs: one containing a structurally normal embryo and the other containing di-thoracic parapagus conjoined twins. This case highlights the critical role of ultrasound imaging in the embryonic period to accurately identify complex multifetal pregnancies and to facilitate timely counseling and clinical decision-making. A review of the literature is included to provide context and management considerations for this rare condition.
单绒毛膜双膜三胞胎是非常罕见的,是由一个受精卵的多次分裂事件引起的。本报告提出了最早的超声诊断的MCDA三胞胎连体,在妊娠8周和5天,在患者接受体外受精与单胚胎移植。高分辨率经阴道超声显示单绒毛膜双羊膜配置与两个羊膜囊:一个包含一个结构正常的胚胎,另一个包含双胸斜腹连体双胞胎。本病例强调了超声成像在胚胎期的关键作用,以准确识别复杂的多胎妊娠,促进及时咨询和临床决策。回顾文献包括提供背景和管理考虑这种罕见的条件。
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引用次数: 0
Rapid enlargement of a tubo-ovarian abscess in a patient with cervical cancer and multiple uterine fibroids: A case report 宫颈癌合并多发性子宫肌瘤患者输卵管卵巢脓肿迅速增大1例
IF 0.6 Q4 OBSTETRICS & GYNECOLOGY Pub Date : 2026-01-06 DOI: 10.1016/j.crwh.2026.e00784
Yuki Yamazawa , Takayoshi Iijima , Daisuke Shigenaga , Tamaki Cho , Yuichi Imai , Taichi Mizushima , Etsuko Miyagi
Locally advanced cervical cancer can be complicated by infections such as pyometra and tubo-ovarian abscess (TOA), although the pathogenesis of TOA is not fully understood. This report presents a case of TOA that rapidly enlarged in a patient with cervical cancer and multiple intramural uterine fibroids. A 61-year-old primigravida was diagnosed with stage IIB cervical cancer, classified as cT2bN0M0, squamous cell carcinoma, complicated by multiple fibroids. Concurrent chemoradiotherapy (CCRT) was planned, and the patient was admitted three weeks after her initial visit with lower abdominal pain. Computed tomography revealed an 8 cm TOA, pyometra, and an enlarged appendix. Conservative treatment with trans-cervical drainage and intravenous antibiotics was unsuccessful. Surgical drainage with bilateral adnexectomy and appendectomy was therefore performed. Bacteroides fragilis was identified in intra-abdominal pus cultures, consistent with findings from cervical drainage, suggesting that the TOA developed secondary to pyometra. One month after surgery, CCRT was resumed and completed without complications. TOA associated with cervical cancer can enlarge rapidly and may require surgical drainage. In patients with locally advanced cervical cancer and multiple uterine fibroids, the potentially increased risk of TOA should be considered.
局部晚期宫颈癌可并发脓脓和输卵管卵巢脓肿(TOA)等感染,尽管TOA的发病机制尚不完全清楚。本报告报告一例迅速扩大的TOA患者宫颈癌和多发性子宫肌瘤。一例61岁的原发女性被诊断为IIB期宫颈癌,分类为cT2bN0M0,鳞状细胞癌,合并多发性肌瘤。计划同步放化疗(CCRT),患者在首次就诊后三周因下腹部疼痛入院。计算机断层显示一个8厘米的TOA,脓膜肿大,阑尾肿大。经颈椎引流及静脉注射抗生素的保守治疗均未成功。手术引流双侧附件切除和阑尾切除术。在腹内脓液培养中发现了脆弱拟杆菌,与宫颈引流的结果一致,表明TOA继发于脓膜肿大。术后1个月恢复CCRT,无并发症。与宫颈癌相关的TOA可迅速扩大,可能需要手术引流。对于局部晚期宫颈癌和多发性子宫肌瘤患者,应考虑TOA的潜在风险增加。
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引用次数: 0
Outcomes of subsequent pregnancies following modified one-step conservative uterine surgery (MOSCUS) in the management of placenta accreta spectrum: Two case reports and a narrative review of the literature 改良的一步保守子宫手术(MOSCUS)治疗增胎性胎盘后妊娠的结局:两例报告和文献综述
IF 0.6 Q4 OBSTETRICS & GYNECOLOGY Pub Date : 2026-01-05 DOI: 10.1016/j.crwh.2026.e00781
Anh Dinh Bao Vuong , Xuan Trang Nguyen , Xuan Trang Thi Pham , Phuc Nhon Nguyen
Cesarean hysterectomy is a common management approach for placenta accreta spectrum. While conservative uterine management can preserve fertility, outcome data remain limited. This article reports the long-term results of modified one-step conservative uterine surgery (MOSCUS) in two cases of placenta accreta spectrum and reviews the literature on the outcomes of subsequent pregnancies after conservative management of the condition. Two women with a history of placenta accreta spectrum managed with MOSCUS attended a tertiary referral hospital in southern Vietnam with term and near-term pregnancies. The pregnancy outcomes were favorable with elective cesarean delivery. Neither uterine rupture nor recurrent placenta accreta spectrum was observed. The low uterine segment of the myometrial layer was 1–1.5 cm in thickness. The mothers and neonates were discharged uneventfully. The data relating to the subsequent pregnancy outcomes after conservative management reported in the literature spanning 2020–2025 are limited and heterogeneous. Commonly, the materno-fetal outcomes are favorable. The recurrence of placenta accreta spectrum in late pregnancy ranges from 5.5 % to 22.7 %. The major concerns are the increased rate of cesarean section and postpartum hemorrhage. In conclusion, the MOSCUS is a promising method that preserves fertility. A well-resourced antenatal care system with a multidisciplinary team is needed to manage these high-risk pregnancies. Further data are required to strengthen these findings.
剖宫产子宫切除术是常见的治疗方法胎盘增生谱。虽然保守的子宫管理可以保持生育能力,但结果数据仍然有限。本文报道改良的一步保守性子宫手术(MOSCUS)治疗2例增生性胎盘的长期疗效,并对保守治疗后的妊娠结局进行文献回顾。在MOSCUS管理下,两名有胎盘增生史的妇女在越南南部的一家三级转诊医院接受了足月和近期妊娠。择期剖宫产妊娠结局良好。未见子宫破裂或复发性胎盘增生谱。子宫下层肌层厚度为1 ~ 1.5 cm。母亲和新生儿平安出院。文献中报道的2020-2025年保守治疗后妊娠结局的相关数据有限且不均匀。通常,母胎结局是有利的。妊娠后期胎盘增生的复发率为5.5% ~ 22.7%。主要的担忧是剖宫产率和产后出血的增加。综上所述,MOSCUS是一种很有前途的保留生育力的方法。需要一个资源充足的产前保健系统和一个多学科团队来管理这些高危妊娠。需要进一步的数据来加强这些发现。
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引用次数: 0
Subdermal contraceptive implant migration to the pulmonary vasculature: A case report 皮下避孕植入物迁移至肺血管:1例报告
IF 0.6 Q4 OBSTETRICS & GYNECOLOGY Pub Date : 2026-01-05 DOI: 10.1016/j.crwh.2026.e00782
Alejandra Tellez Aguilera , Maria Fernanda Zalapa Gómez , Eliana López Zamora , Fernanda Isabel Velázquez Vega , Rogelio A. Lozano Esparza , Victor Sánchez Sotelo , Jorge Aguilar Castillo , José Carlos Alberto Martínez Ramírez
Subdermal implants are highly effective long-acting reversible contraceptives. Rarely, they may migrate intravascularly. This report concerns the case of a 22-year-old woman who presented for removal of a non-palpable etonogestrel implant. Imaging revealed migration to the pulmonary vasculature. Surgical consultation confirmed intravascular embolization to the basal anterior segmental artery of the left lower lobe. Extraction of the implant was performed without complications. Subdermal contraceptive implant embolization into the pulmonary vasculature is an emerging iatrogenic complication. The clinical relevance of this complication lies not only in its potential for pulmonary damage but also in its diagnostic challenge and management complexity. While endovascular retrieval should be considered the first-line approach, especially in cases detected early, in the present case this was not feasible due to endothelialization; thoracotomy ensured safe removal. Pulmonary migration of contraceptive implants is rare but potentially serious. Delayed diagnosis may preclude endovascular removal.
皮下植入是一种高效、长效、可逆的避孕药。极少情况下,它们可在血管内迁移。本报告涉及的情况下,22岁的妇女谁提出去除不可触及的依托孕酮植入物。影像学显示向肺血管转移。外科会诊证实有左下叶基底前段动脉血管内栓塞。种植体的拔出无并发症。皮下避孕植入物栓塞到肺血管是一个新兴的医源性并发症。该并发症的临床意义不仅在于其潜在的肺损伤,而且在于其诊断挑战和管理的复杂性。虽然血管内回收应该被认为是一线方法,特别是在早期发现的病例中,但在本病例中,由于内皮化,这是不可行的;开胸手术确保安全取出。避孕植入物的肺迁移是罕见的,但潜在的严重。延迟诊断可能会妨碍血管内切除。
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引用次数: 0
Congenital factor VII deficiency as a cause of postpartum hemorrhage: A case report 先天性第七因子缺乏引起产后出血1例报告
IF 0.6 Q4 OBSTETRICS & GYNECOLOGY Pub Date : 2026-01-03 DOI: 10.1016/j.crwh.2026.e00779
Janine Russeth Hernández Zanata , Marco Antonio Gámez Garza , Ignacio Uriel Macias Paz , Elias Ledezma Flores , René Anselmo Del Ángel De León , José Eugenio Guerra Cárdenas
Obstetric hemorrhage is one of the leading causes of maternal morbidity and mortality worldwide. However, coagulation disorders as an etiology are rare, with a prevalence of less than 1 %. This report concerns the case of a 24-year-old patient with no previous history of bleeding who presented with postpartum hemorrhage at 38.6 weeks of pregnancy after a normal vaginal delivery. The hemorrhage was refractory to the use of uterotonics and compression maneuvers. In the absence of uterine atony, retained products of conception, or obvious trauma, the possibility of an underlying coagulopathy was considered. Initial studies showed an isolated prolongation of prothrombin time, with activated partial thromboplastin time within normal parameters. A correction test with a normal plasma pool was performed, which showed complete correction of prothrombin time. Specific factor quantification confirmed a severe and isolated factor VII deficiency.
产科出血是全世界孕产妇发病和死亡的主要原因之一。然而,凝血功能障碍作为病因是罕见的,患病率不到1%。本报告涉及一位24岁无出血史的患者,在正常阴道分娩后妊娠38.6周出现产后出血。出血对子宫强直和压迫手法的使用是难治的。在没有子宫张力、妊娠产物保留或明显创伤的情况下,考虑潜在凝血功能障碍的可能性。最初的研究显示一个孤立的延长凝血酶原时间,与活化部分凝血活酶时间在正常参数。用正常血浆池进行校正试验,显示凝血酶原时间完全校正。特异性因子定量证实了严重和孤立的因子7缺乏症。
{"title":"Congenital factor VII deficiency as a cause of postpartum hemorrhage: A case report","authors":"Janine Russeth Hernández Zanata ,&nbsp;Marco Antonio Gámez Garza ,&nbsp;Ignacio Uriel Macias Paz ,&nbsp;Elias Ledezma Flores ,&nbsp;René Anselmo Del Ángel De León ,&nbsp;José Eugenio Guerra Cárdenas","doi":"10.1016/j.crwh.2026.e00779","DOIUrl":"10.1016/j.crwh.2026.e00779","url":null,"abstract":"<div><div>Obstetric hemorrhage is one of the leading causes of maternal morbidity and mortality worldwide. However, coagulation disorders as an etiology are rare, with a prevalence of less than 1 %. This report concerns the case of a 24-year-old patient with no previous history of bleeding who presented with postpartum hemorrhage at 38.6 weeks of pregnancy after a normal vaginal delivery. The hemorrhage was refractory to the use of uterotonics and compression maneuvers. In the absence of uterine atony, retained products of conception, or obvious trauma, the possibility of an underlying coagulopathy was considered. Initial studies showed an isolated prolongation of prothrombin time, with activated partial thromboplastin time within normal parameters. A correction test with a normal plasma pool was performed, which showed complete correction of prothrombin time. Specific factor quantification confirmed a severe and isolated factor VII deficiency.</div></div>","PeriodicalId":9657,"journal":{"name":"Case Reports in Women's Health","volume":"49 ","pages":"Article e00779"},"PeriodicalIF":0.6,"publicationDate":"2026-01-03","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145921304","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Twin-twin transfusion syndrome in a dichorionic-diamniotic gestation with post-laser amniotic band sequence: A case report 双绒毛膜-双羊膜妊娠伴激光后羊膜带序列双胎输血综合征1例
IF 0.6 Q4 OBSTETRICS & GYNECOLOGY Pub Date : 2026-01-03 DOI: 10.1016/j.crwh.2026.e00783
Melissa Chambers, Madushka Y. De Zoysa , Tamera Hatfield
Twin-twin transfusion syndrome most commonly develops in monochorionic-diamniotic twin pregnancies but rarely has been documented in dichorionic pregnancies. Twin-twin transfusion syndrome can often be successfully treated with fetoscopic laser surgery; sequelae are infrequent but can include chorion-amnion membrane separation, preterm rupture of membranes, preterm delivery, neurodevelopmental delay, and, rarely, amniotic band syndrome.
This report concerns the case of a 30-year-old nulligravid woman who presented for routine anatomy evaluation in the setting of a dichorionic-diamniotic monozygotic twin pregnancy. On initial evaluation, selective growth restriction with discordant amniotic fluid was noted, concerning for the development of twin-twin transfusion syndrome. On subsequent evaluation, she was diagnosed with stage 2 twin-twin transfusion syndrome and underwent successful fetoscopic laser ablation at 20 weeks of gestation. Ultimately, the patient underwent cesarean section at 29 weeks for labor after rupture of membranes. The postnatal course was complicated by amniotic band syndrome in one of the neonates.
This case highlights twin-twin transfusion syndrome diagnosed in the rare setting of a dichorionic-diamniotic monozygotic twin pregnancy and a rare postoperative complication of amniotic band syndrome after fetoscopic laser surgery.
双胎输血综合征最常见于单绒毛膜-双绒毛膜双胎妊娠,但很少见于双绒毛膜妊娠。双胎输血综合征通常可以通过胎儿镜激光手术成功治疗;后遗症不常见,但可包括绒毛膜-羊膜分离、胎膜早破、早产、神经发育迟缓,以及罕见的羊膜带综合征。本报告涉及的情况下,30岁无妊娠妇女谁提出了常规解剖评估设置双绒毛膜-双羊膜单卵双胎妊娠。在初步评估中,注意到羊水不一致导致的选择性生长限制,这与双胞胎输血综合征的发展有关。在随后的评估中,她被诊断为2期双胎输血综合征,并在妊娠20周成功接受了胎儿镜激光消融。最终,患者在29周时因胎膜破裂接受了剖宫产。其中1例新生儿出现羊膜带综合征。本病例强调了在罕见的双绒毛膜-双羊膜单卵双胞胎妊娠中诊断出的双胞胎输血综合征和胎儿镜激光手术后罕见的羊膜带综合征的术后并发症。
{"title":"Twin-twin transfusion syndrome in a dichorionic-diamniotic gestation with post-laser amniotic band sequence: A case report","authors":"Melissa Chambers,&nbsp;Madushka Y. De Zoysa ,&nbsp;Tamera Hatfield","doi":"10.1016/j.crwh.2026.e00783","DOIUrl":"10.1016/j.crwh.2026.e00783","url":null,"abstract":"<div><div>Twin-twin transfusion syndrome most commonly develops in monochorionic-diamniotic twin pregnancies but rarely has been documented in dichorionic pregnancies. Twin-twin transfusion syndrome can often be successfully treated with fetoscopic laser surgery; sequelae are infrequent but can include chorion-amnion membrane separation, preterm rupture of membranes, preterm delivery, neurodevelopmental delay, and, rarely, amniotic band syndrome.</div><div>This report concerns the case of a 30-year-old nulligravid woman who presented for routine anatomy evaluation in the setting of a dichorionic-diamniotic monozygotic twin pregnancy. On initial evaluation, selective growth restriction with discordant amniotic fluid was noted, concerning for the development of twin-twin transfusion syndrome. On subsequent evaluation, she was diagnosed with stage 2 twin-twin transfusion syndrome and underwent successful fetoscopic laser ablation at 20 weeks of gestation. Ultimately, the patient underwent cesarean section at 29 weeks for labor after rupture of membranes. The postnatal course was complicated by amniotic band syndrome in one of the neonates.</div><div>This case highlights twin-twin transfusion syndrome diagnosed in the rare setting of a dichorionic-diamniotic monozygotic twin pregnancy and a rare postoperative complication of amniotic band syndrome after fetoscopic laser surgery.</div></div>","PeriodicalId":9657,"journal":{"name":"Case Reports in Women's Health","volume":"49 ","pages":"Article e00783"},"PeriodicalIF":0.6,"publicationDate":"2026-01-03","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"146073688","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Autoimmune syndrome induced by adjuvants (ASIA) following urethral sling placement: A case report 尿道吊带放置后佐剂诱导的自身免疫综合征(ASIA): 1例报告
IF 0.6 Q4 OBSTETRICS & GYNECOLOGY Pub Date : 2025-12-24 DOI: 10.1016/j.crwh.2025.e00778
Muhammed A.M. Hammad , Gustavo Gryzinski , Evelyn Minji Pak , Alexander Bell , Gamal Ghoniem
A 39-year-old woman developed debilitating systemic symptoms following the placement of a synthetic mid-urethral sling for stress urinary incontinence. Previously in good health, she experienced sepsis and adrenal crisis immediately postoperatively, followed by persistent symptoms including fatigue, postural orthostatic tachycardia syndrome (POTS), neuropathic pain, cognitive dysfunction, autonomic instability, and recurrent infections. Despite extensive multispecialty evaluations, no definitive diagnosis was initially reached. Laboratory testing later revealed positive ANA and mild immune dysregulation. Given her complex autoimmune history, strong family predisposition, and the temporal association with mesh implantation, her presentation was suspected to be consistent with autoimmune syndrome induced by adjuvants (ASIA). She elected to undergo surgical removal of the synthetic sling with placement of an autologous rectus fascia pubovaginal sling. Postoperatively, the patient experienced significant resolution of her symptoms, restored bladder function, and improved quality of life. This case demonstrates a temporal association consistent with ASIA, with complete symptom resolution by 3 months post-explant and sustained well-being at 1 year.
一名39岁女性在放置合成尿道中吊带治疗压力性尿失禁后出现衰弱的全身症状。先前健康状况良好,但术后立即出现败血症和肾上腺危机,随后出现持续症状,包括疲劳、体位性心动过速综合征(POTS)、神经性疼痛、认知功能障碍、自主神经不稳定和复发性感染。尽管进行了广泛的多专业评估,但最初没有得出明确的诊断。后来的实验室检测显示ANA阳性和轻度免疫失调。考虑到她复杂的自身免疫性病史,强烈的家族易感性,以及与补片植入的时间关联,她的表现被怀疑与佐剂诱导的自身免疫性综合征一致(ASIA)。她选择手术切除合成吊带,置入自体直肌筋膜耻骨阴道吊带。术后,患者症状明显缓解,膀胱功能恢复,生活质量提高。该病例表现出与亚洲相一致的时间相关性,在移植后3个月症状完全缓解,并在1年内保持健康。
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引用次数: 0
Small bowel volvulus secondary to torsion of a mature cystic teratoma in the first trimester of pregnancy: A case report 妊娠早期成熟囊性畸胎瘤继发于扭转的小肠扭转1例报告
IF 0.6 Q4 OBSTETRICS & GYNECOLOGY Pub Date : 2025-12-24 DOI: 10.1016/j.crwh.2025.e00776
Wondwosen Mengist Dereje , Biniam Gezahagn zewude , Gashaw Tesfa Aragaw , Meredin Nuru Seyide , Asmare Getaneh Aynishet , Misganaw Abere Worku , Samuel Addisu Abera , Gebremariam Maru Yemru , Alem Demissie Bogale , Asratu Getnet Amare , Fasil Tadesse Ashagrie
Small bowel volvulus is a rare but potentially life-threatening surgical emergency. Its occurrence in association with ovarian cyst torsion during pregnancy is exceedingly rare, with few cases reported. To the authors' best knowledge, this case represents the first documented instance occurring in the first trimester.
A 37-year-old woman (gravida 3, para 2) at 12 weeks +2 days of gestation was referred with a 16-h history of crampy abdominal pain, initially infraumbilical and later diffuse, accompanied by multiple episodes of vomiting, which progressed from ingested matter to bilious, and 12 h of progressive abdominal distension.
On presentation, she appeared acutely ill and in severe pain, with abdominal examination revealing generalized peritonitis. She was promptly started on intravenous antibiotics and fluid resuscitation, and an emergency laparotomy was performed. Intraoperatively, a torsioned adnexal mass, gangrenous right ovary, fallopian tube, and a segment of small bowel were identified and resected. The patient left the operating room with stable vital signs and was subsequently transferred to the ward, where she recovered well. Six months later, she delivered a healthy 3.5 kg female infant via repeat cesarean section, with no complications.
Although small bowel volvulus is rare, it must be considered in patients with intestinal obstruction. Delayed recognition can cause ischemia, necrosis, and perforation, so maintaining suspicion, performing timely investigations, and initiating early surgical intervention are essential to improve outcomes and reduce morbidity and mortality.
小肠扭转是一种罕见但可能危及生命的外科急症。它的发生与卵巢囊肿扭转妊娠期间是非常罕见的,少数病例报道。据作者所知,该病例是第一例发生在妊娠早期的病例。一名37岁妇女(妊娠3期,第2段),妊娠12周+2天,因16小时痉挛性腹痛病史就诊,最初是脐下腹痛,后来弥漫性腹痛,伴有多次呕吐,从摄入物质发展到胆汁,12小时进行性腹胀。在就诊时,她表现出急性不适和剧烈疼痛,腹部检查显示广泛性腹膜炎。她立即开始静脉注射抗生素和液体复苏,并进行了紧急剖腹手术。术中发现了一个扭转的附件肿块、坏疽的右卵巢、输卵管和一段小肠,并予以切除。患者出院时生命体征稳定,随后转至病房,恢复良好。6个月后,她通过重复剖宫产产下一名体重3.5公斤的女婴,无并发症。虽然小肠扭转是罕见的,但在肠梗阻患者中必须加以考虑。延迟识别可导致缺血、坏死和穿孔,因此保持怀疑、及时调查和早期手术干预对改善预后和降低发病率和死亡率至关重要。
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引用次数: 0
Pregnancy care and intrapartum management of a woman with high-level cervical spinal cord injury and neurogenic bladder: a case report 高位颈脊髓损伤伴神经源性膀胱1例妊娠护理及产时处理
IF 0.6 Q4 OBSTETRICS & GYNECOLOGY Pub Date : 2025-12-23 DOI: 10.1016/j.crwh.2025.e00777
Monchai Suntipap , Thanathip Samitinthu , Potsanop Kassayanan , Tanapat Pansaksiri , Kasidis Nontaprom
Pregnancy in women with high-level cervical spinal cord injury presents complex challenges, particularly related to autonomic instability, neurogenic bladder dysfunction, and risks of autonomic dysreflexia. Optimal management requires coordinated multidisciplinary care and individualized delivery planning. The case is presented of a 32-year-old woman (gravida 4, para 1) with a chronic spinal cord injury involving the sixth and seventh cervical levels, with neurogenic bladder and bilateral vesicoureteral reflux. Her urodynamic profile evolved from detrusor areflexia to reduced compliance with terminal detrusor overactivity, managed with clean intermittent catheterization. Pregnancy was closely monitored with multidisciplinary collaboration. At 38 weeks and 3 days of gestation, she presented in spontaneous active labor with stable hemodynamics and no features of autonomic dysreflexia. Continuous bladder drainage was instituted, and rapid cervical progression precluded neuraxial anesthesia. A supervised vaginal delivery was achieved in a semi-recumbent position without autonomic instability. A healthy male neonate was delivered with Apgar scores of 9 and 9. Postpartum recovery was uncomplicated, including postpartum tubal ligation and structured bladder management with temporary Foley drainage followed by resumption of clean intermittent catheterization. Renal surveillance and early outpatient follow-up confirmed stable maternal and neonatal outcomes. This case demonstrates that vaginal delivery can be safely accomplished in select women with high-level cervical spinal cord injury when multidisciplinary care, optimized bladder management, and vigilant intrapartum monitoring are available. Individualized, condition-based decision-making should guide the mode of delivery rather than neurological level alone.
高水平颈脊髓损伤妇女的妊娠带来了复杂的挑战,特别是与自主神经不稳定、神经源性膀胱功能障碍和自主神经反射障碍的风险有关。最佳管理需要协调多学科护理和个性化交付计划。该病例是一名32岁妇女(妊娠4,第1段),慢性脊髓损伤累及第6和第7颈椎段,伴有神经源性膀胱和双侧膀胱输尿管反流。她的尿动力学特征从逼尿肌反射到晚期逼尿肌过度活动的依从性降低,并通过清洁的间歇导尿进行管理。多学科合作密切监测妊娠情况。妊娠38周零3天,产妇为主动产程,血流动力学稳定,无自主神经反射障碍。持续膀胱引流,颈椎快速进展排除了神经轴麻醉。在监督下阴道分娩是在半卧位,没有自主神经不稳定。一名健康男性新生儿出生时,Apgar评分分别为9和9。产后恢复并不复杂,包括产后输卵管结扎和结构化膀胱管理,临时Foley引流,随后恢复清洁间歇导尿。肾脏监测和早期门诊随访证实了稳定的产妇和新生儿结局。该病例表明,在多学科护理、优化膀胱管理和警惕的产时监测的情况下,阴道分娩可以安全地完成对高水平颈脊髓损伤妇女的选择。个性化的、基于条件的决策应该指导分娩方式,而不是仅仅从神经层面来指导。
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引用次数: 0
期刊
Case Reports in Women's Health
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