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Vaginal Calculus Formation on Exposed Midurethral Sling Mesh. 暴露的尿道中段吊带网形成阴道结石。
Q4 OBSTETRICS & GYNECOLOGY Pub Date : 2024-03-16 eCollection Date: 2024-01-01 DOI: 10.1155/2024/8287400
Adam J Langer, Zenab Saeed, Elizabeth Barrett, Rose A Maxwell, David N Dhanraj, Geoffrey D Towers, Eyra A Agudu

The presence of a vaginal calculus is a rare clinical entity which may develop in the setting of vaginal urinary stagnation. Numerous factors contribute to stone formation, and management can be complicated by variations in size, location of the stone, and location of adjacent structures. Generally, once diagnosed, vaginal calculi should be removed and surrounding anatomy should be evaluated thoroughly for secondary fistula, erosion, or presence of an instituting foreign body. This report presents a case of vaginal calculus formation on exposed midurethral sling mesh in an elderly patient with hemorrhagic cystitis. This report emphasizes contributing pathophysiology, diagnostic factors, and treatment.

阴道结石是一种罕见的临床症状,可能在阴道尿液淤积的情况下出现。导致结石形成的因素有很多,结石的大小、位置和邻近结构的位置都会使处理变得复杂。一般来说,一旦确诊为阴道结石,应立即将其取出,并彻底评估周围的解剖结构,看是否有继发性瘘管、侵蚀或异物存在。本报告介绍了一例患有出血性膀胱炎的老年患者,其阴道结石形成于暴露的尿道中段吊带网片上。本报告强调了病理生理学、诊断因素和治疗方法。
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引用次数: 0
Acute Abdomen in Pregnancy due to Idiopathic Chylous Ascites. 特发性乳糜腹水导致的妊娠期急性腹部。
IF 0.6 Q4 OBSTETRICS & GYNECOLOGY Pub Date : 2024-02-29 eCollection Date: 2024-01-01 DOI: 10.1155/2024/8898451
Claudia Epelde, Fátima Saravia, Mónica Aguinaga, Ane Toledo, Arantza Lekuona, Mikel Gorostidi

Chylous ascites results from the leakage of lymph rich in lipids into the peritoneal cavity and represents an exceedingly rare event in the course of pregnancy. While there are numerous documented instances of this pathology manifesting with hypogastric or diffuse abdominal pain, our report highlights a unique presentation involving a 35-week pregnant woman experiencing severe epigastric pain unrelated to pregnancy-induced hypertension or other gastrointestinal disorders. Major acute obstetric pathologies were ruled out, and there was no evidence of fetal distress. Due to uncontrolled pain with an unidentified etiology and an unfavorable Bishop score, an urgent cesarean section was performed. A copious amount of milky fluid was observed during the surgery, subsequently confirmed as chylous in nature. Both the newborn and the mother had positive outcomes postsurgery. Although it is usually a benign condition, it is important for healthcare professionals to be aware of this entity in order to provide timely medical care and administer appropriate treatment.

乳糜腹水是富含脂质的淋巴液渗入腹腔所致,在妊娠过程中极为罕见。这种病理现象表现为下腹或弥漫性腹痛的病例不胜枚举,而我们的报告则强调了一种独特的表现形式,即一名怀孕 35 周的孕妇出现剧烈上腹痛,与妊娠高血压或其他胃肠道疾病无关。排除了主要的产科急性病症,也没有胎儿窘迫的证据。由于疼痛无法控制,病因不明,且比绍普评分不理想,医生紧急实施了剖腹产手术。手术中观察到大量乳白色液体,随后证实为乳糜液。新生儿和母亲术后均恢复良好。虽然乳糜泻通常是一种良性病症,但医护人员仍有必要了解这种病症,以便及时提供医疗护理和适当的治疗。
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引用次数: 0
Well-Differentiated Liposarcoma That Increased in Size after Menopause: A Case Report and a Review of the Literature. 绝经后体积增大的分化良好脂肪肉瘤:病例报告和文献综述。
Q4 OBSTETRICS & GYNECOLOGY Pub Date : 2024-02-24 eCollection Date: 2024-01-01 DOI: 10.1155/2024/7599714
Tatsuji Hoshino, Yoshihiro Takada, Ayako Sugihara, Masato Kinugasa, Yoshiyuki Tsuji

This study reports a case of uterine liposarcoma together with a literature review. At 52 years old, our patient was diagnosed with lipoleiomyoma by MRI. A mass (39 × 32 × 41 mm3) protruding from the anterior wall of the uterine body was observed. When the patient was 58, her previous doctor found that the tumor had grown, and she was referred to the gynecology department of our hospital. On MRI, the major diameter was 1.23-fold longer and the volume was 1.85-fold higher compared with the prior imaging findings. Diffusion-weighted images revealed no significant anomalous signals. Thus, malignant tumors were included in the differential diagnosis. The patient consented to total abdominal hysterectomy and bilateral salpingo-oophorectomy. The mass on the anterior wall remained completely in the myometrium. No implantation was found in the abdominal cavity, and ascites was not detected. No bleeding or necrosis was observed on the cut surface. Histopathologically, differences in the sizes of adipocytes and stromal cells were identified. There were irregularities in the nuclear findings. The immunohistochemical findings were as follows: CDK4 (+), desmin (+), S100p (-), and Ki - 67 = 1%. Therefore, a diagnosis of well-differentiated liposarcoma was rendered. The lesion was localized in the uterus, and it was completely removed during surgery. Well-differentiated liposarcoma of uterine primary has no possibility of recurrence following complete resection, and thus, the patient underwent follow-up without additional treatment. No metastasis or recurrence has been observed for 10 months after surgery.

本研究报告了一例子宫脂肪肉瘤病例,并对相关文献进行了综述。患者 52 岁,经核磁共振检查确诊为脂肪组织肌瘤。患者的子宫体前壁有一个突出的肿块(39 × 32 × 41 mm3)。患者 58 岁时,她之前的医生发现肿瘤长大了,于是将她转诊到我院妇科。核磁共振成像显示,与之前的成像结果相比,肿瘤的大直径长了 1.23 倍,体积增大了 1.85 倍。弥散加权成像未发现明显异常信号。因此,恶性肿瘤被纳入鉴别诊断。患者同意接受全腹子宫切除术和双侧输卵管切除术。前壁的肿块完全留在子宫肌层中。腹腔内未发现种植,也未发现腹水。切口表面未发现出血或坏死。从组织病理学角度看,脂肪细胞和基质细胞的大小存在差异。细胞核结果不规则。免疫组化结果如下:CDK4(+)、desmin(+)、S100p(-)和 Ki - 67 = 1%。因此,诊断结果为分化良好的脂肪肉瘤。病灶位于子宫内,手术中将其完全切除。子宫原发的分化良好的脂肪肉瘤在完全切除后没有复发的可能,因此,患者接受了后续治疗,没有接受额外的治疗。术后 10 个月未发现转移或复发。
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引用次数: 0
Ovarian Torsion in a Young Adolescent with Rokitansky Syndrome. 一名患有罗基坦斯基综合征的青少年的卵巢扭转。
Q4 OBSTETRICS & GYNECOLOGY Pub Date : 2024-02-22 eCollection Date: 2024-01-01 DOI: 10.1155/2024/1305476
Francesco Fedele, Giovanna Esposito, Andrea Busnelli, Fabio Parazzini

A case report of a premenarcheal patient with ovarian torsion and mullerian agenesis is presented. A 12-year-old prepubertal girl is presented with severe right lower quadrant abdominal pain and mild rebound. Laparoscopy showed mullerian agenesis and twisted right adnexa. Detorsion and cystectomy of the right ovary were done, and the ovary was fixed to the pelvic sidewall. The postoperative course was uneventful. An association between the lax attachment of the adnexa and torsion may be a contributing factor in this condition.

本病例报告了一名患有卵巢扭转和穆勒氏管缺失的初潮前患者。一名 12 岁的青春期前女孩因严重的右下腹疼痛和轻度反跳就诊。腹腔镜检查显示穆勒氏管发育不全和右侧附件扭转。患者接受了右卵巢剥离和囊肿切除术,并将卵巢固定在盆腔侧壁上。术后恢复顺利。附件附着松弛与扭转之间的关联可能是导致这种情况的一个因素。
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引用次数: 0
A Case of Painful Growing Abdominal Wall Mass during Pregnancy Requiring Resection in the Second Trimester 一例妊娠期腹壁肿块不断增大且疼痛难忍,需在妊娠第二孕期切除的病例
Q4 OBSTETRICS & GYNECOLOGY Pub Date : 2024-01-08 DOI: 10.1155/2024/5881260
S. Stemmer, Cintia Gomes, E. Cardonick
Desmoid fibromatosis (DF) is a rare and locally aggressive neoplasm. We present a case of a 28-year-old previously healthy multigravida who noticed a lump in her abdomen near the umbilicus two months before becoming pregnant. It underwent rapid growth during pregnancy, causing pain and discomfort. Targeted ultrasound of the area showed an irregular mass measuring 0.9×1.7×1.4 cm. The origin of the mass was unclear, suggesting a connection with the intra-abdominal contents. An MRI done three weeks later revealed a subcutaneous ovoid mass measuring 3.0×2.3×3.0 cm, which was significantly larger. Due to pain and rapid growth, surgical resection was done at 25 weeks of pregnancy. Histopathological examination revealed a desmoid tumor. The patient had an uneventful recovery and term vaginal delivery without complications. Hence, our case serves as evidence that DF tumors can be surgically managed during pregnancy with minimal to no complications.
脱模性纤维瘤病(DF)是一种罕见的局部侵袭性肿瘤。我们介绍了一例 28 岁的多胎孕妇,她在怀孕前两个月发现腹部靠近脐部有一个肿块。肿块在怀孕期间迅速增大,引起疼痛和不适。对该部位进行的定向超声波检查显示,该处有一个 0.9×1.7×1.4 厘米的不规则肿块。肿块的来源不清,提示与腹腔内容物有关。三周后的核磁共振成像显示,皮下卵圆形肿块大小为 3.0×2.3×3.0 厘米,明显增大。由于疼痛和生长迅速,在怀孕 25 周时进行了手术切除。组织病理学检查显示为脱模瘤。患者术后恢复顺利,经阴道分娩,无并发症。因此,我们的病例证明,DF 肿瘤可以在妊娠期间通过手术治疗,并发症极少甚至没有。
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引用次数: 0
A Rare Case of Neurosyphilis with Calvaria Osteitis Presenting in Pregnancy 一例罕见的妊娠期神经梅毒伴钙化性骨炎病例
Q4 OBSTETRICS & GYNECOLOGY Pub Date : 2023-12-19 DOI: 10.1155/2023/8856775
Gisella M. Newbery, Christine E. Henricks, Julie A. Vircks, A. Colina, David C. Mundy
Background. The incidence of syphilis throughout the world is increasing. Rates in pregnancy are similarly rising, presenting risks of an untreated syphilis infection that can be detrimental to the mother and fetus. Although routine screening for syphilis infections is recommended at the initial prenatal visit, there is a lack of universal agreement on rescreening pregnant people and approximately 50% of syphilis cases are asymptomatic in the general population. Furthermore, some symptoms of syphilis can overlap with nonspecific pregnancy-related symptoms. Meanwhile, Treponema pallidum can spread to various maternal and fetoplacental tissues quickly after infection and occur at any stage of syphilis. Case. A 26-year-old gravida 5 para 2 presented with a new onset headache and visual and auditory changes at 23 weeks of gestation. A computerized tomography scan revealed numerous ill-defined lytic lesions throughout the calvarium, suspicious for syphilitic osteitis. She tested positive for syphilis antibodies with a rapid plasma reagin (RPR) titer of 1 : 32. Cerebrospinal fluid evaluation from a lumbar puncture resulted in reactive fluorescent treponemal antibody (FTA) testing. She was diagnosed with secondary syphilis with osteitis and neuro and otic components. She completed 14 days of intravenous aqueous crystalline penicillin G with additional benzathine penicillin G 2.4 million units intramuscular weekly for two weeks. There was no evidence of congenital syphilis on neonatal examination. Conclusion. Syphilitic osteitis and neuro, otic, or ocular syphilis infections occur rarely in the nonpregnant population, and therefore, little data in pregnancy is available to inform outcomes in these specific disease states. It is of paramount importance to complete appropriate syphilis screening, recognize symptoms, and consider utilizing rescreen protocols to ensure prompt infection identification and treatment. For neuro, otic, and ocular syphilis, aqueous crystalline penicillin G (as opposed to benzathine penicillin G) is required to achieve treponemicidal concentrations in those physiologic compartments. There is no agreement as to the appropriate treatment regimen for the rare finding of syphilitic osteitis.
背景。梅毒在全世界的发病率不断上升。妊娠期梅毒感染率也同样在上升,梅毒感染未经治疗可能会对母亲和胎儿造成危害。虽然建议在初次产前检查时对梅毒感染进行常规筛查,但对孕妇的再筛查缺乏普遍共识,在普通人群中约有 50%的梅毒病例是无症状的。此外,梅毒的某些症状可能与非特异性妊娠相关症状重叠。同时,苍白螺旋体可在感染后迅速扩散到各种母体和胎盘组织,并发生在梅毒的任何阶段。病例一名 26 岁的孕 5 停 2 期妇女在妊娠 23 周时出现新发头痛、视听改变。计算机断层扫描发现整个小腿有许多界限不清的溶解性病变,怀疑是梅毒性骨炎。她的梅毒抗体检测呈阳性,快速血浆试剂(RPR)滴度为 1 :32.腰椎穿刺的脑脊液评估结果显示,荧光三腺抗体(FTA)检测呈反应性。她被诊断为继发性梅毒,伴有骨炎、神经和耳部感染。她接受了为期14天的晶体青霉素G水溶液静脉注射,并在两周内每周追加苄星青霉素G 240万单位肌肉注射。新生儿检查没有发现先天性梅毒。结论梅毒性骨炎和神经、耳部或眼部梅毒感染很少发生在非孕期人群中,因此,几乎没有孕期数据可以为这些特殊疾病的治疗结果提供参考。最重要的是完成适当的梅毒筛查、识别症状并考虑使用重筛方案,以确保及时发现和治疗感染。对于神经梅毒、耳梅毒和眼梅毒,需要使用水性结晶青霉素G(而非苄星青霉素G),以在这些生理区域达到杀三联体浓度。对于梅毒性骨炎这一罕见病症的适当治疗方案,目前尚无一致意见。
{"title":"A Rare Case of Neurosyphilis with Calvaria Osteitis Presenting in Pregnancy","authors":"Gisella M. Newbery, Christine E. Henricks, Julie A. Vircks, A. Colina, David C. Mundy","doi":"10.1155/2023/8856775","DOIUrl":"https://doi.org/10.1155/2023/8856775","url":null,"abstract":"Background. The incidence of syphilis throughout the world is increasing. Rates in pregnancy are similarly rising, presenting risks of an untreated syphilis infection that can be detrimental to the mother and fetus. Although routine screening for syphilis infections is recommended at the initial prenatal visit, there is a lack of universal agreement on rescreening pregnant people and approximately 50% of syphilis cases are asymptomatic in the general population. Furthermore, some symptoms of syphilis can overlap with nonspecific pregnancy-related symptoms. Meanwhile, Treponema pallidum can spread to various maternal and fetoplacental tissues quickly after infection and occur at any stage of syphilis. Case. A 26-year-old gravida 5 para 2 presented with a new onset headache and visual and auditory changes at 23 weeks of gestation. A computerized tomography scan revealed numerous ill-defined lytic lesions throughout the calvarium, suspicious for syphilitic osteitis. She tested positive for syphilis antibodies with a rapid plasma reagin (RPR) titer of 1 : 32. Cerebrospinal fluid evaluation from a lumbar puncture resulted in reactive fluorescent treponemal antibody (FTA) testing. She was diagnosed with secondary syphilis with osteitis and neuro and otic components. She completed 14 days of intravenous aqueous crystalline penicillin G with additional benzathine penicillin G 2.4 million units intramuscular weekly for two weeks. There was no evidence of congenital syphilis on neonatal examination. Conclusion. Syphilitic osteitis and neuro, otic, or ocular syphilis infections occur rarely in the nonpregnant population, and therefore, little data in pregnancy is available to inform outcomes in these specific disease states. It is of paramount importance to complete appropriate syphilis screening, recognize symptoms, and consider utilizing rescreen protocols to ensure prompt infection identification and treatment. For neuro, otic, and ocular syphilis, aqueous crystalline penicillin G (as opposed to benzathine penicillin G) is required to achieve treponemicidal concentrations in those physiologic compartments. There is no agreement as to the appropriate treatment regimen for the rare finding of syphilitic osteitis.","PeriodicalId":9610,"journal":{"name":"Case Reports in Obstetrics and Gynecology","volume":"119 34","pages":""},"PeriodicalIF":0.0,"publicationDate":"2023-12-19","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"138959699","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
Lethal Neural Tube Defects: Reports of Anencephaly and Craniorachischisis Cases and Literature Review 致命的神经管缺陷:无脑畸形和颅骨畸形病例报告及文献综述
Q4 OBSTETRICS & GYNECOLOGY Pub Date : 2023-12-19 DOI: 10.1155/2023/4017625
A. Lema, Jemila Salih Suleyman
Neural tube defects are serious birth defects of the central nervous system that result from a multifaceted disruption of normal embryogenesis of the nervous system. Although largely preventable, they nonetheless pose a serious threat to global morbidity, disability, mortality, and financial expenses. Despite this, it has been neglected and has only been the subject of limited research until recently. Furthermore, surveillance efforts for neural tube defects remain limited, and no decline in defects has been documented in less developed countries. Here, we report two cases of craniorachischisis and one case of discordant twins for anencephaly. Moreover, the relevant works of literature that are necessary to understand and address this unrelenting phenomenon are provided.
神经管畸形是中枢神经系统的严重先天缺陷,是神经系统正常胚胎发育受到多方面破坏的结果。尽管在很大程度上是可以预防的,但它们对全球的发病率、残疾、死亡率和经济支出构成了严重威胁。尽管如此,神经管畸形一直被忽视,直到最近才进行了有限的研究。此外,对神经管畸形的监测工作仍然有限,在欠发达国家也没有记录到神经管畸形的减少。在此,我们报告了两例颅内畸形和一例无脑畸形不协调双胞胎。此外,我们还提供了相关的文献资料,这些资料对于理解和解决这一屡禁不止的现象十分必要。
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引用次数: 0
A Case of Ruptured Exophytic Uterine Artery Pseudoaneurysm without Specific Risk Factors That Manifested Seven Days after Vaginal Delivery. 阴道分娩后7天无特殊危险因素的子宫外生性动脉假性动脉瘤破裂1例。
Q4 OBSTETRICS & GYNECOLOGY Pub Date : 2023-11-25 eCollection Date: 2023-01-01 DOI: 10.1155/2023/1637463
Masatake Toshimitsu, Takayuki Iriyama, Jiro Sato, Osamu Abe, Mari Ichinose, Seisuke Sayama, Takahiro Seyama, Kenbun Sone, Keiichi Kumasawa, Yutaka Osuga

A uterine artery pseudoaneurysm (UAP) is a life-threatening complication during pregnancy and postpartum. Early diagnosis of exophytic UAP rupture is difficult due to the absence of vaginal bleeding. This study reports the case of a 31-year-old postpartum woman who presented with abdominal pain and fever seven days after vaginal delivery, without symptoms of maternal shock. Ultrasonography revealed a ruptured exophytic UAP with hemoperitoneum, which was confirmed using computed tomography. Interventional radiology confirmed that the site of the pseudoaneurysm was at the level of the uterine artery bifurcation, and embolization was performed immediately after diagnosis using a coil and n-butyl-2-cyanoacrylate. The patient's symptoms were relieved, and she was discharged 12 days after the embolization. At eight months postpartum, the UAP was not visible on transvaginal ultrasonography. Exophytic UAP can occur even in the absence of specific risk factors such as cesarean section or endometriosis, and the UAP may not necessarily rupture immediately after delivery. Obstetricians must remain aware of the possibility of exophytic UAP rupture manifesting as abdominal pain with postpartum fever, rather than as unstable vital signs. This is the first report of an exophytic UAP that occurred at the level of the uterine artery bifurcation. Identification of the sites where exophytic UAP can occur can aid in the early diagnosis of the condition.

子宫动脉假性动脉瘤(UAP)是妊娠和产后危及生命的并发症。由于没有阴道出血,外生性UAP破裂的早期诊断是困难的。本研究报告了一例31岁的产后妇女,阴道分娩后7天出现腹痛和发烧,无产妇休克症状。超声检查显示外生性UAP破裂伴腹膜出血,经计算机断层扫描证实。介入放射学证实假性动脉瘤位于子宫动脉分叉处,诊断后立即用线圈和正丁-2-氰基丙烯酸酯栓塞。患者症状缓解,栓塞12天后出院。产后8个月,经阴道超声检查未见UAP。即使没有特定的危险因素,如剖宫产或子宫内膜异位症,外生性子宫内膜异位症也可能发生,而且子宫内膜异位症不一定在分娩后立即破裂。产科医生必须保持警惕外源性UAP破裂的可能性,表现为腹痛和产后发烧,而不是不稳定的生命体征。这是首次报道发生在子宫动脉分叉水平的外生性UAP。确定外生性UAP可能发生的部位有助于该病的早期诊断。
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引用次数: 0
Malignant Transformation of Unknown Duration of an Ovarian Mature Cystic Teratoma Presenting as a Trocar Recurrence in a Young Patient: A Case Report and Literature Review. 一个年轻的卵巢成熟囊性畸胎瘤以套管针复发为表现的恶性转化时间不明:一个病例报告和文献复习。
Q4 OBSTETRICS & GYNECOLOGY Pub Date : 2023-11-21 eCollection Date: 2023-01-01 DOI: 10.1155/2023/8875092
Tomohiro Okuda, Yoko Uda, Shiho Sakai, Taishi Harada

Although laparoscopic cystectomy is a safe and effective management strategy for ovarian mature cystic teratoma (MCT) in pediatric and adolescent patients, it has been challenged because of its association with a higher risk of intraoperative spillage leading to chemical peritonitis, adhesion formation, and iatrogenic implantation of malignant cells. Here, we report a rare case of a 23-year-old female patient with MCT tissue during laparoscopic ovarian cystectomy that remained in the peritoneum, possibly becoming malignant thereafter. Intraoperatively, the cyst's contents leaked into the abdominal cavity. The abdominal cavity was thoroughly cleaned before the operation was completed. Pathological examination revealed an MCT without malignant findings. The patient's postoperative course was uneventful. Although the excised tissue was benign, the patient presented with a mass at the trocar wound (upper suprapubic area) 2 years after initial surgery. Biopsy results indicated squamous cell carcinoma. Moreover, peritoneal and bladder invasions were diagnosed. She subsequently experienced symptoms of cancerous peritonitis. Achieving a complete cure through surgery alone was deemed difficult; however, successful neoadjuvant chemotherapy and tumor reduction surgery kept her alive up until the publication of this case report, 3 years since diagnosis with squamous cell carcinoma. This case indicates that malignant transformation of MCTs can occur at any age.

尽管腹腔镜膀胱切除术是一种安全有效的治疗儿科和青少年卵巢成熟囊性畸胎瘤(MCT)的方法,但由于其术中溢漏导致化学腹膜炎、粘连形成和恶性细胞医源性植入的风险较高,因此一直受到挑战。在此,我们报告一例罕见的23岁女性患者,在腹腔镜卵巢囊肿切除术中,MCT组织残留在腹膜中,此后可能成为恶性肿瘤。术中,囊肿内容物漏入腹腔。手术完成前腹腔已彻底清洁。病理检查显示MCT未见恶性。病人的术后过程平安无事。虽然切除的组织是良性的,但患者在首次手术2年后在套管针伤口(耻骨上区)出现肿块。活检结果提示鳞状细胞癌。此外,还诊断出腹膜和膀胱浸润。她随后出现癌性腹膜炎的症状。仅仅通过手术完全治愈被认为是困难的;然而,成功的新辅助化疗和肿瘤缩小手术使她活了下来,直到本病例报告发表,自诊断为鳞状细胞癌3年以来。这个病例表明mct的恶性转化可以发生在任何年龄。
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引用次数: 0
Placenta Accreta Spectrum with Ureteral Invasion due to Progression of Cesarean Scar Pregnancy. 剖宫产瘢痕妊娠进展引起输尿管侵犯的胎盘增生谱。
Q4 OBSTETRICS & GYNECOLOGY Pub Date : 2023-10-07 eCollection Date: 2023-01-01 DOI: 10.1155/2023/9065978
Nana Yara, Yoshino Kinjyo, Yukiko Chinen, Tadatsugu Kinjo, Keiko Mekaru

Expectant management is not recommended for cesarean scar pregnancies because they are often associated with placenta accreta, cesarean hysterectomy, and massive life-threatening hemorrhages during delivery. Herein, we report a case of placenta accreta spectrum with ureteral invasion due to the progression of a cesarean scar pregnancy. Case. A 41-year-old woman, with a history of three cesarean sections and two miscarriages, was referred to our hospital at 25 weeks of gestation with a diagnosis of placenta accreta spectrum and bladder invasion. Although the gestational sac was located anterior to the lower uterine segment, a cesarean-scar pregnancy was not diagnosed. A cesarean hysterectomy was performed at 31 weeks of gestation with the placement of an aortic balloon. The placenta was found to adhere to the ureter with more than the expected parenchymal tissue displacement (FIGO Classification 3b). The ureter was not obstructed and was preserved by leaving the placenta slightly on the ureteral side. Postoperatively, a ureteral stent was placed because of the ureteral stricture in the area where the placenta had adhered. Two months after surgery, the ureteral stent was removed after observing an improvement in stenosis. An adherent placenta due to continued cesarean scar pregnancy should be managed by assuming placental invasion beyond the parenchyma into the ureter.

不建议对剖宫产疤痕妊娠进行预期治疗,因为它们通常与胎盘植入、剖宫产子宫切除术和分娩期间危及生命的大出血有关。在此,我们报告了一例因剖宫产瘢痕妊娠进展而引起的胎盘植入谱伴输尿管侵犯的病例。案例一名41岁的女性,有三次剖宫产和两次流产的病史,在妊娠25周时被转诊至我院,诊断为胎盘植入谱和膀胱侵犯。尽管孕囊位于子宫下段前方,但未诊断为剖宫产瘢痕妊娠。在妊娠31周时进行剖宫产子宫切除术,放置主动脉球囊。发现胎盘粘附在输尿管上,实质组织移位超过预期(FIGO分类3b)。输尿管没有阻塞,通过将胎盘稍微留在输尿管侧而得以保留。术后,由于胎盘粘连区域的输尿管狭窄,放置了输尿管支架。术后两个月,在观察到狭窄情况有所改善后,取出输尿管支架。持续剖宫产瘢痕妊娠引起的粘连性胎盘应通过假定胎盘侵入实质以外的输尿管来处理。
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引用次数: 0
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Case Reports in Obstetrics and Gynecology
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