Case Reports in Obstetrics and Gynecology最新文献_第8页

Paracolpium Leiomyoma Misdiagnosed as Endometriosis: Case Report and Surgical Technique of a Laparoscopic Approach. 鞍旁平滑肌瘤误诊为子宫内膜异位症:1例报告及腹腔镜手术技术。

Case Reports in Obstetrics and Gynecology Pub Date : 2022-01-01 DOI: 10.1155/2022/7931391

Nilton de Nadai Filho, Claudio Peixoto Crispi Junior, Marlon de Freitas Fonseca

引用次数: 0

Zinc Deficiency-Associated Dysgeusia Preventing the Improvement of Severe Hyperemesis Gravidarum. 缺锌相关的厌食症预防重度妊娠剧吐的改善。

Case Reports in Obstetrics and Gynecology Pub Date : 2022-01-01 DOI: 10.1155/2022/7486501

Shohei Tanabe, Sachiyo Sugino, Kotaro Ichida, Kiyoshi Niiya, Syuji Morishima

引用次数: 0

Mixed Intervillositis in SARS-CoV-2 Infection Associated with Fetal Death: A Case Report. 与胎儿死亡相关的SARS-CoV-2感染混合性绒毛间炎1例报告

Case Reports in Obstetrics and Gynecology Pub Date : 2022-01-01 DOI: 10.1155/2022/5404952

Boban Gjakov, Darja Kopač, Mateja Vukmanič Pohar, Miha Lučovnik

引用次数: 0

A Case of Uterine Lymphangioleiomyomatosis Complicated by Tuberous Sclerosis Complex. 子宫淋巴管平滑肌瘤病合并结节性硬化症1例。

Case Reports in Obstetrics and Gynecology Pub Date : 2022-01-01 DOI: 10.1155/2022/2893975

Kaori Yamada, Yukio Yamanishi, Junichi Aratake, Nanayo Sasagasako, Yoshihide Inayama, Rei Gou, Atsuko Kawamura, Megumi Yamanishi, Kenzo Kosaka

{"title":"A Case of Uterine Lymphangioleiomyomatosis Complicated by Tuberous Sclerosis Complex.","authors":"Kaori Yamada, Yukio Yamanishi, Junichi Aratake, Nanayo Sasagasako, Yoshihide Inayama, Rei Gou, Atsuko Kawamura, Megumi Yamanishi, Kenzo Kosaka","doi":"10.1155/2022/2893975","DOIUrl":"https://doi.org/10.1155/2022/2893975","url":null,"abstract":"Lymphangioleiomyomatosis (LAM) is one of the presentations of perivascular epithelioid cell neoplasm that is frequently complicated by tuberous sclerosis complex (TSC). Here, we report an uncommon case of uterine LAM treated with everolimus, which is a mechanistic target of rapamycin (mTOR) inhibitor. A 42-year-old female patient (gravida 0) with a history of TSC presented with abdominal pain. Pelvic magnetic resonance imaging showed multiple masses in the uterine myometrium, suggesting tumors that may contain internal hemorrhagic components. The lesions were suspected as the root cause of her symptoms. After everolimus was administered for a previously diagnosed renal angiolipoma, her uterine tumors temporarily decreased in size. Subsequently, laparoscopic hysterectomy and bilateral salpingectomy were performed since she could not tolerate everolimus for a long period due to the medication's side effects. Furthermore, the patient was diagnosed with LAM through histopathological examination after surgical resection. Therefore, it is advisable to suspect and investigate uterine LAM when a patient with a history of TSC presents with irregular genital bleeding or abdominal pain. Moreover, mTOR inhibitors may be a treatment option, in addition to surgery, in cases of uterine LAM exacerbation.","PeriodicalId":9610,"journal":{"name":"Case Reports in Obstetrics and Gynecology","volume":"2022 ","pages":"2893975"},"PeriodicalIF":0.0,"publicationDate":"2022-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9767712/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"10428285","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

引用次数: 0

Advanced Ovarian Pregnancy: A Case Report of Misdiagnosis and Surgical Outcomes. 晚期卵巢妊娠1例误诊及手术结果分析。

Case Reports in Obstetrics and Gynecology Pub Date : 2022-01-01 DOI: 10.1155/2022/8856078

Noppamart Whangteeranon, Pang Pinyochotiwong

引用次数: 0

A Successful Pregnancy in a Hemihysterectomized Patient-A Case Report. 半子宫切除术患者成功妊娠1例报告。

Case Reports in Obstetrics and Gynecology Pub Date : 2022-01-01 DOI: 10.1155/2022/4627241

Sofia Jovina Domingues, Luísa Pinto

{"title":"A Successful Pregnancy in a Hemihysterectomized Patient-A Case Report.","authors":"Sofia Jovina Domingues, Luísa Pinto","doi":"10.1155/2022/4627241","DOIUrl":"https://doi.org/10.1155/2022/4627241","url":null,"abstract":"Introduction: Didelphys uterus, two separate uterine horns or a double uterus with two separate cervices, is one of several congenital uterine anomalies (CUA), accounting for 5% of CUA. CUA could be associated with dysmenorrhea, pelvic pain, and decreased fertility. During pregnancy, it has been associated with higher risk of miscarriage, preterm birth, malpresentation, and fetal growth restriction. There still is insufficient evidence on the efficacy and safety of surgical interventions in CUA, including hemihysterectomy, in what improvement of reproductive performance is concerned.Objective: The aim of the present case report is to review the literature and complement information on pregnancy outcomes after hemihysterectomy, contributing to a better counseling of women planning a pregnancy under these circumstances. Case Presentation. This paper case reports a successful pregnancy in a woman previously submitted to a hemihysterectomy and removal of a vaginal septum by hysteroscopy, due to a symptomatic didelphys uterus. An ipsilateral renal agenesis was also present. A cesarean was performed at 38 weeks' gestation and a healthy baby was born. Discussion. This paper reports an exceptional clinical situation, with only 9 cases described in the last 6 decades. As in previously reported cases, a cesarean was performed at term, resulting in a live childbirth. In these cases, a higher live birth rate and a lower incidence of preterm deliveries was found, comparing with uterine didelphys pregnancies.Conclusion: Understanding both the exact nature of a uterine anomaly before a surgical treatment and the prognosis for a future pregnancy after the intervention are of paramount importance for precise counseling of future parents.","PeriodicalId":9610,"journal":{"name":"Case Reports in Obstetrics and Gynecology","volume":"2022 ","pages":"4627241"},"PeriodicalIF":0.0,"publicationDate":"2022-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9763001/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"10420046","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

引用次数: 0

A Case of Primary Signet-Ring Cell Cervical Carcinoma Treated with Chemoradiation, Brachytherapy, and Adjuvant Hysterectomy. 放化疗、近距离放疗及辅助子宫切除术治疗原发性印戒细胞宫颈癌1例。

Case Reports in Obstetrics and Gynecology Pub Date : 2021-12-27 eCollection Date: 2021-01-01 DOI: 10.1155/2021/5544015

Nicole Salmen, Dominic LaBella, Kenneth Strumpf, Wiley Douglas Bunn, Paul Aridgides

{"title":"A Case of Primary Signet-Ring Cell Cervical Carcinoma Treated with Chemoradiation, Brachytherapy, and Adjuvant Hysterectomy.","authors":"Nicole Salmen, Dominic LaBella, Kenneth Strumpf, Wiley Douglas Bunn, Paul Aridgides","doi":"10.1155/2021/5544015","DOIUrl":"https://doi.org/10.1155/2021/5544015","url":null,"abstract":"Primary signet-ring cell carcinoma of the uterine cervix is a rare subtype of cervical mucinous adenocarcinoma. Approximately 20 cases of primary signet-ring cell carcinoma of the cervix have been reported. Pathologic examination shows that adenocarcinomas with mucin accumulation in intracytoplasmic vacuoles displacing the nucleus indicate signet-ring cell carcinoma. A thorough metastatic workup is needed both for staging and to rule out gastrointestinal tract origin. Due to the rarity of the disease, both the true incidence and optimal management are unknown. Herein, the authors present a case of stage 1B3 primary signet-ring cell cervical carcinoma treated with combined chemotherapy and radiation (including external beam radiation and brachytherapy), followed by resection for residual disease. This case is consistent with limited reports where all surviving patients received surgery as well as 1 surviving patient with bulky disease required with chemoradiation and adjuvant hysterectomy.","PeriodicalId":9610,"journal":{"name":"Case Reports in Obstetrics and Gynecology","volume":"2021 ","pages":"5544015"},"PeriodicalIF":0.0,"publicationDate":"2021-12-27","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8723868/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"39788035","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

引用次数: 1

A Pregnancy Case of Primary Mediastinal Large B Cell Lymphoma with Superior Vena Cava Syndrome. 妊娠原发性纵隔大B细胞淋巴瘤合并上腔静脉综合征1例。

Case Reports in Obstetrics and Gynecology Pub Date : 2021-12-22 eCollection Date: 2021-01-01 DOI: 10.1155/2021/3438230

Lauren Brownhalls, Ann Gillett, Yasmin Whately, Keisuke Tanaka

引用次数: 0

Low-Malignant Schwannoma of the Cervix in Pregnancy: A Case Report and Literature Systematic Review. 妊娠期宫颈低恶性神经鞘瘤1例报告及文献系统回顾。

Case Reports in Obstetrics and Gynecology Pub Date : 2021-12-09 eCollection Date: 2021-01-01 DOI: 10.1155/2021/6806960

Giada M Almirante, Francesco Cantatore, Gianluca Taccagni, Massimo Candiani, Massimo Origoni

{"title":"Low-Malignant Schwannoma of the Cervix in Pregnancy: A Case Report and Literature Systematic Review.","authors":"Giada M Almirante, Francesco Cantatore, Gianluca Taccagni, Massimo Candiani, Massimo Origoni","doi":"10.1155/2021/6806960","DOIUrl":"https://doi.org/10.1155/2021/6806960","url":null,"abstract":"Primary cervical melanocytic schwannomas, arising from the sympathetic chain, are very rare pigmented neural sheath tumors that, both grossly and clinically, are often misdiagnosed with other more frequent lesions of the uterine cervix. Literature review accounts for seventeen published cases of schwannomas of the cervix, ten of which are malignant and seven benign. Pathological examination with immunostaining techniques is essential for the correct diagnosis of these tumors. We report a case of primary cervical schwannoma in a 32-year-old female who was referred to our department at 13 weeks of gestation with a diagnosis of malignant melanoma of the cervix. Pathological review detailed a neoplasm with a myxoid spindle cell component and a minority of small epithelioid cells, with a low-malignant potential proliferation index: morphological and immunocytochemical findings were compatible with the diagnosis of nerve sheath tumor, type schwannoma. The patient underwent a vaginal trachelectomy and a prophylactic Shirodkar's cerclage. Pregnancy was carried on without any negative event. The patient delivered by a caesarean section a healthy female newborn. Placental histology was negative. After 6 years from the first diagnosis, the patient is healthy and disease free.","PeriodicalId":9610,"journal":{"name":"Case Reports in Obstetrics and Gynecology","volume":"2021 ","pages":"6806960"},"PeriodicalIF":0.0,"publicationDate":"2021-12-09","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8677399/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"39827978","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

引用次数: 1

Isolated Fallopian Tube Torsion: A Rare Entity. 孤立性输卵管扭转：罕见病例。

Case Reports in Obstetrics and Gynecology Pub Date : 2021-11-30 eCollection Date: 2021-01-01 DOI: 10.1155/2021/3872201

Indranil Banerjee, Yatin Thakur, Gargi Mukherjee, Jitendra Jadhav, Amita Sahare

引用次数: 0