Pub Date : 2024-08-02DOI: 10.1016/j.jpag.2024.07.008
Samuel Soares Coutinho, Luana Darc de Menezes Braga, Mylena Evilyn Sousa Costa, Mariana Oliveira Veloso, Ana Paula Negreiros Nunes Alves, Edmar Maciel Lima Júnior, Zenilda Vieira Bruno, Manoel Odorico de Moraes Filho, Carlos Roberto Koscky Paier, Felipe Augusto Rocha Rodrigues, Leonardo Robson Pinheiro Sobreira Bezerra
Background: Gonadal dysgenesis, a genetic condition characterized by incomplete of defective formation of the gonads, can present with vaginal agenesis in individuals with 46, XY karyotype.
Case: We report an innovative intervention in the management of vaginal agenesis in a 19-year-old female with gonadal dysgenesis. Despite initial attempts with vaginal dilators, the patient presented unresponsive, leading to the adoption of a neovaginoplasty using Nile Tilapia Fish Skin (NTFS) as graft. The procedure, based on the McIndoe technique, involved the creation of a 10 cm x 3 cm vaginal canal with an NTFS-wrapped acrylic mold without complications.
Conclusion: The use of NTFS as a graft for neovaginoplasty in gonadal dysgenesis, a novel approach not previously reported in medical literature for this diagnosis, demonstrated favorable outcomes in terms of functionality and patient well-being.
{"title":"Neovaginoplasty With Nile Tilapia Skin Graft in A Patient With Gonadal Dysgenesis: A Case Report.","authors":"Samuel Soares Coutinho, Luana Darc de Menezes Braga, Mylena Evilyn Sousa Costa, Mariana Oliveira Veloso, Ana Paula Negreiros Nunes Alves, Edmar Maciel Lima Júnior, Zenilda Vieira Bruno, Manoel Odorico de Moraes Filho, Carlos Roberto Koscky Paier, Felipe Augusto Rocha Rodrigues, Leonardo Robson Pinheiro Sobreira Bezerra","doi":"10.1016/j.jpag.2024.07.008","DOIUrl":"10.1016/j.jpag.2024.07.008","url":null,"abstract":"<p><strong>Background: </strong>Gonadal dysgenesis, a genetic condition characterized by incomplete of defective formation of the gonads, can present with vaginal agenesis in individuals with 46, XY karyotype.</p><p><strong>Case: </strong>We report an innovative intervention in the management of vaginal agenesis in a 19-year-old female with gonadal dysgenesis. Despite initial attempts with vaginal dilators, the patient presented unresponsive, leading to the adoption of a neovaginoplasty using Nile Tilapia Fish Skin (NTFS) as graft. The procedure, based on the McIndoe technique, involved the creation of a 10 cm x 3 cm vaginal canal with an NTFS-wrapped acrylic mold without complications.</p><p><strong>Conclusion: </strong>The use of NTFS as a graft for neovaginoplasty in gonadal dysgenesis, a novel approach not previously reported in medical literature for this diagnosis, demonstrated favorable outcomes in terms of functionality and patient well-being.</p>","PeriodicalId":16708,"journal":{"name":"Journal of pediatric and adolescent gynecology","volume":" ","pages":""},"PeriodicalIF":1.7,"publicationDate":"2024-08-02","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141889559","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2024-08-02DOI: 10.1016/j.jpag.2024.07.006
Heather Appelbaum
Minimally invasive surgery (MIS) techniques, including vaginoscopy, laparoscopy and robotic-assisted surgery (RAS), have revolutionized the field of gynecology, offering numerous benefits such as reduced postoperative pain, shorter hospital stays, and faster recovery. While these techniques are widely employed in adult gynecologic surgery, their application in pediatric and adolescent patients requires careful consideration due to anatomical differences, patient size, and specific surgical requirements in children. Various aspects of MIS in pediatric and adolescent gynecology, including patient positioning, laparoscopic and robotic instrument choices, trocar placement, surgical techniques, and perioperative pediatric adaptations to MIS are discussed. The findings highlight the unique challenges and opportunities in performing MIS for pediatric and adolescent patients undergoing gyn surgery, emphasizing the need for specialized training and multidisciplinary collaboration.
微创手术(MIS)技术,包括阴道镜、腹腔镜和机器人辅助手术(RAS),为妇科领域带来了革命性的变化,具有减少术后疼痛、缩短住院时间和加快康复等诸多优点。虽然这些技术被广泛应用于成人妇科手术,但由于解剖学差异、患者体型以及儿童的特殊手术要求,在儿童和青少年患者中应用这些技术还需慎重考虑。本文讨论了 MIS 在小儿和青少年妇科中的各个方面,包括患者定位、腹腔镜和机器人器械的选择、套管放置、手术技巧以及围手术期小儿对 MIS 的适应性。研究结果突显了为接受妇科手术的儿童和青少年患者实施 MIS 所面临的独特挑战和机遇,强调了专业培训和多学科合作的必要性。
{"title":"Perioperative and Operative Considerations for Minimally Invasive Surgery in Pediatric and Adolescent Gynecology.","authors":"Heather Appelbaum","doi":"10.1016/j.jpag.2024.07.006","DOIUrl":"https://doi.org/10.1016/j.jpag.2024.07.006","url":null,"abstract":"<p><p>Minimally invasive surgery (MIS) techniques, including vaginoscopy, laparoscopy and robotic-assisted surgery (RAS), have revolutionized the field of gynecology, offering numerous benefits such as reduced postoperative pain, shorter hospital stays, and faster recovery. While these techniques are widely employed in adult gynecologic surgery, their application in pediatric and adolescent patients requires careful consideration due to anatomical differences, patient size, and specific surgical requirements in children. Various aspects of MIS in pediatric and adolescent gynecology, including patient positioning, laparoscopic and robotic instrument choices, trocar placement, surgical techniques, and perioperative pediatric adaptations to MIS are discussed. The findings highlight the unique challenges and opportunities in performing MIS for pediatric and adolescent patients undergoing gyn surgery, emphasizing the need for specialized training and multidisciplinary collaboration.</p>","PeriodicalId":16708,"journal":{"name":"Journal of pediatric and adolescent gynecology","volume":" ","pages":""},"PeriodicalIF":1.7,"publicationDate":"2024-08-02","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141889561","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2024-08-02DOI: 10.1016/j.jpag.2024.07.009
Kyle M. Devins MD , Allan M. Goldstein MD , Amanda V. French MD
This is a case report of a 10-year-old with Ollier disease and an ovarian mass. Ollier disease, a rare disorder characterized by multiple enchondromas resulting in bone deformities, has been occasionally associated with ovarian juvenile granulosa cell tumor. This patient developed signs of precocious puberty and was found to have an ovarian tumor; however, pathology revealed a mixed sex-cord stromal tumor with components of juvenile granulosa and Sertoli-Leydig cell tumor. Tumor genomic testing revealed an IDH1 mutation. Mixed sex-cord stromal tumors of this type, also called “gynandroblastomas,” have been associated with DICER1 mutations and DICER1 tumor predisposition syndrome but never with Ollier disease. Our findings expand the known spectrum of syndromic associations with this tumor type, with implications for tumor screening.
{"title":"A Rare Ovarian Mixed Sex Cord Stromal Tumor in a Patient with Ollier Disease: A Case Report","authors":"Kyle M. Devins MD , Allan M. Goldstein MD , Amanda V. French MD","doi":"10.1016/j.jpag.2024.07.009","DOIUrl":"10.1016/j.jpag.2024.07.009","url":null,"abstract":"<div><div>This is a case report of a 10-year-old with Ollier disease and an ovarian mass. Ollier disease, a rare disorder characterized by multiple enchondromas resulting in bone deformities, has been occasionally associated with ovarian juvenile granulosa cell tumor. This patient developed signs of precocious puberty and was found to have an ovarian tumor; however, pathology revealed a mixed sex-cord stromal tumor with components of juvenile granulosa and Sertoli-Leydig cell tumor. Tumor genomic testing revealed an <em>IDH1</em> mutation. Mixed sex-cord stromal tumors of this type, also called “gynandroblastomas,” have been associated with <em>DICER1</em> mutations and <em>DICER1</em> tumor predisposition syndrome but never with Ollier disease. Our findings expand the known spectrum of syndromic associations with this tumor type, with implications for tumor screening.</div></div>","PeriodicalId":16708,"journal":{"name":"Journal of pediatric and adolescent gynecology","volume":"37 6","pages":"Pages 629-631"},"PeriodicalIF":1.7,"publicationDate":"2024-08-02","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141889558","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2024-08-02DOI: 10.1016/j.jpag.2024.07.005
Inês Tj Oliveira, Pedro V Pinto, João Fmal Bernardes
Study objectives: Our aim was to review the evidence concerning the non-invasive diagnosis of endometriosis in adolescents.
Methods: A systematic review was written following the SWiM reporting guidelines. The study research was made across three databases (MEDLINE/PubMed, Scopus, and Web of Science) to identify articles about the adolescent population and the diagnosis of endometriosis through non-invasive methods. The search included the keywords "endometriosis," "adolescents," "diagnosis," "ultrasound," and "MRI." Only English-language articles were considered, and those published prior to 2000 were excluded. The established outcomes focused on clinical symptoms, ultrasound (US), and magnetic resonance imaging (MRI) findings suggestive of endometriosis.
Results: We included 26 articles, mostly comprising case series and cross-sectional studies. The pooled analysis involved 2,299 female adolescents (age range 8-25 years old) with clinically suspected, imaged, and/or surgically confirmed endometriosis. The most frequently reported symptom was dysmenorrhea, followed by chronic pelvic pain. Among adolescents clinically suspected of endometriosis undergoing ultrasound (US), 32.8% exhibited at least one sign of endometriosis. Of the 167 patients with ultrasound-diagnosed endometriosis, 48.5% had deep infiltrating endometriosis (DIE), and 45.5% had an endometrioma detected. Three studies assessed MRI findings, revealing that 49.8% presented with signs of endometriosis.
Conclusions: Dysmenorrhea and chronic pelvic pain stand out as key symptoms of adolescent endometriosis. Although their diagnostic accuracy varies, US and MRI have emerged as valuable tools for diagnosing the disease. While the US may have limitations, especially in detecting subtle lesions, MRI shows promise, even in cases with normal previous ultrasounds. Early recognition and proactive diagnosis are crucial for improving the management of endometriosis in adolescents.
研究目的我们的目的是回顾有关青少年子宫内膜异位症非侵入性诊断的证据:方法:根据 SWiM 报告指南撰写了一篇系统性综述。该研究通过三个数据库(MEDLINE/PubMed、Scopus 和 Web of Science)进行研究,以确定有关青少年人群和通过非侵入性方法诊断子宫内膜异位症的文章。搜索关键词包括 "子宫内膜异位症"、"青少年"、"诊断"、"超声波 "和 "核磁共振成像"。仅考虑英语文章,并排除了 2000 年以前发表的文章。研究结果主要集中在提示子宫内膜异位症的临床症状、超声波(US)和磁共振成像(MRI)结果:我们共纳入了 26 篇文章,其中大部分是病例系列和横断面研究。汇总分析涉及 2299 名临床怀疑、影像检查和/或手术证实患有子宫内膜异位症的女性青少年(年龄范围为 8-25 岁)。最常见的症状是痛经,其次是慢性盆腔疼痛。在接受超声检查(US)的临床疑似子宫内膜异位症的青少年中,32.8%的人至少表现出一种子宫内膜异位症的症状。在 167 名超声诊断为子宫内膜异位症的患者中,48.5% 患有深部浸润性子宫内膜异位症(DIE),45.5% 患有子宫内膜瘤。三项研究对核磁共振成像结果进行了评估,结果显示49.8%的患者有子宫内膜异位症的迹象:结论:痛经和慢性盆腔疼痛是青少年子宫内膜异位症的主要症状。尽管诊断准确率不一,但 US 和 MRI 已成为诊断该疾病的重要工具。虽然 US 可能存在局限性,尤其是在检测微小病灶方面,但 MRI 却显示出良好的前景,即使是之前超声波检查正常的病例也不例外。早期识别和积极诊断对于改善青少年子宫内膜异位症的治疗至关重要。
{"title":"Non-invasive diagnosis of endometriosis in adolescents and young female adults: a systematic review.","authors":"Inês Tj Oliveira, Pedro V Pinto, João Fmal Bernardes","doi":"10.1016/j.jpag.2024.07.005","DOIUrl":"https://doi.org/10.1016/j.jpag.2024.07.005","url":null,"abstract":"<p><strong>Study objectives: </strong>Our aim was to review the evidence concerning the non-invasive diagnosis of endometriosis in adolescents.</p><p><strong>Methods: </strong>A systematic review was written following the SWiM reporting guidelines. The study research was made across three databases (MEDLINE/PubMed, Scopus, and Web of Science) to identify articles about the adolescent population and the diagnosis of endometriosis through non-invasive methods. The search included the keywords \"endometriosis,\" \"adolescents,\" \"diagnosis,\" \"ultrasound,\" and \"MRI.\" Only English-language articles were considered, and those published prior to 2000 were excluded. The established outcomes focused on clinical symptoms, ultrasound (US), and magnetic resonance imaging (MRI) findings suggestive of endometriosis.</p><p><strong>Results: </strong>We included 26 articles, mostly comprising case series and cross-sectional studies. The pooled analysis involved 2,299 female adolescents (age range 8-25 years old) with clinically suspected, imaged, and/or surgically confirmed endometriosis. The most frequently reported symptom was dysmenorrhea, followed by chronic pelvic pain. Among adolescents clinically suspected of endometriosis undergoing ultrasound (US), 32.8% exhibited at least one sign of endometriosis. Of the 167 patients with ultrasound-diagnosed endometriosis, 48.5% had deep infiltrating endometriosis (DIE), and 45.5% had an endometrioma detected. Three studies assessed MRI findings, revealing that 49.8% presented with signs of endometriosis.</p><p><strong>Conclusions: </strong>Dysmenorrhea and chronic pelvic pain stand out as key symptoms of adolescent endometriosis. Although their diagnostic accuracy varies, US and MRI have emerged as valuable tools for diagnosing the disease. While the US may have limitations, especially in detecting subtle lesions, MRI shows promise, even in cases with normal previous ultrasounds. Early recognition and proactive diagnosis are crucial for improving the management of endometriosis in adolescents.</p>","PeriodicalId":16708,"journal":{"name":"Journal of pediatric and adolescent gynecology","volume":" ","pages":""},"PeriodicalIF":1.7,"publicationDate":"2024-08-02","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141889560","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2024-08-02DOI: 10.1016/j.jpag.2024.07.004
Chenglu Qin, Pohching Lee, Licong Luo
Objectives: This study aimed to assess the practical application of conventional two-dimensional (2D) pelvic ultrasound in conjunction with three-dimensional (3D) ultrasound for evaluating obstructive Müllerian abnormalities.
Design: Respective study in tertiary referral hospital METHOD: Computerized stored data was used to collect surgical confirmed obstructive Müllerian anomalies cases between December 2022 and October 2023 with presurgical imagings being evaluated. Acute presentation with abdominal pain and clinical suspicion of obstructive Müllerian abnormality were required for inclusion. All study participants underwent pelvic ultrasound prior to the definitive surgery, with or without a repeat MRI if one was performed previous to admission. Those situations where both MRI and ultrasound were not conducted were excluded, such as the transverse vaginal septum, imperforate hymen, iatrogenic cervical injury or Müllerian malformation alone without obstructive outflow anomalies like didelphys, bicornuate, or septate uterus.
Main outcomes measures: The concordance between the surgically confirmed diagnosis and the pelvic ultrasound was reported in 27 of 29 women (93.1%). In contrast, only 24 of 29 cases were correctly diagnosed with MRI in this study (82.8%). This pilot study presents a comparison of two techniques, with a specific focus on obstructive Müllerian anomalies. The use of pelvic ultrasound not only assisted in our surgical practice but also significantly improved patient-doctor counseling.
Conclusion: In managing obstructive Müllerian abnormalities, 3D-enhanced conventional pelvic ultrasound was found effective in diagnosis and was comparable to MRI.
{"title":"The Comparison between Three-dimensional enhanced Conventional Pelvic Ultrasound and Magnetic Resonance Imaging in the Evaluation of Obstructive Müllerian Anomalies and its Concordance with Surgical Diagnosis.","authors":"Chenglu Qin, Pohching Lee, Licong Luo","doi":"10.1016/j.jpag.2024.07.004","DOIUrl":"https://doi.org/10.1016/j.jpag.2024.07.004","url":null,"abstract":"<p><strong>Objectives: </strong>This study aimed to assess the practical application of conventional two-dimensional (2D) pelvic ultrasound in conjunction with three-dimensional (3D) ultrasound for evaluating obstructive Müllerian abnormalities.</p><p><strong>Design: </strong>Respective study in tertiary referral hospital METHOD: Computerized stored data was used to collect surgical confirmed obstructive Müllerian anomalies cases between December 2022 and October 2023 with presurgical imagings being evaluated. Acute presentation with abdominal pain and clinical suspicion of obstructive Müllerian abnormality were required for inclusion. All study participants underwent pelvic ultrasound prior to the definitive surgery, with or without a repeat MRI if one was performed previous to admission. Those situations where both MRI and ultrasound were not conducted were excluded, such as the transverse vaginal septum, imperforate hymen, iatrogenic cervical injury or Müllerian malformation alone without obstructive outflow anomalies like didelphys, bicornuate, or septate uterus.</p><p><strong>Main outcomes measures: </strong>The concordance between the surgically confirmed diagnosis and the pelvic ultrasound was reported in 27 of 29 women (93.1%). In contrast, only 24 of 29 cases were correctly diagnosed with MRI in this study (82.8%). This pilot study presents a comparison of two techniques, with a specific focus on obstructive Müllerian anomalies. The use of pelvic ultrasound not only assisted in our surgical practice but also significantly improved patient-doctor counseling.</p><p><strong>Conclusion: </strong>In managing obstructive Müllerian abnormalities, 3D-enhanced conventional pelvic ultrasound was found effective in diagnosis and was comparable to MRI.</p>","PeriodicalId":16708,"journal":{"name":"Journal of pediatric and adolescent gynecology","volume":" ","pages":""},"PeriodicalIF":1.7,"publicationDate":"2024-08-02","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141889562","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2024-07-20DOI: 10.1016/j.jpag.2024.07.002
R.U. Gaikaiwari MBBS (Hons) , C. Prinsloo MBBS (Hons) , S.R. Grover MBBS, FRANZCOG, MD, FFPMANZCA , I. Wright MBBS, DCH, MRCP(UK)Paeds, FRACP , N. Drever MBBS, BMedSci, FRANZCOG
Study Objective
Mayer-Rokitansky-Küster-Hauser (MRKH) syndrome is characterized by the congenital absence of the uterus and vagina, sometimes with associated extragenital anomalies. Currently, there is limited literature on pelvic pain and comorbid pain syndromes in people with MRKH. The aims of this scoping review were to summarize existing literature on pelvic and generalized persistent pain syndromes associated with MRKH and to identify knowledge gaps for further research into this field.
Methods
This scoping review followed the Joanna Briggs Institute framework. The population of interest was patients with a diagnosis of MRKH. MEDLINE, CINAHL, Scopus, Cochrane, Embase, and Emcare databases were searched. Articles that did not meet the inclusion criteria or critical appraisal standards were excluded. The resultant articles were reviewed by 2 independent researchers, and a third was used in cases of disagreement. A descriptive analytical method was used for data analysis.
Results
We screened 3348 articles for eligibility. Of these, 39 articles, which described 1353 cases of MRKH, met the criteria. Four studies described baseline pelvic pain in MRKH, 19 described acute presentations, and 13 described postintervention pain levels.
Conclusion
Despite the paucity of research, this review found that cyclic pelvic pain was mostly present in women with uterine remnants, whereas pelvic pain in those without remnants was poorly understood. There were no studies exploring generalized persistent pain syndromes in MRKH. Further cross-sectional studies are needed to elucidate the prevalence and levels of pain syndromes in MRKH.
{"title":"Experiences of Pelvic and Generalized Persistent Pain Syndromes in MRKH: A Scoping Review","authors":"R.U. Gaikaiwari MBBS (Hons) , C. Prinsloo MBBS (Hons) , S.R. Grover MBBS, FRANZCOG, MD, FFPMANZCA , I. Wright MBBS, DCH, MRCP(UK)Paeds, FRACP , N. Drever MBBS, BMedSci, FRANZCOG","doi":"10.1016/j.jpag.2024.07.002","DOIUrl":"10.1016/j.jpag.2024.07.002","url":null,"abstract":"<div><h3>Study Objective</h3><p>Mayer-Rokitansky-Küster-Hauser (MRKH) syndrome is characterized by the congenital absence of the uterus and vagina, sometimes with associated extragenital anomalies. Currently, there is limited literature on pelvic pain and comorbid pain syndromes in people with MRKH. The aims of this scoping review were to summarize existing literature on pelvic and generalized persistent pain syndromes associated with MRKH and to identify knowledge gaps for further research into this field.</p></div><div><h3>Methods</h3><p>This scoping review followed the Joanna Briggs Institute framework. The population of interest was patients with a diagnosis of MRKH. MEDLINE, CINAHL, Scopus, Cochrane, Embase, and Emcare databases were searched. Articles that did not meet the inclusion criteria or critical appraisal standards were excluded. The resultant articles were reviewed by 2 independent researchers, and a third was used in cases of disagreement. A descriptive analytical method was used for data analysis.</p></div><div><h3>Results</h3><p>We screened 3348 articles for eligibility. Of these, 39 articles, which described 1353 cases of MRKH, met the criteria. Four studies described baseline pelvic pain in MRKH, 19 described acute presentations, and 13 described postintervention pain levels.</p></div><div><h3>Conclusion</h3><p>Despite the paucity of research, this review found that cyclic pelvic pain was mostly present in women with uterine remnants, whereas pelvic pain in those without remnants was poorly understood. There were no studies exploring generalized persistent pain syndromes in MRKH. Further cross-sectional studies are needed to elucidate the prevalence and levels of pain syndromes in MRKH.</p></div>","PeriodicalId":16708,"journal":{"name":"Journal of pediatric and adolescent gynecology","volume":"37 5","pages":"Pages 477-494"},"PeriodicalIF":1.7,"publicationDate":"2024-07-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.sciencedirect.com/science/article/pii/S1083318824002547/pdfft?md5=afc4e110156725144d8f2db3a35e56cf&pid=1-s2.0-S1083318824002547-main.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141748377","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2024-07-17DOI: 10.1016/j.jpag.2024.07.001
{"title":"Composing a Life as a Pediatric and Adolescent Gynecologist","authors":"","doi":"10.1016/j.jpag.2024.07.001","DOIUrl":"10.1016/j.jpag.2024.07.001","url":null,"abstract":"","PeriodicalId":16708,"journal":{"name":"Journal of pediatric and adolescent gynecology","volume":"37 4","pages":"Pages 381-382"},"PeriodicalIF":1.7,"publicationDate":"2024-07-17","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141639315","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2024-07-14DOI: 10.1016/j.jpag.2024.07.003
Jasneet Aulakh BS, Erin E. Isaacson MD, Sarah D. Compton PhD, MPH, Monica W. Rosen MD
Study Objective
Mature ovarian dermoid cysts (ODCs) are the most common benign ovarian tumors diagnosed in children. However, there is minimal data on management of ODCs in premenarchal patients. This study assesses characteristics associated with expectant (EM) vs surgical (SM) management in premenarchal patients and the growth rate of ODCs in EM patients at a single institution.
Methods
Forty-four premenarchal patients, either post-surgical with pathologically-confirmed ODC or having radiologic findings consistent with ODCs, were included. Data collected included demographics, cyst characteristics, imaging findings, presence of symptoms, surgical procedure performed, and ovarian torsion occurrence.
Results
Patient age at diagnosis was similar between groups (SM: 8.8 vs EM: 8.0, P = .55). At presentation, 36 patients (82%) underwent SM and 8 (18%) underwent EM. There was a significant difference in cyst size between groups (SM: 8.9 cm vs EM: 3.6 cm, P = .004). Of SM patients, 30% underwent oophorectomy vs cystectomy, with a significant difference in ODC size between procedures (11.8 cm vs 7.7 cm, P = .016). Of EM patients, 75% had at least one and 60% had three follow-up ultrasounds, with average follow-up timeframes of 3.7 and 27 months respectively. Average yearly ODC growth rate for the latter group was 0.8 cm.
Conclusion
The average yearly growth rate of ODCs in premenarchal patients within our institution was slower than in older cohorts, and both age and cyst size played significant roles in determining surgical procedure. Continued study on EM in premenarchal ODCs will help define parameters for recommending SM vs EM in this population.
研究目的成熟卵巢皮样囊肿(ODC)是儿童中最常见的良性卵巢肿瘤。然而,有关孕前患者卵巢皮样囊肿治疗的数据极少。本研究评估了单个医疗机构对初产妇患者进行预期治疗(EM)和手术治疗(SM)的相关特征,以及EM患者ODC的生长率:方法:纳入了44名初产妇患者,他们要么是手术后经病理证实患有ODC,要么是放射学检查结果与ODC一致。收集的数据包括人口统计学特征、囊肿特征、影像学检查结果、有无症状、手术过程和卵巢扭转发生情况:两组患者确诊时的年龄相似(SM:8.8 岁 vs. EM:8.0 岁,P=.55)。就诊时,36 名患者(82%)接受了 SM,8 名患者(18%)接受了 EM。两组患者的囊肿大小存在明显差异(SM:8.9 厘米 vs. EM:3.6 厘米,P=.004)。在SM患者中,30%接受了卵巢切除术与囊肿切除术,两种手术的ODC大小差异显著(11.8厘米 vs. 7.7厘米,P=.016)。在EM患者中,75%的患者至少接受过一次超声随访,60%的患者接受过三次超声随访,平均随访时间分别为3.7个月和27个月。后一组患者的ODC年平均增长率为0.8厘米:结论:与年龄较大的人群相比,我院初产妇患者卵巢早衰的年平均生长速度较慢,年龄和囊肿大小在决定手术方式时起着重要作用。对初产妇ODC的EM继续研究将有助于确定在这一人群中推荐SM与EM的参数。
{"title":"Ovarian Dermoid Cyst Trajectory in Premenarchal Girls","authors":"Jasneet Aulakh BS, Erin E. Isaacson MD, Sarah D. Compton PhD, MPH, Monica W. Rosen MD","doi":"10.1016/j.jpag.2024.07.003","DOIUrl":"10.1016/j.jpag.2024.07.003","url":null,"abstract":"<div><h3>Study Objective</h3><p>Mature ovarian dermoid cysts (ODCs) are the most common benign ovarian tumors diagnosed in children. However, there is minimal data on management of ODCs in premenarchal patients. This study assesses characteristics associated with expectant (EM) vs surgical (SM) management in premenarchal patients and the growth rate of ODCs in EM patients at a single institution.</p></div><div><h3>Methods</h3><p>Forty-four premenarchal patients, either post-surgical with pathologically-confirmed ODC or having radiologic findings consistent with ODCs, were included. Data collected included demographics, cyst characteristics, imaging findings, presence of symptoms, surgical procedure performed, and ovarian torsion occurrence.</p></div><div><h3>Results</h3><p>Patient age at diagnosis was similar between groups (SM: 8.8 vs EM: 8.0, <em>P</em> = .55). At presentation, 36 patients (82%) underwent SM and 8 (18%) underwent EM. There was a significant difference in cyst size between groups (SM: 8.9 cm vs EM: 3.6 cm, <em>P</em> = .004). Of SM patients, 30% underwent oophorectomy vs cystectomy, with a significant difference in ODC size between procedures (11.8 cm vs 7.7 cm, <em>P</em> = .016). Of EM patients, 75% had at least one and 60% had three follow-up ultrasounds, with average follow-up timeframes of 3.7 and 27 months respectively. Average yearly ODC growth rate for the latter group was 0.8 cm.</p></div><div><h3>Conclusion</h3><p>The average yearly growth rate of ODCs in premenarchal patients within our institution was slower than in older cohorts, and both age and cyst size played significant roles in determining surgical procedure. Continued study on EM in premenarchal ODCs will help define parameters for recommending SM vs EM in this population.</p></div>","PeriodicalId":16708,"journal":{"name":"Journal of pediatric and adolescent gynecology","volume":"37 5","pages":"Pages 495-499"},"PeriodicalIF":1.7,"publicationDate":"2024-07-14","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141620216","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2024-07-14DOI: 10.1016/j.jpag.2024.06.009
Maria D. Ash MD, MA(Ed) , Ian S. Watson MS , Lauren E. Matera DO , Ashley M. Ebersole MD, MS , Heather L. Stewart MD , Emily Price BSN, RN , Johanna Taylor MSN, APN , Elise D. Berlan MD, MPH , Andrea E. Bonny MD
Purpose
To visualize contraceptive choice pathways among adolescent and young adults (AYA) designated female at birth (DFAB) as a means of exploring the relationships between current contraceptive use, desired contraceptive, and ultimately, chosen contraceptive method.
Methods
A retrospective cross-sectional study was conducted of AYA DFAB (N = 2369), aged 14-24 years, presenting for initial visit at a contraceptive clinic with standardized efficacy-based counseling. Sankey diagrams were utilized to visualize patient flow through the contraceptive decision-making process. Outcomes of interest were current contraceptive method, desired contraceptive prior to contraceptive counseling, and then chosen contraception. Chi-Square tests were conducted to quantify the strength of the relationships identified by the Sankey diagrams.
Results
Sankey diagrams demonstrated a fair amount of change from current contraceptive to desired contraceptive and from current contraceptive to chosen contraceptive. A stronger relationship was evident between desired contraceptive method and chosen method; most patients did not change their desired contraceptive after receiving counseling except AYA who were undecided about their desired contraceptive who flowed variably into all available methods. Chi-Square test assessing the association between desired and chosen contraceptive method was significant at P-value < .001, validating the patterns identified with the Sankey diagrams.
Discussion
We identified distinct contraceptive decision-making pathways among AYA which could inform the framework for a more tailored counseling approach. These findings are aligned with national medical organizations’ recommendations for provision of non-coercive, patient-centered contraceptive counseling to promote adolescent reproductive autonomy.
{"title":"An Exploration of Contraceptive Choice Pathways in Adolescents and Young Adults","authors":"Maria D. Ash MD, MA(Ed) , Ian S. Watson MS , Lauren E. Matera DO , Ashley M. Ebersole MD, MS , Heather L. Stewart MD , Emily Price BSN, RN , Johanna Taylor MSN, APN , Elise D. Berlan MD, MPH , Andrea E. Bonny MD","doi":"10.1016/j.jpag.2024.06.009","DOIUrl":"10.1016/j.jpag.2024.06.009","url":null,"abstract":"<div><h3>Purpose</h3><p>To visualize contraceptive choice pathways among adolescent and young adults (AYA) designated female at birth (DFAB) as a means of exploring the relationships between current contraceptive use, desired contraceptive, and ultimately, chosen contraceptive method.</p></div><div><h3>Methods</h3><p>A retrospective cross-sectional study was conducted of AYA DFAB (<em>N</em> = 2369), aged 14-24 years, presenting for initial visit at a contraceptive clinic with standardized efficacy-based counseling. Sankey diagrams were utilized to visualize patient flow through the contraceptive decision-making process. Outcomes of interest were current contraceptive method, desired contraceptive prior to contraceptive counseling, and then chosen contraception. Chi-Square tests were conducted to quantify the strength of the relationships identified by the Sankey diagrams.</p></div><div><h3>Results</h3><p>Sankey diagrams demonstrated a fair amount of change from current contraceptive to desired contraceptive and from current contraceptive to chosen contraceptive. A stronger relationship was evident between desired contraceptive method and chosen method; most patients did not change their desired contraceptive after receiving counseling except AYA who were undecided about their desired contraceptive who flowed variably into all available methods. Chi-Square test assessing the association between desired and chosen contraceptive method was significant at <em>P</em>-value < .001, validating the patterns identified with the Sankey diagrams.</p></div><div><h3>Discussion</h3><p>We identified distinct contraceptive decision-making pathways among AYA which could inform the framework for a more tailored counseling approach. These findings are aligned with national medical organizations’ recommendations for provision of non-coercive, patient-centered contraceptive counseling to promote adolescent reproductive autonomy.</p></div>","PeriodicalId":16708,"journal":{"name":"Journal of pediatric and adolescent gynecology","volume":"37 5","pages":"Pages 505-509"},"PeriodicalIF":1.7,"publicationDate":"2024-07-14","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141603746","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2024-06-25DOI: 10.1016/j.jpag.2024.06.005
Background
Prepubertal vaginal bleeding is a common presentation for pediatric adolescent gynecologists with a broad differential diagnosis that historically may not have included complex lymphatic anomalies. However, given recent consensus criteria and imaging capabilities, this may be a condition that pediatric adolescent gynecologists see more frequently in the future.
Case
We present a case of a 5-year-old pre-pubertal girl whose only presenting symptoms of a rare complex lymphatic anomaly was copious vaginal bleeding. After three vaginoscopies, two hysteroscopies, two pelvic MRIs, and a percutaneous ultrasound guided core needle biopsy, this patient was eventually diagnosed with Kaposiform lymphangiomatosis at age 9 years-old, and she is now being treated medically with sirolimus, a mammalian target of rapamycin (mTOR) inhibitor, with improvement in her symptoms.
Summary and conclusion
Complex lymphatic anomalies should be considered after initial and secondary workups for pre-pubertal vaginal bleeding or copious vaginal discharge are negative. Furthermore, this case illustrates the value of pelvic MRI in the setting of unknown cause of vaginal bleeding when typical workup is negative.
{"title":"Kaposiform Lymphangiomatosis as a Cause of Vaginal Bleeding & Discharge: A Case Report","authors":"","doi":"10.1016/j.jpag.2024.06.005","DOIUrl":"10.1016/j.jpag.2024.06.005","url":null,"abstract":"<div><h3>Background</h3><div>Prepubertal vaginal bleeding is a common presentation for pediatric adolescent gynecologists with a broad differential diagnosis that historically may not have included complex lymphatic anomalies. However, given recent consensus criteria and imaging capabilities, this may be a condition that pediatric adolescent gynecologists see more frequently in the future.</div></div><div><h3>Case</h3><div>We present a case of a 5-year-old pre-pubertal girl whose only presenting symptoms of a rare complex lymphatic anomaly was copious vaginal bleeding. After three vaginoscopies, two hysteroscopies, two pelvic MRIs, and a percutaneous ultrasound guided core needle biopsy, this patient was eventually diagnosed with Kaposiform lymphangiomatosis at age 9 years-old, and she is now being treated medically with sirolimus, a mammalian target of rapamycin (mTOR) inhibitor, with improvement in her symptoms.</div></div><div><h3>Summary and conclusion</h3><div>Complex lymphatic anomalies should be considered after initial and secondary workups for pre-pubertal vaginal bleeding or copious vaginal discharge are negative. Furthermore, this case illustrates the value of pelvic MRI in the setting of unknown cause of vaginal bleeding when typical workup is negative.</div></div>","PeriodicalId":16708,"journal":{"name":"Journal of pediatric and adolescent gynecology","volume":"37 6","pages":"Pages 625-628"},"PeriodicalIF":1.7,"publicationDate":"2024-06-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141468872","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}