https://jogeca.com/index.php/jogeca/issue/feed Journal of Obstetrics and Gynaecology of Eastern and Central Africa 2025-07-01T03:14:13+00:00 Editor-in-Chief editor-in-chief@jogeca.com Open Journal Systems <p><em><span style="font-weight: 400;">JOGECA </span></em><span style="font-weight: 400;">publishes original, peer-reviewed, research and reviews in Obstetrics and Gynecology. It also publishes work in basic and translational science relevant to reproductive biology and medicine. </span><em><span style="font-weight: 400;">JOGECA </span></em><span style="font-weight: 400;">provides a portal for work that fall under but not limited to Fetomaternal Medicine, Adolescent Health and Sexuality, Family Planning and Contraception, Gynecological Oncology, Fertility and Endocrinology, Urogynecology, Health Policy and Implementation Science, Information Technology in Health, Developmental Biology, Genomics, and Basic and Translational Science research.</span></p> https://jogeca.com/index.php/jogeca/article/view/270 Phyllodes tumor, cardiovascular and chronic renal disease in a young lady on hormone replacement therapy: A case report 2024-11-25T11:24:12+00:00 Lauryn Mengesa lauryn.mengesa@gmail.com Daki Dido dakidido@gmail.com Dorcus Muchiri Muchiri.dorcus@gmail.com Philomena Owende akothowende@yahoo.com <p><strong>Background:</strong> Hormonal replacement therapy (HRT) has been associated with an<br />increased risk of developing breast cancer. The level of risk varies with different types of<br />HRT and the duration of use. Phyllodes tumor accounts for less than 1% of all breast<br />neoplasms and is associated with Li-Fraumeni syndrome.<br /><strong>Case presentation:</strong> A 37-year-old nulliparous woman presented with a left breast lump.<br />Histological examination revealed a spindle cell neoplasm consistent with a malignant<br />phyllodes tumor. She was diagnosed at age of 12 with ovarian dysgerminoma, had<br />subtotal hysterectomy and right oophorectomy, radiotherapy and chemotherapy. She<br />has been on HRT with conjugated equine estrogens for 13 years and tibolone for the<br />last 5 years. Following the diagnosis of phyllodes tumor, a mastectomy was performed,<br />and HRT was changed to vaginal estrogen gel.<br /><strong>Conclusion:</strong> Hormonal replacement therapy may pose a risk for certain types of breast<br />cancer, especially with prolonged use of combined therapy. Patients who develop<br />cancers early in life, as well as those on HRT, require close follow-up and adequate<br />patient education with an emphasis on self-breast examination. Sensitization of<br />healthcare providers and patients on the value of genetic screening would facilitate<br />early identification of such patients and follow-up at high-risk clinics.</p> 2025-06-30T00:00:00+00:00 Copyright (c) 2025 The authors. https://jogeca.com/index.php/jogeca/article/view/381 Type 2 cesarean section scar pregnancy managed by hysteroscopic resection and methotrexate: A case report 2025-07-01T03:14:03+00:00 Charles Muteshi murwa2006@yahoo.co.uk Kimani Morris morri.kimani@aku.edu Samuel Mukono samuel.mukono@aku.edu <p class="western" align="justify"><span style="font-size: small;"><span style="color: #000000;"><span style="font-family: Times New Roman, serif;"><span style="font-size: medium;"><span lang="en-US"><strong>Background:</strong></span></span></span></span> <span style="color: #000000;"><span style="font-family: Quadraat;"><span lang="en-US">Diagnosis and management of cesarean scar ectopic pregnancy (CSP) remain challeng</span></span></span><span style="font-family: Quadraat;"><span lang="en-US">ing</span></span><span style="font-family: Quadraat;"><span lang="en-US">. We describe ultrasound diagnosis followed by hysteroscopic resection and methotrexate administration. </span></span></span></p> <p class="western" lang="en-US" align="justify"><span style="font-family: Quadraat;"><span style="font-size: small;"><span style="font-family: Times New Roman, serif;"><span style="font-size: medium;"><strong>Case presentation: </strong></span></span>A 42-year-old woman, para 2+1, presented with 8 weeks of amenorrhea and vaginal bleeding. She had two previous cesarean deliveries. Initial ultrasound suggested an incomplete miscarriage and beta human chorionic gonadotropin (β-HCG) was 46,129 mIU/ml. After failed medical management, repeat ultrasound diagnosed CSP. Hysteroscopic resection was performed, and she received methotrexate, resulting ß-HCG resolution.</span></span></p> <p class="western" lang="en-US" align="justify"><span style="font-family: Quadraat;"><span style="font-size: small;"><span style="font-family: Times New Roman, serif;"><span style="font-size: medium;"><strong>Conclusion: </strong></span></span>Though rare, CSP should be entertained in any woman presenting with vaginal bleeding with a history of cesarean delivery. Hysteroscopic resection with methotrexate provides good fertility-preserving modality for management. </span></span></p> <p class="western" lang="en-US" align="justify"><span style="font-family: Quadraat;"><span style="font-size: small;"><span style="font-family: Times New Roman, serif;"><span style="font-size: medium;"><strong>Keywords</strong></span></span><span style="font-family: Times New Roman, serif;"><span style="font-size: medium;">: </span></span>cesarean scar ectopic pregnancy; hysteroscopic resection; methotrexate</span></span></p> 2025-06-30T00:00:00+00:00 Copyright (c) 2025 The authors. https://jogeca.com/index.php/jogeca/article/view/16 Obstructive Hemivagina with Ipsilateral Renal Agenesis in a 16-year-old Diabetic African Girl: a case report 2025-07-01T03:14:13+00:00 JOEL OOKO OJWANDO jojwando@students.uonbi.ac.ke Ephantus Wachira Murage muragew@savannahhealth.co.ke Weston Wakasiaka Khisa westonkhisa@yahoo.com Rita Akoth Arogo ritakoth680@gmail.com <p class="western" align="justify"><span style="font-size: small;"><span style="color: #000000;"><span style="font-family: Times New Roman, serif;"><span style="font-size: medium;"><span lang="en-US"><strong>Background: </strong></span></span></span></span><span style="color: #000000;"><span style="font-family: Quadraat;"><span lang="en-US">The obstructed hemivagina with ipsilateral renal agenesis (OHVIRA) syndrome is a type of Müllerian duct anomaly (MDA) resulting from abnormal development of Müllerian ducts. Its features typically become apparent at puberty when girls present with menstrual abnormalities. </span></span></span><span style="color: #000000;"><span style="font-family: Quadraat;">The varied presentation of MDAs presents diagnostic and management challenges. </span></span></span></p> <p class="western" align="justify"><span style="font-family: Quadraat;"><span style="font-size: small;"><span style="color: #000000;"><span style="font-family: Times New Roman, serif;"><span style="font-size: medium;"><strong>Case presentation:</strong></span></span></span> <span style="color: #000000;">A 16-year-old diabetic African girl presented to Savannah Healthcare with cyclical lower abdominal pain and foul-smelling per vagina discharge. Magnetic resonance imaging (MRI) showed complete duplication of the uterus, cervix, and vagina (uterine didelphys) with an obstructed left hemivagina with hematocolpos. The septum obstructing the hemivagina was resected with drainage of the hematocolpos. A follow-up abdominal renal ultrasound showed the absence of the left kidney. </span></span></span></p> <p class="western" align="justify"><span style="font-family: Quadraat;"><span style="font-size: small;"><span style="color: #000000;"><span style="font-family: Times New Roman, serif;"><span style="font-size: medium;"><strong>Conclusion: </strong></span></span></span><span style="color: #000000;">Careful clinical examination and MRI are essential for diagnosing OHVIRA syndrome. Prompt surgical intervention improves outcomes.</span></span></span></p> 2025-06-30T00:00:00+00:00 Copyright (c) 2025 The authors.