PRIMARY OVARIAN INSUFFICIENCY, A CHALLENGING DIAGNOSIS. A CASE SERIES

Sahil Omar, Mital Vaya, K. Omanwa
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Abstract

INTRODUCTION Primary ovarian insufficiency is rare, affecting 1-2% of those under 40 with only 0.1% of cases below 30 years. Etiology is mainly idiopathic, however chromosomal defects, autoimmune processes, and iatrogenic causes are associated. Symptoms are those of menopause but of intermittent durations and severities; and management targets the symptoms and complication prevention. CASE PRESENTATION We present two 18-year-old patients of African and Indian descent with an eight and five-month history of amenorrhea respectively with otherwise unremarkable history and physical exams. Investigation showed elevated FSH levels of 45.07 and 88.73 mIU/ml done four weeks apart in the first patient and 68.69 in the second patient. All other parameters were normal. DISCUSSION Aetiology is mainly idiopathic. 10-12% of diagnosed patients have chromosomal abnormalities such as Turner’s syndrome, fragile X syndrome, and genetic permutations of FMR 1 gene. Autoimmune causes are mainly autoimmune adrenal diseases. Autoimmune thyroiditis, Dermatomyosistis and Diabetes Mellitus type 1 also show association. Mumps Oophritis is the main infectious cause. Laparoscopic surgical procedures that involve the ovaries or affect their blood supply, pelvic radiotherapy, and chemotherapy all comprise the iatrogenic causes. Lifestyle and environmental factors such as smoking and heavy metals exposure also contribute. Diagnosis is by serum FSH levels of above 25 IU/l in two separate readings four weeks apart with a four-month history of amenorrhea occurring before 40 Years. Both patients were under 30 and met the criteria. Management involves hormone replacement therapy for symptoms, prevention and treatment of osteoporosis, oocyte donation for infertility, and counseling for both the psychological impact of the disease and the numerous complications living with the disease. CONCLUSION Multidisciplinary  care is necessary for management of this rare and challenging illness
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原发性卵巢功能不全,一个具有挑战性的诊断。病例系列
简介:原发性卵巢功能不全非常罕见,在 40 岁以下的人群中发病率为 1-2%,30 岁以下仅占 0.1%。病因主要是特发性的,但也与染色体缺陷、自身免疫过程和先天性原因有关。症状与更年期相同,但持续时间和严重程度时有时无;治疗以症状和预防并发症为目标。病例介绍 我们为您介绍两名分别闭经 8 个月和 5 个月的 18 岁非洲裔和印度裔患者,他们的病史和体检结果均无异常。检查结果显示,第一名患者的前列腺素水平升高,分别为 45.07 和 88.73 mIU/ml,相隔四周;第二名患者的前列腺素水平升高,分别为 68.69 mIU/ml。其他指标均正常。讨论 病因主要是特发性的。10%-12%的确诊患者存在染色体异常,如特纳综合征、脆性 X 综合征和 FMR 1 基因的遗传变异。自身免疫原因主要是自身免疫性肾上腺疾病。自身免疫性甲状腺炎、皮肌炎和 1 型糖尿病也与此有关联。腮腺炎性输卵管炎是主要的感染性病因。涉及卵巢或影响卵巢血液供应的腹腔镜手术、盆腔放疗和化疗都是先天性原因。吸烟和接触重金属等生活方式和环境因素也是诱因之一。诊断的依据是相隔四周两次读取的血清 FSH 水平均高于 25 IU/l,且在 40 岁之前有四个月的闭经史。两名患者均不到 30 岁,符合标准。治疗包括针对症状的激素替代疗法、骨质疏松症的预防和治疗、治疗不孕症的卵母细胞捐献,以及针对该疾病的心理影响和众多并发症的心理咨询。结论 在治疗这种罕见且具有挑战性的疾病时,需要多学科护理
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