异位综合征,右心,肾盂输尿管梗阻,子宫内膜异位症,肺动脉高压的成人先天性心脏缺陷:1例报告。

IF 0.9 Q3 MEDICINE, GENERAL & INTERNAL Journal of Medical Case Reports Pub Date : 2025-01-20 DOI:10.1186/s13256-025-05043-2
Ahmad Al-Bitar, Mhd Ammar Zalzaleh, Hussien Al Helbawi, Mohammad Hossein Morteza
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引用次数: 0

摘要

背景:异位的特征是胸部和/或腹部器官的异常定位,导致各种生理和血流动力学影响。先天性心脏病涉及心脏或胸部主要血管的结构不规则,导致功能障碍。病例介绍:我们报告了一位26岁的阿拉伯女性患者,其复杂的病史包括异位、右心、先天性心脏病和输尿管肾盂连接处梗阻,在她出生后的第一年被诊断出来,随后在她20岁出头时被确认为子宫内膜异位症。据报道,这种疾病的组合在现有文献中是独一无二的。患者因与饮食或排便无关的严重弥漫性腹痛并伴有恶心而寻求急救。疼痛局限于特定区域,并向肩部放射。尽管尝试用激素疗法缓解腹痛,但她的症状持续存在。经检查,没有立即手术或医疗紧急情况,导致症状管理与抗痉挛药物和建议专家随访。讨论了患者的心脏状况,包括紫绀和相关并发症,以及她过去的手术和与心血管健康相关的诊断结果。结论:本病例强调了在年轻个体中管理复杂医疗条件的挑战,强调了多学科护理和长期随访的必要性,以确保患者的最佳生活质量。跨学科的方法对于异位患者的综合护理至关重要,因为他们可能会出现影响不同器官系统的广泛解剖异常。临床医生需要充分了解异位综合征的复杂性及其不同的表现,以提供有效和个性化的护理。
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Heterotaxy syndrome, dextrocardia, ureteropelvic obstruction, endometriosis, and pulmonary hypertension in an adult with congenital heart defects: a case report.

Background: Heterotaxia is characterized by an abnormal positioning of the thoracic and/or abdominal organs, resulting in various physiological and hemodynamic implications. Congenital heart disease involves structural irregularities in the heart or major vessels within the chest, leading to functional challenges.

Case presentation: We present a 26-year-old Arab female patient with a complex medical history involving heterotaxy, dextrocardia, congenital heart disease, and ureteropelvic junction obstruction diagnosed in her first year of life, followed by the identification of endometriosis in her early twenties. This combination of disorders is reportedly unique in existing literature. The patient sought emergency care for severe diffuse abdominal pain unrelated to diet or bowel movements, accompanied by nausea. The pain was localized in specific areas and radiated to the shoulder. Despite treatment attempts with hormonal therapy for abdominal pain relief, her symptoms persisted. Upon examination, no immediate surgical or medical emergencies were noted, leading to symptom management with antispasmodics and recommendations for specialist follow-ups. The patient's cardiac condition, including cyanosis and related complications, was discussed along with her past surgeries and diagnostic findings related to her cardiovascular health.

Conclusion: This case emphasizes the challenges of managing complex medical conditions in a young individual, highlighting the need for multidisciplinary care and long-term follow-up to ensure the best possible quality of life for the patient. An interdisciplinary approach is crucial for the comprehensive care of patients with heterotaxy, as they may present with a wide range of anatomical abnormalities affecting different organ systems. Clinicians need to be well informed about the complexities of heterotaxy syndromes and their diverse manifestations to provide effective and personalized care.

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来源期刊
Journal of Medical Case Reports
Journal of Medical Case Reports Medicine-Medicine (all)
CiteScore
1.50
自引率
0.00%
发文量
436
期刊介绍: JMCR is an open access, peer-reviewed online journal that will consider any original case report that expands the field of general medical knowledge. Reports should show one of the following: 1. Unreported or unusual side effects or adverse interactions involving medications 2. Unexpected or unusual presentations of a disease 3. New associations or variations in disease processes 4. Presentations, diagnoses and/or management of new and emerging diseases 5. An unexpected association between diseases or symptoms 6. An unexpected event in the course of observing or treating a patient 7. Findings that shed new light on the possible pathogenesis of a disease or an adverse effect
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