胎儿的"胆结石"仍然是一个未解之. 案件系列 案件系列
Dan Boitor Borza1, Cristina Ioana Rotar2, Mihaela Oancea3
11st Obstetrics and Gynecology Department UMF Cluj-Napoca. danboitor@yahoo.com.
Medical ultrasonography
|November 6, 2023
概括
胎儿胆囊中的回声产物含量是一种罕见的,偶然的发现. 这种情况似乎是良性的,回声产生的内容往往在出生后自发地消失,没有并发症.
科学领域:
- 周围生理学 周围生理学
- 胎儿医学 胎儿医学
- 儿科胃肠病学 儿科胃肠病学
背景情况:
- 胎儿胆囊 (ECFG) 中的回声含量是第三个三个月的超声波期间不常见的偶然发现.
- ECFG的病因,临床过程和长期预后在很大程度上是未知的.
- 这项研究旨在描述患有ECFG的胎儿的人口,临床和超声波特征.
研究的目的:
- 为了描述胎儿胆囊回声素含量的特征.
- 调查诊断出ECFG的胎儿的临床过程和结果.
- 为了解决这种情况的管理提供了洞察力.
主要方法:
- 回顾性单中心研究.
- 纳入标准:怀孕患者在2022年3月至2023年4月期间通过超声波检测出ECFG.
- 收集的数据:产妇年龄,妊娠年龄,超声检测结果 (回声发作焦点,污泥),出生体重,分娩方式和新生儿结局.
主要成果:
- 确定了四个ECFG病例.
- 诊断时母亲的平均年龄:27.5岁;平均妊娠年龄:36.5周.
- 超声波主要显示了多个超高性焦点;一个病例也含有污泥. 平均焦点长度:3.375毫米.
- 所有胎儿都是在满期分娩的;平均出生体重: 3082.5 g.
- 在所有出生后的新生儿中,ECFG自发消失.
- 在随访期间,没有新生儿出现消化系统症状或并发症.
结论:
- ECFG是一种鲜为人知的疾病,其病因和后果不明确.
- 在超声波期间定期检查胎儿胆囊可能有助于检测.
- 这种情况似乎是良性的,通常在出生后自发消失.
- 患有ECFG的无症状新生儿可以通过警的等待方法来管理.
相关概念视频
01:28Urinary Tract Calculi I: Introduction
16
Renal calculi, or kidney stones, are solid deposits of minerals and salts formed inside the kidneys. In medical terminology, "calculus" refers to the stone itself, while "lithiasis" describes the process of stone formation. Depending on their location within the urinary system, these stones may be classified as either urolithiasis, when situated within the urinary tract, or nephrolithiasis, when located within the kidneys. Each term signifies the specific impact of the stone.Predisposition...
16
01:26Diseases of the Liver and Gallbladder
579
Liver and gallbladder diseases are a significant health concern, with prominent conditions including cirrhosis, hepatitis, non-alcoholic fatty liver disease (NAFLD), and gallstones. Jaundice is a common manifestation of liver and biliary disease.
Cirrhosis is characterized by the scarring of hepatic lobules in the liver, which are replaced by fibrous tissue, affecting the liver's normal functioning. NAFLD, on the other hand, is caused by an excessive build-up of fat in the liver, not...
Cirrhosis is characterized by the scarring of hepatic lobules in the liver, which are replaced by fibrous tissue, affecting the liver's normal functioning. NAFLD, on the other hand, is caused by an excessive build-up of fat in the liver, not...
579
01:20Inborn Errors of Metabolism
166
Phenylketonuria (PKU) is a protein metabolism disorder characterized by high blood levels of the amino acid phenylalanine. This results from a mutation in the gene responsible for phenylalanine hydroxylase, an enzyme that converts phenylalanine into tyrosine. When this enzyme is deficient, phenylalanine builds up in the blood, leading to symptoms such as vomiting, rashes, seizures, growth deficiency, and severe mental retardation. An early diagnosis and a diet restricting phenylalanine intake...
166