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相关概念视频

Mismatch Repair01:36

Mismatch Repair

Overview
Viral Mutations00:36

Viral Mutations

A mutation is a change in the sequence of bases of DNA or RNA in a genome. Some mutations occur during replication of the genome due to errors made by the polymerase enzymes that replicate DNA or RNA. Unlike DNA polymerase, RNA polymerase is prone to errors because it is not capable of “proofreading” its work. Viruses with RNA-based genomes, like HIV, therefore accrue mutations faster than viruses with DNA-based genomes. Because mutation and recombination provide the raw material for adaptive...
Amyloid Fibrils03:03

Amyloid Fibrils

Amyloid fibrils are aggregates of misfolded proteins.  Under most circumstances, misfolded proteins are either refolded by chaperone proteins or degraded by the proteasome. However, in the case of a mutation or a disease, these proteins can accumulate to form large clusters and often further assemble to form elongated fibers, called fibrils. 
Amyloid deposits were observed as early as 1639 in the liver and the spleen.   In 1854, Rudolph Virchow performed iodine staining, normally used to...
Mismatch Repair01:20

Mismatch Repair

Organisms are capable of detecting and fixing nucleotide mismatches that occur during DNA replication. This sophisticated process requires identifying the new strand and replacing the erroneous bases with correct nucleotides. Mismatch repair is coordinated by many proteins in both prokaryotes and eukaryotes.
The Mutator Protein Family Plays a Key Role in DNA Mismatch Repair
The human genome has more than 3 billion base pairs of DNA per cell. Prior to cell division, that vast amount of genetic...
Skin Diseases and Disorders01:23

Skin Diseases and Disorders

Skin is the first line of defense and encounters a variety of microbes. Some pathogenic strains are often the cause of a broad range of infections of the skin and other body systems. These conditions can affect people of all ages and may have different causes, including genetic factors, infections, autoimmune reactions, environmental factors, and lifestyle choices.
Gram-positive Staphylococcus spp. and Streptococcus spp. are responsible for many of the most common skin infections. However, many...
Appendicitis01:19

Appendicitis

Appendicitis is an acute inflammatory condition of the vermiform appendix, most commonly caused by obstruction of its lumen. The appendix is a narrow, blind-ended pouch that extends from the cecum, making it particularly prone to obstruction. Causes include fecaliths, lymphoid hyperplasia (often after viral infections), parasites, tumors, or foreign bodies. This obstruction initiates a cascade of pathological changes.Luminal Obstruction and Early InflammationAfter obstruction, normal mucosal...

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Diagnosis of Neoplasia in Barrett’s Esophagus using Vital-dye Enhanced Fluorescence Imaging
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意外的粘膜下病变与潜在的恶性病变.

Wei-Na Jing1, Du He2, Jin-Lin Yang1

  • 1Gastroenterology and Hepatology, West China Hospital, Sichuan University, China.

Revista espanola de enfermedades digestivas
|June 4, 2024
PubMed
概括

逆转性多发性息肉 (IHP) 是一种罕见的胃病变. 一个病例揭示了患有腺癌的IHP,强调需要仔细评估侵袭深度以有效管理.

科学领域:

  • 胃肠病学 胃肠病学
  • 病理学 病理学 病理学
  • 在瘤学瘤学.

背景情况:

  • 逆转性多发性聚合体 (IHP) 的特征是胃粘膜侵入子粘膜.
  • 虽然通常是良性的,但IHP的恶性转变率很低 (0.02%).
  • 内镜呈现有所不同,通常以亚粘膜病变的形式出现.

研究的目的:

  • 报告一种罕见的逆转型多聚体 (IHP) 病例与同时发生的腺癌.
  • 讨论癌症IHP的诊断挑战和管理考虑.
  • 强调在这种情况下准确确定入侵深度的重要性.

主要方法:

  • 消化管胃管腺镜 (EGD) 用于初步检测病变.
  • 内镜超声波 (EUS) 用于粘膜下表征.
  • 内镜切除后进行了他的病理学和免疫组织化学分析.

主要成果:

  • 在胃底部发现了一个带有独特的针孔状孔的下膜病变.
  • 在EUS中,发现了异质的,低声的粘膜下体质.
  • 病理学证实了病变是带有腺癌的逆转型多聚体 (IHP).
  • 癌症成分的入侵深度被认为是一个关键和有争议的测量.

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结论:

  • 这一案例凸显了逆转型多重塑性息肉 (IHP) 中恶性瘤的潜力.
  • 准确评估入侵深度对于适当的分阶段和治疗计划至关重要.
  • 需要进一步的研究来规范癌症IHP的测量和管理.