不可避免的基底细胞癌 (戈林-戈尔茨综合征):一个偶然的发现
Mahesh Kaggare Puttaraju1, Meera Theenathayalan2
1Oral Medicine and Radiology, JSS Academy of Higher Education and Research, Mysore, Karnataka, India dr.kpmahesh@jssuni.edu.in.
BMJ case reports
|August 22, 2024
概括
戈林-戈尔茨综合征或基底细胞神经综合征,呈现出骨问题,囊和皮肤神经. 先进的数字成像技术有助于诊断这种罕见的疾病,如病例报告所示.
科学领域:
- 口腔医学是指口腔医学.
- 放射学 放射学是一门学科.
- 遗传学 遗传学 是一个
背景情况:
- 戈林-戈尔茨综合征 (基底细胞神经综合征) 是一种罕见的遗传疾病.
- 它的特征是骨异常,牙生瘤和基底细胞瘤.
- 准确的诊断依赖于临床和放射学标准,口腔和面症状是关键指标.
研究的目的:
- 突出高级数字成像在诊断戈林-戈尔茨综合征中的重要性.
- 提出一个诊断为戈林-戈尔茨综合征的病人的病例报告.
- 强调口腔医学和放射学专家在早期检测中的作用.
主要方法:
- 一个20多岁末的男性患者的病例报告.
- 临床检查和例行放射检查.
- 组织病理学评估和先进的数字成像 (例如,CBCT).
主要成果:
- 偶然发现了上和下区域的多种囊性病变.
- 患者呈现出缺失牙和无症状的口腔面部胀.
- 先进的成像证实了囊性病变的程度,有助于诊断.
结论:
- 先进的数字成像显著提高了Gorlin-Goltz综合征的诊断准确度.
- 早期诊断对于管理骨和口腔症状至关重要.
- 包括口腔医学和放射学在内的多学科合作至关重要.
相关概念视频
The Retinoblastoma Gene
4.1K
Tumor suppressor genes are normal genes that can slow down cell division, repair DNA mistakes, or program the cells for apoptosis in case of irreparable damage. Hence, they play an essential role in preventing the proliferation of damaged cells.
The first-ever tumor suppressor gene called Rb was identified in retinoblastoma - a rare eye tumor in children. In inherited forms of the disease, a child inherits one defective copy of the Rb gene, which predisposes them to retinoblastoma. However,...
The first-ever tumor suppressor gene called Rb was identified in retinoblastoma - a rare eye tumor in children. In inherited forms of the disease, a child inherits one defective copy of the Rb gene, which predisposes them to retinoblastoma. However,...
4.1K
Skin Cancer
4.0K
Skin cancer is a type of cancer that occurs when there is an abnormal growth of skin cells, usually triggered by damage to the DNA within the skin cells. It is primarily caused by exposure to ultraviolet (UV) radiation from the sun or artificial sources like tanning beds. Skin cancer is the most common type of cancer worldwide, and its incidence continues to rise.
Basal Cell Carcinoma (BCC): BCC is the most common type of skin cancer, accounting for about 80% of cases. It typically develops in...
Basal Cell Carcinoma (BCC): BCC is the most common type of skin cancer, accounting for about 80% of cases. It typically develops in...
4.0K
Pleiotropy
40.3K
Pleiotropy is the phenomenon in which a single gene impacts multiple, seemingly unrelated phenotypic traits. For example, defects in the SOX10 gene cause Waardenburg Syndrome Type 4, or WS4, which can cause defects in pigmentation, hearing impairments, and an absence of intestinal contractions necessary for elimination. This diversity of phenotypes results from the expression pattern of SOX10 in early embryonic and fetal development. SOX10 is found in neural crest cells that form melanocytes,...
40.3K
Notch Signaling Pathway
4.2K
The Notch signaling pathway is a major intracellular signaling pathway that is highly conserved over a broad spectrum of metazoan species. It stands unique from other intracellular signaling mechanisms in animals because notch protein itself acts as the receptor as well as the primary signaling molecule.
The Notch gene came into the limelight in 1914 after the discovery that its mutation in Drosophila melanogaster leads to a serrated (or "notched") wing margin phenotype. It was not...
The Notch gene came into the limelight in 1914 after the discovery that its mutation in Drosophila melanogaster leads to a serrated (or "notched") wing margin phenotype. It was not...
4.2K
Abnormal Proliferation
4.5K
Under normal conditions, most adult cells remain in a non-proliferative state unless stimulated by internal or external factors to replace lost cells. Abnormal cell proliferation is a condition in which the cell's growth exceeds and is uncoordinated with normal cells. In such situations, cell division persists in the same excessive manner even after cessation of the stimuli, leading to persistent tumors. The tumor arises from the damaged cells that replicate to pass the damage to the...
4.5K


