[一个林奇综合征与穆尔-托雷综合征的病例]
Takehiro Shiraishi1, Yoshiko Mori, Noriyasu Chika
1Dept. of Digestive Tract and General Surgery, Saitama Medical Center, Saitama Medical University.
Gan to kagaku ryoho. Cancer & chemotherapy
|February 14, 2025
概括
穆尔-托雷综合征 (MTS) 是一种罕见的脂质和内脏瘤疾病,是林奇综合征 (LS) 的一种变体. 对LS的监测应包括皮肤瘤,正如这位患者所证明的那样.
科学领域:
- 在瘤学瘤学.
- 皮肤病学 皮肤病学
- 遗传学 是一个遗传学.
背景情况:
- 穆尔-托雷综合征 (MTS) 的特征是脂质瘤和内脏恶性瘤.
- MTS被认为是林奇综合征 (LS) 的表型变体.
研究的目的:
- 突出林奇综合征患者皮肤监测的重要性.
- 为了说明一个患有已知的LS的患者MTS的表现.
主要方法:
- 一个58岁的女性患者的病例报告.
- 审查患者的病史,包括子宫内膜腺癌和乳腺癌.
- 多基因小组测试揭示了MSH2致病变体.
- 对切除的皮内结节进行组织病理学检查.
主要成果:
- 根据MSH2变体和内脏恶性瘤病史诊断出林奇综合征的患者.
- 在监测中发现的脂质腺瘤,符合MTS的标准.
- 证明LS可以表现为皮肤发现.
结论:
- 林奇综合征监测应包括对皮肤瘤的查.
- 在LS患者中早期检测脂质瘤对于综合管理至关重要.
- 这个案例强调了LS和MTS之间的联系,强调了综合患者护理.
更多相关视频
09:08Isolating Human Peripheral Blood Mononuclear Cells and CD4+ T cells from Sézary Syndrome Patients for Transcriptomic Profiling
Published on: October 14, 2021
5.3K
06:48Fingerprinting Cardiolipin in Leukocytes by Mass Spectrometry for a Rapid Diagnosis of Barth Syndrome
Published on: March 23, 2022
2.3K
相关概念视频
Pleiotropy
39.5K
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,...
39.5K
mTOR Signaling and Cancer Progression
3.7K
The mammalian target of rapamycin or mTOR protein was discovered in 1994 due to its direct interaction with rapamycin. The protein gets its name from a yeast homolog called TOR. The mTOR protein complex in mammalian cells plays a major role in balancing anabolic processes such as the synthesis of proteins, lipids, and nucleotides and catabolic processes, such as autophagy in response to environmental cues, such as availability of nutrients and growth factors.
The mTOR pathway or the...
The mTOR pathway or the...
3.7K
lncRNA - Long Non-coding RNAs
8.5K
In humans, more than 80% of the genome gets transcribed. However, only around 2% of the genome codes for proteins. The remaining part produces non-coding RNAs which includes ribosomal RNAs, transfer RNAs, telomerase RNAs, and regulatory RNAs, among other types. A large number of regulatory non-coding RNAs have been classified into two groups depending upon their length – small non-coding RNAs, such as microRNA, which are less than 200 nucleotides in length, and long non-coding RNA...
8.5K
Abnormal Proliferation
4.4K
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...
4.4K
Loss of Tumor Suppressor Gene Functions
4.7K
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.
When the tumor suppressor genes develop mutations or are lost, cells start growing out of control, leading to cancer. However, a single functional copy of the tumor suppressor gene is enough for the cells to maintain their normal functions and cell...
When the tumor suppressor genes develop mutations or are lost, cells start growing out of control, leading to cancer. However, a single functional copy of the tumor suppressor gene is enough for the cells to maintain their normal functions and cell...
4.7K
Lethal Alleles
14.6K
Agouti: A Lethal Allele
Lucien Cuénot discovered lethal alleles in 1905 while studying the inheritance of coat color in mice. The agouti gene is responsible for the color of the coat in mice. This gene codes for an agouti-signaling protein, which is responsible for melanin distribution in mammals. The wild-type allele gives rise to gray-brown coat color in mice, while the mutant allele gives rise to yellow coat color. In addition to coat color, the agouti gene is associated with the yellow...
Lucien Cuénot discovered lethal alleles in 1905 while studying the inheritance of coat color in mice. The agouti gene is responsible for the color of the coat in mice. This gene codes for an agouti-signaling protein, which is responsible for melanin distribution in mammals. The wild-type allele gives rise to gray-brown coat color in mice, while the mutant allele gives rise to yellow coat color. In addition to coat color, the agouti gene is associated with the yellow...
14.6K
