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病例报告:RAS 病中的进行性中央传导性淋巴异常。两例病例报告,包括通过 MEK 抑制进行的成功治疗。

Case Report: Progressive central conducting lymphatic abnormalities in the RASopathies. Two case reports, including successful treatment by MEK inhibition.

作者信息

Gordon Kristiana, Moore Matthew, Van Zanten Malou, Pearce Julian, Itkin Maxim, Madden Brendan, Ratnam Lakshmi, Mortimer Peter S, Nagaraja Rani, Mansour Sahar

机构信息

Lymphovascular Research Unit, Molecular and Clinical Sciences Research Institute, University of London, London, United Kingdom.

Lymphovascular Clinic, St. George's University Hospitals NHS Foundation Trust, London, United Kingdom.

出版信息

Front Genet. 2022 Sep 27;13:1001105. doi: 10.3389/fgene.2022.1001105. eCollection 2022.

DOI:10.3389/fgene.2022.1001105
PMID:36238151
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9550924/
Abstract

The RASopathies are a group of genetic conditions resulting from mutations within the RAS/mitogen-activated protein kinase (RAS-MAPK) pathway. Lymphatic abnormalities are commonly associated with these conditions, however central conducting lymphatic abnormalities (CCLA) have only recently been described. CCLAs may be progressive and can result in devastating systemic sequelae, such as recurrent chylothoraces, chylopericardium and chylous ascites which can cause significant morbidity and even mortality. Improvements in imaging modalities of the central lymphatics have enhanced our understanding of these complex abnormalities. Management is challenging and have mainly consisted of diuretics and invasive mechanical drainages. We describe two adult males with Noonan syndrome with a severe and progressive CCLA. In one patient we report the therapeutic role of targeted molecular therapy with the MEK inhibitor 'Trametinib', which has resulted in dramatic, and sustained, clinical improvement. The successful use of MEK inhibition highlights the importance of understanding the molecular cause of lymphatic abnormalities and utilising targeted therapies to improve quality of life and potentially life expectancy.

摘要

RAS 病是一组由 RAS/丝裂原活化蛋白激酶(RAS-MAPK)信号通路中的突变引起的遗传疾病。淋巴系统异常通常与这些疾病相关,然而,中枢传导性淋巴系统异常(CCLA)直到最近才被描述。CCLA 可能会进展,并可能导致严重的全身后遗症,如复发性乳糜胸、乳糜心包和乳糜性腹水,这些可能会导致显著的发病率甚至死亡率。中枢淋巴管成像方式的改进增强了我们对这些复杂异常的理解。治疗具有挑战性,主要包括利尿剂和侵入性机械引流。我们描述了两名患有严重进行性 CCLA 的努南综合征成年男性。在一名患者中,我们报告了使用 MEK 抑制剂“曲美替尼”进行靶向分子治疗的治疗作用,该治疗已导致显著且持续的临床改善。MEK 抑制的成功应用凸显了了解淋巴系统异常的分子原因并利用靶向治疗来改善生活质量和潜在延长预期寿命的重要性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5691/9550924/a0c53673c63e/fgene-13-1001105-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5691/9550924/356d006772c7/fgene-13-1001105-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5691/9550924/7793d413b172/fgene-13-1001105-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5691/9550924/982dd549de38/fgene-13-1001105-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5691/9550924/cd823f1fd3ac/fgene-13-1001105-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5691/9550924/a0c53673c63e/fgene-13-1001105-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5691/9550924/356d006772c7/fgene-13-1001105-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5691/9550924/7793d413b172/fgene-13-1001105-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5691/9550924/982dd549de38/fgene-13-1001105-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5691/9550924/cd823f1fd3ac/fgene-13-1001105-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5691/9550924/a0c53673c63e/fgene-13-1001105-g005.jpg

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