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骨科学在复杂淋巴畸形中的应用。

Osteopathy in Complex Lymphatic Anomalies.

机构信息

Department of Anatomy and Neurobiology, Northeast Ohio Medical University (NEOMED), Rootstown, OH 44272, USA.

Musculoskeletal Research Group, Northeast Ohio Medical University (NEOMED), Rootstown, OH 44272, USA.

出版信息

Int J Mol Sci. 2022 Jul 26;23(15):8258. doi: 10.3390/ijms23158258.

DOI:10.3390/ijms23158258
PMID:35897834
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9332568/
Abstract

Complex Lymphatic Anomalies (CLA) are lymphatic malformations with idiopathic bone and soft tissue involvement. The extent of the abnormal lymphatic presentation and boney invasion varies between subtypes of CLA. The etiology of these diseases has proven to be extremely elusive due to their rarity and irregular progression. In this review, we compiled literature on each of the four primary CLA subtypes and discuss their clinical presentation, lymphatic invasion, osseous profile, and regulatory pathways associated with abnormal bone loss caused by the lymphatic invasion. We highlight key proliferation and differentiation pathways shared between lymphatics and bone and how these systems may interact with each other to stimulate lymphangiogenesis and cause bone loss.

摘要

复杂淋巴管畸形(CLA)是一种具有特发性骨和软组织受累的淋巴管畸形。异常淋巴管表现和骨质侵犯的程度在 CLA 的不同亚型之间有所不同。由于这些疾病的罕见性和不规则进展,其病因已被证明极其难以捉摸。在这篇综述中,我们汇集了关于四种主要 CLA 亚型的文献,并讨论了它们的临床表现、淋巴管侵犯、骨骼特征以及与淋巴管侵犯引起的骨丢失相关的调节途径。我们强调了淋巴管和骨骼之间共同的增殖和分化途径,以及这些系统如何相互作用以刺激淋巴管生成并导致骨丢失。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0ed4/9332568/744fd2b228dc/ijms-23-08258-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0ed4/9332568/e0478e2d2b56/ijms-23-08258-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0ed4/9332568/e788c04cc54f/ijms-23-08258-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0ed4/9332568/3885b3fe4ae6/ijms-23-08258-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0ed4/9332568/744fd2b228dc/ijms-23-08258-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0ed4/9332568/e0478e2d2b56/ijms-23-08258-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0ed4/9332568/e788c04cc54f/ijms-23-08258-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0ed4/9332568/3885b3fe4ae6/ijms-23-08258-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0ed4/9332568/744fd2b228dc/ijms-23-08258-g004.jpg

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2
Extracellular HSP90α Induces MyD88-IRAK Complex-Associated IKKα/β-NF-κB/IRF3 and JAK2/TYK2-STAT-3 Signaling in Macrophages for Tumor-Promoting M2-Polarization.细胞外 HSP90α 诱导巨噬细胞中 MyD88-IRAK 复合物相关的 IKKα/β-NF-κB/IRF3 和 JAK2/TYK2-STAT3 信号转导,促进肿瘤的 M2 极化。
Cells. 2022 Jan 11;11(2):229. doi: 10.3390/cells11020229.
3
Recent Progress in Lymphangioma.
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Cells. 2023 Oct 18;12(20):2482. doi: 10.3390/cells12202482.
4
Interaction Between Blood Vasculatures and Lymphatic Vasculatures During Inflammation.炎症过程中血管与淋巴管之间的相互作用。
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