Low lymphatic vessel density associates with chronic rhinosinusitis with nasal polyps

医学 淋巴系统 鼻息肉 淋巴管 淋巴管新生 血管性血友病因子 病理 淋巴管内皮 上颌窦 内皮 解剖 内科学 癌症 血小板 转移
作者
Annika Luukkainen,M. Seppälä,Jutta Renkonen,Jaana Hagström,Heini Huhtala,Markus Rautiainen,Jyri Myller,Timo Paavonen,Annemarei Ranta,T. Torkkeli,Sanna Toppila‐Salmi
出处
期刊:Rhinology [European Rhinologic Society]
卷期号:55 (2): 181-191 被引量:7
标识
DOI:10.4193/rhin16.007
摘要

Chronic rhinosinusitis with and without nasal polyps (CRSwNP and CRSsNP) and antrochoanal polyps (ACP) are different upper airway inflammation phenotypes with different pathomechanisms. In order to understand the development of tissue edema, the present study aimed to evaluate lymphatic vessel density in CRSsNP, CRSwNP and ACP.120 retrospective nasal and maxillary sinus specimens were stained immunohistochemically with a von Willebrand factor polyclonal antibody recognizing vascular and lymphatic endothelium, and with a podoplanin monoclonal antibody recognizing lymphatic endothelium. Vessels were studied by microscopy in a blinded fashion, and the vessel density and the relative density of lymphatic vessels were calculated. Patient characteristic factors and follow-up data of in average 9 years were collected from patient records.In the nasal cavity, the low absolute and relative density of vessels and of lymphatic vessels was associated with CRSwNP and ACP tissues compared to control inferior turbinate. This was observed also in the inflammatory hotspot area. In the maxillary sinus, lower absolute and relative density of lymphatic vessels associated with the CRSwNP phenotype. High lymphatic vessel density in polyp tissue associated with the need for revision CRS-surgery. As a conclusion, low density of lymphatic vessels distinguished patients with CRSwNP not only in the hotspot area of polyp tissue, but also in maxillary sinus mucosa. Yet, higher lymphatic vessel density seems to associate with polyp recurrence. Further studies are still needed to explore if formation of nasal polyps could be diminished by intranasal therapeutics affecting lymphangiogenesis.
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