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回顾性分析同时患有肺动脉高压混合型和疑似肺毛细血管血管瘤病的犬猫与以细前肺动脉高压为主的动物。

Retrospective analysis of dogs and cats with a mixed form of pulmonary hypertension and suspected pulmonary capillary hemangiomatosis in comparison to animals with predomination of precapillary pulmonary hypertension.

机构信息

Veterinary clinic "Belij Klyk", Moscow, Russian Federation.

出版信息

Open Vet J. 2024 May;14(5):1216-1223. doi: 10.5455/OVJ.2024.v14.i5.17. Epub 2024 May 31.

Abstract

BACKGROUND

Pulmonary capillary hemangiomatosis (PCH) is an idiopathic disease with the anomalous proliferation of a small capillary-like vessel in the pulmonary tissue, which can lead to a severe form of PH. There are only several cases of PCH described in veterinary literature: 27 cases in dogs and 2 cases in cats. In veterinary medicine, PH is mostly recognized as a consequence of left heart failure as a progression of the postcapillary PH to the precapillary form. PCH is mostly described as a primary disease, but resistant postcapillary PH with the high possibility of pulmonary edema raises speculation that PCH could be a secondary malformation to the left heart disease.

AIM

Discover the features associated with the shift between left- and right-sided heart disease in the context of PH development.

METHODS

Retrospective analysis of materials from cats and dogs with histological markers of PCH (sPCH) versus those with right heart failure (RHF).

RESULTS

Animals with histological and immunohistochemistry markers of PCH had a previous history of disease with left heart volume overload. There were no differences between the groups in radiography and gross pathology. Histologically, pulmonary fibrosis and arteriopathy could be found in RHF; in sPCH-a duplication of capillaries in alveolar septa and bizarre proliferation in surrounding structures.

CONCLUSION

PCH could be a secondary pattern of vascular remodeling due to volume overload.

摘要

背景

肺毛细血管血管瘤病(PCH)是一种特发性疾病,其特征是肺组织中小毛细血管样血管异常增殖,可导致严重的 PH 形式。兽医文献中仅描述了几例 PCH:犬 27 例,猫 2 例。在兽医医学中,PH 主要被认为是左心衰竭的后果,是后向 PH 向前向 PH 进展的结果。PCH 主要被描述为原发性疾病,但对毛细血管后 PH 的抵抗力较高,肺水肿的可能性较大,这使得人们推测 PCH 可能是左心疾病的继发性畸形。

目的

发现 PH 发展过程中与左心和右心疾病转移相关的特征。

方法

对具有 PCH 组织学标志物(sPCH)的猫和犬与具有右心衰竭(RHF)的材料进行回顾性分析。

结果

具有 PCH 组织学和免疫组织化学标志物的动物有左心容量超负荷的既往病史。两组在放射学和大体病理学方面没有差异。组织学上,RHF 可发现肺纤维化和小动脉病变;sPCH 则在肺泡隔毛细血管复制和周围结构奇异增殖。

结论

PCH 可能是由于容量超负荷导致的血管重塑的继发性模式。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4ad8/11199750/6e904b9df421/OpenVetJ-14-1216-g001.jpg

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