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双腔右心室导致的进行性右心室梗阻,通过合并的先天性室间隔缺损引起分流逆转,并在一只犬中继发红细胞增多症。

Progressive Right Ventricular Obstruction Caused by a Double-Chambered Right Ventricle Resulting in Shunt-Reversal via a Concomitant Congenital Ventricular Septal Defect and Subsequent Erythrocytosis in a Dog.

作者信息

Szatmári Viktor, Dirven Mark, Aupperle-Lellbach Heike

机构信息

Clinical Sciences, Faculty of Veterinary Medicine, Utrecht University, 3584CM Utrecht, The Netherlands.

Laboklin GMBH & CO.KG, 97688 Bad Kissingen, Germany.

出版信息

Vet Sci. 2023 Feb 21;10(3):174. doi: 10.3390/vetsci10030174.

Abstract

A 3-year-old Chihuahua was presented because of exercise intolerance, respiratory distress, and syncopal episodes. At the age of 10 weeks, the dog was diagnosed with a congenital small left-to-right shunting ventricular septal defect and a mild right ventricular outflow tract obstruction via echocardiography. At that time, the dog was asymptomatic, but the breeder's veterinarian heard a murmur. Both cardiac defects were judged to be clinically non-relevant at that time. However, at 3 years of age, echocardiography revealed a severe right ventricular obstruction, known as a double-chambered right ventricle, along with right-to-left shunting via the ventricular septal defect. Because of chronic hypoxemia due to the right-to-left shunting, erythrocytosis developed. Flow reversal via the shunt was caused by a progressively worsening right ventricular obstruction leading to a supra-systemic right ventricular systolic pressure. Because of the poor prognosis, the dog was euthanized, and the heart was submitted for post-mortem examination. Gross pathologic findings revealed the close proximity of the right ventricular obstructive lesion to the ventricular septal defect. Histopathology revealed localized muscular hypertrophy and severe endocardial fibrosis. The suspected pathogenesis of the progressive obstruction was infiltrative myocardial fibrosis due to turbulent blood flow from the left-to-right shunting ventricular septal defect, as described in humans.

摘要

一只3岁的吉娃娃犬因运动不耐受、呼吸窘迫和晕厥发作前来就诊。10周龄时,通过超声心动图诊断该犬患有先天性左向右分流的小型室间隔缺损和轻度右心室流出道梗阻。当时,该犬无症状,但繁育者的兽医听到了杂音。当时判断这两种心脏缺陷在临床上均无关联。然而,3岁时,超声心动图显示存在严重的右心室梗阻,即双腔右心室,同时伴有通过室间隔缺损的右向左分流。由于右向左分流导致慢性低氧血症,出现了红细胞增多症。分流处的血流逆转是由右心室梗阻逐渐加重导致右心室收缩压超过体循环压力引起的。由于预后不良,该犬实施了安乐死,并将心脏送检进行尸检。大体病理检查发现右心室梗阻性病变与室间隔缺损紧邻。组织病理学显示局部肌肉肥大和严重的心内膜纤维化。如人类所述,渐进性梗阻的推测发病机制是由于室间隔缺损左向右分流产生的湍流导致浸润性心肌纤维化。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7288/10053892/07fd12890d60/vetsci-10-00174-g001.jpg

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