Henry Perrine, Schiavo Luca, Owen Laura, McCallum Katie E
Department of Veterinary Medicine, Queen's Veterinary School Hospital, Cambridge, UK.
JFMS Open Rep. 2021 Sep 29;7(2):20551169211045642. doi: 10.1177/20551169211045642. eCollection 2021 Jul-Dec.
A 5-month-old entire male domestic shorthair kitten was referred for investigation of a month-long history of urinary incontinence. Clinical examination, baseline blood work and imaging (plain radiography and ultrasonography) were unremarkable. Urinalysis documented a urinary tract infection and a retrograde urethrocystogram revealed an outpouching of the pelvic urethra. Surgical exploration revealed the absence of the dorsal portion of the urethral wall in this section of pelvic urethra, replaced by an epithelial lined expanded 'pouch'. The ventral aspect of the urethra appeared grossly normal. A modified perineal urethrostomy was performed to create an anastomosis of the urethral pouch to the skin of the perineum alongside conventional castration. The kitten made a full recovery and the incontinence resolved within 48 h. A congenital urethral diverticulum and secondary urinary tract infection were deemed the most likely aetiology in this case.
Urethral diverticuli are a rare condition in veterinary medicine. To our knowledge, it has only been reported in two dogs and presumptively in one cat, all of which made a complete recovery after surgical intervention. The present case reports an unusual urethral deformity as a potential differential diagnosis for lower urinary tract signs in a young cat.
一只5个月大的未绝育雄性家猫短毛小猫因长达一个月的尿失禁病史被转诊进行检查。临床检查、基础血液检查和影像学检查(X线平片和超声检查)均无异常。尿液分析显示存在尿路感染,逆行尿道膀胱造影显示盆腔尿道有一个憩室。手术探查发现盆腔尿道的这一段尿道壁背侧部分缺失,取而代之的是一个内衬上皮的扩张“囊袋”。尿道腹侧外观大体正常。在进行常规去势手术的同时,实施了改良会阴尿道造口术,以使尿道囊袋与会阴皮肤吻合。小猫完全康复,尿失禁在48小时内得到解决。先天性尿道憩室和继发性尿路感染被认为是该病例最可能的病因。
尿道憩室在兽医学中是一种罕见病症。据我们所知,仅在两只犬类中报道过,在一只猫中疑似存在,所有这些病例在手术干预后均完全康复。本病例报告了一种不寻常的尿道畸形,作为幼猫下尿路症状的潜在鉴别诊断。