J Am Vet Med Assoc. 2022 Mar 8;260(11):1-5. doi: 10.2460/javma.21.06.0272.
A 10-month-old male crossbred dog presented with a 4-week history of polyuria and polydipsia and a 6-month history of vomiting.
Clinical examination revealed abdominal pain and right-sided nephromegaly. Biochemistry was within normal limits. Diagnostic imaging showed a well-defined, unilateral renal mass containing anechoic fluid consistent with a simple renal cyst (SRC).
The cyst was drained under ultrasonographic guidance but recurred 3 months later, concomitant with recurrence of the previously reported clinical signs. The cyst was then deroofed, fulgurated, and omentalized under laparoscopy by use of a 3-port technique. The resected cystic wall was histopathologically consistent with an SRC, presumptively congenital. The dog showed a good recovery with resolution of clinical signs. Renal function was normal at last follow-up, conducted 2 years postoperatively, without evidence of recurrent disease.
To our knowledge, this was the first report of a symptomatic juvenile SRC of presumptively congenital origin in a dog treated successfully by laparoscopic deroofing, fulguration, and omentalization. The polyuria, polydipsia, chronic vomiting, and abdominal pain may all have been related to space-occupying effects of the cyst, as these symptoms resolved post-treatment. Results of long-term follow-up advocate for this durable cure of SRC by use of laparoscopic procedures, especially when compared to simple drainage of the cyst, as the latter initially failed in the present case.
一只 10 月龄雄性杂交犬,表现为多尿和多饮史 4 周,呕吐史 6 个月。
临床检查发现腹痛和右侧肾肿大。生化检查在正常范围内。诊断性影像学检查显示一个边界清楚的单侧肾肿块,内含与单纯性肾囊肿(SRC)一致的无回声液体。
囊肿在超声引导下引流,但 3 个月后再次复发,同时伴有先前报告的临床症状复发。然后通过腹腔镜使用 3 孔技术对囊肿进行去顶、电灼和网膜化。切除的囊壁组织病理学上与 SRC 一致,推测为先天性的。狗狗术后恢复良好,临床症状缓解。最后一次随访时肾功能正常,术后 2 年,无疾病复发的证据。
据我们所知,这是首例经腹腔镜去顶、电灼和网膜化成功治疗的、具有先天性起源的、有症状的幼年 SRC 犬。多尿、多饮、慢性呕吐和腹痛可能都与囊肿的占位效应有关,因为这些症状在治疗后得到缓解。长期随访结果支持使用腹腔镜手术治疗 SRC,特别是与囊肿的单纯引流相比,因为在本病例中,囊肿单纯引流最初失败。