背景
据估计,犬先天性疾病的发病率在新生犬中高达6.95%(1–3)。多种环境因素对胚胎发育过程中的发育畸形有直接影响,包括遗传因素、药物、重金属、毒素、感染和营养不良。多种犬品种均可受影响(2)。总体而言,可区分三种类型的异常:染色体异常、性腺异常和表型性别异常。每种异常均可导致不同的表型改变(4)。
在胚胎发育过程中,苗勒管发育为输卵管、子宫、宫颈和子宫阴道管的后段。形成的宫颈构成子宫与阴道之间的连接处。阴道前庭由泌尿生殖窦发育而来。处女膜由阴道管后端与前庭连接而形成。在犬中,这种上皮分离通常在出生时消失(5–7)。
处女膜闭锁可表现为背腹侧膜或环形狭窄。当阴道被处女膜完全封闭时,此状况称为处女膜闭锁。这可导致子宫和阴道分泌物积聚,引起阴道积液。该区域胚胎发育过程中发生的任何错误均可导致远端生殖道的各种异常(6, 8–12)。
这些区域的其他先天性异常包括阴道发育不全、阴道隔和前庭阴道狭窄。除无症状病例外,生殖道异常可引起非常不同的症状,如反复泌尿系统感染、尿失禁、阴道炎、阴道分泌物、不孕、无法自然繁殖和难产。所描述的阴道积液症状包括排尿困难、痛性尿淋沥、尿频、里急后重和腹痛(6, 7, 11–15)。
本病例报告旨在描述一只疑似创伤诱导的继发性阴道闭锁及由此导致的阴道积液患犬的临床表现、影像学发现、手术干预和结局。
病例介绍
一只3.5岁、体重5.2 kg的已绝育雌性吉娃娃混种犬因痛性尿淋沥就诊于柏林Valera小动物诊所。该犬最初由匈牙利一家动物福利组织救助。因难产,该犬于6个月前被绝育。自6周前抵达德国以来,她表现出滴尿和痛性尿淋沥。这些临床症状是否以及何时在匈牙利已经出现尚不清楚。既往使用抗生素(不详物质)和镇痛药(不详物质)治疗无效。
除腹部张力增加外,一般临床检查无异常。所有血液参数均在参考范围内。腹部X线片显示膀胱向头侧移位,降结肠因盆腔内软组织衰减团块而受压(图1)。
[图:腹部X线片,左侧位-侧位观:盆腔内软组织衰减团块**,使尿管移位]
腹部超声检查显示一个边界清晰的无回声结构,位于膀胱尾背侧。该结构无法归属于特定器官。膀胱本身含有自由漂浮的颗粒状成分(图2)。
[图:腹部超声检查:膀胱内可见游离漂浮的颗粒状内容物*;膀胱尾侧可见]
作为诊断和初始治疗步骤,放置了导尿管。外尿道口尺寸严重缩小(直径1 mm)。尿液分析显示活跃沉渣含有白细胞和红细胞,怀疑存在细菌。随后的微生物学检查证实存在多重耐药菌。
对边界清晰的充液结构进行细针抽吸, revealed 为漏出液,无恶性肿瘤迹象。
在全身麻醉下(前用药:美沙酮0.2 mg/kg IV(Insistor 10 mg/ml,盐酸美沙酮,Chanelle Pharma)和右美托咪定2 mcg/kg IV(Dexdomitor 0.5 mg/ml,盐酸右美托咪定,Vetoquinol GmbH);诱导:丙泊酚IV(Proposure,丙泊酚,Le Vet Beheer B.V.,荷兰);维持:异氟烷吸入(Isofluran CP 1 ml/ml,异氟烷,CP-Pharma Handelsgesellschaft mbH)),进行了计算机断层扫描。诊断为阴道积液(图3)。
[图:(A、B)计算机断层扫描,矢状面观:直肠**与尿道***之间可见管状低密度结构*,伴]
阴道镜检查显示阴唇外观正常,但阴道前庭缺失,前庭阴道连接处直径缩小,符合阴道闭锁。外尿道口解剖位置正确,但被一个茎状团块遮挡(图4)。
[图:(A、B)带蒂团块*,使用直径1 mm导管显示尿道外口。]
放置新导尿管(直径1 mm),并在高压下逆行注入30 ml 1:1稀释的Xenetix 300(碘比醇300 mg碘/ml,Guerbet),以评估是否存在尿道狭窄。外尿道口后方尿道显著扩张(图5)。怀疑该带蒂团块阻塞尿流,因此使用电外科镊将其切除(图6)。
[图:(A、B)X线片,左侧位-侧位观:30 ml造影剂(1:1稀释的Xenetix 300(碘比醇300 mg碘/m]
[图:切除带蒂团块,使用1 mm导管显示尿道外口。]
在内镜控制下扩大尿道外口,并置入12号French Foley导尿管。新鲜化阴门背侧缘,用简单间断缝合将其与尿道黏膜对合。组织病理学分析显示为纤维性息肉伴轻度黏膜增生。
术后,患者接受Sterofundin ISO IV恒速输注(40 ml/kg/24 h;B. Braun Vet Care GmbH)、美洛昔康(0.1 mg/kg口服,每日一次,连用7天;Melosus 1.5 mg/ml,美洛昔康,Cp-Pharma Handelsgesellschaft GmbH)和呋喃妥因(5 mg/kg口服,每日两次,连用14天;Nifurantin 50 mg,呋喃妥因,Apogepha Arzneimittel GmbH),根据药敏结果选用。术后4天拔除导管。观察2个月排尿正常。阴道镜检查确认无伤口愈合并发症。
第9周出现里急后重,主要影响排便,并在1周内显著加重。肛周区域肿胀,并出现直肠脱垂。直肠检查发现一个波动性肿块,怀疑对应于最初诊断的阴道积液。第二次经腹部超声检查未显示与之前检查相比的任何其他变化。因此,认为重复计算机断层扫描不必要。相反,在手术干预前重新评估了第一次计算机断层扫描。
为确定是否存在诊断影像可能遗漏的其他伴随组织改变,并尝试对阴道积液进行一期手术切除,选择诊断性剖腹术而非外阴切开术。
将先前描述的麻醉方案与硬膜外麻醉(甲哌卡因4 mg/kg;Intra-Epicain,盐酸甲哌卡因,Dechra Veterinary Products Deutschland GmbH,以及两次芬太尼静脉推注;每次推注2 mcg/kg;Fentadon 50 mcg/ml,枸橼酸芬太尼,Dechra Veterinary Products Deutschland GmbH)联合使用。术前及整个手术过程中每90分钟给予阿莫西林/克拉维酸(20 mg/kg静脉注射;AmoxClav HEXAL® 500/100 mg,Hexal AG)。阶段性低血压用多巴胺治疗(5 mg/kg/min静脉注射;Dopamin Fresenius 50 mg/5 ml,盐酸多巴胺,Fresenius Kabi Deutschland GmbH)。
膀胱粘连于大网膜。阴道积液无法通过剖腹术切除。按层适当关闭腹部切口后,行外阴切开术。
显示尿道开口,顺利置入导尿管(Ø 1 mm)。阴道积液表现为尿道颅背侧一个坚实、有弹性的黏膜突出物(图7)。
[图:外阴切开术:置入1 mm导尿管,并显示尿道。* 阴道积液。]
用11号手术刀片穿刺切开阴道积液。排出大量黏液脓性液体。采集微生物学拭子样本。随后,用无菌乳酸林格氏液冲洗开放部分。扩大穿刺切口,置入12号French Foley导尿管后,使用Monosyn (4-0)单针缝合在阴道积液膜与阴道黏膜之间创建5 mm造口(图8)。然后按层适当关闭外阴切开切口。
[图:外阴切开术:在扩大阴道积液黏膜之间的造口后,置入12 French Foley导管]
术后,患者接受晶体液静脉输注治疗,并辅以芬太尼(Fentadon 50 mcg/ml,枸橼酸芬太尼,Dechra Veterinary Products Deutschland GmbH)和氯胺酮(Ketamin 10%,盐酸氯胺酮,WDT – Wirtschaftsgenossenschaft Deutscher Tierärzte eG),初始安乃近30 mg/kg静脉注射每日三次(Metamizol WDT,500 mg/kg,安乃近钠,WDT – Wirtschaftsgenossenschaft Deutscher Tierärzte eG),随后美洛昔康0.1 mg/kg口服每日一次(Melosus 1.5 mg/ml,美洛昔康,Cp-Pharma Handelsgesellschaft GmbH)和阿莫西林/克拉维酸10 mg/kg口服每日两次(Amoxiclav 40/10 mg,阿莫西林三水合物,克拉维酸钾,CP-Pharma Handelsgesellschaft GmbH)。
2天后患犬出院,排尿正常。阴道积液微生物学检查阴性。在2年随访时,患者仍无症状。
讨论
阴道积液是兽医中一种罕见的先天性畸形。它尤其与处女膜闭锁或前庭阴道连接缺失合并发生(9, 11, 12, 14–18)。共发表了8篇涉及10只犬的病例报告(表1),描述了旨在解决典型临床症状(如排尿困难、痛性尿淋沥和里急后重)的临床症状谱、诊断步骤和治疗干预(11, 12, 15–17)。
Table 1. Summary of case reports in veterinary medicine: hydrocolpos.
| Case number | Literature | Signalment | Clinical signs | Diagnostics | Diagnosis | Therapy | Clinical course |
|---|---|---|---|---|---|---|---|
| 1 | Palm et al. ( 12 ) | Chihuahua mix, 15 months old, spayed | Dysuria, stranguria, dyschezia, occasional urinary incontinence | Abdominal ultrasonography, computed tomography, cystourethroscopy, vaginoscopy, fluoroscopy | Congenital imperforate vestibulovaginal connection with secondary hydrocolpos | Initial laparotomy with ovariohysterectomy; after 1.5 months, endoscopic perforation of the vestibulovaginal connection using a guidewire, ballon dilation of the cervical stenosis, enhancement of the opening (2 cm) via laser, rinsing | Initial improvement; after 1 month, recurrence of hydrocolpos; second intervention recommended; euthanasia; no pathohistological examination |
| 2 | Palm et al. ( 12 ) | Mixed-breed dog, 14 months old, spayed | Strangury, dysuria, urinary incontinence, dyschezia, tenesmus | Abdominal ultrasonography, fine-needle aspiration, cystourethroscopy, vaginoscopy | Congenital imperforate vestibulovaginal connection with secondary hydrocolpos | Endoscopic perforation using biopsy forceps, enhancement of the opening via laser (1,5 cm) | Endoscopic control after 2 weeks (unremarkable); long-term outcome: no clinical signs for 6 years |
| 3 | Viehoff and Sjollema ( 11 ) | Maltese, 2 years old, intact female | No clinical symptoms; incidental finding during ovariohysterectomy | Vaginoscopy, retrograde vagino-urethrocystography, abdominal sonography | Congenital vaginal obstruction at the level of the vestibulovaginal connection with secondary hydrocolpos (fibrotic connection) | Laparotomy with omentalization (not successful); episiotomy and anastomosis of the caudal vagina and the vestibule | At 24 months postoperatively, the patient remained clinically unremarkable with no recurrence |
| 4 | Viehoff and Sjollema ( 11 ) | Golden Retriever, 1 year old, intact female | Tenesmus; minimal vaginal discharge during first heat | Abdominal ultrasonography, retrograde vagino-urethrocystography | Congenital complete obstruction between the vestibule and the caudal vagina (vaginal agenesia) with secondary hydrocolpos | Ovariohysterectomy and episiotomy with a tension-free anastomosis of the vagina and the vestibule | At 15 months post- operatively, the patient remained clinically unremarkable |
| 5 | Kim et al. ( 9 ) | Shih-Tzu, 9 years old, intact female | Abdominal pain, abdominal distension, fever, anorexia, no proestrus bleeding observed since birth, subsequent urinary incontinence | Abdominal radiography, abdominal ultrasonography, explorative laparotomy, vaginoscopy | Persistent hymen with secondary pyocolpos; postoperative recurrent pyocolpos | Ovariohysterectomy and splenectomy; initial hymenotomy; 1 month later, endoscopic dissection of the hymen and lavage | 1 month after laparotomy, blunted pyocolpos; development of peritonitis and sepsis after endoscopic dissection of the hymen; death 3 days after surgery |
| 6 | Tsumagari et al. ( 16 ) | Golden Retriever, 38 months old, intact female | Dysuria, dyschezia | Vaginoscopy, abdominal radiography, abdominal ultrasonography | Imperforate hymen with hydrocolpos and a vaginal polyp | Ovariohysterectomy/partial vaginectomy; dissection of the hymen via episiotomy | 3 weeks post- surgery, normal micturition; 20 months after surgery, urinary incontinence |
| 7 | Gee et al. ( 14 ) | Bullmastiff, 14 months old, female, intact | Seven months of intermittent vaginitis since the first heat, mucopurulent vaginal discharge, vulvar swelling | Abdominal radiography, barium enema, explorative laparotomy | Segmental aplasia of the Müllerian duct system (9 cm obstruction of the cranial vagina) with secondary hydrometra/hydrocolpos | Surgical resection of the aplastic vaginal segment; end-to-end anastomosis of the vagina; intraoperative drainage of the uterus | No postoperative complications; 30 months later, successful gestation (8 puppies); no further complications |
| 8 | Alonge et al. ( 18 ) | Labrador Retriever, 1 year old, intact female | Vaginal discharge, mild apathy, a single episode of vomiting | Abdominal ultrasonography, explorative laparotomy | Congenital malformation of the tunica muscularis of the cranial vagina with secondary hematopyocolpos (vaginal ectasia due to muscular disorganization) | Ovariohysterectomy and partial vaginectomy with vaginoplasty | No postoperative complications; vaginal discharge few days later; 12 months later, the patient remained clinically unremarkable |
| 9 | Blackford et al. ( 15 ) | Dachshund, 8 years old, neutered | Acute, painful perineal bulge, dysuria, pollakiuria, tenesmus, dyschezia | Computed tomography, vaginoscopy | Imperforate hymen with secondary hydrocolpos | Perforation of the membrane; endoscopic removal of the remaining hymen | Clinical signs resolved; at the 2-month follow-up, the patient remained clinically unremarkable |
| 10 | Kim et al. ( 17 ) | Shih Tzu, 5 years old, partially neutered | Initial presentation: 2 days of anorexia and apathy; 50 days post-surgery: dysuria, dyschezia, pollakiuria, and infertility | Abdominal radiography, abdominal ultrasonography, laparotomy | First diagnosis: bilateral ureterolithiasis with hydronephrosis (left > right), pyometra, and azotemia. Second diagnosis: pyocolpos due to an imperforate hymen and vestibulovaginal stenosis | 1. First surgery: left-sided nephroureterectomy, right-sided ureterotomy with stent implantation, and hysterectomy. 2. Second surgery (50 days later): Cruciform incision of the hymen, drainage of the pyocolpos, resection of the stenotic area, vestibulovaginal anastomosis via episiotomy, and removal of the ureteral stent | Post-surgery, no clinical signs; normal micturition and defecation; no relapse |
这10只犬在信号特征方面差异很大。各种体型和品种的犬,包括吉娃娃和斗牛獒,均可发生阴道积液,与去势状态[未去势(n=6)(9, 11, 14, 16, 18)、已绝育(n=2)和已去势(n=2)(12, 15, 17)]和年龄(1至9岁)无关。大多数犬,如本病例,表现为排尿障碍(6/10;表1),其次为排便困难(5/10)、阴道分泌物(3/10)和里急后重(2/10)。仅有一只犬无临床症状。该先天性异常是在卵巢子宫切除术中偶然发现的。
与本病例不同,所有这些犬的阴道积液均由先天性异常所致,包括前庭阴道连接不通(11, 12)、阴道闭锁(11)、苗勒管系统节段性发育不全(14)、肌层先天性畸形(18)或持久性或不通的处女膜(9, 15–17)。
如本病例所怀疑的,创伤诱导的继发性阴道闭锁导致阴道积液此前尚未见描述。在我们这只犬中,预先存在的完全性阴道闭锁伴处女膜不通或前庭阴道连接缺失似乎不太可能,因为交配成功。关于可能预先存在的阴道先天性畸形(如不完全性阴道闭锁)、交配相关损伤、难产期间的产科并发症或手术过程的详细信息无法获得。因此,仍有可能轻微的先存异常或软组织创伤导致了继发性阴道闭锁,进而引起阴道积液。
一般而言,分娩相关损伤或外科干预引起的并发症可导致组织撕裂,随后发生纤维化过程,造成功能性或完全性狭窄,如继发性阴道闭锁。
此外,人类医学中有一篇病例报告描述了产科损伤后创伤诱导的阴道闭锁和阴道积血,支持这一假说(19)。该女性通过负压吸引助产分娩,分娩后5个月出现腹痛、闭经和尿潴留等临床症状。通过手术干预修复阴道并开放阴道积血后,临床症状完全缓解。在本病例中,腹部超声检查和阴道镜检查足以建立诊断。
这不适用于我们的病例,超声检查显示一个来源不明的充满液体的结构。
进一步的诊断技术,如使用或不使用造影剂的X线摄影、透视、阴道镜检查、计算机断层扫描和剖腹探查术,是诊断阴道积液的成熟工具(表1)(9, 11, 12, 14–18)。计算机断层扫描、阴道镜检查和逆行膀胱造影对本犬的畸形进行了精确描述。
最初选择微创外科手术,是因为怀疑尿道外口区域息肉可能是排尿障碍的主要原因,且微创干预足以解决临床症状。逆行膀胱尿道造影支持这一点,显示尿道外口近端尿道腔扩张,无证据表明阴道积液本身造成尿道外压性压迫。
临床进展强烈支持这一初始理由。手术切除息肉并扩大尿道外口后,排尿障碍完全缓解且未复发。然而,患者随后再次就诊时仅表现为严重里急后重、肛周肿胀和直肠脱垂。
临床症状的这一转变表明,阴道息肉和阴道积液代表了两个不同的、尽管解剖上相邻的机械性问题。息肉直接在尿道外口引起局灶性机械性尿流梗阻,而逐渐扩张的阴道积液在骨盆腔内对直肠施加严重的背侧机械压力,最终引发严重里急后重。尿道通畅性未受影响。
阴道息肉是黏液样子上皮区的反应性增生,由雌激素诱导。已知这些息肉可引起排尿障碍。与本病例不同,绝育和手术切除此类息肉通常可永久缓解临床症状(20)。
本病例中息肉的存在提示整体疾病进展背后有两种可能的病理机制。首先,预先存在的息肉可能在分娩期间作为骨盆腔内的机械性梗阻,直接导致初始难产,随后引起产伤和继发性阴道闭锁。或者,尿道口周围前庭黏膜的严重分娩相关撕裂可能刺激增生性肉芽组织形成,导致息肉形成和纤维化闭塞,最终引起阴道积液。
仅有一篇病例报告描述了一只表现为排尿困难与排便困难的犬同时发生囊性息肉与阴道积液(16)。在该报告中,一只38月龄母犬有治疗过的阴道炎与囊性结石病史,在发情前期未出现血性分泌物。最终诊断通过阴道内镜完成,发现完整处女膜位于外尿道口头侧,并伴有囊性息肉。该患犬的治愈性治疗需要开腹探查与卵巢子宫切除术,联合会阴切开术以切开处女膜(16)。
阴道息肉与阴道积液的并发构成了本病例诊断与治疗的复杂性。
如文献所记载,即使不存在并发息肉,确立阴道积液的 definitive 诊断也可能尤为困难。初始误诊或延迟诊断屡有报道。例如,在一例中,该病最初被误诊为子宫残端积脓。2周后因持续性里急后重与排便困难而重新评估,最终才正确诊断为阴道积液(12)。在另一篇报告中,卵巢子宫切除术中偶然发现阴道严重扩张,但阴道积液的 definitive 诊断仅在术后4周才确立,当时患犬经会阴切开术成功治愈(11)。此外,一例特别复杂的病例因严重子宫积脓与肾积水而 initially 行肾输尿管切除术与子宫切除术。阴道积液仅在50天后当该母犬出现严重排便困难与排尿困难时才被诊断(17)。
本病例中临床症状的缓解通过手术排空阴道积液并经会阴切开术在阴道积液黏膜与阴道黏膜之间建立造口而实现。即使在该操作2年后,该犬仍无症状。
文献回顾证实了这一假设:仅引流阴道积液即为充分的治疗干预(表1)。在总结的病例报告中,成功治疗通过部分阴道切除术、处女膜穿孔、通过吻合术恢复前庭阴道连接,或处女膜穿孔后球囊扩张实现,伴或不伴会阴切开术。开腹探查联合卵巢子宫切除术或大网膜化无效(9, 11)。在一篇报告中,初次开腹探查联合术中阴道冲洗未能评估处女膜通畅性,导致1个月后残端积脓复发。因此需要第二次内镜操作以切开持续存在的处女膜并排空液体。然而,该患犬最终在操作后3天死于脓毒症(9)。关于长期结局,仅有一只患犬在术后20个月出现尿失禁(16)。另一只接受阴道端端吻合术治疗的患犬成功妊娠,并在30个月后分娩8只健康幼犬(14)。
本病例报告的主要局限性在于可获得的该犬病史信息有限。关于交配前是否存在潜在较轻的先天性阴道畸形,或该犬在难产之前或紧接难产之后的排尿行为,均一无所知。从抵达德国后的第一天起,该犬即表现出排尿障碍。与人类病例相比,排尿障碍在出生后几乎相同的时间范围内发生:人类病例为分娩后五个月(19),本病例为难产后约六个月。
尽管阴道闭锁及由此导致的阴道积液的 definitive 发病机制无法确定,但本病例表明,对于产科并发症后出现持续性里急后重、排便困难与排尿困难的犬,应将阴道积液视为鉴别诊断。联合使用影像学工具可促进诊断。长期而言,侵入性手术治疗是最有希望的治疗选择。本病例中的犬在操作2年后仍无症状。
结论
据作者所知,这是首篇描述疑似继发性、创伤性诱导的阴道闭锁与阴道积液的病例报告。通过会阴切开术在阴道积液与阴道腔之间建立造口以引流阴道积液,是本病例中的有效治疗。
致谢
我谨衷心感谢所有共同作者的支持,以及Abby的主人给予她机会的奉献。
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伦理声明
根据当地法规和机构要求,涉及人类的研究无需伦理批准。根据国家法规和机构要求,本研究无需参与者或其法定监护人/近亲属签署书面知情同意书。根据当地法规和机构要求,涉及动物的研究无需伦理批准,因为本病例是在我们的兽医诊所就诊的,并非动物实验。本病例报告包含了所有必要的诊断和治疗。已获得动物主人书面知情同意,同意其动物参与本研究。
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CL:撰写——原始草稿。TR:撰写——原始草稿。SR-M:撰写——原始草稿。
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Background
Canine congenital disorders have been estimated to occur in up to 6.95% of newborn dogs (1–3). Various environmental factors have a direct impact on developmental malformations during embryogenesis, including genetic factors, drugs, heavy metals, toxins, infections, and malnutrition. Various dog breeds can be affected (2). Overall, three types of abnormalities can be distinguished: chromosomal, gonadal, and phenotypic sex abnormalities. Each of these can cause various phenotypical alterations (4).
During embryonic development, the Müllerian ducts develop into the fallopian tubes, uterus, cervix, and the caudal section of the uterovaginal canal. The resulting cervix forms the junction between the uterus and vagina. The vestibule of the vagina develops from the urogenital sinus. The hymen is formed by connecting the caudal end of the vaginal canal and the vestibule. In dogs, this epithelial separation usually disappears at birth (5–7).
An imperforate hymen can occur as a dorsoventral membrane or as a circular stricture. When the vagina is completely closed by the hymen, this condition is referred to as hymenal atresia. This can lead to the accumulation of fluid due to uterine and vaginal secretions, resulting in hydrocolpos. Any error that occur during embryonic development in this area can lead to various abnormalities in the distal reproductive tract (6, 8–12).
Other congenital abnormalities of these areas include vaginal aplasia, vaginal septa, and vestibulovaginal strictures. In addition to asymptomatic cases, abnormalities of the genital tract can cause very different symptoms, such as recurrent urinary tract infections, urinary incontinence, vaginitis, vaginal discharge, infertility, inability to reproduce naturally, and dystocia. The described symptoms of hydrocolpos include dysuria, stranguria, pollakiuria, tenesmus, and abdominal pain (6, 7, 11–15).
The aim of this case report was to describe the clinical presentation, imaging findings, surgical interventions, and outcomes in a dog with suspected trauma-induced secondary vaginal atresia and the resulting hydrocolpos.
Case presentation
A 3.5-year-old, 5.2-kg, neutered female Chihuahua mix was presented to the Valera Clinic for Small Animals, Berlin, due to stranguria. The dog had originally been rescued by an animal welfare organization in Hungary. Due to dystocia, the dog was neutered 6 months previously. Since arriving in Germany 6 weeks before presentation, she had exhibited urinary dribbling and stranguria. Whether and when these clinical signs had already occurred in Hungary is unknown. Previous treatment with antibiotics (unknown substance) and analgesics (unknown substance) had no effect.
Apart from increased abdominal tension, the general clinical examination was unremarkable. All blood parameters were within the reference range. Abdominal radiographs revealed a cranially displaced urinary bladder and constriction of the descending colon due to an intrapelvic soft-tissue attenuating mass (Figure 1).
[图:Abdominal radiograph, left lateral-lateral view: an intrapelvic mass of soft-tissue attenuation**, displacing the urinar]
Abdominal ultrasonography revealed a well-marginated, anechoic structure located caudodorsal to the urinary bladder. This structure could not be assigned to a specific organ. The urinary bladder itself contained free-floating, corpuscular components (Figure 2).
[图:Abdominal ultrasonography: the urinary bladder with free-floating corpuscular content*; caudal to the urinary bladder, a]
As a diagnostic and initial therapeutic step, a urinary catheter was placed. The size of the ostium urethrae externum was heavily reduced (Ø 1 mm). Urine analysis revealed active sediment containing leukocytes and erythrocytes, with suspected bacterial presence. Subsequent microbiological examination confirmed the presence of multidrug-resistant bacteria.
Fine-needle aspiration of the well-marginated, fluid-filled structure revealed a transudate, with no hints of malignancy.
Under general anesthesia (premedication: methadone 0.2 mg/kg IV (Insistor 10 mg/ml, methadone hydrochloride, Chanelle Pharma) and dexmedetomidine 2 mcg/kg IV (Dexdomitor 0.5 mg/ml, dexmedetomidine hydrochloride, Vetoquinol GmbH); induction: propofol IV (Proposure, Propofol, Le Vet Beheer B.V., the Netherlands); and maintenance: isofluran inhalation (Isofluran CP 1 ml/ml, Isofluran, CP-Pharma Handelsgesellschaft mbH), computed tomography was performed. Hydrocolpos was diagnosed (Figure 3).
[图:(A, B ) Computed tomography, sagittal view: a tubular, hypodense structure * between the rectum ** and urethra *** , wit]
Vaginoscopy revealed that the labia appeared normal, but the vestibule of the vagina was absent, and the diameter of the vestibulovaginal junction was reduced, consistent with vaginal atresia. The ostium urethrae externum was anatomically in the correct position, but it was obscured by a stem-shaped mass (Figure 4).
[图:(A, B) Pedunculated mass * with visualization of the ostium urethrae externum using a catheter of Ø 1 mm.]
A new urinary catheter (Ø 1 mm) was placed, and 30 ml of 1:1 diluted Xenetix 300 (Iobitridol 300 mg Jod/ml, Guerbet) was instilled retrogradely under high pressure to evaluate the presence of a urethral stricture. The urethra was significantly dilated behind the ostium urethrae externum (Figure 5). It was suspected that this pedunculated mass was obstructing urinary outflow and was therefore removed using electrosurgical tweezers (Figure 6).
[图:(A, B ) Radiograph, left lateral-lateral view: 30 ml of contrast agent (1:1 diluted Xenetix 300 (Iobitridol 300 mg Jod/m]
[图:Removal of the pedunculated mass with visualization of the ostium urethrae externum using a 1-mm catheter.]
The ostium urethrae externum was widened under endoscopic control, and a 12-French Foley catheter was inserted. The dorsal vulvar margin was freshened and apposed to the urethral mucosa using simple interrupted sutures. Histopathological analysis revealed a fibrotic polyp with mild mucosal hyperplasia.
Postoperatively, the patient received a constant rate infusion of Sterofundin ISO IV (40 ml/kg/24 h; B. Braun Vet Care GmbH), meloxicam (0.1 mg/kg PO once daily for 7 days; Melosus 1.5 mg/ml, meloxicam, Cp-Pharma Handelsgesellschaft GmbH), and nitrofurantoin (5 mg/kg PO twice daily for 14 days; Nifurantin 50 mg, nitrofurantoin, Apogepha Arzneimittel GmbH) according to the antibiogram. The catheter was removed 4 days postoperatively. Normal micturition was observed for 2 months. No wound-healing complications occurred, as confirmed by vaginoscopy.
In the 9th week, tenesmus developed, which primarily affected defecation and worsened significantly within 1 week. The perianal area was swollen, and a rectal prolapse was present. Rectal examination revealed a fluctuant mass, which was suspected to correspond to the initially diagnosed hydrocolpos. A second transabdominal ultrasonographic examination did not show any other changes compared to the previous examinations. Thus, repeat computed tomography was deemed unnecessary. Instead, the first computed tomography scan was re-evaluated before surgical intervention.
To determine whether any additional concomitant tissue alterations, which could have been missed on diagnostic imaging, were present and to attempt primary surgical resection of the hydrocolpos, a diagnostic laparotomy was chosen over episiotomy.
The previously described anesthetic protocol was combined with epidural anesthesia (mepivacaine 4 mg/kg; Intra-Epicain, mepivacaine hydrochloride, Dechra Veterinary Products Deutschland GmbH, and two boluses of fentanyl IV; 2 mcg/kg per bolus; Fentadon 50 mcg/ml, fentanyl citrate, Dechra Veterinary Products Deutschland GmbH). Amoxicillin/clavulanic acid (20 mg/kg IV; AmoxClav HEXAL® 500/100 mg, Hexal AG) was administered preoperatively and every 90 min throughout the surgery. Phased hypotension was treated with dopamine (5 mg/kg/min IV; Dopamin Fresenius 50 mg/5 ml, dopamine hydrochloride, Fresenius Kabi Deutschland GmbH).
The urinary bladder was adherent to the omentum. The hydrocolpos could not be resected via laparotomy. After layer-appropriate wound closure of the abdominal incision, an episiotomy was performed.
The urethral opening was visualized, and a urinary catheter (Ø 1 mm) was inserted without resistance. The hydrocolpos presented as a firm, elastic protrusion of the mucous membrane located craniodorsal to the urethra (Figure 7).
[图:Episiotomy: insertion of a 1-mm urinary catheter, and visualization of the urethra. * Hydrocolpos.]
The hydrocolpos was opened by puncture incision using a 11-scalpel blade. A large amount of mucopurulent fluid was evacuated. A microbiological swab sample was collected. Afterward, the opened part was rinsed with sterile Ringer's lactate solution. The puncture incision was widened, and after inserting a 12-French Foley catheter, a 5-mm stoma was created between the hydrocolpos membrane and the vaginal mucosa using single sutures with Monosyn (4-0) (Figure 8). A layer-appropriate wound closure of the episiotomy incision was then performed.
[图:Episiotomy: insertion of a 12-French Foley catheter after widening the stoma between the mucous membrane of the hydrocol]
Postoperatively, the patient received intravenous infusion therapy with a crystalloid solution supplemented with fentanyl (Fentadon 50 mcg/ml, Fentanylcitrate, Dechra Veterinary Products Deutschland GmbH) and ketamine (Ketamin 10%, Ketaminhydrochlorid, WDT – Wirtschaftsgenossenschaft Deutscher Tierärzte eG), initially 30 mg/kg metamizole three times daily IV (Metamizol WDT, 500 mg/kg, Metamizol-Natrium, WDT – Wirtschaftsgenossenschaft Deutscher Tierärzte eG), followed by 0.1 mg/kg meloxicam once daily PO (Melosus 1.5 mg/ml, Meloxicam, Cp-Pharma Handelsgesellschaft GmbH) and 10 mg/kg amoxicillin/clavulanic acid two times daily PO (Amoxiclav 40/10 mg, Amoxicillin-Trihydrat, Kalium-Clavulanat) CP-Pharma Handelsgesellschaft GmbH).
The dog was discharged 2 days later with normal micturition. Microbiological examination of the hydrocolpos fluid was negative. At the 2-year follow-up, the patient remained asymptomatic.
Discussion
Hydrocolpos is a rare congenital malformation in veterinary medicine. It occurs particularly in combination with an imperforate hymen or a missing vestibulovaginal connection (9, 11, 12, 14–18). In total, eight case reports involving 10 dogs have been published (Table 1), describing a spectrum of clinical signs, diagnostic steps, and therapeutic interventions aimed at resolving typical clinical signs such as stranguria, dysuria, and tenesmus (11, 12, 15–17).
Table 1. Summary of case reports in veterinary medicine: hydrocolpos.
| Case number | Literature | Signalment | Clinical signs | Diagnostics | Diagnosis | Therapy | Clinical course |
|---|---|---|---|---|---|---|---|
| 1 | Palm et al. ( 12 ) | Chihuahua mix, 15 months old, spayed | Dysuria, stranguria, dyschezia, occasional urinary incontinence | Abdominal ultrasonography, computed tomography, cystourethroscopy, vaginoscopy, fluoroscopy | Congenital imperforate vestibulovaginal connection with secondary hydrocolpos | Initial laparotomy with ovariohysterectomy; after 1.5 months, endoscopic perforation of the vestibulovaginal connection using a guidewire, ballon dilation of the cervical stenosis, enhancement of the opening (2 cm) via laser, rinsing | Initial improvement; after 1 month, recurrence of hydrocolpos; second intervention recommended; euthanasia; no pathohistological examination |
| 2 | Palm et al. ( 12 ) | Mixed-breed dog, 14 months old, spayed | Strangury, dysuria, urinary incontinence, dyschezia, tenesmus | Abdominal ultrasonography, fine-needle aspiration, cystourethroscopy, vaginoscopy | Congenital imperforate vestibulovaginal connection with secondary hydrocolpos | Endoscopic perforation using biopsy forceps, enhancement of the opening via laser (1,5 cm) | Endoscopic control after 2 weeks (unremarkable); long-term outcome: no clinical signs for 6 years |
| 3 | Viehoff and Sjollema ( 11 ) | Maltese, 2 years old, intact female | No clinical symptoms; incidental finding during ovariohysterectomy | Vaginoscopy, retrograde vagino-urethrocystography, abdominal sonography | Congenital vaginal obstruction at the level of the vestibulovaginal connection with secondary hydrocolpos (fibrotic connection) | Laparotomy with omentalization (not successful); episiotomy and anastomosis of the caudal vagina and the vestibule | At 24 months postoperatively, the patient remained clinically unremarkable with no recurrence |
| 4 | Viehoff and Sjollema ( 11 ) | Golden Retriever, 1 year old, intact female | Tenesmus; minimal vaginal discharge during first heat | Abdominal ultrasonography, retrograde vagino-urethrocystography | Congenital complete obstruction between the vestibule and the caudal vagina (vaginal agenesia) with secondary hydrocolpos | Ovariohysterectomy and episiotomy with a tension-free anastomosis of the vagina and the vestibule | At 15 months post- operatively, the patient remained clinically unremarkable |
| 5 | Kim et al. ( 9 ) | Shih-Tzu, 9 years old, intact female | Abdominal pain, abdominal distension, fever, anorexia, no proestrus bleeding observed since birth, subsequent urinary incontinence | Abdominal radiography, abdominal ultrasonography, explorative laparotomy, vaginoscopy | Persistent hymen with secondary pyocolpos; postoperative recurrent pyocolpos | Ovariohysterectomy and splenectomy; initial hymenotomy; 1 month later, endoscopic dissection of the hymen and lavage | 1 month after laparotomy, blunted pyocolpos; development of peritonitis and sepsis after endoscopic dissection of the hymen; death 3 days after surgery |
| 6 | Tsumagari et al. ( 16 ) | Golden Retriever, 38 months old, intact female | Dysuria, dyschezia | Vaginoscopy, abdominal radiography, abdominal ultrasonography | Imperforate hymen with hydrocolpos and a vaginal polyp | Ovariohysterectomy/partial vaginectomy; dissection of the hymen via episiotomy | 3 weeks post- surgery, normal micturition; 20 months after surgery, urinary incontinence |
| 7 | Gee et al. ( 14 ) | Bullmastiff, 14 months old, female, intact | Seven months of intermittent vaginitis since the first heat, mucopurulent vaginal discharge, vulvar swelling | Abdominal radiography, barium enema, explorative laparotomy | Segmental aplasia of the Müllerian duct system (9 cm obstruction of the cranial vagina) with secondary hydrometra/hydrocolpos | Surgical resection of the aplastic vaginal segment; end-to-end anastomosis of the vagina; intraoperative drainage of the uterus | No postoperative complications; 30 months later, successful gestation (8 puppies); no further complications |
| 8 | Alonge et al. ( 18 ) | Labrador Retriever, 1 year old, intact female | Vaginal discharge, mild apathy, a single episode of vomiting | Abdominal ultrasonography, explorative laparotomy | Congenital malformation of the tunica muscularis of the cranial vagina with secondary hematopyocolpos (vaginal ectasia due to muscular disorganization) | Ovariohysterectomy and partial vaginectomy with vaginoplasty | No postoperative complications; vaginal discharge few days later; 12 months later, the patient remained clinically unremarkable |
| 9 | Blackford et al. ( 15 ) | Dachshund, 8 years old, neutered | Acute, painful perineal bulge, dysuria, pollakiuria, tenesmus, dyschezia | Computed tomography, vaginoscopy | Imperforate hymen with secondary hydrocolpos | Perforation of the membrane; endoscopic removal of the remaining hymen | Clinical signs resolved; at the 2-month follow-up, the patient remained clinically unremarkable |
| 10 | Kim et al. ( 17 ) | Shih Tzu, 5 years old, partially neutered | Initial presentation: 2 days of anorexia and apathy; 50 days post-surgery: dysuria, dyschezia, pollakiuria, and infertility | Abdominal radiography, abdominal ultrasonography, laparotomy | First diagnosis: bilateral ureterolithiasis with hydronephrosis (left > right), pyometra, and azotemia. Second diagnosis: pyocolpos due to an imperforate hymen and vestibulovaginal stenosis | 1. First surgery: left-sided nephroureterectomy, right-sided ureterotomy with stent implantation, and hysterectomy. 2. Second surgery (50 days later): Cruciform incision of the hymen, drainage of the pyocolpos, resection of the stenotic area, vestibulovaginal anastomosis via episiotomy, and removal of the ureteral stent | Post-surgery, no clinical signs; normal micturition and defecation; no relapse |
These 10 dogs differed greatly in terms of signalment. Dogs of various sizes and breeds, including Chihuahua and Bullmastiff, can be affected by hydrocolpos, regardless of castration status [intact (n = 6) (9, 11, 14, 16, 18), spayed (n = 2), and neutered (n = 2) (12, 15, 17)] and age (1 to 9 years). Most dogs, as in the present case, exhibited micturition disorders (6/10; Table 1), followed by dyschezia (5/10), vaginal discharge (3/10), and tenesmus (2/10). Only one dog showed no clinical signs. The congenital abnormality was an incidental finding during ovariohysterectomy.
In contrast to the present case, all of these dogs developed hydrocolpos due to a congenital anomaly, including an imperforate vestibulovaginal connection (11, 12), vaginal atresia (11), segmental aplasia of the Müllerian duct system (14), congenital malformation of the tunica muscularis (18), or a persistent or imperforate hymen (9, 15–17).
Trauma-induced secondary vaginal atresia resulting in hydrocolpos, as was suspected in the present case, has not been previously described. Pre-existing complete vaginal atresia associated with an imperforate hymen or a missing vestibulovaginal connection seems to be unlikely in our dog because mating was successful. Detailed information regarding possible pre-existing vaginal congenital malformations, such as incomplete vaginal atresia, mating-related injuries, obstetric complications during dystocia, or the course of surgery, was unavailable. Therefore, it remains possible that minor pre-existing anomalies or soft-tissue trauma could have led to secondary vaginal atresia and, consequently, hydrocolpos.
In general, childbirth-related injuries or complications arising from surgical interventions can lead to tissue lacerations followed by fibrotic processes, causing functional or complete stenosis such as secondary vaginal atresia.
In addition, one case report in human medicine describes trauma-induced vaginal atresia and hematocolpos after obstetric injury, supporting this hypothesis (19). The woman had delivered her child by ventouse-assisted delivery and, 5 months after childbirth, developed clinical signs such as abdominal pain, amenorrhea, and urinary retention. Surgical intervention to restore the vagina and opening the hematocolpos led to complete resolution of the clinical signs. Abdominal ultrasonography and vaginoscopy were sufficient to establish the diagnosis in this case.
This does not apply to our case, where ultrasonography revealed a fluid-filled structure of unclear origin.
Further diagnostic techniques, such as radiography with or without contrast agents, fluoroscopy, vaginoscopy, computed tomography, and exploratory laparotomy, are well-described tools for diagnosing hydrocolpos (Table 1) (9, 11, 12, 14–18). Computed tomography, vaginoscopy, and retrograde cystography led to a precise description of the malformation in the present dog.
A minimally invasive surgical procedure was initially chosen because it was suspected that the polyp in the area of the ostium urethrae externum could be the main cause of the micturition disorder and that a minimally invasive intervention would be sufficient to resolve clinical signs. This was supported by retrograde cystourethrography, which demonstrated a dilated urethral lumen proximal to the external urethral ostium, with no evidence of extrinsic urethral compression by the hydrocolpos itself.
The clinical progression strongly supported this initial rationale. After the surgical removal of the polyp and widening of the ostium urethrae externum, the micturition disorder resolved completely and did not recur. However, the subsequent re-presentation of the patient was characterized exclusively by severe tenesmus, perianal swelling, and rectal prolapse.
This shift in clinical signs indicates that the vaginal polyp and the hydrocolpos represented two distinct, albeit anatomically adjacent, mechanical issues. While the polyp caused a focal mechanical urinary outflow obstruction directly at the ostium urethrae externum, the progressively expanding hydrocolpos exerted strict dorsal mechanical pressure on the rectum within the pelvic canal, ultimately triggering severe tenesmus. Urethral patency was not compromised.
A vaginal polyp is a reactive hyperplasia of the myxoid subepithelial zone, which is induced by estrogen. These polyps are well known to cause micturition disorders. In contrast to our case, spaying and surgically removing such polyps usually result in permanent resolution of the clinical signs (20).
The presence of the polyp in our case suggests two plausible pathological mechanisms underlying the overall disease progression. First, the pre-existing polyp may have acted as a mechanical obstruction within the pelvic canal during parturition, directly causing the initial dystocia, which subsequently resulted in birth trauma and secondary vaginal atresia. Alternatively, severe birth-related laceration of the vestibular mucosa surrounding the urethral opening may have stimulated the formation of hyperplastic granulation tissue, resulting in polyp formation and fibrotic occlusion, ultimately leading to hydrocolpos.
Only one case report has described the simultaneous occurrence of a cystic polyp and hydrocolpos in a dog presenting with dysuria and dyschezia (16). In that report, a 38-month-old bitch with a medical history of treated vaginitis and cystic calculi showed an absence of bloody discharge during proestrus. The final diagnosis was achieved via vaginal endoscopy, revealing an intact hymen located cranial to the external urethral orifice alongside a cystic polyp. Curative treatment in that patient required an exploratory laparotomy with ovariohysterectomy, combined with an episiotomy to dissect the hymen (16).
The concurrence of a vaginal polyp and hydrocolpos accounts for the diagnostic and therapeutic complexity of this case.
As documented in the literature, establishing a definitive diagnosis of hydrocolpos can be particularly challenging, even in the absence of a concurrent polyp. Initial misdiagnosis or delayed diagnosis has been frequently reported. For instance, in one case, the condition was initially misdiagnosed as stump pyometra. A re-evaluation performed 2 weeks later due to persistent stranguria and tenesmus finally led to the correct diagnosis of hydrocolpos (12). In another report, a severely distended vagina was noted incidentally during ovariohysterectomy, but the definitive diagnosis of hydrocolpos was only established 4 weeks postoperatively, when the patient was successfully treated by episiotomy (11). Furthermore, a particularly complex case involved an initial nephroureterectomy and hysterectomy performed due to severe pyometra and hydronephrosis. Hydrocolpos was only diagnosed 50 days later when the bitch presented with severe dyschezia and dysuria (17).
Resolution of the clinical signs in the presented case was achieved by surgically emptying the hydrocolpos and creating a stoma between the mucous membrane of the hydrocolpos and the vaginal mucosa via episiotomy. Even 2 years after the procedure, the dog remained asymptomatic.
A review of the literature confirms the assumption that only the drainage of hydrocolpos is an adequate therapeutic intervention (Table 1). In the summarized case reports, successful treatment was achieved by partial vaginectomy, perforation of the hymen, restoration of the vestibulovaginal connection by anastomosis, or hymenal perforation followed by balloon dilatation, with or without episiotomy. Exploratory laparotomy with ovariohysterectomy or omentalization was ineffective (9, 11). In one report, an initial laparotomy with intraoperative vaginal flushing failed to evaluate hymenal patency, leading to recurrence of stump pyocolpos 1 month later. A second endoscopic procedure was therefore required to dissect the persistent hymen and evacuate the fluid. However, the patient ultimately succumbed to sepsis 3 days after the procedure (9). Regarding long-term outcomes, only one patient developed urinary incontinence 20 months postoperatively (16). Another patient treated with an end-to-end vaginal anastomosis achieved a successful pregnancy and delivered eight healthy puppies 30 months later (14).
A main limitation of this case report is the limited information available regarding the medical history of the dog. Nothing is known about the presence of potentially less severe congenital vaginal malformations prior to mating or the dog's micturition behavior before or immediately after dystocia. From the first day after arrival in Germany, the dog exhibited micturition disorders. In comparison to the human case, micturition disorders occurred in nearly the same time frame after birth: five months after childbirth in the human case (19) and approximately six months after dystocia in the presented case.
Although the definitive pathogenesis of the vaginal atresia and resulting hydrocolpos could not be determined, this case shows that hydrocolpos should be considered a differential diagnosis in dogs with persistent stranguria, tenesmus, and dyschezia after obstetric complications. A combination of imaging tools can facilitate the diagnosis. In the long term, invasive surgical treatment represents the most promising treatment option. The dog presented in this case remained asymptomatic 2 years after the procedure.
Conclusion
To the best of the authors' knowledge, this is the first case report describing suspected secondary, traumatically induced vaginal atresia and hydrocolpos. Drainage of the hydrocolpos by creating a stoma between the hydrocolpos and the vaginal canal via episiotomy was an effective treatment in the presented case.
Acknowledgments
I would like to sincerely thank all the co-authors for their support and Abby's owner for her dedication to giving her a chance.
Funding Statement
The author(s) declared that financial support was not received for this work and/or its publication.
Footnotes
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Data availability statement
The original contributions presented in the study are included in the article/supplementary material, further inquiries can be directed to the corresponding author.
Ethics statement
Ethical approval was not required for the study involving humans in accordance with the local legislation and institutional requirements. Written informed consent to participate in this study was not required from the participants or the participants' legal guardians/next of kin in accordance with the national legislation and the institutional requirements. Ethical approval was not required for the studies involving animals in accordance with the local legislation and institutional requirements because this case was presented in our veterinary clinic, it was not an animal experiment. The case report includes all the necessary diagnostics und treatments. Written informed consent was obtained from the owners for the participation of their animals in this study.
Author contributions
CL: Writing – original draft. TR: Writing – original draft. SR-M: Writing – original draft.
Conflict of interest
The author(s) declared that this work was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.
Generative AI statement
The author(s) declared that Generative AI was not used in the creation of this manuscript.
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References
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Associated Data
Data Availability Statement
The original contributions presented in the study are included in the article/supplementary material, further inquiries can be directed to the corresponding author.
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