Hydranencephaly in a foal

Hydranencephaly is well recognised in several domestic animals, especially ruminants, but is virtually unknown in the horse. This case report describes a premature filly foal that on the day of delivery was found with a severe neurological disorder that initially improved but then progressively worsened. The foal was subjected to euthanasia on humane grounds and post mortem examination revealed somewhat asymmetric but bilateral destruction of the telencephalon identified as hydranencephaly. The possible causes of hydranencephaly in foals are discussed.     

Retrograde intussusception of the descending colon secondary to multiple colonic hamartomas in a neonatal foal

A neonatal Thoroughbred filly presented with a 3-h history of abdominal pain and distention that failed to respond to medical treatment. Diagnostic evaluation, including abdominal ultrasound, barium enema and proctoscopy, was suggestive of atresia coli. Exploratory laparotomy revealed a pedunculated mass in the wall of the diaphragmatic flexure of the ascending colon. The mass, subsequently diagnosed as a hamartoma, was attached to a smaller hamartoma by a fibrous pedicle originating from the descending colon. The descending colon had intussuscepted retrograde into the ascending colon along the fibrous band. The filly was euthanised due to poor prognosis.     

An unusual cause of colic in a neonatal foal

A case of a neonatal foal with acute colic and respiratory distress is described. The foal presented with signs of acute colic and was treated medically. The foal did not respond to treatment and 2 h after admission the foal began to demonstrate signs of respiratory distress. Thoracic and abdominal radiographs were obtained and a diagnosis of a diaphragmatic hernia was made. Surgical repair of the hernia was recommended but the owner declined and the foal was subjected to euthanasia. Post mortem findings confirmed the diagnosis and revealed that the defect was of congenital origin. Congenital diaphragmatic hernia is an unusual cause of colic in a neonatal foal.     

Surgical repair of a congenital lateral abdominal wall hernia in a neonatal foal

A 16‐hour‐old Quarter Horse filly presented for evaluation of a soft mass in the right caudoventral lateral abdominal wall. Radiography and ultrasonography confirmed the presence of a nonreducible lateral abdominal wall hernia with small intestine located between the skin and body wall. The size of the defect itself could not be imaged and the filly was taken to surgery. A 4 cm vertical defect that appeared congenital was found in the transverse abdominal muscle and was repaired by primary apposition. This case report describes the repair and outcome of this unusual type of congenital hernia.     

Small colon obstruction by an ovarian pedicle as an acquired condition in a foal

This report describes the clinical course and the surgical findings in a 7‐day‐old foal referred for signs of abdominal pain. The foal underwent abdominal celiotomy due to the degree of pain unresponsive to medical treatment and, upon exploration, an ovarian pedicle was found to be wrapped around the small colon. The lesion was corrected, the foal recovered well from anaesthesia, and a 4 month follow‐up revealed no other signs of abdominal pain or complications.     

Resuscitation of an anaesthetised foal with uroperitoneum and ventricular asystole

A 2‐day‐old male Quarter Horse foal was diagnosed with uroperitoneum and ruptured bladder. Intravenous fluid therapy was initiated prior to anaesthesia and repeated unsuccessful attempts were made to drain the abdomen of accumulated urine. Prior to anaesthesia the foal exhibited clinical signs of abdominal compartment syndrome. When anaesthetised the accumulated urine was drained by free flow through a small abdominal stab incision after aseptic site preparation. A few minutes later electrocardiography indicated second degree atrioventricular block which progressed into third degree atrioventricular block and ventricular asystole. The foal was resuscitated by closed chest compressions, mechanical ventilation, sympathomimetic and antimuscarinergic drugs. When anaesthetising these neonatal patients one must be prepared to handle potentially fatal cardiac arrhythmias and, prior to surgery, the danger posed by increased intra‐abdominal pressure should be weighed against the need for diluting plasma potassium.     

Computed tomographic myelography of a foal with discospondylitis and extradural spinal cord compression due to a vertebral abscess

A one‐month‐old Quarter Horse colt presented with progressive gait abnormalities and weakness. The foal was ataxic at presentation. Radiography identified focal endplate irregularities and lysis at C6–7. Radiographic diagnosis was discospondylitis. Computed tomographic myelography was performed immediately following euthanasia and identified an extradural compressive spinal cord lesion corresponding to the site of discospondylitis. Post mortem examination findings included abscess formation at the C6–7 intervertebral space with osteomyelitis extending into the adjacent physes and subchondral bone of caudal C6 and cranial C7. The vertebral abscess extended into the ventral spinal canal at C6–7 and was identified as the cause of extradural spinal cord compression. Salmonella sp. was cultured and isolated from purulent exudate at the intervertebral space. Computed tomographic myelography has not been previously reported for assessment of discospondylitis in horses and was successful at accurately characterising spinal cord compression in addition to osteolytic changes associated with discospondylitis.     

Surgical management of an extrahepatic portosystemic shunt in a foal: A multidisciplinary problem

A 5‐week‐old American Miniature filly was referred due to intermittent neurological signs of 4 weeks' duration. Clinicopathological findings showed increased ammonia and bile acids in venous blood samples. Abdominal ultrasonography detailed a portosystemic shunt (PSS). The foal underwent laparotomy and operative mesenteric portovenography, which further defined the PSS as extrahepatic portocaval in configuration. The PSS was occluded and intraoperative portovenography confirmed successful shunt occlusion. The foal made a good recovery from surgery and had a successful showing career until she succumbed to colic just over 3 years after surgery.     

Equine laryngeal dysplasia as a cause of acute respiratory distress in a neonatal foal

Equine laryngeal dysplasia (ELD) is a congenital disorder caused by hypoplasia or aplasia of the structures derived from the fourth and possibly sixth branchial arches. The severity of the clinical signs varies widely, and depends on which structures are involved and the extent of the defect. In most cases, affected horses present with abnormal respiratory noise during exercise and poor performance. Manifestation of the disease in foals is very rare. This case report describes an unusual presentation of ELD in a neonatal foal. The foal presented with severe respiratory distress and weakness. Equine laryngeal dysplasia was suspected on endoscopy and later confirmed on post mortem examination of the larynx. To the best of our knowledge, this is the first report describing ELD as a cause of respiratory distress in a neonatal foal.     

Traumatic sacral fracture following dystocia in a Thoroughbred foal

A Thoroughbred colt with a history of dystocia was referred for further management of suspected hypoxia. The foal showed signs of neonatal maladjustment syndrome and hindlimb paralysis. Radiography revealed the presence of a severe lumbosacral injury. The foal was subjected to euthanasia due to a hopeless prognosis. Computed tomography was performed post‐mortem and revealed a type I Salter Harris fracture of the cranial physis of the first sacral vertebra.     

Cervical vertebral anomaly and ventricular septal defect in an Arabian foal

A male Arabian foal born with a cervical mass and no apparent clinical signs presented with a cervical vertebral anomaly and ventricular septal defect. Both congenital anomalies were diagnosed at age 3 weeks and rechecked at age 6 months with radiographs and ultrasonographic studies respectively. At 11 months, in addition to radiographs and Doppler ultrasonographic studies, a contrast ultrasonographic study and post mortem myelographic and computed tomographic studies of the cervical vertebral column revealed the appearance of this rare cervical vertebral anomaly and the severity of the ventricular septal defect. To the authors' knowledge, in the Arabian foal, both conditions have not been reported simultaneously in the same patient.     

Splenic rupture and splenectomy in a foal

A 45‐day‐old foal was presented for abdominal pain. Examination revealed the presence of haemoabdomen. An exploratory celiotomy was performed that revealed a large tear on the visceral surface of the spleen. A splenectomy was performed without rib resection. An abdominal wall hernia and leucocytosis had developed by 6 weeks post surgery. A second celiotomy to repair the hernia and explore the cause of the leucocytosis was performed 10 weeks after the first surgery. A portion of the caecum and colon had become adhered to the body wall at the site of the hernia; these areas were resected and the hernia repaired with a polypropylene mesh. The filly made a good recovery and is currently in training. Splenic rupture should be considered in any horse showing signs of abdominal pain with ultrasonographic findings consistent with haemoabdomen.     

Osteomyelitis of the scapulohumeral joint associated with Rhodococcus equi and unresponsive to antibiotherapy in a foal

This case report describes the treatment and outcome of a 3.5-month-old lame foal, with a history of pneumonia associated with Rhodococcus equi. Clinical examination identified osteomyelitis of the scapulohumeral joint. The unusual location of the Rhodococcus equi osteomyelitis unresponsive to prevention and adequate treatment led to euthanasia of the patient. Post-mortem findings confirmed bronchopneumonia due to Rhodococcus equi as well as the osteomyelitis of the scapulohumeral joint. This case highlights that Rhodococcus equi should be considered as a pathogen in extrapulmonary locations such as septic arthritis and osteomyelitis in foals with history of bronchopneumonia. Early and aggressive treatment should be considered.     

Clinical presentation and surgical repair of traumatic lateral patellar luxation associated with a complete tear of the vastus medialis muscle in a neonatal Cob foal

Patellar luxation associated with traumatic injury is rare in the horse, and surgical correction has not been adequately described. This case report describes the clinical findings associated with traumatic lateral patellar luxation in a 2-day-old cob colt, and the technique used for successful surgical repair. A combination of computed tomography (CT), radiography and ultrasound was used to diagnose lateral luxation of the patella due to a complete tear of the vastus medialis muscle. All patellar ligaments were intact and no congenital abnormalities associated with the patellar luxation were present. Surgical correction of the patellar luxation was achieved using a lateral release of the patella performed by transection of the lateral femoropatellar ligament along with overlying fascia, and stabilisation of the patella by medial imbrication of the medial patellar ligament and parapatellar fascia to the distal tendon of the sartorius muscle. Radiographs at 18 weeks of age showed the patella in a normal position in a well-developed trochlear groove. At 1 year of age the foal was walking and trotting sound, with normal range of motion of the affected stifle.     

Complex stifle injury in a foal

A 130 kg, 60-day-old Quarter Horse male foal presented with bilateral stifle effusion and severe left hindlimb lameness. Clinical examination and imaging including radiography, ultrasound and computed tomography revealed bilateral stifle trauma. Specifically, disruption of the left medial meniscus and deep bone injury to the left medial femoral condyle (MFC) were detected, and bilateral injury to the origin of the cranial cruciate ligaments was suspected. Treatment consisted of stall rest and joint injection with corticosteroids, however there was little improvement in lameness. Due to the poor prognosis for soundness, the foal was subject to euthanasia 10 weeks after initial presentation. Post-mortem examination supported the left medial meniscus and MFC injuries and revealed avulsions of the origin of the cranial cruciate ligaments (complete on the left and partial on the right) from the lateral femoral condyle. Histopathology of the left stifle joint revealed varying depths of MFC osteochondral injury and severe left medial meniscus damage.     

Primary malignant melanoma in the oesophagus of a foal

A 2‐month‐old filly was evaluated for severe colic. Ultrasound, abdominocentesis and physical examination findings prompted an abdominal exploratory surgery. Perforation of the stomach was discovered during the surgery. The filly was humanely subjected to euthanasia under anaesthesia and post mortem examination was performed. In addition to gastric and duodenal ulceration, a thickened, black area of the proximal oesophagus was discovered. Histopathology of the lesion revealed primary malignant melanoma. Although rare, primary melanoma can occur in noncutaneous locations.     

A single umbilical artery and omphalophlebitis in an Arabian foal

In women, a single umbilical artery has been associated with congenital abnormalities and post-natal problems for the infant. This paper describes a case of a single umbilical artery in the amniotic portion of an abnormally long umbilical cord of a recipient mare carrying an Arabian foal. In this case, the single umbilical artery did not appear to be associated with congenital abnormalities that resulted in fetal demise or serious post-partum problems. However, the placenta showed signs, both during gestation and after delivery, of disturbances in its fluid dynamics, and omphalophlebitis developed in the foal at age one week. How such cord anomalies might disturb fluid homeostasis in the placenta or bias the foal to umbilical infection remains to be determined. Notwithstanding, careful examination of the umbilical cord at birth could alert attending veterinary clinicians to be particularly discerning in their examination of the umbilicus.