Primary lymphoedema in a kitten

Primary lymphoedema refers to a swelling of a part or parts of the body due to a congenital defect in the lymphatic system. Recently, the patent blue violet dye test has been described as a means of confirming the diagnosis in dogs. This case report demonstrates that the dye test is a simple and useful diagnostic test for the diagnosis of primary lymphoedema In the cat also.     

Atresia coli in a nine-week-old kitten

A case of blind-end atresia coli in a kitten surviving for 66 days is presented. Human cases of intestinal atresia are often attributed to injuries sustained in utero to a previously normal fetus. Neither clinical nor autopsy findings gave conclusive evidence regarding the aetiology of the condition in the kitten; the only sibling affected from a litter of five. The case is interesting because the kitten survived nine weeks without any clinical signs other than abdominal distension.     

Glomerulocystic kidney disease in a kitten

A 4-month-old 1-kg female Siamese-Manx cross kitten was evaluated because of renomegaly and renal failure. Ultrasonography and cytologic examination of a renal aspirate failed to provide an antemortem diagnosis. Histologic lesions included diffuse cystic dilatation of all tubules and Bowman's spaces in the renal cortex and occasional small glomerular tufts; the lesions were similar to those of glomerulocystic kidney disease of humans. Glomerulocystic kidney disease is a rare cause of early-onset renal failure, but should be considered when renomegaly is detected, cysts are not detected in the kidney by ultrasonography, and cytologic examination of a renal aspirate is nondiagnostic.     

Cerebral phaeohyphomycosis in a Birman kitten

Extract

A 6-month-old female Birman kitten was presented for long-lasting and repeated seizures. It initially had some response to treatment but deteriorated and was euthanised. At necropsy, the brain was swollen and some of the caudal cerebellum was compressed into the foramen magnum. The right cerebral hemisphere was enlarged and had a round, dark, 5 mm-diameter focus on the dorsal surface of the rostral sigmoid gyrus of the frontal cerebrum. There were smaller dark areas extending caudally into the endomarginal gyrus. When the fixed brain was sliced transversely, the lesions were grey-coloured or translucent and involved most of the rostral half of the right cerebral hemisphere. Histologically, there was severe, extensive pyogranulomatous inflammation with some interspersed areas of spongiosus and oedema. Within the granulomas were variable numbers of branching, pigmented, thin-walled, septate fungal hyphae. Cladosporium bantianum (trichoides) was isolated from the brain. This is the most frequent agent reported from cases of cerebral phaeohyphomycosis.     

Congenital diabetes insipidus in a kitten

Congenital diabetes insipidus in an 8-week-old, female longhair kitten is described. The mean urine specific gravity was 1–006; this remained unchanged after water deprivation but rose following intramuscular injection of vasopressin tannate. Pathological examination suggested pituitary malformation as the cause of the condition.     

Congenital lobar emphysema in a kitten

A five‐month‐old ragdoll cat presented with severe respiratory signs, unresponsive to medical therapy. Hyperinflation of the right middle lung lobe was diagnosed with radiography and computed tomography. Lung lobectomy following a median sternotomy led to full recovery. Histopathological analysis revealed lobar emphysema and, based on the animal's age, congenital lobar emphysema was considered the most likely diagnosis.     

Spongiform neurodegenerative disease in a Persian kitten

A congenital encephalopathy with spongiform degeneration and prominent neuronal apoptosis was observed in a 4-month-old Persian male cat with a history of depressed mental status and ataxia. On clinical examination, signs included right head tilt, ventroflexion of the head and neck, and tetraparesis. Histological examination of the central nervous system revealed multifocal, bilateral and symmetrical vacuolar degeneration of the neuropil, mainly involving the cerebellar and vestibular nuclei area, the caudal colliculi, the mesencephalic nuclei, the tegmental area and the deeper layer of the cerebral cortex. Accumulation of phosphorylated neurofilaments was detected in neuronal perikarya of the deep cortical layers, hippocampus and thalamus. Numerous pyknotic and apoptotic neurons were also observed in the cerebral cortex. These neuropathological changes differ from those observed in previous reports of spongiform degeneration of the grey matter in cats and were suggestive of a congenital neurodegenerative disease.     

Suspect osteogenesis imperfecta in a male kitten

A 4.5-month-old, male domestic shorthair was presented with bilateral femoral fractures after falling from a low height. Radiographs revealed reduced radio-opacity and thin cortices of all long bones. A presumptive diagnosis of osteodystrophy, secondary to osteogenesis imperfecta, was made on postmortem examination.     

Unilateral forelimb partial aphalangia in a kitten

Congenital limb deformities are rarely reported in the cat. The macroscopic and radiographic features of aphalangia are described in a 2-month-old male kitten showing a shortened limb that ended, at the level of the carpus, in a stump without digits. A nail was present at the level of the first phalanx and on the palmar surface only two footpads were present. The radiographs showed an absence of phalanges. The first metacarpal and the proximal and distal phalanges of digit 1 were present. The deformed metacarpal bones were reduced in length; the carpal bones were incompletely ossified. This defect is a rare condition in many animal species. To the author's knowledge, the congenital fore limb deformity described here is the first documented case in a cat.     

Ataxia in a kitten treated with griseofulvin

A 12-week-old male domestic shorthair kitten developed ataxia, fever, leukopenia, and thrombocytopenia during treatment with griseofulvin for superficial dermatophytosis. The fever and hematologic changes resolved promptly with withdrawal of the drug, but the ataxia continued unchanged. Persistent ataxia may represent a previously unrecognized idiosyncratic reaction to griseofulvin in cats.     

Congenital supravalvular aortic stenosis in a kitten

A three-month-old, male intact Norwegian forest cat without any clinical signs was referred to the cardiology service of the author’s teaching hospital for evaluation of a cardiac murmur. The murmur was systolic with an intensity of 4 out of 6 with the point of maximal intensity at the left heart base. Echocardiography revealed a moderate mitral valve regurgitation and a moderate dynamic left ventricular outflow tract obstruction both resulting from systolic anterior motion of the mitral valve (SAM). Moreover, left ventricular concentric hypertrophy was noted. Oral atenolol therapy was initiated. Recheck examination 3.5 months later revealed unchanged murmur characteristics in the still asymptomatic kitten. Echocardiography showed no SAM, but there was a severe fixed aortic stenosis apparent caused by a discrete supravalvular lesion, 4 mm distal to the valve, with an hourglass morphology. Supravalvular aortic stenosis is a rare congenital anomaly in cats, which has not been reported antemortem yet.     

Type III hemifacial microsomia in a kitten

The case described herein presented with craniofacial malformations resembling hemifacial microsomia (HFM), a congenital disorder described in humans. To our knowledge, this is the first reported case of HFM in a domestic cat.