|
|
(14 intermediate revisions by 5 users not shown) |
Line 1: |
Line 1: |
− | {{Unfinished}}
| + | #REDIRECT[[Key-Gaskell Syndrome]] |
− | | |
− | Also known as Feline Key-Gaskell Syndrome and Feline Autonomic Polygangliopathy.
| |
− | | |
− | Part of a syndrome of generalised autonomic neuropathy. It has been observed throughout Western Europe and The United States.
| |
− | | |
− | ==Signalment==
| |
− | * Historically reported most frequently in cats but now also in dogs
| |
− | * Usually seen in younger dogs
| |
− | * No sex predisposition
| |
− | * In a recent study of dogs confirmed as having dysautonomia those raised and housed in rural environments appeared to be at greater risk (56/65 dogs) for dysautonomia than dogs from the city
| |
− | * Labrador Retrievers may have a breed predisposition
| |
− | | |
− | ==Description==
| |
− | * Degenerative lesions of the autonomic ganglia, spinal cord intermediate grey columns and sympathetic axons
| |
− | * Aetiology still largely idiopathic
| |
− | | |
− | ==Diagnosis==
| |
− | ===Clinical Signs===
| |
− | Those of a generalised autonomic dysfuntion of the gastrointestinal and urinary tracts. Those associated with the oesophagus include:
| |
− | * Regurgitation
| |
− | * Megaoesophagus
| |
− | * Oesophageal hypotmotility
| |
− | The most frequent clinical signs associated with the syndrome are depression, anorexia, constipation, regurgitation or vomiting and incontinence (faecal and urinary) less frequently.
| |
− | | |
− | ===Physical Examination===
| |
− | Findings associated with the GI system include:
| |
− | * Dry mucous membranes
| |
− | * Intestinal distension
| |
− | | |
− | ===Radiography===
| |
− | ====Plain Radiography====
| |
− | Oesophageal dilatation may be observed.
| |
− | ====Contrast Radiography====
| |
− | Oesophageal hypomotility may be evident on barium contrast study.
| |
− | | |
− | ===Histological Findings===
| |
− | Chromatolytic degeneration in autonomic ganglia, spinal cord intermediate grey columns and some sympathetic axons.
| |
− | | |
− | ===Pharmalogical Testing===
| |
− | * Topical ocular administration of dilute pilocarpine - miosis implies a postive result. However, not all dogs will respond. Response is dependent on damage to the postganglionic parasympathetic neuron that results in supersensitivity of the iris muscle dogs.
| |
− | * IV or SC administration of atropine (a parasympatholytic)
| |
− | * ID administration of histamine - the wheal and flare response may be dampened in those with dysautonomia
| |
− | | |
− | | |
− | ==Differential Diagnosis==
| |
− | There are few differentials on presentation of the many manifestations of the disease. However, early in the course of disease other causes of megaoesophagus need to be considered.
| |
− | | |
− | | |
− | ==Treatment==
| |
− | ===Supportive===
| |
− | Including elevated feeding, gastrostomy tube feedings or total paranteral nutrition.
| |
− | ===Parasympathomimetic Drugs===
| |
− | Some dogs may show minor improvement on initiation of for example, bethanechol, metoclopramide.
| |
− | | |
− | | |
− | ==Prognosis==
| |
− | Guarded to poor. Recovery rates in the cat are reported as 20-40%, however this may take 2-12 months. In the dog recovery rates are lower. Despite recovery many are also left with residual impairment including intermittent regurgitation.
| |