Difference between revisions of "Muscles Developmental - Pathology"

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#REDIRECT[[:Category:Muscles - Developmental Pathology]]
 
 
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|backcolour =CDE472
 
|linkpage =Musculoskeletal System - Pathology
 
|linktext =Musculoskeletal System
 
|maplink = Musculoskeletal System (Content Map) - Pathology
 
|pagetype =Pathology
 
|sublink1=Muscles - Pathology
 
|subtext1=MUSCLES
 
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===Congenital diaphragmatic defects===
 
 
 
*Clefts may lead to [[Peritoneal Cavity Developmental - Pathology#Pleuroperitoneal diaphragmatic hernia|herniation]] of abdominal organs into thoracic cavity in any species
 
 
 
 
 
===Myofibrillar hypoplasia===
 
 
 
*In piglets
 
* = '''Splayleg'''
 
*May spontaneously resolve
 
*Unknown cause
 
*Responsible for significant deaths
 
 
 
 
 
===Hyperplasia of muscle fibres===
 
 
 
*In calves and lambs
 
*'''“Double muscling”'''
 
**Increased number of myofibres in affected muscle (thighs, rump, loin)
 
**Predisposes to dystocia
 
 
 
 
 
===Muscular dystrophies===
 
 
 
*Inherited group of degenerative muscular diseases
 
*Progressive muscle weakness and wasting
 
*Usually due to a genetic fault -> muscular protein deficiency
 
**Duchenne MD in humans due to dystrophin deficiency also present in some animals
 
**Dystrophin gene mutations reported in the Golden Retriever, Rottweiler, German shorthaired pointer and Irish terrier ''etc.''
 
*Inadequate [[Muscle Regeneration - Anatomy & Physiology|regeneration]], [[Muscles Hyperplastic and Neoplastic - Pathology#Hypertrophy|compensatory hypertrophy]]
 
*More about [[Muscular dystrophy]]
 
 
 
 
 
===Glycogen storage diseases===
 
 
 
*Caused by a deficiency of an enzyme
 
*See [[General Pathology - Degenerations and Infiltrations#Glycogen infiltration|general pathology]]
 
*Type II glycogenosis
 
**Deficiency of acid maltase
 
**In Shorthorn cattle
 
**Muscular weakness and incoordination
 
**Glycogen stored in skeletal muscle, heart and CNS
 
**Type I and II muscle fibres contain glycogen vacuoles
 
*Type III glycogenosis
 
**Deficiency of debranching enzyme
 
**In dogs
 
**Causes [[Myocardial - Pathology#Hypertrophic cardiomyopathy|hypertrophic cardiomyopathy]] and hepatomegaly
 
**Glycogen in skeletal and cardiac muscle, neurons nad hepatocytes
 
 
 
 
 
===Steatosis===
 
 
 
*Also called '''lipomatosis'''
 
*In cattle, sheep and pigs
 
*Fat replaces lost muscle fibres
 
*Pale muscle, bilaterally symmetrical
 
*No clinical significance
 
*Noticed at slaughter or necropsy
 
 
 
 
 
===Myasthenia gravis (MG)===
 
 
 
*'''Acquired'''
 
**Autoimmune disease
 
***Antibodies directed against acetyl choline receptors
 
**Associated with [[Thymus - Pathology|thymomas]], [[Oesophagus - Pathology#Congenital Achalasia - Megaoesophagus|megaoesophagus]] and dysphagia
 
**In adult dogs
 
*'''Congenital'''
 
**Inherited deficiency in acetyl choline receptors
 
**Rare
 
**Newfoundland, Jack Russel Terrier, Springer Spaniels – genetic predisposition
 
**In dogs – 4 DLA genes recognized: DLA-12, DLA-88, DLA-79 and DLA-64
 
**Associated with HLA gene in humans
 
**No antibodies against acetyl choline receptors in serum
 
**Non-specific muscle [[Muscles Degenerative - Pathology#Atrophy|disuse atrophy]] and fibrosis or no changes on histology
 
*Both forms manifest as weakness which worsens on exercise
 
 
 
===Canine dermatomyositis===
 
 
 
*Hereditary in Collies and Shetland sheepdgs
 
*Lesions resemble [[Muscles Inflammatory - Pathology#Canine polymyositis|canine polymyositis]]
 
*Also degeneration of blood vessels -> muscle [[Muscles Degenerative - Pathology#Ischaemia|microinfarcts]]
 
*Usually generalised but temporalis and other masticatory muscles may be involved the most
 
*Microscopically: inclusion bodies in endothelial cells
 
*Also involves [[Skin Immunologic - Pathology#Dermatomyositis|skin]]
 
 
 
===[[Muscles Degenerative - Pathology#Porcine stress syndrome|Porcine stress syndrome]]===
 

Latest revision as of 17:39, 3 March 2011