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| Predicate | Object |
|---|---|
| rdf:type | |
| lifeskim:mentions | |
| pubmed:issue |
4
|
| pubmed:dateCreated |
1989-9-12
|
| pubmed:abstractText |
In a histological and fine structural study of right atrial biopsy specimens from 31 patients with rheumatic heart disease (RHD), aged 7 to 46 years, and 11 patients with congenital heart disease (CHD), aged 3 to 36 years, nerve fibers or endings were seen by electron microscopy in 11 specimens. There was concurrence of ordinary axons along with terminals bearing pale cholinergic or dark adrenergic synaptic vesicles. Smaller and denser cholinergic vesicles suggested proliferation followed by exhaustion of such nerve endings. The closest proximity of nerve terminal to muscle fiber was about 100 nm. In one RHD specimen a "specific terminal cell" was present between a nerve ending and muscle fiber; in another a possible neuromuscular contact was developing at the surface of a regenerating small muscle fiber with a few myofilaments. Unmyelinated axons amidst increased subendocardial and subepicardial collagen, with prominent fibroblasts and depleted muscle fibers, were seen more frequently in specimens of CHD. Loss of myofibrils and accumulation of mitochondria, with infrequent formation of lipofuscin bodies, characterized degenerating muscle fibers in CHD also, although to a lesser degree than in RHD (reported earlier, 1985). The myocardial blood vessels in CHD tended to have pale swollen endothelial cells and narrowed lumen. The most severely affected cases of CHD were those with (1) a very wide atrial septal defect (ASD), (2) ventricular septal defect (VSD) with vegetations near the defect, (3) infundibular pulmonary stenosis, and (4) Fallot's tetralogy.
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| pubmed:language |
eng
|
| pubmed:journal | |
| pubmed:citationSubset |
IM
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| pubmed:status |
MEDLINE
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| pubmed:issn |
0191-3123
|
| pubmed:author | |
| pubmed:issnType |
Print
|
| pubmed:volume |
13
|
| pubmed:owner |
NLM
|
| pubmed:authorsComplete |
Y
|
| pubmed:pagination |
413-31
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| pubmed:dateRevised |
2009-6-26
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| pubmed:meshHeading |
pubmed-meshheading:2763378-Adolescent,
pubmed-meshheading:2763378-Adult,
pubmed-meshheading:2763378-Autonomic Nervous System,
pubmed-meshheading:2763378-Axons,
pubmed-meshheading:2763378-Child,
pubmed-meshheading:2763378-Child, Preschool,
pubmed-meshheading:2763378-Cytoplasm,
pubmed-meshheading:2763378-Female,
pubmed-meshheading:2763378-Heart,
pubmed-meshheading:2763378-Heart Defects, Congenital,
pubmed-meshheading:2763378-Humans,
pubmed-meshheading:2763378-Male,
pubmed-meshheading:2763378-Microscopy, Electron,
pubmed-meshheading:2763378-Middle Aged,
pubmed-meshheading:2763378-Myocardium,
pubmed-meshheading:2763378-Nerve Endings,
pubmed-meshheading:2763378-Nerve Fibers,
pubmed-meshheading:2763378-Rheumatic Heart Disease,
pubmed-meshheading:2763378-Schwann Cells
|
| pubmed:articleTitle |
Fine structure of A: autonomic nerve fibers and terminals in human myocardium; and B: myocardial changes in congenital heart disease.
|
| pubmed:affiliation |
Department of Neuropathology and Applied Biology, Bombay Hospital, India.
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| pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
|