Immunocytochemistry of paragangliomas?value of staining for S-100 protein and glial fibrillary acid protein in diagnosis and prognosis

1991 ◽  
Vol 18 (5) ◽  
pp. 453-458 ◽  
Author(s):  
E. ACHILLES ◽  
B.-C. PADBERG ◽  
K. HOLL ◽  
G. KLÖPPEL ◽  
S. SCHRÖDER
1988 ◽  
Vol 119 (1) ◽  
pp. 16-20 ◽  
Author(s):  
P. J. Coates ◽  
I. Doniach

Abstract. The development of the folliculo-stellate cell in human fetal pituitaries has been investigated by immunocytochemical methods for S-100 protein and glial fibrillary acid protein. S-100 positivity was first observed in pars intermedia cells in a 13-week fetus. Staining with this antiserum is seen in cells of the pars distalis after 15 weeks. Glial fibrillary acid protein was not apparent until 18 weeks, when only cells in the pars intermedia were stained. These cells were not seen in the pars distalis before 28 weeks' gestation, but were present in a 39-week specimen and in a 5 day old baby. In most pituitaries examined, cells staining for S-100 and glial fibrillary acid protein were more concentrated in the pars intermedia than the pars distalis. These results suggest that folliculo-stellate cells in the human pituitary originate in the neurally associated facet of the pars intermedia and pass through this lobe to reach the pars distalis. Since these cells stain for glial related antigens, they may be a modified form of glial cell and arise in the neuroectoderm. Evidence for this hypothesis is given by a lack of both S-100 and glial fibrillary acid protein in the pituitaries of three anencephalic pituitaries. Differences in the timing of S-100 and glial fibrillary acid protein immunoreactivity may be related to either developmental aspects of the folliculo-stellate cell, or to the presence of two distinct cell types.


1996 ◽  
Vol 33 (6) ◽  
pp. 727-730 ◽  
Author(s):  
N. Kirchhof ◽  
W. Scheidemann ◽  
W. Baumgärtner

Multiple neurofibromas, schwannomas, and hyperplastic enteric plexuses were observed in the distal jejunum and ileum of a 6-year-old pinto gelding. The animal was presented because of an acute episode of colic. Three meters of distal small intestine, partially incarcerated in the epiploic foramen, were surgically removed. Numerous tumor nodules up to 10 mm in diameter were found adjacent to a Meckel's diverticulum, predominantly located in the subserosa of a hypertrophic segment. Histologically, tumors were well demarcated and composed of interlacing fascicles formed by spindloid cells. Adjacent enteric plexuses were hyperplastic. Immunohistochemically, all tumors were positive for vimentin and S-100. Desmin immunoreactivity was only observed in larger tumors (>500 μm). Glial fibrillary acid protein was demonstrated nearly exclusively in smaller ones. Immunostaining for neurofilament was restricted to entrapped ganglion cells. Based on conventional light microscopic examination and immunohistochemical evaluation, the lesion was diagnosed as multiple benign peripheral nerve sheath tumors in the small intestine.


2001 ◽  
Vol 38 (6) ◽  
pp. 689-697 ◽  
Author(s):  
F. Del Piero ◽  
B. A. Summers ◽  
J. F. Cummings ◽  
G. Mandelli ◽  
E. A. Blomme

Eleven gastrointestinal neoplasms from 10 aged horses and 1 pony were examined grossly, histologically, immunohistochemically, and (in two cases) ultrastructurally. Clinical signs were associated with two neoplasms, and the other nine tumors were incidental findings at laparotomy or necropsy. The neoplasms were solitary (9/11) or multifocal (2/11), well demarcated, serosal or mural masses of stomach (1), jejunum (1), ileum (3), cecum (5), and/or colon (2). Microscopic examination revealed discrete spindle cells arranged in compact patterns with fascicles and whorls or cribriform pattern with fascicles and rare palisades, often with a myxoid interstitial matrix. Three tumors infiltrated between the muscularis interna and the muscularis externa at the myenteric plexi. All neoplasms were vimentin positive, 3/11 were S-100 positive, 2/11 were muscle actin positive, and no neoplasm was positive for glial fibrillary acid protein, desmin, factor VIII, chromogranin, or neuron-specific enolase. Of the two tumors studied ultrastructurally, one contained an admixture of smooth muscle cells and cells resembling Schwann cells, and the second was populated by homogeneous fusiform mesenchymal cells separated by homogeneous matrix. Gastrointestinal stromal tumors (GIST) have been recognized in humans, more recently in dogs and nonhuman primates, and now in equids. Most of these tumors are comprised of a loosely arranged network of spindled cells separated by myxoid matrix. GIST may be composed of myogenic, neurogenic, combined myogenic and neurogenic, and undifferentiated mesenchymal cells.


1988 ◽  
Vol 3 (2) ◽  
pp. 129-134 ◽  
Author(s):  
S. Senatore ◽  
L. Zizzi ◽  
D. D'Astore ◽  
G. Saccani Jotti ◽  
M. Gabrielli

The immunocytochemical phenotype was evaluated in a case of Merkel cell carcinoma of the skin. Intermediate filaments, i.e. neurofilament, glial fibrillary acid protein, cytokeratins, keratin and panfilament as well as S-100 protein, calcitonin and epithelial membrane antigen were detected by immunoperoxidase methods. Nodular positivity for neurofilament was observed. The remaining intermediate filaments and other markers were negative. Thus the origin of Merkel cell carcinoma appears uncertain and this tumor probably has neuroendocrine activity.


2003 ◽  
Vol 40 (1) ◽  
pp. 97-102 ◽  
Author(s):  
B. Porter ◽  
A. DeLahunta ◽  
B. Summers

Gliomatosis cerebri is a well-recognized entity in human medicine characterized by unusually widespread infiltration of the neuraxis by neoplastic glial cells with relative preservation of brain architecture. This report describes the pathologic features of the disease in six dogs. The dogs ranged from 3 to 9 years of age (mean 6.1 years) without evidence of breed predilection; five of the six dogs were neutered or intact males. The clinical findings were mixed (including depression, circling, cranial nerve deficits), reflecting the diffuse nature of the disease. Histologically, there was remarkably diffuse infiltration of the white and gray matter of the brain by small numbers of elongated neoplastic cells. Areas of greater cellularity formed grossly visible lesions in four cases. Anisocytosis and pleomorphism were greater in areas of higher cellularity. Other features of tumor growth included subpial accumulation, neuronal satellitosis, perivascular cuffing, and tropism for cranial nerve and brain stem nuclei. Neoplastic cells were negative on immunohistochemical stains for glial fibrillary acid protein (GFAP) and leukocyte markers, reflecting the uncertain histogenesis of these unusual neoplasms.


1996 ◽  
Vol 39 ◽  
pp. 207-207
Author(s):  
Paul G Ekert ◽  
Neil MacLusky ◽  
Larry Becker ◽  
Martin Post ◽  
A. Keith Tanswell

2021 ◽  
Author(s):  
Sierra A. Codeluppi ◽  
Dipashree Chatterjee ◽  
Thomas D. Prevot ◽  
Keith A. Misquitta ◽  
Etienne Sibille ◽  
...  

AbstractBackgroundNeuromorphological changes are consistently reported in the prefrontal cortex (PFC) of patients with stress-related disorders and in rodent stress models, but the effects of stress on astrocyte morphology and potential link to behavioral deficits are relatively unknown.MethodsTo answer these questions, transgenic mice expressing green fluorescent protein (GFP) under the glial fibrillary acid protein (GFAP) promotor were subjected to 7, 21 or 35 days of chronic restraint stress (CRS). CRS behavioral effects on anhedonia- and anxiety-like behaviours were measured using the sucrose intake and the PhenoTyper tests, respectively. PFC GFP+ or GFAP+ cells morphology was assessed using Sholl analysis and associations with behavior were determined using correlation analysis.ResultsCRS-exposed mice displayed anxiety-like behavior at 7, 21 and 35 days and anhedonia-like behavior at 35 days. Analysis of GFAP+ cell morphology revealed significant atrophy of distal processes following 21 and 35 days of CRS. CRS induced similar decreases in intersections at distal radii for GFP+ cells, accompanied by increased proximal processes. Additionally, the number of intersections at the most distal radius step significantly correlated with time spent in the shelter zone in the PhenoTyper test (r=-0.581, p<0.01) for GFP+ cells and with behavioural emotionality calculated by z-scoring all behavioral measured deficits, for both GFAP+ and GFP+ cells (r=-0.400, p<0.05; r=-0.399, p<0.05).ConclusionChronic stress exposure induces a progressive atrophy of cortical astroglial cells, potentially contributing to maladaptive neuroplastic changes associated with stress-related disorders.


2018 ◽  
Vol 205 (2) ◽  
pp. 105-119
Author(s):  
Rasha B. Abd-ellatief ◽  
Heba K. Mohamed ◽  
Hassan I. Kotb

To our knowledge, this is the first study which investigates the induction of neuroinflammation in rats using an acidic-saline model of fibromyalgia. It is well known that the hippocampus has a fundamental role in pain perception, and astrocytes play a crucial role in pain signaling. Our aim is to evaluate the ability of dexmedetomidine to attenuate the inflammatory responses induced in astrocytes. In a group of healthy rats, induction of chronic muscle pain by intramuscular injection of 100 µL of acidic saline on days 0 and 5 resulted in peripheral sensitization (measured using the von Frey test) and significant (p < 0.05) increases in IL-1β (160.2 ± 1.1 to 335.2 ± 1.8), IL-6 (100.1 ± 1.4 to 202.4 ± 1.1), and TNF-α (60.0 ± 0.7 to 115.5 ± 1). Light and electron microscopy revealed degenerative changes in the hippocampus and reactive astrogliosis. Immunohistochemistry showed increased expression of glial fibrillary acid protein and inducible nitric oxide synthase. Surprisingly, treatment with a single dose of an α2-adrenergic agonist, dexmedetomidine (5 µg/kg i.p.), attenuated these changes. This trial suggests that dexmedetomidine possibly directly acts on astrocytes, and a peripheral action is also suggested.


Genomics ◽  
1991 ◽  
Vol 10 (4) ◽  
pp. 1087-1089 ◽  
Author(s):  
Elise Brownell ◽  
Alice S. Lee ◽  
Susan K. Pekar ◽  
Dimitrina Pravtcheva ◽  
Frank H. Ruddle ◽  
...  

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