Document Detail


Differential expression of desmosomal glycoproteins in keratoacanthoma and squamous cell carcinoma of the skin: an immunohistochemical aid to diagnosis.
MedLine Citation:
PMID:  8891017     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
The distinction between keratoacanthoma and squamous cell carcinoma is a common dermatopathological dilemma. Although the mainstay of the diagnosis is still clinico-pathological correlation, many dermatopathologists now include keratoacanthomas in the spectrum of squamous cell carcinomas. Recent reports, however, have pointed out that keratoacanthoma is "deficient squamous cell carcinoma" since it loses the expression of bcl-2 antigen, consistent with initiation of apoptosis, i.e. its involution. Electron microscope studies performed in keratoacanthomas and squamous cell carcinomas also revealed significantly reduced desmosomes in squamous cell carcinoma, but not in keratoacanthoma. A series of 38 keratoacanthomas and 62 squamous cell carcinomas of the skin (28 well-differentiated, 21 moderately differentiated and 13 poorly differentiated) were stained immunohistochemically with the monoclonal antibody 32-2B to desmosomal glycoproteins desmoglein 1 and desmoglein 3. Thirty-five keratoacanthomas showed extensive pericellular desmoglein expression. Three keratoacanthomas and 20 squamous cell carcinomas (19 well-differentiated, 1 moderately differentiated) showed focal staining, and in 11 squamous cell carcinomas (2 moderately differentiated, 9 poorly differentiated) the staining was negative. The remaining 31 squamous cell carcinomas (9 well differentiated, 18 moderately differentiated, 4 poorly differentiated) showed juxtanuclear staining. None of the squamous cell carcinomas exhibited the extensive pericellular pattern found in keratoacanthomas. Assessment of staining intensity, by 3 independent examiners, revealed a strong negative correlation between desmoglein expression and degree of dysplasia in the squamous cell carcinomas (p < 0.01). This antibody therefore clearly distinguishes these tumours and may be of value in the differential diagnosis of keratoacanthoma and squamous cell carcinomas in routine histopathology.
Authors:
A L Krunic; D R Garrod; N P Smith; G S Orchard; O B Cvijetic
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Publication Detail:
Type:  Journal Article    
Journal Detail:
Title:  Acta dermato-venereologica     Volume:  76     ISSN:  0001-5555     ISO Abbreviation:  Acta Derm. Venereol.     Publication Date:  1996 Sep 
Date Detail:
Created Date:  1997-03-04     Completed Date:  1997-03-04     Revised Date:  2005-11-17    
Medline Journal Info:
Nlm Unique ID:  0370310     Medline TA:  Acta Derm Venereol     Country:  NORWAY    
Other Details:
Languages:  eng     Pagination:  394-8     Citation Subset:  IM    
Affiliation:
Dermatologic Surgery Unit, Duke University Medical Center, Durham, North Carolina, USA.
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MeSH Terms
Descriptor/Qualifier:
Autoantigens / analysis*
Cadherins / analysis*
Carcinoma, Squamous Cell / diagnosis*
Cytoskeletal Proteins / analysis*
Desmoglein 1
Desmoglein 3
Desmogleins
Desmoplakins
Desmosomes / chemistry*
Diagnosis, Differential
Humans
Immunohistochemistry
Keratoacanthoma / diagnosis*
Skin Diseases / diagnosis*
Skin Neoplasms / diagnosis*
Chemical
Reg. No./Substance:
0/Autoantigens; 0/Cadherins; 0/Cytoskeletal Proteins; 0/DSG1 protein, human; 0/DSG3 protein, human; 0/Desmoglein 1; 0/Desmoglein 3; 0/Desmogleins; 0/Desmoplakins
Comments/Corrections
Erratum In:
Acta Derm Venereol 1996 Nov;76(6):504

From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine


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