Literature DB >> 2438926

Comparison of cytokeratin expression in primary and metastatic carcinomas. Diagnostic application in surgical pathology.

K D Shah, S S Tabibzadeh, M A Gerber.   

Abstract

Metastatic poorly differentiated carcinomas often represent diagnostic difficulties in surgical pathology. Therefore, the expression of cytokeratins of different molecular weights (54, 57, and 66 kd) were compared in paraffin sections of 37 primary carcinomas with their lymph node metastases by an avidin-biotin complex (ABC) method, using monoclonal antibodies. The epithelial tumors consisted of 16 squamous cell carcinomas (SCCs) and 17 adenocarcinomas with different degrees of differentiation (well, moderately, or poorly differentiated), a renal cell carcinoma, a hepatocellular carcinoma, a transitional cell carcinoma of the bladder, and a carcinoid tumor of the stomach. The primary and metastatic tumors showed the same cytokeratin profiles. All SCCs and their metastases were positive for 57-kd cytokeratin and negative for 54-kd cytokeratin. All adenocarcinomas and their metastases were positive for 54-kd cytokeratin and negative for 66-kd cytokeratin. The extent of reactions varied with the differentiation of the carcinomas, with well-differentiated tumors showing more diffuse staining. Cases of lymphoma, sarcoma, and melanoma were negative for the three types of cytokeratins. The results indicate that identification of different molecular weight cytokeratins may be used to distinguish poorly differentiated SCCs from poorly differentiated adenocarcinomas, even in metastatic tumors. In addition, demonstration of these cytokeratins is useful in substantiating presence and identity of small foci of metastases in lymph nodes.

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Year:  1987        PMID: 2438926     DOI: 10.1093/ajcp/87.6.708

Source DB:  PubMed          Journal:  Am J Clin Pathol        ISSN: 0002-9173            Impact factor:   2.493


  5 in total

1.  The limited difference between keratin patterns of squamous cell carcinomas and adenocarcinomas is explicable by both cell lineage and state of differentiation of tumour cells.

Authors:  E B van Dorst; G N van Muijen; S V Litvinov; G J Fleuren
Journal:  J Clin Pathol       Date:  1998-09       Impact factor: 3.411

2.  Immunohistochemistry of cytokeratin proteins in squamous and transitional cell lesions of the urinary tract.

Authors:  M F Tungekar; K C Gatter; M S Al-Adnani
Journal:  J Clin Pathol       Date:  1988-12       Impact factor: 3.411

3.  Keratin expression in chemically induced mouse lung adenomas.

Authors:  W T Gunning; P J Goldblatt; G D Stoner
Journal:  Am J Pathol       Date:  1992-01       Impact factor: 4.307

4.  Cytokeratin 20 in human carcinomas. A new histodiagnostic marker detected by monoclonal antibodies.

Authors:  R Moll; A Löwe; J Laufer; W W Franke
Journal:  Am J Pathol       Date:  1992-02       Impact factor: 4.307

5.  A histopathological and ultrastructural study of eccrine porocarcinoma with special reference to its subtypes.

Authors:  O Yamamoto; J Haratake; S Yokoyama; S Imayama; M Asahi
Journal:  Virchows Arch A Pathol Anat Histopathol       Date:  1992
  5 in total

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