Carbonic anhydrase IX (CAIX) does not differentiate between benign and malignant mesothelium.

@article{Ananthanarayanan2014CarbonicAI,
  title={Carbonic anhydrase IX (CAIX) does not differentiate between benign and malignant mesothelium.},
  author={Vijayalakshmi Ananthanarayanan and Maria S. Tretiakova and Aliya N. Husain and Thomas Krausz and Tatjana Antic},
  journal={American journal of clinical pathology},
  year={2014},
  volume={142 1},
  pages={
          82-7
        }
}
OBJECTIVES To examine carbonic anhydrase IX (CAIX), a marker of renal cell carcinoma that recently has been described in malignant effusions. METHODS Pleural and peritoneal fluids with the following diagnoses-reactive (n = 23), carcinoma (n = 17), and "suspicious for mesothelioma" (n = 4)-were immunostained for CAIX, calretinin, Ber-EP4, and MOC31. A tissue microarray of epithelioid (n = 27) and sarcomatoid (n = 8) mesotheliomas and three cases of benign mesothelium were also immunostained… 
1 Citations
Genomic Alterations in Undifferentiated Malignant Tumors with Rhabdoid Phenotype and Loss of BRG1 Immunoexpression Identified by Fine Needle Aspirates
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TLDR
It is demonstrated that CAIX is sensitive for mccRCC within the lung and a novel immunohistochemical marker for mesothelial proliferations, notably mesothelioma.
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TLDR
CAIX expression is more common in clear cell RCC than other renal tumor types and is associated with grade and an association between CAIX expression and grade in primary clear cell carcinomas was found.
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TLDR
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TLDR
The aim was to evaluate the utility of CAIX expression for the detection of malignant pleural effusions by enzyme‐linked immunosorbent assay (ELISA) and immunocytochemistry.
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TLDR
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TLDR
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TLDR
Key morphologic clues and a focused immunohistochemical panel, including CK7, α-methylacyl coenzyme A racemase (AMACR), TFE3, cathepsin K, and carbonic anhydrase IX (CAIX), now allow most resected RCCs with papillary architecture and clear cells to be accurately classified.
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TLDR
Taken together, CAIX expression and VHL mutational status are able to stratify patients with clear cell RCC into distinct groups with regards to clinicopathological variables and prognosis, with low CAix expression and absence of VHL mutation being associated with a poor Clinicopathological phenotype and diminished survival.
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