KL-6/MUC-1 sebagai Penanda Penyakit Paru Interstisial

Authors

  • Juliani Dewi Laboratorium Rampal Diagnostika, Malang, Indonesia

DOI:

https://doi.org/10.55175/cdk.v45i1.845

Keywords:

Penyakit paru interstitial, Krebs Von De Lungen-6 (KL-6), marker potensial

Abstract

Penyakit paru interstisial ditandai dengan inflamasi dan fibrosis interstitium paru, yang merupakan kerusakan dan/atau regenerasi pneumosit tipe II. Diagnosisnya membutuhkan HRCT (high resolution computed tomography), bronkoskopi, dan/atau biopsi paru yang cukup invasif. Krebs Von De Lungen-6 (KL-6), glikoprotein musinous dengan berat molekul 200 kD, yang disekresi oleh pneumosit tipe II dan sel-sel epitel bronkiolar sangat menjanjikan untuk dijadikan marker yang potensial dan kurang invasif bagi kelainan paru interstitial ini.

 

Interstitial lung diseases are marked by inflammation and fibrosis in the interstitium, a damage and/or regeneration of type II pneumocytes. HCRT (high resolution computed tomography), bronchoscopy, and/or invasive lung biopsy are needed for diagnosis. Krebs Von De Lungen-6 (KL-6), a mucinous, 200 kD molecule weight glycoproteins, secreted by a type II pneumocytes and bronchiolar epithel cells is very promising as a potential and less invasive marker for this interstitial lung diseases.

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References

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Published

02-01-2018

How to Cite

Dewi, J. (2018). KL-6/MUC-1 sebagai Penanda Penyakit Paru Interstisial. Cermin Dunia Kedokteran, 45(1), 67–70. https://doi.org/10.55175/cdk.v45i1.845