Pneumologie 1999; 53(10): 493-498
DOI: 10.1055/s-1999-9040
ÜBERSICHT
Georg Thieme Verlag Stuttgart ·New York

Pathogenesis of Malignant Pleural Effusions and Talc Pleurodesis[1]

V. B. Antony
  • Professor of Medicine and Pediatrics, Indiana University School of Medicine, USA
Further Information

Publication History

Publication Date:
31 December 1999 (online)

In this review I hope to cover two critical areas, namely the mechanism of formation of malignant pleural effusions and the treatment of malignant pleural effusions via pleurodesis. The pathogenesis of malignant pleural effusions involves several steps. These allow the malignant cell to separate from the primary tumor, dock onto the area of the metastatic site, transmigrate through the pleural membrane and initiate autocrine proliferation. The role of several factors including integrins and hyaluronan will be described. I will use the role of the glycosaminoglycan, hyaluronan, and its interaction with the CD44 receptor to illustrate the mechanisms of metastatic tumor formation on the pleural surface.

Since talc pleurodesis remains the mainstay of treatment for malignant pleural effusions, this review will discuss the inflammatory responses induced by talc and the mechanisms of talc induced fibrosis. The concept that the normal mesothelium plays a critical role in the development of pleural fibrosis will be introduced. The possibility that talc may serve other functions besides the induction of pleural fibrosis will be discussed.

1 Herrn Prof. Dr. R. Loddenkemper, Berlin, zum 60. Geburtstag gewidmet

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1 Herrn Prof. Dr. R. Loddenkemper, Berlin, zum 60. Geburtstag gewidmet

MD Veena B. Antony

Professor of Medicine and Pediatrics Indiana University School of Medicine Chief, Pulmonary and Critical Care Medicine RL Roudebush VA Medical Center

1481 West 10th Street

Indianapolis, IN 46202

USA

Email: vantony@iupui-edu

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