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Erschienen in: World Journal of Surgery 4/2006

01.04.2006

Benign Peritoneal Cystic Mesothelioma

verfasst von: Jon Arne Søreide, MD, PhD, Kjetil Søreide, MD, Hartwig Körner, MD, PhD, Håvard Søiland, MD, Ole Jacob Greve, MD, Einar Gudlaugsson, MD

Erschienen in: World Journal of Surgery | Ausgabe 4/2006

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Abstract

Background

Benign peritoneal cystic mesothelioma (BPCM) is a rare tumor of unknown origin, most frequently encountered in women of reproductive age. Etiology is unknown; definitions and terminology are confusing, and preoperative diagnosis is difficult. Several differential diagnoses must be considered.

Methods

Based on our own clinical experience and a review of the relevant literature, we address clinical challenges and controversies of importance.

Results

Current literature on BPCM is mostly based on small case reports. Complete surgical resection is recommended if possible. Nevertheless, recurrent disease is not uncommon. Clinical positive effects of various adjuvant medical treatments remain to be shown.

Conclusions

Lack of consistent definitions, various treatment approaches, and mostly short follow-up times make it difficult to draw any firm conclusions from published reports. The natural history of this rare disease is less than well clarified. When possible, in an individual patient, surgical resection with curative intent seems to be the treatment of choice.
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Metadaten
Titel
Benign Peritoneal Cystic Mesothelioma
verfasst von
Jon Arne Søreide, MD, PhD
Kjetil Søreide, MD
Hartwig Körner, MD, PhD
Håvard Søiland, MD
Ole Jacob Greve, MD
Einar Gudlaugsson, MD
Publikationsdatum
01.04.2006
Erschienen in
World Journal of Surgery / Ausgabe 4/2006
Print ISSN: 0364-2313
Elektronische ISSN: 1432-2323
DOI
https://doi.org/10.1007/s00268-005-0639-z

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