Zusammenfassung
Der Pleuraerguss ist ein häufiges pneumologisches und interdisziplinäres Problem.
In Verbindung mit bildgebenden Basisuntersuchungen bleibt die Ergussprobepunktion
zur Transsudat/Exsudat-Diskriminierung der Grundbaustein der Ergussdiagnostik. Die
klassischen Light'schen Kriterien, bestehend aus Eiweiß und LDH (beziehungsweise ihr
Serumwert-Ratio) erweisen sich hierbei mit einer Genauigkeit von 95 % am zuverlässigsten.
Die Ergänzung um das Cholesterin zum Tripletttest kann in Einzelfällen zur verbesserten
Identifikation der Transsudate genutzt werden. In der Regel lösen nur Exsudate als
Hinweis auf direkte pleurale Krankheitsbeteiligung weiteren lokalen Klärungsbedarf
aus. Die bakterielle Pleuritis, der maligne Erguss und die tuberkulöse Pleuritis sind
die wichtigsten Differenzialdiagnosen. Die Thorakozentese ermöglicht mit einer Vielzahl
biochemischer, zytologisch-immunologischer, mikrobiologischer und zunehmend auch innovativer
zellbiologischer Marker in ca. 70 % (- 90 %) eine Diagnose oder wesentliche Einengung
der Diagnose. Bei der bakteriellen Pleuritis ist die Thorakozentese in Bezug auf lokale
Interventionen unmittelbar therapierelevant. Sie liefert ferner eine Plattform für
weiterführende bildgebungs- oder endoskopie-gestützte bioptische Untersuchungen, in
deren Mittelpunkt die internistische Thorakoskopie (Pleuroskopie) steht. Die ungezielte
Stanz- oder Nadelbiopsie ist gleichermaßen bei entzündlichen wie malignen Erkrankungen
zu 40 - 70 % diagnostisch, thorakoskopisch lässt sich der exsudative Pleuraerguss
zu 95 % klären. Maligne Ergüsse können so in Kombination mit den weniger invasiven
Untersuchungen zu 97 % spezifisch diagnostiziert werden, tuberkulöse Ergüsse zu nahezu
100 %. Zusätzliche interventionelle Möglichkeiten im Sinne der vollständigen Drainage
± Pleurodese (Talkpoudrage), ggf. auch Lösung von Kammerung und Verklebung ± Fibrinolyse
charakterisieren die Thorakoskopie bei Durchführung in Lokalanästhesie auf hohem Sicherheitsniveau
auch gegenüber wesentlich aufwendigeren chirurgischen Techniken als Goldstandard im
Management der Pleuraergüsse.
Abstract
Pleural effusion is a common pneumologic and interdisciplinary problem. Transudate/exsudate
discrimination of the pleural fluid by thoracentesis remains the diagnostic basic
algorithm. Regardless of a number of new markers, classical LIGHT's criteria comprising
the pleural fluid protein- and LDH-values (or their serum ratio respectively) reveal
the highest potency with an overall accuracy of 95 %. Expansion to cholesterol-determination
(triplet test) may be helpful to identify transudates in indeterminate cases. The
need for further local diagnostic evaluation is then usually restricted to exudates.
Bacterial pleurisy, malignant and tuberculous effusion are the principal differential
diagnoses. With the use of a variety of conventional biochemical, cytologic, immunologic
and microbiologic investigations, thoracentesis will allow- or substantially narrow-diagnosis
of exudates in about 70 %, with novel cell biological markers in some conditions up
to 90 %. In bacterial pleurisy thoracentesis provides information directly relevant
to management in terms of local interventions. It also constitutes a platform for
more invasive imaging- or endoscopy-guided investigations with a focus on medical
thoracoscopy (pleuroscopy). Blind needle biopsy is diagnostic in a range of 40 - 70
% both in malignancy and inflammatory disease, thoracoscopy may clarify exudative
conditions in about 95 %. Thus malignancy may be specifically diagnosed in 97 % of
cases, tuberculous effusion in virtually 100 %. The value of thoracoscopy is augmented
by interventional options including complete evacuation of the pleural cavity, eventually
followed by talc pleurodesis (“poudrage”) in recurrent effusions or adhesiolysis,
irrigation and fibrinolysis protocols in certain inflammatory conditions. These combined
features as accomplished in local anesthesia on a remarkably high safety level characterise
medical thoracoscopy as a gold standard tool for the management of pleural disease
even in comparison to more elaborate surgical procedures.
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Bereits publizierte Beiträge zu dieser Serie:
- 01
Bildgebende Diagnostik bei Pleuraerkrankungen.
Pneumologie.
2004;
58
238-254
- 02
Pleura: Pathologie nicht-neuroplastischer Erkrankungen.
Pneumologie.
2004;
58
516-524
- 03
Pleuramesotheliom - Pathologie und Pathogenese.
Pneumologie.
2004;
58
670-679
Wolfgang Frank
Klinik III, Pneumologie · Johanniterkrankenhaus im Fläming
Johanniterstr. 1
14929 Treuenbrietzen
Email: frank@johanniter-treuenbrietzen.de