Zusammenfassung
Hintergrund
Das Osteoidosteom ist der dritthäufigste gutartige primäre Knochentumor und verursacht typischerweise starke Nachtschmerzen.
Ziel der Arbeit
Dieser Artikel soll einen umfassenden Überblick über die Epidemiologie, Pathogenese, das histologische und radiologische Bild sowie die diversen Behandlungsoptionen des Osteoidosteoms geben.
Material und Methodik
Präsentiert werden die Ergebnisse eines Literaturüberblicks, die wesentliche Arbeiten zu diesem Thema zusammenfassen.
Ergebnisse
Das Osteoidosteom ist durch einen zentralen Nidus von maximal 1,5 cm Durchmesser mit ausgedehnter Umgebungssklerose charakterisiert. Der Tumor tritt bevorzugt diaphysär an der unteren Extremität auf und manifestiert sich überwiegend zwischen dem 5. und 25. Lebensjahr. Die Schmerzen sind auf eine Prostaglandin-vermittelte Reizung afferenter Nervenfasern zurückzuführen. Neben der Röntgenaufnahme stellt die Computertomographie in Dünnschichttechnik den Goldstandard der Diagnostik dar, sollte jedoch durch magnetresonanztomographische oder nuklearmedizinische Verfahren ergänzt werden. Die konservative Therapie mit langfristiger Einnahme nichtsteroidaler Antirheumatika wird meistens durch die minimal-invasive Radiofrequenzablation als operative Therapie der Wahl ersetzt.
Diskussion
Die Erfolgsrate der Radiofrequenzablation und anderer minimal-invasiver Verfahren in der Behandlung des Osteoidosteoms ist hoch, Therapiekosten und Hospitalisierungsdauer sind niedrig. Daher ist die offene Herdausräumung seltenen Indikationen vorbehalten und die En-bloc-Resektion nur wiederholten Lokalrezidiven.
Abstract
Background
Osteoid osteoma is the third most common benign bone tumor and typically induces pain that is worse at night.
Objective
To identify the epidemiological, pathogenetic, histological and radiological characteristics of osteoid osteoma and to present the broad variety of treatment options.
Material and methods
This review article summarizes relevant clinical studies and meta-analyses on this topic.
Results
Osteoid osteoma is characterized by a central nidus smaller than 1.5 cm in diameter with surrounding bone sclerosis. In the majority of cases, the tumor occurs in the long bones of the lower extremities and is predominantly manifested in patients aged between 5 and 25 years. Pain is mediated by prostaglandins, which stimulate afferent peripheral nerve fibers. Besides plain radiographs, thin-section computed tomography represents the gold standard of diagnostics but should be complemented by magnetic resonance or nuclear medicine imaging modalities. The conservative treatment consists of long-term therapy with non-steroidal anti-inflammatory drugs. Minimally invasive radiofrequency ablation of the nidus is the current operative treatment of choice.
Conclusion
Success rates of radiofrequency ablation and other minimally invasive procedures are high while treatment costs and length of hospital stay are low. Thus, open surgical curettage is reserved for rare indications and en bloc excision of the nidus should only be performed in cases of recurrent lesions.
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P. Orth und D. Kohn geben an, dass kein Interessenkonflikt besteht.
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Orth, P., Kohn, D. Diagnostik und Therapie des Osteoidosteoms. Orthopäde 46, 510–521 (2017). https://doi.org/10.1007/s00132-017-3428-0
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DOI: https://doi.org/10.1007/s00132-017-3428-0