Patients with thymomas have an increased risk of developing additional malignancies: lack of immunological surveillance?

Granato F, Ambrosio M R, Spina D, Lazzi S, Rocca B J, Voltolini L, Bongiolatti S, Luzzi L, Gotti G, Leoncini L & Tosi P 
(2012) Histopathology 60, 270–277 
Patients with thymomas have an increased risk of developing additional malignancies: lack of immunological surveillance? Aims:  To assess th...

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Veröffentlicht in:Histopathology 2012-02, Vol.60 (3), p.437-442
Hauptverfasser: Granato, Felice, Ambrosio, Maria R, Spina, Donatella, Lazzi, Stefano, Rocca, Bruno J, Voltolini, Luca, Bongiolatti, Stefano, Luzzi, Luca, Gotti, Giuseppe, Leoncini, Lorenzo, Tosi, Piero
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Sprache:eng
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Zusammenfassung:Granato F, Ambrosio M R, Spina D, Lazzi S, Rocca B J, Voltolini L, Bongiolatti S, Luzzi L, Gotti G, Leoncini L & Tosi P 
(2012) Histopathology 60, 270–277 
Patients with thymomas have an increased risk of developing additional malignancies: lack of immunological surveillance? Aims:  To assess the risk, for patients with thymoma, of developing an additional malignancy (AM). Methods and results:  We studied 68 patients with thymomas. Based on the World Health Organization classification, the tumours were categorised as A, AB or B (B1, B2, B3) thymomas. Control populations comprised 114 patients with colorectal cancer, 108 patients with lymphoma and 123 patients with thyroid carcinoma. Patients with thymomas showed a higher risk of developing an AM (22 of 68 patients versus 11 of 114, eight of 108, and eight of 123 patients, respectively; P = 0.0002). The association between thymomas and AMs was related to the thymoma histotype, with B1, B2, B3 and AB tumours showing a higher risk of developing an AM than A thymomas (P = 0.0474). Conclusions:  Patients affected by thymomas showed a significantly higher risk of developing additional malignancies than those in the control groups, and cases that exhibited a predominantly cortical component were more likely to develop other neoplasms. This may be related to the functions of cortical thymic epithelial cells in providing for T lymphocyte maturation through interaction with major histocompatibility complexes.
ISSN:0309-0167
1365-2559
DOI:10.1111/j.1365-2559.2011.04111.x