Primitive Neuroectodermal Tumor as a Differential Diagnosis of CD56-Positive Tumors in Adults

A 33-year-old Japanese man was referred to our hospital after a huge intrapelvic tumor with bilateral hydronephrosis was found following persistent lumbago. Natural killer/T-cell lymphoma was suspected due to positive immunostaining for CD56, but CHOP therapy was ineffective. Re-evaluation of the tu...

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Veröffentlicht in:Internal Medicine 2009, Vol.48(15), pp.1267-1272
Hauptverfasser: Nagaya, Tadanobu, Tanaka, Naoki, Kamijo, Atsushi, Joshita, Satoru, Nakazawa, Koh, Miyabayashi, Hideharu, Yoneda, Suguru, Ito, Tetsuya, Komatsu, Michiharu, Tanaka, Eiji, Kitano, Kiyoshi
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Sprache:eng
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Zusammenfassung:A 33-year-old Japanese man was referred to our hospital after a huge intrapelvic tumor with bilateral hydronephrosis was found following persistent lumbago. Natural killer/T-cell lymphoma was suspected due to positive immunostaining for CD56, but CHOP therapy was ineffective. Re-evaluation of the tumor cells showed that they were positive for CD99, neuron-specific enolase, and synaptophysin and had a t(11 ; 22) (q24 ; q12) translocation, leading to the revised diagnosis of primitive neuroectodermal tumor (PNET). Systemic chemotherapies and radiation therapy were added to surgical resection, and no recurrence has been detected for 3 years. Taken together, PNET may be considered in adult patients with CD56-positive tumors.
ISSN:0918-2918
1349-7235
DOI:10.2169/internalmedicine.48.1980