Primary carcinoid tumor of the testis: A rare case
Abstract
Neuroendocrine tumors most commonly occur in the gastrointestinal tract, lungs and pancreas. Primary testicular neuroendocrine tumors are rare, constituting 0.23% of all testicular tumors. A 35-year-old man presented to urology department with a painless left scrotal mass. He had no history of trauma. Scrotal Doppler ultrasonography revealed a 2×1.5 cm, well-circumscribed, solid lesion. Tumor marker levels were normal and staging computed tomography demonstrated no evidence of metastasis. The patient subsequently underwent left radical orchiectomy. The orchiectomy material, grossly showed a 1.4x1.2 cm, well-circumscribed, yellow, solid mass. On histopathologic examination, primary testicular carcinoid tumors cannot be distinguished from well-differentiated neuroendocrine carcinoma. The diagnosis of a primary testicular carcinoid tumor was made after ruling out an extratesticular neuroendocrine tumor using clinical and radiological data. This rare case is presented with clinical, morphological and immunohistochemical features.
Keywords
Kaynakça
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Ayrıntılar
Birincil Dil
İngilizce
Konular
Sağlık Kurumları Yönetimi
Bölüm
Olgu Sunumu
Yazarlar
Gülruh Büberal
*
0000-0002-8241-1553
Türkiye
Banu Sarsik
0000-0003-4775-3942
Türkiye
Adnan Şimşir
0000-0002-0681-0325
Türkiye
Sadık Tamsel
0000-0001-8749-782X
Türkiye
Sait Şen
0000-0002-1100-6657
Türkiye
Yayımlanma Tarihi
14 Eylül 2018
Gönderilme Tarihi
2 Ekim 2017
Kabul Tarihi
15 Kasım 2017
Yayımlandığı Sayı
Yıl 2018 Cilt: 57 Sayı: 3