A spontaneous seminoma in a 3 yr old male koi carp Cyprinus carpio L. is described. The animal, presenting a symmetric abdominal enlargement, showed a celomatic multinodular, whiteyellowish and firm mass that infiltrated the liver and the intestine wall. Histologically, the neoplasm was non-encapsulated and poorly demarcated, showed invasive growth and was characterized by a lobular architecture, subdivided by abundant fibro-connective septa. Large necrotic and calcified areas together with small aggregates of residual spermatids were present. We diagnosed a classical seminoma with a diffuse pattern. Neoplastic cells cross-reacted with vimentin, placental alkaline phosphatase, and c-KIT. An immunohistochemical phenotypization of the tumor was performed to exclude other celomatic neoplasms and to compare this seminoma with those reported in mammals and humans.
KEY WORDS: Seminoma · Koi carp · Histology · Immunohistochemistry
Resale or republication not permitted without written consent of the publisherDis Aquat Org 92: [83][84][85][86][87][88] 2010 The tumor is described histopathologically, and an immunohistochemical phenotypization was performed to exclude other celomatic neoplasms such as hepatic or intestinal carcinoma and lymphoma and to study similarities with mammalian and human seminoma.
MATERIALS AND METHODSA 3 yr old male koi carp Cyprinus carpio L. with gross pathological symptoms consisting of a symmetrical abdominal enlargement was examined histologically and immunohistochemically. The first 2 yr, the fish was kept in a farm with natural reproduction in Italy. It was then kept for 1 yr with other koi carp in a pet shop tank, during which period it was not treated with chemicals.Immediately after death, the animal was sent to the Servizio di Anatomia Patologica, Deparment of Veterinary Public Health and Animal Pathology, Faculty of Veterinary, Bologna, Italy, for further investigation. A complete necropsy was performed, and parts of the neoplastic mass and liver, intestine, swim bladder, kidney, gills, skin, and muscle were removed and fixed in 10% formalin or Bouin's fixative for histological examination. Sections were stained with hematoxylin and eosin (H&E). Additional samples of the mass were stained with periodic acid-Schiff (PAS) to detect the presence of glycogen in gonocytes. For immunohistochemistry, only formalin-fixed tissue samples from the mass were used. Immunohistochemistry was performed with antibodies against cytokeratin (1:50, clone AE1/AE3; Dako), vimentin (prediluted, clone V9; Novocastra), c-KIT (1:600, polyclonal; Dako), placental alkaline phosphatase (PLAP) (1:25, clone 8A9; Dako), alpha-fetoprotein (AFP) (prediluted, clone C3; BioGenex Laboratories), estrogen receptor (ER) (prediluted, clone SP1; Ventana Medical Systems), neuronspecific enolase (NSE) (1:1600, clone AB-1; NeoMarkers), calretinin (1:100, clone AB-1; NeoMarkers), CD3 (1:75, clone F7.2.38; Dako), CD79α (1:10, clone HM57; Dako), CD45RA (1:20, clone 4KB5; Dako). A mammal positive control and a non-diseas...