Clear Cell Carcinoid Tumor of the Gallbladder

Author:

Konishi Eiichi1,Nakashima Yasuaki1,Smyrk Thomas C.1,Masuda Seiji1

Affiliation:

1. From the Department of Laboratory Medicine, Saiseikai Kyoto Hospital, Nagaokakyo, Japan (Dr Konishi); Laboratory of Anatomic Pathology, Kyoto University Hospital, Kyoto, Japan (Dr Nakashima); Department of Laboratory Medicine and Pathology, Mayo Clinic, Rochester, Minn (Dr Smyrk); and Department of Surgery, Kyowa Hospital, Kyoto, Japan (Dr Masuda)

Abstract

Abstract A golden yellow polyp was detected in the gallbladder of a 64-year-old man who presented with epigastric pain. The lesion was composed of clear polygonal cells arranged in a trabecular and glandular pattern. The tumor invaded through the wall into the perimuscular subserosal layer. Immunohistochemical stains showed that neoplastic cells were positive for chromogranin A, synaptophysin, somatostatin, gastrin, and pancreatic polypeptide and negative for glucagon, serotonin, insulin, S100 protein, and inhibin. This tumor resembles the recently described clear cell endocrine tumors of the gallbladder and pancreas that are associated with von Hippel-Lindau disease. Our patient, however, had neither personal nor family history indicative of von Hippel-Lindau disease. Furthermore, published accounts of clear cell endocrine tumors in von Hippel-Lindau disease describe immunoreactivity for inhibin; the current case was negative for the disease. There may be a subtype of clear cell carcinoid tumor not associated with von Hippel-Lindau disease, which is characterized by its lack of immunoreactivity against inhibin.

Publisher

Archives of Pathology and Laboratory Medicine

Subject

Medical Laboratory Technology,General Medicine,Pathology and Forensic Medicine

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