Adenomatoid Tumor of the Right Adrenal Gland: A Case Report
Authors:
J. Koreň; P. Čunderlík
Authors‘ workplace:
Banská Bystrica
; Oddelenie patológie, Fakultná nemocnica s poliklinikou F. D. Roosevelta
Published in:
Čes.-slov. Patol., 41, 2005, No. 3, p. 111-114
Category:
Original Article
Overview
Adenomatoid tumor of adrenal gland is a very rare primary tumor with favourable prognosis. The mesothelial origin of this tumor was confirmed by multiple studies of various authors. This origin was proven by immunohistochemical and ultrastructural examinations. In our case report, we present an interesting case of the adenomatoid tumor of the right adrenal gland in a 55-year-old woman. Our case is the second well-documented case of this tumor occurring in a female adult patient. We emphasize the presence of an intraluminal thread-like bridging strands, generally considered to be a characteristic histologic feature of this tumor, which have not yet been reported in literature in adenomatoid tumor located in adrenal glands.
Key words:
adenomatoid tumor – adrenal gland – mesothelial origin – intraluminal bridges – immunohistochemistry – electron microscopy
Labels
Anatomical pathology Forensic medical examiner ToxicologyArticle was published in
Czecho-Slovak Pathology
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2005 Issue 3
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