TY - JOUR
T1 - Synchronous ileal neuroendocrine tumor and ovarian steroid cell tumor present in a female with hyperandrogenism
AU - Gray, Stephanie
AU - Chen, Yongxin
AU - Litton, Tyler
AU - Jallad, Bassel
AU - Poddar, Nishant
AU - Hoff, John T.
AU - Schroeder, Katie
AU - Taylor, Jason
AU - Veerapong, Jula
AU - Lai, Jin Ping
N1 - Publisher Copyright:
© 2016 International Society of Gynecological Pathologists.
PY - 2016/11/1
Y1 - 2016/11/1
N2 - Well-differentiated neuroendocrine tumors (NET) of the ileum are generally slow-growing tumors with metastatic potential that may cause systemic symptoms from the secretion of serotonin, cortisol, and other biologically active substances. Likewise, steroid cell tumors of the ovary are slow-growing tumors that cause systemic symptoms from the functional production of androgens, estrogens, and other hormones. To the best of our knowledge, synchronous ileal NET and ovarian steroid cell tumors have not been previously reported in the English literature. We present a case of a 59-yr-old woman with 2 primary tumors that were found incidentally: a Stage III (T2N1M0) 1.6 cm well-differentiated NET (NET G 2) of the terminal ileum with metastasis to a mesenteric lymph node and a 2.4 cm steroid cell tumor of the left ovary. The patient had suffered from hyperandrogenism for several years before diagnosis of an ovarian steroid cell tumor, but had no symptoms attributable to the NET. From review of the literature, this is the first case description of these 2 primaries arising in the same individual.
AB - Well-differentiated neuroendocrine tumors (NET) of the ileum are generally slow-growing tumors with metastatic potential that may cause systemic symptoms from the secretion of serotonin, cortisol, and other biologically active substances. Likewise, steroid cell tumors of the ovary are slow-growing tumors that cause systemic symptoms from the functional production of androgens, estrogens, and other hormones. To the best of our knowledge, synchronous ileal NET and ovarian steroid cell tumors have not been previously reported in the English literature. We present a case of a 59-yr-old woman with 2 primary tumors that were found incidentally: a Stage III (T2N1M0) 1.6 cm well-differentiated NET (NET G 2) of the terminal ileum with metastasis to a mesenteric lymph node and a 2.4 cm steroid cell tumor of the left ovary. The patient had suffered from hyperandrogenism for several years before diagnosis of an ovarian steroid cell tumor, but had no symptoms attributable to the NET. From review of the literature, this is the first case description of these 2 primaries arising in the same individual.
KW - Hyperandrogenism
KW - Ileal neuroendocrine tumor
KW - Ovarian steroid cell tumor
KW - Steroid cell tumor not otherwise specified
KW - Synchronous
KW - Testosterone
KW - Well-differentiated neuroendocrine tumor
UR - http://www.scopus.com/inward/record.url?scp=84966696471&partnerID=8YFLogxK
U2 - 10.1097/PGP.0000000000000285
DO - 10.1097/PGP.0000000000000285
M3 - Article
C2 - 27167674
AN - SCOPUS:84966696471
SN - 0277-1691
VL - 35
SP - 554
EP - 560
JO - International Journal of Gynecological Pathology
JF - International Journal of Gynecological Pathology
IS - 6
ER -