A Case of Adrenal Cortical Tumor Without Endocrinological Symptoms

1941 ◽  
Vol 45 (5) ◽  
pp. 785-794 ◽  
Author(s):  
Martin J. Loeb
PEDIATRICS ◽  
1973 ◽  
Vol 51 (4) ◽  
pp. 705-709
Author(s):  
Juan J. Gershanik ◽  
Miles Elmore ◽  
Abner H. Levkoff

A neonate with hypertension, hyperglycemia, glycosuria, and an abdominal mass had, at postmortem examination, an adrenal cortical tumor, multiple microscopic ganglioneuromas of the contralateral adrenal gland, and toxoplasmosis. The possibility of a common linkage among these three entities is discussed.


1965 ◽  
Vol 119 (1) ◽  
pp. 126-131 ◽  
Author(s):  
W. J. Lossow ◽  
G. Shyamala ◽  
S. Shah ◽  
I. L. Chaikoff

1978 ◽  
Vol 11 (1-3) ◽  
pp. 75-88 ◽  
Author(s):  
PRISCILLA MATTSON ◽  
JEROME KOWAL

1987 ◽  
Vol 67 (2) ◽  
pp. 304-306 ◽  
Author(s):  
Stefano Esposito ◽  
Piervittorio Nardi

✓ Lipomas of the infundibulum are extremely rare and may not be recognized radiologically, even on computerized tomography (CT) scanning, if the tumor is less than 20 mm in diameter. A questionable CT diagnosis in the presence of endocrinological symptoms may justify an operation by microsurgical technique on the retrochiasmatic region. In the case reported, microsurgical removal of a small infundibular lipoma was successfully accomplished.


Endocrinology ◽  
1986 ◽  
Vol 118 (5) ◽  
pp. 1897-1905 ◽  
Author(s):  
DAVID S. DUCH ◽  
JEFFREY H. WOOLF ◽  
MARK P. EDELSTEIN ◽  
O. HUMBERTO VIVEROS ◽  
MARTHA A. ABOU-DONIA ◽  
...  

Author(s):  
David S. Duch ◽  
Jeffrey H. Woolf ◽  
Mark P. Edelstein ◽  
O. Humberto Viveros ◽  
Martha M. Abou-Donia ◽  
...  

Sign in / Sign up

Export Citation Format

Share Document