Imaging for the Differential Diagnosis of Cushing’s Syndrome: MRI, CT, and Isotopic Scanning

2010 ◽  
pp. 91-103
Author(s):  
Wouter W. de Herder ◽  
Richard A. Feelders
1989 ◽  
Vol 120 (3_Suppl) ◽  
pp. S113 ◽  
Author(s):  
C. JAURSCH-HANCKE ◽  
B. ALLOLIO ◽  
M. REINCKE ◽  
W. WINKELMANN

The Lancet ◽  
1986 ◽  
Vol 328 (8511) ◽  
pp. 871 ◽  
Author(s):  
T.A. Howlett ◽  
A. Grossman ◽  
L.H. Rees ◽  
G.M. Besser

2010 ◽  
pp. OR14-5-OR14-5
Author(s):  
G Page-Wilson ◽  
PU Freda ◽  
TP Jacobs ◽  
AG Khandji ◽  
JN Bruce ◽  
...  

2006 ◽  
Vol 154 (6) ◽  
pp. 807-811 ◽  
Author(s):  
Malebranche Berardo C Cunha Neto ◽  
Márcio Carlos Machado ◽  
Flávia Mesquita ◽  
Nina Rosa de Castro Musolino ◽  
Andrea Cecília Toscanini ◽  
...  

Thymic hyperplasia has been described after the resolution of hypercortisolism from several etiologies, causing great diagnostic dilemmas. We describe a case where the catheterization of the thymic vein was essential for the differential diagnosis of a thymic enlargement in an adrenalectomized patient with ACTH-dependent Cushing’s syndrome. The patient was a 48-year-old female with clinical and laboratorial data suggesting Cushing’s disease. She underwent a transsphenoidal surgery with no tumor visualization and no remission of the syndrome. Histopathological studies disclosed a normal pituitary. She underwent a bilateral adrenalectomy and 8 months later a chest CT showed an increase of left thymic lobe, which was previously non-existent. After a negative 111In-pentetreotide scintigraphy, the patient underwent simultaneous and bilateral catheterism of the petrosus sinuses and catheterization of the thymic and inominate veins and no ACTH gradient was shown among the sites of collection. She did not undergo thoracotomy and a follow-up was established. During the evolution, there was a spontaneous regression of the thymic lesion 38 months after the diagnosis. The ACTH gradient during the catheterization of thymic vein was essential for the differential diagnosis of the thymic enlargement tumor after hypercortisolism resolution in ACTH-dependent Cushing’s syndrome, especially in this case, where the ACTH source was occult, thus avoiding an invasive surgical procedure for a benign entity with spontaneous resolution.


Pituitary ◽  
2016 ◽  
Vol 19 (5) ◽  
pp. 488-495 ◽  
Author(s):  
Mattia Barbot ◽  
Laura Trementino ◽  
Marialuisa Zilio ◽  
Filippo Ceccato ◽  
Nora Albiger ◽  
...  

1992 ◽  
Vol 55 (3) ◽  
pp. 264-268 ◽  
Author(s):  
Marco Boscaro ◽  
Annalisa Rampazzo ◽  
Agostino Paoletta ◽  
Paola Roseano ◽  
Uberto Pagotto ◽  
...  

1971 ◽  
Vol 67 (4) ◽  
pp. 625-633 ◽  
Author(s):  
A. C. M. Vingerhoeds ◽  
P. J. der Kinderen ◽  
J. H. H. Thijssen ◽  
F. Schwarz

ABSTRACT A patient is described in whom an ACTH-producing bronchial carcinoid tumour was found eighteen months after bilateral adrenalectomy for Cushing's syndrome. A critical review is given of laboratory methods used in the differential diagnosis of ectopic Cushing's syndrome. Finally a course of action is suggested by which such unnecessary ablative surgery might be avoided.


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