Xanthogranulomatous Hypophysitis Mimicking a Pituitary Neoplasm

2004 ◽  
Vol 15 (4) ◽  
pp. 351-358 ◽  
Author(s):  
Shunichi Yokoyama ◽  
Toshiaki Sano ◽  
Kenichiro Tajitsu ◽  
Kazuhiro Kusumoto
Keyword(s):  
JAMA ◽  
1925 ◽  
Vol 85 (7) ◽  
pp. 513
Author(s):  
IRVING H. PARDEE

Neurosurgery ◽  
2015 ◽  
Vol 76 (5) ◽  
pp. 616-622 ◽  
Author(s):  
Antonio Di Ieva ◽  
Jennilee M. Davidson ◽  
Luis V. Syro ◽  
Fabio Rotondo ◽  
Julian F. Montoya ◽  
...  

Abstract Crooke's cell adenomas are a rare type of pituitary neoplasm. They produce adrenocorticotropic hormone causing Cushing's disease or may be endocrinologically silent. These tumors are usually invasive, may exhibit aggressive clinical behavior, and often recur with a low success of cure after reoperation and/or radiotherapy. Due to their rarity, they present great difficulties in assessing prognosis, treatment, and clinical management. Neurosurgeons and physicians dealing with pituitary adenomas diagnosed as Crooke's cell adenomas have to be aware of their potential clinical aggressiveness to plan strict follow-up of patients and eventual multimodality treatment. We review here the published cases of Crooke's cell tumors, as well as the clinical and histopathological characteristics of these unusual neoplasms.


1978 ◽  
Vol 48 (1) ◽  
pp. 23-28 ◽  
Author(s):  
James N. Domingue ◽  
S. Douglas Wing ◽  
Charles B. Wilson

✓ Seventeen cases of coexisting secreting pituitary adenomas and partially empty sellas are presented. The location of the cisternal invagination into the sella was not helpful in predicting the location of the tumor. In patients with endocrine indication of a secreting pituitary neoplasm, the finding of a partially empty sella should not contradict the diagnosis.


2006 ◽  
Vol 65 (4) ◽  
pp. 552-553 ◽  
Author(s):  
Luis V. Syro ◽  
Humberto Uribe ◽  
Luis C. Penagos ◽  
Leon D. Ortiz ◽  
Camilo E. Fadul ◽  
...  

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