Zobrazeno 1 - 10
of 241
pro vyhledávání: '"Granulomatous hypophysitis"'
Autor:
Mohammad Mahdi Rabiei, Kaveh Ebrahimzadeh, Zahra Davoudi, Farahnaz Bidari Zerehpoosh, Farid Javandoust Gharehbagh, Roghayeh Sedaghati, Legha Lotfollahi, Fatemeh Kalhor, Ilad Alavi Darazam
Publikováno v:
BMC Neurology, Vol 23, Iss 1, Pp 1-6 (2023)
Abstract Background Granulomatous hypophysitis is a rare disease that presents with chronic inflammation of the pituitary gland. In this study, we reported a case of granulomatous hypophysitis associated with a pituitary abscess. Case presentation A
Externí odkaz:
https://doaj.org/article/eb487d0b5bcd434fa527afecb954331d
Autor:
Guive Sharifi, Mohammad Reza Mohajeri-Tehrani, Behrouz Navabakhsh, Bagher Larijani, Touraj Valeh
Publikováno v:
Journal of Medical Case Reports, Vol 13, Iss 1, Pp 1-4 (2019)
Abstract Background Inflammation of the pituitary gland can occur in a variety of primary or secondary disorders. Idiopathic granulomatous hypophysitis is a rare inflammatory disease of the pituitary gland that can closely mimic a pituitary adenoma c
Externí odkaz:
https://doaj.org/article/5426358e258a4abeb3ddc604ba7f25a8
Akademický článek
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Autor:
Bahar K. Force, Tiphanie P. Vogel, Dang M. Nguyen, Kent A. Heck, Sherly Sebastian, Mas Takashima, Daniel Yoshor, Susan L. Samson
Publikováno v:
Frontiers in Endocrinology, Vol 11 (2020)
Background: Hypophysitis is primary or idiopathic or secondary to another disease process. The histologic subtypes of hypophysitis are lymphocytic, granulomatous, xanthomatous, xanthogranulomatous, or IgG4-related. Granulomatous hypophysitis is the s
Externí odkaz:
https://doaj.org/article/191bda5723dc4f99a6d2135758fad685
Publikováno v:
Indian Journal of Pathology and Microbiology, Vol 61, Iss 3, Pp 389-392 (2018)
Hypophysitis of the pituitary gland is a rare inflammatory disorder and broadly classified as primary and secondary hypophysitis. Primary hypophysitis is mainly of lymphocytic, granulomatous, and xanthomatous types. Among the various primary hypophys
Externí odkaz:
https://doaj.org/article/41e2c1efa8904906a44946a9c86c09f8
Akademický článek
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Publikováno v:
Journal of the ASEAN Federation of Endocrine Societies, Vol 34, Iss 2 (2019)
Granulomatous hypophysitis is an extremely rare condition, with no established definitive treatment. An elderly Asian woman was diagnosed to have recurrent granulomatous hypophysitis 5 years after transsphenoidal surgery. No other intervention was do
Externí odkaz:
https://doaj.org/article/9dcfb35658664fb192e63cecc6e4b4bb
Akademický článek
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Publikováno v:
Cogent Medicine, Vol 5, Iss 1 (2018)
Hypophysitis is a pituitary inflammatory disorder commonly misdiagnosed and treated as a pituitary macroadenoma. Occurring at an incidence of 1 case to 9 million people into lymphocytic, granulomatous, _histopathologically_ per year, it is further cl
Externí odkaz:
https://doaj.org/article/b76001598ab749bb86a7fd62c33e7a32
Autor:
Abhay Gundgurthi, Sandeep Kharb, M K Garg, K S Brar, Reena Bharwaj, Srishti Gupta, H C Pathak
Publikováno v:
Indian Journal of Endocrinology and Metabolism, Vol 16, Iss 5, Pp 846-849 (2012)
We report a case of 41-year-old lady who presented with chronic headache of 6-month duration and a sellar mass with a suprasellar extension on imaging, which was interpreted as pituitary macroadenoma. She had normal pituitary function and visual peri
Externí odkaz:
https://doaj.org/article/41e3fe7690544ddfbafc0b70a72e474b