Case of an atypical pituitary abscess

Zachary W. Bloomer; Treyce S. Knee; Zachary S. Rubin; Thanh Duc Hoang

doi:10.1136/bcr-2021-246776

Case of an atypical pituitary abscess

Zachary W. Bloomer
, Treyce S. Knee
, Zachary S. Rubin
, Thanh Duc Hoang^*

^*Corresponding author for this work

Medicine

Research output: Contribution to journal › Article › peer-review

5 Scopus citations

Abstract

A pituitary abscess is a rare intrasellar infection. Correct identification can be challenging preoperatively given its non-specific symptoms and imaging findings. We report a case of a young woman presenting with secondary amenorrhea, visual field deficits and a 2.6 cm pituitary lesion diagnosed to be a craniopharyngioma. A concomitant unexpected pituitary abscess was diagnosed intraoperatively without associated meningeal symptoms.

Original language	English
Article number	e246776
Journal	BMJ Case Reports
Volume	14
Issue number	11
DOIs	https://doi.org/10.1136/bcr-2021-246776
State	Published - 30 Nov 2021

Keywords

endocrine system
headache (including migraines)
infections
neuroendocrinology
pituitary disorders

Access to Document

10.1136/bcr-2021-246776

Cite this

@article{b1fa81d0f3bf4c3286431eab19f08dfc,

title = "Case of an atypical pituitary abscess",

abstract = "A pituitary abscess is a rare intrasellar infection. Correct identification can be challenging preoperatively given its non-specific symptoms and imaging findings. We report a case of a young woman presenting with secondary amenorrhea, visual field deficits and a 2.6 cm pituitary lesion diagnosed to be a craniopharyngioma. A concomitant unexpected pituitary abscess was diagnosed intraoperatively without associated meningeal symptoms.",

keywords = "endocrine system, headache (including migraines), infections, neuroendocrinology, pituitary disorders",

author = "Bloomer, \{Zachary W.\} and Knee, \{Treyce S.\} and Rubin, \{Zachary S.\} and Hoang, \{Thanh Duc\}",

note = "Publisher Copyright: {\textcopyright} BMJ Publishing Group Limited 2021. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ.",

year = "2021",

month = nov,

day = "30",

doi = "10.1136/bcr-2021-246776",

language = "English",

volume = "14",

journal = "BMJ Case Reports",

issn = "1757-790X",

publisher = "BMJ Publishing Group",

number = "11",

}

TY - JOUR

T1 - Case of an atypical pituitary abscess

AU - Bloomer, Zachary W.

AU - Knee, Treyce S.

AU - Rubin, Zachary S.

AU - Hoang, Thanh Duc

N1 - Publisher Copyright: © BMJ Publishing Group Limited 2021. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ.

PY - 2021/11/30

Y1 - 2021/11/30

N2 - A pituitary abscess is a rare intrasellar infection. Correct identification can be challenging preoperatively given its non-specific symptoms and imaging findings. We report a case of a young woman presenting with secondary amenorrhea, visual field deficits and a 2.6 cm pituitary lesion diagnosed to be a craniopharyngioma. A concomitant unexpected pituitary abscess was diagnosed intraoperatively without associated meningeal symptoms.

AB - A pituitary abscess is a rare intrasellar infection. Correct identification can be challenging preoperatively given its non-specific symptoms and imaging findings. We report a case of a young woman presenting with secondary amenorrhea, visual field deficits and a 2.6 cm pituitary lesion diagnosed to be a craniopharyngioma. A concomitant unexpected pituitary abscess was diagnosed intraoperatively without associated meningeal symptoms.

KW - endocrine system

KW - headache (including migraines)

KW - infections

KW - neuroendocrinology

KW - pituitary disorders

UR - https://www.scopus.com/pages/publications/85120676189

U2 - 10.1136/bcr-2021-246776

DO - 10.1136/bcr-2021-246776

M3 - Article

C2 - 34848428

AN - SCOPUS:85120676189

SN - 1757-790X

VL - 14

JO - BMJ Case Reports

JF - BMJ Case Reports

IS - 11

M1 - e246776

ER -

Case of an atypical pituitary abscess

Abstract

Keywords

Access to Document

Fingerprint

Cite this