Xanthomatous Hypophysitis Mimicking a Pituitary Adenoma: Case Report and Review of the Literature
Background. Hypophysitis is an inflammatory disease of the pituitary gland that may mimic pituitary tumors clinically and radiologically. Case Description. We report a case of a xanthomatous hypophysitis initially diagnosed as pituitary adenoma. A 31-year-old woman presented with headache, diabetes...
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doaj-cf724e29e0ea4f52b4767fc1a58b07982020-11-24T23:18:48ZengHindawi LimitedJournal of Oncology1687-84501687-84692010-01-01201010.1155/2010/195323195323Xanthomatous Hypophysitis Mimicking a Pituitary Adenoma: Case Report and Review of the LiteratureLaura Aste0Mattia Bellinzona1Veronica Meleddu2Graziella Farci3Cristina Manieli4Umberto Godano5Department of Neurosurgery, Brotzu Hospital, Via Peretti 1, 09100 Cagliari, ItalyDepartment of Neurosurgery, Brotzu Hospital, Via Peretti 1, 09100 Cagliari, ItalyDepartment of Neurosurgery, Brotzu Hospital, Via Peretti 1, 09100 Cagliari, ItalyDepartment of Pathological Anatomy, Brotzu Hospital, 09100 Cagliari, ItalyDepartment of Pathological Anatomy, Brotzu Hospital, 09100 Cagliari, ItalyDepartment of Neurosurgery, Brotzu Hospital, Via Peretti 1, 09100 Cagliari, ItalyBackground. Hypophysitis is an inflammatory disease of the pituitary gland that may mimic pituitary tumors clinically and radiologically. Case Description. We report a case of a xanthomatous hypophysitis initially diagnosed as pituitary adenoma. A 31-year-old woman presented with headache, diabetes insipidus, and amenorrhea. A head CT scan showed no intrasellar changes, while an MRI scan showed a sellar cystic mass. An endocrinological work up revealed mild hypocortisolism and diabetes insipidus (DI). Transsphenoidal surgery was performed. The intraoperative histological examination suggested a pituitary adenoma. The removed tissue showed central necrosis surrounded by accumulation of foamy cells and xanthomatous epithelioid cells. The patient made an uneventful postoperative recovery, Nevertheless, DI persisted and the adenohypophysis hypofunction did not recover. Conclusion. We describe an unusual inflammatory lesion of the pituitary gland mimicking an adenoma. A high level of clinical suspicion of inflammatory disorders is necessary for correct diagnosis and optimal management.http://dx.doi.org/10.1155/2010/195323 |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Laura Aste Mattia Bellinzona Veronica Meleddu Graziella Farci Cristina Manieli Umberto Godano |
spellingShingle |
Laura Aste Mattia Bellinzona Veronica Meleddu Graziella Farci Cristina Manieli Umberto Godano Xanthomatous Hypophysitis Mimicking a Pituitary Adenoma: Case Report and Review of the Literature Journal of Oncology |
author_facet |
Laura Aste Mattia Bellinzona Veronica Meleddu Graziella Farci Cristina Manieli Umberto Godano |
author_sort |
Laura Aste |
title |
Xanthomatous Hypophysitis Mimicking a Pituitary Adenoma: Case Report and Review of the Literature |
title_short |
Xanthomatous Hypophysitis Mimicking a Pituitary Adenoma: Case Report and Review of the Literature |
title_full |
Xanthomatous Hypophysitis Mimicking a Pituitary Adenoma: Case Report and Review of the Literature |
title_fullStr |
Xanthomatous Hypophysitis Mimicking a Pituitary Adenoma: Case Report and Review of the Literature |
title_full_unstemmed |
Xanthomatous Hypophysitis Mimicking a Pituitary Adenoma: Case Report and Review of the Literature |
title_sort |
xanthomatous hypophysitis mimicking a pituitary adenoma: case report and review of the literature |
publisher |
Hindawi Limited |
series |
Journal of Oncology |
issn |
1687-8450 1687-8469 |
publishDate |
2010-01-01 |
description |
Background. Hypophysitis is an inflammatory disease of the pituitary gland that may mimic pituitary tumors clinically and radiologically. Case Description. We report a case of a xanthomatous hypophysitis initially diagnosed as pituitary adenoma. A 31-year-old woman presented with headache, diabetes insipidus, and amenorrhea. A head CT scan showed no intrasellar changes, while an MRI scan showed a sellar cystic mass. An endocrinological work up revealed mild hypocortisolism and diabetes insipidus (DI). Transsphenoidal surgery was performed. The intraoperative histological examination suggested a pituitary adenoma. The removed tissue showed central necrosis surrounded by accumulation of foamy cells and xanthomatous epithelioid cells. The patient made an uneventful postoperative recovery, Nevertheless, DI persisted and the adenohypophysis hypofunction did not recover. Conclusion. We describe an unusual inflammatory lesion of the pituitary gland mimicking an adenoma. A high level of clinical suspicion of inflammatory disorders is necessary for correct diagnosis and optimal management. |
url |
http://dx.doi.org/10.1155/2010/195323 |
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