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- Publisher Website: 10.3171/jns.2004.101.2.0262
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- PMID: 15309917
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Article: Primary hypophysitis: A single-center experience in 16 cases
Title | Primary hypophysitis: A single-center experience in 16 cases |
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Authors | |
Keywords | Hypophysitis Pituitary Steroids radiosurgery Transsphenoidal surgery |
Issue Date | 2004 |
Publisher | American Association of Neurological Surgeons. The Journal's web site is located at http://www.thejns-net.org |
Citation | Journal Of Neurosurgery, 2004, v. 101 n. 2, p. 262-271 How to Cite? |
Abstract | Object. The authors review their experience in the treatment of 16 patients with primary hypophysitis. Methods. A retrospective study was undertaken to review cases of primary hypophysitis. The mean age of the patients was 47 years and there was an equal distribution of sexes. Recent pregnancy and underlying autoimmunity were noted in 50% of the patients. Two patients had undergone previous transsphenoidal operations at other centers, one for prolactinoma and another for hypophysitis. Headache, anterior pituitary deficiency, and suprasellar mass lesions were the most common presenting features. The initial presumptive diagnosis was pituitary adenoma in six patients (37.5%) and inflammatory hypophysitis in 10 (62.5%). Five patients received initial medical therapy for hypophysitis; although three (60%) responded satisfactorily, two (40%) did not and later underwent surgery. Altogether 13 patients (81.2%) underwent transsphenoidal surgery. The histological diagnoses were lymphocytic hypophysitis in 10 (76.9%) and granulomatous hypophysitis in three (23.1%) of the surgically treated patients. A coexistent Rathke cleft cyst was noted in one patient. There was no death in this series. One patient experienced postoperative cerebrospinal fluid leakage and meningitis. One patient had bilateral internal carotid artery occlusion secondary to inflammatory involvement of the cavernous sinuses and arteritis. This patient recovered and is capable of independent functional activities. Conclusions. All surgical patients experienced improvement in their headache and/or visual field defects and none had visual deterioration. None of the patients experienced any improvement in endocrine function and all required long-term hormone replacement. Transsphenoidal surgery was a safe and effective treatment especially for visual and pressure symptoms. A postoperative recurrence developed in two patients (15.4%) and the treatment modalities included steroid therapy, repeated surgery, and radiosurgery. |
Persistent Identifier | http://hdl.handle.net/10722/172904 |
ISSN | 2023 Impact Factor: 3.5 2023 SCImago Journal Rankings: 1.173 |
ISI Accession Number ID | |
References |
DC Field | Value | Language |
---|---|---|
dc.contributor.author | Leung, GKK | en_US |
dc.contributor.author | Lopes, MBS | en_US |
dc.contributor.author | Thorner, MO | en_US |
dc.contributor.author | Vance, ML | en_US |
dc.contributor.author | Laws Jr, ER | en_US |
dc.date.accessioned | 2012-10-30T06:25:43Z | - |
dc.date.available | 2012-10-30T06:25:43Z | - |
dc.date.issued | 2004 | en_US |
dc.identifier.citation | Journal Of Neurosurgery, 2004, v. 101 n. 2, p. 262-271 | en_US |
dc.identifier.issn | 0022-3085 | en_US |
dc.identifier.uri | http://hdl.handle.net/10722/172904 | - |
dc.description.abstract | Object. The authors review their experience in the treatment of 16 patients with primary hypophysitis. Methods. A retrospective study was undertaken to review cases of primary hypophysitis. The mean age of the patients was 47 years and there was an equal distribution of sexes. Recent pregnancy and underlying autoimmunity were noted in 50% of the patients. Two patients had undergone previous transsphenoidal operations at other centers, one for prolactinoma and another for hypophysitis. Headache, anterior pituitary deficiency, and suprasellar mass lesions were the most common presenting features. The initial presumptive diagnosis was pituitary adenoma in six patients (37.5%) and inflammatory hypophysitis in 10 (62.5%). Five patients received initial medical therapy for hypophysitis; although three (60%) responded satisfactorily, two (40%) did not and later underwent surgery. Altogether 13 patients (81.2%) underwent transsphenoidal surgery. The histological diagnoses were lymphocytic hypophysitis in 10 (76.9%) and granulomatous hypophysitis in three (23.1%) of the surgically treated patients. A coexistent Rathke cleft cyst was noted in one patient. There was no death in this series. One patient experienced postoperative cerebrospinal fluid leakage and meningitis. One patient had bilateral internal carotid artery occlusion secondary to inflammatory involvement of the cavernous sinuses and arteritis. This patient recovered and is capable of independent functional activities. Conclusions. All surgical patients experienced improvement in their headache and/or visual field defects and none had visual deterioration. None of the patients experienced any improvement in endocrine function and all required long-term hormone replacement. Transsphenoidal surgery was a safe and effective treatment especially for visual and pressure symptoms. A postoperative recurrence developed in two patients (15.4%) and the treatment modalities included steroid therapy, repeated surgery, and radiosurgery. | en_US |
dc.language | eng | en_US |
dc.publisher | American Association of Neurological Surgeons. The Journal's web site is located at http://www.thejns-net.org | en_US |
dc.relation.ispartof | Journal of Neurosurgery | en_US |
dc.subject | Hypophysitis | - |
dc.subject | Pituitary | - |
dc.subject | Steroids radiosurgery | - |
dc.subject | Transsphenoidal surgery | - |
dc.subject.mesh | Adult | en_US |
dc.subject.mesh | Aged | en_US |
dc.subject.mesh | Female | en_US |
dc.subject.mesh | Giant Cell Arteritis - Complications | en_US |
dc.subject.mesh | Granulomatous Disease, Chronic - Complications | en_US |
dc.subject.mesh | Graves Disease - Complications | en_US |
dc.subject.mesh | Humans | en_US |
dc.subject.mesh | Hydrocortisone - Blood | en_US |
dc.subject.mesh | Hypothyroidism - Complications | en_US |
dc.subject.mesh | Inflammation - Pathology - Surgery | en_US |
dc.subject.mesh | Magnetic Resonance Imaging | en_US |
dc.subject.mesh | Male | en_US |
dc.subject.mesh | Middle Aged | en_US |
dc.subject.mesh | Pituitary Diseases - Diagnosis - Surgery - Therapy | en_US |
dc.subject.mesh | Pituitary Gland - Metabolism - Pathology - Surgery | en_US |
dc.subject.mesh | Pituitary Neoplasms - Complications | en_US |
dc.subject.mesh | Postoperative Complications | en_US |
dc.subject.mesh | Prolactinoma - Complications | en_US |
dc.subject.mesh | Radiosurgery | en_US |
dc.subject.mesh | Retrospective Studies | en_US |
dc.subject.mesh | Steroids - Therapeutic Use | en_US |
dc.title | Primary hypophysitis: A single-center experience in 16 cases | en_US |
dc.type | Article | en_US |
dc.identifier.email | Leung, GKK: gilberto@hkucc.hku.hk | en_US |
dc.identifier.authority | Leung, GKK=rp00522 | en_US |
dc.description.nature | link_to_subscribed_fulltext | en_US |
dc.identifier.doi | 10.3171/jns.2004.101.2.0262 | - |
dc.identifier.pmid | 15309917 | - |
dc.identifier.scopus | eid_2-s2.0-3242806709 | en_US |
dc.relation.references | http://www.scopus.com/mlt/select.url?eid=2-s2.0-3242806709&selection=ref&src=s&origin=recordpage | en_US |
dc.identifier.volume | 101 | en_US |
dc.identifier.issue | 2 | en_US |
dc.identifier.spage | 262 | en_US |
dc.identifier.epage | 271 | en_US |
dc.identifier.isi | WOS:000223000600014 | - |
dc.publisher.place | United States | en_US |
dc.identifier.scopusauthorid | Leung, GKK=35965118200 | en_US |
dc.identifier.scopusauthorid | Lopes, MBS=35479962200 | en_US |
dc.identifier.scopusauthorid | Thorner, MO=7102935307 | en_US |
dc.identifier.scopusauthorid | Vance, ML=7102823154 | en_US |
dc.identifier.scopusauthorid | Laws Jr, ER=25950075000 | en_US |
dc.identifier.issnl | 0022-3085 | - |