Hypophysitis: a single-center case series

被引:52
|
作者
Imber, Brandon S. [1 ]
Lee, Han S. [2 ]
Kunwar, Sandeep [1 ,3 ]
Blevins, Lewis S. [1 ,3 ]
Aghi, Manish K. [1 ,3 ]
机构
[1] Univ Calif San Francisco, Dept Neurol Surg, San Francisco, CA 94143 USA
[2] Univ Calif San Francisco, Div Neuropathol, Dept Anat Pathol, San Francisco, CA 94143 USA
[3] Univ Calif San Francisco, Calif Ctr Pituitary Disorders, San Francisco, CA 94143 USA
关键词
Autoimmune hypophysitis; Pituitary inflammation; Sellar mass; Stalk thickening; Granulomatous; Lymphocytic; RATHKES CLEFT CYST; CENTRAL DIABETES-INSIPIDUS; LYMPHOCYTIC HYPOPHYSITIS; LYMPHOMATOID GRANULOMATOSIS; AUTOIMMUNE HYPOPHYSITIS; INFLAMMATORY PSEUDOTUMOR; IGG4-RELATED HYPOPHYSITIS; ANTIPITUITARY ANTIBODIES; TRANSSPHENOIDAL SURGERY; AZATHIOPRINE;
D O I
10.1007/s11102-014-0622-5
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
The authors review their treatment experience and summarize clinical outcomes for patients with hypophysitis over the past 15 years. A retrospective analysis was conducted on patients with lymphocytic, granulomatous or IgG4-related hypophysitis treated from 1997 to 2014 at a single academic center. Patients' medical records were reviewed and binary logistic regression analysis was used to assess whether various clinical parameters were associated with improved outcomes including endocrine function, radiographic appearance and disease recurrence. Twenty-one patients (13 women and 8 men) were identified with a median diagnosis age of 37.4 years. All but two patients (90 %) were diagnosed histopathologically and the remaining two were diagnosed clinically with lymphocytic hypophysitis. 16 patients (76 %) had lymphocytic hypophysitis, 3 (14 %) had granulomatous hypophysitis, 1 (5 %) had IgG4-related hypophysitis and 1 (5 %) had mixed lymphocytic-granulomatous. Patients presented with various symptoms of expanding sellar mass with most common signs including headache (57 %), polyuria/polydipsia (52 %), vision changes (52 %) and amenorrhea or decreased libido (48 %). Pre-treatment endocrine evaluation revealed that 12 (57 %) patients had complete anterior hypopituitarism, 11 patients (52 %) had diabetes insipidus, ten patients (48 %) had mild hyperprolactinemia and three patients (14 %) had isolated endocrine axis deficiencies with partial gland function. We observed a broad diversity in pre-treatment imaging with common findings including uniform contrast enhancement (62 %), thickened infundibulum (57 %) and loss of hypophysis bright spot on T1 imaging (43 %). Patients were treated with steroids and hormone supplementation as needed. 16 patients (76 %) had recorded post-treatment MRI scans which revealed that half had radiographic improvement and half had stable or worsened post-treatment imaging. Only female gender was found to significantly predict improved odds of post-steroid radiographic improvement. For post-treatment endocrine evaluation, six patients (29 %) did not have an evaluation on record, four patients (19 %) had some improvement in at least one axis, seven patients (33 %) had stable but non-worsened endocrine function and four patients (19 %) had worsened endocrine function post-steroids. Hypophysitis is an increasingly recognized diagnosis that can present with a broad array of radiographic and clinical features. Surgical biopsy can be helpful to make definitive diagnosis and may guide treatment decision-making.
引用
收藏
页码:630 / 641
页数:12
相关论文
共 50 条
  • [1] Hypophysitis: a single-center case series
    Brandon S. Imber
    Han S. Lee
    Sandeep Kunwar
    Lewis S. Blevins
    Manish K. Aghi
    Pituitary, 2015, 18 : 630 - 641
  • [2] Primary and Ipilimumab-induced Hypophysitis: A Single-center Case Series
    Atkins, Paul
    Ur, Ehud
    ENDOCRINE RESEARCH, 2020, 45 (04) : 246 - 253
  • [3] Kounis syndrome: a single-center case series
    Canale, Claudia
    Fracasso, Giulia
    Masoero, Giovanni
    Gnecco, Giovanni
    Chiarella, Francesco
    Brunelli, Claudio
    Porto, Italo
    EUROPEAN HEART JOURNAL SUPPLEMENTS, 2019, 21 (0J) : J153 - J153
  • [4] Plasmapheresis in thyrotoxicosis: a single-center case series
    I. Rami
    D. Zerrouki
    I. Assarrar
    S. Rouf
    H. Latrech
    Journal of Medical Case Reports, 18
  • [5] Levosimendan: A retrospective single-center case series
    Berry, William T.
    Hewson, Russell W.
    Langrish, Chris J.
    Mckenzie, Catherine A.
    Barrett, Nicholas A.
    JOURNAL OF CRITICAL CARE, 2013, 28 (06) : 1075 - 1078
  • [6] Castleman disease: A single-center case series
    Pribyl, Kyle
    Vakayil, Victor
    Farooqi, Najiha
    Arora, Nivedita
    Kreitz, Benjamin
    Ikramuddin, Salman
    Linden, Michael A.
    Harmon, James
    INTERNATIONAL JOURNAL OF SURGERY CASE REPORTS, 2021, 80
  • [7] GammaTile for Gliomas: A Single-Center Case Series
    Budnick, Hailey C.
    Richardson, Angela M.
    Shiue, Kevin
    Watson, Gordon
    Ng, Sook K.
    Le, Yi
    Shah, Mitesh, V
    CUREUS JOURNAL OF MEDICAL SCIENCE, 2021, 13 (11)
  • [8] Plasmapheresis in thyrotoxicosis: a single-center case series
    Rami, I.
    Zerrouki, D.
    Assarrar, I.
    Rouf, S.
    Latrech, H.
    JOURNAL OF MEDICAL CASE REPORTS, 2024, 18 (01)
  • [9] Primary hypophysitis: a single-center experience in 16 cases
    Leung, GKK
    Lopes, MBS
    Thorner, MO
    Vance, ML
    Laws, ER
    JOURNAL OF NEUROSURGERY, 2004, 101 (02) : 262 - 271
  • [10] Retrospective, single-center case series of neonatal lupus
    Wang, Yixin Ally
    Sibbald, Cathryn
    Moon, Amanda T.
    PEDIATRIC DERMATOLOGY, 2020, 37 (03) : 484 - 489