Literature DB >> 27581598

Primary pituitary lymphoma: an update of the literature.

A Tarabay1, G Cossu1, M Berhouma2, M Levivier1, R T Daniel1, M Messerer3.   

Abstract

Primary intracranial lymphomas (Weller et al. in Neuro Oncol 14(12):1481-1484, 2012) are an emerging disease and an isolated localization in the pituitary gland i.e. primary pituitary lymphoma (PPL) represents a rare condition. We present an update of the most recent evidence for PPL through a systematic review of the literature. A systematic literature review was conducted using PubMed database up to October 2015. The population was defined as immunocompetent patients with a pathologically confirmed diagnosis of PPL. Patients' characteristics, clinical presentation, radiological features, pathology reports, adjuvant treatment and follow-up data were analyzed. We reported one case of PPL and included our data in this analysis. A total of 33 cases of PPL were identified, including ours. A slight not significant female prevalence was evident, with a mean age of 59 years at diagnosis. Visual troubles and headaches were the most common presenting symptoms. About 80 % of patients presented a cranial nerve (CN) deficit. The most frequently involved were the II and III CN. Anterior hypopituitarism was present in 70 % of cases and a diabetes insipidus in 36 % of cases. PPL was rarely limited to the sella and most often extended to the suprasellar and parasellar space. 70 % of cases underwent resection, 21 % a biopsy. A B-cell lymphoma was isolated in 82 % of cases, a T-cell lymphoma in 15 % and a NK/T cell lymphoma in one case. Overall mean survival rate was 14.4 months (95 % confidence interval 9.0-19.8 months) and there was no difference in terms of survival rates when patients were stratified according to the treatment they received. PPL is an emerging clinical entity. Literature data are too scarce to allow the definition of specific protocols of treatment and the management is based on the guidelines present for PCNSL. The role of surgery aiming at a complete resection of PPL should be reevaluated in wider studies including only this category of patients, to establish the real role of each therapeutic strategy.

Entities:  

Keywords:  Chemotherapy; Endoscopic endonasal surgery; Primary central nervous system lymphoma; Primary pituitary lymphoma; Radiotherapy; Sellar mass; Trans-sphenoidal surgery

Mesh:

Year:  2016        PMID: 27581598     DOI: 10.1007/s11060-016-2249-z

Source DB:  PubMed          Journal:  J Neurooncol        ISSN: 0167-594X            Impact factor:   4.130


  52 in total

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Authors:  Michael Weller; Peter Martus; Patrick Roth; Eckhard Thiel; Agnieszka Korfel
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Journal:  Endocr J       Date:  2005-10       Impact factor: 2.349

Review 6.  First-line treatment and outcome of elderly patients with primary central nervous system lymphoma (PCNSL)--a systematic review and individual patient data meta-analysis.

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Journal:  Cancer       Date:  1988-12-01       Impact factor: 6.860

Review 9.  Extranodal NK/T-cell lymphoma presenting as a pituitary mass. Case report and review of the literature.

Authors:  James K Liu; Christina Sayama; Steven S Chin; William T Couldwell
Journal:  J Neurosurg       Date:  2007-09       Impact factor: 5.115

Review 10.  Primary pituitary lymphoma: idiopathic anasarca with relapse in bone marrow only.

Authors:  Soley Bayraktar; Wilfredo Bassini; Mark Goodman
Journal:  Acta Haematol       Date:  2010       Impact factor: 2.195

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  8 in total

1.  Endoscopic Endonasal Trans-sphenoidal Approach: Minimally Invasive Surgery for Pituitary Adenomas.

Authors:  Mahmoud Messerer; Giulia Cossu; Mercy George; Roy Thomas Daniel
Journal:  J Vis Exp       Date:  2018-01-17       Impact factor: 1.355

2.  Primary central nervous system lymphoma involving the hypothalamic-pituitary axis: a case series and pooled analysis.

Authors:  Dong-Won Shin; Jeong Hoon Kim; Young-Hoon Kim; Young Hyun Cho; Seok Ho Hong
Journal:  J Neurooncol       Date:  2020-03-27       Impact factor: 4.130

3.  Methotrexate-associated lymphoproliferative disorder with hypopituitarism and central diabetes insipidus.

Authors:  Misaki Aoshima; Koji Nagayama; Kei Takeshita; Hiroshi Ajima; Sakurako Orikasa; Ayana Iwazaki; Hiroaki Takatori; Yutaka Oki
Journal:  Endocrinol Diabetes Metab Case Rep       Date:  2019-10-12

4.  Coexistence of Pituitary Adenoma and Primary Pituitary Lymphoma: A Case Report and Review of the Literature.

Authors:  Shangjun Ren; Qingyang Lu; Yilei Xiao; Yiming Zhang; Lianqun Zhang; Bin Li; Mengyou Li
Journal:  Front Surg       Date:  2022-03-16

5.  A UNIQUE CASE OF CENTRAL HYPOPITUITARISM AND CENTRAL DIABETES INSIPIDUS CAUSED BY DIFFUSE LARGE B-CELL LYMPHOMA.

Authors:  Jason A Stegink; Vishal Sehgal; Manige Konig
Journal:  AACE Clin Case Rep       Date:  2019-01-30

6.  Primary Pituitary Lymphoma in Immunocompetent Patients: A Report on Two Case Studies and the Review of Literature.

Authors:  Lian Duan; Jie Liu; Yan Zhang; Lijia Cui; Xiao Zhai; Boju Pan; Lin Lu; Hui Pan; Yong Yao; Huijuan Zhu
Journal:  Front Endocrinol (Lausanne)       Date:  2021-02-04       Impact factor: 5.555

7.  Case Report: Identification of Potential Prognosis-Related TP53 Mutation and BCL6-LPP Fusion in Primary Pituitary Lymphoma by Next Generation Sequencing: Two Cases.

Authors:  Yi Zhang; Liyuan Ma; Jie Liu; Huijuan Zhu; Lin Lu; Kan Deng; Wenbin Ma; Hui Pan; Renzhi Wang; Yong Yao
Journal:  Front Endocrinol (Lausanne)       Date:  2021-07-26       Impact factor: 5.555

8.  41-year-old male with a pituitary mass.

Authors:  Wenjuan Wen; Leiming Wang; Mengyou Li; Peijin Li; Yubo Ren; Xuedong Zhang
Journal:  Brain Pathol       Date:  2021-07-19       Impact factor: 6.508

  8 in total

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