“The human body is the best picture of the human soul.” – Tony Robbins

 

 

PNA Medical Corner:

Endogenous Cushing’s and Cancer

Dr. Maria Fleseriu

This month the PNA Medical Corner features a study co-authored by Maria Fleseriu, a  longtime member of the PNA and Professor of Endocrinology and Neurological Surgery and Director of the Pituitary Center at Oregon Health & Science University.  The study finds that endogenous Cushing’s Syndrome is linked to higher risk of cancer.

Eur J Endocrinol

2024 Jul 27:lvae098.

 doi: 10.1093/ejendo/lvae098. Online ahead of print.

Endogenous Cushing’s Syndrome and Cancer Risk

Yaron Rudman 1 2Maria Fleseriu 3Laura Dery 2Hiba Masri-Iraqi 1 2Liat Sasson 1 2Tzipora Shochat 4Shiri Kushnir 5Ilan Shimon 1 2Amit Akirov 1 2

Affiliations Expand

Abstract

Objective: Cancer incidence in patients with endogenous Cushing’s syndrome (CS) has never been established. We aimed to assess the cancer risk in patients with CS, as compared with individually matched controls.

Design: A nationwide retrospective matched-cohort study of patients with endogenous CS diagnosed between 2000-2023, using the database of Clalit Health Services in Israel.

Methods: Patients with adrenal carcinoma or ectopic CS were excluded. Patients with CS were matched in a 1:5 ratio, with controls individually matched for age, sex, socioeconomic status, and body mass index. The primary outcome was defined as the first diagnosis of any malignancy following a CS diagnosis. Risk of malignancy was calculated using the Cox proportional hazards model with death as a competing event.

Results: A total of 609 patients with CS and 3018 controls were included [mean age at diagnosis, 48.0±17.2 years; 2371 (65.4%) women]. The median follow-up 14.7 years (IQR, 9.9-20.2 years).Patients with CS had an increased cancer risk, with hazard ratio (HR) of 1.78 (95% CI 1.44-2.20), compared with their matched controls. The risk of malignancy was elevated in patients with Cushing’s disease (251 cases and 1246 controls; HR 1.65, 95% CI 1.15-2.36) and in patients with adrenal CS (200 cases and 991 controls; HR 2.36, 95% CI 1.70-3.29). The increased cancer risk in patients with CS persists after exclusion of thyroid malignancies.

Conclusion: Endogenous CS is associated with increased malignancy risk. These findings underscore the need for further research to establish recommendations for cancer screening in this population.

Keywords: Adrenal; Cancer; Cushing’s disease; Cushing’s syndrome; Malignancy; Pituitary.

© The Author(s) 2024. Published by Oxford University Press on behalf of European Society of Endocrinology. All rights reserved. For commercial re-use, please contact [email protected] for reprints and translation rights for reprints. All other permissions can be obtained through our RightsLink service via the Permissions link on the article page on our site—for further information please contact [email protected].

 

Reversing vision loss with successful pituitary tumor surgery

Pituitary tumors often cause vision problems. That’s because the optic nerves, which connect the eye to the brain, are located just on top of the pituitary gland. Pituitary tumors can grow

in a way that causes them to compress the optic nerves, leading to vision loss.

 

“Often the visual loss starts with the peripheral vision and is quite subtle,” says Mayo Clinic neurosurgeon Dr. Maria Peris Celda. “Pituitary tumors usually grow slowly and over time, people can get used to the visual loss. They may not notice the problem until the larger tumor affects their central vision.”

 

Fortunately, vision loss is often reversed once the tumor is surgically removed. The most common procedure is endoscopic endonasal transsphenoidal surgery. The endoscope, a small surgical camera, and surgical instruments are placed through the nostrils to access the tumor through the sinuses.


“We don’t have to make any incisions in the face,” Dr. Peris Celda says. “Very often, the visual loss either improves or is completely resolved after the operation.” Mayo Clinic was among the first institutions to extensively research the endoscopic through-the-nose approach. Now standard practice, the procedure lowers discomfort and usually requires only an overnight stay in the hospital.

 

ENT nose and sinus surgeons work alongside neurosurgeons during these procedures. For challenging cases, patients can benefit from the care provided by neuro-ophthalmologists: subspecialists who treat vision issues linked to neurological conditions.

 

Successful pituitary tumor surgery requires detailed imaging. “The pituitary gland is located in a delicate area, surrounded by very important blood vessels and nerves,” Dr. Peris Celda says. “Using the latest MRI technology allows us to understand the relationship between the tumor, brain and other important structures.”

 

Vision problems are just one type of complication that pituitary tumors can cause. “A specialized team that focuses on skull base diseases can help provide patients with the best possible outcomes and return to normal quality of life,” Dr. Peris Celda says.

 

Mayo Clinic is one of the leading pituitary centers in the U.S.  For more information, please visit careinfo.mayoclinic.org/pituitary-tumor 

 

 

Featured News and Updates

News Articles February 2026

Omics data on pituitary tumors catalogued

A recent study reviewed scientific studies on omics data generated in pituitary tumors.  The data has been catalogued to make future research projects easier. Read more: https://www.eurekalert.org/news-releases/1114907

 

Pituitary cells and intracranial germ cell tumors

A new study looks at role of pituitary cells in the genesis of intracranial germ cell tumors, given that primordial germ cell-like cells reside in the pituitary. The authors call for more study. Read more: https://www.nature.com/articles/s41598-026-38060-2

 

Benefits of surgery for adrenal Cushing’s

An study in Lancet Diabetes and Endocrinology finds that surgery is more effective at controlling cortisol in patients with adrenal Cushing’s disease compared to a conservative management approach. Read the article in Cushing’s Disease News: https://cushingsdiseasenews.com/news/surgery-offers-best-cortisol-control-adrenal-cushings-syndrome/

 

Doctors say online influencers spread fear about cortisol

An article in the Associated Press looks at a trend online where influencers focus on the stress hormone cortisol. Some may raise people’s anxiety levels and push them to get unnecessary tests. Read more: https://apnews.com/article/cortisol-supplement-endocrinology-cushing-stress-0f6f6b8df2d11e2560d4e7562f522998

Research Articles

Research Articles February 2026

Pituitary tumors
Preoperative Metabolic Predictors of Granulation Subtypes in Somatotroph Tumors: A Multicenter Retrospective Cohort Study.

Chen L, Wang J, Zeng A, Akter F, Wang S, Liu S, Hu W, Yao S, Margetis K, Wang Z, Liu H, Wang X.CNS Neurosci Ther. 2026 Feb;32(2):e70774. doi: 10.1002/cns.70774.

 

Radiotherapy regimens and concurrent Cabergoline use for non-functioning pituitary neuroendocrine tumors: a large, single-center cohort.

Mauro GP, Rebello LG, Da Róz LM, Gico VC, Weltman E, de Souza EC, Batista RL, da Cunha Neto MBC, Villar RC.Endocrine. 2026 Feb 3;91(1):60. doi: 10.1007/s12020-025-04473-8.

 

Pediatric craniopharyngioma: when hypoglycemia reveals a brain tumor. Illustrative case.

Hmamouche OM, Hammoud M, Lakhdar F, Benzagmout M, Chakour K, Chaoui El Faiz M.J Neurosurg Case Lessons. 2026 Feb 2;11(5):CASE25727. doi: 10.3171/CASE25727. Print 2026 Feb 2.

 

Incidental 18F-Flortaucipir Uptake in Pituitary Macroadenoma.

Xiong M, Liu Y, Luo X, Jiang SN.Clin Nucl Med. 2026 Jan 22. doi: 10.1097/RLU.0000000000006313. Online ahead of print.

 

Exploring the Genetic Correlation Between Pituitary Adenomas and Psychiatric Disorders: Insights From Genome-Wide Association Studies.

Yang Z, Maimaiti A, Wu J, Zhou Z, Ding C, Sun H, Li S.J Craniofac Surg. 2026 Feb 2. doi: 10.1097/SCS.0000000000012474. Online ahead of print.

 

A Case Report of Growth Hormone-Secreting Pituitary Adenoma Complicated by Apoplexy With Atypical Clinical Presentation.

Hariri BA, Faizan M, Balintona R Jr, Elhassan MOE, Salameh S, Mohammad IH, Qasem AM.Case Rep Med. 2026 Jan 30;2026:4124145. doi: 10.1155/carm/4124145. eCollection 2026.

 

Lugol’s solution for preoperative management of a TSH/GH-secreting pituitary adenoma with suboptimal response to octreotide: a case report.

Peng G, Lei X, Leng W, Wu F, Xie L, Long M, Chen L.Front Endocrinol (Lausanne). 2026 Jan 15;16:1698948. doi: 10.3389/fendo.2025.1698948. eCollection 2025.

 

Optical coherence tomography in preoperative workup and visual outcome of pituitary macroadenomas.

Dal Fabbro M, Moura FC, Atihe C, Sampaio MH, Garmes HM.Surg Neurol Int. 2025 Dec 19;16:533. doi: 10.25259/SNI_908_2025. eCollection 2025.

 

Mixed gangliocytoma-pituitary neuroendocrine tumour: clinical, immunohistochemical, and molecular genetic profiles in a series of four patients.

Dalakas K, Engström BE, Tebani A, Bontell TO, Larsson A, Nord H, Lindskog C, Pontén F, Boldt HB, Ragnarsson O, Casar-Borota O.Acta Neuropathol Commun. 2026 Jan 30. doi: 10.1186/s40478-026-02225-x. Online ahead of print.


Exploring the Dynamic Interaction Between Pituitary Neuroendocrine Tumors (Pit-NETs) Cells and Their Angiogenic Microenvironment by Using the MIB1 Labeling Index, VEGF Expression and Digital Image Analysis.

Cozma M, Cimpean AM, Parnov M, Corlan AS, Stratulat S, Fala P, Melnic E.Curr Issues Mol Biol. 2025 Dec 25;48(1):27. doi: 10.3390/cimb48010027.

 

Pediatric and Adult Craniopharyngioma: A 37-Year Experience at a National Referral Center.

Hernández MI, Ibeas C, Fernández JP, Ivanovic-Zuvic D, Gómez M, Gutiérrez D, Valenzuela S, Okuma C.Clin Endocrinol (Oxf). 2026 Jan 30. doi: 10.1111/cen.70103. Online ahead of print.

 

Oxidative Phosphorylation in Silent Pituitary Adenomas: A Multiomics Perspective.

Chen Y, Zhao Q, Wang X, Wang X, Guo Y.Int J Endocrinol. 2026 Jan 28;2026:8488950. doi: 10.1155/ije/8488950. eCollection 2026.


A novel germline CDH23 variant as a likely cause of an ultra-giant prolactinoma.

Albasri E, Alghamdi B, Murugan AK, Othman E, Alotaibi S, Dababo MA, Alfares A, Alzahrani AS.Orphanet J Rare Dis. 2026 Jan 29;21(1):32. doi: 10.1186/s13023-025-04161-w.

 

Pituitary Surgery

Endoscopic Endonasal Approach With Extradural Posterior Clinoidectomy and Upper Clivectomy for Retrochiasmatic Craniopharyngiomas.

Morisako H, Nagahama A, Ikegami M, Sasaki T, Kulkarni AV, Hazunga R, Ichinose T, Teranishi Y, Goto T.Oper Neurosurg. 2026 Feb 3. doi: 10.1227/ons.0000000000001905. Online ahead of print.

 

Ultrasound-guided percutaneous versus trans-nasal pterygopalatine fossa block in endoscopic trans-sphenoidal pituitary gland surgery: a randomized controlled trial.

Saad DH, Ahmed AMM, ElKholy WM, Bakr MM.BMC Anesthesiol. 2026 Feb 2. doi: 10.1186/s12871-026-03618-0. Online ahead of print.

 

Cushing’s Disease
New Sparks and Spots: Molecular Imaging with Positron Emission Tomography Will Change Management of Cushing’s Disease.

Reincke M, Apaydin T, Kakashvili M, Albert NL, Thorsteinsdottir J, Schweizer JROL, Theodoropoulou M, Schilbach K, Völter F.Endocrinol Metab (Seoul). 2026 Feb 3. doi: 10.3803/EnM.2025.2728. Online ahead of print.

 

Recurrent Pituitary Adenoma Causing Cushing’s Disease in a Patient With Lynch Syndrome.

Bares V, Netuka D.Cureus. 2026 Jan 27;18(1):e102414. doi: 10.7759/cureus.102414. eCollection 2026 Jan.


Psychological Recovery after treatment of Cushing syndrome.

Pereira AM, Stenvers DJ.J Clin Endocrinol Metab. 2026 Jan 28:dgag034. doi: 10.1210/clinem/dgag034. Online ahead of print.

 

Radiation Therapy

Low Incidence of New-Onset Hypopituitarism After High-Precision Stereotactic Radiation Therapy of Sellar and Perisellar Lesions.

Heer A, Schneider M, Boström JP, Pinkawa M, Kovács A, Weller J, Bischoff J, Fries CM, Boström A, Fenske WK.Adv Radiat Oncol. 2025 Oct 31;11(3):101933. doi: 10.1016/j.adro.2025.101933. eCollection 2026 Mar.

 

Hormonal Health
Neurologic Complications of Endocrine Disorders.

Mustafa R.Continuum (Minneap Minn). 2026 Feb;32(1):105-130. doi: 10.1212/cont.0000000000001658. Epub 2026 Feb 3.


PPP1R12A Mutation Presenting With Congenital Jejunal Atresia and Short Stature: A Pediatric Endocrinology Case Report.

Saul R, David M, Frasch J, Sanchez-Lara PA, Schweiger BM.Case Rep Pediatr. 2026 Jan 28;2026:2247764. doi: 10.1155/crpe/2247764. eCollection 2026.


Identification of a novel KISS1R (GPR54) gene variant (c.505+2T>G) in a patient with congenital hypogonadotropic hypogonadism: A case report and literature review.

Menekse B, Ucgul E, Bakir A, Hepsen S, Ozturk Unsal I, Kizilgul M, Araki T, Cakal E.Exp Ther Med. 2026 Jan 16;31(3):71. doi: 10.3892/etm.2026.13066. eCollection 2026 Mar.


Oxytocin Deficiency in Childhood and Adolescence: Clinical Features, Diagnostic Challenges and Therapeutic Perspectives.

Paparella R, Bei A, Bernabei I, Fiorentini C, Iafrate N, Lucibello R, Marchetti L, Pastore F, Maglione V, Niceta M, Fiore M, Caronti B, Vitali M, Pucarelli I, Tarani L.Curr Issues Mol Biol. 2025 Nov 25;47(12):982. doi: 10.3390/cimb47120982.

 

Isolated Menarche and Empty Sella Turca: A Rare Pediatric Case.

Vieira M, Azevedo IA, Rangel MA, Campos RA, Leite AL.Cureus. 2025 Dec 28;17(12):e100275. doi: 10.7759/cureus.100275. eCollection 2025 Dec.

 

 

 

 

Count on your Xeris CareConnection™ Team for unparalleled Cushing’s Support

Cushing’s can be challenging, but there is support so patients can feel like themselves again. The main goal of treating Cushing’s is to get cortisol levels back to normal. This Pituitary Awareness Month, Xeris Pharmaceuticals® is highlighting the importance of one-on-one support for patients living with Cushing’s Syndrome and support for HCPs treating Cushing’s Syndrome.

Sign up to get dedicated support:

Patients: Sign up for support | Recorlev® (levoketoconazole)

HCP’s: Connect with Xeris support | RECORLEV® (levoketoconazole)

Have more questions? Call for more support at 1-844-444-RCLV (7258)

Copyright © 2024 Pituitary Network Association All rights reserved.

Disclaimer: PNA does not engage in the practice of medicine. It is not a medical authority, nor does it claim to have medical expertise. In all cases, PNA recommends that you consult your own physician regarding any course of treatment or medication.

Our mailing address is:
Pituitary Network Association
P.O. Box 1958
Thousand Oaks, CA 91358
(805) 499-9973 Phone - (805) 480-0633 Fax
Email [email protected]

You are receiving this Newsletter because you have shown interest in receiving information about our activities.

If you do not want to receive any more emails from PNA, Unsubscribe.