“As I see it, every day you do one of two things: build health or produce disease in yourself.” – Adelle Davis

PNA Spotlight: Dr. Noa Tal

Noa Tal, MD, is a neuroendocrinologist with the Pituitary Disorders Center at Pacific Neuroscience Institute in Santa Monica, California.  Dr. Tal graduated from medical school at Tel Aviv University School of Medicine. She did a residency in internal medicine at Montefiore Medical Center in the Bronx in New York. Later she completed a fellowship in endocrinology at Cedars-Sinai Medical Center in Los Angeles, California. Her research focuses on improving the understanding of clinical outcomes in patients with pituitary disorders, with particular emphasis on long-term outcomes and quality of life.

She was kind enough to answer some questions from the PNA. Her answers follow.

What is your current position?

I’m a neuroendocrinologist working at Pacific Neuroscience Institute at St John’s in Santa Monica. I see patients with pituitary-related disorders both in the outpatient setting for follow-up visits and in the hospital when they are undergoing surgery.

Tell me about your education.

I completed my undergraduate studies in neuroscience at Bar-Ilan University near Tel Aviv, where I met my husband. I then attended medical school at Tel Aviv University. My husband later pursued postdoctoral research in neuroscience at Columbia University, which led us to move to the United States. I completed my internal medicine residency at Montefiore Medical Center in New York, followed by an endocrinology fellowship at Cedars-Sinai in Los Angeles.

Read More Here

 

The Power of Practice: 3D Modeling for Pituitary Surgery

In fields from music to sports, rehearsal isn’t just skill-building. It’s foundational to success when the moment to perform arrives. The same is true in medicine. For Mayo Clinic neurosurgeons operating on the extremely delicate pituitary gland, practicing before the actual procedure creates familiarity with complex tumors, often leading to more successful outcomes.

That preparation is especially critical because real-life surgery varies from patient to patient. “No two people have the exact same anatomy,” says Bernard R. Bendok, M.D., Neurosurgeon and Chair of Neurosurgery at Mayo Clinic in Arizona. “Differences in the pituitary gland, surrounding bone, nearby arteries, and membranes all influence how a surgeon approaches each case.”

To bridge that gap, Mayo Clinic is increasingly using advanced 3D modeling—both physical and virtual—to help surgeons plan and rehearse procedures before entering the operating room.

Surgeons have long used mental mapping to build a three-dimensional understanding of a patient’s anatomy from imaging scans. “A good surgeon is able, after reviewing a lot of scans, to build a 3D model in their mind,” Dr. Bendok explains. “Now, 3D printing takes that a step further.” These models replicate patient anatomy using materials that mimic both soft tissue and bone, allowing surgeons to study and even simulate the procedure in advance.

The benefit is simple but powerful: familiarity. By the time surgery begins, the anatomy is no longer entirely new. Surgeons can recognize key landmarks and confirm what they expected to see. As Dr. Bendok puts it, the goal is to “register what you imagined with what’s actually in the field.”

ENT surgeons play a critical role in pituitary tumor removal during endoscopic endonasal surgery. Dr. Devyani Lal, Division Chair of Rhinology and endoscopic surgeon at Mayo Clinic, says, “Patient-specific 3D models give the team a shared view of the route to the gland, helping anticipate challenges, map key landmarks, and align on the safest approach before surgery begins.”

Beyond physical models, Mayo Clinic is also leveraging virtual reality. Using 3D holographic imaging, surgeons can explore anatomy in an immersive environment, including areas where tissue may be more fragile. “Being very gentle and knowing how to avoid injury becomes paramount,” Dr. Bendok says, especially in cases where scar tissue or distortion makes navigation more complex.

These tools are also used for full-team surgical rehearsals. In some cases, surgeons, anesthesiologists, and nurses simulate entire procedures together, including potential complications. “We integrate these models into surgical rehearsal and scenario simulation,” Dr. Bendok says. “When a complication occurs, you learn how to work your way out of a challenge.” The goal is not just to prevent complications, but to ensure the team is prepared to respond effectively if they arise.

This kind of preparation mirrors other high-performance fields. “The goal of surgery is to be proactive and not reactive,” he explains. Like athletes studying opponents or musicians rehearsing difficult passages, surgeons benefit from anticipating what comes next.

For patients, this preparation can translate into meaningful differences in outcomes. Pituitary surgery often requires removing tumors while preserving the function of the gland itself, which is a delicate balance. Advances in imaging and modeling now allow surgeons to better understand how a tumor has displaced or compressed the pituitary, helping guide a more strategic approach.

“One of our goals is to preserve pituitary function,” Dr. Bendok says. “Understanding that in three dimensions allows you to be strategic about how you remove the tumor.” The result can be more complete tumor removal and better hormonal outcomes for patients.

Perhaps most importantly, these technologies are accelerating the learning curve for surgeons and improving collaboration across institutions. Complex cases can be shared, studied, and even rehearsed remotely, expanding access to expertise.

“My outcomes today are much better than they were 10 years ago. That’s experience,” Dr. Bendok says. “But we can accelerate that by engaging physical and virtual models.”

In the end, what may look effortless in the operating room is anything but. Like a finely tuned performance, it’s the result of preparation, repetition, and precision—before the first incision is ever made.

PNA Medical Corner: PNA Medical Corner: Adamantinomatous craniopharyngioma

This month in the PNA Medical Corner we are proud to feature a study co-authored by eleven members of the PNA: Drs. Maria Peris-Celda, Andrew Little, Paul Gardner, Georgios Zenonos, Juan Fernandez-Miranda, Adam Mamelak, Willliam Couldwell, Daniel Prevedello, Nathan Zwagerman, Varun Kshettry, and Jamie Van Gompel. This is the largest group of PNA-affiliated doctors collaborating on a study that PNA staff can ever recall seeing!  The study looks at adamantinomatous craniopharyngioma and finds that surgery achieved gross-total resection in fewer than half of patients.

Adamantinomatous craniopharyngioma: outcomes from a US multicenter registry cohort (RAPID consortium study)

Yuki Shinya 1Sandhya R Palit 1Maria Peris Celda 1Andrew S Little 2Mark A Pacult 2Paul Gardner 3Georgios Zenonos 3James Evans 4Juan Fernandez-Miranda 5Adam Mamelak 6Robert C Rennert 7William T Couldwell 7Gabriel Zada 8Albert H Kim 9Julie M Silverstein 10Won Kim 11Marvin Bergsneider 11Kyle C Wu 12Daniel M Prevedello 12Nathan Zwagerman 13Stephanie Cheok 13Michael P Catalino 14Varun R Kshettry 15Michael Karsy 16Jamie J Van Gompel 1

Affiliations Expand

Abstract

Objective: Adamantinomatous craniopharyngioma (ACP) is a rare type of brain tumor that affects a wide age range, from children to older adults. Due to the rarity of the disease, existing studies are predominantly limited to single-center or single-surgeon experiences, often lacking statistical power and generalizability. The aim of this study was to address this gap by providing a comprehensive analysis of ACP outcomes based on a large multicenter cohort from the Registry of Adenomas of the Pituitary and Related Disorders (RAPID).

Methods: This multicenter retrospective cohort study was conducted via the RAPID consortium and assessed patients with histologically confirmed ACP treated surgically between August 2000 and November 2024 at high-volume pituitary centers across the United States.

Results: Among the 359 patients (206 male, median age at primary surgery of 47 years) included in the analysis, 76% underwent endoscopic transsphenoidal surgery and 22% underwent craniotomy. Gross-total resection was achieved in 45% and subtotal resection in 47%. Notably, 120 of 311 patients (39%) presented with preoperative hypothalamic-pituitary axis dysfunction. Following all treatments, permanent hypothyroidism was reported in 40% of patients, adrenal insufficiency in 33%, and arginine vasopressin deficiency in 19%. Of 263 patients who underwent primary surgery, radiation therapy was administered in 84 (32%). Progression-free survival (PFS) declined from 66% at 1 year to 31% at 6 years. In the multivariable analysis, independent predictors of worse PFS included subtotal resection (HR 0.22, 95% CI 0.11-0.42; p = 0.001), partial resection (HR 0.11, 95% CI 0.04-0.28, p = 0.001), larger tumor size (HR 0.77, 95% CI 0.64-0.94; p = 0.009), and tumor extension beyond the sella and suprasellar regions (HR 0.21, 95% CI 0.06-0.74; p = 0.016). Primary surgery and salvage surgery groups showed comparable PFS.

Conclusions: In this large multicenter cohort study, gross-total resection was achieved in fewer than half of patients and was independently associated with improved PFS. Approximately one-third of patients underwent radiation therapy after primary surgery. These findings provide robust evidence supporting the prognostic value of extent of resection and inform contemporary treatment algorithms for ACP. The high incidence of postoperative endocrinopathy underscores the need for individualized multidisciplinary long-term care. While the retrospective design is a limitation, the multicenter approach enhances the generalizability of these results.

Keywords: RAPID consortium; adamantinomatous type; cohort overview; craniopharyngioma; multicenter study; oncology; pituitary surgery; skull base; surgical outcomes; tumor.

 

Featured News and Updates

News Articles May 2026

Getting mental health care help for patients with acromegaly

An article in Everyday Health features tips from a marriage and family therapist for people diagnosed with acromegaly on how to cope with the emotional effects of the disease.  The author even recommends the PNA! Read more: https://www.everydayhealth.com/hormones-metabolic-disorders/getting-support-for-acromegaly/

 

Spinal fractures and Cushing’s disease

An article in Cushing’s Disease News looks at an Italian study that found that vertebral fractures can occur early-on in Cushing’s patients, and were more severe in men and in people with high morning levesl of cortisol.

Read more:  https://cushingsdiseasenews.com/news/spinal-fractures-occur-early-cushings-disease-study-finds/

Pituitary patient misdiagnosed for 20 years

A study featured on Cureus.com presents the case of a 65-year-old woman with a pituitary tumor who was misdiagnosed for two decades. Doctors thought she had primary hypothyroidism and prescrived Levothyroxine. Read more: https://www.cureus.com/articles/464786-thyroid-stimulating-hormone-tsh-secreting-pituitary-tumor-misdiagnosed-for-20-years-possible-effect-of-long-term-treatment-with-thyroid-hormone#!/medications

Study proposes standardized protocol for imaging in acromegaly

A study in the Journal of Clinical Endocrinology & Metabolism says that imaging for patients with acromegaly differs widely among medical centers and proposes “a standardized, tiered approach… guided by individual patient features and tailored to the anticipated therapeutic approach. An online tool, which can be adapted to the clinical context, is provided as an aid to decision-making.” Read more: https://academic.oup.com/jcem/advance-article/doi/10.1210/clinem/dgag179/8661978?searchresult=1

 

Research Articles

Research Articles May 2026

Pituitary Tumors

Astragaloside IV targets TUBB4B to inhibit proliferation and promote apoptosis of pituitary tumor cells via the STMN1/ERK pathway.

Li J, Qu Y, Zhang W, Yang Z, Zeng Y, Xu J, Xie K, Liu Q.Int J Mol Med. 2026 Jun;57(6):151. doi: 10.3892/ijmm.2026.5822. Epub 2026 Apr 3.

 

[Endocrine inactive pituitary microadenomas: current data on natural history and follow-up approaches].

Dzhatieva DN, Pigarova EA, Dzeranova LK.Zh Vopr Neirokhir Im N N Burdenko. 2026;90(2):98-102. doi: 10.17116/neiro20269002198.


[Impact of cabergoline on fibrosis in prolactinoma].

Matsueva IA, Paltsev AA, Guseva KA, Tsoy UA, Grineva EN.Zh Vopr Neirokhir Im N N Burdenko. 2026;90(2):85-91. doi: 10.17116/neiro20269002185.


[Hypothalamic obesity in adults with craniopharyngiomas: prevalence and risk factors before and after neurosurgical treatment].

Klochkova IS, Astafyeva LI, Kutin MA, Konovalov AN, Sidneva YG, Shkarubo AN, Kalinin PL.Zh Vopr Neirokhir Im N N Burdenko. 2026;90(2):77-84. doi: 10.17116/neiro20269002177.

 

Gonadal recovery in men with prolactinomas on cabergoline: 6-month testosterone levels as a predictor of testosterone replacement timing.

Fedai NK, Uzun N, Bostan H, Kizilgul M, Demirci T, Cakal E, Ucan B.Hormones (Athens). 2026 Apr 2. doi: 10.1007/s42000-026-00766-3. Online ahead of print.


Visual outcomes after pituitary adenoma surgery: Associated factors and longitudinal progression in a prospective single-centre study.

Lozouet M, Saadoun A, Ménard A, Aldea S, Jaoude SA, Heran F, Yavchitz A, Philibert M, Chauvet D.Clin Neurol Neurosurg. 2026 Mar 28;267:109409. doi: 10.1016/j.clineuro.2026.109409. Online ahead of print.

 

Machine Learning-Based models in prediction of Ki-67 in pituitary adenoma: A systematic review and Meta-Analysis.

Hajikarimloo B, Mohammadzadeh I, Tos SM, Bahri A, Sabaghian A, Habibi MA.Endocrine. 2026 Apr 1;91(1):118. doi: 10.1007/s12020-026-04590-y.

 

Pituitary disorders

Recurrent pituitary apoplexy: experience from a national registry and review of the literature.

Biagetti B, Cordero Asanza E, Iglesias P, Camara R, Asla Q, Vicente A, Martinez-Saez E, Sarria-Estrada S, Puig-Domingo M, Araujo-Castro M.Ther Adv Endocrinol Metab. 2026 Mar 28;17:20420188261434641. doi: 10.1177/20420188261434641. eCollection 2026.


Post-Traumatic Pituitary Stalk Transection Syndrome.

Albusaidi R, AlHatmi A, Al Shidhani A, Al-Ajmi E.Sultan Qaboos Univ Med J. 2026 Mar 7;26(1):230-232. doi: 10.18295/2075-0528.2977. eCollection 2026.


The impact of a non-functioning pituitary adenoma on life – A qualitative study of patients’ experiences.

Al-Shamkhi N, Edén Engström B, Rask E, Anderzén-Carlsson A.PLoS One. 2026 Mar 31;21(3):e0345909. doi: 10.1371/journal.pone.0345909. eCollection 2026.

 

Combined surgery and proton radiotherapy in the management of craniopharyngiomas: an update with paradigmatic and challenging case scenarios.

Valeri F, Zoli M, Lillo S, Tengattini F, Colombo F, Pasquini E, Salierno G, Carretta A, D’Ambrosio L, Babaei D, Agosti E, Mattogno PP, Fontanella MM, Lauretti L, Mazzatenta D, Doglietto F, Iannalfi A.Neurosurg Rev. 2026 Mar 31;49(1):331. doi: 10.1007/s10143-026-04258-1.

 

Cushing’s

Traditional Chinese Medicine in Cushing’s Syndrome: A Narrative Review of Pathophysiology and Potential Therapeutic Effects.

Chen B, He C, Han L, Wang H, Ma Y, Wang R, Cai X.Onco Targets Ther. 2026 Feb 6;19:571776. doi: 10.2147/OTT.S571776. eCollection 2026.

 

Symptom management with osilodrostat in multiple endocrine neoplasia type 1 with a Cushing syndrome presentation.

Jamal HF.JCEM Case Rep. 2026 Mar 31;4(4):luag039. doi: 10.1210/jcemcr/luag039. eCollection 2026 Apr.


Persistent remission after steroidogenesis inhibitor discontinuation in Cushing disease: a case series.

Mangone A, Sala E, Carosi G, Sindaco GD, Mungari R, Cremaschi A, Petria I, Noschese G, Lotito V, Mantovani G, Ferrante E.Pituitary. 2026 Apr 1;29(2):68. doi: 10.1007/s11102-026-01668-8.

 

Clinical characteristics, diagnosis, and treatment of Cushing’s syndrome: analysis of a multicenter registry in Antioquia, Colombia.

Rivera-Martínez WA, Ramírez Castaño MJ, Cruz Calderón S, Díaz Posada NA, Gutiérrez Restrepo J, Román-González A, Aristizábal Henao N, Castaño Ceballos PA, Tobón Ospina CI, Donado Gómez JH, López Pompey N, Builes-Montaño CE.Ther Adv Endocrinol Metab. 2026 Mar 28;17:20420188261434078. doi: 10.1177/20420188261434078. eCollection 2026.


Prevalence of Metabolic Dysfunction Associated Steatotic Liver Disease in Craniopharyngioma Patients Using Non-Invasive Investigations.

Nitya AAV, Ghosh J, Taneja S, Singla V, Kalra N, Dutta P.Indian J Endocrinol Metab. 2026 Jan-Feb;30(1):79-84. doi: 10.4103/ijem.ijem_821_25. Epub 2026 Feb 27.


A proposed classification and scoring system predicting gross total resection of recurrent and residual pituitary adenoma: a retrospective study.

Quan W, Zhao DW, Li L, Chen HR, Wang L, Hu SL, Hu R.World Neurosurg. 2026 Mar 28:124958. doi: 10.1016/j.wneu.2026.124958. Online ahead of print.PMID: 41912140

 

 

Acromegaly

Meningoencephalitis and secondary pituitary abscess in a 16-year-old patient with gigantism.

Wissa M, Strenger V, Weinhandl G, Braun H, Wolfsberger S, Micko A.JCEM Case Rep. 2026 Apr 1;4(4):luag032. doi: 10.1210/jcemcr/luag032. eCollection 2026 Apr.

 

The silent surden: Alexithymia and quality of life in acromegaly patients.

Soltanova L, Aygun AB, Kocaman BB, Muradov I, Taze SS, Turan S, Kadioglu P, Durcan E.Endocrine. 2026 Apr 2;91(1):135. doi: 10.1007/s12020-026-04606-7.

 

To test or not to test: what we have learnt from 50 years of dynamic testing in acromegaly.

De Marinis L, Chiloiro S, Mancini A, Giambò P, Giampietro A, Bianchi A, Pontecorvi A, Giustina A.Pituitary. 2026 Mar 31;29(2):67. doi: 10.1007/s11102-026-01649-x.


Acromegaly is Associated with an Increased Incidence of Primary Malignant Tumors: Data from a National Study in Sweden.

Tsatsaris E, Robèrt J, Burman P, Berinder K, Bonelli L, Dahlqvist P, Höybye C, Ragnarsson O, Vouzouneraki K, Åkerman AK, Ekman B, Engström BE.J Clin Endocrinol Metab. 2026 Mar 30:dgag137. doi: 10.1210/clinem/dgag137. Online ahead of print.PMID: 41913644

 

Acromegaly-Physiopathology and etiology.

Castinetti F.Vitam Horm. 2026;131:83-102. doi: 10.1016/bs.vh.2026.01.001. Epub 2026 Jan 28.PMID: 41912301 Review.

 

Co-secreting pituitary adenomas in acromegaly: Classification, diagnosis, and treatment strategies.

Biagetti B, Araujo-Castro M.Vitam Horm. 2026;131:41-57. doi: 10.1016/bs.vh.2025.06.002. Epub 2025 Dec 3.


Acromegaly and histopathology.

Caballero GA, Ribalta T, Aldecoa I.Vitam Horm. 2026;131:293-334. doi: 10.1016/bs.vh.2025.10.007. Epub 2025 Nov 13.PMID: 41912298 Review.


New molecular markers of response to medical therapy in acromegaly.

Raventós A, Gil J, Marques-Pamies M, de Pedro-Campos P, Puente de la Vega C, Picó A, Lamas C, Delgado E, Menéndez E, Serra G, Bernabéu I, Villar R, Ferri J, Mariaca K, Martínez R, Marazuela M, Araujo-Castro M, Biagetti B, Jordà M, Valassi E, Puig-Domingo M; ACROMICS investigators.Vitam Horm. 2026;131:265-292. doi: 10.1016/bs.vh.2025.10.006. Epub 2025 Nov 12.

 

Acromegaly and genetics.

de Lapiscina IM, Baquero C, Castaño L.Vitam Horm. 2026;131:235-263. doi: 10.1016/bs.vh.2025.10.008. Epub 2025 Dec 16.PMID: 41912295 Review.

 

Gigantism.

Donato S, Regala C, Marques P.Vitam Horm. 2026;131:195-234. doi: 10.1016/bs.vh.2025.10.005. Epub 2026 Feb 16.PMID: 41912294 Review.

 

Hormonal Health

Male testosterone synthesis disorders: oxidative stress pathways, regulatory mechanisms, potential of antioxidant therapy, and botanical medicine prospects.

Wu H, Jian MT, Ning G, Li BN, Peng AJ, Wang HY, Tang X, Zhou X.Asian J Androl. 2026 Apr 3. doi: 10.4103/aja2025105. Online ahead of print.

 

From the perspective of prolactin: a view on obesity.

Wang Y, Luo D, Fang G, Ge M, Huang Y, Deng H.Front Endocrinol (Lausanne). 2026 Mar 16;17:1762596. doi: 10.3389/fendo.2026.1762596. eCollection 2026.

 

Gonadotropins Across the Lifespan: Their role in the Neurodevelopment-Neurodegeneration Continuum.

Galbraith JA, Elhassan MZ, Rocha JF, Al Mozani TA, Fredericks CA.Yale J Biol Med. 2026 Mar 31;99(1):199-215. doi: 10.59249/EVST3084. eCollection 2026 Mar.

 

Neonatal Hypopituitarism.

Dayno AN, Crowley J, Bamba V, Bhoj EJK, Shekdar K, McCormack SE.Neoreviews. 2026 Apr 1;27(4):e211-e221. doi: 10.1542/neo.27-4-002.

 

Unconventional Uses of Human Growth Hormone.

Lisbona-Buzali M, Edid-Jaris G, Alegre-Lifshitz A, Mercado-Medrez S, Taniguchi-Ponciano K, Marrero-Rodriguez D, Mercado M.Arch Med Res. 2026 Mar 30;57(5):103412. doi: 10.1016/j.arcmed.2026.103412. Online ahead of print.PMID: 41915988 Review.

 

Comment on: Oxytocin: a neglected hormone in pituitary disease – From function to the diagnosis of a deficiency, resulting clinical relevance, and potential treatment options in endocrinology.

Elia A.Arch Endocrinol Metab. 2026 Jun 1;70(3):e260025. doi: 10.20945/2359-4292-2026-0025.

 

TRH can stimulate the release of two POMC-derived pituitary hormones, ACTH and MSH, in medaka.

Yamakawa M, Gajbhiye DS, Golan M, Kanda S.Endocrinology. 2026 Mar 30:bqag037. doi: 10.1210/endocr/bqag037. Online ahead of print.

 

 

 

 

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)

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