Roderick J. Bligh-Clifton

Roderick J. Bligh-Clifton

PhD, MBBS (hons), BSC (med), FRACP, FFSc (RCPA)

Endocrinologist

27+ years of Experience

Male📍 St Leonards

About of Roderick J. Bligh-Clifton

Roderick J. Bligh-Clifton is an Endocrinologist based in St Leonards, NSW, Australia.


Endocrinology can be a bit of a tricky space because it covers hormones, glands, and how the body uses energy. In day-to-day work, he looks after people with common issues like thyroid problems and ongoing hormone imbalances. He also helps with more complex conditions, including calcium and phosphate problems, adrenal gland disorders, and issues linked to the pituitary or hypothalamus.


Over time, patients often come in after scans, blood tests, or after symptoms have been hanging around for a while. In many cases that means working out what’s driving things like tiredness, weight changes, feeling weak, headaches, or blood pressure concerns. He also sees people with genetic or inherited endocrine conditions, where careful checking and long-term planning matter.


Some of the rarer problems he deals with include tumours of hormone-making glands, thyroid cancers of different types, and adrenal conditions such as pheochromocytoma and other adrenal tumours. He also helps when people have trouble with things like osteoporosis and bone thinning, and when calcium levels are too high or too low. At times, that can also connect with kidney issues, since hormones and kidneys often affect each other.


Roderick has more than 27 years of experience. That sort of time in the field helps in the way he thinks through symptoms and results. He’s used to managing change too, because hormone levels can move around and treatment plans may need fine-tuning.


His education includes a PhD focused on the genetics of thyroid disorders from the University of Cambridge (1999). He also has an MBBS from the University of Sydney (1993) and a BSc (med) from the University of Sydney (1990). He is a Fellow of the Royal Australasian College of Physicians (FRACP, 2004) and a Fellow of the Royal College of Pathologists of Australasia (FFSc, 2011).


Because of that research background, genetics is a big part of how he approaches some endocrine conditions, especially where thyroid disease runs in families or where inherited syndromes are possible. He brings that practical research mindset to clinic, helping people understand what the tests mean and what the next steps might look like.


Clinical trials information isn’t listed, but care focuses on clear decisions, steady follow-up, and making sure patients feel supported while treatment is getting underway.

Education

  • PhD — PhD in the genetics of thyroid disorders; University of Cambridge; 1999
  • MBBS — Medical degree (Bachelor of Medicine, Bachelor of Surgery); University of Sydney; 1993
  • BSc (Med) — Undergraduate medical sciences; University of Sydney; 1990
  • FRACP — Fellowship of the Royal Australasian College of Physicians; 2004
  • FFSc (RCPA) — Fellowship of the Royal College of Pathologists of Australasia; 2011

Services & Conditions Treated

PheochromocytomaAdrenal CancerHypervitaminosis DMedullary Thyroid CarcinomaMultiple Endocrine NeoplasiaMultiple Endocrine Neoplasia Type 2Neural Crest TumorNeuroendocrine TumorPapillary Thyroid CancerThyroid CancerAnaplastic Thyroid CancerCongenital HypothyroidismGastrointestinal Stromal TumorGlycogen Storage Disease Type 6HypercalcemiaHyperparathyroidismHyperthyroidismHypophosphatemiaHypothyroidismMalnutritionMilk-Alkali SyndromeNephrocalcinosisOsteomalaciaOsteoporosisParathyroid AdenomaParathyroidectomyRicketsThyroidectomyAdrenal Gland AdenomaAdrenocortical CarcinomaAscitesBrain TumorCalcinosisChronic Kidney DiseaseCraniopharyngiomaCushing's diseaseDiabetic KetoacidosisEnd-Stage Renal Disease (ESRD)Exocrine Pancreatic InsufficiencyFamilial Glucocorticoid DeficiencyFamilial Isolated HyperparathyroidismFibromatosisFollicular Thyroid CancerGanglioneuromaHashimoto ThyroiditisHeadacheHypertensionHypoparathyroidismHypopituitarismHypothalamic TumorLangerhans Cell HistiocytosisLymphofollicular HyperplasiaMelanomaMenopauseMultiple Endocrine Neoplasia Type 1Nelson SyndromeNeonatal HypothyroidismOvarian CancerPancreatectomyPancreatic CancerPancreatic Islet Cell TumorPancreaticoduodenectomyParathyroid CancerPituitary TumorPneumoniaPostmenopausal OsteoporosisProlactinomaRenal Cell Carcinoma (RCC)Teratoma of the MediastinumThyroid NoduleType 1 Diabetes (T1D)Uterine FibroidsX-Linked Hypophosphatemia

Publications

5 total
Pheochromocytoma in MEN2.

Recent results in cancer research. Fortschritte der Krebsforschung. Progres dans les recherches sur le cancer • March 19, 2025

Matti Gild, Kimchi Do, Venessa H Tsang, Lyndal Tacon, Roderick Clifton Bligh, Bruce Robinson

Pheochromocytomas (PCs) are rare neuroendocrine tumors found in 20-50% of MEN2 patients. MEN2-related PCs are more often bilateral, identified at a younger age and have a low metastatic potential. They secrete epinephrine as the predominant catecholamine, along with its metabolite metanephrine, and lesser amounts of norepinephrine and normetanephrine. The advent of molecular diagnostic tools has enhanced the identification and stratification of these tumors, revealing a strong genotype-phenotype correlation which is crucial for screening and managing patients. Evaluation involves a combination of structural (CT/MRI) and functional imaging. MIBG remains helpful for PC assessment but novel PET ligands (18F-DOPA, 68Ga-DOTATATE, 18F-FDG) aid in the detection of extra-adrenal paragangliomas, recurrence, and metastatic disease. The treatment paradigm has shifted toward personalized medicine, incorporating genetic insights to tailor interventions, particularly surgical approaches and novel therapeutics such as radiolabeling of somatostatin analogs with lutetium and tyrosine kinase inhibitors.

Hyperglycemia in patients treated with immune checkpoint inhibitors: key clinical challenges and multidisciplinary consensus recommendations.

Journal For Immunotherapy Of Cancer • May 15, 2025

Linda Wu, Venessa Tsang, Roderick Clifton Bligh, Matteo Carlino, Tim Tse, Yiting Huang, Meredith Oatley, Ngai Cheung, Georgina Long, Alexander Menzies, Jenny Gunton

Immune checkpoint inhibitors (ICIs) have an expanding role in the management of numerous cancers. Hyperglycaemia is commonly seen in patients treated with ICIs. However, the differential diagnosis for hyperglycaemia is broad, and incorrect diagnosis can have serious consequences. Herein we review the available literature on causes of hyperglycaemia in ICI treated patients and expert guidelines on management and provide an updated synthesis of expert multidisciplinary recommendations. Our key recommendations are as follows: Intensity of screening for hyperglycaemia should be based on a patient's risk level, including assessment of factors such as corticosteroid use, pre-existing diabetes, baseline HbA1c and fasting blood glucose levels (BGL). People with new onset hyperglycaemia should undergo initial assessment to determine severity and aetiology, including bedside capillary BGL, and formal bloods including lipase, C-peptide with matching glucose, electrolytes and renal function and in some cases type 1 diabetes autoantibodies. People with BGL >15mmol/L (or those receiving SGLT2 inhibitors with BGL >10mmol/L) should additionally have ketones measured. Patients with a high risk of diabetic ketoacidosis (BGL>15 mmol/L, ketones >2 mmol/L) and/or risk of hyperosmolar hyperglycaemic state (BGL persistently >20 mmol/L or reading 'HI') should be referred directly to hospital for emergency assessment and management. Further management of hyperglycaemia should be tailored to the underlying cause(s).

Exercise for Postmenopausal Bone Health - Can We Raise the Bar?

Current Osteoporosis Reports • March 10, 2025

Shejil Kumar, Cassandra Smith, Roderick Clifton Bligh, Belinda Beck, Christian Girgis

Objective: This review summarises the latest evidence on effects of exercise on falls prevention, bone mineral density (BMD) and fragility fracture risk in postmenopausal women, explores hypotheses underpinning exercise-mediated effects on BMD and sheds light on innovative concepts to better understand and harness the skeletal benefits of exercise. Results: Multimodal exercise programs incorporating challenging balance exercises can prevent falls. Emerging clinical trial evidence indicates supervised progressive high-intensity resistance and impact training (HiRIT) is efficacious in increasing lumbar spine BMD and is safe and well-tolerated in postmenopausal women with osteoporosis/osteopenia. There remains uncertainty regarding durability of this load-induced osteogenic response and safety in patients with recent fractures. Muscle-derived myokines and small circulating extracellular vesicles have emerged as potential sources of exercise-induced muscle-bone crosstalk but require validation in postmenopausal women. Exercise has the potential for multi-modal skeletal benefits with i) HiRIT to build bone, and ii) challenging balance exercises to prevent falls, and ultimately fractures. The therapeutic effect of such exercise in combination with osteoporosis pharmacotherapy should be considered in future trials.

Approach to the Patient with Metastatic Pheochromocytoma and Paraganglioma.

The Journal Of Clinical Endocrinology And Metabolism • February 15, 2025

Hussam Alkaissi, David Taieb, Frank Lin, Jaydira Del Rivero, Katharina Wang, Roderick Clifton Bligh, Karel Pacak

Pheochromocytomas and paragangliomas (PPGLs) are rare neural crest-derived tumors with malignant potential and a highly variable natural history, where some patients achieve a cure through surgical resection, while others experience an aggressive and protracted disease course characterized by recurrence and metastasis. While currently no definitive curative treatment exists for metastatic PPGL, ongoing trials and advances in biology of the disease present a beacon of hope. We present a case that illustrates a 15-year treatment journey, illustrating the complexity of metastatic PPGL treatment with different modalities, each with distinct efficacy and toxicity profiles. The choice of treatment is often an art, as much as it is based on evidence, as the clinician must balance among several factors, including tumor-related (pace of progression, tumor burden) and patient-related (functional status, symptoms, general health) ones. Through a stepwise approach, this discussion aims to provide insights into the evolving landscape of metastatic PPGL management.

Adjuvant External Beam Radiotherapy Reduces Local Recurrence in Poorly Differentiated Thyroid Cancer : A Multicenter Retrospective Cohort Study Describing Outcomes in the Treatment of Resectable Poorly Differentiated Thyroid Cancer.

Annals Of Surgical Oncology • February 03, 2025

Pascal K Jonker, Jan Koetje, John Turchini, Jia Feng Lin, Anthony Gill, Thomas Eade, Ahmad Aniss, Roderick Clifton Bligh, Bettien Van Hemel, Diana Learoyd, Hans H Verbeek, Thera Links, Bruce Robinson, Venessa Tsang, Stanley Sidhu, Schelto Kruijff, Mark Sywak

Background: Poorly differentiated thyroid carcinoma (PDTC) accounts for 5% of all thyroid cancers and is responsible for a large proportion of thyroid cancer-related deaths. The optimal treatment approach is not clear. This study aimed to evaluate the effect of postoperative intensity-modulated radiotherapy (IMRT) on the treatment of resectable PDTC. Additionally, treatment-related morbidity, characteristics of 131I-refractory disease, and factors affecting survival were assessed. Methods: The study included consecutive PDTC cases from 1997 to 2018, defined according to Turin criteria and treated in two tertiary referral centers. Surgery, IMRT, 131I, and systemic therapies were administered based on multidisciplinary team recommendations. The primary study outcome was 5-year local control after IMRT in cases with positive resection margins (micro- and macroscopic). The secondary outcomes were treatment-related morbidity within 30-days after completion of treatment (Clavien-Dindo and Common Terminology Criteria for Adverse Events [CTC-AE] 5.0), 131I-refractory disease characteristics using standardized definitions, and factors influencing survival. Results: Among 51 PDTC cases, 53% presented with metastatic disease. Adjuvant IMRT improved 5-year local control (100% vs. 17.5%; p = 0.02), with a higher number of grades 1 to 3 complications (p = 0.005) versus cases without IMRT. Within 13 months, 131I-refractory disease occurred in 62.7% of the patients and was more common in non-survivors (86.6% vs. 52.8%; p = 0.01). Positive resection margins and extrathyroidal extension were associated with poor survival in the univariate analysis, but were not significant in the multiple regression analysis. Conclusions: Adjuvant IMRT may reduce thyroid bed recurrence in resectable PDTC with positive resection margins, but is associated with increased treatment-related complications. 131I-refractory disease occurs frequently, with non-survivors progressing earlier to 131I resistance.

Frequently Asked Questions

Where is Dr Roderick Bligh-Clifton based and how can I find him?
Dr Roderick Bligh-Clifton is based in St Leonards, NSW. If you’re looking for an endocrinologist, you can check his profile for practice details and contact information to arrange an appointment.
What services does Dr Bligh-Clifton offer?
He provides care for a wide range of endocrine conditions and related procedures, including thyroid and parathyroid disorders, adrenal gland issues, neuroendocrine tumours, multiple endocrine neoplasia syndromes, and associated imaging or surgical planning where relevant.
Which conditions can he help with?
He can help with conditions such as hyperthyroidism and hypothyroidism, thyroid nodules and cancer, parathyroid disease, adrenal disorders, diabetes-related concerns, osteoporosis, and various endocrine tumours and syndromes.
How do I book an appointment with him?
To book an appointment, contact the practice through the listed channels on his profile. If you have urgent concerns, call the clinic or your local GP for guidance on next steps.
What should I bring to my first consultation?
Bring any relevant medical records, current medications, and recent test results related to thyroid, parathyroid, adrenal, or other endocrine concerns to help the appointment run smoothly.
Does he perform procedures or surgical planning for thyroid or parathyroid conditions?
The profile notes services and procedures in the endocrine field; for specifics on surgical procedures like thyroidectomy or parathyroidectomy, please confirm during your consultation or with the clinic directly.
What languages does he use or communicate in?
The profile lists languages as not specified; please contact the clinic to confirm language support and any interpreter services if needed.

Contact Information

St Leonards, NSW, Australia

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Memberships

  • Fellow of the Royal Australasian College of Physicians (FRACP)
  • Fellow of the Faculty of Science, Royal College of Pathologists of Australasia (FFSc RCPA)
  • the Endocrine Society of Australia (ESA)
  • Adult Medicine Division (AMD) Council (RACP)
  • Journal of the Endocrine Society
  • European Thyroid Journal