Searchable abstracts of presentations at key conferences in endocrinology

ea0019p256 | Pituitary | SFEBES2009

A case of FSH secreting pituitary adenoma

Muralidhara Koteshwara , Vaughan Nick

A 43-year-old, previously well Asian male was found to have a large intrasellar mass when investigated with an MRI brain for a history of reduced hearing. He had no other clinical history. His visual fields were normal. The tumour had extended to the suprasellar cistern but there was no optic nerve compression. Pre-operative biochemistry showed mild panhypopituitarism with a 0900 a.m. cortisol of 135 mmols/l, a free T4 of 8.5 pmols/l, a free T3 of 3.2 pmo...

ea0077p147 | Adrenal and Cardiovascular | SFEBES2021

Autonomous cortisol secretion (ACS) in other overt functioning adrenal adenoma: two case reports

Zheng Dongling , Kyaw Ye , Muralidhara Koteshwara

Incidentally discovered adrenal masses on abdominal imaging for unrelated reasons have a prevalence of 1-7%. A great majority of these are non-functioning adenomas, but 5-30% are associated with autonomous cortisol secretion (ACS), which is mainly subclinical, and 1-5% with phaeochromocytoma or Conn’s syndrome. Here we report two cases of overt functioning adrenal adenoma with coexisting ACS. We could not find any other reports of such cases in the literature.<p class...

ea0077p124 | Thyroid | SFEBES2021

Two Unusual Cases of Subacute Thyroiditis (SAT) and management

Zheng Dongling , Muralidhara Koteshwara , Theofanoyiannis Panayiotis

Subacute thyroiditis (SAT) is a self-limited inflammatory condition of the thyroid characterised by a clinical course of hyperthyroidism, hypothyroidism, and then return to normal thyroid function. The inflammation is thought to be triggered by a viral infection and is usually treated with anti-inflammatory medications and steroids. Recurrences can uncommonly occur and could be difficult to manage. There are some promising reports of the role of Colchicine in managing recurren...

ea0050ep021 | Adrenal and Steroids | SFEBES2017

Shortcomings of the short Synacthen test; a near miss case of Addison’s disease

Sharma Aditi , Avari Parizad , Muralidhara Koteshwara

We present a case of a middle-aged lady with clinical features suspicious of Addisons, however an initial false negative short synacthen test (SST), resulted in delay of diagnosis.Case: A 62-year-old lady presented to ED with a month history of generalised malaise, weakness, dizziness and vomiting. She had a background of type2 diabetes mellitus, previous left parathyroidectomy for primary hyperparathyroidism and B-thalassaemia trait. Admission bloods in...

ea0050ep021 | Adrenal and Steroids | SFEBES2017

Shortcomings of the short Synacthen test; a near miss case of Addison’s disease

Sharma Aditi , Avari Parizad , Muralidhara Koteshwara

We present a case of a middle-aged lady with clinical features suspicious of Addisons, however an initial false negative short synacthen test (SST), resulted in delay of diagnosis.Case: A 62-year-old lady presented to ED with a month history of generalised malaise, weakness, dizziness and vomiting. She had a background of type2 diabetes mellitus, previous left parathyroidectomy for primary hyperparathyroidism and B-thalassaemia trait. Admission bloods in...

ea0082wc1 | Workshop C: Disorders of the thyroid gland | SFEEU2022

Subclinical hyperthyroidism and its many facets; a presentation with severe thyroid eye disease

Shepherd Carol , Muralidhara Koteshwara , Kyaw Ye

Case History: A 70-year-old man of Chinese origin presents with a two-month history of worsening visual acuity and double vision. He denied systemic symptoms apart from marginal weight loss. Other medical history includes stable asthma, treated with inhalers. He has a niece and nephew with thyroid disease. He is an ex-smoker, retired accountant, and drinks occasional alcohol. On examination, he was normotensive with a body mass index of 22 kg/m2 however was found to...

ea0050ep030 | Bone and Calcium | SFEBES2017

Hypercalcaemic crisis secondary to a large cystic parathyroid adenoma

Jacobs Alana , Wijetilleka Sajini , Sharma Aditi , Muralidhara Koteshwara

We report the case of an 82-year-old lady who was admitted with hypercalaemic crisis (adjusted Calcium 4.82 mmol/L) and acute kidney injury (creatinine 169 micromol/L). PTH was 295 pmol/L, raising the suspicion of an underlying parathyroid carcinoma. She had no palpable neck mass. Her ALP was 131 IU/L and Vitamin D 73 nmol/L; myeloma screen was negative and chest radiograph showed no pathology. A DEXA scan revealed osteoporosis. The hypercalcaemic crisis...

ea0050ep030 | Bone and Calcium | SFEBES2017

Hypercalcaemic crisis secondary to a large cystic parathyroid adenoma

Jacobs Alana , Wijetilleka Sajini , Sharma Aditi , Muralidhara Koteshwara

We report the case of an 82-year-old lady who was admitted with hypercalaemic crisis (adjusted Calcium 4.82 mmol/L) and acute kidney injury (creatinine 169 micromol/L). PTH was 295 pmol/L, raising the suspicion of an underlying parathyroid carcinoma. She had no palpable neck mass. Her ALP was 131 IU/L and Vitamin D 73 nmol/L; myeloma screen was negative and chest radiograph showed no pathology. A DEXA scan revealed osteoporosis. The hypercalcaemic crisis...

ea0015p194 | Growth and development | SFEBES2008

A case of Gorlin-Goltz syndrome with delayed puberty

Muralidhara Koteshwara , Kumar Jesse , Barnes Dennis , Goulden Peter

We report a case of a 20-year-old male with a clinical profile of Gorlin-Goltz syndrome with delayed puberty. This 20-year-old man had learning disablitiy, macrocephaly and multiple jaw cysts. His other clinical features included agenesis of the carpus callosum, obesity and multiple cutaneous lesions suggestive of angiolipomata. His pubertal development was delayed although a LHRH test done at the age of 16 showed a normal response. Radiological features included macrocephaly,...

ea0056p57 | Adrenal cortex (to include Cushing's) | ECE2018

A case of adrenal Cushing’s syndrome initially presenting with diabetic ketoacidosis

Nogueira Edson , Muralidhara Koteshwara , Rahman Mushtaqur , Darko Daniel , Seechurn Shivshankar

A 49-year-old female was admitted to medical HDU with diabetes ketoacidosis (DKA) and newly diagnosed diabetes. Six months previously she was diagnosed with malignant hypertension. She had poorly controlled blood pressure despite treatment with four anti-hypertensives, which were her only regular medication. She had never used any medications or creams containing glucocorticoids. She had no history of hypokalaemia and reported no use of liquorice. She recently attended an outp...