Searchable abstracts of presentations at key conferences in endocrinology

ea0059p129 | Neuroendocrinology and pituitary | SFEBES2018

The Utility of the high dose Short Synacthen test in pituitary patients who failed the ITT but have a low pre-test likelihood of ACTH deficiency

Muhammad Zia Ul Hussnain Hafiz , Agha Amar

The Insulin tolerance test (ITT) is regarded as the gold-standard for diagnosing ACTH deficiency but some normal subjects do not exhibit an adequate cortisol response to hypoglycaemia. Identification of false fail cases in pituitary patients is important so as to avoid unnecessary treatment with glucocorticoids. Two hundred consecutive ITTs in pituitary patients were analysed. Twenty six (13 males) failed the ITT and subsequently have a Short Synacthen test (SST). 20 patients ...

ea0038p481 | Thyroid | SFEBES2015

Recurrent Hashimoto’s encephalopathy: a case report of reversible coma and status epilepticus

Agha Adnan , Htun Htwe , Ahmed Adeeba

Background: Steroid-responsive encephalopathy associated with autoimmune thyroiditis (SREAT) also known as Hashimoto’s encephalopathy (HE), is a rare immune-mediated complication independent of functional status of thyroid, which leads to either stroke-like symptoms, or presents as diffuse progressive symptoms of altered mental status, seizures, and cognitive dysfunction. Here we present a case of SREAT in a female with recurrent episodes.Case histo...

ea0011p106 | Clinical case reports | ECE2006

Parathyroid carcinoma in multiple endocrine neoplasia (MEN) type 1: two case reports

Agha A , Carpenter R , Bhattacharya S , Monson JP

Hyperparathyroidism occurs in most patients with MEN Type 1 but the association of MEN type-1 with parathyroid carcinoma has only been described previously in one patient. In this report, we describe two further cases of parathyroid carcinoma presenting in association of MEN type 1 syndrome.The first patient was a 69-year-old woman who presented with severe hyperparathyroidism and tracheal compression by a mediastinal mass which was shown histologically ...

ea0007p284 | Clinical case reports | BES2004

Late recovery of pituitary function following traumatic brain injury

Ryan J , Agha A , Sherlock M , Thompson C

Anterior pituitary dysfunction is a well-recognized complication of traumatic brain injury (TBI) but recovery is an exceptional event, with only three previously published case reports.We report a case of a 25 year old man who suffered severe TBI in a road traffic accident in 1997. His neurological recovery was slow and incomplete with significant cognitive deficit and recurrent seizures. He developed polyphagia and his weight increased by 20 Kilograms i...

ea0005p182 | Neuroendocrinology and Behaviour | BES2003

Hypopituitarism following cranial irradiation for non-pituitary brain tumours

Agha A , O'Connor S , Rogers B , Thompson C

There is little information on the effects on pituitary function of cranial irradiation for non-pituitary tumours. We have studied anterior and posterior pituitary function in 17 patients (6 males), with a median age 19 years (range 5-48) at the time of radiotherapy. 16 patients had primary brain tumours and one had acute lymphocytic leukaemia. The patients were selected by the radiotherapists for investigation . Pituitary functions were assessed at a median of 60 months (rang...

ea0062p10 | Poster Presentations | EU2019

Metabolic encephalopathy secondary to diabetic ketoacidosis

Tomkins Maria , Richard McCormack , Karen O'Connell , Agha Amar , Merwick Aine

Case presentation: A 35-year-old man presented to the emergency department (ED) in a confused and agitated state. His past medical history was significant for poorly controlled type 1 diabetes, complicated by background diabetic retinopathy. He was taking basal/bolus insulin and had a history of diabetic ketoacidosis (DKA) eleven years prior. He also had multiple sclerosis however disengaged with neurology services and was non-compliant with interferon therapy. Prior to admiss...

ea0063p535 | Diabetes, Obesity and Metabolism 2 | ECE2019

Metabolic encephalopathy secondary to diabetic ketoacidosis

Tomkins Maria , McCormack Richard , O'Connell Karen , Agha Amar , Merwick Aine

Case presentation: A 35-year-old man presented to the emergency department (ED) in a confused and agitated state. His past medical history was significant for poorly controlled type 1 diabetes, complicated by background diabetic retinopathy. He was taking basal/bolus insulin and had a history of diabetic ketoacidosis (DKA) eleven years prior. He also had multiple sclerosis however disengaged with neurology services and was non-compliant with interferon therapy. Prior to admiss...

ea0044ep42 | (1) | SFEBES2016

Birds of a feather flock together: Maternally inherited diabetes and Deafness AND Mitochondrial encephalopathy lactic acidosis and stroke like episodes

Agha Adnan , Ansari Yousuf , Bajwa Hammad , Webber Jonathan

Introduction: The mutation at m. 3243 adenine to guanine (A>G) in mitochondrial encoded transfer-RNA Leucine 1 (MTTL1) gene is the single most prevalent disease-causing mitochondrial DNA (MtDNA) mutation, with carrier status of 1:400 in our general population. The distinct disease phenotype is dependent on the level of heteroplasmy of wild-type vs mutation-type mtDNA in the specific target tissues, ranging from Maternally inherited diabetes and Deafness (MIDD) to mitochond...

ea0044ep54 | (1) | SFEBES2016

A rare case of type 2 diabetes for 35 years on metformin who developed insulinoma and diazoxide induced renal failure

Alam Muhammad , Agha Adnan , Bajwa Hammad , Mtemrerwa Brian

Background: Insulinoma in a pre existing patient of type diabetes is extremely rare presentation.Methods: We are presenting a a rare case of insulinoma in a pre existing case of type 2 diabetes. A 73 years old patient with type 2 diabetes for 35 years presented to endocrine clinic with hypoglycaemic symptoms ultimatley diagnosed with insulinoma and patient developed renal failure with diazoxide treatment.Result: A 73 years old chin...

ea0059ep31 | Bone and calcium | SFEBES2018

Multiple vertebral fragility fractures following pregnancy

Sharma Aditi , Agha-Jaffar Rochan , Cox Jeremy , Comninos Alexander N

We present the case of a 35-year-old woman who was well until pregnancy 4y previously in Israel. Her antenatal course was uncomplicated. She breastfed postpartum and a few months into this she experienced acute back pain on reaching for a nappy. MRI demonstrated six vertebral fractures. DEXA scan confirmed osteoporosis (lumbar T-score −4.3, hip T-score −3.3). She received a single dose of denosumab. She moved to the UK 2y later and was referred to our Endocrine Bon...