Searchable abstracts of presentations at key conferences in endocrinology

ea0032p1122 | Thyroid cancer | ECE2013

Diagnostic validity of thyroid ultrasonography in thyroid nodules

Ram Nanik , Saima S , Ahmed Saqib , Anwer Zahid , Islam Najmul

Introduction: A thyroid ultrasound scan is recommended in the assessment of any suspected thyroid nodule. The ultrasound characteristics of nodules have been shown to be useful in assessing their malignant potential. The aim of this study is to determine diagnostic validity of thyroid ultrasound in differentiating benign and malignant thyroid nodule.Material and Methods: It was cross-sectional study, conducted at XXXX Hospital from August 2011 to July 20...

ea0015p4 | Bone | SFEBES2008

Why do we need to think of differential diagnosis?

Myint Thaung , Srinivasan Ram , Randall Jo , Huston Nigel

Fourth-two years old female patient was diagnosed with carcinoma left breast in 2003. She had mastectomy of left breast and axillary clearance followed by adjuvant radiotherapy and chemotherapy. Histology showed ER positive. She was commenced on anastrozole. She suffered from back pain in 2005. Investigations revealed she had spinal metastases as well as left ureteric stone and hydronephrosis of left kidney. She had a left ureteric stent and her back pain was relived. USG kidn...

ea0013p60 | Clinical practice/governance and case reports | SFEBES2007

Short Synacthen Test (Standard and Low dose): Do we need multiple cortisol samples?

Kela Ram , Tahrani Abd , Varughese George , Clayton R , Hanna FWF

Aim: This study was aimed to assess the need for multiple cortisol samples in ruling out adrenal insufficiency by standard dose Short Synacthen Tests (SST) and Low Dose Short Synacthen Tests (LDSST).Method: We assessed the lab results of 767 patients who attended Metabolic Unit of a University Hospital in the UK from 1999 to 2006 for assessment of adrenal reserve. In LDSST, serum cortisol was measured at 0, 30 and 40 min after administration of 1 mcg of ...

ea0073ep156 | Pituitary and Neuroendocrinology | ECE2021

Functional pituitary gonadotroph adenoma in male patients: a case study

Ram Nanik , Ali Khan Sajjad , Das Bhagwan , Islam Najmul

BackgroundPituitary gonadotroph adenomas are common but very rarely do they secrete biologically active luteinizing hormone (LH) and follicle-stimulating hormone (FSH). There have been case studies reporting high sex hormones (testosterone/estrogen) in the presence of high or normal LH and FSH.Case presentationHere we report two cases who presented with visual disturbance and headache at a tertiary care hospi...

ea0094p14 | Adrenal and Cardiovascular | SFEBES2023

Evaluation of inpatient hyponatremia: if formal recognition (coding) of hyponatremia makes a difference in management and outcomes

Aung Ei Thuzar , Balafshan Tala , Bujawansa Sumudu , Narayanan Ram Prakash

Introduction: Hyponatremia is a common electrolyte disorder in clinical practice. We did a retrospective analysis of 100 patients admitted between Jan 2019 to June 2019 with moderate hyponatremia (Na-125-129 mmol/l) to see if there was a difference in management and outcome of the patients who were formally coded as hyponatremia and those who were not coded as such.Results: Mean age was 74 years in the coded group (n...

ea0099p480 | Diabetes, Obesity, Metabolism and Nutrition | ECE2024

Tolvaptan fortnightly can reduce hyponatraemia related inpatient admissions

Chaudhary Aparna , Sullivan Heather , Balafshan Tala , Prakash Narayanan Ram

Hyponatremia generally defined as a serum sodium of less than 135 mmol/l is the most common type of electrolyte imbalance found in older adults. Its mild to moderate forms can predispose patients to falls, fatigue and a general decline. Severe hyponatremia can contribute to seizures, confusion and death. We present a case of a 70-year-old lady with severe symptomatic chronic hyponatremia secondary to SIADH. She also had progressive Alzheimer’s dementia, anxiety, T1DM, hyp...

ea0081ep878 | Reproductive and Developmental Endocrinology | ECE2022

Characteristics of male idiopathic hypogonadotropic hypogonadism (IHH) patients

Saleem Muhammad , Ram Nanik , Khan Sajjad Ali , Mustansir Mehdi Khan Muhammad

Background: Idiopathic Hypogonadotropic Hypogonadism (IHH) is a condition caused by deficiency or insensitivity to gonadotropin-releasing hormone where the pathology behind the mechanism is unknown and no secondary causes of hypogonadotropic hypogonadism are present. The condition not only effect sexual characteristic but can affect the physical and psychosocial development of a patient therefore making its prompt diagnoses and treatment necessary. The purpose of this study wa...

ea0086p39 | Bone and Calcium | SFEBES2022

An unusual case of severe hypercalcaemia due to treatment resistant Graves’ disease

Thuzar Aung Ei , Sheokand Ajasra , Prakash Narayanan Ram , Balafshan Tala , McNulty Sid , Furlong Niall , Bujawansa Sumudu

A 32-years-old lady was admitted with raised calcium. She had palpitation, sweating, 3 stones weight loss and neck swelling. She was diagnosed with Graves’ disease 5 months ago. Her mother had history of thyroid disease but no family history of hypercalcaemia. She had a small goitre and lid lag on examination. On admission, adjusted calcium was 3.04 mmol/l. PTH was < 0.5 pmol/l. Phosphate, vitamin-D, kidney functions, cortisol, myeloma screen and ACE levels ...

ea0086p341 | Metabolism, Obesity and Diabetes | SFEBES2022

New onset diabetes triggered by use of growth hormone secretogogue for body building, a case report

Thuzar Aung Ei , Sheokand Ajasra , Westall Samuel , Balafshan Tala , Prakash Narayanan Ram , Bujawansa Sumudu

Introduction: Growth hormone secretogogues (GHS) are popular among body building communities as muscle bulking agents. We present an interesting case of new onset diabetes induced by a combination of GHS and selective androgen receptor modulators (SARMs).Case report: A 34-years body builder was referred by his GP due to a 3-week history of polyuria, polydipsia and fatigue. He had recently used one cycle of a combination tablet which contained Ibutamoren ...

ea0065p249 | Metabolism and Obesity | SFEBES2019

‘H’ syndrome; a rare case with novel symptoms

Shah Shanty , DSilva Deborah , Arunachalam Col. , Ganesh MK , Shenoy Ram , Sudeep K

Background: ‘H’ syndrome is a rare autosomal recessive disorder characterised by hyperpigmentation, hypertrichosis, hepatosplenomegaly, hearing loss, hypogonadism, hyperglycaemia (insulin-dependent diabetes), hallux valgus and low height (short stature) and systemic inflammation. Caused by mutations in SLC29A3 gene located on chromosome 10q23 which encodes the human equilibrative nucleoside transporter 3 (hENT3). We report this case to highlight the rarity of the Syn...