Searchable abstracts of presentations at key conferences in endocrinology

ea0038p431 | Steroids | SFEBES2015

A severe case of ectopic ACTH presenting with Cushing’s syndrome with hypokalaemia, hypomagnesemia, hypophosphatemia, hyponatraemia and hypocalcaemia

Qureshi Sheharyar , Gray Anna , Adjmal Nisha , Farooq Junaid , Padinjakara Noushad

: We present a case of 79 year old lady who presented to hospital with symptoms of polyuria and polydipsia requiring admission for level 3 care. She reported no bowel symptoms or alcohol usage. Her past medical history showed that she suffered from T2DM, Epilepsy, Asthma, Hypertension and Chronic Kidney disease. Her biochemistry revealed a combination of Hyperglycaemia, Hypokalaemia, Hypomagnesemia, Hypophosphatemia, Hyponatremia and Hypocalcaemia. Her medications revealed no ...

ea0021p189 | Endocrine tumours and neoplasia | SFEBES2009

Laparoscopic versus open adrenalectomy and adjuvant mitotane in adrenocortical carcinoma

Ali Sarah , Qureshi Asjid , Clarke Ian , Palazzo Fausto

Introduction: Adrenocortical carcinoma (ACC) is an uncommon aggressive malignancy. Despite surgical resection, recurrence rates are high. Two areas of contention currently involve treatment of ACC: the role of laparoscopic surgery in removal of large, potentially malignant tumours and the role of Mitotane. We present a case of a large adrenal tumour, later confirmed as ACC, where initially laparoscopic adrenalectomy was considered, and adjuvant Mitotane has been given despite ...

ea0019p264 | Pituitary | SFEBES2009

Hypogonadism secondary to hyperprolactinaemia: successful treatment and its adverse consequences….

Bujawansa S , Narayanan RP , Rimmer M , Qureshi Z , Heald A

Background: It is well known that care must be taken in initiating testosterone replacement in individuals with historically low androgen levels. However less is reported about the influence of restoration of normal endogenous testosterone production on behaviour.Here, we report the how adverse sequelae of successful treatment of secondary hypogonadism were managed through a joint approach.Case report: A 34-year-old Business Accoun...

ea0008p78 | Reproduction | SFE2004

Androgens inhibit atresia and retard early development of ovarian follicles: a model for PCOS?

Qureshi AI , Bano G , Whitehead S , Nussey SS , Mason HD

BackgroundPCOS is the commonest endocrinopathy in women. PCO are typified by increased ovarian follicles. The aetiology is unknown, but may be due either to enhanced follicular growth, reduced atresia, or both. Hyperandrogenism is almost universal either clinically or biochemically and in primates and sheep androgen excess in-utero produces ovaries phenotypically identical to those in PCOS. There have been no analyses of the effects of androgens on early...

ea0007p181 | Reproduction | BES2004

The CAM technique and follicle development

Qureshi A , Bano G , Whitehead S , Nussey S , Mason H

BackgroundCurrent techniques to study the early stages of follicular development (i)in vitro(/i) are handicapped by the spontaneous wholesale transition of primordial to primary follicles and by primary follicle arrest. We have circumvented this problem by culturing fragments of ovarian cortical tissue on the chorioallantoic membrane (CAM) of chick embryos and shown it to be successful for the (i)in ovo(/i) culture of cortical slices from a variety of sp...

ea0007p277 | Clinical case reports | BES2004

A diagnostic pitfall: concomitant occurrence of macroprolactinaemia and a non-secreting pituitary adenoma

Krishnan U , Qureshi M , Burrows J , Labib M , Fiad T

We present the case of a 49 year old man who initially presented to his GP with complaints of tiredness, weight gain and tingling in his right hand. GP requested thyroid hormone measurements which showed FT4 level of 3.4 picomoles per litre and TSH 10.89 milli international units per litre. The inappropriately low TSH level raised the possibility of central hypothyroidism and triggered further investigations which revealed a low level for GH, LH, FSH, testosterone and cortisol...

ea0006p57 | Reproduction | SFE2003

Ovarian follicle culture: an old technique revisited

Qureshi A , Bano G , Whitehead S , Nussey S , Mason H

Current techniques to study (i)in vitro(/i) the early stages of follicular development are handicapped by the spontaneous wholesale transition of primordial to primary follicles. Implantation of ovarian tissue into SCID mice is possible but expensive. We have, therefore, adapted a model first described in 1958. Fragments of ovarian cortex are implanted on the chorioallantoic membrane (CAM) of 5-6 day old fertilised chick eggs. The membrane is rich in blood vessels and results ...

ea0081ep436 | Diabetes, Obesity, Metabolism and Nutrition | ECE2022

Insulinoma with Poland Syndrome

Ahmed Suhail , Qureshi Saba , Raza Qureshi Shahzeel , Ajay Joshua , Ahmed Khan Shahid , Botoros George , Kumar Satis , Dashora Umesh Kumar

23-year-old scaffolder, fit and well, presented several times to A&E with episodes of fitting which comprised of an energy surge followed by typical neuroglycopenic and autonomic signs of hypoglycaemia. He was only found to be hypoglycaemic after a severe episode where paramedics were called to his home and discovered his blood sugars to be 1.8 mmol/l with a serum insulin was measurable. His symptoms were moderately relieved by eating a combination of sugary food like hone...

ea0086p191 | Bone and Calcium | SFEBES2022

A case of Familial hypocalciuric hypercalcemia with markedly elevated serum calcium

Ahmed Suhail , Mizanour Rahman Muhammad , Raza Qureshi Shahzeel , Ahmed Khan Shahid , Qureshi Saba , Botros George , Kumar Satis , Kumar Dashora Umesh

A 50-year-old lady presented with fatigue, tiredness and constipation, has more than twenty years history of hypercalcemia. She was clinically and biochemically diagnosed as familial hypocalciuric hypercalcemia with high calcium, normal parathormone, low urinary calcium, low fractional excretion of calcium, positive family history. Genetic confirmation was done by positive molecular genetic analysis of CASR gene. She has persistent high calcium level ranging between 2.8 and 3....

ea0077p231 | Neuroendocrinology and Pituitary | SFEBES2021

A challenging adrenal incidentaloma

Mantega Michele , Ronneberger Ruth , Baldeweg Stephanie , Grieve Joan , Seechurn Shivshankar , Qureshi Asjid

Case History: 69 years old gentleman was referred to endocrinology for investigation of a benign appearing left incidental adrenal adenoma (1cm) after being investigated for abdominal pain. He had a past medical history of an abdominal aortic aneurysm (AAA), type 2 diabetes mellitus and hypertension.Investigations: Initial endocrine investigations revealed normal 24h urinary free cortisol levels (twice), metanephrines and ARR. His overnight dexamethasone...