Searchable abstracts of presentations at key conferences in endocrinology

ea0062wa1 | Workshop A: Disorders of the hypothalamus and pituitary | EU2019

A rare case of diabetes insipidus and breathlessness…

Andrabi Syed Basharat , Bano Gul

Langerhans cell (LCH) histiocytosis occurs in 1 per 560,000 adults with variable manifestations. It has a high rate of misdiagnosis due to its variable presentation and rarity. It is even more rare that it presents with simultaneous and multiple endocrine dysfunction early in the course of disease. We report a case of Langhans Cell Histiocytosis in an adult male presenting with central Diabetes Insipidus, Hypergonadotrophic Hypogonadism and pulmonary disease. A 36 year old mal...

ea0065p426 | Thyroid | SFEBES2019

A reversible cause of pulmonary hypertension

Andrabi Syed Basharat , Kurera Isuri , Maltese Giuseppe , Bano Gul

Graves’ disease is one of the reversible causes of pulmonary hypertension (PAH). The association was first reported in 1980. Studies have suggested an elevated pulmonary artery systolic pressure in about 36% of patients with Graves’ disease by Doppler echocardiography. We report a case of Graves disease associated with pulmonary hypertension in a young female.Case report: A 41 year old female presented with history of worsening breathless and p...

ea0062p22 | Poster Presentations | EU2019

A rare variant of Hashimoto’s thyroiditis

Eid Hatem , Andrabi Basharat , Kurera I , Bano G

Hashimoto’s thyroiditis (HT) is the most common inflammatory condition of the thyroid gland. In addition to the classic variant of HT, several other subtypes have been identified, such as the fibrous variant (HTFV).Case history: A 38 years old man noticed a rapidly enlarging lump in his neck month ago. This resulted in discomfort with choking sensation and mild dysphagia. He mentioned weight loss, tiredness and night sweats. He was a smoker and dran...

ea0062p23 | Poster Presentations | EU2019

Pancreatic lesions in von Hippel–Lindau (vHL) disease: A diagnostic and management challenges

Kurera I , Andrabi B , Ismail R , Snape K , Bano G

vHL disease is commonly inherited in an autosomal dominant fashion. Pancreatic lesions in vHL are generally asymptomatic or associated with mild nonspecific symptoms.Case history: A 40 year old Asian female was seen in genetic/endocrine clinic for Predictive vHL mutation. She was married to her first cousin and had a 19 years old daughter. Her sister was diagnosed with vHL in Canada. She presented with Renal cell carcinoma and renal cysts. Her mother die...

ea0063ep147 | Thyroid | ECE2019

A rare variant of Hashimoto’s thyroiditis

Eid Hatem , Andrabi Basharat , Kurera I , Bano G

Hashimoto’s thyroiditis (HT) is the most common inflammatory condition of the thyroid gland. In addition to the classic variant of HT, several other subtypes have been identified, such as the fibrous variant (HTFV).Case history: A 38 years old man noticed a rapidly enlarging lump in his neck month ago. This resulted in discomfort with choking sensation and mild dysphagia. He mentioned weight loss, tiredness and night sweats. He was a smoker and dran...

ea0065p334 | Neuroendocrinology | SFEBES2019

Co-secreting TSH and growth hormone pituitary adenoma

Eid Hatem , Andrabi B , Ismail R , Nizar H , Maltese G , Bano G

The co-existence of thyrotropin (TSH) and growth hormone (GH) secreting pituitary adenoma is exceedingly rare. Less than 15 cases having been reported.Case report: A 75 years’ old man presented with new-onset atrial fibrillation. He had high FT4 with normal TSH. His ultrasound scan of the neck showed a solitary nodule. He had ablation twice and was started on bisoprolol and anticoagulant. He had an MRI scan for headaches and this showed a pituitary ...

ea0062p18 | Poster Presentations | EU2019

A rare cause of hypercalcemia and nephrolithiasis

Andrabi Syed Basharat , Kurera Isuri , Maltese Guisseppe , Snape Katie , Bano Gul

We present a 67 years old male originally from Cyprus who presented with Hypercalcemia. He had renal calculi twice and required Laparoscopic procedure. In his family history his 3 siblings had confirmed raised calcium and PTH and 2 other siblings had renal calculi. One of his brother, had surgery for primary hyperparathyroidism twice but no parathyroid adenoma was found and his calcium remained high. Patients’ calcium was 2.81 mmol/l (2.15–2.50), 25 HVD 82 nmol/l (75...