Searchable abstracts of presentations at key conferences in endocrinology

ea0077p128 | Thyroid | SFEBES2021

A case of Transient Neonatal Thyrotoxicosis born to mother with Graves’ Disease

Musharraf Adeel , Kandaswamy Leelavathy , Krishnasamy Senthil-Kumar

Neonatal autoimmune hyperthyroidism is rare but potentially fatal condition. It occurs in 1-5% of infants born to pregnant mothers with Graves’ disease (GD). We present a case of transient neonatal thyrotoxicosis born to pregnant women with GD and high TSH Receptor antibodies. 42 years pregnant lady was referred to Antenatal Endocrine clinic at Walsall Manor Hospital in 15th week of pregnancy with symptoms of Thyrotoxicosis. She has GD and was taking Propylthio...

ea0050ep007 | Adrenal and Steroids | SFEBES2017

Respiratory muscle weakness and diaphragmatic failure secondary to cushing’s syndrome

Gherman-Ciolac Carolina , Kandaswamy Leelavathy , Hatta Fara , Buch Harit

Respiratory muscle weakness and diaphragmatic failure is a rare presentation of hypercortisolism. We report a case of Cushing’s syndrome in a 60-year-old female with history of rheumatoid arthritis, biliary cirrhosis and hypothyroidism. She presented to the Respiratory Physicians with progressive worsening of shortness of breath. Clinical assessment excluded infective pathology, cardiac failure or asthma. Pulmonary function tests (PFT) showed re...

ea0050ep007 | Adrenal and Steroids | SFEBES2017

Respiratory muscle weakness and diaphragmatic failure secondary to cushing’s syndrome

Gherman-Ciolac Carolina , Kandaswamy Leelavathy , Hatta Fara , Buch Harit

Respiratory muscle weakness and diaphragmatic failure is a rare presentation of hypercortisolism. We report a case of Cushing’s syndrome in a 60-year-old female with history of rheumatoid arthritis, biliary cirrhosis and hypothyroidism. She presented to the Respiratory Physicians with progressive worsening of shortness of breath. Clinical assessment excluded infective pathology, cardiac failure or asthma. Pulmonary function tests (PFT) showed re...

ea0038p378 | Reproduction | SFEBES2015

Importance of social support and implications of gender reassignment in congenital adrenal hyperplasia due to 3-β hydroxysteroid deficiency

Kandaswamy Leelavathy , Raghavan Rajeev , Cherukuri Vijay Nandini , Buch Harit

Introduction: 3-β-hydroxysteroid dehydrogenase (3BHSD) deficiency is a rare genetic disorder of steroid biosynthesis that results in decreased production of all three groups of adrenal steroids, which include mineralocorticoids, glucocorticoids, and sex steroids.Case presentation: An infant was born with ambiguous genitalia in 1975 to a conservative Muslim family and was registered as male. The child was hospitalised with addisonian crisis on the el...

ea0044p57 | Bone and Calcium | SFEBES2016

Initial experience of a newly established intra-operative PTH service

Lekkakou Leoni , Kandaswamy Leelavathy , Rolli Alain , Ford Claire , Garnham Andrew , Spinou Catherine , Liew Lenny , Buch Harit

Background: A minimally invasive approach to primary hyperparathyroidism (PHPT) is equivalent to bilateral exploration when intraoperative parathyroid hormone (iPTH) monitoring is used. We have recently established an iPTH service jointly with Surgical and Clinical Chemistry teams and the aim of the study was to evaluate our initial results with its use.Patients and methods: We collected data from 18 operations for PHPT from October 2015, including one r...

ea0038p79 | Clinical practice/governance and case reports | SFEBES2015

Somatotroph adenoma localised with composite 11C-methionine PET/MRI: a cost effective solution

Kandaswamy Leelavathy , Lekkakou Leoni , Koulouri Olympia , Gurnell Mark , Buch Harit , Viswanath Ananth

Background: Although, the diagnostic accuracy of magnetic resonance imaging (MRI) has increased in recent years, it may fail to detect secretory adenoma in a few patients with GH excess. Managing such patients with acromegaly can be challenging. We present a case where 11C-methionine PET/CT co-registered with SPGR/volume MRI proved to be helpful in identifying GH secreting pituitary adenoma.Case history: A 42-year-old male was referred by surg...