Searchable abstracts of presentations at key conferences in endocrinology

ea0038p112 | Clinical practice/governance and case reports | SFEBES2015

Carbarmazepine and Cushing’s: a cautionary tale of assay interference mimicking disease

Tisdale Mie Mie , Swords Francesca

We present two cases, with apparently confirmed Cushing’s. Detailed clinical evaluation did not support the diagnosis, and carbamezepine interference was finally confirmed in both patients.Case 1: A 44-year-old man presented to a nephrologist with malignant hypertension. Routine investigation for secondary causes revealed hyperreninaemia with marked disparity of kidney size suggestive of renal infarction. 24 h urinary free cortisols (UFCs) were also...

ea0038p448 | Thyroid | SFEBES2015

Management of amiodarone induced thyrotoxicosis within the United Kingdom: is it time for a consensus guideline? A single centre retrospective review

Tisdale Mie Mie , Swords Francesca , Ahluwalia Rupa

Introduction: Amiodarone induced thyrotoxicosis (AIT) remains a diagnostic and therapeutic challenge. Broadly, AIT is classified as type 1 (underlying latent thyroid disorder) or type 2 (destructive thyroiditis). Despite being an on-going clinical conundrum, there is no U.K. wide guidance on management of AIT. We report a retrospective review of recent cases treated within our department as AIT.Methods: Data was collected for all patients referred to our...

ea0050ep014 | Adrenal and Steroids | SFEBES2017

Delayed diagnosis of neurofibromatosis type 1 associated phaeochromocytoma and intussuscepting sigmoid adenocarcinoma

Tisdale Mie Mie , Burgess Neil , Stearns Adam , Lopez Berenice , Sadah Jaan , Myint Khin Swe

Background: Neurofibromatosis type 1 (NF1) related Phaeochromocytoma is a rare endocrine disorder and diagnosis is frequently delayed. NF1 is frequently associated with gastro-intestinal stromal tumour but also reported with adenocarcinoma (rare genetic MLH1 mutation). We presented a case where diagnosis of phaeochromocytoma was delayed 5 years after initial symptoms and only incidentally found on scanning at the time of his presentation with colonic...

ea0050ep014 | Adrenal and Steroids | SFEBES2017

Delayed diagnosis of neurofibromatosis type 1 associated phaeochromocytoma and intussuscepting sigmoid adenocarcinoma

Tisdale Mie Mie , Burgess Neil , Stearns Adam , Lopez Berenice , Sadah Jaan , Myint Khin Swe

Background: Neurofibromatosis type 1 (NF1) related Phaeochromocytoma is a rare endocrine disorder and diagnosis is frequently delayed. NF1 is frequently associated with gastro-intestinal stromal tumour but also reported with adenocarcinoma (rare genetic MLH1 mutation). We presented a case where diagnosis of phaeochromocytoma was delayed 5 years after initial symptoms and only incidentally found on scanning at the time of his presentation with colonic...

ea0038p56 | Clinical practice/governance and case reports | SFEBES2015

Phaeochromocytoma in pregnancy: good luck and judgement lead to a successful outcome

Tisdale Mie Mie , Burgess Neil , McKelvey Alastair , O'Hare Debbie , Swords Francesca

Phaeochromocytoma during pregnancy is extremely rare with a frequency of 0.002% pregnancies. However, the risks for the pregnant patient with this tumour are extremely high: with maternal and foetal mortality up to 50% if undiagnosed. In contrast, early diagnosis and treatment during pregnancy decrease the maternal and foetal mortality to <5 and 15% respectively.A 37-year-old female underwent abdominal imaging to investigate iron deficiency anaemia. ...