Searchable abstracts of presentations at key conferences in endocrinology

ea0082p1 | Poster Presentations | SFEEU2022

Pseudohypoparathyroidism presenting with extensive bone lytic lesion histology proven Brown tumours

Eltayeb Randa , Sahoo Saroj , ISLAM Quazi , Eldigair Hiba , Armeni Eleni , Patel Dipesh , Karra Efthimia , Yousseif Ahmed , Khoo Bernard

Summary: 59-year-old female diagnosed at the age of 41 in 2004 with pseudohypoparathyroidism (PHP) initially presenting with raised PTH 152 pmol/l (1.6-6.9), Phosphate 1.91 mmol/l (0.87-1.45), adjusted calcium 1.90 mmol/l (2.20-2.60), raised ALP 600 units/l (0-129) and low vitamin D 29 nmol/l. Since diagnosis started on alfacalcidol 1 mg daily and Calcichew-D3. Investigations by hepatology team in the view of persistently raised ALP showed normal liver ultrasound, Fibroscan an...

ea0082p32 | Poster Presentations | SFEEU2022

Pituitary Apoplexy presenting with acute hyponatraemia

Islam Quazi , Sahoo Saroj , Naeem Ammara , Eldigair Hiba , Mehta Jay , Khoo Bernard , Karra Efthimia , Yousseif Ahmed , Patel Dipesh , Armeni Elena

Case history: 48-years old man, with no comorbidities, presented to A&E due to global headache of 20 days duration, with associated intermittent vomiting, but no photophobia, cranial nerve impairment, neck pain or visual disturbance. The first head-scan (CT, computed tomography) was unremarkable, hence was discharged with safety advises. One week later, he represented to A&E with similar complaints. On enquiries, he mentioned to be reviewed by an optician 6 months ago,...

ea0086p249 | Neuroendocrinology and Pituitary | SFEBES2022

Acute hypoglycemia as the presenting manifestation secondary to pituitary metastasis in a patient with malignant melanoma

Sahoo Saroj , Eltayeb Randa , Islam Quazi , Naeem Ammara , Patel Dipesh , Yousseif Ahmed , Armeni Eleni , Karra Efthimia , Khoo Bernard , Grossman Ashley

Introduction: Pituitary metastasis (PM) is a rare condition and associated with a reduced life-span. The most common primary sites are breast and lung, followed by thyroid and renal cell carcinoma. Patients with PM are mostly asymptomatic and incidentally discovered during neuroimaging. Characteristic symptoms are reported in <20% and most commonly include visual involvement, diabetes insipidus, and panhypopituitarism. We here describe a case with malignant melanoma (MM) w...

ea0090p297 | Calcium and Bone | ECE2023

Chronic hypoparathyroidism is associated with skeletal muscle dysfunction and restrictive lung disease

Sahoo Saroj , Anush Babu Takasi , Hashim Zia , Neyaz Zafar , Mani Vinita E. , Jain Neeraj , Bhatia Eesh , Mishra Anjali

Introduction: Whether patients with non-surgical hypoparathyroidism have skeletal muscle dysfunction is not studied. It is also not known if skeletal muscle dysfunction involves respiratory muscles and results in a restrictive lung disease (RLD).Aim: To assess skeletal muscle and pulmonary function in patients with non-surgical hypoparathyroidism, who were asymptomatic for overt muscle and lung diseases.Methods: Thirty patients wit...

ea0090p469 | Reproductive and Developmental Endocrinology | ECE2023

Gestational thyrotoxicosis due to molar pregnancy complicated by pre-eclampsia

Mansukhbhai Shekhda Kalyan , Zlatkin Vladislav , Kumar Sahoo Saroj , Tamjidul Islam Quazi , Naeem Ammara , Nwokolo Munachiso , Yousseif Ahmed , Karra Efthimia , Patel Dipesh , Khoo Bernard , Armeni Eleni

Introduction: Gestational trophoblastic disease (GTD) is a group of disorders arising from abnormal proliferation of placental trophoblasts. Hydatiform mole (molar pregnancy) is a premalignant condition which is further devided in to partial and complete mole. Incidence of molar pregnancy is estimated to be 1 in 1000 pregnancies. Hyperthyroidism is one of the rare complications of molar pregnancy which, if not detected and treated, can lead to adverse consequences. We describe...

ea0090ep108 | Adrenal and Cardiovascular Endocrinology | ECE2023

Adrenocortical Carcinoma presenting as florid Cushing’s Syndrome

Islam Quazi , Armeni Eleni , Naeem Ammara , Nwokolo Munachiso , Shekhda Kalyan , Karra Efthimia , Khoo Bernard , Patel Dipesh , Sahoo Saroj Kumar , Yousseif Ahmed

Introduction: Adrenocortical Carcinoma (ACC) is a rare endocrine neoplasm with poor prognosis, and an estimated incidence of approximately 2.5/1,000,000 patients. The functional state of these tumors varies from non-secretory (20%) to non-secretory. The latter category is subdivided into glucocorticoid-producing (45%) or glucocorticoid-androgen producing (45%) or androgen-producing only (10%). We report a case of a 35-year-old lady who initially presented with symptoms of Cush...

ea0091wd15 | Workshop D: Disorders of the adrenal gland | SFEEU2023

Uncovering the Rare: Managing a case of ‘Cushing’s Crisis’

Islam Quazi , Armeni Eleni , Khoo Bernard , Mladenova Irinia , Naeem Ammara , Patel Dipesh , Sahoo Saroj , Shekhda Kalyan , Yousseif Ahmed , Grossman Ashley , Karra Efthimia

Introduction: Cushing’s syndrome is a rare endocrine disorder characterized by excess cortisol secretion. It can be caused by various etiologies, including ACTH-dependent and ACTH-independent forms. We report a case of a 78-year-old male who presented with severe hypertension, refractory hypokalemia, and severe hypercortisolaemia, diagnosed with ACTH-dependent Cushing’s syndrome with bilateral adrenal hyperplasia.Case Presentation: A 78-year-ol...

ea0094p43 | Bone and Calcium | SFEBES2023

Paradoxical severe hypercalcemia in a male bodybuilder with rhabdomyolysis: A case report

Islam Quazi , Armeni Eleni , Eltayeb Randa , Grossman Ashley , Khoo Bernard , Mladenova Irina , Patel Dipesh , Sahoo Saroj , Shekhda Kalyan , Yousseif Ahmed , Karra Efthimia

Paradoxical severe hypercalcemia is a rare phenomenon observed in some patients in delayed phase following rhabdomyolysis. We present a case of 33-year-old male who developed severe hypercalcemia following successful treatment of rhabdomyolysis. Patient was admitted with agitation and disinhibition, was intubated in A&E due to metabolic acidosis (pH 6.7), hyperkalemia (K+ 7.3 mmol/l), lactic acidosis (23 mmol/l), and pyrexia (40°C). Toxicology screening shown presence...

ea0094p189 | Bone and Calcium | SFEBES2023

Resistant hypocalcaemia in a patient with prostatic adenocarcinoma with extensive osteoblastic metastasis

Sahoo Saroj , Armeni Eleni , Bouloux Pierre , Grossman Ashley , Islam Quazi , Karra Eftimia , Khoo Bernard , Naeem Ammara , Nwokolo Muna , Patel Dipesh , Shekhda Kalyan , Silverwood Clare , Yousseif Ahmed

Introduction: Hypocalcaemia is rare in patients with malignancy, occurring in <2% of patients with malignancy. Osteoblastic bone metastases as an aetiology of hypocalcaemia are further rare.Case description: A 75-year-old male presented to emergency with back pain, and immobility. He was diagnosed to have prostate cancer in 2019. A bone scan in April 2022 showed extensive sclerotic metastases involving axial and prox...