Searchable abstracts of presentations at key conferences in endocrinology

ea0092ps1-10-08 | Basic Thyroid Gland, Iodine & Autoimmunity Basic | ETA2023

Thyroid-Resident memory T-cells specific for SARS-COV-2 are enriched in patients with thyroid disorders related to covid-19

Carelli Elena , Silvestri Ylenia , Clemente Francesca , Moschetti Giorgia , Maioli Sara , Espadas de Aris Alejandro , Torelli Rosanna , Longhi Elena , De Feo Tullia , Salvi Mario , Mantovani Giovanna , Arosio Maura , Bombaci Mauro , Pesce Elisa , Grifantini Renata , Abrignani Sergio , Geginat Jens , Muller Ilaria

Objectives: SARS CoV-2 infections have been associated with the onset of classic subacute thyroiditis (SAT) or atypical SAT, observed in 10-15% of patients hospitalized for severe COVID19 disease (COV-A-SAT) and characterized by absence of neck pain, mild thyrotoxicosis associated with non-thyroidal illness syndrome and thyroiditis-like areas which may persist in the thyroid gland up to 12 months following SARS-CoV-2 infection, despite normalization of thyroid function. Little...

ea0090p213 | Thyroid | ECE2023

Patients with Covid-19 induced atypical thyroiditis have thyroid-resident memory T-cells specific for SARS-CoV-2

Muller Ilaria , Silvestri Ylenia , Clemente Francesca , Maioli Sara , Carelli Elena , Moschetti Giorgia , Espadas Alejandro , De Feo Tullia , Mantovani Giovanna , Arosio Maura , Bombaci Mauro , Pesce Elisa , Grifantini Renata , Abrignani Sergio , Salvi Mario , Geginat Jens

Background: The severe acute respiratory syndrome coronavirus-2 (SARS-CoV-2) pandemic disease (Covid-19) is associated with the onset of thyroid dysfunction via multiple mechanisms. Patients hospitalised for severe Covid-19 disease may develop painless atypical thyroiditis coexisting with non-thyroidal illness syndrome, which determines transient thyrotoxicosis with quick restoration of euthyroidism during the following weeks. However signs of thyroiditis at ultrasound and sci...

ea0009p182 | Clinical | BES2005

Familial expansile osteolysis (FEO): a rare cause of tooth loss

Thomas R , Welbury R , Wallace R , Parr J , Hughes A , Pearce S , Cheetham T

Familial expansile osteolysis is a rare autosomal dominant disorder of bone, first described in a kindred from Northern Ireland in 1988. There are histological similarities to Paget's disease but the disorder typically presents in the young.Case report: Our patient presented at 15 years of age with sensorineural hearing loss, skeletal pain, gingival hypertrophy and mobile teeth. Neither parent was similarly affected. Radiographs demonstrated tooth root r...

ea0090ep786 | Pituitary and Neuroendocrinology | ECE2023

De-escalation treatment with pasireotide for aggressive acromegaly: A long-term experience

Menotti Sara , Giampietro Antonella , Chiloiro Sabrina , Pontecorvi Alfredo , De Marinis Laura , Bianchi Antonio

Introduction: Pasireotide long acting release (LAR) is approved for second line treatment of acromegaly. We present 3 patients with aggressive acromegaly treated with a personalized de-escalation approach.Case 1: A 61-year-old female affected by acromegaly reisistant on first-line SSAs. In 2015 therapy was switched to pasireotide LAR 60 mg every 28 days. After two years, the IGF-I level touched the lower age range and therapy was downscaled to pasireotid...

ea0029p349 | Clinical case reports - Pituitary/Adrenal | ICEECE2012

A case of acromegaly without clear evidence of pituitary adenoma or ectopic GH/GHRH secreting tumors

Fibbi B. , Maggioli C. , Vannucci L. , De Feo M. , Petrone L. , Cilotti A. , Forti G. , Pupilli C.

Introduction: Acromegaly secondary to an extrapituitary source of GH or GHRH is rare, usually associated with bronchial/thymic carcinoids, neuroendocrine enteropancreatic tumors or extrasellar somatotropinomas. Few series of acromegalic patients with negative pituitary imaging and lack of an ectopic source are reported in the literature.Methods: We report the clinical history and the laboratory and imaging results of an acromegalic woman with no clear ev...

ea0029p1318 | Paediatric endocrinology | ICEECE2012

Psychiatric symptoms in Addison's crisis in childhood: the complexity of diagnosis

Maggioli C. , Maseroli E. , Dirindelli P. , Stefanini M. , Innocenti E. , Pupilli C. , Petrone L. , Forti G. , De Feo M.

Introduction: Since Addison disease is relatively rare and difficult to recognize in childhood delayed diagnosis is common. Patients with adrenal insufficiency generally show hypotension, hypoglycaemia, hyponatriemia, but can also manifest mild symptoms like chronic fatigue, nausea, vomiting, weight loss, recurring abdominal pain and psychiatric symptoms. In this regard mild disturbances in mood, motivation and behavior represent the main clinical features showing a prevalence...

ea0029p1792 | Thyroid cancer | ICEECE2012

Circulating BRAFV600E in the diagnosis and follow up of differentiated thyroid cancer

Pupilli C. , Pinzani P. , Salvianti F. , Fibbi B. , Rossi M. , Petrone L. , De Feo M. , Forti G.

Introduction: Although overall accuracy of fine needle aspiration (FNA) in identifying thyroid cancer is considered excellent, 20–30% of aspirates do not allow definitive diagnosis of malignancy. Proto-oncogene somatic mutations such as BRAFV600E in FNA strongly suggest the presence of malignancy. However, only few studies reported the use of circulating BRAFV600E-mutated alleles in plasma as an useful marker for non invasive diagnosis and follow up of this disease.<p...

ea0099ep161 | Pituitary and Neuroendocrinology | ECE2024

Kallmann-de morsier syndrome: about a case

Souissi Mariem , Fadia Boubaker , Elomma Mrabet Houcem , Dimassi Oumaima , Wafa Alaya , Mohamed Habib Sfar

Introduction: Kallmann-de Morsier Syndrome is a rare genetic disorder characterized by the combination of hypogonadotropic hypogonadism and anosmia or hyposmia. It is more prevalent in males compared to females. In this case report, we present the case of an adolescent with Kallmann-de Morsier Syndrome.Case Presentation: An 18-year-old patient was referred to our endocrinology clinic by gynecologists for the investigation of pubertal delay. The patient&#...

ea0084ps3-11-103 | Case Reports | ETA2022

Suspicious thyroid nodule in de quervain’s thyroiditis

Sorina Martin Carmen , Dumea Bianca , Parfeni Ovidiu , Mustata Theodor , Sirbu Anca , Fica Simona

Introduction: De Quervain’s thyroiditis, also known as subacute granulomatous thyroiditis, is a self-limiting inflammatory disorder of the thyroid gland. It is presumed to be caused by a viral infection and many patients have a history of an upper respiratory infection 2-8 weeks prior to the onset of thyroiditis. It is the most common cause for neck pain or discomfort, and it usually has a predictable course of thyroid function evolution. On ultrasonography the thyroid gl...

ea0021oc5.2 | Steroids and thyroid | SFEBES2009

De novo cortisol synthesis by primary human keratinocytes

Hannen Rosalind , Michael Anthony , Burrin Jacky , Philpott Micheal

Cortisol-based therapy is still the most potent anti-inflammatory treatment available for skin conditions such as psoriasis and atopic dermatitis. Previous studies have demonstrated the presence of components of the steroidogenic pathway in keratinocytes, though surprisingly none have reported that these cells, which form up to 90% of the epidermis are able to synthesise cortisol1,2. Here, we demonstrate that primary human keratinocytes (PHK) are capable of de no...