Searchable abstracts of presentations at key conferences in endocrinology

ea0090ep841 | Pituitary and Neuroendocrinology | ECE2023

Sheehan’s syndrome presenting as post-partum depression : a case report

Qasdi Ikrame , Echchad Lamya , Ouirar Hasna , Elmazuni Zainab , Rifai Kaoutar , Hinde Iraqi , Gharbi Mohamedelhassan

Introduction: Sheehan’s syndrome or Simmond’s disease is a partial or complete postpartum hypopituitarism caused by pituitary infraction and necrosis that usually occurs as a complication of massive postpartum hemorrhage or severe hypotension during or after labor and delivery. We present the case of Sheehan’s syndrome presenting postpartum depression. Case: A 40 years old woman, referred to our department by her psychiatrist for explorati...

ea0035p856 | Pituitary Clinical (<emphasis role="italic">Generously supported by IPSEN</emphasis>) | ECE2014

GH replacement therapy during pregnancy in a patient with Sheehan's syndrome

Karaca Zuleyha , Tanriverdi Fatih , Uludag Semih Zeki , Ozgun Tuncay , Unluhizarci Kursad , Kelestimur Fahrettin

Introduction: Appropriate replacement therapy of not only gonadotrophins, but other deficient pituitary hormones is important in patients with hypopituitarism for a successful pregnancy. Data regarding GH replacement therapy during pregnancy is limited. We would like to present a case with panhypopituitarism including severe GH deficiency due to Sheehan’s syndrome, who achieved successful pregnancy with GH replacement therapy in the first half of pregnancy.<p class="a...

ea0029p393 | Clinical case reports - Pituitary/Adrenal | ICEECE2012

Recovery of prolactin function following spontaneous pregnancy in a patient with Sheehan’s syndrome

Laway B. , Mir S.

Introduction: Sheehan’s syndrome presents with hypopituitarism of variable severity after parturition usually preceded by post partum hemorrhage. Recovery of lactotroph function after initial insult has not been reported in the literature.Case report: A 41-year woman delivered her 1st child in 1994 at the age of 25 years, complicated by profuse vaginal bleeding and received two blood transfusions at a city hospital. She had lactation failure ...

ea0037ep712 | Pituitary: clinical | ECE2015

Sheehan's syndrome: a clinical, biochemical, hormonal, radiological, bone mineral density, and quality of life assessment

Razi Syed Mohd , Gutch Manish , Kumar Sukriti , Gupta Abhinav , Gupta Keshav Kumar

Background: Sheehan’s syndrome or postpartum pituitary necrosis though rare, is still remains one of the commonest causes of hypopituitarism in the developing parts of world like Indian subcontinent. The clinical presentation is often variable and frequently accompanied by hypogonadism which leads to low bone density due to loss of bone protective effect of oestrogen.Aims: To find out the bone mineral density and the quality of life (QoL) i...

ea0081p769 | Late-Breaking | ECE2022

Coexistence of hypopituitarism caused by Sheehan′s syndrome and Hashimoto′s thyroiditis. A case report, review of literature.

Kermaj Marjeta , Zaimi Irsa , Guni Mirjeta , Shkurti Adela , Fureraj Thanas , Ylli Agron

Introduction: Hypopituitarism due to Sheehan′s syndrome is a rare complication and its diagnosis is often overlooked. The vast majority of people with hypothyroidism have primary hypothyroidism, often due to Hashimoto’s thyroiditis. Coexistence of hypopituitarism and primary hypothyroidism, may accelerate clinical manifestations, mainly those associated with hypothyroidism. Hashimoto′s Thyroiditis with concomitant hypopituitarism is rare but has been described...

ea0049ep937 | Pituitary - Clinical | ECE2017

Four decades without diagnosis: Sheehan‘s syndrome, a retrospective analysis

Gokalp Deniz , Alpagat Gulistan , Tuzcu Alpaslan Kemal , Bahceci Mithat , Tuzcu Sadiye , Yakut Fatime , Yildirim Azat

Aim: Sheehan‘s syndrome (SS) remains a frequent cause of hypopituitarism in undeveloped and developing countries, but due to improvements in obstetric care, it is rare in developed countries. We aimed to share the results of a retrospective study analyzing the demographic, clinical, imaging, and hormonal characteristics of a large group of patients with SS, and also increase awareness of this syndrome especially in developed countries.Methods: The m...

ea0049ep996 | Pituitary - Clinical | ECE2017

Sheehan syndrome presenting 21 years later as severe heart failure

Ferreira Ana Goncalves , Alegria Sofia , Cordeiro Maria Carlos , Portugal Jorge

Introduction: Sheehan syndrome (SS) is caused by postpartum necrosis of the pituitary gland, associated with significant haemorrhage during or after delivery. It is rare in developed countries, but still frequent in underdeveloped ones. We present a rare presentation of this syndrome.Clinical case: A 48 years old black woman presented at the emergency department for long term fatigue and dyspnea that worsened a few days before. Her physical examination r...

ea0090ep750 | Pituitary and Neuroendocrinology | ECE2023

Sheehan syndrome revealed by acute adrenal insufficiency 3 months after the delivery

Laamouri Rihab , Smagala Agnes , Niculina Racolta

Introduction: Sheehan syndrome (SS) is a hemorrhagic necrosis of the pituitary gland responsible of anterior pituitary insufficiency. It occurs in a context of cerebral hypo flow due to a rapid blood pressure drop and/or acute hemorrhagia. We report a case of SS revealed by acute corticotropic insufficiency.Case report: A sunday morning 34 years-old woman consulted the emergency department for of a fatigue and diarrhea. She reported a 7 kg weight-loss in...

ea0041ep268 | Clinical case reports - Pituitary/Adrenal | ECE2016

Delayed diagnosis of isolated postpartum TSH deficiency: Sheehan’s syndrome or lymphocytic hypophysitis?

Iuliana Pascu , Minodora Betivoiu , Alexandra Nila , Sorina Martin , Simona Fica

Introduction: Sheehan’s syndrome (SS) is a rare complication of postpartum hemorrhage resulting in varying degrees of pituitary insufficiency. The diagnosis of SS has often been overlooked and thus delayed for many years due to its nonspecific signs and symptoms. Lymphocytic hypophysitis (LL) is also an uncommon autoimmune disorder that has to be suspected in women with recent delivery presenting with changes of one or more pituitary hormone secretions, especially when as...

ea0014p613 | (1) | ECE2007

Effect of hormone replacement therapy apart from growth hormone on the endothelial functions in patients with Sheehan’s syndrome

Bahceci Mithat , Pasa Semir , Akay Hatice O , Tuzcu Alpaslan , Arikan Senay , Gokalp Deniz

Aim: To examine the endothelial functions of patients with Sheehan syndrome (SS) and to eveluate the effects of hormone replacement treatment except growth hormone on endothelial functions.Subjects and methods: Twenty-four patients with Sheehan syndrome (PSS) aged 40.83±6.43 yr and 25 healthy control women aged 41.13±6.51 yr (C) were included. Endothelial functions were evaluated with high resolution ultrasonography (flow mediated dilatation:FM...