Results 1 to 10 of about 12,834 (118)

Stiff-person syndrome mimic secondary to hypopituitarism: a case report and literature review [PDF]

open access: yesFrontiers in Endocrinology
IntroductionFlexion contracture has been reported to be associated with hypopituitarism and hypoadrenalism. We reported a case of a patient who presented with stiff-person syndrome (SPS) mimic secondary to prolactinoma-associated hypopituitarism.MethodsA
Menghan Zheng   +8 more
doaj   +2 more sources

Hyperprolactinemia and Hypopituitarism in Acromegaly and Effect of Pituitary Surgery: Long-Term Follow-up on 529 Patients

open access: yesFrontiers in Endocrinology, 2022
PurposeStudies on hyperprolactinemia and hypopituitarism in acromegaly are limited. We aimed to analyze the preoperative status, postoperative alterations, and correlated factors of hyperprolactinemia and hypopituitarism in acromegaly patients ...
Xiaopeng Guo   +57 more
doaj   +1 more source

Decreased mannan-binding lectin level in adults with hypopituitarism; dependence on appropriate hormone replacement therapies

open access: yesFrontiers in Immunology, 2023
BackgroundMannan-binding lectin (MBL) is a main component of the lectin pathway of the complement system. Although there are some studies showing links between endocrine and immune systems, the ones concerning hypopituitarism are limited. The aim of this
Aleksandra E. Matusiak   +5 more
doaj   +1 more source

Hypereosinophilia is a predictive biomarker of immune checkpoint inhibitor-induced hypopituitarism in patients with renal cell carcinoma

open access: yesBMC Endocrine Disorders, 2022
Background This study aimed to evaluate whether hypereosinophilia is a clinical biomarker of immune checkpoint inhibitor-induced hypopituitarism in patients with renal cell carcinoma treated with nivolumab plus ipilimumab.
Hodaka Yamada   +11 more
doaj   +1 more source

Lipid profile and response to statin therapy in patients with hypopituitarism

open access: yesArchives of Endocrinology and Metabolism, 2020
Objective: Dyslipidemia is prevalent among patients with hypopituitarism, especially in those with growth hormone (GH) deficiency. This study aimed to evaluate the response to statin therapy among adult patients with dyslipidemia and hypopituitarism ...
Graziela Rissetti   +5 more
doaj   +1 more source

Cholestasis and hypercalcemia secondary to panhypopituitarism in a newborn

open access: yesThe Turkish Journal of Pediatrics, 2017
Cholestatic hepatitis and hypercalcemia are rare features of hypopituitarism in newborns. So diagnosis of hypopituitarism is frequently delayed.
Fatma Dursun   +2 more
doaj   +1 more source

Management of hypopituitarism: a perspective from the Brazilian Society of Endocrinology and Metabolism

open access: yesArchives of Endocrinology and Metabolism, 2021
Hypopituitarism is a disorder characterized by insufficient secretion of one or more pituitary hormones. New etiologies of hypopituitarism have been recently described, including head trauma, cerebral hemorrhage, and drug-induced hypophysitis.
Heraldo Mendes Garmes   +16 more
doaj   +1 more source

Advances in understanding hypopituitarism [version 1; referees: 2 approved]

open access: yesF1000Research, 2017
The understanding of hypopituitarism has increased over the last three years. This review provides an overview of the most important recent findings. Most of the recent research in hypopituitarism has focused on genetics.
Mareike R. Stieg   +3 more
doaj   +1 more source

Acute Secondary Adrenal Insufficiency Misdiagnosed as Acute Cholecystitis

open access: yesCase Reports in Endocrinology, 2021
Hypopituitarism refers to insufficient secretion of the pituitary hormones. Patients with acute adrenocorticotropic hormone (ACTH) deficiency may be presented with fatigue, dizziness, orthostatic hypotension, hypoglycemia, nausea, vomiting, or ...
Moslem Sedaghattalab   +1 more
doaj   +1 more source

Genetic diagnosis of congenital hypopituitarism by a target gene panel: novel pathogenic variants in GLI2, OTX2 and GHRHR

open access: yesEndocrine Connections, 2019
Aim: Congenital hypopituitarism has an incidence of 1:3500–10,000 births and is defined by the impaired production of pituitary hormones. Early diagnosis has an impact on management and genetic counselling.
Marilena Nakaguma   +12 more
doaj   +1 more source

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