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Sarcoidosis is an immune-mediated multisystem condition of unknown etiology, characterized by non-caseating granulomatous inflammation. While it commonly affects the lungs and the reticuloendothelial system, it can affect any organ. Most of such cases involve the central nervous system, but the condition rarely presents with symptoms related to hypothalamic-pituitary dysfunction.
View Article and Find Full Text PDF[Pituicitoma in a patient with neurofibromatosis type 1].
Medicina (B Aires)
December 2024
División de Endocrinología y Metabolismo, Hospital General de Agudos José María Ramos Mejía, Buenos Aires, Argentina. E-mail:
Pituicytoma is a rare low degree tumor that arises from pituicytes in the infundibulum and posterior pituitary gland. As they do not have characteristic radiological features, they can be misdiagnosed as pituitary adenoma, meningioma, or craniopharyngioma. Clinically, patients can present with hormonal disturbances, headaches and visual field defects.
View Article and Find Full Text PDFEndoscopic endonasal resection of a craniopharyngioma in a 23-month-old patient: illustrative case.
J Neurosurg Case Lessons
December 2024
Departments of Neurological Surgery, University of Washington, Seattle, Washington.
Background: Treatment of pediatric craniopharyngioma requires a multidisciplinary approach to counsel patients and families on the spectrum of treatment options, including biopsy, radiation, and/or resection. Gross-total resection can avoid radiation and its long-term comorbidities. In very young patients, this is of particular importance but is especially challenging because of anatomical considerations.
View Article and Find Full Text PDFCushing Disease in a Patient with Double Pituitary Adenomas Complicated with Diabetes Insipidus: A Case Report.
J ASEAN Fed Endocr Soc
December 2024
Faculty of Medicine, Universiti Kebangsaan Malaysia.
Managing a patient with both pituitary hypersecretory and hyposecretory manifestations may be perplexing. We report a 14-year-old female who presented with weight gain, polyuria and polydipsia. Biochemical results were consistent with Cushing disease with central diabetes insipidus.
View Article and Find Full Text PDFPanhypopituitarism and diabetes insipidus secondary to hypothalamic glioblastoma multiforme.
Med Clin (Barc)
November 2024
Servicio de Medicina Interna, Hospital Universitario Marqués de Valdecilla, Santander, España.
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