Publications by authors named "A Case McCormack"

Purpose: Rathke's cleft cysts (RCC) are present in up to 20% of autopsy studies but only a minority necessitate surgical treatment. Inflammation of RCC is thought to be significant in three processes: the development of classical symptoms, a predisposition to rupture or apoplexy, and increasing the rate of RCC recurrence. We aim to characterize clinical presentation, histological and radiological findings in patients with surgically managed RCC.

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Article Synopsis
  • Engineering 3D tissue-like structures is challenging in regenerative medicine, but new self-healing, viscoplastic fluids help with this by allowing easier printing of bioinks.
  • Researchers developed gellan gum granular gels that can be used as suspension media for 3D bioprinting, demonstrating effective printing at various temperatures and with low yield stresses.
  • The study shows that these gels support cell-laden droplet printing for over a week and can create hydrogel features, highlighting their advantages in biofabrication due to their ease of use, speed, and ability to crosslink.
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Non-Functioning Pituitary Adenomas (pituitary neuroendocrine tumours) (NFPA) have a profound detrimental effect of patient-reported health-related quality of life (QOL). Elucidating the underlying mechanisms by which NFPA influence patients' emotional physical and psychosocial wellbeing would provide the foundation for therapeutic strategies to optimise patient outcomes. A systematic review of the literature was performed in accordance with the PRISMA statement.

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Objectives: Early removal of chest tubes reduces pain and morbidity. This study aimed to remove chest tubes immediately after robotic pulmonary resection with complete thoracic lymphadenectomy by administering ice cream to rule out chylothorax.

Methods: This quality improvement study utilized prospectively gathered data from one thoracic surgeon.

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Investigation and management of hypotonic polyura is a common challenge in clinical endocrinology. The three main causes, recently renamed to arginine vasopressin deficiency (AVP-D, formerly central diabetes insipidus), AVP-resistance (AVP-R, formerly nephrogenic diabetes insipidus), and primary polydipsia (PP) require accurate diagnosis as management differs for each. This new nomenclature more accurately reflects pathophysiology, and has now been adopted by the Systemised Nomenclature of Medicine (SNOMED).

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