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Predicting dopamine agonist resistance in patients with macroprolactinoma is essential for clinicians to prevent treatment failure and subsequent complications such as medication-induced cerebrospinal fluid (CSF) rhinorrhea. We evaluated the features of patients with cabergoline resistance and CSF rhinorrhea in patients with prolactinomas with prolactin levels ≥1000 ng/mL. A total of 140 patients who were newly diagnosed with prolactinoma secreting only prolactin ≥1000 ng/mL and treated with cabergoline for the first time were included in this study. Based on the hormonal and radiologic response of the prolactinoma, the patients were divided into responders and non-responders. Non-responders (36/140, 25.8%) included a higher number of patients receiving hormone replacement than responders (responders, (%) = 12(11.5) vs. non-responders = 13(36.1), = 0.001). In propensity score matching analysis, patients who developed CSF rhinorrhea presented more frequent hormone deficiency than responders regardless of initial cabergoline dose. Hormone deficiency was associated with a greater odds ratio for the risk of non-responders (adjusted odds ratio = 5.13, 95% CI 1.96-13.46, = 0.001). Cabergoline was effective in bioactive macroprolactinoma. Furthermore, initial cabergoline dose was not significantly associated with long-term responsiveness and development of CSF rhinorrhea but the hypopituitarism was independently associated with an increased risk of cabergoline resistance and CSF rhinorrhea.
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http://dx.doi.org/10.3390/cancers13215374 | DOI Listing |
J Neurosurg Case Lessons
September 2025
Lewis Katz School of Medicine, Temple University, Philadelphia, Pennsylvania.
Background: Traumatic brain injury involving destruction of the mastoid bone leading to a large defect in the middle fossa floor or posterior fossa dura can necessitate delayed or multistep repairs or reconstruction of the middle fossa floor because of a CSF leak and rhinorrhea. Delayed repair may be associated with CNS infection. Reconstruction using a temporalis myofascial flap has been described in delayed reconstruction cases with CSF leak.
View Article and Find Full Text PDFMaedica (Bucur)
June 2025
Department of Internal Medicine, General Hospital "G. Hatzikosta" of Ioannina, Ioannina, Greece.
Cerebrospinal fluid (CSF) rhinorrhea is a relatively rare medical condition characterized by the drainage of CSF through the nasal cavity. Cerebrospinal fluid leakage can be attributed to a plethora of different causes, mostly traumatic or iatrogenic, but it can also be spontaneous. Due to its rare entity, CSF rhinorrhea is often a diagnostic trap and can be misdiagnosed and mistreated as rhinosinusitis or allergic rhinitis.
View Article and Find Full Text PDFZh Vopr Neirokhir Im N N Burdenko
August 2025
Burdenko Neurosurgical Center, Moscow, Russia.
Unlabelled: The combination of basal encephalocele with craniosynostosis is a rare clinical situation. Few observations of these two pathologies combination are described in the literature. Objective: to analyze own sample of patients to determine possible causes of encephalocele formation and surgical treatment strategy.
View Article and Find Full Text PDFEur Arch Otorhinolaryngol
August 2025
Department of Otorhinolaryngology Head and Neck Surgery, The first affiliated hospital, Jiangxi Medical College, Nanchang University, Nanchang, 330006, China.
Objectives: The goal of this study was to analyze the surgical efficacy and application value of using autologous materials (pedicled nasal mucosal flaps) as the main repair material for cerebrospinal fluid rhinorrhea under nasal endoscopy in our department in the past 5 years.
Methods: A retrospective analysis was conducted on patients who underwent cerebrospinal fluid rhinorrhea repair at our department between 1st February 2019 to 28th February 2024. Preoperative nasal endoscopy, computed tomography (CT) and/or magnetic resonance imaging (MRI) was performed to determine the location of the leak.
Ear Nose Throat J
August 2025
Department of Otolaryngology, University of Florida College of Medicine, Gainesville, FL, USA.
The main objective of this report was to describe a very unique clinical case of a post-traumatic temporal bone encephalocele with lateral ventricle herniation. This report involves a 60 year-old male who initially presented with right-sided hearing loss, otorrhea, and clear rhinorrhea with metallic taste and a history of a temporal bone fracture managed conservatively 6 years prior to presentation. Computed tomography (CT) revealed a large right tegmen defect and magnetic resonance imaging demonstrated herniation of a significantly-distended lateral ventricle into the mastoid cavity.
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