The preoperative hypocycloidal sellar tomograms, angiograms, and pneumoencephalograms of 100 patients being evaluated for prolactin-secreting pituitary adenomas were reviewed and the results correlated with surgical findings at transsphenoidal exploration. The majority (53%) of tumors encountered were microadenomas. Although sellar volume was normal in 72%, sellar shape on tomography was abnormal in 96%; the location of the tumor within the sella could be predicted by means of tomography alone in 88%. Low volume pneumoencephalography was a reliable method for determining suprasellar extension in 19% of cases and in demonstrating arachnoidal diverticulae in 24%, a finding of great importance to the surgeon planning a transsphenoidal exploration. The use of internal carotid angiography to predict lateral tumor extension proved unreliable. Tumor blush was demonstrated only in larger lesions. No vascular anomalies that would contraindicate transsphenoidal exploration were encountered in this group of patients with hyperprolactinemia.
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http://dx.doi.org/10.2214/ajr.134.4.707 | DOI Listing |
Endocrinol Diabetes Metab Case Rep
October 2024
Summary: Paediatric pituitary adenomas are rare in children and adolescents and differ from adults in both clinical presentation and management. We present the case of a 14-year-old female with primary amenorrhoea secondary to a macroprolactinoma, showing a modest radiological and biochemical response to dopamine agonist (DA) therapy. Despite a 10-month duration of increasing DA therapy, initial symptoms of primary amenorrhoea and hyperprolactinaemia persisted, with new symptoms of weight gain, lethargy and low mood.
View Article and Find Full Text PDFEndocrine
December 2024
Department of Neurosurgery, Dongfang Affiliated Hospital of Xiamen University, School of Medicine, Xiamen University, Xiamen, China.
Purpose: The growth hormone (GH) level on postoperative day one (POD1), i.e., POD1GH, holds significant value in assessing surgical efficacy and predicting long-term remission in patients with acromegaly.
View Article and Find Full Text PDFWorld Neurosurg
December 2024
Department of Neurosurgery, Third Affiliated Hospital of Sun Yat-sen University, Sun Yat-sen University, Guangzhou, China. Electronic address:
Background: Chiasmatic cavernous hemangioma (CCH) is a rare disease. Most cases are treated with surgical resection through approaches such as pterional and orbitozygomatic craniotomy. However, with advancements in surgical technique and heightened patient demand for improved postoperative quality of life, there have been reports in recent years exploring more minimally invasive surgical approaches, such as the subfrontal trans-eyebrow keyhole and endoscopic endonasal transsphenoidal approach.
View Article and Find Full Text PDFNeurosurg Rev
November 2024
Department of Neurosurgery, Hospital Universitario 12 de Octubre; Departamento de Cirugía, Facultad de Medicina, Universidad Complutense de Madrid, Instituto de Investigaciones Sanitarias 12 de Octubre, imas12, Madrid, 28041, Spain.
Cureus
October 2024
Endocrinology, Diabetes, and Metabolism, Centro Hospitalar Universitário de Santo António, Unidade Local de Saúde de Santo António, Porto, PRT.
Cushing disease (CD), a rare endocrine disorder characterized by a pituitary adenoma that secretes excess adrenocorticotropic hormone (ACTH), leads to overproduction of cortisol by the adrenal glands and, depending on severity and duration, manifests with a broad spectrum of clinical signs and symptoms, ranging from classical features to more common conditions seen in the general population. Discovery of molecular and pathogenic mechanisms related to the development of CD tumors has increased in recent years, almost two-thirds of the somatic variants cases have been linked to the USP8 gene, while very rare germline variants in MEN1 and AIP genes have been associated with pituitary adenomas. Variants affecting the RET proto-oncogene, which encodes a receptor tyrosine kinase involved in cell growth and differentiation, are implicated in the development of medullary thyroid carcinoma (MTC) and its hereditary form, multiple endocrine neoplasia type 2 (MEN2).
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