Aim: We have evaluated the anatomic measurements on sellar area of patients who were radiologically diagnosed with empty sella to determine the relation between the amount of pressure on the adenohypophysis and hormonal imbalances.
Materials And Methods: Sixty-one cases were diagnosed with empty sella and had hormone tests and hypophysis magnetic resonance (MR). The cases were categorized into two groups - patients with hypophyseal hormone anomaly and patients without hormone anomaly. We have measured interclinoid distance, anteroposterior distance from the anterior diaphragm sella to the pituitary stalk, depth of the sella turcica, craniocaudal distance of the optic chiasm from the diaphragm sella, the heights of the right and left adenohypophysis, subcutaneous fat thickness measured orthogonal to the coronal suture and posteriorly at the level of C2-C3 for two groups on hypophysis and cranial MR imaging MRI.
Results: Twenty-five hormone-positive cases (40.9%) (hormone test were abnormal) and 36 hormone-negative cases (59.1%) (hormone tests were normal) were included in the study. The most common hormone abnormality was thyroid-stimulating hormone, T3 and T4 deficiency in 12 cases (48%) and increase in prolactin level in 7 cases (28%). Right adenohypophysis height was 1.54 ± 0.840 mm for the 1 group, and 1.96 ± 0.83 mm for the 2 group. The left adenohypophysis height was 1.66 ± 0.80 mm for the 1 group, and 1.94 ± 0.94 mm for the 2 group. It was found out that the thickness at right and left side in the hormone-positive group diminished significantly.
Conclusion: Adenohypophysis height and distance between stalk and optic nerve were good determiner for hormone defect.
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http://dx.doi.org/10.4103/ajns.AJNS_50_18 | DOI Listing |
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 PDFMult Scler Relat Disord
December 2024
Department of Pediatric Neurology, Children´s Hospital Datteln, University Witten/Herdecke, Datteln, Germany. Electronic address:
Background: Fulminant idiopathic intracranial hypertension (IIH) is characterized by headache, rapid decrease of vision and elevated CSF-opening pressure.
Objective: To delineate a subgroup of MOGAD mimicking fulminant IIH.
Methods: In this case series children with MOGAD with vision loss, optic disc swelling and elevated CSF opening pressure, initially diagnosed with fulminant IIH, were included.
J Neuroophthalmol
November 2024
Ruiz Department of Ophthalmology and Visual Science (ALC, AZC, O-oA), McGovern Medical School at UTHealth Houston, Houston, Texas; Robert Cizik Eye Clinic (ALC, AZC, O-oA), Houston, Texas; and Texas Children's Hospital (JLM, RPP), Baylor College of Medicine, Houston, Texas.
Background: Pseudotumor cerebri (PTC) syndrome is a disorder of increased intracranial pressure, most commonly affecting overweight women of childbearing age. Malignant PTC (MPTC) is a rare presentation that involves rapidly worsening vision, often necessitating surgical intervention to prevent permanent vision loss. The goal of this study was to determine whether radiographic findings of PTC are predictive of MPTC and the final visual outcome.
View Article and Find Full Text PDFJ Neurol Sci
November 2024
Thrombosis and Hemostasis Institute, Sheba Medical Center, Tel-Hashomer, Ramat Gan, Israel. Affiliated with Tel Aviv University, Faculty of Medical and Health Sciences, Tel Aviv, Israel. Electronic address:
Arch Endocrinol Metab
October 2024
University of Novi Sad Faculty of Medicine Novi Sad Serbia University of Novi Sad, Faculty of Medicine, Novi Sad, Serbia.
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