Results 71 to 80 of about 2,447 (143)

Pancreatic Tail Schwannoma in a 44-Year-Old Male: A Case Report and Literature Review

open access: yesCase Reports in Oncological Medicine, 2013
Pancreatic schwannomas are exceedingly uncommon neoplasms. According to a recent study in 2012, less than 50 cases of pancreatic schwannoma have been described in the English literature over the past thirty years.
Ahmed Abu-Zaid   +5 more
doaj   +1 more source

Management of giant adrenal schwannoma

open access: yesInternational Surgery Journal, 2019
Adrenal schwannoma is a rare differential of adrenal incidentaloma with scarce literature available at present. Adrenal schwannomas are usually non-secreting tumours but can very rarely secrete catecholamines. Specimen of our patient was 14 cm in diameter and weighed 900 gm which is the largest adrenal schwannoma in literature.
Ajit Oberoi   +4 more
openaire   +2 more sources

Clinical and Demographic Characteristics of 78 Patients with Adrenal Incidentaloma [Adrenal Insidentalomali 78 Hastanin Demografik ve Klinik Ozellikleri]

open access: yesMedicine Science, 2015
Adrenal incidentalomas (AIs) are adrenal lesions detected on abdominal imaging procedures or abdominal laparotomy that had been performed for unrelated reasons.
Faruk Kilinc   +5 more
doaj   +1 more source

Melanotic Schwannomas Are Rarely Seen Pigmented Tumors with Unpredictable Prognosis and Challenging Diagnosis

open access: yesCase Reports in Pathology, 2017
Melanotic Schwannoma (MS) is rarely seen and potentially malignant neoplasm that is categorized as a variant of Schwannoma. MS most frequently involves intracranial structures followed by posterior nerve roots in the spinal canal.
Elif Keskin   +3 more
doaj   +1 more source

Adrenal schwannoma: A case report of an unusual incidentaloma. [PDF]

open access: yesInt J Surg Case Rep, 2021
Timilsina S   +7 more
europepmc   +1 more source

Ganglioneuroma in a child with hereditary spherocytosis

open access: yesThe Turkish Journal of Pediatrics, 2012
Hereditary spherocytosis (HS) is the most frequent cause of congenital hemolytic anemia. Extramedullary hematopoiesis (EMH) mimicking a mass may develop in the lymph nodes, kidneys, pleura, mediastinum, adrenal gland, and in particular the spleen ...
Haci Ahmet Demir   +5 more
doaj  

UEG Week 2025 Moderated Posters

open access: yes
United European Gastroenterology Journal, Volume 13, Issue S8, Page S189-S802, October 2025.
wiley   +1 more source

ePoster

open access: yes
European Journal of Neurology, Volume 32, Issue S1, June 2025.
wiley   +1 more source

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