Results 51 to 60 of about 396,713 (282)
Clinical Case Reports, 2023 Key Clinical Message Parathyroid lipoadenoma is a rare type of parathyroid adenoma, described as a single parathyroid adenoma with more than 50% fat on histologic examination and an unknown etiology, which is one of the rare causes of primary ...
Yihan Wang, Yan Chen, Yantao Fu
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Secondary hyperparathyroidism due to multiple parathyroid carcinomas in a patient with chronic hemodialysis: a case report [PDF]
Kosin Medical Journal, 2022 Parathyroid carcinoma (PC) in cases of secondary or tertiary hyperparathyroidism is relatively uncommon, and only a few case reports have described this entity.
Soree Ryang +5 more
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Autopsy and Case Reports, 2021 Background: Hemangiomas are benign neoplasms of capillary proliferation that arise from a developmental anomaly where angioblastic mesenchyme fails to form canals.
Odille Mejia +4 more
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Intraoperative neuromonitoring versus visual nerve identification for prevention of recurrent laryngeal nerve injury in adults undergoing thyroid surgery [PDF]
, 2016 This is a protocol for a Cochrane Review (Intervention). The objectives are as follows: To assess the effects of intraoperative neuromonitoring (IONM) versus visual nerve identification for prevention of recurrent laryngeal nerve injury in adults ...
Abraha, Iosief +7 more
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Journal of the Belgian Society of Radiology, 2013 Background: A 32-year-old woman with palpable neck mass and clinical presentation of hypercalcemic crisis and primary hyperparathyroidism was referred to radiology and nuclear medicine departments for imaging studies.
A Dilli, SS Gultekin, UY Ayaz
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Ectopic parathyroid adenoma in the upper anterior mediastinum
Journal of the Belgian Society of Radiology, 2011 Background: A 66-year-old man, known with nephrocalcinosis in his medical history, was complaining of weight loss, pain at the level of the kidneys and at the right hip. Clinical examination revealed no additional abnormalities.
W Verwimp, P Bracke, H Degryse
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The association between tumor-infiltrating lymphocytes (TILs) and metastatic course in neuroendocrine neoplasms. [PDF]
, 2016 A moderate lymphocytic infiltration was found in about 25% of these well-differentiated neoplasms, all of which had no distant metastases to liver or pulmonary hilar lymph nodes during a follow-up period >10 years; mild or absent lymphocytic ...
FARINETTI, Alberto +3 more
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A late diagnosis of MEN 1 Syndrome in a young patient initially pre-senting with nephrolithiasis
Liječnički vjesnik, 2023 Multiple Endocrine Neoplasms Type 1 (MEN 1), originally called Wermer Syndrome, is a rare hereditary condition caused by mutations in the MEN1 tumor suppressor gene.
Ana Čala, Tina Dušek
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Chromogranin A: From Laboratory to Clinical Aspects of Patients with Neuroendocrine Tumors [PDF]
, 2018 Background. Neuroendocrine tumors (NETs) are characterized by having behavior and prognosis that depend upon tumor histology, primary site, staging, and proliferative index.
Baldelli, Roberto +8 more
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Frontiers in Endocrinology, 2018 Thyroid tumors usually present as masses in the thyroid gland. While the majority of these tumors represent neoplasms of thyroid tissues, mainly of follicular epithelial cell differentiation, the differential diagnosis includes other lesions, such as C ...
Sylvia L. Asa +3 more
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