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| http://dx.doi.org/10.4322/acr.2024.505 | DOI Listing |
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Characterisation of Kürsteiner canals of parathyroid: imparting relevance to a one-and-a-quarter-century-old concept.
Histopathology
February 2025
Department of Pathology, University of Pittsburgh Medical Center, Pittsburgh, PA, USA.
Article Synopsis
- Kürsteiner canals (KC) are embryological remnants linked to parathyroid and thymic development, with ongoing research aimed at understanding their role in various parathyroid lesions and cysts.
- A study evaluated 62 cystic and 22 non-cystic parathyroid lesions over a 12-year period, identifying distinct KC phenotypes in relation to the presence of parathyroid hormone (PTH).
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Oxf Med Case Reports
September 2024
Division of Anatomic Pathology and Histology, Catholic University of Sacred Heart, Largo Agostino Gemelli, 8, 00168, Rome, Italy.
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- - A 32-year-old man with MEN1 syndrome presented with multiple health issues, including hyperparathyroidism, but no prolactin or growth hormone-secreting tumors were found.
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Non-functioning parathyroid cyst presenting as a neck mass.
Autops Case Rep
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Post Graduate Institute of Medical Education and Research (PGIMER), Department of Histopathology, Chandigarh, India.
[Non-functioning parathyroid cysts].
Khirurgiia (Mosk)
February 2024
Sechenov First Moscow State Medical University (Sechenov University), Moscow, Russia.
Objective: To study the features of clinical course, diagnosis and treatment of true non-functioning parathyroid cysts.
Material And Methods: We retrospectively analyzed 18 patients with non-functioning true parathyroid cysts. Inclusion criteria: US-confirmed anechoic lesion of the neck without tissue component, cytological data on cystic lesion, high cystic parathyroid hormone and no laboratory signs of hyperparathyroidism.
Two cases of pancreatic neuroendocrine tumors with ectopic ACTH syndrome during their disease course.
Clin J Gastroenterol
April 2024
Department of Medicine and Bioregulatory Science, Graduate School of Medical Sciences, Kyushu University, 3-1-1 Maidashi, Higashi-Ku, Fukuoka, 812-8582, Japan.
Pancreatic neuroendocrine tumors (PanNETs) are rare malignant tumors that occur in the pancreas. They are divided into functioning and non-functioning tumors based on the presence or absence of their specific hormonal hyper-expression symptoms. Adrenocorticotropic hormone (ACTH)-producing PanNETs are rare, functional tumors, and their clinical characteristics and outcomes have not been well reported.
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