Results 91 to 100 of about 1,506,220 (180)

Clinical suspicion and parathyroid carcinoma management

São Paulo Medical Journal
CONTEXT AND OBJECTIVE: Adequate management of parathyroid carcinoma apparently relates to the surgeon’s ability to identify it at the first operation.
Fabio Luiz de Menezes Montenegro, Marcos Roberto Tavares, Marcelo Doria Durazzo, Claudio Roberto Cernea, Anói Castro Cordeiro, Alberto Rosseti Ferraz   +5 more
doaj   +1 more source

Parathyroid carcinoma: The importance of high clinical suspicion for a correct management [PDF]

, 2012
Background. Parathyroid carcinoma is an infrequent clinical entity whose diagnosis is very challenge. Indeed a pre-operative or intraoperative diagnosis of parathyroid carcinoma is reported in less than half cases described in the literature.
Gabriele Ricci, Angelo Serao, Livio Paganelli, ASSENZA, Marco, Marco Barreca, Pierluigi Marini, Gianluca Liotta, Giovanni Tufodandria   +7 more
core   +1 more source

Expression of parathyroid hormone-related protein in gastrointestinal malignancies. [PDF]

, 2006
Parathyroid hormone-related protein (PTHrP) is a peptide hormone which, when abundantly produced by certain tumours, and released into the systemic circulation, stimulates via an endocrine-like pathway, bone resorption and renal calcium reabsorption, by ...
McStay, M.K.G.
core  

First Case of Mature Teratoma and Yolk Sac Testis Tumor Associated to Inherited MEN-1 Syndrome

Frontiers in Endocrinology, 2019
Introduction: Multiple endocrine neoplasia type 1 (MEN1) is an autosomal dominantly inherited endocrine tumor syndrome characterized by the development of cancer in various endocrine organs, particularly in the pituitary, parathyroid and pancreas ...
Sabrina Chiloiro, Ettore Domenico Capoluongo, Giovanni Schinzari, Paola Concolino, Ernesto Rossi, Maurizio Martini, Alessandra Cocomazzi, Giuseppe Grande, Domenico Milardi, Brigida Anna Maiorano, Antonella Giampietro, Guido Rindi, Alfredo Pontecorvi, Laura De Marinis, Antonio Bianchi   +14 more
doaj   +1 more source

Atypical ovarian carcinoid tumor with widespread skeletal metastases: a case report of multiple endocrine neoplasia type 1 in a young woman

BMC Cancer, 2019
Background Multiple endocrine neoplasia type 1 (MEN1) is a rare autosomal dominant inherited condition affecting multiple endocrine organs, resulting in significant morbidity and decreased life expectancy.
Lei Lou, Lixia Zhou, Wenyan Wang, Huina Li, Yuehong Li   +4 more
doaj   +1 more source

Case Report: Management of multiple brown tumors after kidney transplantation

Frontiers in Endocrinology
Brown tumor is usually caused by primary or secondary hyperparathyroidism but is exceptionally rare after kidney transplantation. Their rarity and atypical pathological features make diagnosis and treatment particularly challenging.
Qingyi Sun, Yafei Bai, Ruman Chen, Hong Li   +3 more
doaj   +1 more source

Inherited Deletion of 1q, Hyperparathyroidism and Signs of Y-chromosomal Influence in a Patient with Turner Syndrome

JCRPE, 2019
We report a detailed phenotypic, cytogenetic and molecular characterization of a patient prenatally diagnosed with Turner syndrome (TS). In addition to having typical TS clinical characteristics including webbed neck, high arched palate and coarctation ...
Alejandro F. Siller, Alex Shimony, Marwan Shinawi, Ina Amarillo, Louis P. Dehner, Katherine Semenkovich, Ana María Arbeláez   +6 more
doaj   +1 more source

Evaluation of the metabolism properties of choline kinase alpha in neoplasms of the parathyroid glands. A pilot study

Ожирение и метаболизм, 2019
BACKGROUND: Primary hyperparathyroidism (PHPT) is a widespread endocrine disease characterized by excessive production of parathyroid hormone (PTH) due to parathyroid gland hyperplasia (PGH) or tumor lesions (adenoma or cancer of the parathyroid gland ...
Natalia G. Mokrysheva, Iya A. Voronkova, Julia A. Krupinova, Mikhail B. Dolgushin, Larisa E. Gurevch, Akgul A. Odzharova, Sergey N. Kuznetsov, Irina V. Kryukova   +7 more
doaj   +1 more source

Parathyroid Cancer

, 2012
Parathyroid carcinoma is a rare endocrine malignancy derived from the parenchymal cells of the parathyroid glands. It is usually associated with more severe and profound clinical and laboratory manifestations than its more common benign counterparts. Its
IACOBONE, MAURIZIO, HENRY JF
core   +1 more source

A family case report of parathyroid carcinoma associated with CDC73 mutation in hyperparathyroidism-jaw tumor syndrome

Frontiers in Endocrinology
BackgroundHereditary primary hyperparathyroidism (PHPT) accounts for 5-10% of all PHPT cases, necessitating genetic testing for diagnosis and management.
Yian Gu, Yuanyuan Ye, Hua Shu, Lina Chang, Yinghui Xie, Fengao Li, Tiehong Zhu, Ming Liu, Qing He   +8 more
doaj   +1 more source