Results 81 to 90 of about 50,666 (222)

Who can safely discontinue lifelong follow‐up among patients with sporadic pheochromocytoma and paraganglioma?

Journal of Internal Medicine, EarlyView.
Background Current guidelines recommend at least 10 years of follow‐up for all pheochromocytoma and paraganglioma (PPGL) patients and lifelong monitoring for high‐risk individuals. Nonetheless, data identifying patients who may not require routine lifelong follow‐up are scarce.
Min Jeong Park, Seung Shin Park, Won Woong Kim, Su‐Jin Kim, Yu‐Mi Lee, Kyu Eun Lee, Tae‐Yon Sung, Jae‐Kyung Won, Dong Eun Song, Jung‐Min Koh, Sara Talvacchio, Tamara Prodanov, Hussam Alkaissi, Karel Pacak, Seung Hun Lee, Jung Hee Kim   +15 more
wiley   +1 more source

SDHB-Associated Paraganglioma in a Pediatric Patient and Literature Review on Hereditary Pheochromocytoma-Paraganglioma Syndromes

Case Reports in Endocrinology, 2014
Pheochromocytoma and paraganglioma are rare in the pediatric population occurring in approximately 1 in 50,000 children. While some cases are sporadic, they have commonly been associated with syndromes such as von Hippel-Lindau, multiple endocrine ...
Heather Choat, Kerri Derrevere, Lisa Knight, Whitney Brown, Elizabeth H. Mack   +4 more
doaj   +1 more source

Robot assisted laparoscopic excision of a paraganglioma: new therapeutic approach

International Brazilian Journal of Urology, 2014
The Paraganglioma is the most common extra-adrenal pheochromocytoma arising from neural crest (1) (It will better to write: The paraganglioma is an extra-adrenal pheocromocytoma arising from the neural crest. 10% of pheocromocytomas are extra-adrenal and
G. Cochetti, E. Cottini, F. Barillaro, E. Lepri, A. Boni, S. Pohja, E. Mearini   +6 more
doaj   +1 more source

Genetic testing and surveillance guidelines in hereditary pheochromocytoma and paraganglioma

Journal of Internal Medicine, 2018
Pheochromocytoma and paraganglioma (PPGL) are rare tumours and at least 30% are part of hereditary syndromes. Approximately 20% of hereditary PPGL are caused by pathogenic germ line variants in genes of the succinate dehydrogenase complex (SDHx), TMEM127
A. Muth, J. Crona, O. Gimm, A. Elmgren, K. Filipsson, M. S. Askmalm, J. Sandstedt, M. Tengvar, E. Tham, E. Tham   +9 more
semanticscholar   +1 more source

[Retroperitoneal paraganglioma].

Boletin. Sociedad de Cirugia del Uruguay, 1998
Presented at session 13th July ...
Rodríguez Juanotena, Jorge, Pavlotzky, Marcos, Giuria, Frederik   +2 more
openaire   +2 more sources

Quality of Life After Surgical Treatment of Head and Neck Paragangliomas

Head &Neck, Volume 48, Issue 4, Page 941-949, April 2026.
ABSTRACT Background Head and neck paragangliomas (HNPGLs) are rare neuroendocrine tumors and often arise in the head and neck. Due to their localization, the tumor and its surgical treatment pose a risk for cranial nerve impairments. Few studies have focused on the health‐related quality of life (HRQOL) in patients with HNPGLs and their relation to ...
Christina Sauter, Philipp Erhart, Dittmar Böckler, Patrick Schuler, Peter K. Plinkert, Ralph Hohenberger   +5 more
wiley   +1 more source

Review of Pediatric Pheochromocytoma and Paraganglioma

Frontiers in Pediatrics, 2017
Pheochromocytoma (PCC) and paraganglioma (PGL) are rare chromaffin cell tumors which secrete catecholamines and form part of the family of neuroendocrine tumors.
R. Bholah, T. Bunchman
semanticscholar   +1 more source

Dysphagia Characteristics in High Versus Low Vagal Unilateral Vocal Fold Paralysis

The Laryngoscope, Volume 136, Issue 4, Page 1800-1807, April 2026.
High vagal etiology of unilateral vocal fold paralysis (UVFP) is linked to greater swallowing dysfunction compared to low vagal etiology of UVFP, with higher rates of premature spillage, pharyngeal residue, penetration and aspiration on instrumental swallow assessment; and higher prevalence of diet and behavioral modifications recommended.
Madeline Miles Marker, Liam W. Gallagher, Aanish Puri, Jesse Hoffmeister, Scott Lunos, Heather Erickson, Gina Cruciani, Joslyn Kahn, Stephanie Misono, Raluca Gray   +9 more
wiley   +1 more source

Malignant Potential of Temporal Bone Paragangliomas With Reference to GAPP System

Laryngoscope Investigative Otolaryngology, Volume 11, Issue 2, April 2026.
ABSTRACT Objectives To evaluate the temporal bone paragangliomas (so‐called glomus tumors, TB‐PGLs) via the Grading System for Adrenal Pheochromocytoma and Paraganglioma (GAPP) and succinate dehydrogenase subunit B (SDHB) immunohistochemistry, and to discuss their implications for postoperative follow‐up and treatment strategies. Methods This report is
Noritaka Komune, Midori Taniguchi, Yutaro Kida, Ryosuke Kuga, Daisuke Kuga, Koichi Arimura, Yoshinori Fujiwara, Hidetaka Yamamoto, Yoshinao Oda, Koji Yoshimoto, Takashi Nakagawa   +10 more
wiley   +1 more source

Effectiveness of 18F-FDG PET/CT in finding lung metastasis from a retroperitoneal paraganglioma [PDF]

Asia Oceania Journal of Nuclear Medicine and Biology
A 50-year-old woman was diagnosed with iron deficiency anemia on general medical examination. Further, contrast-enhanced abdominal CT and magnetic resonance imaging revealed a large hypervascular mass with internal degeneration and necrosis in the ...
Tomonori Chikasue, Seiji Kurata, Shuji Nagata, Shuichi Tanoue, Akiko Sumi, Mizuki Gobaru, Toru Hisaka, Toshihiro Hashiguchi, Takuya Furuta, Jun Akiba, Kiminori Fujimoto, Toshi Abe   +11 more
doaj   +1 more source