Results 151 to 160 of about 35,965 (199)
Some of the next articles are maybe not open access.

Gangliocytic paraganglioma

The American Journal of Surgical Pathology, 1977
Six cases of upper intestinal gangliocytic paraganglioma, five in the duodenum and one in the jejunum, are reported. Three histologic patterns, each comparable to patterns in paraganglioma, ganglioneuroma, or carcinoid-islet cell tumor, are mixed in varying proportions.
R J, Reed, P J, Caroca, J C, Harkin
openaire   +2 more sources

Paraganglioma in sella

Journal of Neuro-Oncology, 2005
We report a very rare case of a paraganglioma arising from sellar and suprasellar region which has been treated with radiotherapy following multiple surgeries.
Faruk, Zorlu   +4 more
openaire   +2 more sources

Paraganglioma in the orbit

Journal of Cancer Research and Clinical Oncology, 1980
A 56-year-old Japanese woman was treated surgically for orbital paraganglioma. She had had proptosis of the left eye and lowered visual acuity. Papilledema and many retinochoroidal folds were seen. CT-scan demonstrated a tumor shadow on the optic nerve in the muscle cone.
T, Amemiya, M, Kadoya
openaire   +2 more sources

Orbital Paraganglioma

Journal of Craniofacial Surgery, 2019
Background: Paragangliomas are groups of neuroendocrine neoplasms originating from neural crest cells throughout the body, but are rarely observed within the orbit. Case report: Two patients, a 4-year-old male and 27-year-old female, presented with a slow-growing proptosis.
Binbin, Zhu, Jianhua, Yan
openaire   +2 more sources

Thyroid Paraganglioma

Annals of Otology, Rhinology and Laryngology, 1992
Paraganglioma of the thyroid gland is a rare neoplasm. Only eight cases have previously been reported. The neoplasm was confined to the thyroid in all but two patients; laryngeal involvement was seen in one and tracheal involvement in another. A review of these previously reported cases is presented along with the details of an additional case with ...
R E, Brownlee, W W, Shockley
exaly   +3 more sources

Metastatic paraganglioma

BMJ Case Reports, 2023
A man in his 70s, with a history of a glomus jugulare paraganglioma diagnosed 18 years ago, presented with an unprovoked deep vein thrombosis (DVT). The paraganglioma had been treated by radiotherapy, and yearly scans had not shown any progression since treatment.
Daniela Harmsworth   +3 more
openaire   +2 more sources

Familial paraganglioma

European Archives of Oto-Rhino-Laryngology, 2005
Paragangliomas are unusual tumors that are sometimes familial. We treated a family who exhibited multiple head and neck paragangliomas (HNPGs) and pheochromocytomas. The purpose was to determine the clinical characteristics of paragangliomas with familial history and to define a better standardized proceeding in the management of these tumors. Patients
A Cemal Umit, Işik   +5 more
openaire   +2 more sources

Paragangliomas of the Neck

Archives of Surgery, 1992
Between 1967 and 1990 inclusive, 28 patients with paragangliomas of the neck were diagnosed at the University of Alabama at Birmingham Affiliated Hospitals. There were 11 men and 17 women, whose ages ranged from 12 to 76 years (mean, 47 years). Tumor locations included the carotid bodies (19 cases), the vagus nerves (three), supraglottic larynx (two ...
G B, Bishop   +4 more
openaire   +2 more sources

Paraganglioma of the tongue

Journal of Oral and Maxillofacial Surgery, 1990
The paraganglia are derived from neural crest cells and arise in association with autonomic ganglia throughout the body. Glenner and Grimley’ divided the extraadrenal paraganglion system on an anatomic and histologic basis into several groups: 1) branchiomeric paraganglia, closely related to arteries and cranial nerves in the head and neck and superior
J, Lustmann, M, Ulmansky
openaire   +2 more sources

Home - About - Disclaimer - Privacy