A rare case of lynch syndrome in a patient with metastatic malignant paraganglioma with SDHA mutation

2020 ◽  
Author(s):  
Blanco Jessica Ares ◽  
Pedro Pujante ◽  
Raul Rodriguez ◽  
Soraya Lanes ◽  
Elías Delgado ◽  
...  
Keyword(s):  
Lynch Syndrome ◽  
Rare Case ◽  
Malignant Paraganglioma

scholarly journals SAT-322 An Extremely Rare Case of Intrathyroidal Malignant Paraganglioma in an Elderly Woman

2019 ◽  
Vol 3 (Supplement_1) ◽  
Author(s):  
Thomas Fandel ◽  
Joselito Cabaccan ◽  
Jessica Gosnell ◽  
Nicole Tyer
Keyword(s):  
Rare Case ◽  
Elderly Woman ◽  
Malignant Paraganglioma

scholarly journals A rare case of malignant paraganglioma of urinary bladder

2015 ◽  
Vol 58 (2) ◽  
pp. 235 ◽  
Author(s):  
VinayaB Shah ◽  
AmitT Bhandare
Keyword(s):  
Urinary Bladder ◽  
Rare Case ◽  
Malignant Paraganglioma

scholarly journals Primary supratentorial intracerebral malignant paraganglioma

2015 ◽  
Vol 42 (S1) ◽  
pp. S47-S47
Author(s):  
AA Ahmed ◽  
B Lach ◽  
E Kachur ◽  
A Cenic
Keyword(s):  
Neural Crest ◽  
Surgical Resection ◽  
Rare Case ◽  
Neuroendocrine Tumours ◽  
Gangliocytic Paraganglioma ◽  
Intracranial Metastasis ◽  
Malignant Paraganglioma ◽  
Complete Surgical Resection ◽  
Benign Tumours ◽  
Work Up

Paragangliomas are extra-adrenal neuroendocrine tumours that derive from neural crest. They are benign tumours in general but few cases had shown their tendency to metastasize. Malignant forms have been reported previously with intracranial metastasis from duodenal origin but primary intracranial origin represent a rare and unusual location for such tumours. We report a rare case for a 48 year old lady who presented with symptomatic right sided insular mass with negative metastatic work up. A complete surgical resection had been done with an unexpected diagnosis of primary gangliocytic paraganglioma with malignant features.

Malignant Paraganglioma (Pheochromocytoma) of the Urinary Bladder: Report of a Case and Review of the Literature

PEDIATRICS ◽  
1979 ◽  
Vol 63 (6) ◽  
pp. 879-885
Author(s):  
James J. Meyer ◽  
Shashikant M. Sane ◽  
Robert M. Drake
Keyword(s):  
Lymph Node ◽  
Surgical Treatment ◽  
Urinary Bladder ◽  
Rare Case ◽  
Clinical Symptoms ◽  
Review Of The Literature ◽  
Malignant Paraganglioma ◽  
Better Than

A rare case of malignant paraganglioma of the urinary bladder with metastasis to a lymph node in a 12-year-old girl is reported, and eight other previously recorded cases are reviewed. Headache, fainting, and hypertention initiated by voiding were the most prominent clinical symptoms. Hematuria was Present in three cases and aided cystoscopy were most diagnostic. Cystography, pelvic angiogtaphy, and cystoscopy were most diagnostic. Segmental cystectomy, when feasible. was the preferred surgical treatment. The prognosis was slightly better than for other forms of extraadrenal pheochromocytomas.

Identification of Pulmonary Deposits from a Sandpaper Worker: A Study by Electron Microscopy and X-Ray Microanalysis

1982 ◽  
Vol 40 ◽  
pp. 52-53
Author(s):  
S. K. Peng ◽  
M.A. Egy ◽  
J. K. Singh ◽  
M.B. Bishop
Keyword(s):  
Electron Microscopy ◽  
Environmental Pollution ◽  
Rare Case ◽  
Interstitial Fibrosis ◽  
X Ray ◽  
Documented Case ◽  
Etiologic Agents ◽  
Pulmonary Interstitial Fibrosis ◽  
Gold Miners ◽  
Pulmonary Changes

Electron microscopy and energy dispersive x-ray microanalysis (EDXA) are found to be very useful tools for identification of etiologic agents in pneumoconiosis or interstitial pulmonary disorders. Pulmonary interstitial fibrosis and granulomatosis are frequently associated with occupational and environmental pollution. Numerous reports of pneumoconiosis in various occupations such as coal and gold miners are presented in the literature. However, there is no known documented case of pulmonary changes in workers in the sandpaper industry. This study reports a rare case of pulmonary granulomatosis containing deposits from abrasives of sandpaper diagnosed by using EDXA.

Predicting Lynch Syndrome Propensity to Cancer

2006 ◽  
Vol 39 (21) ◽  
pp. 52
Author(s):  
MARY ANN MOON
Keyword(s):  
Lynch Syndrome
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