Total: 11 |
|
PMID (PMCID) | ||
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30829863 |
FEMALE | Middle Aged |
68Ga-DOTANOC PET/CT in an Atypical Extraskeletal Paravertebral Hemangioma Mimicking as Neurogenic Tumor in a Known Case of Breast Cancer. | ||
Vadi SK, Mittal BR, Parihar AS, Kumar R, Singh H, Singh G. Clin Nucl Med. 2019;44(5):e364-e366. |
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Ga-DOTANOC PET/CT is well documented in evaluation of well-differentiated neuroendocrine tumors and in other lesions with somatostatin receptor expression such as pheochromocytoma, paraganglioma, neuroblastoma, meningioma, and mesenchymal tumors causing oncogenic osteomalacia. | ||
28409892 |
FEMALE | |
Failure of MIBG scan to detect metastases in SDHB-mutated pediatric metastatic pheochromocytoma. | ||
Sait S, Pandit-Taskar N, Modak S. Pediatr Blood Cancer. 2017;64(11):. |
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123 I-meta-iodo benzyl guanidine (MIBG) scans are considered the gold standard imaging in neuroblastoma; however, flouro deoxy glucose positron emission tomography (FDG-PET) scans have increased sensitivity in adults with pheochromocytoma/paraganglioma. | ||
30263028 |
OTHER | |
Composite Paraganglioma and Neuroblastoma of the Urinary Bladder: A Rare Histopathological Entity. | ||
Lacefield E, Raheem OA, Cox R, Davis R, Kamel MH. Curr Urol. 2015;8(4):208-211. |
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This report presents the case of a composite paraganglioma and neuroblastoma in a 45 year-old male who presented with dysuria and flank pain. | ||
30263028 |
OTHER | |
Composite Paraganglioma and Neuroblastoma of the Urinary Bladder: A Rare Histopathological Entity. | ||
Lacefield E, Raheem OA, Cox R, Davis R, Kamel MH. Curr Urol. 2015;8(4):208-211. |
||
Composite Paraganglioma and Neuroblastoma of the Urinary Bladder: A Rare Histopathological Entity. | ||
30263028 |
OTHER | |
Composite Paraganglioma and Neuroblastoma of the Urinary Bladder: A Rare Histopathological Entity. | ||
Lacefield E, Raheem OA, Cox R, Davis R, Kamel MH. Curr Urol. 2015;8(4):208-211. |
||
Following partial cystectomy and bilateral pelvic lymph node dissection, pathology confirmed a composite tumor consisting of paraganglioma and neuroblastoma. | ||
20503330 |
MIXED_SAMPLE | Adult |
Paraganglioma, neuroblastoma, and a SDHB mutation: Resolution of a 30-year-old mystery. | ||
Schimke RN, Collins DL, Stolle CA. Am J Med Genet A. 2010;152A(6):1531-5. |
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Paraganglioma, neuroblastoma, and a SDHB mutation: Resolution of a 30-year-old mystery. | ||
21092109 (2997098) |
OTHER | |
Radiological and pathological findings of a metastatic composite paraganglioma with neuroblastoma in a man: a case report. | ||
Fritzsche FR, Bode PK, Koch S, Frauenfelder T. J Med Case Rep. 2010;4:374. |
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Radiological and pathological findings of a metastatic composite paraganglioma with neuroblastoma in a man: a case report. | ||
21092109 (2997098) |
OTHER | |
Radiological and pathological findings of a metastatic composite paraganglioma with neuroblastoma in a man: a case report. | ||
Fritzsche FR, Bode PK, Koch S, Frauenfelder T. J Med Case Rep. 2010;4:374. |
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The final histopathological workup revealed a composite paraganglioma with neuroblastoma. | ||
19598001 |
FEMALE | Middle Aged |
Extra-adrenal composite paraganglioma with ganglioneuroma component presenting as a pancreatic mass. | ||
Inzani F, Rindi G, Tamborrino E, Cobelli R, Bordi C. Endocr Pathol. 2009;20(3):191-5. |
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Paragangliomas may have composite forms in which they combine features of a typical paraganglioma with those of a neural component consisting of either neuroblastoma, ganglioneuroblastoma, or ganglioneuroma. | ||
15087676 |
FEMALE | |
Unusual chromaffin cell differentiation of a neuroblastoma after chemotherapy and radiotherapy: report of an autopsy case with immunohistochemical evaluations. | ||
Miyauchi J, Kiyotani C, Shioda Y, Kumagai M, Honna T, Matsuoka K, Masaki H, Aiba M, Hata J, Tsunematsu Y. Am J Surg Pathol. 2004;28(4):548-53. |
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This case confirms that neuroblastomas in childhood can transform into pheochromocytoma/paraganglioma-like tumors under special conditions. | ||
2716185 |
MALE | |
[An autopsied case of malignant paraganglioma of the posterior thoracic cavity]. | ||
Kitazawa S, Maeda S, Horio M, Sugiyama T. Gan No Rinsho. 1989;35(4):486-92. |
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These results indicate that a paraganglioma originating from the aortic sympathetic paraganglia had similar features of a carcinoid and a neuroblastoma. |