The Grading system for Adrenal Pheochromocytoma and Paraganglioma (GAPP) was proposed for predicting the metastatic potential of pheochromocytoma and paraganglioma to overcome the limitations of the Pheochromocytoma of the Adrenal Scaled Score (PASS). However, to date, no study validating the GAPP has been conducted, and previous studies did not include mutations in the succinate dehydrogenase type B (SDHB) gene in the score calculation. In this retrospective cohort study, we validated the prediction ability of GAPP and assessed whether it would be improved by inclusion of the loss of SDHB immunohistochemical staining.We divided the tumors into non-metastatic and metastatic groups based on the presence of synchronous or metachronous metasta...
Background: Pheochromocytomas and paragangliomas (PPGLs) have a heterogeneous prognosis, the basis o...
OBJECTIVE: Pheochromocytomas and paragangliomas (PPGL) are relatively rare and mostly benign tumours...
ObjectiveThe aim was to formulate clinical practice guidelines for pheochromocytoma and paragangliom...
<p>Correlation of the Grading system for Adrenal Pheochromocytoma and Paraganglioma (GAPP) score, Ph...
Pheochromocytomas (PCCs) and abdominal paragangliomas (PGLs), collectively abbreviated PPGLs, are ne...
Pheochromocytoma (PCC) and sympathetic paraganglioma (PGL) are rare neuroendocrine tumors characteri...
Pheochromocytomas (PCCs) and abdominal paragangliomas (PGLs), collectively abbreviated PPGL, are bel...
Morphologic determination of the malignant potential of adrenal pheochromocytoma is a challenging pr...
phaeochromocytoma and paraganglioma (GAPP). The tumours were scored based on as 5.5G2.6 years. The s...
Background: Pheochromocytomas and paragangliomas (PPGL) have up to 20% rate of metastatic disease th...
Many malignant tumors initially appear benign but subsequently exhibit extensive metastases. Early i...
Pheochromocytomas/Paragangliomas (PPGLs) and adrenocortical tumors are rare neoplasms with significa...
Item does not contain fulltextOBJECTIVE: Testing for succinate dehydrogenase subunit B (SDHB) mutati...
Malignant pheochromocytomas/paragangliomas are rare tumors with a poor prognosis. Malignancy is diag...
Evaluation of the malignant potential of phaeochromocytomas in the absence of metastases presents a ...
Background: Pheochromocytomas and paragangliomas (PPGLs) have a heterogeneous prognosis, the basis o...
OBJECTIVE: Pheochromocytomas and paragangliomas (PPGL) are relatively rare and mostly benign tumours...
ObjectiveThe aim was to formulate clinical practice guidelines for pheochromocytoma and paragangliom...
<p>Correlation of the Grading system for Adrenal Pheochromocytoma and Paraganglioma (GAPP) score, Ph...
Pheochromocytomas (PCCs) and abdominal paragangliomas (PGLs), collectively abbreviated PPGLs, are ne...
Pheochromocytoma (PCC) and sympathetic paraganglioma (PGL) are rare neuroendocrine tumors characteri...
Pheochromocytomas (PCCs) and abdominal paragangliomas (PGLs), collectively abbreviated PPGL, are bel...
Morphologic determination of the malignant potential of adrenal pheochromocytoma is a challenging pr...
phaeochromocytoma and paraganglioma (GAPP). The tumours were scored based on as 5.5G2.6 years. The s...
Background: Pheochromocytomas and paragangliomas (PPGL) have up to 20% rate of metastatic disease th...
Many malignant tumors initially appear benign but subsequently exhibit extensive metastases. Early i...
Pheochromocytomas/Paragangliomas (PPGLs) and adrenocortical tumors are rare neoplasms with significa...
Item does not contain fulltextOBJECTIVE: Testing for succinate dehydrogenase subunit B (SDHB) mutati...
Malignant pheochromocytomas/paragangliomas are rare tumors with a poor prognosis. Malignancy is diag...
Evaluation of the malignant potential of phaeochromocytomas in the absence of metastases presents a ...
Background: Pheochromocytomas and paragangliomas (PPGLs) have a heterogeneous prognosis, the basis o...
OBJECTIVE: Pheochromocytomas and paragangliomas (PPGL) are relatively rare and mostly benign tumours...
ObjectiveThe aim was to formulate clinical practice guidelines for pheochromocytoma and paragangliom...