eRAM
encyclopedia of Rare Disease Annotation for Precision Medicine
| Disease | pheochromocytoma |
| Comorbidity | C0030421|paraganglioma |
| Sentences | 6 |
| PubMedID- 26359568 | A 22-year-old woman with rapidly progressing metastatic paraganglioma due to hereditary paraganglioma-pheochromocytoma syndrome from an sdhb mutation, who recurred after neoadjuvant chemotherapy, was found to be mibg avid. |
| PubMedID- 25275255 | pheochromocytoma may coexist with paraganglioma and when paraganglioma is diagnosed, the patient should be screened for pheochromocytoma too, especially in people with hypertension. |
| PubMedID- 26359562 | A 26-year-old woman with a 5-year history of metastatic paraganglioma due to hereditary paraganglioma-pheochromocytoma syndrome with sdhb mutation, who had failed multiple treatment regimens and had transfusion dependent pancytopenia, presented with progressive liver and bone metastases. |
| PubMedID- 20664475 | pheochromocytomas, intra-adrenal paraganglioma, and extra-adrenal sympathetic and parasympathetic paragangliomas are neuroendocrine tumors derived from adrenal chromaffin cells or similar cells in extra-adrenal sympathetic and parasympathetic paraganglia, respectively. |
| PubMedID- 25918656 | pheochromocytoma, along with paraganglioma, is a chromaffin neuroendocrine tumor that secretes catecholamine, which mostly manifests characteristic symptoms including headache, hypertension, and palpitation. |
| PubMedID- 24499341 | Surgical outcome of laparoscopic surgery, including laparoendoscopic single-site surgery, for retroperitoneal paraganglioma compared with adrenal pheochromocytoma. |
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