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eRAM

encyclopedia of Rare Disease Annotation for Precision Medicine




Disease neurofibromatosis type 1
Comorbidity C0031511|pheochromocytoma
Sentences 9
PubMedID- 21042801 The aim of the study was to evaluate the prevalence of pheochromocytoma (pheo) in patients with neurofibromatosis type 1 (nf1), and to analyze the behavior of some anthropometric and cardiovascular parameters.
PubMedID- 25039695 Case of pheochromocytoma associated with neurofibromatosis type 1 developing postoperative hypertension.
PubMedID- 25130111 It is well known that neurofibromatosis type 1 (nf1) is uncommonly associated with pheochromocytoma development and also, to a larger extent, with gastrointestinal stromal tumors (gists).
PubMedID- 23287063 Multiple gastrointestinal stromal tumors and pheochromocytoma in a patient with von recklinghausen's disease.
PubMedID- 23235276 pheochromocytoma occurs in 0.1-5.7% of patients with neurofibromatosis type 1 (nf1), while dopamine-secreting pheochromocytoma is rare.
PubMedID- 24640818 We discuss the characteristics of pheochromocytoma associated with neurofibromatosis type 1 via reversible cardiac dysfunction.
PubMedID- 24518181 pheochromocytoma in neurofibromatosis type 1: when should it be suspected.
PubMedID- 20219130 pheochromocytoma associated with neurofibromatosis type 1: concepts and current trends.
PubMedID- 22145147 The combination of pheochromocytoma with neurofibromatosis is rarely reported in the literature.

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