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eRAM

encyclopedia of Rare Disease Annotation for Precision Medicine




Disease multiple endocrine neoplasia type 2
Comorbidity C0031511|pheochromocytoma
Sentences 8
PubMedID- 22107743 Unilateral subtotal adrenalectomy for pheochromocytoma in multiple endocrine neoplasia type 2 patients: a feasible surgical strategy.
PubMedID- 24169328 Objective: to explore the clinical patterns and clinical significance for ret screening in adrenal pheochromocytoma (pheo) associated with multiple endocrine neoplasia type 2a (men2a).
PubMedID- 23961501 We also are reporting the largest described case of pheochromocytoma associated with men2a from india.
PubMedID- 24981168 We reported two cases of bilateral pheochromocytoma associated with men 2 syndrome cured by simultaneous bilateral laparoscopic adrenalectomy.
PubMedID- 24449023 multiple endocrine neoplasia type 2 (men2) is an autosomal, dominantly inherited disorder manifesting various combinations of medullary thyroid carcinoma (mtc) and pheochromocytoma, with hyperparathyroidism (men2a) or neuromas of the enteric autonomic nerve cells (men2b).
PubMedID- 24571990 Surgical treatment of pheochromocytoma in men 2.
PubMedID- 21453592 Discussion: the benefits of laparoscopic adrenalectomy for a single lesion are well documented in the literature; this type of intervention is indicated in cases of pheochromocytoma in patients with men 2b.
PubMedID- 22614196 pheochromocytoma in multiple endocrine neoplasia type 2a: positive 123i mibg with negative ct and equivocal 131i mibg imaging.

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