eRAM
encyclopedia of Rare Disease Annotation for Precision Medicine
| Disease | acromegaly |
| Symptom | C0032000|pituitary adenoma |
| Sentences | 6 |
| PubMedID- 24447924 | It is characterized by cm, extracardiac myxomas (mucosal and cutaneous), osteochondromyxoma, spotty skin pigmentation, myxomatous tumors of the breast, ductal adenoma of breast, blue nevi, endocrine overactivity and tumors (hypercortisolism, pituitary adenoma with acromegaly or gigantism, thyroid tumors, testicular large cell calcifying sertoli cell tumors (lccst) and psammomatous melanotic schwannoma (pms)) and paradoxical positive response of urinary glucocorticoids to dexamethasone administration (ppnad) during liddle’s test . |
| PubMedID- 26071586 | Methods: the paraffin embedded pituitary adenoma tissue sections of 28 patients with acromegaly who were diagnosed as monohormonal growth hormone (gh) secreting adenomas were immunostained for eag1 using the avidin-biotin-peroxidase complex method. |
| PubMedID- 24101276 | acromegaly associated with mixed pituitary adenoma-gangliocytoma and rathke's cleft cyst. |
| PubMedID- 22029034 | acromegaly with no pituitary adenoma and no evidence of ectopic source. |
| PubMedID- 23512282 | We conclude from this case and a literature review that double endocrinologically active pituitary adenomas leading to acromegaly and cushing's disease may occur. |
| PubMedID- 21744088 | Somatotroph pituitary adenoma with acromegaly and autosomal dominant polycystic kidney disease: sstr5 polymorphism and pkd1 mutation. |
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