A well documented sporadic case of multiple endocrine adenomatosis (MEA) type I, with the pituitary tumour presenting as a prolactinoma, is described in a 28-year-old female. Primary amenorrhoea, resulting from hyperprolactinaemia, was the first symptom of the polyglandular neoplasia. A gastrinoma was re-moved from the head of the pancreas and latent hyper-parathyroidism appeared to be present. Treatment with bromocriptine was poorly tolerated; neuro-surgical intervention was refused by the patient. The possibility that a serum prolactin determination may be useful in detecting pituitary involvement in MEA deserves consideration
Fourteen patients presented with arrested pubertal development associated with prolactin-secreting p...
IntroductionThe diagnosis of pituitary carcinoma is very rare, requires the evidence of metastatic d...
Prolactinomas account for approximately 50% of all pituitary adenomas coming to medical attention an...
Combined prolactin (PRL) and growth hormone (GH) secretion by a single pituitary tumor can occur in ...
Combined prolactin (PRL) and growth hormone (GH) secretion by a single pituitary tumor can occur in ...
We report the case of a patient presenting amenorrhea, hyperprolactinemia, headache and nuclear magn...
Prolactinoma is an adenoma arising from the lactotroph cells of the pituitary gland that secrete pro...
We describe three cases of multiple endocrine neoplasia type I (Wermer’s syndrome) associating a pit...
We report an unusual case of multiple endocrine neoplasia (MEN-1) presenting with hyperinsulinemia, ...
Summary: We report a case of synchronous bilateral pi-tuitary adenomas in a patient with multiple en...
We briefly review the characteristics of pituitary tumors associated with multiple endocrine neoplas...
This review summarizes knowledge on pathology of proliferative lesions of the pituitary gland in mul...
Introduction. Approximately one third of pituitary adenomas are manifested neither by specific sympt...
A 54-year-old man had gastrinoma, parathyroid hyperplasia and pituitary tumor. His family history in...
Introduction: The diagnosis of pituitary carcinoma is very rare, requires the evidence of metastatic...
Fourteen patients presented with arrested pubertal development associated with prolactin-secreting p...
IntroductionThe diagnosis of pituitary carcinoma is very rare, requires the evidence of metastatic d...
Prolactinomas account for approximately 50% of all pituitary adenomas coming to medical attention an...
Combined prolactin (PRL) and growth hormone (GH) secretion by a single pituitary tumor can occur in ...
Combined prolactin (PRL) and growth hormone (GH) secretion by a single pituitary tumor can occur in ...
We report the case of a patient presenting amenorrhea, hyperprolactinemia, headache and nuclear magn...
Prolactinoma is an adenoma arising from the lactotroph cells of the pituitary gland that secrete pro...
We describe three cases of multiple endocrine neoplasia type I (Wermer’s syndrome) associating a pit...
We report an unusual case of multiple endocrine neoplasia (MEN-1) presenting with hyperinsulinemia, ...
Summary: We report a case of synchronous bilateral pi-tuitary adenomas in a patient with multiple en...
We briefly review the characteristics of pituitary tumors associated with multiple endocrine neoplas...
This review summarizes knowledge on pathology of proliferative lesions of the pituitary gland in mul...
Introduction. Approximately one third of pituitary adenomas are manifested neither by specific sympt...
A 54-year-old man had gastrinoma, parathyroid hyperplasia and pituitary tumor. His family history in...
Introduction: The diagnosis of pituitary carcinoma is very rare, requires the evidence of metastatic...
Fourteen patients presented with arrested pubertal development associated with prolactin-secreting p...
IntroductionThe diagnosis of pituitary carcinoma is very rare, requires the evidence of metastatic d...
Prolactinomas account for approximately 50% of all pituitary adenomas coming to medical attention an...