No abstract available.
Neuropeptides* ; Pituitary Hormones*

No abstract available.
Neuropeptides* ; Pituitary Hormones*

The concentration of TSH receptor autoantibodies (TRAB) was determined by a radioreceptor assay kit (RRA) in serum collected from 30 normal adults (15 males and 15 females). The results showed that the overall mean level of TRAB is 1.360.57u/l. The mean level is 1.49+/-0.67u/l in men and is 1.22+/-0.44u/l in women. There was not significant difference between man and women in TRAB level.
Autoantibodies ; Pituitary Hormones ; Thyrotropin ; adult

The tumors containing ganglion cells are rare in the pituitary gland. These tumors are divided into two groups. The first group is the cases of mixed gangliocytoma-adenoma that contained both gangliocytoma and pituitary adenoma elements in the same tumor and the second group is those of gangliocytoma that contained only gangliocytoma element. Since the first description by Kiyono in 1926, 45 cases have been reported. The most common presentation of these tumors is acromegaly and the cases of Cushings disease and galactorrhea-amenorrhea also have been reported. In immunohistochemical study, hypothalamic-releasing hormones are stained in gangliocytoma cells and adenohypophyseal hormones are stained in adenoma cells. The releasing hormones stained in gangliocytoma element and the pituitary hormones stained in adenoma elements are usually closely related but unrelated cases also have been reported. We report a case of a 41 year-old lady with acromegaly which was diagnosed as mixed gangliocytoma-adenoma after surgical removal of the pituitary tumor.
Acromegaly* ; Adenoma ; Adult ; Ganglion Cysts ; Ganglioneuroma ; Humans ; Pituitary Gland* ; Pituitary Hormones ; Pituitary Hormones, Anterior ; Pituitary Neoplasms

TSH secreting pituitary adenoma is a very rare disease, but it should be carefully suspected in patients with the lack of inhibition of TSH levels in the presence of increased thyroid hormones. The clinical manifestations are similar to those of hyperthyroidism, so TSH secreting pituitary adenoma can be easily misdiagnosed as hyperthyroidism resulting in inappropriate treatment. Surgery is the treatment of choice and the long-acting somatostatin analogs are effective in reducing TSH secretion with consequent restoration of the euthyroid state in the majority. Recently, development of neuroradiological techniques and better recognition of TSH-secreting adenomas increase the rate of diagnosis as microadenoma and improve surgical cure rate in patients with TSH secreting pituitary adenoma.
Adenoma ; Humans ; Hyperthyroidism ; Pituitary Neoplasms ; Rare Diseases ; Somatostatin ; Thyroid Hormones

From October 1981 to August 1982, a program of plasma gonadotropin (FSH & LH) and testosterone measurement was undertaken in 33 cases of prepubertal cryptorchid boys. Radioimmunoassay resulted in the following findings. 1. The mean values of each FSH, LH and testosterone in unilateral prepubertal cryptorchid boys did not show a correlation with chronologic age. 2. There were no differences in the value of FSH and LH between unilateral cryptorchid boys and Canadian healthy boys, except for a decrement in cryptorchid boys in age group from 6 to 8 and from 8 to 10. No differences in the values of testosterone through the whole age group were observed. It seems to be indicated that the study of histopathology of the testis and of pituitary hormones especially via the stimulation test is helpful for further evaluation of pathogenesis of cryptorchidism in hormonal approach.
Cryptorchidism ; Gonadotropins* ; Humans ; Male ; Pituitary Hormones ; Plasma ; Radioimmunoassay ; Testis ; Testosterone*

Following irradiation with 2.45GHz microwave, pituitary hormonal changes in rabbits were observed. A 30 rabbits (New Zealand, White, Male) were used for the experiments, 10 for each experiment immediately following one two and four weeks after irradiation with amount of 2.4 Joule/cm2, 4.8 Joule/cm2 and 7.2 Joule/cm2 respectively. The following are the results of the study as a conclusion. The secretion of cortisol hormone increased immediately after the exposure and then decrease to below that of the control group until two weeks afterwards, followed by recovery phase with secretion level approaching that of the central group in 4 weeks. Lutenizing hormone showed a tendency of increase from the first week of exposure, rather than immediately after, lasting up to over four weeks, In the irradiation group for 30 min, however, the increase began immediately after the exposure. The secretion of of growth hormone showed an insignificant, increase after the second and fourth weeks over the control group. The duration of exposure did not have much effect on the hormonal secretion. Thyroid stimulating hormone showed a different pattern changes: increase of immediately after exposure, decreased in two weeks, and then approaching the level of the control group after four weeks.
Growth Hormone* ; Hydrocortisone ; Microwaves* ; Pituitary Hormones ; Rabbits* ; Thyroid Gland* ; Thyrotropin

Tuberculous meningitis is a well-known cause of hypothalamic pituitary dysfunction. However, deficiencies of anterior pituitary hormones may only become evident years after recovery because symptoms are of insidious-onset and nonspecific. Pituitary hormones are essential for normal growth and sexual development in childhood, and for maintenance of healthy body composition. In addition, pituitary hormones and vitamin D are important for cardiovascular and bone health. Although evidence of the relationship between hypovitaminosis D and hypopituitarism is limited, some studies suggested that the incidence of vitamin D deficiency increased in hypopituitarism. We describe herein an unusual case of hypopituitarism and severe hypovitaminosis D presenting as osteoporotic fracture after cured tuberculous meningitis.
Body Composition ; Hypopituitarism* ; Incidence ; Osteoporotic Fractures* ; Pituitary Hormones ; Pituitary Hormones, Anterior ; Sexual Development ; Tuberculosis, Meningeal* ; Vitamin D ; Vitamin D Deficiency

A long-held belief is that pituitary hormones bind to their cognate receptors in classical target glands to actuate their manifold functions. However, a number of studies have shown that multiple types of pituitary hormone receptors are widely expressed in non-classical target organs. Each pituitary gland-derived hormone exhibits a wide range of nonconventional biological effects in these non-classical target organs. Herein, the extra biological functions of pituitary hormones, thyroid-stimulating hormone, follicle-stimulating hormone, luteinizing hormone, adrenocorticotrophic hormone, and prolactin when they act on non-classical organs were summarized, defined by the novel concept of an "atypical pituitary hormone-target tissue axis." This novel proposal explains the pathomechanisms of abnormal glucose and lipid metabolism, obesity, hypertension, fatty liver, and atherosclerosis while offering a more comprehensive and systematic insights into the coordinated regulation of environmental factors, genetic factors, and neuroendocrine hormones on human biological functions. The continued exploration of the physiology of the "atypical pituitary hormone-target tissue axis" could enable the identification of novel therapeutic targets for metabolic diseases.
Humans ; Pituitary Hormones/metabolism* ; Luteinizing Hormone ; Follicle Stimulating Hormone ; Prolactin ; Pituitary Gland/metabolism*

Objective: To investigate the clinicopathological characteristics of plurihormonal PIT1-lineage pituitary neuroendocrine tumors. Methods: Forty-eight plurihormonal PIT1-lineage tumors were collected between January 2018 and April 2022 from the pathological database of Sanbo Brain Hospital, Capital Medical University. The related clinical and imaging data were retrieved. H&E, immunohistochemical and special stains were performed. Results: Out of the 48 plurihormonal PIT1-lineage tumors included, 13 cases were mature PIT1-lineage tumors and 35 cases were immature PIT1-lineage tumors. There were some obvious clinicopathological differences between the two groups. Clinically, the mature plurihormonal PIT1-lineage tumor mostly had endocrine symptoms due to increased hormone production, while a small number of immature PIT1-lineage tumors had endocrine symptoms accompanied by low-level increased serum pituitary hormone; patients with the immature PIT1-lineage tumors were younger than the mature PIT1-lineage tumors; the immature PIT1-lineage tumors were larger in size and more likely invasive in imaging. Histopathologically, the mature PIT1-lineage tumors were composed of large eosinophilic cells with high proportion of growth hormone expression, while the immature PIT1-lineage tumors consisted of chromophobe cells with a relatively higher expression of prolactin; the mature PIT1-lineage tumors had consistently diffuse cytoplasmic positive staining for keratin, while the immature PIT1-lineage tumors had various expression for keratin; the immature PIT1-lineage tumors showed more mitotic figures and higher Ki-67 proliferation index; in addition, 25.0% (12/48) of PIT1-positive plurihormonal tumors showed abnormal positive staining for gonadotropin hormones. There was no significant difference in the progression-free survival between the two groups (P=0.648) by Kaplan-Meier analysis. Conclusions: Plurihormonal PIT1-lineage tumor belongs to a rare type of PIT1-lineage pituitary neuroendocrine tumors, most of which are of immature lineage. Clinically increased symptoms owing to pituitary hormone secretion, histopathologically increased number of eosinophilic tumor cells with high proportion of growth hormone expression, diffusely cytoplasmic keratin staining and low proliferative activity can help differentiate the mature plurihormonal PIT1-lineage tumors from the immature PIT1-lineage tumors. The immature PIT1-lineage tumors have more complicated clinicopathological characteristics.
Humans ; Neuroendocrine Tumors ; Pituitary Neoplasms/pathology* ; Pituitary Hormones ; Growth Hormone/metabolism* ; Keratins