Acromegaly causes: Difference between revisions

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==Overview==
==Overview==
Common causes of acromegaly include pituitary adenoma, acidophil stem cell adenomas, pleurihormonal adenoma. Less common causes of acromegaly include GHRH secreting tumors as hypothalamic tumors, small cell lung cancer, adrenal adenoma, and pheochromocytoma. Other causes include GH secreting tumors as lymphoma and pancreatic islet cell tumor.  
Common causes of acromegaly include [[pituitary adenoma]], acidophil [[stem cell]] adenomas, pleurihormonal adenoma. Less common causes of acromegaly include GHRH secreting tumors as hypothalamic tumors, small cell lung cancer, adrenal adenoma, and pheochromocytoma. Other causes include GH secreting tumors as lymphoma and pancreatic islet cell tumor.  


==Causes==
==Causes==

Revision as of 14:16, 14 August 2017

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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief: Ahmed Elsaiey, MBBCH [2]

Overview

Common causes of acromegaly include pituitary adenoma, acidophil stem cell adenomas, pleurihormonal adenoma. Less common causes of acromegaly include GHRH secreting tumors as hypothalamic tumors, small cell lung cancer, adrenal adenoma, and pheochromocytoma. Other causes include GH secreting tumors as lymphoma and pancreatic islet cell tumor.

Causes

Common Causes

Acromegaly may be caused by:

  • Pituitary adenoma:[1]
    • The pituitary adenoma is a benign tumor in the pituitary gland and it resembles the most common cause of acromegaly.
    • The pituitary adenoma is responsible for excessive secretion of the growth hormone and the insulin like growth factor-1.
    • Some of the pituitary adenomas have a slow progression and may not be noticed for years.
  • Other types of pituitary adenoma causing acromegaly:
    • Mixed growth hormone and prolactin cell adenomas
    • Acidophil stem cell adenomas
    • Mammosomatotroph cell adenomas
    • Pleurihormonal adenomas

Less Common Causes

Less common causes of acromegaly include:[1]

  • Hypothalamic tumors which secrete Growth Hormone Releasing Hormone (GHRH).
  • Ectopic tumor secretion of GHRH. These tumors include the following:
    • Small cell lung cancer
    • Adrenal adenoma
    • Pheochromocytoma
    • Thyroid carcinoma
  • Ectopic tumor secretion of GH. These tumors include the following:
    • Lymphoma
    • Pancreatic islet cell tumor

Genetic Causes

  • Acromegaly is caused by a mutation in the guanine nucleotide stimulatory protein gene which is responsible for pituitary adenomas.[2]

Causes by Organ System

Cardiovascular No underlying causes
Chemical/Poisoning No underlying causes
Dental No underlying causes
Dermatologic No underlying causes
Drug Side Effect No underlying causes
Ear Nose Throat No underlying causes
Endocrine Pituitary adenoma, Adrenal adenoma, Pancreatic islet cell tumor, Pheochromocytoma, Thyroid carcinoma,
Environmental No underlying causes
Gastroenterologic No underlying causes
Genetic No underlying causes
Hematologic No underlying causes
Iatrogenic No underlying causes
Infectious Disease No underlying causes
Musculoskeletal/Orthopedic No underlying causes
Neurologic No underlying causes
Nutritional/Metabolic No underlying causes
Obstetric/Gynecologic No underlying causes
Oncologic No underlying causes
Ophthalmologic No underlying causes
Overdose/Toxicity No underlying causes
Psychiatric No underlying causes
Pulmonary Small cell lung cancer
Renal/Electrolyte No underlying causes
Rheumatology/Immunology/Allergy No underlying causes
Sexual No underlying causes
Trauma No underlying causes
Urologic No underlying causes
Miscellaneous No underlying causes

Causes in Alphabetical Order

List the causes of the disease in alphabetical order.

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References

  1. 1.0 1.1 Melmed S, Braunstein GD, Horvath E, Ezrin C, Kovacs K (1983). "Pathophysiology of acromegaly". Endocr Rev. 4 (3): 271–90. doi:10.1210/edrv-4-3-271. PMID 6354702.
  2. Landis CA, Masters SB, Spada A, Pace AM, Bourne HR, Vallar L (1989). "GTPase inhibiting mutations activate the alpha chain of Gs and stimulate adenylyl cyclase in human pituitary tumours". Nature. 340 (6236): 692–6. doi:10.1038/340692a0. PMID 2549426.


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