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Pituitary adenoma
Classification and external resources
ICD-10 D35.2
ICD-9 237.0
ICD-O: M8140/0
MedlinePlus 000704
eMedicine neuro/312
MeSH D010911

Pituitary adenomas are tumors that occur in the pituitary gland, and account for about 10% of intracranial neoplasms. They often remain undiagnosed, and small pituitary tumors have an estimated prevalence of 16.7% (14.4% in autopsy studies and 22.5% in radiologic studies).[1][2]

Contents

[edit] Types

Pituitary tumors were, historically, classed as basophilic, acidophilic, or chromophobic on the basis of whether or not they took up the stains hematoxylin and eosin. This classification has fallen into disuse, in favor of a classification based on what type of hormone is secreted by the tumor (though tumors which do not secrete any active hormone ("non-functioning tumors") are still sometimes called "chromophobic").


At present, classification of pituitary tumors is based on plasma hormone levels or immunohistochemical staining:

Type of adenoma Secretion Staining Pathology
corticotrophic adenomas secrete adrenocorticotropic hormone (ACTH) and pro-opiomelanocortin (POMC) basophilic Cushing's disease
somatotrophic adenomas secrete growth hormone (GH) acidophilic acromegaly (gigantism)
thyrotrophic adenomas (rare) secrete thyroid-stimulating hormone (TSH) basophilic occasionally hyperthyroidism[3], usually doesn't cause symptoms
gonadotrophic adenomas secrete luteinizing hormone (LH), follicle-stimulating hormone (FSH) and their subunits basophilic usually doesn't cause symptoms
lactrotrophic adenomas or prolactinomas (most common) secrete prolactin acidophilic galactorrhea, hypogonadism, amenorrhea, infertility, and impotence
null cell adenomas do not secrete hormones may stain positive for synaptophysin

[edit] Diagnosis

The diagnosis is generally entertained either on the basis of visual difficulties arising from the compression of the optic nerve by the tumor, or on the basis of manifestations of excess hormone secretion: the specifics depend on the type of hormone. The specific area of the visual pathway at which compression by these tumours occurs is at the optic chiasma.

The anatomy of this structure causes pressure on it to produce a defect in the temporal visual field on both sides, a condition called bitemporal hemianopia. Lateral expansion of a pituitary adenoma can also compress the abducens nerve, causing a lateral rectus palsy.

Tumors which cause visual difficulty are likely to be macroadenoma greater than 10 mm in diameter; tumors less than 10 mm are microadenoma.

Some tumors secrete more than one hormone, the most common combination being GH and prolactin.

Prolactinomas are frequently diagnosed during pregnancy, when the hormone progesterone increases the tumor's growth rate. Headaches may be present. Women and men can both present with decreased libido. The diagnosis is confirmed by testing hormone levels, and by radiographic imaging of the pituitary (for example, by CT scan or MRI).

[edit] Treatment

Treatment options depend on the type of tumor and on its size:

  • Prolactinomas are most often treated with bromocriptine or more recently, cabergoline or quinagolide which, unlike bromocriptine, decreases tumor size as well as alleviates symptoms, both dopamine agonists, and followed by serial imaging to detect any increase in size. Treatment where the tumor is large can be with radiation therapy or surgery, and patients generally respond well. Efforts have been made to use a progesterone antagonist for the treatment of prolactinomas, but so far have not proved successful.
  • Thyrotrophic adenomas respond to octreotide, a long-acting somatostatin analog, in many but not all cases according to a review of the medical literature. Unlike prolactinomas, thyrotrophic adenomas characteristically respond poorly to dopamine agonist treatment.[3]
  • Surgery is a common treatment for pituitary tumors. Trans-sphenoidal adenectomy surgery can often remove the tumor without affecting other parts of the brain. Endoscopic surgery has become common recently. [4]

[edit] Additional images

[edit] References

  1. ^ Ezzat S, Asa SL, Couldwell WT, Barr CE, Dodge WE, Vance ML, McCutcheon IE. (August 2004). "The prevalence of pituitary adenomas: a systematic review". Cancer 101 (3): 613–9. doi:10.1002/cncr.20412. PMID 15274075. 
  2. ^ Asa SL (August 2008). "Practical pituitary pathology: what does the pathologist need to know?". Arch. Pathol. Lab. Med. 132 (8): 1231–40. PMID 18684022. http://journals.allenpress.com/jrnlserv/?request=get-abstract&issn=0003-9985&volume=132&page=1231. Retrieved 2008-09-03. 
  3. ^ a b Chanson P, Weintraub BD, Harris AG (August 1993). "Octreotide therapy for thyroid-stimulating hormone-secreting pituitary adenomas. A follow-up of 52 patients". Ann. Intern. Med. 119 (3): 236–40. PMID 8323093. http://www.annals.org/cgi/pmidlookup?view=long&pmid=8323093. Retrieved 2008-09-03. 
  4. ^ [1] American Cancer Society. "Detailed guide: Pituitary tumor. Surgery." Retrieved January 10, 2008

[edit] External links




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