Pinealoma
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| Pinealoma Classification and external resources |
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| Pineocytoma | |
| ICD-10 | D44.5 |
| ICD-9 | 237.1, 194.4 |
| ICD-O: | M9360/1 |
| DiseasesDB | 10044 |
| eMedicine | med/2911 |
| MeSH | D010871 |
Pinealoma is a tumor of the pineal gland.
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[edit] Presentation
The pineal gland produces the hormone melatonin which plays a role in regulating circadian rhythms. A pinealoma may disrupt production of this hormone, and insomnia may result.
Frequently, paralysis of upward gaze along with several ocular findings known collectively as Parinaud's syndrome are the only physical symptom seen. This is caused by the compression of the vertical gaze center in the midbrain tectum at the level of the superior colliculus and cranial nerve III. Patients may also present with pupillary disturbances and eyelid retraction (Collier's sign).
A pinealoma may cause interruption of hypothalamic inhibiting pathways, sometimes leading to beta-hCG secretion and consequent Leydig's cell stimulation.
Other symptoms may include hydrocephalus, gait disturbances, and precocious puberty.
[edit] Etiology
Pinealomas can be due to proliferation of primary pineocytes (pineocytomas, pineoblastomas), astrocytes (astrocytoma), or germ cells (germinoma).[1] Germinomas are the most common tumor in the pineal gland.
[edit] Prognosis
Of the different types of pinealomas, the type with the most favorable prognosis is the pineocytoma. [2]
[edit] References
- ^ eMedicine - Germinoma, Central Nervous System : Article by Daniel D Mais, MD. Retrieved on 2007-12-03.
- ^ Deshmukh VR, Smith KA, Rekate HL, Coons S, Spetzler RF (2004). "Diagnosis and management of pineocytomas". Neurosurgery 55 (2): 349–55; discussion 355–7. PMID 15271241.
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