Craniopharyngioma
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| Craniopharyngioma Classification and external resources | |
| Craniopharyngioma | |
| ICD-10 | D44.4 |
| ICD-9 | 237.0 |
| ICD-O: | 9350/1 |
| DiseasesDB | 3153 |
| MedlinePlus | 000345 |
| eMedicine | radio/196 |
| MeSH | D003397 |
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Craniopharyngioma is a type of tumor that comprises 9% of all pediatric brain tumors. They usually occur in children between 5 and 10 years of age.[1]
It has a point prevalence of approximately 2/100,000.[1]
They are also known as Rathke pouch tumors, hypophyseal duct tumors, or adamantinomas.
Presentation
They are very slow growing tumors. They arise from the cells along the pituitary stalk. They are classified as benign.[1]
Craniopharyngioma is a rare, usually suprasellar[1] neoplasm, which may be cystic, that develops from the nests of epithelium derived from Rathke's pouch.
Histology
The histologic pattern consists of nesting of squamous epithelium bordered by radially arranged cells. It is frequently accompanied by calcium deposition and have a microscopic papillary architecture.
Possible symptoms
- Anorexia
- Balance disorder
- Dry skin
- Fatigue
- Fever
- Headache (obstructive hydrocephalus)
- Lethargy
- Myxedema
- Nausea
- Short stature
- Polydipsia
- Polyuria (diabetes insipidus)
- Vision loss (bitemporal hemianopsia)
- Vomiting
- Weight gain
- amenorrhea
References
External links
Nervous tissue tumors (ICD-O 9350-9589) | |
|---|---|
| Miscellaneous tumors (9350-9379) | Craniopharyngioma - Pinealoma - Chordoma |
| Glioma (9380-9489) | Gliomatosis cerebri - Oligoastrocytoma - Choroid plexus papilloma - Ependymoma - Astrocytoma (Pilocytic astrocytoma, Glioblastoma multiforme) - Dysembryoplastic neuroepithelial tumour - Oligodendroglioma - Medulloblastoma - Primitive neuroectodermal tumor |
| Neuroepitheliomatous (9490-9529) | Ganglioneuroma - Neuroblastoma - Atypical teratoid rhabdoid tumor - Retinoblastoma - Esthesioneuroblastoma |
| Meningiomas (9530-9539) | Meningioma |
| Nerve sheath tumor (9540-9579) | Neurofibroma (Neurofibrosarcoma, Neurofibromatosis) - Schwannoma - Neurinoma - Acoustic neuroma - Neuroma |
| see also brain tumors (though not all brain tumors are of nervous tissue) | |
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Acknowledgement and Attribution Regarding Sources of Content
Some of the initial content on this page may be incorporated in part from copyleft sources in the public domain including wikis such as Wikipedia and AskDrWiki. Drug information for patients came from the The National Library of Medicine. Infectious disease information may have come from the Centers for Disease Control (CDC). Differential Diagnoses are drawn from clinicians as well as an amalgamation of 3 sources: 1.The Disease Database; 2. Kahan, Scott, Smith, Ellen G. In A Page: Signs and Symptoms. Malden, Massachusetts: Blackwell Publishing, 2004:3; 3. Sailer, Christian, Wasner, Susanne. Differential Diagnosis Pocket. Hermosa Beach, CA: Borm Bruckmeir Publishing LLC, 2002:7 .

