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Hypothalamic Neoplasms
Research News and Information
Definition of 'Hypothalamic Neoplasms'Benign and malignant tumors of the HYPOTHALAMUS. Pilocytic astrocytomas and hamartomas are relatively frequent histologic types. Neoplasms of the hypothalamus frequently originate from adjacent structures, including the OPTIC CHIASM, optic nerve (see OPTIC NERVE NEOPLASMS), and pituitary gland (see PITUITARY NEOPLASMS). Relatively frequent clinical manifestations include visual loss, developmental delay, macrocephaly, and precocious puberty. (From Devita et al., Cancer: Principles and Practice of Oncology, 5th ed, p2051) |
Saturday, November 21, 2009
13 Dec 2009
Frasier syndrome is characterized by a 46 XY disorder of sex development, nephropathy, and increased risk for gonadoblastoma due to Wilms tumor 1(WT1) mutation in the donor splice site of intron-9, resulting in the splice form +KTS. Germ cell tumors ... Read more...
Safety aspects of GH replacement.
12 Aug 2009
In adults, GH replacement therapy will often be maintained for decades. Owing to the long duration of GH replacement in many adults, it is essential to establish the long-term safety aspects of the treatment. In this review, studies that have ... Read more...
Endoscopic disconnection of hypothalamic astrocytoma causing gelastic epilepsy. Case report.
30 Jul 2009
The authors report on a case of juvenile pilocytic astrocytoma (JPA) and concomitant hypothalamic hamartoma (HH) with gelastic epilepsy that was successfully treated with endoscopic disconnection. This 6-year-old girl presented with prolonged, ... Read more...
Latest indexed articles for 'Hypothalamic Neoplasms'
These are the very latest articles for this heading:
- Bilateral gonadoblastoma with dysgerminoma and pilocytic astrocytoma with WT1 GT-IVS9 mutation: A 46 XY phenotypic female with Frasier syndrome.
13 Dec 2009 - Safety aspects of GH replacement.
12 Aug 2009 - Clinical Centers of Excellence: Seizure disorders. Barrow Neurological Institute.
5 Aug 2009 - Endoscopic disconnection of hypothalamic astrocytoma causing gelastic epilepsy. Case report.
30 Jul 2009 - Hypothalamic lipoma associated with severe obesity. Report of 2 cases.
30 Jul 2009 - [A successful surgical case of a hypothalamic hamartoma with gelastic seizure: a case report]
30 Jul 2009 - [Secondary hypopituitarism due to hypothalamic metastasis from small cell lung cancer]
9 Jun 2009 - [Clinical and imaging features of hypothalamic hamartoma in children]
29 Apr 2009 - Tumor stabilization under treatment with imatinib in progressive hypothalamic-chiasmatic glioma.
30 Mar 2009 - Hypothalamic lymphoma with symptoms mimicking pituitary apoplexy.
14 Mar 2009 - Chemotherapy with cisplatin and vincristine for optic pathway/hypothalamic astrocytoma in young children.
15 Feb 2009 - Mixed germ cell tumor of the pituitary-hypothalamic region presenting as craniopharyngioma: case report and review of the literature.
29 Nov 2008 - Suprasellar hemangioblastoma.
29 Nov 2008 - Bicarbonate contributes to GABAA receptor-mediated neuronal excitation in surgically resected human hypothalamic hamartomas.
18 Nov 2008 - Cognition before and after chemotherapy alone in children with chiasmatic-hypothalamic tumors.
12 Nov 2008 - Underlying pathogenesis and proper treatments of traumatic subdural hygromas.
29 Sep 2008 - Radiological classification of optic pathway gliomas: experience of a modified functional classification system.
29 Sep 2008 - Hypothalamic papillary tumor in a patient with tuberous sclerosis.
29 Sep 2008 - Loss of myelinated retinal nerve fibers from chronic papilledema.
30 Aug 2008 - Clinicopathological features and global genomic copy number alterations of pilomyxoid astrocytoma in the hypothalamus/optic pathway: comparative analysis with pilocytic astrocytoma using array-based comparative genomic hybridization.
9 Jul 2008
See a longer list of these articles.
Technical information about 'Hypothalamic Neoplasms'
Definition: Benign and malignant tumors of the HYPOTHALAMUS. Pilocytic astrocytomas and hamartomas are relatively frequent histologic types. Neoplasms of the hypothalamus frequently originate from adjacent structures, including the OPTIC CHIASM, optic nerve (see OPTIC NERVE NEOPLASMS), and pituitary gland (see PITUITARY NEOPLASMS). Relatively frequent clinical manifestations include visual loss, developmental delay, macrocephaly, and precocious puberty. (From Devita et al., Cancer: Principles and Practice of Oncology, 5th ed, p2051)
Descriptor UI: D007029
Alternative terms: Hypothalamic Neoplasms; Hypothalamus Neoplasms; Hypothalamus Neoplasm; Neoplasm, Hypothalamus; Tumors, Hypothalamus; Hypothalamus Tumor; Hypothalamus Tumors; Tumor, Hypothalamus; Neoplasms, Hypothalamus; Hypothalamic Tumors; Hypothalamic Tumor; Tumor, Hypothalamic; Tumors, Hypothalamic; Neoplasms, Hypothalamic; Hypothalamic Neoplasm; Neoplasm, Hypothalamic; Hypothalamic Cancer; Cancer, Hypothalamic; Cancers, Hypothalamic; Hypothalamic Cancers; Hypothalamic Neoplasms, Malignant; Hypothalamic Neoplasm, Malignant; Malignant Hypothalamic Neoplasm; Neoplasm, Malignant Hypothalamic; Neoplasms, Malignant Hypothalamic; Malignant Hypothalamic Neoplasms; Neoplasms, Hypothalamic, Malignant; Hypothalamic-Pituitary Neoplasms; Hypothalamic Pituitary Neoplasms; Hypothalamic-Pituitary Neoplasm; Neoplasm, Hypothalamic-Pituitary; Neoplasms, Hypothalamo-Neurohypophysial Region; Neoplasms, Hypothalamo Neurohypophysial Region; Hypothalamo-Neurohypophysial Region Neoplasms; Hypothalamo Neurohypophysial Region Neoplasms; Hypothalamo-Neurohypophysial Region Neoplasm; Neoplasm, Hypothalamo-Neurohypophysial Region; Neoplasms, Hypothalamic-Pituitary; Neoplasms, Hypothalamic Pituitary; Hypothalamic Teratomas; Hypothalamic Teratoma; Teratoma, Hypothalamic; Teratomas, Hypothalamic; Hypothalamic-Chiasmatic Neoplasms; Hypothalamic Chiasmatic Neoplasms; Hypothalamic-Chiasmatic Neoplasm; Neoplasm, Hypothalamic-Chiasmatic; Neoplasms, Hypothalamic-Chiasmatic; Neoplasms, Hypothalamic Chiasmatic; Benign Hypothalamic Neoplasms; Benign Hypothalamic Neoplasm; Neoplasm, Benign Hypothalamic; Neoplasms, Hypothalamic, Benign; Hypothalamic Neoplasms, Benign;
Allowable Qualifiers: blood; blood supply; cerebrospinal fluid; chemically induced; classification; complications; congenital; diagnosis; diet therapy; drug therapy; economics; embryology; enzymology; ethnology; etiology; genetics; history; immunology; metabolism; microbiology; mortality; nursing; epidemiology; parasitology; pathology; physiopathology; prevention & control; psychology; radiography; radionuclide imaging; radiotherapy; rehabilitation; secondary; secretion; surgery; therapy; ultrastructure; urine; veterinary; ultrasonography; chemistry; virology;
Tree Number: C04.588.614.250.195.885.500; C10.228.140.211.885.500; C10.228.140.617.477; C10.551.240.250.700.500;
History Note: 1981
Technical Notes: coord IM with site in hypothalamus (IM) + histol type of neopl (IM)