| IRP | immunoreactive plasma; immunoreactive proinsulin; incus replacement prosthesis; insulin-releasing po... |
|---|---|
| IRT | immunoreactive trypsin; interresponse time; interstitial radiotherapy |
| IS | ileal segment; immediate sensitivity; immune serum; immunosuppression; impingement syndrome; incenti... |
| ISF | interstitial fluid |
| ISFV | interstitial fluid volume |
| primary brain tumour | <neurology, oncology> May be subdivided into primary brain tumours and the more common, secondary brain tumours. Primary brain tumours (for example astrocytoma, craniopharyngioma, glioma, ependymoma, neuroglioma, oligodendroglioma, glioblastoma multiforme, meningioma, medulloblastoma) arise from the uncontrolled proliferation of cells within the brain. Secondary brain tumours occur from the spread of cancer into the brain from a distant cancerous organ (metastasis). Common symptoms of a brain tumour include headache, nausea, vomiting, seizures, change in mentation, neurologic symptoms and loss of memory. (06 Mar 1998) |
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| primary tumour | <oncology> The mass of tumour cells at the original site of the neoplastic event from the primary tumour metastasis will lead to the establishment of secondary tumours. (18 Nov 1997) |
| primitive neuroectodermal tumour | A designation used to refer to a group of morphologically similar embryonal neoplasms that arise in intracranial and peripheral sites of the nervous system and which may show various degrees of cellular differentiation; includes medulloblastoma, pineoblastoma, etc. (05 Mar 2000) |
| sand tumour | <tumour> A firm cellular neoplasm derived from fibrous tissue of the meninges, choroid plexus, and certain other structures associated with the brain, characterised by the formation of multiple, discrete, concentrically laminated, calcareous bodies (psammoma bodies); most of these neoplasms are histologically benign, but may lead to severe symptoms as a result of compressing the brain. Synonym: angiolithic sarcoma, sand tumour, Virchow's psammoma. (05 Mar 2000) |
| heterologous tumour | A tumour composed of a tissue unlike that from which it springs. (05 Mar 2000) |
| histoid tumour | Old term for a tumour composed of a single type of differentiated tissue. (05 Mar 2000) |
| secondary tumour | <oncology> A tumour that develops as a result of metastasis or spreads beyond the original cancer. (09 Oct 1997) |
| homologous tumour | <oncology> Any tumour which is composed of the same tissue as that in which it arose. (09 Oct 1997) |
| sex cord-stromal tumour | A malignant neoplasm of the ovary or testis. These tumours differentiate toward sex cords (in embryonic gonads) in the form of female (i.e., granulosa and theca) cells, male (i.e., sertoli and leydig) cells, or indifferent elements. In the ovary, sex cord-stromal tumours comprise 5% of all ovarian neoplasms. In the testes, leydig and sertoli cell tumours comprise about 5% of all testicular neoplasms, 10% of which behave in a malignant fashion. (12 Dec 1998) |
| hylic tumour | <tumour> A neoplasm of pulp tissue, resulting from proliferation of elements derived from the embryonic pulp of epiblastic origin. Synonym: hylic tumour. Origin: G. Hyle, stuff, crude matter, + -oma, tumour (05 Mar 2000) |
| smooth muscle tumour | A tumour composed of smooth muscle tissue, as opposed to leiomyoma, a tumour derived from smooth muscle. (12 Dec 1998) |
| solid tumour | A cancer that originates in organ or tissue other than bone marrow or the lymph system. (16 Dec 1997) |
| solitary fibrous tumour | A benign tumour of fibrous tissue which usually arises in the pleural space on other sites. Synonym: benign mesothelioma. (05 Mar 2000) |
| spinal cord tumour | A spinal cord tumour is a aggregate if cells that form a mass that can compress the spinal cord. Spinal cord tumours may arise from local structures (for example meninges) or from a cancer from a distant site (i.e. Metastasis). Regardless of the aetiology, all spinal cord tumours cause symptoms from compression on the spinal cord, surrounding nerve roots or blood vessels that supply the cord. Symptoms are variable with the extent and the level of the spinal cord tumour. Common symptoms include back pain that may radiate, numbness and tingling to the lower extremities, muscle weakness in the legs, difficulty walking and loss of bowel and bladder control (incontinence). (27 Sep 1997) |
| spinal tumour | A spinal cord tumour is a aggregate if cells that form a mass that can compress the spinal cord. Spinal cord tumours may arise from local structures (for example meninges) or from a cancer from a distant site (i.e. Metastasis). Regardless of the aetiology, all spinal cord tumours cause symptoms from compression on the spinal cord, surrounding nerve roots or blood vessels that supply the cord. Symptoms are variable with the extent and the level of the spinal cord tumour. Common symptoms include back pain that may radiate, numbness and tingling to the lower extremities, muscle weakness in the legs, difficulty walking and loss of bowel and bladder control (incontinence). (27 Sep 1997) |