| CMAP | compound muscle (or motor) action potential |
|---|---|
| CPM | circumference of papillary muscle |
| CTM | cardiotachometer; Chlortrimeton; cricothyroid muscle; computed tomographic myelography |
| DMC | demeclocycline; di(p-chlorophenyl)methylcarbinol; direct microscopic count; duration of muscle contr... |
| DMR | depolarizing muscle relaxant; Diploma in Medical Radiology |
| haarscheibe tumour | Dominantly inherited or nonfamilial elliptical parafollicular mesenchymal hamartomas. Synonym: haarscheibe tumour. (05 Mar 2000) |
|---|---|
| crown gall tumour | A disease which afflicts dicot plants, caused by the bacteria Agrobacterium tumefaciens. The disease causes large tumours to form in the roots or in the stems nearest the roots, deforming the plant along its base (where it meets the ground). (09 Oct 1997) |
| potato tumour of neck | A firm nodular mass in the neck, usually a carotid body tumour (chemodectoma). (05 Mar 2000) |
| Pott's puffy tumour | A circumscribed swelling of the scalp indicating an underlying osteitis of the skull or an extradural abscess. (05 Mar 2000) |
| pregnancy tumour | A pyogenic granuloma developing on the gingiva during pregnancy; thought to be related to hormonally altered response of the oral mucous membranes to local irritants such as bacterial plaque on adjacent teeth. Synonym: pregnancy tumour. (05 Mar 2000) |
| 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) |
| 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) |
| hilar cell tumour of ovary | A small benign masculinizing ovarian tumour derived from hilar cells, which resemble Leydig cells of the testis. (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) |
| Hurthle cell tumour | A neoplasm of the thyroid gland composed of polyhedral acidophilic cells, thought by some to be oncocytes; it may be benign or malignant, the behaviour of the latter depending on the general microscopic pattern, whether follicular, papillary, or undifferentiated. See: Hurthle cell adenoma. Synonym: Hurthle cell carcinoma. (05 Mar 2000) |