| WC | ward clerk; water closet; Weber-Christian [syndrome]; wheel chair; white cell; white cell casts; whi... |
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| MEN | Multiple Endocrine Neoplasia ; AD Trait 1. MEN Type I(= Wermer Syndro... |
| NK cell | Natural Killer cell |
| RS cell | Reed Sternberg cell |
| Tc cell | cytotoxic T cell |
| Wilms' tumour | A malignant renal tumour of young children, composed of small spindle cells and various other types of tissue, including tubules and, in some cases, structures resembling foetal glomeruli, and striated muscle and cartilage. Often inherited as an autosomal dominant trait . Synonym: adenomyosarcoma, embryoma of the kidney, nephroblastoma. (05 Mar 2000) |
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| wing-beating tumour | A coarse, irregular tumour that is most prominent when the limbs are held outstretched, reminiscent of a bird flapping its wings; due to up and down excursion of arm at abducted shoulder. Seen mainly with Wilson's disease. (05 Mar 2000) |
| mucoepidermoid tumour | A malignant epithelial tumour of glandular tissue, especially the salivary glands, characterised by acini with mucus-producing cells and by the presence of malignant squamous elements. most mucoepidermoid tumours are low-grade lesions readily cured by adequate excision. They may appear in any age group. They grow slowly. If high-grade, they behave aggressively, widely infiltrating the salivary gland and producing lymph node and distant metastases. (12 Dec 1998) |
| congenital sinus tumour | <radiology> Midline depression or tract, lined with stratified squamous epithelium, most common sites: lumbosacral area, occiput, epidermoid or dermoid cyst anywhere along tract (12 Dec 1998) |
| connective tumour | <oncology> Any tumour of the connective tissue group, such as osteoma, fibroma, sarcoma. (05 Mar 2000) |
| pontine angle tumour | A tumour in the angle formed by the cerebellum and the lateral pons, often refers to an acoustic schwannoma. (05 Mar 2000) |
| 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) |