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REMA repetitive excess mixed anhydride
TMA tetramethylammonium; thrombotic microangiopathy; thyroid microsomal antibody; transcortical mixed ap...
KMLE ÀÚµ¿ÃßÃâ ÀÇÇоà¾î »çÀü À¯»ç °Ë»ö °á°ú : 5 ÆäÀÌÁö: 11
MECLR mixed epidermal cell - T lymphocyte reaction
MFO mixed function oxidase system
MLR mixed leucocyte response
MLTC mixed leukocyte tumor cell culture
(MLR mixed lymphocyte culture
CancerWEB ¿µ¿µ ÀÇÇлçÀü À¯»ç °Ë»ö °á°ú : 15 ÆäÀÌÁö: 11
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)
sertoli cell tumour A rare benign tumour of the testis that histologically resembles the foetal testis. There are three varieties: diffuse stromal, mixed (stromal and epithelial), and tubular (epithelial). Sertoli cells in the epithelial elements may produce oestrogen and cause feminization.
(12 Dec 1998)
sertoli-leydig cell tumour An ovarian tumour usually of low-grade malignancy occurring most frequently in the third and fourth decades, with 75% seen in women under 40. It is rare, representing less than .02% of ovarian cancers. The tumour typically produces androgens with virilization being noted in 70-85% of the patients. (holland et al., cancer medicine, 3d ed, p1684)
(12 Dec 1998)
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)
squamous odontogenic tumour A benign epithelial odontogenic tumour thought to arise from the epithelial cell rests of Malassez; appears clinically as a radiolucent lesion closely associated with the tooth root and histologically as islands of squamous epithelium enclosed by a peripheral layer of flattened cells.
(05 Mar 2000)
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