| 영문 | ovarian cysts | 한글 | 난소낭 |
|---|---|---|---|
| 설명 | 난소에 발생한 낭. 여기에는 단순한 물혹인 낭이 있고 종양성 낭이 있다. 낭이란, 막으로 둘러 싸여져 있으며, 안에는 액체가 차있는 병터를 말한다. 이런 낭형태의 종양으로는 피부모양낭종(dermoid cyst), 낭샘종(cystadenoma) 등이 있다. 이들의 감별진단은 환자의 예후에 결정적이므로 반드시 시행되어야 하나, 그 방법은 수술에 의해서 낭종을 절제하여 병리학적으로 구분하는 수밖에 없다. |
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| 영문 | ovarian cancer | 한글 | 난소암 |
|---|---|---|---|
| 설명 | 여성의 난소에 발생하는 암. 부인과종양으로서 50세 이상 여성악성종양의 약 18%를 차지한다. 종양은 대개 복부 깊숙히 위치하므로 종양이 많이 진행된 상태에서 발견되는 수가 많으며, 또한 종양의 초기에는 증상이 거의 없는 경우가 많아 더욱 조기발견이 어렵다. 아주 다양한 종류의 암이 발생하며, 예후도 각기 그 종양의 종류에 따라 다르다. 대표적인 암으로 장성낭샘암종(serous cystadenocarcinoma), 점액낭샘암종(mucinous cystadenocarcinoma), 종자세포종(germinoma 등이 있다. 치료는 수술적 치료가 선행되어야 하지만, 많이 진행되어 이미 다른 조직으로 전이가 이루어진 상태에서는 화학요법이 선택적으로 사용된다. |
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| OCAA | Ovarian Cystadenocarcinoma Associated Antigen; Serous Mucinous Ovarian Tumor에만 나타남 |
|---|---|
| POF | pattern of failure; position of function; premature ovarian failure; primary ovarian failure; pyruva... |
| PCOS | Poly-Cystic Ovary(Ovarian) Syndrome |
| TOA | Tubo-Ovarian Abscess |
| HBOC | hereditary breast-ovarian cancer |
| MMT | Mixed Mullerian Tumours |
|---|---|
| CHO | Chinese Hamster Ovarian |
| COH | Compensatory ovarian hypertrophy |
| COH | Controlled ovarian hyperstimulation |
| EOC | Epithelial Ovarian Cancer |
| ovarian tumours | <radiology> Before age 45 most likely to be 98% benign, 2/3 of cancers in ages 40 - 65 yrs see also: ovarian stromal tumours (12 Dec 1998) |
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| ovarian stromal tumours | <radiology> Age 20 - 50 yrs, 20% of all ovarian tumours, fibroma / fibrosarcoma, granulosa-theca cell tumour, with or without oestrogens most likely to be precocious puberty, endometrial hyperplasia/carcinoma, fibrocystic breast disease, Sertoli-Leydig cell tumour, aka: arrhenoblastoma, with or without androgens most likely to be masculinization, may be mixed type (12 Dec 1998) |
|---|---|
| benign liver tumours | <radiology> EPITHELIAL TUMORS, nodular transformation, focal nodular hyperplasia, hepatocellular adenoma, MESENCHYMAL TUMORS, lipoma, myelolipoma, angiomyolipoma, leiomyoma, infantile haemangioendothelioma, haemangioma, benign mesothelioma, MIXED TISSUE TUMORS, mesenchymal hamartoma, benign teratoma, MISCELLANEOUS, adrenal rest tumours, pancreatic rest (12 Dec 1998) |
| brain tumours | Can be malignant or benign and can occur at any age. Primary brain tumours initially form in the brain tissue. Secondary brain tumours are cancers that have spread to the brain tissue (metastasized) from tissue elsewhere in the body. (12 Dec 1998) |
| pancreatic isleT-cell tumours | <radiology> Insulinoma (beta-cell), usually solitary, 85% benign, gastrinoma, small, slow-growing, multiple, 60% malignant, Zollinger-Ellison syndrome: mult. Intractable ulcers, VIPoma, vasoactive intestinal peptide (VIP), WDHA syndrome: watery diarrhoea, hypokalaemia, achlorhydria, Verner-Morrison syndrome, glucagonoma, hyperglycaemia, migratory necrolytic erythema APUDomas, associated with MEN-1 (12 Dec 1998) |
| malignant liver tumours | <radiology> EPITHELIAL TUMORS, hepatocellular, hepatoblastoma (7%), hepatocellular carcinoma (HCC) (75%), cholangiocellular (6%), cholangiocarcinomarcinoma, cystadenocarcinoma, MESENCHYMAL TUMORS, tumours of blood vessels, angiosarcoma, haemangioendothelioma, other tumours, embryonal sarcoma, fibrosarcoma, TUMORS OF MUSCLE TISSUE, leiomyosarcoma, rhabdomyosarcoma, MISCELLANEOUS, carcinosarcoma, teratoma, yolk sac tumour, carcinoid, squamous carcinoma, primary lymphoma see: benign liver tumours (12 Dec 1998) |
| venereal tumours, veterinary | Tumours most commonly seen on or near the genitalia. They are venereal, most likely transmitted through transplantation of cells by contact. Metastases have been reported. Spontaneous regression may occur. (12 Dec 1998) |
| giant cell tumours | Tumours of bone tissue or synovial or other soft tissue characterised by the presence of giant cells. The most common are giant cell tumour of tendon sheath and giant cell tumour of bone. (12 Dec 1998) |
| pineal region tumours | Type of brain tumours. (12 Dec 1998) |
| pineal tumours | <radiology> SIGNS: aqueductal obstruction most likely to be hydrocephalus, paralysis of upward gaze (due to pressure on quarigeminal plate), precocious puberty, symptoms of hypothalamic, thalamic, cerebellar or pyramidal lesion TYPES: germ-cell (teratoid) tumours, teratoma, germinoma / atypical teratoma, endodermal sinus (yolk sac) tumour, choriocarcinoma, pineal-cell tumours, pineocytoma, pineo---, others, glioma, ganglioneuroma, ganglioglioma (12 Dec 1998) |
| plant tumours | A localised proliferation of plant tissue forming a swelling or outgrowth, commonly with a characteristic shape and unlike any organ of the normal plant. Plant tumours or galls usually form in response to the action of a pathogen or a pest. (12 Dec 1998) |
| posterior fossa tumours | <radiology> Midline, medulloblastoma (hyperdense, enhances), astrocytoma (hypodense, enhances), 4th ventricle, ependymoma (most common, slow-growing, expands ventricle), medulloblastoma (usually obliterates ventricular cavity), choroid plexus papilloma (more common in lateral ventricles) (12 Dec 1998) |
| primitive neuroectodermal tumours | A type of brain tumour. Prenatal diagnosis: diagnosis before birth. Methods for prenatal diagnosis include ultrasound (of the uterus, placenta and developing foetus), chorionic villus sampling to obtain tissue for chromosome or biochemical analysis, amniocentesis to obtain amniotic fluid for the analysis of chromosmes, enzymes, DNA, etc. A growing number of birth defects and diseases are now amenable to prenatal diagnosis. Also called antenatal diagnosis. (12 Dec 1998) |
| nerve sheath tumours | Tumours arising in the sheath surrounding the axon of some nerve cells and formed by the plasma membrane of schwann cells in the peripheral nervous sytem and by oligodendrocytes in the central nervous system. Neurofibromas and neurilemmomas are the most commonly occurring tumours of this type. (12 Dec 1998) |
| neuroectodermal tumours | Malignant neoplasms arising in the neuroectoderm, the portion of the ectoderm of the early embryo that gives rise to the central and peripheral nervous systems, including some glial cells. (12 Dec 1998) |
| neuroendocrine tumours | Tumours whose cells possess secretory granules and originate from the neuroectoderm, i.e., the cells of the ectoblast or epiblast that program the neuroendocrine system. Common properties across most neuroendocrine tumours include ectopic hormone production (often via apud cells), the presence of tumour-associated antigens, and isozyme composition. (12 Dec 1998) |
제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
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제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
|---|