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"diffuse nontoxic goiter"¿¡ ´ëÇÑ °Ë»ö °á°úÀÔ´Ï´Ù. °Ë»ö °á°ú º¸´Â µµÁß¿¡ Tab ۸¦ ´©¸£½Ã¸é °Ë»ö âÀÌ ¼±Åõ˴ϴÙ.
À̰ÍÀ» ¿øÇϼ̽À´Ï±î?
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  • ¿µ¹®
    ÇѱÛ
  • follicular goiter
    ¼ÒÆ÷°©»ó»ùÁ¾
  • familial goiter
    °¡Á·¼º°©»ó»ùÁ¾
  • goiter
    °©»ó»ùÁ¾, °©»ó¼±Á¾, °íÀÌÅÍ
  • intrathoracic goiter
    °¡½¿³»°©»ó»ùÁ¾
  • intratracheal goiter
    ±â°ü³»°©»ó»ùÁ¾
  • lingual goiter
    Çô°©»ó»ùÁ¾
  • lymphadenoid goiter
    ¸²ÇÁ»ùÁ¾¸ð¾ç°©»ó»ùÁ¾
  • lymphomatous goiter
    ¸²ÇÁÁ¾°©»ó»ùÁ¾
  • nodular goiter
    °áÀý°©»ó»ùÁ¾
  • plunging goiter
    À̵¿°©»ó»ùÁ¾
  • retrosternal goiter
    º¹Àå»ÀµÚ°©»ó»ùÁ¾
  • retrovascular goiter
    Ç÷°üµÚ°©»ó»ùÁ¾
  • sporadic goiter
    »ê¹ß°©»ó»ùÁ¾, »ê¹ß°íÀÌÅÍ
  • substernal goiter
    º¹Àå»À¹Ø°©»ó»ùÁ¾, Èä°ñÇϰíÀÌÅÍ
  • simple goiter
    ´Ü¼ø°©»ó»ùÁ¾, ´Ü¼ø°íÀÌÅÍ
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  • ¿µ¹®
    ÇѱÛ
  • goiter
    °©»ó»ùÁ¾, ¹æÆÐ»ùÁ¾
  • intrathoracic goiter
    °¡½¿³»°©»ó»ùÁ¾, °¡½¿³»¹æÆÐ»ùÁ¾
  • intratracheal goiter
    ±â°ü³»°©»ó»ùÁ¾, ±â°ü³»¹æÆÐ»ùÁ¾
  • lingual goiter
    Çô°©»ó»ùÁ¾, Çô¹æÆÐ»ùÁ¾
  • lymphadenoid goiter
    ¸²ÇÁ»ùÁ¾¸ð¾ç°©»ó»ùÁ¾, ¸²ÇÁ»ùÁ¾¸ð¾ç¹æÆÐ»ùÁ¾
  • lymphomatous goiter
    ¸²ÇÁÁ¾°©»ó»ùÁ¾, ¸²ÇÁÁ¾¹æÆÐ»ùÁ¾
  • nodular goiter
    °áÀý°©»ó»ùÁ¾, °áÀý¹æÆÐ»ùÁ¾
  • plunging goiter
    (¢¡diving goiter) À̵¿°©»ó»ùÁ¾, À̵¿¹æÆÐ»ùÁ¾
  • retrosternal goiter
    º¹Àå»ÀµÚ°©»ó»ùÁ¾, º¹Àå»ÀµÚ¹æÆÐ»ùÁ¾
  • retrovascular goiter
    Ç÷°üµÚ°©»ó»ùÁ¾, Ç÷°üµÚ¹æÆÐ»ùÁ¾
  • simple goiter
    ´Ü¼ø°©»ó»ùÁ¾, ´Ü¼ø¹æÆÐ»ùÁ¾
  • sporadic goiter
    »ê¹ß°©»ó»ùÁ¾, »ê¹ß¹æÆÐ»ùÁ¾
  • subacute diffuse glomerulonephritis
    ¾Æ±Þ¼º»êÀçÅ丮ÄáÆÏ¿°, ¾Æ±Þ¼º¹ü¹ß»ç±¸Ã¼½Å¿°
  • substernal goiter
    º¹Àå»À¹Ø°©»ó»ùÁ¾, º¹Àå»À¹Ø¹æÆÐ»ùÁ¾
  • progressive diffuse keratoderma
    ±¤¹üÀ§ÁøÇà°¢ÁúÇǺÎÁõ
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  • diffuse exfoliative erythroderma
    ¹Ì¸¸¼º<¹ü¹ß¼º> ¹Ú¸®¼º È«ÇÇÁõ.
  • diffuse external otitis
    ¹ü¹ß(¼º) ¿ÜÀ̵µ¿°
  • diffuse familial comedo
    ±¤¹üÀ§ °¡Á·¼º ¸éÆ÷
  • diffuse fascitis
  • diffuse granulomatosis
    ¹Ì¸¸¼º À°¾ÆÁ¾(Áõ).
  • diffuse inflammation
    ¹Ì¸¸¼º ¿°Áõ.
  • diffuse interstitial keratitis
    ±¤¹üÀ§°£Áú°¢¸·¿°, ¹Ì¸¸¼º°£Áú°¢¸·¿°
  • diffuse interstitial pneumonia
    ¹Ì¸¸¼º °£Áú¼º Æó·Å.
  • diffuse interstitial pulmonary disease
    ¹Ì¸¸¼º °£Áú¼º ÆóÁúȯ
  • diffuse interstitial pulmonary fibrosis
    ¹Ì¸¸¼º °£Áú¼º Æó¼¶À¯Áõ.
  • diffuse intravascular coagulation
    ¹ü¹ß¼º Ç÷°ü³»ÀÀ°í.
  • diffuse intravascular coagulopathy
    ¹ü¹ß¼º Ç÷°ü³» ÀÀ°íº´Áõ.
  • diffuse intravascular coagulopathy
    ¹Ì¸¸¼º ¹ü¹ß¼º Ç÷°ü³» ÀÀ°íº´Áõ.
  • diffuse labyrinthitis
    ¹Ì¸¸(¼º) ³»ÀÌ¿°, ¹Ì¸¸(¼º) ¹Ì·Î
  • diffuse pericementitis
    ¹Ì¸¸¼º Ä¡±Ù¸·¿°(¡­öÍÐÆØ¯æú).
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DILS Diffuse Infiltrative Lymphocytosis Syndrome
DISH Diffuse Idiopathic Skeletal Hyperostosis
DL Diffuse Lymphoblastic
DMLH Diffuse Mixed Lymphocytic Histiocytic
DPDL Diffuse Poorly Differentiated Lymphocytic
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DIT Diffuse Intimal Thickening
DLBCL Diffuse Large B-cell Lymphoma
DLBD Diffuse Lewy body disease
DNIC diffuse noxious inhibitory control
DA Diffuse adherence
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endemic goiter Goiter, usually of simple type, prevalent in certain regions where dietary intake of iodine is suboptimal.
(05 Mar 2000)
exophthalmic goiter Any of the various forms of hyperthyroidism in which the thyroid gland is enlarged and exophthalmos is present.
(05 Mar 2000)
familial goiter A group of heritable thyroid disorders in which goiter is commonly apparent first during childhood; often associated with skeletal and/or mental retardation, and with other signs of hypothyroidism that may develop with age. Various types of familial goiter have been identified: 1) iodide transport defect, in which the gland is unable to concentrate iodide; 2) organification defect, in which the iodination of tyrosine is defective; 3) Pendred's syndrome; 4) coupling defect, in which cretinism results from defective coupling of iodotyrosines to form iodothyronines; 5) iodotyrosine deiodinase defect, in which deiodination of iodotyrosine is defective, considerable glandular loss of these hormonal precursors occurs, and cretinism may be present; 6) plasma iodoprotein disorder, in which an abnormal iodinated serum protein that is insoluble in acidic butanol is present; 7) hereditary hyperthyroidism.
(05 Mar 2000)
fibrous goiter A firm hyperplasia of the thyroid and its capsule.
(05 Mar 2000)
follicular goiter A form of goiter in which there is a great increase in the follicles with proliferation of the epithelium.
Synonym: follicular goiter.
(05 Mar 2000)
lingual goiter A tumour of thyroid tissue involving the embryonic rudiment at the base of the tongue.
(05 Mar 2000)
lymphadenoid goiter <endocrinology> Inflammation of the thyroid gland without the formation of pus. Noninfectious nonbacterial thyroid inflammation.
(27 Sep 1997)
cerebral sclerosis, diffuse Diffuse progressive degeneration of the white matter of the brain, accompanied by mental deterioration, severe motor disturbances, and early death.
(12 Dec 1998)
chronic diffuse sclerosing osteomyelitis A proliferative reaction of bone to a low-grade infection of the jaws; most often seen in middle-aged or older black women as extensive, often bilateral radio-opacities of the mandible and maxilla.
(05 Mar 2000)
hyperostosis, diffuse idiopathic skeletal A disease of elderly men characterised by large osteophytes that bridge vertebrae and ossification of ligaments and tendon insertions.
(12 Dec 1998)
diffuse Not definitely limited or localised, widely distributed.
Origin: L. Dis = apart, fundere = to pour
(18 Nov 1997)
diffuse abdominal calcification <radiology> Ovarian cystadenocarcinoma (psammomatous Calcium), pseudomyxoma peritonei, pseudomucinous cystadenoma of ovary, mucocele of appendix, undifferentiated abdominal malignancy, TB peritonitis, oil granulomata, meconium peritonitis
(12 Dec 1998)
diffuse abscess A collection of pus not circumscribed by a well-defined capsule.
(05 Mar 2000)
diffuse aneurysm An aneurysm that has enlarged and spread to the surrounding tissues in consequence of rupture of its walls.
Synonym: consecutive aneurysm.
(05 Mar 2000)
diffuse angiokeratoma <disease> Lysosomal storage disease caused by a deficiency of alpha-galactosidase a and resulting in an accumulation of globotriaosylceramide in the renal and cardiovascular systems.
The disease is characterised by telangiectatic skin lesions, renal failure, and disturbances of the cardiovascular, gastrointestinal, and central nervous systems.
Inheritance: x-linked.
(08 Mar 2000)
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