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neoplázia endokrinná mnohopočetná, typ 2b
SYS d018814 LBL 00000cz--a2200000o--4500 005 20250606214148.1 008 940523|||anznnbabn-----------|-a|a------ 040 $b slo $a DNLM $d BA006 065 $a C04.588.322.400.510 065 $a C04.651.600.510 065 $a C04.700.630.510 065 $a C16.320.700.630.510 065 $a C19.344.400.510 066 $a 01 $c 03 150 $a neoplázia endokrinná mnohopočetná, typ 2b $x BL $x BS $x CF $x CH $x CI $x CL $x CN $x CO $x DG $x DH $x DI $x DT $x EC $x EH $x EM $x EN $x EP $x ET $x GE $x HI $x IM $x ME $x MI $x MO $x NU $x PA $x PC $x PP $x PS $x PX $x RH $x RT $x SC $x SU $x TH $x UL $x UR $x VE $x VI $2 slo 450 $w v $a MEN 2b $2 eng 450 $w v $a MEN 3 $2 eng 450 $w v $a Neoplasia, Multiple Endocrine Type 2b $2 eng 450 $w v $a Neoplasms, Multiple Endocrine Type 2b $2 eng 450 $w v $a nádory endokrinné mnohopočetné, typ 2b $2 slo 450 $w v $a MEN2b $2 slo 450 $w v $a MEN 2b $2 slo 450 $w v $a MEN 3 $2 slo 550 $7 sllk_us_auth*d010673 $Y Pheochromocytoma $w b $a feochromocytóm 550 $7 sllk_us_auth*d018276 $Y Carcinoma, Medullary $w b $a karcinóm medulárny 665 $a 1995; MEA III & MEN III see NEOPLASMS, MULTIPLE ENDOCRINE 1983-1994 $2 eng 665 $a Multiple Endocrine Neoplasia (1975-1994) $2 eng 680 9-
$i Similar to MEN2A, it is also caused by mutations of the MEN2 gene, also known as the RET proto-oncogene. Its clinical symptoms include medullary carcinoma (CARCINOMA, MEDULLARY) of THYROID GLAND and PHEOCHROMOCYTOMA of ADRENAL MEDULLA (50%). Unlike MEN2a, MEN2b does not involve PARATHYROID NEOPLASMS. It can be distinguished from MEN2A by its neural abnormalities such as mucosal NEUROMAS on EYELIDS; LIP; and TONGUE, and ganglioneuromatosis of GASTROINTESTINAL TRACT leading to MEGACOLON. It is an autosomal dominant inherited disease. $2 eng 680 $a coordinate IM with specific endocrine/neoplasm pre-coordinates (IM) + specific histological type (IM) if pertinent $2 eng 750 -2
$a Multiple Endocrine Neoplasia Type 2b $2 eng 980 $x M
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