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Path T4 M/c
M/C
| Question | Answer |
|---|---|
| m/c AML | Drugs |
| m/c child/adol CA | ALL |
| m/c 25-60 CA | CML |
| M/c in adults >50yo | MDS |
| m/c Caribbean & Japan | HTLV |
| m/c Asia, SA | EBV nasopharyngeal lymphoma |
| M/c 1* malignant tumor of bone | Mult Myeloma |
| m/c ca in ♂, old, AA>Cauc, US>Asia | PROSTATIC ADENOCARCINOMA |
| M/c pure GCT | Seminoma |
| m/c ≤3yo, ↑AFP | YST (lace-like pattern |
| M/c sites: ovaries/FT’s, uterine lig, rectovag sep, pelvic peritoneum | ENDOMETRIOSIS |
| M/c ovarian malignancy in girls, <35yo | GCT |
| M/c breast, GI | BrCA, GI |
| (m/c) ENDOMETRIAL CARCINOMA | Endometrioid adeno-ca |
| M/c Benign ENDOMETRIAL TUMORS | endometrial stromal nodule |
| m/c condition of ♀ br | FIBROCYSTIC CHANGES |
| m/c benign tumor of br | Fibroadenoma |
| m/c invasive brCA | Infil duct ca |
| m/c Lymphatic spread of BrCA | nodes of axilla & internal mammary a |
| m/c IV. INVASIVE CERVICAL CANCER | large cell nonkeratinizing SCC |
| m/c - Metachromatic leukodystrophy | late infantile form |
| M/c urea cycle d/o | Ornithine transcarbamylase def: X-linked Dom |
| M/c affected: Irish, Scottish | PKU |
| M/c affected: N European | MCADD |
| M/c from 21-OHase def; ↑Italian | Congenital Adrenal Hyperplasia |
| M/c MR | Trisomy 21: 1/700 |
| m/c cause of hypogonadism in ♂ | 47, XXY (KLINEFELTER) |
| M/c inherited cause of MR | FRAGILE X SYNDROME: 1/4k-M, 1/8k-F |
| m/c, most severe LHON | G11778A |
Created by:
mcafej02
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