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