Neoplasm
Neoplasm |Cell type |Characteristics |Malignant Potential/Prognosis |Risk factors/epidemiology | |
|Ovarian – Surface Epithelial Tumors (65-70% of ovarian neoplasms) – tumor marker = CA-125 |
| | |Frequently bilateral | |(Risk factors for all ovarian neoplasms: |
|Serous tumors |Ciliated epithelium |S. cystadenoma: unilocular or paucilocular cyst(s) lined by simple serous ep. |Benign to malignant, dep. on type |nulliparity, low parity, family history) |
| | |Borderline s. tumor: complex papillary growth pattern w/atypia, psammoma bodies, | |Most common ovarian neoplasms (40%). |
| | |no stromal invasion | |Benign: 40 yrs. |
| | |Less often bilateral; multilocular; large. | | |
|Mucinous tumors |Resemble intestinal or |M. cystadenoma: 80% |Benign to malignant, dep. on type |As above, but 10-15% of ovarian neoplasms.|
| |endocervical epithelium |Borderline M. tumor: 10%; ↑complexity, glandular/papillary growth w/atypia, | | |
| | |stratification of cells. May resemble colon adenoma. | | |
| | |M. adenocarcinoma: 10%; as above, more complex, w/ stromal invasion. Rarely a/w | | |
| | |pseudomyxoma peritonei (malignant mucinous ascites). | | |
|Endometrioid tumors |Resemble endometrial |May show squamous metaplasia. | | |
| |gland epith. |E. adenofibromas and borderline e. tumors are rare. |Most are malignant. |As above |
| | |E. adenocarcinoma: 40% bilateral, 15% coexist w/ endometriosis; solid, not | | |
| | |mucinous. | | |
|Clear cell tumors |Variant of above |40% are bilateral |All are high grade, aggressive, | |
|(adenocarcinoma) | |Cells have clear cytoplasm or “hobnail” morphology (apical nucleus). |rarely survive 5 years. |As above |
|Transitional cell tumor |Resemble bladder |Brenner tumor most common: nests of transitional epith. in fibrotic stroma, may be|Benign | |
| |urothelium |a/w mucinous tumor. 90% unilateral. | |As above |
|Ovarian – Sex Cord-Stromal Tumors (10% of ovarian neoplasms) |
|Granulosa cell tumor |Granulosa |Usually unilateral; estrogenic; may present w/post-menopausal bleeding or |Malignant but indolent course in |May occur at any age, most (2/3) |
| | |precocious puberty, rupture & hemoperitoneum. |5-25%; |post-menopausal |
| | |Small cells w/grooved “coffee-bean” nuclei; microfollicles (Call-Exner bodies) |Risk of endomet. | |
| | | |hyperplasia/carcinoma | |
|Thecoma-fibroma |Theca |90% unilateral; estrogenic (→AUB) |Risk of endomet. | |
| | |Solid stromal tumor, plump spindle cells w/cytoplasmic lipid droplets (Oil-red-O +|hyperplasia/carcinoma | |
| | |) | | |
|Sertoli-Leydig cell tumor |Sertoli & Leydig |Tubules & solid cords of cells, resemble immature testis; 50% androgenic, |Depends on differentiation & stage | |
| | |virilizing. Well to poorly differentiated. | | |
|Ovarian – Germ Cell Tumors (15-20% of ovarian neoplasms) |
|Dysgerminoma |Primitive germ cells |Analogous to seminoma in testis; Sheets of large, prim. germ cells, intervening |Radiosensitive, so good prognosis |(GCT’s in those under 35 yrs. Most common|
| | |stroma w/ lymphs, occ. syncytiotrophoblastic giant cells; hCG in ................
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