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50 Cards in this Set

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  • Back
Low grade ovarian tumor, 30% are bilateral, can spread locally via peritoneum, mutations in K-Ras or BRAF oncogene with rare mutation in p53
Serous Adenocarcinoma
High grade ovarian tumor with mutation in p53, but lacks mutations in K-ras or BRAF, usually arises in women with BRACA 1 or 2, 60% are bilateral, invasive peritoneal spread with rapidly progressive course.
Serous Adenocarcinoma (high-grade)
Ovarian tumor, occurs in middle-adult life, 80% are benign, commonly have K-ras mutation, characterized by lining with tall columnar epithelial cells
Mucinous Tumor
This tumor occurs from 40-70 years old, are cystic with solid component, ppl with low parity or BRCA 1 or 2 are at higher risk, stromal invasion, and psammonma bodies.
Serous Carcinoma
About 30% of tumors, usually in middle life, can be very large, are multilocular with tenacious mucin filling cysts, and smoking is a risk factor.
Mucinous Cystadenomas
This tumor causes extensive mucinous ascites with cystic epithelial implants on peritoneal surfaces, appendix is source.
Pseudomyxomatous Peritonei
This timor may coexist with endometriosis, or endometrial hyperplasia/carcinoma. 40% are bilateral. Commonly have mutations in PTEN and K-ras.
Endometriod Tumor
This tumor is considered a variant of endometrioid carcinoma, of mullerian origin, 40% bilateral, has hobnail cell.
Clear Cell Adenocarcinoma
Tumor characterized by large epithelial cells with abundant clear cytoplasm similar to hypersecretory gestational endometrium.
Clear cell adenocarcinoma
This is a solid tumor composed of epithelial cells resembling those of the urinary tract (transitional cells). Usually found incidently, 6% are bilateral.
Brenner Tumor
Adenofibroma in which the epithelial component consists of nests of transitional-type epithelial cells. Has Walthard rests, usually benign.
Brenner Tumor
Cystic tumor containing sebaceous material and hair. Are all XX and benign. Are bilateral in 15% of cases. Often present with abdominal or pelvic pain. Has glands, hair shafts, skin, teeth and other adnexal structures.
Mature Teratoma
This rare tumor is composed of embryonal and immature fetal tissue. It is usually found in prepubertal young women, often presents with abdominal or pelvic pain, has neuroepithelium. Carries risk for subsequent malignant extra-ovarian spread.
Immature teratoma
This monodermal teratoma has thyroid tissue and may be associated with papillary thyroid carcinoma
Monodermal Teratoma
Tumor contains primitive neuroepithelium and usually presents in the 2nd decade of life.
Immature malignant teratoma
Primordial germ cell tumor, has fibrous septa with lymphocytes, responsive to chemotherapy, may occur in patients with gonadal dygenesis, may have elevated levels of chorionic gonadotropin and syncytiotrophoblastic giant cells.
Dysgerminoma
Expresses Oct3, Oct4, and c-KIT
Dysgerminoma
Germ cell tumor with reticular arrangement of primitive round cells with papillary structures. Rich in AFP and alpha 1 -antitrypsin. Most patients are children or young women with pelvic pain and rapidly developing pelvic mass.
Yolk Sac tumor
This germ cell tumor has a chacteristic glomerulus-like structure composed of a central blood vessel enveloped by germ cells (schiller Duval bodies). Usually appear in a single ovary but grow rapidly and aggressively.
Yolk Sac tumor
The ovarian primary tumors are aggressive and generally metastasize widely through the bloodstream to the lungs, liver, bone etc. Composed of malignant placental-like tissue. Have high levels of HCG. Usually exist in combination with other germ cell tumors.
Choriocarcinoma
This tumor is solid, spherical, or slightly lobulated, encapsulated, and associated with right hydrothorax and ascites
Fibroma
Composed of well-differentiated fibroblasts and interspersed collagenous tissue with focal areas of thecal differentiation.
Fibroma
Triad consisting of ovarian tumor, right hydrothorax, and ascites.
Meig's Syndrome
These tumors are potentially malignant, cause virilization, occur in 2nd and 3rd decades, are unilateral, and have crystals of reinke.
Sertoli-Leydig cell tumors
Systemic syndrome characterized by widespread maternal endothelial dysfunction, usually occurs in the last trimester of pregnancy and is caused by placental ischemia due to impaired vasodilation- causes maternal hypertension
Preeclampsia
Presents in pregnant women with hypertension, proteinuria and edema
Preeclampsia- if seizures are present it is eclampsia
This is a life-threatening obstetric complication usually associated with preeclampsia, characterized by hemolytic anemia, elevated liver enzymes, and low platelets. May preceed DIC
HELLP Syndrome
This complication of pregnancy will have elevated fibrin degradation products and elevated lactate dehydrogenase (marker for hemolysis)
HELLP Syndrome
This condition is characterized by abnormal vaginal bleeding, honeycombed and abnormally enlarged uterus, and a snowstorm appearance on sonogram.
Complete Hyatidaform Mole
This condition has cystic swelling of chorionic villi and proliferation of chorionic epithelium, is the most common precursor of choriocarcinoma and has highly elevated hCG levels.
Complete Hyatidaform Mole
This condition is a cystic swelling of chorionic villi and epihelium that has some fetal parts and abnormal placental tissue
Incomplete Hyatidaform Mole
Occurs during the first month of breast feeding, associated with staph or strep infection, breasts are erythematous and painful. In the beginning, only one duct system or sector of the breast is involved
Acute mastitis
This nonproliferative change in the breast causes a lumpy, bumpy feel that causes the breast to appear dense with cysts on radiography.
Fibrocystic breast change
Has three characteristics
1. Cystic change with apocrine metaplasia
2. Fibrosis
3. Adenosis
Fibrocystic Breast Change
A benign condition that produces an excess of tissue growth in the lobules of the breast
Sclerosing Adenosis
This condition causes multiple, small, firm tender lumps in the breast. Presents with recurring pain that tends to be linked to the menstrual cycle. Can be seen as a radiologic density or calcification.
Sclerosing Adenosis
On histologic examination, this condition causes doubling of the acini in the ducts with prominent myoepithelial cells.
Sclerosing Adenosis
This is the most common benign tumor of the breast, occurs in the 20s and 30s, are multiple and bilateral, and usually presents with a palpable mass in younger women and a mammographic density/calcification in older women
Fibroadenoma
This breast tumor grows as spherical nodules that are usually sharply circumscribed and freely movable.
Fibroadenoma
This breast tumor is most common in women in their 40s or 50s. Typically presents with a palpable, firm mass that can increase significantly in size in just a few weeks. It is distinguished from fibroadenomas by its cellularity, mitotic rate, nuclear polymorphism, stromal overgrowth and infiltrative borders.
Phylloides Tumor
This is an extension of ductal carcinoma in situ into lactiferous ducts and skin of the nipple.
Paget's Disease of the Breast
Presents with scaling red rash similar to eczema that starts at the nipple and spreads to include the areola with nipple retraction - ductal carcinoma in situ that spreads along duct to the external skin
Paget's Disease of the Breast
Erythematous breast with dimpling like an orange due to fixed openings of the sweat glands. The underlying carcinoma is usually diffusely infiltrative and typically doesn't form a discrete palpable mass
Inflammatory Breast Carcinoma
This condition is often associated with either ovarian or adrenal tumor. The principle features are obesity, anovulation or amenorrhea, acne and hirsutism. Gynocologic u/s looks for small ovarian follicles and may have thickened, white smooth outer surface of the ovary
Polycystic ovarian syndrome
This condition is characterized by an ovarian tumor with ascites and pleural effusion. Has elevated CA-125 tumor marker
Meigs Syndrome
This is an uncommon tumor commonly associated with cancer of the appendix. Known for its production of mucus in the abdominal cavity that rarely spreads through the abdominal cavity. Its characterized by mucin and scattered cancer cells in the abdomen but not in the liver or other sites of mets.
Psuedomyxoma Peritoneri
This condition is associated with abdominal pain and distension, digestive disorders and diagnosis is confirmed by cystic epithelial implants on the peritoneal surfaces, adhesions, and frequently mucinous tumors of the ovaries,
Psuedomyxoma Peritoneri
Syndrome includes flushing and diarhhea, heart failure and bronchoconstriction. The most useful initial test is the 24 hour urine levels of 5-hydroxyindolacetic acid (a product of serotonin metabolism)
Carcinoid Syndrome
Rare form of mature teratoma that contains mostly thyroid tissue- leads to hyperthyroidism and are usually benign. Immunohistochemical staining for thyroglobulin
Struma Ovarii
Metastatic ovarian malignancy whose primary site arose in the GI tract or breast. Has signet ring cells. Patient presents with abdominal pain, bloating, vaginal bleeding, and pain during intercourse.
Krukenberg Tumor