Testicular Yolk Sac Tumor Adults

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Testicular Yolk Sac Tumor Adults

High Alpha- Fetoprotein Levels LIVESTRONG. COMAlpha- fetoprotein, or AFP, is a protein found normally in abundance in the developing fetus. Only very low levels of the protein are present in healthy children and adults, except for pregnant women. Elevated blood levels of AFP can be associated with liver disease, certain kinds of cancer and abnormal pregnancies. Alpha- fetoprotein is a major protein produced by the fetal yolk sac, a part of the early embryo that eventually disappears, and the fetal liver.

Some of this protein leaks into the amniotic fluid and across the placenta, resulting in typically elevated AFP levels in pregnant women. Newborns have very high AFP levels, which drop rapidly over the first few months of life to the very low levels seen in children and adults, according to Lab Tests Online.

Also called endodermal sinus tumor of Teilum (endoderm is embryonic layer closest to yolk sac) Numerous patterns that recapitulate the yolk sac, allantois and extra. Alpha fetoprotein or AFP as a tumor marker in blood for liver cancer and certain types of testicular cancer. 20.1 IME List MedDRA Code SOC Name PT Name Comment Primary SOC Change 10078862 Blood and lymphatic system disorders Hyperleukocytosis X 10078778 IDH differentiation. UpToDate, electronic clinical resource tool for physicians and patients that provides information on Adult Primary Care and Internal Medicine, Allergy and Immunology.

Information for understanding testicular cancer. Statistics, Signs and Symptoms, Risk Factors, Diagnosis and Testing, Types, Staging and Treatments. Looking for online definition of tumor in the Medical Dictionary? tumor explanation free. What is tumor? Meaning of tumor medical term. What does tumor mean? A teratoma is a tumor made up of several different types of tissue, such as hair, muscle, or bone. They typically form in the ovaries, testicles, or tailbone and less.

Normal adult levels are less than 6 ng/m. L, but can vary between different laboratories performing the test. Liver cells are the main source of AFP found in healthy non- pregnant people. Mild to moderate elevations of AFP blood levels are seen with cirrhosis, viral hepatitis, other causes of chronic liver damage and normal pregnancy. Repair and regeneration of liver cells with liver disease results in release of additional AFP into the bloodstream, and AFP from the fetus leads to the higher levels seen in pregnant women. The rise in AFP in these conditions is typically less than 5. L and can fluctuate with the activity of the disease or the stage of pregnancy, according to the Family Practice Notebook.

Small numbers of healthy people also have higher than expected AFP levels on an inherited basis and should not be confused with evidence of disease. A woman’s AFP level rises in a predictable manner throughout pregnancy as the fetus grows but can be altered by problems with the pregnancy. By comparing the woman’s measured AFP level to the average level of all women at the same gestational age, the result can be used as a screening test for possible problems in the developing fetus, according to Mayo Medical Laboratories.

Abnormally high AFP levels indicate the possibility of a neural tube defect, or abnormality of the baby’s developing brain and spinal cord, as well as other developmental abnormalities, congenital kidney disease or increased risk of fetal loss. The test is not diagnostic, but indicates further evaluation should be performed. Higher AFP levels are also seen normally in multiple pregnancies, such as with twins or triplets, and accurate dating of gestational age is critical for comparison purposes in screening.

Certain tumors can produce elevated AFP blood levels, particularly hepatocellular carcinoma, or primary liver cancer, and some types of testicular and ovarian cancer. AFP is elevated in about 8.

The high AFP levels associated with a tumor should return to normal following successful treatment, with rising levels after treatment indicating new tumor growth or recurrence. People with cirrhosis and chronic hepatitis have an increased risk of developing liver cancer, and if their already moderately elevated AFP levels increase suddenly the change could indicate the emergence of cancer. Abnormal results should always be discussed with a health care practitioner.

AFP is a tumor marker for liver and testicular cancer. Alpha Fetoprotein Tumor MarkerAlpha fetoprotein (AFP) is a 6.

D single chain polypeptide which is similar in size and structure to human serum albumin. In human embryos, AFP is first made in the yolk sac and later in the fetal liver.

As the fetal liver matures, it gradually switches to albumin synthesis. In the fetus, AFP synthesis gradually declines to the normal adult range by 6 to 1. During pregnancy, AFP levels in maternal serum rise steadily to a peak of approximately 5. L at about 3. 2 weeks of gestation. Thereafter, they decline until term.

As a tumor marker, AFP is useful in detecting germ cell tumors of the ovary and testis, primary hepatocellular carcinoma in adults, and hepatoblastoma in children. AFP is not specific for these cancers. In addition to the elevations seen during pregnancy, serum values can be high in patients with a variety of liver diseases. Modest elevations of AFP occur in about 2. The highest values are seen in acute viral hepatitis, which may reach 5.

L. AFP levels begin to rise, when transaminases are beginning to decline, suggesting that AFP synthesis is related to hepatocellular regeneration. Chronic elevations in patients with cirrhosis may also reflect ongoing necrosis and regeneration. AFP levels are useful in screening for liver cancer in areas of high incidence, such as Southeast Asia, South Africa, China, and Alaska. The sensitivity of AFP for hepatoma is 6. AFP levels greater than 3. L are found in asymptomatic individuals with small, surgically resectable tumors. The most common cause of false positive AFP elevations is pregnancy.

General population screening in countries, such as the U. S., where the incidence of hepatoma is much lower, is not as effective. However, selective screening of high risk groups, such as patients with cirrhosis, chronic active hepatitis, and hemochromatosis is probably warranted. AFP levels are useful in distinguishing hepatocellular carcinoma from benign hepatic disorders in symptomatic patients. The magnitude of AFP elevation is helpful in assessing the likelihood of cancer. Serum AFP concentrations above 5.

L are essentially diagnostic of an AFP producing cancer. One half of the cases of hepatoma have AFP levels > 1. L at diagnosis. A tumor must be > 3 cm in diameter to produce an AFP level of this magnitude. Serial measurements are useful since elevations secondary to nonmalignant diseases are usually temporary, while increases secondary to malignancies continue to increase. In benign liver disease, AFP levels are usually elevated only transiently, tend to rise only during the regenerative phase after peak elevation of liver enzymes, and rarely exceed 5.

L. Pretreatment AFP levels in hepatoma patients do not significantly correlate with response to therapy or survival time. Posttreatment AFP levels correlate well with response to therapy.

Failure of AFP levels to return to normal after surgery indicates incomplete resection or the presence of metastases. The half- life of serum AFP is approximately 5 days. The failure of AFP levels to decline at this rate suggests residual cancer. AFP levels also correlate with response to chemotherapy. Serial measurements of AFP can be used to detect relapses before they become clinically apparent. The seminiferous tubules contain two cell populations: supporting (Sertoli) cells and spermatogenic cells (spermatogonia). Clusters of Leydig cells, which secrete androgens, are embedded in the interstitial stroma.

Ninety five percent of all primary testicular tumors arise from germinal cells and 5% arise from Sertoli and Leydig cells. Germinal neoplasms are divided into seminoma and nonseminomatous germ cell tumors. Seminoma is the most common germinal cancer, accounting for 4. Germ cell tumors are best diagnosed using a combination of AFP and beta h. CG, since these tumors may be comprised of mixtures of seminoma, yolk sac, and embryonal carcinoma cells. AFP is produced by embryonal carcinoma, teratocarcinoma, yolk sac tumor, or compbined tumors. It is usually not produced by pure seminomas.

CG is produced by choriocarcinomas, 6. Seminomas that secrete h. CG usually produce serum levels less than 1. U/m. L.% Patients with Elevated h. CG or AFP Cancerh. CGAFPEither. Seminoma. Seminoma w/ metastasis.

Embryonal. 60. 70. Choriocarcinoma. 10.

Yolk Sac. 25. 75. Teratoma, mature. The sensitivity of AFP for non- seminomatous germ cell testicular tumors is 5. CG is 3. 0 to 6. 0%, and the sensitivity of both exceeds 6. Therefore, the combined use of AFP and h. CG is more effective than either marker alone. Serum levels may reach very high values; AFP may reach 8.

L and hc. G may reach one million U/m. L. The pattern of tumor marker positivity may also aid in the differential diagnosis of germ cell tumors.

Elevation of AFP in any tumor considered a pure seminoma by biopsy, should be reevaluated for germ cell elements, since this may influence therapeutic decisions.

Teratoma - Wikipedia. Teratoma. Micrograph of a teratoma showing tissue from all three germ layers: mesoderm (immature cartilage - left- upper), endoderm (gastrointestinal glands - center- bottom) and ectoderm (epidermis - right)Specialty.

Gynecology, oncology. Symptoms. Minimal, painless lump[1][2]Complications. Ovarian torsion, testicular torsion, hydrops fetalis[2][3][1]Types. Mature, immature[4]Causes. Unknown[2]Diagnostic method. Tissue biopsy[2]Similar conditions.

Lipoma, dermoid, myelomeningocele[5]Treatment. Surgery, chemotherapy[5][6]Frequency. A teratoma is a tumor made up of several different types of tissue, such as hair, muscle, or bone.[4] They typically form in the ovaries, testicles, or tailbone and less commonly in other areas.[4] Symptoms may be minimal if the tumor is small.[2] A testicular teratoma may present as a painless lump.[1] Complications may include ovarian torsion, testicular torsion, or hydrops fetalis.[3][1][2]They are a type of germ cell tumor (a tumor that begins in the cells that give rise to sperm or eggs).[4][8] They are divided into two types mature and immature.[4] Mature teratomas include dermoid cysts and are generally benign.[8] Immature teratomas may be cancerous.[4][9] Most ovarian teratomas are mature.[1. In adults, testicular teratomas are generally cancerous.[1. Definitive diagnosis is based on a tissue biopsy.[2]Treatment of tailbone, testicular, and ovarian teratomas is generally by surgery.[5][6][1. Testicular and immature ovarian teratomas are also frequently treated with chemotherapy.[1.

Teratomas occur in the tailbone in about 1 in 3. Best Places For Young Adults To Live In Florida on this page. Females are affected more often than males.[5] Ovarian teratomas represent about a quarter of ovarian tumors and are typically noticed during middle age.[1. Testicular teratomas represent almost half of testicular cancers.[1. They can occur in both children and adults.[1. The term comes from the Greek words for "monster" and "tumor".[1. Signs and symptoms[edit]Teratomas maybe found in babies, children, and adults.

Teratomas of embryonal origin are most often found in babies at birth, in young children, and, since the advent of ultrasound imaging, in fetuses. The most commonly diagnosed fetal teratomas are sacrococcygeal teratoma (Altman types I, II, and III) and cervical (neck) teratoma. Because these teratomas project from the fetal body into the surrounding amniotic fluid, they can be seen during routine prenatal ultrasound exams. Teratomas within the fetal body are less easily seen with ultrasound; for these, MRI of the pregnant uterus is more informative.[1. Complications[edit]Teratomas are not dangerous for the fetus unless there is either a mass effect or a large amount of blood flow through the tumor (known as vascular steal).

The mass effect frequently consists of obstruction of normal passage of fluids from surrounding organs. The vascular steal can place a strain on the growing heart of the fetus, even resulting in heart failure, and thus must be monitored by fetal echocardiography. Teratomas can cause an autoimmune illness called Anti N- methyl- D- aspartate (NMDA) Receptor Encephalitis.

After surgery, there is a risk of regrowth in place, or in nearby organs.[1. Mature teratoma[edit]. Mature teratoma of the mediastinum. A horizontal slice of the resected tumor reveals fibrofatty tissue, calcified areas, and a few cystic spaces lined with smooth membrane and containing a hair. In the left lower corner, the involved B5 bronchus is evident. A mature teratoma is a grade 0 teratoma. Mature teratomas are highly variable in form and histology, and may be solid, cystic, or a combination of solid and cystic.

A mature teratoma often contains several different types of tissue such as skin, muscle, and bone. Skin may surround a cyst and grow abundant hair (see dermoid cyst).

Mature teratomas generally are benign; malignant mature teratomas are of several distinct types. Dermoid cyst[edit]. A small (4 cm) dermoid cyst of an ovary, discovered during a C- section.

A dermoid cyst is a mature cystic teratoma containing hair (sometimes very abundant) and other structures characteristic of normal skin and other tissues derived from the ectoderm. The term is most often applied to teratoma on the skull sutures and in the ovaries of females. Fetus in fetu and fetiform teratoma[edit]Fetus in fetu and fetiform teratoma are rare forms of mature teratoma that include one or more components resembling a malformed fetus. Both forms may contain or appear to contain complete organ systems, even major body parts such as torso or limbs. Fetus in fetu differs from fetiform teratoma in having an apparent spine and bilateral symmetry.[1. Most authorities agree that fetiform teratomas are highly developed mature teratomas; the natural history of fetus in fetu is controversial.[1.