Monday, November 17, 2008

Time to Decorate for the Holidays


























Christmas starts in September in the Philippines.The San Juan medical Center joins in the celebration.It is a tradition to hold annual decorating contest in different areas of the hospital based on the theme agreed upon by the superiors.The decorations comes from cheap and recycled materials that can be found in each area.It is during these times that the creativity and innovativeness of the employees come out.I am a real admirer of their artistry- a true Filipino ingenuity.

Sunday, November 16, 2008

cat on wheel



















A cat on the wheel

we attended the POGS convention






mga gamit ko sa pagduduty.ballpen,kape,tissue,hair brush,wallet,cologne,sunblock

SJMC OBGYN Dept

























our picture in the Phil Obstetrics and Gynecology Society Convention souvenir program

Tuesday, November 11, 2008

Congenital hypothyroidism

From Wikipedia, the free encyclopedia
.
Congenital hypothyroidism
Classification and external resources
ICD-10 E00., E03.0, E03.1
ICD-9 243
Congenital hypothyroidism (CHT) is a condition of thyroid hormone deficiency present at birth. Approximately 1 in 4000 newborn infants has a severe deficiency of thyroid function, while even more have mild or partial degrees. If untreated for several months after birth, severe congenital hypothyroidism can lead to growth failure and permanent mental retardation. Treatment consists of a daily dose of thyroid hormone (thyroxine) by mouth. Because the treatment is simple, effective, and inexpensive, nearly all of the developed world practices newborn screening to detect and treat congenital hypothyroidism in the first weeks of life.




Causes
Around the world, the most common cause of congenital hypothyroidism is iodine deficiency, but in most of the developed world and areas of adequate environmental iodine, cases are due to a combination of known and unknown causes. Most commonly there is a defect of development of the thyroid gland itself, resulting in an absent (athyreosis) or underdeveloped (hypoplastic) gland. A hypoplastic gland may develop higher in the neck or even in the back of the tongue. A gland in the wrong place is referred to as ectopic, and an ectopic gland at the base or back of the tongue is a lingual thyroid. Some of these cases of developmentally abnormal glands result from genetic defects, and some are "sporadic," with no identifiable cause. One Japanese study found a statistical correlation between certain organochlorine insecticides and dioxin-like chemicals in maternal milk samples and congenital hypothyroidism.[1]

Congenital hypothyroidism can also occur due to genetic defects of thyroxine or triiodothyronine synthesis within a structurally normal gland. Among specific defects are thyrotropin (TSH) resistance, iodine trapping defect, organification defect, thyroglobulin, and iodotyrosine deiodinase deficiency. In a small proportion of cases of congenital hypothyroidism, the defect is due to a deficiency of thyroid stimulating hormone, either isolated or as part of congenital hypopituitarism.

In some instances, hypothyroidism detected by screening may be transient. The most common cause of this is the presence of maternal antibodies which temporarily impair thyroid function for several weeks.

Cretinism is an old term for the state of mental and physical retardation resulting from untreated congenital hypothyroidism, usually due to iodine deficiency from birth because of low iodine levels in the soil and local food sources. The term, like so many other 19th century medical terms, acquired pejorative connotations as it became used in lay speech. It is now rarely used by physicians.


Diagnostic evaluation
In the developed world, nearly all cases of congenital hypothyroidism are detected by the newborn screening program. These are based on measurement of TSH or thyroxine (T4) on the second or third day of life. If the TSH is high, or the T4 low, the infant's doctor and parents are called and a referral to a pediatric endocrinologist is recommended to confirm the diagnosis and initiate treatment. Often a technetium thyroid scan is performed to detect a structurally abnormal gland.


Treatment
The goal of newborn screening programs is to detect and start treatment within the first 1-2 weeks of life. Treatment consists of a daily dose of thyroxine, available as a small tablet. The generic name is levothyroxine, and several brands are available. Commonly used brands in North America are Synthroid, Levoxyl, Unithroid, and Levothroid. The tablet is crushed and given to the infant with a small amount of water or milk. The most commonly recommended dose range is 10-15 μg/kg daily, typically 37.5 or 44 μg.[2] Within a few weeks, the T4 and TSH levels are rechecked to confirm that they are being normalized by treatment. As the child grows up, these levels are checked regularly to maintain the right dose. The dose increases as the child grows.


Symptoms
Infants born with congenital hypothyroidism may show no effects, or may display mild effects that often go unrecognized as a problem: excessive sleeping, reduced interest in nursing, poor muscle tone, low or hoarse cry, infrequent bowel movements, exaggerated jaundice, and low body temperature. If fetal deficiency was severe because of complete absence (athyreosis) of the gland, physical features may include a larger anterior fontanel, persistence of a posterior fontanel, an umbilical hernia, and a large tongue (macroglossia).

In the era before newborn screening, less than half of cases of severe hypothyroidism were recognized in the first month of life. As the months proceeded, these infants would grow poorly and be delayed in their development. By several years of age, they would display the recognizable facial and body features of cretinism. Persistence of severe, untreated hypothyroidism resulted in severe mental impairment, with an IQ below 80 in the majority. Most of these children eventually ended up in institutional care.


Prognosis
Most children born with congenital hypothyroidism and correctly treated with thyroxine grow and develop normally in all respects. Even most of those with athyreosis and undetectable T4 levels at birth develop with normal intelligence, although as a population academic performance tends to be below that of siblings and mild learning problems occur in some.[3]

Congenital hypothyroidism is the most common preventable cause of mental retardation. Few treatments in the practice of medicine provide as large a benefit for as small an effort.

Tuesday, October 14, 2008

Friday, October 10, 2008

SAN JUAN CITY 101

PINAGLABANAN IN 1946
































PINAGLABANAN MONUMENT







N.DOMINGO STREET





















SAN JUAN CITY HALL





N.DOMINGO,IN FRONT OF CITY HALL

















SAN JUAN CITY PLAZA

















SAN JUAN ELEMENTARY SCHOOL





LOKAL NG SAN JUAN

BEHIND THE MASKS

ARE THE IMPISH SMILES OF BUDDING GREAT SURGEONS!!!!

SURGICAL INSTRUMENTS

SUBSEROUS MYOMA



present!!!


this kind of machine is a waste of the government money.I signed in yesterday but since I was on 24-hour duty , i was not supposed to sign out until today. I again placed my ID in front of the white box shown there, but what happened was it still signed me in.They said that i still have to sign in the attendance log book.How ignorant whoever thought of this!!!

Wednesday, October 8, 2008

best pomelo in the world



Aside from being the pasalubong of my idol Dr Fernando when he went to Davao, pomelo from Davao is the sweetest in the world.

Tuesday, October 7, 2008

SABI NI SIR BAWAL ANG HALTER SA OPD



















PANO BA YAN?MAGPAPAPAYAT PA NAMAN AKO PARA MAKAPAGSUOT NITO.Nagreact daw ba?

Monday, October 6, 2008

GESTATIONAL DIABETES MANAGEMENT


In some prospective studies, treatment of gestational diabetes has resulted in a decrease in shoulder dystocia (a frequently discussed perinatal outcome), but cesarean delivery has not been shown to reduce perinatal morbidity. Patients diagnosed with gestational diabetes should monitor their blood glucose levels, exercise, and undergo nutrition counseling for the purpose of maintaining normoglycemia. The commonly accepted treatment goal is to maintain a fasting capillary blood glucose level of less than 95 to 105 mg per dL (5.3 to 5.8 mmol per L); the ambiguity (i.e., the range) is due to imperfect data. The postprandial treatment goal should be a capillary blood glucose level of less than 140 mg per dL (7.8 mmol per L) at one hour and less than 120 mg per dL (6.7 mmol per L) at two hours. Patients not meeting these goals with dietary changes alone should begin insulin therapy. In patients with well-controlled diabetes, there is no need to pursue delivery before 40 weeks of gestation. In patients who require insulin or have other comorbid conditions, it is appropriate to begin antenatal screening with nonstress tests and an amniotic fluid index at 32 weeks of gestation. (Am Fam Physician 2003;68:1767-72,1775-6. Copyright© 2003 American Academy of Family Physicians.).

Screening for gestational diabetes mellitus is widely practiced despite lack of evidence that it prevents adverse perinatal outcomes. Although the disorder affects approximately 2.5 percent of pregnant women and has been the subject of extensive research, its diagnosis and management continue to be debated.
Definition and Complications
Gestational diabetes mellitus is defined as glucose intolerance that begins, or is first recognized, during pregnancy. A wide range of complications is associated with the disorder. For the mother, gestational diabetes increases the risk of preeclampsia, cesarean delivery, and future type 2 diabetes. In the fetus or neonate, the disorder is associated with higher rates of perinatal mortality, macrosomia, birth trauma, hyperbilirubinemia, and neonatal hypoglycemia. Some studies have found an association between gestational diabetes and increased perinatal mortality rates, but other studies have shown no increased risk.
Diagnosis of Gestational Diabetes
Patients do not have to fast before a 50-g, one-hour glucose challenge test.
Initial screening for gestational diabetes is accomplished by performing a 50-g, one-hour glucose challenge test at 24 to 28 weeks of gestation. Patients do not have to fast for this test. To be considered normal, serum or plasma glucose values should be less than 130 mg per dL (7.2 mmol per L) or less than 140 mg per dL (7.8 mmol per L). Using a value of 130 mg per dL or higher will increase the sensitivity of the test from 80 to 90 percent and decrease its specificity, compared with using a value of 140 mg per dL or higher. Thus, the lower screening level of 130 mg per dL identifies more patients with gestational diabetes at the cost of more false-positive results. Current recommendations from the American Diabetes Association (ADA) and the American College of Obstetricians and Gynecologists (ACOG) accept either value for defining an abnormal initial screening result. [Reference 4--Evidence level C, consensus/expert opinion; Reference 15--Evidence level C, consensus/expert opinion]
An abnormal one-hour screening test should be followed by a 100-g, three-hour venous serum or plasma glucose tolerance test. After the patient has been on an unrestricted diet for three days, venous blood samples are obtained following an overnight fast, and then one, two, and three hours after an oral 100-g glucose load. During the test period, patients should remain seated and should not smoke. Two or more abnormal values are diagnostic for gestational diabetes.
The diagnostic criteria from the National Diabetes Data Group (NDDG) have been used most often, but some centers rely on the Carpenter and Coustan criteria, which set the cutoff for normal at lower values (Table 1).Compared with the NDDG criteria, the Carpenter and Coustan criteria lead to a diagnosis of gestational diabetes in 54 percent more pregnant women, with an increased cost and no compelling evidence of improved perinatal outcomes. While the ADA supports use of the stricter criteria, the most recent ACOG practice bulletin supports the use of either criteria set.Whole blood glucose values are approximately 10 to 15 percent lower than serum or plasma values.[corrected]

TABLE 1 Criteria for Abnormal Result on 100-g, Three-Hour Oral Glucose Tolerance Tests in Pregnant Women*
Blood sample

National Diabetes Data Group / Carpenter and Coustan
Fasting
105 mg per dL (5.8 mmol per L) / 95 mg per dL (5.3 mmol per L)
1-hour
190 mg per dL (10.5 mmol per L) / 180 mg per dL (10.0 mmol per L)
2-hour
165 mg per dL (9.2 mmol per L) / 155 mg per dL (8.6 mmol per L)
3-hour
145 mg per dL (8.0 mmol per L) / 140 mg per dL (7.8 mmol per L)
*--Gestational diabetes mellitus is diagnosed if two or more of the values (venous serum or plasma glucose levels) are met or exceeded.


Management of Gestational Diabetes
BLOOD GLUCOSE MONITORING

In patients requiring insulin therapy, the ideal frequency of glucose monitoring has not been established. A common practice is to check the glucose level four times daily. A first morning glucose level can rule out fasting hyperglycemia, and additional one- or two-hour postprandial values can ensure adequate control.
Postprandial testing is preferable to preprandial testing. In one randomized study comparing postprandial and preprandial blood glucose monitoring in patients with gestational diabetes who required insulin therapy, those who measured their glucose levels after meals had larger drops in A1c (-3.0 versus -0.6 percent, P <.001), gave birth to infants with lower birth weights (3,469 g [7 lb, 10 oz] versus 3,848 g [8 lb, 7 oz], P = .01), and had fewer cesarean deliveries (12 versus 42 percent, P = .04).19 [Evidence level B, lower quality RCT] Gestational diabetes is diagnosed when a patient has two or more abnormal values on a fasting 100-g, three-hour glucose tolerance test. There is neither objective evidence nor a clinical guideline to support a frequency for glucose monitoring in patients with diet-controlled gestational diabetes. In these patients, an acceptable practice is to use the four-times-a-day schedule on two days per week and begin more intensive treatment if two values per week exceed the limits. DIET A recent Cochrane review20 found no difference in the prevalence of birth weights greater than 4,000 g (8 lb, 13 oz) or cesarean deliveries in women with gestational diabetes who were randomly assigned to receive primary dietary therapy or no specific treatment. The review concluded that insufficient evidence exists to recommend dietary therapy in patients with altered glucose metabolism. The ideal diet for women with gestational diabetes remains to be defined, and current recommendations are based on expert opinion. The ADA recommends nutrition counseling (with a registered dietitian, if possible) and a diet that adequately meets the needs of pregnancy but restricts carbohydrates to 35 to 40 percent of daily calories. Caloric restriction should be approached with caution, because two studies have reported a relationship between elevated maternal serum ketone levels and reduced psychomotor development and IQ at three to nine years of age in the offspring of mothers with gestational diabetes.For patients with a body mass index greater than 30 kg per m2, the ADA suggests lowering daily caloric intake by 30 to 33 percent (to approximately 25 kcal per kg of actual weight per day), which avoids ketonemia. Regular exercise has been shown to improve glycemic control in women with gestational diabetes, but it has not been shown to affect perinatal outcomes.

INSULIN
Most,but not all,prospective trials involving insulin therapy in women with gestational diabetes have shown a reduction in the incidence of neonatal macrosomia. Therefore, insulin therapy traditionally has been started when capillary blood glucose levels exceed 105 mg per dL (5.8 mmol per L) in the fasting state and 120 mg per dL (6.7 mmol per L) two hours after meals. These cutoff values are derived from guidelines for managing insulin in pregnant women who have type 1 diabetes. A more aggressive goal of a fasting capillary blood glucose level below 95 mg per dL (5.3 mmol per L) is supported by a prospective study of 471 women with gestational diabetes that showed a decrease in large-for-gestational-age neonates, from 28.6 to 10.3 percent (relative risk, 5.99; 95 percent confidence interval, 1.37 to 8.88), in the women with fasting blood glucose levels of 95 to 105 mg per dL who were treated, respectively, with diet or insulin; the study reported no data on additional birth outcomes.[Evidence level B, nonrandomized observational study] This more conservative goal is recommended in the most recent ACOG practice bulletin on gestational diabetes. Because of variable and imperfect data on this point, it is acceptable to use either cutoff value for fasting glucose testing.
Women with gestational diabetes should be screened for diabetes six weeks postpartum and annually thereafter.
One prospective nonrandomized study of 445 patients has shown a reduction in operative deliveries and birth trauma in women with gestational diabetes who are treated with insulin. However, the findings of this study remain to be demonstrated in an adequately powered RCT.
There are no specific studies declaring one type of insulin or a certain regimen as superior in affecting any perinatal outcome. A common initial dosage is 0.7 units per kg per day, with one dose consisting of two thirds of the total amount given in the morning and one dose consisting of one third of the total amount given in the evening. One third of each dose is given as regular insulin, and the remaining two thirds as NPH insulin. A recent study of 42 women with gestational diabetes supports the safety of very-short-acting insulin lispro, which can be used with once-daily extended insulin ultralente. The simplest regimen that will control blood glucose levels is the best.
Physicians should expect to increase the insulin dosage as the pregnancy progresses and insulin resistance increases. No published guidelines are available to help family physicians treat patients with gestational diabetes who require insulin. When necessary, collaborative care with an obstetrician or perinatologist is advisable.
ORAL HYPOGLYCEMIC MEDICATIONS
Use of oral hypoglycemic agents to treat gestational diabetes has not been recommended because of concerns about potential teratogenicity and transport of glucose across the placenta (causing prolonged neonatal hypoglycemia). Although first-generation hypoglycemic agents (chlorpropamide [Diabinese], tolbutamide [Orinase]) have been shown to cross the placenta, recent in vitro and in vivo evidence has determined that glyburide (Micronase) does not enter the fetal circulation.A recent RCT comparing the use of glyburide and insulin in women with gestational diabetes demonstrated that glyburide therapy resulted in comparable maternal outcomes (e.g., glycemic control, cesarean deliveries) and neonatal outcomes (e.g., macrosomia, hypoglycemia, intensive care unit admissions). Glyburide therapy was not started before 11weeks of gestation and was not detected in any of the neonatal cord blood samples. Preliminary evidence from this trial suggests that glyburide may be a safe, effective alternative to insulin in the management of gestational diabetes.
The ACOG and the ADA agree that glyburide should not be prescribed for the treatment of gestational diabetes until additional RCTs support its safety and effectiveness. Despite these recommendations, many physicians are using glyburide in this setting because of its ease of use compared with insulin. In a recent prospective cohort study of patients with polycystic ovary syndrome, metformin therapy has been shown to decrease the subsequent incidence of gestational diabetes, reduce first-trimester miscarriage rates, and result in no apparent increase in congenital anomalies. RCTs are needed to demonstrate the safety and effectiveness of metformin (Glucophage) in pregnancy before use of this medication is warranted for the treatment of gestational diabetes.
ANTEPARTUM FETAL ASSESSMENT
Data on gestational diabetes and an increased risk of fetal demise are conflicting. The 2001 ACOG practice bulletin15 concludes that evidence is insufficient to determine the optimal antepartum testing regimen in women with gestational diabetes who have relatively normal glucose levels on diet therapy and no other perinatal risk factors. Acceptable practice patterns for monitoring pregnancies complicated by gestational diabetes range from testing all women beginning at 32 weeks of gestation to no testing until 40 weeks of gestation.
The ACOG recommends antenatal testing for patients whose blood glucose levels are not well controlled, who require insulin therapy, or who have concomitant hypertension. The antenatal testing can be initiated at 32 weeks of gestation. In this situation, no method of antenatal testing has proved superior to others. Community preference may dictate use of the nonstress test, the modified biophysical profile (i.e., nonstress test and amniotic fluid index), or a full biophysical profile.
TIMING AND ROUTE OF DELIVERY
In gestational diabetes, shoulder dystocia is the complication most anticipated at the time of delivery. In one study, this complication occurred in 31 percent of neonates weighing more than 4,000 g who were delivered vaginally to unclassified mothers with diabetes. No prospective data support the use of cesarean delivery to avoid birth trauma in women who have gestational diabetes. One remaining limiting factor is the 13 percent error rate (± 2 SD) in estimating fetal weight by ultrasonography.
A decision analysis that evaluated the cost and efficacy of a policy of elective cesarean delivery for an estimated fetal weight of 4,500 g (9 lb, 15 oz) in mothers with diabetes found that 443 cesarean deliveries would need to be performed to prevent one case of brachial plexus injury, at a cost of $930,000. A reasonable approach is to offer elective cesarean delivery to the patient with gestational diabetes and an estimated fetal weight of 4,500 g or more, based on the patient's history and pelvimetry, and the patient and physician's discussion about the risks and benefits. There are no indications to pursue delivery before 40 weeks of gestation in patients with good glycemic control unless other maternal or fetal indications are present.
INTRAPARTUM MANAGEMENT
The goal of intrapartum management is to maintain normoglycemia in an effort to prevent neonatal hypoglycemia. Patients with diet-controlled diabetes will not require intrapartum insulin and simply may need to have their glucose level checked on admission for labor and delivery. While patients with insulin-requiring diabetes are in active labor, capillary blood glucose levels should be monitored hourly. Target values are 80 to 110 mg per dL (4.4 to 6.1 mmol per L).

POSTPARTUM MANAGEMENT
Women with gestational diabetes rarely require insulin in the postpartum period. As insulin resistance quickly resolves, so does the need for insulin. Patients with diet-controlled diabetes do not need to have their glucose levels checked after delivery. In patients who required insulin therapy during pregnancy, it is reasonable to check fasting and two-hour postprandial glucose levels before hospital discharge.
Because women with gestational diabetes are at high risk for developing type 2 diabetes in the future, they should be tested for diabetes six weeks after delivery via fasting blood glucose measurements on two occasions or a two-hour oral 75-g glucose tolerance test. Normal values for a two-hour glucose tolerance test are less than 140 mg per dL. Values between 140 and 200 mg per dL (11.1 mmol per L) represent impaired glucose tolerance, and greater than 200 mg per dL are diagnostic of diabetes. Screening for diabetes should be repeated annually thereafter, especially in patients who had elevated fasting blood glucose levels during pregnancy.Breastfeeding improves glycemic control and should be encouraged in women who had gestational diabetes.

Contraception should be discussed, because women who have diabetes during one pregnancy are likely to have the same condition in a subsequent pregnancy. There are no limits on the use of hormonal contraception in patients with a history of gestational diabetes. As previously noted, these women also are at increased risk of developing type 2 diabetes in the future.
Patients should be counseled about diet and exercise. By losing weight and exercising, women can significantly decrease their risk of developing diabetes.

abnormal uterine bleeding algorithm

Sunday, October 5, 2008

madagascar 2

To be sure that you get into a clean bathroom





















GO AND EAT IN MAX OR STARBUCKS.he!he!he!

i Bought CRispy pata in Max'











I bought crispy pata in Max so that we will have a good lunch today.The appeal lies to the succulent taste and crispiness of the toasted exterior of the meat.This is well served with a vinegar dip which is mixed with onion, garlic and soy sauce.You will eat lots of rice,really, if you have this.forget about your diet.

THESE ARE CARDIAC MONITORS


WHAT THE MODERN FILIPINOS DO WHEN NOT BUSY


CHATTING, PLAYING,BLOGGING or checking their account in FRIENDSTER. I also have multiply and facebook, though

A GOOD CUP OF COFFEE...



IS THE BEST COMPANY WHEN YOU ARE ON 24-HOUR DUTY. KEEPS YOU ENERGETIC AND AWAKE

Di po Starex corporation ang may gawa kasi nito



SIRA NA NAMAN ANG ELEVATOR

Saturday, October 4, 2008

ENDOMETRIAL CARCINOMA ,TREATMENT OPTIONS BY STAGE

DERIVED FROM AMERICAN CANCER SOCIETY

Endometrial cancer is often diagnosed when a woman who is having symptoms has an endometrial biopsy or D&C. Tests, such as ultrasound and CT scan, may be done to look for signs that the cancer has spread to lymph nodes or tissues outside of the uterus. Even when these tests show no signs of cancer spread, surgery is needed to stage the cancer. In this operation, the uterus, fallopian tubes, and ovaries are removed (total hysterectomy bilateral salpingo-oophorectomy -- TH/BSO). Lymph nodes from the pelvis and around the aorta are also removed (a pelvic and para-aortic lymph node dissection) and examined for cancer spread. Pelvic washings are obtained. If tests done before surgery show signs that the cancer has spread outside of the uterus, a different surgery may be planned.
Stage I
An endometrial cancer is stage I if the cancer is limited to the body of the uterus and has not spread to lymph nodes or distant sites. If the tumor is endometrioid, standard treatment includes surgery to remove and stage the cancer (see above). The tissues removed at surgery are examined under a microscope in a lab to see how far the cancer has spread. This decides what stage the cancer is in. Treatment after surgery depends upon stage. Surgery and other treatment often differ for cancers that aren't endometrioid - this will be discussed later in this section.
Treatment after complete staging
Stage IA endometrioid cancers are only in the endometrium and have not grown into the myometrium. These cancers most often do not need any further treatment after surgery. If the tumor is grade 3, the doctor may recommend vaginal brachytherapy (VB). Pelvic radiation may be given as well in rare circumstances.
In Stage IB, the cancer has grown less than halfway into the myometrium. Many of these can be observed without further treatment after surgery. For high grade tumors, doctors are more likely to recommend radiation after surgery. Either VB, pelvic radiation, or both can be used.
In stage IC, the cancer has grown more than halfway through the myometrium. After surgery the patient may be watched without further treatment or offered some form of radiation treatment. Either VB, pelvic radiation, or both can be used.
High-grade cancers, such as papillary serous carcinoma or clear cell carcinoma, are more likely to have spread outside of the uterus at the time of diagnosis. Patients with these types of tumors do not do as well as those with lower grade tumors. The surgery may be more extensive if the biopsy done before surgery showed a high-grade cancer, In addition to the TH/BSO and the pelvic and para-aortic lymph node dissections, the omentum is often removed and peritoneal biopsies may be obtained. After surgery, both chemotherapy and radiation therapy are often given to help keep the cancer from coming back. The chemotherapy usually includes the drugs cisplatin and doxorubicin. Sometimes paclitaxel is given as well.
Someone with a uterine carcinosarcoma often has the same type of surgery that is used for high-grade endometrial carcinoma. After surgery, radiation, chemotherapy, or both may be used. The chemotherapy often includes the drugs cisplatin and ifosfamide, sometimes along with paclitaxel.
Patients not staged with surgery
As stated above, standard treatment for endometrial cancer includes surgery to remove and stage the cancer. In some cases, however, the doctor may treat based on the clinical stage (see the section about staging for more details) and radiologic testing.
If the cancer seen on endometrial biopsy or D&C is grade 1 and it looks like the cancer is only in the uterus, the cancer is said to be clinical stage I, grade 1. Because few of these cancers have already spread, some doctors do not feel that full surgical staging is always needed. Often a TH/BSO will be done first. As soon as the uterus is removed, it will be examined to see how deep and far the cancer may have spread. If the cancer is only in the upper two thirds of the body of the uterus and hasn't grown more than halfway through the muscle layer of the uterus, the chance that the cancer has spread is very low. In these cases, the surgeon may not do a LND but instead may remove only a few lymph nodes or none at all. If any of the lymph nodes contains cancer it means that the cancer is stage IIIC and further treatment is needed (treatment of stage IIIC is discussed later). If no lymph nodes were removed (or if there were no cancer cells in the nodes that were removed), treatment after surgery could include observation without further treatment or radiation.
Women who cannot have surgery because of other medical problems are often treated with radiation alone.
Progestin therapy is sometimes used to treat stage I, grade 1 EC in young women with who still want to have children. Progestin treatment can cause the cancer to shrink or even go away for some time, giving the woman a chance to get pregnant. This approach is experimental and can be risky. In some cases, it does not work and the cancer keeps growing. Sometimes the tumor gets smaller or goes away for a while, but then comes back again. Not having surgery right away may give the cancer time to spread outside the uterus. A second opinion from a gynecologic oncologist and pathologist (to confirm the grade of the cancer) before starting progestin therapy is important. Patients need to understand that this is not a standard treatment and may increase risk.
Doctors are more likely to remove some lymph nodes when the biopsy shows that the cancer is a higher grade (2 or 3). If the cancer has spread deeper than half the thickness of the wall of the uterus, then the pelvic and para-aortic lymph nodes are usually sampled.
If the cancer comes back after surgery, it usually does so in the vagina. Many doctors recommend vaginal brachytherapy to prevent this from happening. Others recommend external beam radiation to the whole pelvic area. Certain features make it more likely that the cancer will come back after surgery, such as higher grade, spread to the lower third or outer half of the uterus, growth into lymph or blood vessels, larger tumor size, and patient age over 60. Radiation therapy is often given to reduce the risk of cancer coming back in the vagina or pelvis for cancers with one or more of these features. In patients without these risk factors the chance that the cancer will come back is small and radiation may not be given after surgery. Although giving radiation right after surgery reduces the chance of the cancer growing back in the pelvis, it does not help women live longer than if the radiation is only given when the cancer comes back. There may be less worry if the radiation is given right away, but fewer women will receive radiation if they wait until the cancer returns.
Stage II
When a cancer is stage II, it has spread to the cervix but still has not grown outside of the uterus.
Stage IIA cancers have spread among the gland cells of the cervix, but have not grown into the supporting connective tissue. Most often, the patient first has surgery -- hysterectomy and bilateral salpingo-oophorectomy (BSO), with pelvic and para-aortic lymph node dissection. After surgery, the patient may require no further treatment, or the doctor may recommend radiation therapy with vaginal brachytherapy, pelvic radiation treatments, or both. Treatment after surgery depends on how far the cancer has grown into the muscle layer of the uterus (the myometrium) and the grade of the tumor.
Stage IIB cancers are growing into (invading) the connective tissue of the cervix. One treatment option is to have surgery first, then radiation therapy. The surgery would include a hysterectomy (discussed in the section about treatment), bilateral salpingo-oophorectomy (BSO), and pelvic and para-aortic lymph node dissection (LND). Vaginal brachytherapy and pelvic radiation treatments are given after the patient has recovered from surgery. The other option is radiation therapy first, followed by a simple hysterectomy, BSO, and LND.
The lymph nodes that have been removed are checked for cancer cells. If lymph nodes show cancer, then the cancer is not really a stage II - it is a stage IIIC.
In some cases, a woman with early stage endometrial cancer might be too frail or ill from other diseases to safely have surgery. These women are treated with radiation therapy alone.
For women with high-grade cancers, such as papillary serous carcinoma or clear cell carcinoma, the surgery may include omenetectomy and peritoneal biopsies in addition to the TH/BSO, pelvic and para-aortic lymph node dissections, and pelvic washings. After surgery, chemotherapy, radiation therapy, or both may be given to help keep the cancer from coming back. The chemotherapy usually includes the drugs cisplatin and doxorubicin. Sometimes paclitaxel is given as well.
Someone with a Stage II uterine carcinosarcoma often has the same type of surgery that is used for a high-grade cancer. After surgery, radiation, chemotherapy, or both may be used. The chemotherapy often includes the drugs cisplatin and ifosfamide, sometimes along with paclitaxel.
Stage III
Stage III cancers have spread outside of the uterus.
If the surgeon thinks that all visible cancer can be removed, a hysterectomy with bilateral salpingo-oophorectomy (BSO) is done. Sometimes patients with stage III cancers require a radical hysterectomy. A pelvic and para-aortic lymph node dissection may also occur. Pelvic washings will be obtained and the omentum may be removed. Some doctors will try to remove any remaining cancer (debulking), but doing this hasn't been proven to help patients live longer.
If the surgeon feels that it is not possible to remove all visible cancer, radiation therapy may be given before surgery to remove the cancer. Radiation therapy may shrink the tumor enough to make surgery an option.
Stage IIIA: If the cancer looks like it hasn't spread outside of the uterus, but the pelvic washings show cancer cells, it is stage IIIA. For small, low-grade cancers, no other treatment may be needed after surgery. If the cancer is grade 3, the doctor may recommend further treatment with radiation.
A cancer is also considered stage IIIA when it has spread to other tissues in the pelvis like the fallopian tubes, the ovaries, and the omentum. When this occurs, treatment after surgery may include chemotherapy, radiation, or a combination of both. Radiation is given to the pelvis or to both the abdomen and the pelvis. Sometimes vaginal brachytherapy is used as well.
Stage IIIB: In this stage, the cancer has spread to the vagina. After surgery, stage IIIB may be treated with radiation, with or without chemotherapy.
Stage IIIC: When the cancer has spread to the lymph nodes in the pelvis or around the aorta, it is stage IIIC. Treatment includes surgery, followed by chemotherapy and radiation.
For women with high-grade cancers, such as papillary serous carcinoma or clear cell carcinoma, the surgery may include omenetectomy and peritoneal biopsies in addition to the TH/BSO, pelvic and para-aortic lymph node dissections, and pelvic washings. After surgery, chemotherapy, radiation therapy, or both may be given to help keep the cancer from coming back. The chemotherapy usually includes the drugs cisplatin and doxorubicin. Sometimes paclitaxel is given as well.
Someone with a Stage III uterine carcinosarcoma often has the same type of surgery that is used for a high-grade cancer. After surgery, radiation, chemotherapy, or both may be used. The chemotherapy often includes the drugs cisplatin and ifosfamide, sometimes along with paclitaxel.
Stage IV
Stage IVA: These cancers have grown into the bladder or bowel.
Stage IVB: These cancers have spread to lymph nodes outside of the pelvis or para-aortic area. This stage also includes cancers that have spread to the liver, lungs, or other organs.
The patient may have the best chance if all the cancer that is seen can be removed and biopsies of the abdomen do not show cancer cells. This may be possible if the cancer has only spread to lymph nodes in the abdomen and pelvis. In most cases of stage IV endometrial cancer, the extensive spread of the cancer makes a surgical cure nearly impossible. A hysterectomy and bilateral salpingo-oophorectomy may still be done to prevent excessive bleeding. Radiation therapy may also be used for this reason. When the cancer has spread to other parts of the body, hormone therapy may be used. Drugs used for hormone therapy include progestins and tamoxifen. Aromatase inhibitors may also be useful and are being studied. High-grade cancers and those without detectable progesterone receptors are less likely to respond to hormone therapy.
Combinations of chemotherapy drugs may help for a time in some women with advanced endometrial cancer. The drugs used most often are doxorubicin (Adriamycin), paclitaxel (Taxol), and either cisplatin or carboplatin.. These drugs are often used together in combination. Stage IV carcinosarcoma is often treated with chemotherapy. Cisplatin, ifosfamide, and paclitaxel are the drugs most often used. Women with stage IV endometrial cancer should consider taking part in clinical trials of chemotherapy or other new treatments.
Recurrent endometrial cancer
When a cancer has gone away with treatment, but then comes back later, it is called recurrent. Treatment depends on the amount and location of the cancer. If the recurrent cancer is only in the pelvis, radiation therapy may provide a cure. Women with more extensive recurrences are treated like those with stage IV endometrial cancer. Either hormone therapy or chemotherapy is recommended. Low-grade cancers containing progesterone receptors are more likely to respond well to hormone therapy. Higher-grade cancers and those without detectable receptors are less likely to shrink during hormone therapy, but may respond to chemotherapy. Clinical trials of new treatments are another option.
If patients have other medical conditions that make them unable to have surgery, radiation therapy alone or combined with hormonal therapy is generally used. The outlook for these patients is not as good as those who are able to have surgery.
Last Revised: 07/26/2008

PATHOLOGY REVIEW of the FEMALE REPRODUCTIVE TRACT






NORMAL CERVIX







NORMAL ADULT VAGINAL MUCOSA













NORMAL CERVICAL NONKERATINIZING ENDOMETRIUM







CHRONIC CERVICITIS














CERVICAL DYSPLASIA








SQUAMOUS CELL CARCINOMA, KERATINIZING







STAGE IV CERVICAL CA

















SQUAMOUS CELL CARCINOMA ,CERVIX












SEPTATE UTERUS








PROLIFERATIVE ENDOMETRIUM












SECRETORY ENDOMETRIUM DAY 2







SECRETORY ENDOMETRIUM














ENDOMETRIAL POLYP











ENDOMETRIAL HYPERPLASIA









SIMPLE ENDOMETRIAL HYPERPLASIA


















ENDOMETRIAL ADENOCARCINOMA
















MYOMA














LEIOMYOSARCOMA





















ADENOMYOSIS,GROSS AND MICROSCOPIC















ENDOMETRIOSIS,FALLOPIAN TUBE















ENDOMETRIOSIS











krukenberg tumor
















ENDOMETRIOMA
















GRANULOSA CELL CARCINOMA












DYSGERMINOMA

















GROSS PICTURE OF SEROUS CYSTADENOCARCINOMA



















SEROUS CYSTADENOMA






PSAMMOMA BODIES

















OVARIAN SEROUS CYSTADENOCARCINOMA










BORDERLINE SEROUS CYSTADENOMA








FIBROMA






FIBROTHECOMA
















FOLLICULAR CYST













CORPUS LUTEUM CYST HEMORRHAGICUM,
GROSS AND MICROSCOPIC













THECA LUTEIN CYST














OVARIAN TORSION















ACUTE SALPINGITIS,gonorrhea
















Neisseria gonorrhea, TOA

















DERMOID CYSTS,gross AND Microscopic













TERM UTERUS













2nd TRIMESTER FETUS and UTERUS









TUBAL PREGNANCY









TUBAL PREGNANCY









TUBAL PREGNANCY