hi doctors, can you tell me what is pleomorhic rhabdo sarcoma?

Question

What kind of doctor treats kaposi sarcoma?

Answer 1

Aggressive cancer: Pleomorphic rhabdomyosarcoma. It's a moderately aggressive cancer that seems to arise totally at random. You'd do well to have at least two pathologists sign out on the diagnosis, as there's some tricky mimics. Best wishes.

Answer 2

Pleomorphic RMS: Pleomorphic rhabdomyosarcoma is a very rare primitive sarcoma that derives from skeletal muscle progenitor cells gone haywire. If you have been given a diagnosis of Pleomorphic Rhabdomyosarcoma, it is imperative that you seek out a 2nd opinion from an expert pathologist in sarcoma. I have been trained in sarcoma from MD Anderson Cancer Center and offer free consults [email protected]

Answer 3

Rare, aggressive: A rare aggressive cancer thought to arise in muscle. These have a high propensity to spread early. Patients are best diagnosed and managed with a multidisciplinary approach at a large, referral, sarcoma center such as Sylvester in Miami.

Answer 4

Can be: Left untreated any malignancy can be fatal. We do have treatments for ks but no treatment is 100% effective.

Answer 5

They can be: Kaposi saromas used to be much more lethal two to three decades ago when the aids epidemidic was in full swing. Now with improving treatments and retroviral therapies, the outcomes have improved dramatically so that if you have a "good risk" kaposi's there is a 90% overall survival. The survival is about 50% for those patients with "poor risk" features of ks.

Answer 6

Lots of variety.: The term "spindle cell" sarcoma is a generic descriptive term that doesn't really give enough information. It would be like asking, "i saw a convertible, how fast can it go?" additional testing often reveals exactly what kind of sarcoma, and then once you know that, you can more accurately discuss the prognosis and the treatment.

Answer 7

Depends: It truly depends. Some spindle cell sarcomas can have much more aggressive growth doubling in several weeks to a month or two. Some spindle cell sarcomas can be more indolent doubling in size in three to 6 months.

Answer 8

Not a diagnosis: This is not a diagnosis commonly used and you should have your pathology checked by an expert. I am an MD Anderson trained pathologist with expertise in sarcoma. Please contact if you a free opinion [email protected]

Answer 9

Soft tissue tumor: Sarcomas are uncommon tumors that arise from the soft tissues in your body: muscles, tendons, fat, the lining of your joints, blood vessels, and nerves. They can be very serious, especially if there is a delay in the time to diagnosis.

Answer 10

Highly malignant: Tumors which can arise from any so called mesenchymal tissue & not from epithelial tissues such as skin intestinal lining, i.e. Rhabdomyosarcoma tumor of muscle, osteogenic sarcoma of bone, liposarcoma of fat etc. These tumors are rare +best treated in centers with experience + team of surgeons + oncologists. Treatment may consist of any combination of chemotherapy, surgery + radiation.

Answer 11

Definition: A cancer (i.e., a tumor with a destabilized genome that's likely to invade and destroy locally and/or spread to a remote site) whose cell of origin is mesenchyme (muscle, connective tissue) that is not of bone marrow origin. They range from very tame to extremely aggressive, but all require treatment.

Answer 12

Cancer: Sarcomas are cancers derived from "mesenchymal" tissues, generally referred to as bone and soft tissue. These differ from carcinomas that are derived from epithelial tissue. Sarcomas are less common and tend to behave differently than carcinomas.

Answer 13

Rare cancer: It's a very rare cancer that arises in connective tissues such as bone, muscles, fat. Other cancer types such as breast, lung and prostate cancer are much more common. There are many subtypes of sarcoma. The main treatment of sarcoma is surgical removal of the tumor. Amputation is rarely needed. Sometimes chemotherapy and radiation are also given.

Answer 14

Great Question: Sarcoma is a very rare tumor derived from early progenitor cells gone haywire. These cells normally make up bones, cartilage, muscle, fat, etc. If you have been given a diagnosis of sarcoma, it is imperative that you seek out a 2nd opinion from an expert pathologist in sarcoma. I have been trained in sarcoma from MD Anderson Cancer Center and offer free consults [email protected]

Answer 15

Rare but many types: A very rare cancer of bone or soft tissues. There are over 50 different types. Best diagnosed and managed at a sarcoma center like Sylvester in Miami.

Answer 16

A cancer : Sarcomas are relatively uncommon tumors that arise from connective tissue. Sarcomas can arise from fat, muscle, cartilage, bone or bone marrow. They can show up just about anywhere. They tend to be slower growing tumors and often do not respond well to chemotherapy or radiation treatments. Surgery is often the first and best treatment for soft tissue sarcomas.

Answer 17

It depends.: There are a wide variety of different sarcomas. The most important pieces of information regarding recurrence rates are if the sarcoma is "low grade" or "high grade" (also known as well vs. Poorly differentiated). Also, you should find out the exact kind of sarcoma. For example, is this liposarcoma, or is this a malignant peripheral nerve sheath tumor? Check with your surgeon or oncologist.

Answer 18

Depends : After surgery, sarcoma recurrence will depend upon the type, size, grade, location and the adequacy of the surgery. If tumor was left behind, it will recurr. In the extremities, radiation may allow a closer resection margin with comparable results to a more radical operation. Low grade tumors may recurr late- even over a decade.

Answer 19

Depends on location: Early sarcomas may have no symptoms. Location of the sarcoma produces specific symptoms such as pain (bone, back, limbs); noticeable mass, and genralized symptoms such as weight loss, fatigue, low blood counts, etc, for advanced cancers.

Answer 20

Mass, sometimes pain: The most common finding is an enlarging mass. It is often non-tender but can be painful. But often there are really no symptoms other that the mass itself, .

hi doctors, can you tell me what is pleomorhic rhabdo sarcoma?

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