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Recent News and Articles on the Keywords: soft tissue + tumors + soft  Related to the article below (Last Update: 8/5/2008)

One Fifth Of British Adult Survivors Of Childhood Cancer Smoke ...
Science Daily (press release) -
The relatively high rate of smoking in survivors of Wilms tumor, Hodgkin lymphoma, and soft tissue sarcomas is concerning because previous research suggests ...
Phase 2 Study of IMC-A12 for Advanced Soft Tissue Sarcoma Opens ...
ADMET.net (press release), UK - Jul 8, 2008
Patients with the following types of soft-tissue sarcoma are eligible for study enrolment: Ewing?s sarcoma, peripheral neuroectodermal tumor (PNET), ...IMCL
What If You Do Find a Lump?
FitSugar.com, CA -
Health.com: A soft lump: It's smooth and round (like a grape), and it moves a little when you press on it. This lump may be painful to the touch, ...
Adjuvant Chemotherapy Confirmed Beneficial for Resectable Soft ...
Cancer Consultants, ID - Jul 24, 2008
1 Soft tissue sarcomas are a heterogeneous group of tumors with variable rates of recurrence after complete resection. The role of adjuvant chemotherapy and ...
Misonix Receives FDA Approval of Second Sonatherm(R) Soft Tissue ...
FOXBusiness - Jul 17, 2008
To date, the two Sonatherm Systems are the only HIFU-based soft tissue ablation systems that have received FDA clearance for general surgery. ...MSON
MIMA Cancer Center Becomes First in World to Treat Soft Tissue ...
CNNMoney.com (press release) - Jul 22, 2008
A 72-year-old man with Merkel cell carcinoma was treated for a soft tissue tumor in his thigh, which had developed close to where a similar tumor had been ...VAR
Percutaneous Spine Biopsy: A Meta-Analysis
Journal of Bone and Joint Surgery (subscription) - Aug 1, 2008
In cases in which fluoroscopy cannot identify the lesion or in cases of paraspinal soft-tissue tumors, the use of computed tomography is needed. ...
Smoking among child cancer survivors highest in most at risk group
News-Medical.net, Australia - Aug 3, 2008
The study included almost 2500 survivors of Hodgkin's lymphoma, soft tissue sarcoma or Wilms' tumour. Study author, Dr Clare Frobisher, said: "Although our ...
NH's Miss Outstanding Teen survived rare cancer
The Union Leader, NH -
"Hopefully, we'll be coming back with some good news," says Lyman, who was diagnosed at the age of 13 with soft tissue sarcoma on her right shoulder. ...
Cutting-Edge Care
RedOrbit, TX -
Despite the activity, it is quiet and soothing with soft lighting and a central courtyard, where patients and families can find a few minutes of peace. ...
Source: Google News

[CITATION] Soft Tissue Tumors.
FM Enzinger, SW Weiss, B Chandrasekhar - Plastic and Reconstructive Surgery, 1985

Tumor oxygenation predicts for the likelihood of distant metastases in human soft tissue sarcoma -
DM Brizel - Cancer Research, 1996 - AACR
... brizel@radonc.duke.edu. This study was performed to explore the relationship between
tumor oxygenation and treatment outcome in human soft tissue sarcoma. ...

Long-term results of a prospective randomized trial of adjuvant brachytherapy in soft tissue sarcoma -
PW Pisters, LB Harrison, DH Leung, JM Woodruff, ES … - Journal of Clinical Oncology, 1996 - jcojournal.org
... Hoekstra Isolated Limb Perfusion With Tumor Necrosis Factor {alpha} and Melphalan
for Locally Advanced Soft Tissue Sarcoma: The Value of Adjuvant Radiotherapy ...

Cell proliferation in human soft tissue tumors correlates with platelet-derived growth factor B … -
J Wang - Cancer Research, 1994 - AACR
... B expression and increasing malignant tumor grade (P ... All tumors were also demonstrated
to express the ... autocrine mechanism, in human soft tissue tumors and may ...

Prognostic factors in adult patients with locally controlled soft tissue sarcoma. A study of 546 … -
JM Coindre, P Terrier, NB Bui, F Bonichon, F … - Journal of Clinical Oncology, 1996 - jcojournal.org
... adult patients with locally controlled soft tissue sarcoma (STS) and ... of Cancer Centers
(FNCLCC) Sarcoma Group from ... consisted of complete tumor resection with ...

Management of primary and recurrent soft-tissue sarcoma of the retroperitoneum. -
DP Jaques, DG Coit, SI Hajdu, MF Brennan - Annals of Surgery, 1990 - pubmedcentral.nih.gov
... Tumor grade was a significant predictor of ... partial resection versus unresectable
tumors did not ... and recurrent retroperitoneal soft-tissue sarcoma is indicated. ...

… detection of P-glycoprotein: prognostic correlation in soft tissue sarcoma of childhood -
HS Chan, PS Thorner, G Haddad, V Ling - Journal of Clinical Oncology, 1990 - jco.ascopubs.org
... Soft Tissue Leiomyosarcomas and Malignant Gastrointestinal Stromal Tumors: Differences
in Clinical Outcome and Expression of Multidrug Resistance Proteins J ...

Chromosomal aberrations in soft tissue tumors. Relevance to diagnosis, classification, and molecular … -
C Sreekantaiah, M Ladanyi, E Rodriguez, RS … - American Journal of Pathology, 1994 - ASIP
... malignant soft tissue tumors and found an incidence of specific translocations in
these neoplasms that ranged from 20% to 93% within histological tumor types. ...

The role of multimodality therapy in soft-tissue sarcoma. -
MF Brennan, ES Casper, LB Harrison, MH Shiu, J … - Annals of Surgery, 1991 - pubmedcentral.nih.gov
... Analysis of alterations in the retinoblastoma gene and tumor grade in ... Diagnostic
relevance of clonal cytogenetic aberrations in malignant soft-tissue tumors. ...

[CITATION] THE CLASSIC: The Hazards of Biopsy in Patients with Malignant Primary Bone and Soft-Tissue Tumors. -
HJ Mankin, TA Lange, SS Spanier - Clinical Orthopaedics and Related Research, 2006
... Patients with Malignant Primary Bone and Soft-Tissue Tumors. [SECTION I: SYMPOSIUM
I: Papers Presented at the 2005 Meeting of the Musculoskeletal Tumor Society] ...

Source: Google Scholar
 

Soft Tissue Tumors - Malignant

Malignant soft tissue tumors are known as sarcomas. These tumors form in connective tissues, such as muscles, tendons, ligaments, fat and cartilage.

They are different than the more common cancers (carcinomas), which are malignant tumors that form in organs or glands (e.g., breast, prostate, colon, liver, kidney, lung, thyroid gland, etc). Malignant soft tissue tumors are still serious. They must be treated with great caution.

Fortunately, malignant soft tissue tumors are rare, making up only about 1% of all malignant tumors. Only about 6,000 of these tumors occur each year in the United States.

These types of tumors include:

  • Angiosarcoma
  • Ewing's sarcoma
  • Fibrosarcoma
  • Hemangiopericytoma
  • Liposarcoma

Article continues below and (thank you)

 
  • Malignant fibrous histiocytoma (MFH)
  • Neurosarcoma
  • Rhabdosarcoma
  • Synovial sarcoma

Causes and Risk Factors of Malignant Soft Tissue Tumors

Malignant soft tissue tumors can occur at almost any age, but are most common in individuals between the ages of 50 and 70.

Diagnosing Malignant Soft Tissue Tumors

In diagnosing malignant soft tissue tumors, it is important to know whether or how far the tumor has spread in the body. In more than 90% of patients with a malignant tumor, there are no visible signs the tumor has spread. This does not necessarily mean that the tumor hasn't spread; it may mean that the scattered cells can't be picked up by current medical tests and imaging.

If the tumor has spread, removing the visible part of the tumor will not cure the patient.

An experienced pathologist can examine a sample of the tumor under a microscope. He or she can then group it according to how likely it is to have spread. A tumor that is classed as high grade has a 70 to 90% chance of having spread. A low-grade tumor has less than a 15% chance of spreading.

Treating Malignant Soft Tissue Tumors

There have been important advanced made in the treatment of malignant soft tissue tumors over the past 15 years.

Combining chemotherapy and radiation therapy with surgery has helped prevent tumors from coming back and helped to increase survival rates.

Specialized radiation techniques, improved surgical methods for removing tumors and rebuilding affected parts of the body have meant that 90 to 95% of the people with these aggressive tumors can be treated without amputating limbs.

For low grade tumors, surgery may be the only treatment needed.

 
 
 
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