Ewing's Sarcoma: Difference between revisions
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As a physical therapist, one should be cautious when the symptoms of "growing pains" or a proposed sports injury are out of proportion or abnormal. | As a physical therapist, one should be cautious when the symptoms of "growing pains" or a proposed sports injury are out of proportion or abnormal. | ||
<div class="researchbox">Review an excellent [http://eradiology.bidmc.harvard.edu/LearningLab/musculo/Son.pdf Presentation on Ewings Sarcoma ]</div><div class="researchbox"><span style="line-height: 1.5em;"> | <div class="researchbox">Review an excellent [http://eradiology.bidmc.harvard.edu/LearningLab/musculo/Son.pdf Presentation on Ewings Sarcoma ]</div><div class="researchbox"><span style="line-height: 1.5em;"> by Jen Son and Gilian Lieberman MD</span> </div><div class="researchbox"></div><div class="researchbox"></div><div class="researchbox"> <rss>http://eutils.ncbi.nlm.nih.gov/entrez/eutils/erss.cgi?rss_guid=1VsHRGSo3HX0CgCh0yQTDe7FwEqMdcz0ZoLhJtVqvvv0fjjM7M|charset=UTF-8|short|max=10</rss><span style="line-height: 1.5em;"> </span></div> | ||
== Case Reports/ Case Studies == | == Case Reports/ Case Studies == | ||
Revision as of 04:00, 21 February 2014
Original Editors - Lisa Miville from Bellarmine University's Pathophysiology of Complex Patient Problems project.
Top Contributors - Joseph Dorrell, Lisa Miville, Elaine Lonnemann, Nikhil Benhur Abburi, Jack Tencza, Lucinda hampton, Tessa Larimer, Admin, Vidya Acharya, Khloud Shreif, Kim Jackson, 127.0.0.1, Wendy Walker, WikiSysop and Claire Knott
Definition/Description[edit | edit source]
Ewing’s Sarcoma is a high grade malignant primary tumor that can arise in soft tissue or bone. It is often referred to as a family of tumors known as Ewing family of tumors (EFT).[1][2][3][4] The tumor is named after James Ewing who first discovered the small, blue round cell that was distinct from osteogenic sarcoma.[4] Although any bone can be invovled, the most common are the pelvis, femur, tibia, ulna and metatarsals.[5] Close behind is the ribs and vertebral column.[3] EFT is most common in children between the ages of 5 and 16, and due to recent availability of multi-agent cytostatic approaches and local therapy, the 5 year survival rate has increased from 10% to 70%.[4][6] Prognosis is dependent on metastisis, worsening with widespread involvement. 26% of patients with EFT have metastatic disease: 10% to the lungs, 10% to bone/bone marrow, and 6% combination.[3]
Prevelance[edit | edit source]
Ewing's Sarcoma is the second most common primary malignant bone tumor of children and the fourth most common overall. 80% of these tumors occur in people under the age of 20.
- Youngest reported case of EFT - 5 months old
- Oldest reported case - 77 year old female
- Rarely occurs in the African American or Asian population
- More common in males than females 1.5:1
Characteristics/Clinical Presentation[edit | edit source]
Pain at the affected site is usually the intial symptom.[4] The pain may be worse during exercise or at night and can be
accompanied by swelling or a lump, redness, and warmth (see picture below).[8] The pain is typically intermittent.[5]
It is common to see fatigue, weight loss, decreased appetite, and/or paralysis or incontinence (if the tumor is of spinal origin).[9]The tumor may be present for months before there are any signs or symptoms.
An injury is often what brings attention to the tumor, because bone weakened by disease can break with little force. Kids with EFT can go undiagnosed until an injury from a sport or rough play requires diagnostic imaging.[10]
Medications[edit | edit source]
Chemotherapy medications most commonly used: vincristine (Oncovin), dactinomycin (Actinomycin D), cyclophosphamide (Cytoxan), ifosfamide (Ifex), etoposide (VePeside, VP-16), and doxorubicin (Adriamycin).[4][7][10]
Immuniological approaches, such as the use of cytokines (interleukins, and interferon), are still being researched.[4]
Diagnostic Tests/Lab Tests/Lab Values[edit | edit source]
In order to properly diganose and treat Ewing's Sarcoma many images and tests need to be aquired. The following are often used in combination for the best results: CT scan, bone scan, biopsy to see if there is bone marrow involvement, X-ray, MRI, chest scan, brain MRI or brain scan, and a blood test. It is important to scan the entire body to know whether the tumor is localized or difuse and to ensure removal of all metastatic lesions.[1][11][3]
Etiology/Causes[edit | edit source]
It has been found that 95% of Ewing's tumors are derived from a specific genetic translocation between chromosomes 11 and 22. The molecualr oncogenesis remains unknown.[1][4][10]
Systemic Involvement[edit | edit source]
Ewing's Family of Tumors are highly malignant. It most commonly spreads to the lungs, but it can also metastisize to the kidney, bone marrow, heart, adrenal gland, and other soft tissues.[9] Chemotherapy and radiation, which are most commonly used to treat EFT, have many systemic side effects including hair loss, nausea, vomiting, ulcers, and low blood cell count.
Medical Management (current best evidence)[edit | edit source]
Depending upon location of the tumor and metatstasis, doctors in many specialties help treat EFT. These include orthopedic surgical oncologists, pediatric or adult medical oncologists, radiation oncologists, pathologists, and radiologists. Most patients are treated at major hospital institutions or cancer centers.[3][4][10]
The first line of treatment is chemotherapy, also referred to as cytostatic drug therapy, which is given through an indwelling intravenous catheter. It is done in cycles to let the blood cell count recover inbetween. The second line of treatment, which can be done before or during chemotherapy, is local treatment. Local treatment includes radiation and/or surgery.Radiation can be used instead of surgery if it is too risky or complicated. It decreases the chance of return of the primary tumor. Over serveral weeks, daily treatments of radiation are given.Surgery can be done to remove the primary tumor or metastatic lesions. It can also be done to rebuild a body part or limb. As the child grows, reconstruction therapy will be necessary to lengthen the bone.[3][4][10]
Follow up intervals of 2-4 months for the first 3 years after completion of therapy are recommended for high-grade tumors such as EFT. Follow up every 6 months for year 4 and 5 and annually after that.[3]
Physical Therapy Management (current best evidence)[edit | edit source]
Physical therapy (PT) can be beneficial for victim's of EFT for many reasons and at different stages during the management process.
Pre-operative PT is beneficial when feasible.It should include strengthening of affected limb and aerobic conditioning (precaution: avoid weight bearing on extremity or placing weight distal to extremity in which tumor is located).[12]
Post operative PT is essential but caution must be taken because of the impaired healing process due to chemotherapy. Precautions include: stretching the skin in the area of incision, weight bearing status, lab values (especially platelet count). Some general guidlines include: aerobic conditioning, strengthening, continuous passive range of motion, and aquatic therapy.[12]
If amputation is done, it may take the child several months to learn to use a prosthetic leg or arm. A physical therapist will be able to assist in fitting the prosthesis, teaching the child how to use it, and how to use necessary assistive devices. Children may also have a tissue graft, which the child needs to start moving almost immediately. Physical therapy and rehabilitation is typically recommended for six to twelve weeks post operation.[10]
Alternative/Holistic Management (current best evidence)[edit | edit source]
Although there are plenty of resources describing the use of diet and herbal remedies for curing cancer, there is not sufficient evidence or research to support these treatments.
Differential Diagnosis[edit | edit source]
Osteomyelitis and Ewing's Sarcoma may both present with swelling, redness, low grade fever, and flu-like symptoms. The patient will typically experience intermittent pain with Ewing's Sarcoma versus the constant pain seen with osteomyelitis. The patient may also experience extreme fatigue, weight loss, and loss of appetite with a tumor. Antibiotics will not effect Ewing's Sarcoma, but should help with osteomyelitis. Lab values of Ewing's Sarcoma versus osteomyelitis:
Ewings Sarcoma: elevated lactate dehydrogenase (LDH), possible elevation of sedimentation rate (UCSF childrens hosp)
As a physical therapist, one should be cautious when the symptoms of "growing pains" or a proposed sports injury are out of proportion or abnormal.
Case Reports/ Case Studies[edit | edit source]
add links to case studies here (case studies should be added on new pages using the case study template)
Resources
[edit | edit source]
Recent Related Research (from Pubmed)[edit | edit source]
see tutorial on Adding PubMed Feed
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References[edit | edit source]
see adding references tutorial.
- ↑ 1.0 1.1 1.2 1.3 Goodman, Boissonnault, Fuller. Pathology: Implications for the Physical Therapist. Pennsylvania: Saunders, 2003.
- ↑ 2.0 2.1 Medline Plus. Ewing’s Sarcoma. http://www.nlm.nih.gov/medlineplus/ency/article/001302.htm (accessed Feb 2011).
- ↑ 3.0 3.1 3.2 3.3 3.4 3.5 3.6 3.7 Grimer, Robert, Athanasou, Nick, Gerrand, Craig, Judson, Ian, Lewis, Ian, Morland, Bruce, Peake, David, Seddon, Beatrice, Whelan, Jereamy. UK Guidelines for the Management of Bone Sarcomas. Sarcoma 2010; 1-14. http://www.hindawi.com/journals/srcm/2010/317462/ (accessed 28 Feb 2011).
- ↑ 4.0 4.1 4.2 4.3 4.4 4.5 4.6 4.7 4.8 4.9 Paulussen, Michael. Frohlich, Brigit, Jurgens, Herbert. Ewing Tumour: Incidence, Prognosis, and Treatment Options. Pediatric Drugs 2001; 3(12); 899-913. http://www.ncbi.nlm.nih.gov/pubmed/11772151 (accessed 28 Feb 2011).
- ↑ 5.0 5.1 Elaine Lonneman’s Powerpoint, Oncology. Pathophysiology of Complex Patient Problems. Bellarmine University 2011.
- ↑ 6.0 6.1 Goodman C, Snyder T. Differential Diagnosis for Physical Therapists: Screening for Referral. St. Louis, MO: Saunders Elsevier: 2007
- ↑ 7.0 7.1 Karosas, Ann O. Ewing’s sarcoma. Am J Health-Syst Pharm 2010; 67; 1599-1605. http://www.ajhp.org/content/67/19/1599.full.pdf+html (accessed 28 Feb 2011).
- ↑ Kids Health from Nemours. Ewing Sarcoma. http://kidshealth.org/parent/medical/cancer/ewings.html (accessed 28 Feb 2011).
- ↑ 9.0 9.1 Children’s Hospital Boston. Ewing’s Sarcoma. http://www.childrenshospital.org/az/Site852/mainpageS852P0.html (accessed March 2011)
- ↑ 10.0 10.1 10.2 10.3 10.4 10.5 American Academy of Orthopaedic Surgeons. Ewing’s Sarcoma. http://orthoinfor.aaos.org/topic.cfm?topic=a00082 (accessed 28 Feb 2011).
- ↑ Cite error: Invalid
<ref>tag; no text was provided for refs namedmedline - ↑ 12.0 12.1 Tiley, Karen L. Multidisciplinary Rounds: Limb Salvage Surgery and Bone Marrow Transplant in an Adolescent with Recurrent Ewing’s Sarcoma. Cancer Practice 1995; 3(2); 72-75.
