Sourasky Medical Center (Ichilov)
Ofer Merimsky
Treatment plan for little and young patients is conducted in the specialized Dana Dwek Children’s Hospital which belongs to Sourasky Medical Group.
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Treatment plan for little and young patients is conducted in the specialized Dana Dwek Children’s Hospital which belongs to Sourasky Medical Group.
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Dr. Ofer Merimsly is the best sarcoma, lymphoma, and lung cancer doctor within Israel and in the world. Also specializes in Whipple surgery treatment for patients with pancreatic cancer. Head of the National Center for sarcomas of bone and soft tissues of the Tel Aviv Medical Center Sourasky (Ichilov).
Specialty:
Education and specialization:
Membership:
Dr. Ronit El Hasid is the Head of Pediatric Oncohematology and Oncology at Dana Dwek Children’s Hospital (Sourasky). She specializes in bone marrow and umbilical blood transplantation and has conducted over 300 transplantations and published 50 papers and 40 reports. She is a member of American Association for Hematology and Israeli Society for Pediatric Hematooncology, and has previously practiced in the City of Hope Hospital (Los-Angeles) and other medical centers in Israel.
Dr. Dror Levin is a senior pediatrician and director of the blood disorder and bone cancer (sarcoma) treatment departments at Children's Hospital "Dana" and Medical Center "Sourasky" respectively. He is a specialist in pediatric medicine, hematology, and oncology, with additional experience studying abroad at the Rizzoli Orthopaedic Institute in Italy.
Dr. Jacob Zauberman is a highly experienced neurosurgeon specializing in brain tumors, epilepsy, endoscopic surgeries, and hydrocephalus treatment. He graduated from the Medical Faculty at the Technion in Israel and studied at BYU and Seattle Children's Hospital in the US. He is a member of the Israeli Association of Neurosurgeons, the American Neurosurgical Association, and the American Association for the Surgery of Trauma.
Rhabdomyosarcoma develops from a transversely striated (skeletal) muscle and is a colony of modified muscle cells (myocytes). In a result of a number of successive divisions, tumor elements are simplified and become similar to embryonic cells (precursors of muscles) that are rabdomioblasts. The longer the tumor does not being treat, the worse the prognosis for life is as there is the higher risk of metastasing and organ damage around tumors.
In two-thirds of cases, rhabdomyosarcoma affects the children up to 10 years, mainly boys (girls’ rate is in 2 times lower). Overwhelming majority of the illness cases (90%) is up to the age of 25 years.
Types of rhabdomyosarcoma:
Major risk factors contributing to the development of rhabdomyosarcoma:
Rhabdomyosarcoma usually develops in people with immunodeficiency. People infected with HIV, TB, children with any form of anemia are the most vulnerable. It is necessary to pay attention to the children previously treated with chemotherapy. In some cases, rhabdomyosarcoma develops after leukemia.
Depending on the location of the main tumor, the disease manifests itself as follows:
The symptoms at different stages of rhabdomyosarcoma:
Stage 1 |
Stage 2 |
nearly invisible tumor, no local reactions |
visible (subdermal) tumor, some pain, redding |
Stage 3 |
Stage 4 |
intense pain, enlarged lymph nodes |
damage and dysfunction of organs, metastasing |
Israeli oncologists achieve excellent results even with common processes (3A-B stage):
After the examination of relatives, it turned out that my brother can be a bone marrow donor. We have conducted stem cell transplantation.
Now the boy is 2 years old, he is often sick, but there are no tumor signs anymore. We take drugs (necessary for normal functioning of the transplanted bone marrow).”
Valentina, Turkmenistan
Prediction for patients depends on the process stage. Even at the 4th stage, the five-year survival rate exceeds 30% (alveolar form of the disease). Careful attention to a patient after surgery and intensive chemotherapy allows to achieve full cure in 70% of all patients with rhabdomyosarcoma.
It is recommended to make regular visits to the oncologist (every 2 months during the first year after surgery) and periodic screening of tissues:
Two recent studies allow quick identifying metastases in the process expansion.