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rhabdoid tumor/kuume

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ArtikkelitKliiniset tutkimuksetPatentit
10 tuloksia

Co-existent Rhabdoid Tumor of The Kidney and Brain in a Male Infant: A Rare Case.

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Malignant rhabdoid tumor of the kidney (MRTK) is a rare neoplasm of infancy. We report a case of a nine-month-old male infant who presented to the pediatrics outpatient department with the history of fever, lethargy, and abnormal head movements. On gross examination, the patient had a firm,

Malignant rhabdoid tumor of the liver: case report and literature review.

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A case of malignant rhabdoid tumor (MRT) occurring as a primary hepatic neoplasm in a 12-month-old Japanese female infant is presented. The patient had a slight fever for 2 weeks and presented with a palpable mass in her left hypochondrial region. After admission, the hepatic artery was embolized

[Teratoid/rhabdoid tumor of the central nervous system].

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Teratoid/rhabdoid tumor is a recently introduced infantile brain neoplasm of uncertain origin clinically characterized by a most aggressive course. We describe the case of a 2-year-old boy and a 7-year-old girl, the former presenting with central fever and hemiparesis, while vomiting and headache

Clinical presentation of rhabdoid tumors of the kidney.

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OBJECTIVE We designed this study to differentiate the clinical presentation, particularly the incidence of hematuria, of a rhabdoid tumor of the kidney (RTK), a rare but highly malignant tumor, from a Wilms tumor. METHODS We reviewed patient flow charts from the National Wilms Tumor Study Group and

Successful management of rhabdoid tumor of the liver.

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A 3-year-old male was referred because of fever, abdominal pain, and enlarged abdomen. Magnetic resonance imaging showed a very large lobulated mass involving predominantly the right lobe of liver. Tumor histology was consistent with rhabdoid tumor of the liver. The patient received 3 cycles of

[A case of embryonal rhabdomyosarcoma of the kidney].

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A case of embryonal rhabdomyosarcoma of the left kidney is reported. A 16-year-old boy was admitted with the complaint of left abdominal pain and fever on January 6, 1983. Radiological examination showed a tumor of the left kidney; and, nephrectomy was performed. Histopathologically the entire tumor

Renal Medullary Carcinoma: a Report of the Current Literature.

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We present an updated report of renal medullary carcinoma (RMC), a rare and aggressive condition.There is a majority of male patients, of African descent, in the second or third decade of life. In differential diagnosis, other tumors, such as malignant

Safety of high-dose intravenous mistletoe therapy in pediatric cancer patients: A case series.

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BACKGROUND Long-term survival of children with cancer has reached rates of up to 80%. Nevertheless, continued research devoted to further improvement of survival rates especially for patients with high-risk illnesses is necessary. Recent studies have shown direct positive effects on tumor reduction
Effective treatment for pediatric embryonal brain tumors includes dose-intensive multiagent chemotherapy (DIMAC) followed by high-dose chemotherapy with stem cell rescue (HDCSCR). Use of repeated cycles of DIMAC including high-dose methotrexate (HDMTX) without HDCSCR has not been
Pembrolizumab is approved for the treatment of advanced cancer in adults; however, no information is available on safety and efficacy in paediatric patients. We aimed to establish the recommended phase 2 dose of pembrolizumab and its safety and antitumour activity in advanced
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