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rhabdoid tumor/horečka

Odkaz je uložen do schránky
ČlánkyKlinické testyPatenty
10 Výsledek

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

Články mohou překládat pouze registrovaní uživatelé
Přihlášení Registrace
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.

Články mohou překládat pouze registrovaní uživatelé
Přihlášení Registrace
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].

Články mohou překládat pouze registrovaní uživatelé
Přihlášení Registrace
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.

Články mohou překládat pouze registrovaní uživatelé
Přihlášení Registrace
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.

Články mohou překládat pouze registrovaní uživatelé
Přihlášení Registrace
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].

Články mohou překládat pouze registrovaní uživatelé
Přihlášení Registrace
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.

Články mohou překládat pouze registrovaní uživatelé
Přihlášení Registrace
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.

Články mohou překládat pouze registrovaní uživatelé
Přihlášení Registrace
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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