3 edition of Malignant Neoplasms in Childhood and Adolescence (Monographs in Pediatrics, Vol 18) found in the catalog.
by S. Karger AG (Switzerland)
Written in English
|The Physical Object|
|Number of Pages||396|
Purpose: To examine the clinical presentation, treatment and results in children and adolescents with primary mediastinal (PM) and retroperitoneal (RP) germ cell tumors (GCTs). Methods: The TGM95 trial for malignant GCTs was conducted in France between and to evaluate a strategy adapted to prognostic factors with cisplatin-based chemotherapy and surgical management. COVID Resources. Reliable information about the coronavirus (COVID) is available from the World Health Organization (current situation, international travel).Numerous and frequently-updated resource results are available from this ’s WebJunction has pulled together information and resources to assist library staff as they consider how to handle coronavirus.
Increased risk of second malignant neoplasms in adolescents and young adults with cancer. Jean S. Lee MD. Department of Pediatrics, University of California San Francisco Benioff Children's Hospital San Francisco, San Francisco, California. Search for more papers by this author. Yang Zhang, Karen Goddard, John J. Spinelli, Carolyn Gotay, Mary L. McBride, Risk of Late Mortality and Second Malignant Neoplasms among 5-Year Survivors of Young Adult Cancer: A Report of the Childhood, Adolescent, and Young Adult Cancer Survivors Research Program, Journal of Cancer Epidemiology, //, , (), ().
Two of the 23 malignant tumors developed in the vagina and the others originated in the ovary. In 19 patients unilateral salpingo‐oophorectomy or local excision was done in an attempt for reproductive organ conservation; 4 cases of advanced stage disease were treated with hysterectomy and/or bilateral salpingo‐oophorectomy. The liver is the third-most-common site for intra-abdominal malignancy in children, following adrenal neuroblastoma and wilms tumor. Although the overall incidence of childhood cancer has been slowly increasing since , cancer in children and adolescents is still rare, the incidence of primary malignant liver tumors per year is per million children in the United States [1, 2, 3, 4].
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INTRODUCTION. Each year in the United States, approximat adolescents and young adults (AYAs) ages 15 to 39 years are diagnosed with, die of, invasive cancer. 1 This compares to approximately children aged ≤ 14 years and over million older adults aged (≥40 years) diagnosed annually.
Cancer survival continues to increase, and more than million survivors Cited by: St Jude Children’s Research Hospital Childhood Cancer Survivor Study reported a % cumulative incidence of SMN at 10 years for all kidney tumors, the large majority being Wilms tumor.
SMN cumulative incidence continued to increase at 20 and 30 years to % and % by: Malignant neoplasms in childhood and adolescence. Basel ; New York: Karger, (OCoLC) Online version: Malignant neoplasms in childhood and adolescence. Basel ; New York: Karger, (OCoLC) Document Type: Book: All Authors /.
OBJECTIVE--To assess the relative risk of developing a second malignant neoplasm in people with a diagnosis of cancer in childhood and adolescence.
DESIGN--Register based follow up study. SETTING--Populations of Nordic countries. SUBJECTS, people under the age of 20 with a first malignant neoplasm diagnosed during the period Cited by: Although in the past malignant tumors of epithelial origin were predominant, today the most common type of tumor is rhabdomyosarcoma.
Indeed, % (20/47 cases) of laryngeal malignant tumors in children and adolescents are rhabdomyosarcomas. In all cases in which the cell type was specified they were by: Malignant neoplasm constituted % of orofacial tumours and tumour-like lesions in children and adolescent in our centre.
In agreement with previous reports from Africa, Burkitt's lymphoma is the most common malignant tumour and carcinoma is relative rare in this age group. Journals & Books; Help Malignant pancreatic neoplasms in children and adolescents are rare. The clinical presentation, pathologic characteristics, management, and outcomes at two institutions are discussed.
Regardless of the tumor type, complete surgical resection is the main treatment modality for primary malignant neoplasms in. Purpose: Bladder tumors are rare in children and adolescents.
For this reason, the diagnosis is sometimes delayed in pediatric patients. We aimed to describe the diagnosis, treatment, and follow-up methods of bladder urothelial neoplasms in children and adolescents. The other six children were free of detectable tumor 16 months to 8 years from diagnosis. Chemotherapy with PBVb and actinomycin D+ cyclophosphamide (AC) should be used in the postoperative management of young persons with malignant ovarian tumors.
Adr is of doubtful value and may be considerably toxic. Malignant bone tumors are not common in children, and because these tumors occur most frequently in active adolescents, initial complaints may be attributed to a sports injury or a sprain [MALIGNANT TUMORS IN CHILDHOOD AND YOUTH: DIAGNOSIS AND PROGNOSIS] Dtsch Med J.
Sep 5; [Article in German]. GYNECOLOGY Ovarian neoplasms in childhood and adolescence II. Tumors of non-germ cell origin M. ABELL, PH.D.
HOLTZ, M.D. Ann Arbor, Michigan N E o P L A s M s of gonadal origin maybe divided on a histogenetic basis into 2 major groups representing those of germ cell origin and those from non-germ cell tissues that are both specific and nonspecific for the gonads. The 3 Sertoli cell neoplasms occurred in girls 3, 7, and 8 years of age, and 2 were associated with precocious development.
The 3 arrhenoblastomas, occurring after puberty, produced masculinizing effects. None of the Sertoli-Leydig cell groups of neoplasms behaved in a malignant manner. Abstract Our purpose was to assess the risk of developing a second malignant neoplasm (SMN) after cancer in childhood and adolescence associated with different treatment modalities.
Our investigati. The goal of the current study was to describe the incidence, characteristics, and outcomes of secondary malignant neoplasms (SMNs) in this population.
METHODS Patients aged birth to 40 years at time of primary diagnosis with osteosarcoma and reported to the Surveillance, Epidemiology, and End Results (SEER) program between and were.
Background: Brain metastases of pediatric germ cell tumors are uncommon, and there is limited information regarding their incidence, clinical presentation, response to treatment, and influence on survival.
Methods: The authors reviewed the experience with brain metastases from pediatric germ cell tumors at St. Jude Children's Research Hospital (Memphis, TN) over a year period. Time variations in the risk of cancer following irradiation in childhood.
Radiat Res. Jun; (3)– Olsen JH, Garwicz S, Hertz H, Jonmundsson G, Langmark F, Lanning M, Lie SO, Moe PJ, Møller T, Sankila R, et al. Second malignant neoplasms after cancer in childhood or adolescence.
Esophageal tumors are exceedingly rare in childhood and adolescence. However, they should always be considered when evaluating a pediatric patient who presents with dysphagia. Although both are rare, benign esophageal tumors are more frequent than malignant ones.
Daniel M. Green, Chemotherapy for the Treatment of Children and Adolescents With Malignant Germ Cell Tumors, Journal of Clinical Oncology, /JCO, 26, 20, (. Little information is available regarding the relative frequency of benign and malignant ovarian tumors in children and adolescents.
This series of primary ovarian neoplasms occurring in patients under 20 years of age indicates the comparative frequency of various types of tumors in young patients. Garwicz S, Anderson H, Olsen JH, et al. Second malignant neoplasms after cancer in childhood and adolescence: a population-based case-control study in the 5 Nordic countries.
The Nordic Society for Pediatric Hematology and Oncology. The Association of the Nordic Cancer Registries. Int J Cancer. ; –Primary heart tumors are uncommon in children.
The majority of them are benign, with only 10% malignant. Among malignant cardiac tumors, sarcoma (rhabdomyosarcoma, angiosarcoma, synovial sarcoma) and lymphoma (Burkitt's lymphoma, large B-cell lymphoma, lymphoblastic lymphoma) predominate.
There are .Vascular anomalies include both vascular tumors (benign, borderline and malignant) and vascular malformations (low-flow and high-flow).
Diagnosis and management of vascular anomalies can be challenging, particularly in infancy and childhood. The infantile hemangioma may lead to life-threatening, obstructive and disfiguring complications. In case of required treatment with oral propranolol, the.