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Journal articles on the topic 'Tumors in children'

To see the other types of publications on this topic, follow the link: Tumors in children.

Author: Grafiati

Published: 4 June 2021

Last updated: 30 July 2024

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1

Mathew, George, and Shwetha Jose. "PRIMARY TUMORS AND TUMOR-LIKE LESIONS OF BONE IN CHILDREN." International Journal of Integrative Medical Sciences 4, no. 6 (November 3, 2017): 507–11. http://dx.doi.org/10.16965/ijims.2017.112.

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2

Joaquim, Andrei Fernandes, Enrico Ghizoni, Marcelo Gomes Cordeiro Valadares, Simone Appenzeller, Simone dos Santos Aguiar, and Helder Tedeschi. "Spinal tumors in children." Revista da Associação Médica Brasileira 63, no. 5 (May 2017): 459–65. http://dx.doi.org/10.1590/1806-9282.63.05.459.

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Summary Introduction: Spinal tumors are rare in the pediatric population, presenting many specific peculiarities when compared to adults. We have performed a broad narrative review to describe the most common spinal tumors in children, discussing their main characteristics and management options. Method: The authors have performed an extensive review of the peer-reviewed literature addressing the aforementioned objectives. Results: Multimodality radiological studies (plain films, 3D computed tomography scan and magnetic resonance imaging) are necessary for proper evaluation and differential diagnosis of spinal tumors in children. In selected cases nuclear medicine imaging is used to improve the chances of a more accurate diagnosis. As a general rule, a fine needle biopsy is recommended after radiological evaluation to confirm the tumor's histology. Primary bone tumors can be divided into benign bone tumors, mostly represented by vertebral hemangiomas, osteoid osteomas, osteoblastomas, aneurismal bone cysts, and eosinophilic granulomas, and malign or aggressive tumors, such as Ewing's or osteogenic sarcomas. Secondary bone tumors (spinal metastases) comprise different tumor histologies, and treatment is mainly based on tumor's radiosensitivity. The characteristics and treatment options of the main spinal tumors are discussed in details. Conclusion: Spinal tumors in children are rare lesions that demand a thorough understanding of their main characteristics for their proper management. Understanding the nuances of spinal tumors in children is of paramount importance for improving outcomes and chances of cure.

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3

Akyol, Şefika. "Kidney Tumors in Children." Journal of Pediatric Academy 4, no. 2 (June 22, 2023): 44–49. http://dx.doi.org/10.4274/jpea.2023.237.

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Wilms tumor (WT) is an embryonal tumor of the kidneys. It is associated with many oncogenic genetic aberrations and congenital anomalies. Owing to worldwide clinical research and optimized patient care, curative therapy can be obtained in 90% of diagnosed children with WT. The decision of treatment mainly depends on stage, age, histological type, and genetic markers. Except for WT; congenital mesoblastic nephroma, clear cell sarcoma, malignant rhabdoid tumor, and renal cell carcinoma constitute 5% of kidney tumors. Herein, WT and other tumors of the kidney will be emphasized.

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4

Llempén, Mercedes, Gema Ramírez, Rosa Cabello, and Catalina Márquez. "Adrenocortical tumors in children." Revista Médica de Trujillo 14, no. 3 (August 19, 2019): 152–59. http://dx.doi.org/10.17268/rmt.2019.v14i03.08.

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5

Edwards, Michael S. B., Roger J. Hudgins, Charles B. Wilson, Victor A. Levin, and William M. Wara. "Pineal region tumors in children." Journal of Neurosurgery 68, no. 5 (May 1988): 689–97. http://dx.doi.org/10.3171/jns.1988.68.5.0689.

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✓ The authors believe that the preferred treatment for pineal region tumors in children requires definitive surgery with a histological diagnosis and that a conservative approach consisting of shunting and radiation therapy no longer seems to be appropriate. The results are reported of a retrospective review of the presentation, treatment, and outcome of 36 children under the age of 18 years treated between 1974 and 1986. Eleven children had germinomas (two-cell type), seven had astrocytomas, and the remaining 18 had 15 histologically different tumor types. Surgery was performed on 30 patients; there were no deaths, but a 10% rate of persistent morbidity was found. The median follow-up period was 4 years. Nine (82%) of 11 patients with germinomas are alive without evidence of recurrence; one child died from recurrent tumor in the pineal region and another is presently being treated for recurrent tumor of the spinal cord. Six (86%) of the seven patients with astrocytoma are well after biopsy and radiation therapy. Of the remaining 18 children, five (28%) died from tumor progression. The cerebrospinal fluid (CSF) tumor markers α-fetoprotein and β-human chorionic gonadotropin were helpful in determining the presence of malignant germ-cell tumors, particularly those with a poor prognosis. Magnetic resonance imaging was useful for diagnosis and for planning the operative approach. Magnetic resonance images showed the presence of pineal region tumors in four children with hydrocephalus who had no evidence of tumor on computerized tomography scans. Because the great variety of tumor types found in the pineal region must be treated in different ways and because improved microsurgical and stereotaxic surgical techniques have made mortality and morbidity rates acceptably low, a biopsy diagnosis should be obtained in all patients. Preoperative assessment of CSF tumor markers and cytology is useful for the identification of patients who have a poor prognosis.

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6

Ostwal, Piyush, and Shanbhag Nandan. "SEIZURES IN CHILDREN WITH LOW GRADE GLIOMA." MNJ (Malang Neurology Journal) 7, no. 1 (January 1, 2021): 60–65. http://dx.doi.org/10.21776/ub.mnj.2021.007.01.12.

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Seizures are a common presentation of pediatric brain tumors. The incidence of pediatric brain tumor (Age 0-19 years) ranges from 1.12–5.26 cases per 100,000 persons. Low grade gliomas are an important subgroup of pediatric brain tumors causing epilepsy. Low-grade gliomas are largely slow-growing tumors and the manifestations are dependent on age, location, tumor type, size of tumor and rate of tumor growth. Seizures have been reported in up to 38 % of children with supratentorial tumors. The tumors are identified when work up of patients for epilepsy includes electrophysiological and imaging studies. The primary treatment modality remains surgical excision. Antiepileptic medications are used for control of seizures. Subsequent histopathological diagnosis is important for prognostication. The tumors commonly associated with long-term epilepsy in various studies were ganglioglioma, dysembryoplastic neuroepithelial tumor, pilocytic astrocytoma and pilocytic xanthoastrocytoma. The outcome of surgery with regards to seizure control is generally good. Though concomitantly antiepileptic medications will be needed for most of them. An attempt is made in this review to summarize the epidemiology, clinical features, pathology and treatment aspects of pediatric low grade gliomas presenting with seizures.

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7

Alimoukhamedova, G. A., and Z. Yu Khalimova. "ANDROGEN-SECRETING ADRENAL TUMORS." International Journal of Medical Sciences And Clinical Research 02, no. 04 (April 1, 2022): 16–22. http://dx.doi.org/10.37547/ijmscr/volume02issue04-03.

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The objective of this research was to study clinical peculiarities of androgen-secreting tumors in adrenals dependent on age and gender. Among the patients with various neoplasms in adrenals (n=282), who received out-patient and in-patient treatment in the Republican Specialized Scientific Practical Medical Center of Endocrinology of the Uzbekistan Public Healthcare Ministry within the period from 2000 to 2018, androgen-secreting tumors were diagnosed in 9(3.2%) patients: 3(33.3%) men and 6(66.7%) women aged from 1.7 to 34 years old. As well as in the other groups with adrenal neoplasms, there was double prevailing of women. However, correlation of separate age subgroups was significantly different. In this group of patients specific weight of children increased (55.6%) compared to adults under 44 years old (44.4%). In spite of similar etiopathogenetic basis analysis of clinical manifestations of adrenal androgen-secreting tumors in children and adults revealed some differences. So, performed analysis confirms the presence of several symptoms in children, symptoms which are not observed in adults. On the other hand, somatic disorders in adults are more expressed than in children.

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8

Bartels, Loren J., and Michael Gurucharri. "Pediatric Glomus Tumors." Otolaryngology–Head and Neck Surgery 99, no. 4 (October 1988): 392–95. http://dx.doi.org/10.1177/019459988809900407.

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Glomus tumors of the middle ear are unusual in adults, but exeedingly rare in children. While a dull, red bulging tympanic membrane in the adult may suggest a glomus tumor, it generally signifies infection in the child. This report details our management of a 10-year-old girl afflicted with bilateral chronic middle ear cleft infection that obscured bilateral glomus tumors. Review of the current English language literature reveals seven additional case reports of otologic glomus tumors in children less than fourteen years of age. Two additional cases are presented that were given to the senior author by personal communication, producing a total of 10 cases for review. Glomus tumors in children may be hidden by otitis media and appear more likely to be endocrine active. Failure to cure the lesion is apparent in five of six case reports of children with glomus jugulare tumors; three of these children are reported to have expired. Complete surgical extirpation is advocated for childhood glomus tumors.

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9

Akhaladze, D. G., G. S. Rabaev, and N. S. Grachev. "Cytoreductive surgery and hyperthermic intraperitoneal chemotherapy in children." Pediatric Hematology/Oncology and Immunopathology 18, no. 4 (December 31, 2019): 118–26. http://dx.doi.org/10.24287/1726-1708-2019-18-4-118-126.

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Cytoreductive surgery with hyperthermic intraperitoneal chemotherapy (HIPEC) is treatment of choice for determined group of adult patients. Cytoreduction and HIPEC is usually used in patients with ovarian, gastric and colorectal cancer, appednix cancer, peritoneal mesothelioma and in some tumors of another localization. The experience of cytoreductive surgery and HIPEC in childhood is limited due to the lower frequency of peritoneal carcinomatosis in pediatric population. However, about 30% of malignant tumors in children develop in peritoneal cavity and pelvis. High recurrence rate are typical for these tumors, particularly due to tumor rupture. Taking into consideration low frequency of epithelioid tumors in children HIPEC is used for patients with other tumor types such as desmoplastic small round cell tumor (DSRCT), germ cell tumors, rhabdomyosarcoma and others. The aim o this paper is the review of the literature and present experience analysis of cytoreductive surgery and HIPEC in children.

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10

McAbee, Joseph H., Joseph Modica, Clinton J. Thompson, Alberto Broniscer, Brent Orr, Asim F. Choudhri, Frederick A. Boop, and Paul Klimo. "Cervicomedullary tumors in children." Journal of Neurosurgery: Pediatrics 16, no. 4 (October 2015): 357–66. http://dx.doi.org/10.3171/2015.5.peds14638.

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OBJECT Cervicomedullary tumors (CMTs) represent a heterogeneous group of intrinsic neoplasms that are typically low grade and generally carry a good prognosis. This single-institution study was undertaken to document the outcomes and current treatment philosophy for these challenging neoplasms. METHODS The charts of all pediatric patients with CMTs who received treatment at St. Jude Children’s Research Hospital between January 1988 and May 2013 were retrospectively reviewed. Demographic, surgical, clinical, radiological, pathological, and survival data were collected. Treatment-free survival and overall survival were estimated, and predictors of recurrence were analyzed. RESULTS Thirty-one children (16 boys, 15 girls) with at least 12 months of follow-up data were identified. The median age at diagnosis was 6 years (range 7 months-17 years) and the median follow-up was 4.3 years. Low-grade tumors (Grade I or II) were present in 26 (84%) patients. Thirty patients underwent either a biopsy alone or resection, with the majority of patients undergoing biopsy only (n = 12, 39%) or subtotal resection (n = 14, 45%). Only 4 patients were treated solely with resection; 21 patients received radiotherapy alone or in combination with other treatments. Recurrent tumor developed in 14 children (45%) and 4 died as a result of their malignancy. A high-grade pathological type was the only independent variable that predicted recurrence. The 5- and 10-year treatment-free survival estimates are 64.7% and 45.3%, respectively. The 5- and 10-year overall survival estimate is 86.7%. CONCLUSIONS Children with CMTs typically have low-grade neoplasms and consequently long-term survival, but high risk of recurrence. Therapy should be directed at achieving local tumor control while preserving and even restoring neurological function.

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11

Upton, Joseph, and Christopher Coombs. "VASCULAR TUMORS IN CHILDREN." Hand Clinics 11, no. 2 (May 1995): 307–36. http://dx.doi.org/10.1016/s0749-0712(21)00050-0.

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12

Chatterjee, Sandip, and Uttara Chatterjee. "Intramedullary tumors in children." Journal of Pediatric Neurosciences 6, no. 3 (2011): 86. http://dx.doi.org/10.4103/1817-1745.85718.

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13

Bajčiová, Viera. "Gastrointestinal tumors in children." Onkologie 13, no. 2 (April 5, 2019): 63–68. http://dx.doi.org/10.36290/xon.2019.012.

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14

Litten, Jason B., and Gail E. Tomlinson. "Liver Tumors in Children." Oncologist 13, no. 7 (July 2008): 812–20. http://dx.doi.org/10.1634/theoncologist.2008-0011.

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15

Yildiz, Turan. "Testicular tumors in children." Sakarya Medical Journal 3, no. 1 (2013): 48–50. http://dx.doi.org/10.5505/sakaryamj.2013.54872.

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16

Cohen, Alan R. "Brain Tumors in Children." New England Journal of Medicine 386, no. 20 (May 19, 2022): 1922–31. http://dx.doi.org/10.1056/nejmra2116344.

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17

Ribeiro, R. C., E. L. Michalkiewicz, B. C. Figueiredo, L. DeLacerda, F. Sandrini, M. D. Pianovsky, G. Sampaio, and R. Sandrini. "Adrenocortical tumors in children." Brazilian Journal of Medical and Biological Research 33, no. 10 (October 2000): 1225–34. http://dx.doi.org/10.1590/s0100-879x2000001000013.

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18

Munirulhaq, Muhammad. "Orbital tumors in children." Orbit 8, no. 3 (January 1989): 215–22. http://dx.doi.org/10.3109/01676838909087653.

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19

Nemes, Julianne, and Marie Collins Donahue. "SOLID TUMORS IN CHILDREN." Nursing Clinics of North America 29, no. 4 (December 1994): 585–98. http://dx.doi.org/10.1016/s0029-6465(22)02247-2.

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20

Aronson, Daniel C. "Liver tumors in children." Hepatoma Research 8 (2022): 22. http://dx.doi.org/10.20517/2394-5079.2022.20.

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21

Alter, Craig A., Karuna V. Shekdar, and Laurie E. Cohen. "Pituitary Tumors in Children." Advances in Pediatrics 68 (August 2021): 211–25. http://dx.doi.org/10.1016/j.yapd.2021.05.007.

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22

Ismail-zade, R. S., A. O. Tarasik, A. T. Shimanski, and D. V. Kochubinski. "Desmoid Tumors in Children." Онкопедиатрия 2, no. 2 (2015): 131–38. http://dx.doi.org/10.15690/onco.v2.i2.1344.

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23

CRONEN, PAUL W., and HIRIKATI S. NAGARAJ. "Ovarian Tumors in Children." Southern Medical Journal 81, no. 4 (April 1988): 464–68. http://dx.doi.org/10.1097/00007611-198804000-00014.

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24

Kim, Hae Sol, Ra Joo Im, Hye Eun Kim, Chul Gu Lee, Jeong Meen Seo, and Suk Koo Lee. "Liver Tumors in Children." Journal of the Korean Association of Pediatric Surgeons 13, no. 2 (2007): 144. http://dx.doi.org/10.13029/jkaps.2007.13.2.144.

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25

Samson, T. "Parotid Tumors in Children." AAP Grand Rounds 31, no. 2 (January 31, 2014): 22. http://dx.doi.org/10.1542/gr.31-2-22.

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26

Srinivas, Kannepalli. "ADRENOCORTICAL TUMORS IN CHILDREN." Journal of Evolution of Medical and Dental Sciences 4, no. 70 (August 29, 2015): 12184–86. http://dx.doi.org/10.14260/jemds/2015/1756.

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27

Kline, Nancy E., and Nicole Sevier. "Solid tumors in children." Journal of Pediatric Nursing 18, no. 2 (April 2003): 96–102. http://dx.doi.org/10.1053/jpdn.2003.12.

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28

&NA;. "Solid Tumors in Children." American Journal of Surgical Pathology 14, no. 6 (June 1990): 602. http://dx.doi.org/10.1097/00000478-199006000-00017.

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29

Shields, Carol L., and Jerry A. Shields. "Conjunctival tumors in children." Current Opinion in Ophthalmology 18, no. 5 (September 2007): 351–60. http://dx.doi.org/10.1097/icu.0b013e32823ecfbb.

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30

Oh, Chaeyoun, Joong Kee Youn, Ji-Won Han, Hyun-Young Kim, and Sung-Eun Jung. "Abdominal tumors in children." Medicine 95, no. 46 (November 2016): e5181. http://dx.doi.org/10.1097/md.0000000000005181.

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31

Emre, Sukru, and Greg J. McKenna. "Liver tumors in children." Pediatric Transplantation 8, no. 6 (December 2004): 632–38. http://dx.doi.org/10.1111/j.1399-3046.2004.00268.x.

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32

Pomeroy, Scott L. "Brain tumors in children." Current Opinion in Pediatrics 4, no. 6 (December 1992): 930–34. http://dx.doi.org/10.1097/00008480-199212000-00004.

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33

Packer, Roger J. "Brain tumors in children." Current Opinion in Pediatrics 7, no. 1 (February 1995): 64–72. http://dx.doi.org/10.1097/00008480-199502000-00012.

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34

Packer, Roger J. "Brain tumors in children." Current Opinion in Pediatrics 8, no. 6 (December 1996): 549–57. http://dx.doi.org/10.1097/00008480-199612000-00003.

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35

Pollack, Ian F. "Brain Tumors in Children." New England Journal of Medicine 331, no. 22 (December 1994): 1500–1507. http://dx.doi.org/10.1056/nejm199412013312207.

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36

Abramowicz, S. "Jaw Tumors in Children." Journal of Oral and Maxillofacial Surgery 68, no. 9 (September 2010): e51. http://dx.doi.org/10.1016/j.joms.2010.06.073.

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37

Hornick, Jason L. "Myofibroblastic Tumors in Children." Surgical Pathology Clinics 3, no. 3 (September 2010): 653–88. http://dx.doi.org/10.1016/j.path.2010.06.004.

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38

Kastenberg, Zachary J., and Eric R. Scaife. "Adrenocortical tumors in children." Seminars in Pediatric Surgery 29, no. 3 (June 2020): 150927. http://dx.doi.org/10.1016/j.sempedsurg.2020.150927.

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39

Ladino-Torres, Maria F., and Peter J. Strouse. "Gastrointestinal Tumors in Children." Radiologic Clinics of North America 49, no. 4 (July 2011): 665–77. http://dx.doi.org/10.1016/j.rcl.2011.05.009.

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40

Kadota, Richard P., Judith B. Allen, Gary A. Hartman, and Wayne E. Spruce. "Brain tumors in children." Journal of Pediatrics 114, no. 4 (April 1989): 511–19. http://dx.doi.org/10.1016/s0022-3476(89)80686-9.

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41

Penn, O.D, Sasha, and Mark T. Dunbar, O.D., F.A.A.O. "Orbital tumors in children." Clinical Eye and Vision Care 10, no. 4 (January 1999): 195–204. http://dx.doi.org/10.1016/s0953-4431(98)00023-x.

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42

Stocker, J. Thomas. "Hepatic Tumors in Children." Clinics in Liver Disease 5, no. 1 (February 2001): 259–81. http://dx.doi.org/10.1016/s1089-3261(05)70163-x.

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43

Binning, Mandy, Paul Klimo, Wayne Gluf, and Liliana Goumnerova. "Spinal Tumors in Children." Neurosurgery Clinics of North America 18, no. 4 (October 2007): 631–58. http://dx.doi.org/10.1016/j.nec.2007.07.001.

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44

Fernbach, Sandra K., and Kate A. Feinstein. "Renal tumors in children." Seminars in Roentgenology 30, no. 2 (April 1995): 200–217. http://dx.doi.org/10.1016/s0037-198x(05)80034-3.

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45

Kovalyov, A. I. "Desmold tumors in children." European Journal of Cancer 33 (September 1997): S125—S126. http://dx.doi.org/10.1016/s0959-8049(97)85090-3.

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46

Fleming, Adam J., and Susan N. Chi. "Brain Tumors in Children." Current Problems in Pediatric and Adolescent Health Care 42, no. 4 (April 2012): 80–103. http://dx.doi.org/10.1016/j.cppeds.2011.12.002.

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47

Lee, Seong Wook. "Renal Tumors in Children." Clinical Pediatric Hematology-Oncology 24, no. 1 (April 30, 2017): 21–36. http://dx.doi.org/10.15264/cpho.2017.24.1.21.

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48

Ciftci, Arbay O., Mehmet Emin Şenocak, F. Cahit Tanyel, and Nebil Büyükpamukçu. "Adrenocortical tumors in children." Journal of Pediatric Surgery 36, no. 4 (April 2001): 549–54. http://dx.doi.org/10.1053/jpsu.2001.22280.

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49

Ciftci, Arbay O., Meltem Bingöl-Koloğlu, Mehmet E. Şenocak, F. Cahit Tanyel, Münevver Büyükpamukçu, and Nebil Büyükpamukçu. "Testicular tumors in children." Journal of Pediatric Surgery 36, no. 12 (December 2001): 1796–801. http://dx.doi.org/10.1053/jpsu.2001.28841.

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50

Bullock, John D., Stuart H. Goldberg, and Steven M. Rakes. "ORBITAL TUMORS IN CHILDREN." Ophthalmic Plastic & Reconstructive Surgery 5, no. 1 (March 1989): 13–16. http://dx.doi.org/10.1097/00002341-198903000-00002.

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