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1

Geller, Evan, and Polly S. Kochan. "Renal Neoplasms of Childhood." Radiologic Clinics of North America 49, no. 4 (2011): 689–709. http://dx.doi.org/10.1016/j.rcl.2011.05.003.

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2

Hancock, Betty Jean, Maria Di Lorenzo, Sami Youssef, Salam Yazbeck, Jacques-Edouard Marcotte, and Pierre-Paul Collin. "Childhood primary pulmonary neoplasms." Journal of Pediatric Surgery 28, no. 9 (1993): 1133–36. http://dx.doi.org/10.1016/0022-3468(93)90147-d.

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3

Lala, Shailee V., and Naomi Strubel. "Ovarian neoplasms of childhood." Pediatric Radiology 49, no. 11 (2019): 1463–75. http://dx.doi.org/10.1007/s00247-019-04456-8.

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4

Maniar, Tapan N., Inbal Braunstein, Stephen Keefe, et al. "Childhood ALL and second neoplasms." Cancer Biology & Therapy 6, no. 10 (2007): 1525–31. http://dx.doi.org/10.4161/cbt.6.10.4928.

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5

Lee, Christina Y., Lauren M. Sholl, Bin Zhang, et al. "Atypical Spitzoid Neoplasms in Childhood." American Journal of Dermatopathology 39, no. 3 (2017): 181–86. http://dx.doi.org/10.1097/dad.0000000000000629.

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6

Chung, C. J., V. Bui, Lynn A. Fordham, Jeannie Hill, and Dorothy Bulas. "Malignant intraperitoneal neoplasms of childhood." Pediatric Radiology 28, no. 5 (1998): 317–21. http://dx.doi.org/10.1007/s002470050363.

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7

Eryilmaz Polat, Sanem, Mina Gharibzadeh Hizal, Beste Ozsezen, Gokcen Dilsa Tugcu, and Guzin Cinel. "Childhood Pulmonary Neoplasms in Two Cases." Turkish Thoracic Journal 20, no. -1 (2019): 375. http://dx.doi.org/10.5152/turkthoracj.2019.375.

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8

Armata, Jerzy, and Walentyna Balwierz. "Prognosis in Childhood Second Malignant Neoplasms." Leukemia & Lymphoma 7, no. 4 (1992): 341–42. http://dx.doi.org/10.3109/10428199209049788.

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9

Kennedy, Alexander. "Ovarian Neoplasms in Childhood and Adolescence." Seminars in Reproductive Medicine 6, no. 01 (1988): 79–90. http://dx.doi.org/10.1055/s-2007-1021344.

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10

Varan, Ali, and Rejin Kebudi. "Secondary Malignant Neoplasms After Childhood Cancer." Pediatric Hematology and Oncology 28, no. 5 (2011): 345–53. http://dx.doi.org/10.3109/08880018.2011.553879.

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11

Karow, A., R. Nienhold, P. Lundberg, et al. "Mutational profile of childhood myeloproliferative neoplasms." Leukemia 29, no. 12 (2015): 2407–9. http://dx.doi.org/10.1038/leu.2015.205.

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12

Park, Meerim, Kyung Nam Koh, Bo Eun Kim, Ho Joon Im, Dae-Youn Kim, and Jong Jin Seo. "Pancreatic Neoplasms in Childhood and Adolescence." Journal of Pediatric Hematology/Oncology 33, no. 4 (2011): 295–300. http://dx.doi.org/10.1097/mph.0b013e318206990a.

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13

Zichová, Andrea, Tomáš Eckschlager, Marta Ganevová, Běla Malinová, Aleš Lukš, and Jarmila Kruseová. "Subsequent neoplasms in childhood cancer survivors." Cancer Epidemiology 68 (October 2020): 101779. http://dx.doi.org/10.1016/j.canep.2020.101779.

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14

Grabb, Paul A., L. Dade Lunsford, L. Dade Lunsford, et al. "Stereotactic Radiosurgery for Glial Neoplasms of Childhood." Neurosurgery 38, no. 4 (1996): 696–702. http://dx.doi.org/10.1227/00006123-199604000-00013.

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15

Langabeer, Stephen E., Karl Haslam, and Corrina McMahon. "The molecular landscape of childhood myeloproliferative neoplasms." Leukemia Research 38, no. 8 (2014): 997–98. http://dx.doi.org/10.1016/j.leukres.2014.06.003.

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16

Meadows, Anna T. "Second Malignant Neoplasms in Childhood Cancer Survivors." Journal of the Association of Pediatric Oncology Nurses 6, no. 1 (1989): 7–11. http://dx.doi.org/10.1177/104345428900600103.

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17

Bhattacharya, S., F. D. Lobo, P. K. Pai, and G. K. Pai. "Hepatic neoplasms in childhood - a clinicopathologic study." Pediatric Surgery International 14, no. 1-2 (1998): 51–54. http://dx.doi.org/10.1007/s003830050434.

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18

Klein, G., J. Michaelis, C. Spix, et al. "Second malignant neoplasms after treatment of childhood cancer." European Journal of Cancer 39, no. 6 (2003): 808–17. http://dx.doi.org/10.1016/s0959-8049(02)00875-4.

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19

Wang, Lu, Klaus J. Busam, Ryma Benayed, et al. "Identification of NTRK3 Fusions in Childhood Melanocytic Neoplasms." Journal of Molecular Diagnostics 19, no. 3 (2017): 387–96. http://dx.doi.org/10.1016/j.jmoldx.2016.11.005.

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20

Ajani, MustaphaAkanji, KolawoleOlanrewaju Aramide, TinuadeAdesola Ajani, AyodejiA Salami, and ClementAbu Okolo. "Childhood ovarian neoplasms in Ibadan, South-western Nigeria." Nigerian Medical Journal 57, no. 3 (2016): 164. http://dx.doi.org/10.4103/0300-1652.184061.

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21

Jenkner, Alessandro, Francesca Diomedi Camassei, Renata Boldrini, et al. "111 renal neoplasms of childhood: A clinicopathologic study." Journal of Pediatric Surgery 36, no. 10 (2001): 1522–27. http://dx.doi.org/10.1053/jpsu.2001.27036.

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22

Neglia, Joseph P., Anna T. Meadows, Leslie L. Robison, et al. "Second Neoplasms after Acute Lymphoblastic Leukemia in Childhood." New England Journal of Medicine 325, no. 19 (1991): 1330–36. http://dx.doi.org/10.1056/nejm199111073251902.

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23

Rickert, C. H., Stefan Probst-Cousin, and Filippo Gullotta. "Primary intracranial neoplasms of infancy and early childhood." Child's Nervous System 13, no. 10 (1997): 507–13. http://dx.doi.org/10.1007/s003810050127.

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24

dos Santos-Bueno, Filipe Vicente, Francianne Gomes Andrade, Ingrid Sardou-Cezar, et al. "Childhood Myeloid Neoplasms With PTPN11 Mutations in Brazil." Clinical Lymphoma Myeloma and Leukemia 20, no. 8 (2020): e496-e505. http://dx.doi.org/10.1016/j.clml.2020.04.009.

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25

Yu, Chu-Ling, Emily S. Tonorezos, Chiung-Yu Huang, et al. "Second malignant neoplasms in a nationwide population-based cohort of childhood cancer survivors in Taiwan." Journal of Clinical Oncology 35, no. 15_suppl (2017): 10569. http://dx.doi.org/10.1200/jco.2017.35.15_suppl.10569.

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10569 Background: Childhood cancer survivors have excess risk of second malignant neoplasms, but data are limited in Asian populations. We established a nationwide retrospective cohort of childhood cancer survivors in Taiwan to study the risk of second malignant neoplasms in the population. Methods: Children and adolescents diagnosed with cancer before age 21 years between 1990 and 2011 were identified from the Taiwan Cancer Registry, the national cancer registry in Taiwan. One-year survivors of childhood cancer were ascertained through data linkage with the national death registry. Survivors
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26

Coffin, Cheryl M., and Rita Alaggio. "Adipose and Myxoid Tumors of Childhood and Adolescence." Pediatric and Developmental Pathology 15, no. 1_suppl (2012): 239–54. http://dx.doi.org/10.2350/10-05-0836-pb.1.

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Adipose and myxoid tumors in children are an unusual and challenging group of neoplasms that have some unique aspects in contrast to these tumors in adults. Less than 10% of soft tissue neoplasms in the 1st 2 decades of life have an adipose phenotype and most are benign. The most common are various types of lipoma and lipoblastoma. Liposarcoma in young patients is rare and has a distinctive distribution of histologic subtypes, including classic myxoid liposarcoma, and unusual variants, such as pleomorphic-myxoid liposarcoma. Pathologic examination enhanced by adjunct techniques, such as immuno
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27

Johnston, Derrick L., Michael W. Bishop, Melissa M. Hudson, and Dana W. Giel. "Subsequent Neoplasms in Adult Survivors of Childhood Genitourinary Tumors." Urology 86, no. 4 (2015): 666–75. http://dx.doi.org/10.1016/j.urology.2015.07.022.

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28

CHERULLO, EDWARD E., JONATHAN H. ROSS, ROBERT KAY, and ANDREW C. NOVICK. "RENAL NEOPLASMS IN ADULT SURVIVORS OF CHILDHOOD WILMS TUMOR." Journal of Urology 165, no. 6 Part 1 (2001): 2013–17. http://dx.doi.org/10.1016/s0022-5347(05)66283-0.

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29

Attias, D., R. Lain, G. Rechavi, and M. Jaffe. "#628 Unusual second neoplasms in childhood acute lymphoblastic leukemia." Journal of Pediatric Hematology/Oncology 18, no. 4 (1996): 445. http://dx.doi.org/10.1097/00043426-199611000-00067.

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30

Davis, Jessica L., Linh Matsumura, Douglas A. Weeks, and Megan L. Troxell. "PAX2 Expression in Wilms Tumors and Other Childhood Neoplasms." American Journal of Surgical Pathology 35, no. 8 (2011): 1186–94. http://dx.doi.org/10.1097/pas.0b013e31821d3131.

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31

Messinger, Y. H., L. P. Dehner, D. A. Hill, G. Williams, and J. R. Priest. "Pleuropulmonary Blastoma and its association with other childhood neoplasms." Journal of Clinical Oncology 22, no. 14_suppl (2004): 8542. http://dx.doi.org/10.1200/jco.2004.22.14_suppl.8542.

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32

Schmiegelow, Kjeld, Mette Levinsen, Andishe Attarbashi, et al. "Second Neoplasms After Treatment of Childhood Acute Lymphoblastic Leukemia." Blood 120, no. 21 (2012): 661. http://dx.doi.org/10.1182/blood.v120.21.661.661.

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Abstract Abstract 661 Purpose: The 10-year overall survival (OS) for childhood ALL is now 80% or higher with many contemporary treatment programs. Although, second neoplasms (SMN) after diagnosis of childhood acute lymphoblastic leukemia (ALL) are rare events, toxic death in remission and death due to a SMN may constitute up to one third of all deaths among children with ALL. Previously reported cumulative incidences of SMN have varied between treatment protocols from less than 1% to 10% or more due to differences in the antileukemic therapy and duration and structure of follow-up. Method: 18
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33

Bryant, Victoria A., John Booth, Liina Palm, Michael Ashworth, Thomas S. Jacques, and Neil J. Sebire. "Childhood neoplasms presenting at autopsy: A 20-year experience." Pediatric Blood & Cancer 64, no. 9 (2017): e26474. http://dx.doi.org/10.1002/pbc.26474.

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34

Shulman, Stanford T. "Acyclovir Treatment of Disseminated Varicella in Childhood Malignant Neoplasms." Archives of Pediatrics & Adolescent Medicine 139, no. 2 (1985): 137. http://dx.doi.org/10.1001/archpedi.1985.02140040035021.

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35

Jazbec, Janez, Patricija E?imovi?, and Berta Jereb. "Second neoplasms after treatment of childhood cancer in Slovenia." Pediatric Blood & Cancer 42, no. 7 (2004): 574–81. http://dx.doi.org/10.1002/pbc.20025.

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36

Feig, Stephen A. "Second Malignant Neoplasms after Successful Treatment of Childhood Cancers." Blood Cells, Molecules, and Diseases 27, no. 3 (2001): 662–66. http://dx.doi.org/10.1006/bcmd.2001.0436.

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37

Newton, William A., Anna T. Meadows, Hiroyuki Shimada, Greta R. Bunin, and Gordon F. Vawter. "Bone sarcomas as second malignant neoplasms following childhood cancer." Cancer 67, no. 1 (1991): 193–201. http://dx.doi.org/10.1002/1097-0142(19910101)67:1<193::aid-cncr2820670132>3.0.co;2-b.

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38

Paulino, Arnold MD C., and B. Zach Fowler. "SECONDARY NEOPLASMS AFTER RADIOTHERAPY FOR A CHILDHOOD SOLID TUMOR." Pediatric Hematology and Oncology 22, no. 2 (2005): 89–101. http://dx.doi.org/10.1080/08880010590896459.

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39

Messinger, Y. H., L. P. Dehner, D. A. Hill, G. Williams, and J. R. Priest. "Pleuropulmonary Blastoma and its association with other childhood neoplasms." Journal of Clinical Oncology 22, no. 14_suppl (2004): 8542. http://dx.doi.org/10.1200/jco.2004.22.90140.8542.

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40

Teinturier, C., M. S. Pauchard, L. Brugi�res, P. Landais, J. L. Chaussain, and P. F. Bougn�res. "Clinical and prognostic aspects of adrenocortical neoplasms in childhood." Medical and Pediatric Oncology 32, no. 2 (1999): 106–11. http://dx.doi.org/10.1002/(sici)1096-911x(199902)32:2<106::aid-mpo7>3.0.co;2-j.

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41

Friedman, Debra L., John Whitton, Wendy Leisenring, et al. "Subsequent Neoplasms in 5-Year Survivors of Childhood Cancer: The Childhood Cancer Survivor Study." JNCI: Journal of the National Cancer Institute 102, no. 14 (2010): 1083–95. http://dx.doi.org/10.1093/jnci/djq238.

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42

Neglia, J. P., D. L. Friedman, Y. Yasui, et al. "Second Malignant Neoplasms in Five-Year Survivors of Childhood Cancer: Childhood Cancer Survivor Study." JNCI Journal of the National Cancer Institute 93, no. 8 (2001): 618–29. http://dx.doi.org/10.1093/jnci/93.8.618.

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43

Davies, Stella M. "Subsequent malignant neoplasms in survivors of childhood cancer: Childhood Cancer Survivor Study (CCSS) studies." Pediatric Blood & Cancer 48, no. 7 (2007): 727–30. http://dx.doi.org/10.1002/pbc.21113.

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44

Shahab, Nouval, Arry Rodjani, and Rainy Umbas. "Childhood renal cell carcinoma." Paediatrica Indonesiana 46, no. 2 (2016): 93. http://dx.doi.org/10.14238/pi46.2.2006.93-6.

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Renal cell carcinoma (RCC) in children isseldom found. The incidence of thistumor in childhood is estimated to be 0.1-0.3% out of all neoplasms and 2-7% out ofall malignant renal tumors. The Third NationalCancer Survey reported an incidence of only four casesof RCC per year compared to 117 per year of Wilms’tumor.The incidence of RCC has not been reported inIndonesia. This is the first case of childhood RCCfound in our institution. To the best of our knowl-edge, this is the first report of childhood RCC in In-donesia.
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45

Wijnen, M., M. M. van den Heuvel-Eibrink, M. Medici, R. P. Peeters, A. J. van der Lely, and S. J. C. M. M. Neggers. "Risk factors for subsequent endocrine-related cancer in childhood cancer survivors." Endocrine-Related Cancer 23, no. 6 (2016): R299—R321. http://dx.doi.org/10.1530/erc-16-0113.

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Long-term adverse health conditions, including secondary malignant neoplasms, are common in childhood cancer survivors. Although mortality attributable to secondary malignancies declined over the past decades, the risk for developing a solid secondary malignant neoplasm did not. Endocrine-related malignancies are among the most common secondary malignant neoplasms observed in childhood cancer survivors. In this systematic review, we describe risk factors for secondary malignant neoplasms of the breast and thyroid, since these are the most common secondary endocrine-related malignancies in chil
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46

Bomken, Simon, and Roderick Skinner. "Secondary Malignant Neoplasms Following Haematopoietic Stem Cell Transplantation in Childhood." Children 2, no. 2 (2015): 146–73. http://dx.doi.org/10.3390/children2020146.

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47

Reddy, Kalpana S., and Sherrie L. Perkins. "Advances in the Diagnostic Approach to Childhood Lymphoblastic Malignant Neoplasms." Pathology Patterns Reviews 122, suppl_1 (2004): S3—S18. http://dx.doi.org/10.1309/mqp7ptw7rqpjldl4.

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48

Schmiegelow, Kjeld, Mette Frandsen Levinsen, Andishe Attarbaschi, et al. "Second Malignant Neoplasms After Treatment of Childhood Acute Lymphoblastic Leukemia." Journal of Clinical Oncology 31, no. 19 (2013): 2469–76. http://dx.doi.org/10.1200/jco.2012.47.0500.

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Purpose Second malignant neoplasms (SMNs) after diagnosis of childhood acute lymphoblastic leukemia (ALL) are rare events. Patients and Methods We analyzed data on risk factors and outcomes of 642 children with SMNs occurring after treatment for ALL from 18 collaborative study groups between 1980 and 2007. Results Acute myeloid leukemia (AML; n = 186), myelodysplastic syndrome (MDS; n = 69), and nonmeningioma brain tumor (n = 116) were the most common types of SMNs and had the poorest outcome (5-year survival rate, 18.1% ± 2.9%, 31.1% ± 6.2%, and 18.3% ± 3.8%, respectively). Five-year survival
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49

Savasan, S. "Leukaemia/lymphoma cell microparticles in childhood mature B cell neoplasms." Journal of Clinical Pathology 57, no. 6 (2004): 651–53. http://dx.doi.org/10.1136/jcp.2003.011643.

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50

Bhatia, Smita, Leslie L. Robison, Odile Oberlin, et al. "Breast Cancer and Other Second Neoplasms after Childhood Hodgkin's Disease." New England Journal of Medicine 334, no. 12 (1996): 745–51. http://dx.doi.org/10.1056/nejm199603213341201.

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