The DOI matches its Crossref record; 37 of the 37 references it cites were found in a registry or an index.
Clinical and Outcome Characteristics of Children With Adrenocortical Tumors: A Report From the International Pediatric Adrenocortical Tumor Registry
Open accessAbstract
PURPOSE: We created a registry for pediatric adrenocortical tumors (ACTs), which are rare and are not well characterized. We provide a descriptive analysis of 254 patients registered on the International Pediatric Adrenocortical Tumor Registry. PATIENTS AND METHODS: Between January 1990 and December 2001, 254 patients younger than 20 years of age with newly diagnosed or previously treated ACTs were registered. A histologic diagnosis of ACT was required, although central review was not mandatory. Follow-up information was periodically requested from the referring physician. Treatment was chosen by the primary physician. RESULTS: The overall female-male ratio was 1.6:1, but it varied widely among age groups. The most common presenting sign (84.2%) was virilization. Cushing's syndrome without virilization was uncommon (5.5%). Tumors were completely resected in 83% of patients. Patients with disseminated or residual disease received mitotane, cisplatin, etoposide, and/or doxorubicin, and rarely, radiation therapy. At a median follow-up of 2 years and 5 months, 157 patients (61.8%) survived without evidence of disease and 97 patients (38.2%) had died. The 5-year event-free survival estimate was 54.2% (95% CI, 48.2% to 60.2%). In a multivariate analysis, disease stage, presenting signs of endocrine dysfunction, and age were independently associated with prognosis. CONCLUSION: Childhood ACTs occur predominantly in females and almost always causes clinical signs. Complete resection is required for cure. Residual or metastatic disease carries a poor prognosis. Our results demonstrate the feasibility of a disease-specific database for obtaining meaningful clinical and outcome information.
Overview
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
In the citing paper
“In the adult as well as in the pediatric population, there is a predilection for the female gender (the ratio of female to male ranges from 1.5–2.5:1) (10, 17).”
From Adrenocortical carcinoma (2014) · cites this paper as [17]
In the citing paper
“The fact that 1.3% of all childhood cancers are ACCs as opposed to 0.02% to 0.2% of adult cancers confirms a higher relative incidence early in life (12, 15–17).”
From Adrenocortical carcinoma (2014) · cites this paper as [17]
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Citations
Cites
Nonparametric Estimation from Incomplete Observations
Kaplan, E. L., & Meier, P. (1992) · Springer series in statistics · doi:10.1007/978-1-4612-4380-9_25 · Cited by 45,239
Nonparametric Estimation from Incomplete Observations
Kaplan, E. L., & Meier, P. (1958) · Journal of the American Statistical Association · doi:10.1080/01621459.1958.10501452 · Cited by 39,158
Pathologic features of prognostic significance in adrenocortical carcinoma
Weiss, L. M., Medeiros, L. J., & Vickery, A. L. (1989) · The American Journal of Surgical Pathology · doi:10.1097/00000478-198903000-00004 · Cited by 818 · cited 1×
“These data are consistent with the results of several studies [4,14,26-30] that found tumor size to be associated with prognosis.”
ResultRibeiro, R. C., Sandrini, F., Figueiredo, B., Zambetti, G. P., Michalkiewicz, E., Lafferty, A. R., DeLacerda, L., Rabin, M., Cadwell, C., Sampaio, G., et al. (2001) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.161479898 · Cited by 541
Self-citationTumors associated with p53 germline mutations: a synopsis of 91 families.
Kleihues, P., Schäuble, B., Hausen, A. Z., Estève, J., & Ohgaki, H. (1997) · Europe PMC (PubMed Central) · Cited by 413
Top-down morphogenesis of colorectal tumors
Shih, I., Wang, T., Traverso, G., Romans, K., Hamilton, S. R., Ben‐Sasson, S. A., Kinzler, K. W., & Vogelstein, B. (2001) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.051629398 · Cited by 387
Adrenal Cortical Neoplasms in the Pediatric Population
Wieneke, J. A., Thompson, L. D. �., & Heffess, C. S. (2003) · The American Journal of Surgical Pathology · doi:10.1097/00000478-200307000-00001 · Cited by 350
Adrenocortical Carcinoma: Clinical, Morphologic, and Molecular Characterization
Stojadinovic, A., Ghossein, R. A., Hoos, A., Nissan, A., Marshall, D., Dudas, M. E., Cordon‐Cardo, C., Jaques, D. P., & Brennan, M. F. (2002) · Journal of Clinical Oncology · doi:10.1200/jco.2002.20.4.941 · Cited by 312
A novel mechanism of tumorigenesis involving pH-dependent destabilization of a mutant p53 tetramer
DiGiammarino, E. L., Lee, A. S., Cadwell, C., Zhang, W., Bothner, B. B., Ribeiro, R. C., Zambetti, G. P., & Kriwacki, R. W. (2001) · Nature Structural Biology · doi:10.1038/nsb730 · Cited by 293
Self-citationA population-based case-control study of childhood leukemia in shanghai
Shu, X. O., Gao, Y. T., Tu, J., Zheng, W., Brinton, L. A., Linet, M. S., & Fraumeni, J. F. (1988) · Cancer · doi:10.1002/1097-0142(19880801)62:3 · Cited by 291
Cited by
Sorted by citations
Items 401–500 of 522
Poole, R., & Makaya, T. (2015) · Archives of Disease in Childhood Education & Practice · doi:10.1136/archdischild-2015-309411
Análise em alta resolução (aCGH) de alterações genômicas em tumores de córtex adrenal em crianças
Komechen, H. (2013) · LA Referencia (Red Federada de Repositorios Institucionales de Publicaciones Científicas)
Zancanella, P. (2012) · LA Referencia (Red Federada de Repositorios Institucionales de Publicaciones Científicas)
Identificaçao de marcador embrionário em tumor de córtex adrenal de crianças
Rodrigues, G. A. (2004) · LA Referencia (Red Federada de Repositorios Institucionales de Publicaciones Científicas)
Special Aspects of Cushing’s Syndrome: Childhood
Savage, M. O., Afshar, F., Plowman, N. P., Dias, R. P., Grossman, A. B., & Storr, H. L. (2010) · Humana Press eBooks · doi:10.1007/978-1-60327-449-4_22
Pathologie des corticosurrénales
Raux-Demay, M. C. (2010) · EMC - Pédiatrie - Maladies infectieuses · doi:10.1016/s1637-5017(10)72468-6
A case of a rare adrenocortical tumour mimicking neuroblastoma
Rozario, K. S., Ryan, F. J., & Makaya, T. (2015) · Endocrine Abstracts · doi:10.1530/endoabs.39.ep12
Infantile Virilization Secondary to Malignant Etiology
Dasarwar, N., & Santosh, R. (2016) · Journal of Clinical Case Reports · doi:10.4172/2165-7920.1000780
An 18-Month-Old Boy with Decreasing Height Velocity
Soylu, L., & Chawla, V. (2015) · Pediatric Annals · doi:10.3928/00904481-20151012-04
Stratakis, C. A. (2015) · The Endocrine Society eBooks · doi:10.1210/mtp4.9781936704941.ch50
AÇÃO DE DERIVADOS DO ÁCIDO BETULÍNICO EM CÉLULAS DO TUMOR DE CÓRTEX ADRENAL
Martin, M. M., Yamaguchi, A. A., Ribeiro, P. S., de Figueiredo, B. C., & Bonatto, S. J. R. (2016) · Revista Médica da UFPR · doi:10.5380/rmu.v3i2.45954
Self-citationAdrenal Cortical Cancer from a Regional Cancer Center in South India
Arroju, V. (2016) · International Journal of Sciences · doi:10.18483/ijsci.981
A Rare Presentation of Infantile Virilization Secondary to Malignant Etiology
Nagesh, V. D., Santosh, D. R., & Sravya, N. D. (2016) · Indian Journal of Surgical Oncology · doi:10.1007/s13193-016-0581-6
Hiperkortyzolemia u dzieci - trudny, wielodyscyplinarny problem diagnostyczny i leczniczy
Doleżal-Ołtarzewska, K., Kumorowicz-Kopiec, M., Kruczek, P., Pietrzyk, J. J., Tomasik, P., & Starzyk, J. (2009) · Via Medica Journals
Virilizing adrenocortical oncocytoma in a toddler
Khansa, M. E., Naous, A., Daoud, N., & Rajab, M. (2017) · Journal of Pediatric Surgery Case Reports · doi:10.1016/j.epsc.2017.08.024
Nally, L. M., Conner, E., Paige, S. L., Mooney, K. L., Naber, U., Richards, R. M., & Wright, G. E. (2018) · Journal of Pediatric Endocrinology and Metabolism · doi:10.1515/jpem-2018-0340
Cavalcanti, M. M. (2018) · Digital Library of Theses and Dissertations (Universidade de São Paulo) · doi:10.11606/t.17.2018.tde-24042018-164945
Erkrankungen der endokrinen Drüsen inkl. Diabetes und Wachstumsstörungen
Hiort, O., Kapellen, T. M., Pfäffle, R. W., Raile, K., & Willgerodt, H. (2007) · Elsevier eBooks · doi:10.1016/b978-343723200-8.50021-4
Une tumeur pédiatrique inhabituelle
Moreau, A., Joubert, M., Thomas, C., & Boccon-Gibod, L. A. (2004) · Annales de Pathologie · doi:10.1016/s0242-6498(04)94028-x
Androgen Secreting Adrenal Adenoma – A Case report
Begum, S., Sharmin, F., Biswas, D. C., Jahan, I., & Hossain, M. (2018) · Northern International Medical College Journal · doi:10.3329/nimcj.v10i1.39332
Kletskaya, I. S., Рогожин, Д. В., Коновалов, Д. М., Эктова, А. П., & Kushnir, B. L. (2018) · Pediatric Hematology/Oncology and Immunopathology · doi:10.24287/1726-1708-2018-17-3-111-119
Hauffa, B. P., Binder, G., Bonfig, W., Bettendorf, M., & Dörr, H. G. (2019) · Monatsschrift Kinderheilkunde · doi:10.1007/s00112-019-0697-1
Infantile virilisation caused by an androstenedione-producing adrenal adenoma
McCallion, O., Ravi, K., Fowler, D. J., Wilson, S. R., & Lakhoo, K. (2019) · Journal of Pediatric Surgery Case Reports · doi:10.1016/j.epsc.2019.101265
Pienkowski, C., Cartault, A., & Bar, C. (2019) · Elsevier eBooks · doi:10.1016/b978-2-294-75965-9.00005-2
Cushing’s syndrome as a rare manifestation of adrenal tumours in infants – case report
Badurowicz, J., Stefanowicz, J., Jezierska, M., Janecka, A., Birkholz-Walerzak, D., Gołębiewski, A., Piskunowicz, M., & Świętoń, D. (2019) · Pediatria Polska · doi:10.5114/polp.2019.89869
A rare presentation of adrenal adenoma in infancy: isolated Cushing`s syndrome
Sal, O., Yeğen, G., & Oğuzkurt, P. (2020) · The Turkish Journal of Pediatrics · doi:10.24953/turkjped.2020.01.022
Dome, J. S., Galindo, C. R., Spunt, S. L., & Santana, V. M. (2014) · Elsevier eBooks · doi:10.1016/b978-1-4557-2865-7.00095-3
Allolio, B., & Faßnacht, M. (2015) · Elsevier eBooks · doi:10.1016/b978-0-323-18907-1.00107-4
Lau, S. T., & Caty, M. G. (2006) · Elsevier eBooks · doi:10.1016/b978-0-323-02842-4.50041-3
Adrenal Cortical Neoplasms in Children
Nosé, V. (2018) · Elsevier eBooks · doi:10.1016/b978-0-323-52480-3.50100-1
Factors Affecting Survival in Adrenocortical Cancers: Single-Center Experience
GÜVEN, M., Şimşek, M., & Tuzcu, A. (2020) · Endocrinology research and practice. · doi:10.25179/tjem.2020-74861
Sindrome di Cushing in età pediatrica
Chioma, L., & Cappa, M. (2020) · L Endocrinologo · doi:10.1007/s40619-020-00788-y
Adrenal Cortex Carcinoma: One of the Rarest Retroperitoneal Tumors in children
Hanine, D. (2021) · Research in Pediatrics & Neonatology · doi:10.31031/rpn.2021.05.000618
Análise dos genes ATRX e ZNRF3 como fatores de prognóstico do carcinoma adrenocortical
Balderrama-Brondani, V. (2021) · Digital Library of Theses and Dissertations (Universidade de São Paulo) · doi:10.11606/t.5.2021.tde-28092021-123423
Nebennierentumoren mit Androgen-/Östrogen-Überproduktion
Ladurner, R. (2021) · Springer Reference Medizin · doi:10.1007/978-3-662-61724-3_33-1
ACTH-Independent Cushing’s Syndrome: Adrenocortical Tumors
Fragoso, M. C. B. V., Domenice, S., Latronico, A. C., & Mendonca, B. B. (2010) · Humana Press eBooks · doi:10.1007/978-1-60327-449-4_16
Malignant Adrenal Cortex in Children: About 6 Cases
Hadir, M., Benomar, I., Skiredj, A. A., & Kisra, M. (2022) · SAS Journal of Medicine · doi:10.36347/sasjm.2022.v08i01.004
de Dávila, M. T. G., Galluzzo, L., de, D., & Scheimberg, I. B. (2000) · Cambridge University Press eBooks · doi:10.1017/cbo9781139237000.008
(2011) · Elsevier eBooks · doi:10.1016/b978-1-4377-0755-7.00500-5
von Allmen, D. (2010) · Springer eBooks · doi:10.1007/978-1-4419-6643-8_93
Hoang, P. T., Eric, T., Mace, J., & Hathout, E. H. (2017) · International Journal of Integrative Pediatrics and Environmental Medicine · doi:10.36013/ijipem.v3i0.30
Genetics of Familial Forms of Cortisol-Secreting Adrenal Tumors and Hyperplasias
Drougat, L., & Stratakis, C. A. (2018) · Elsevier eBooks · doi:10.1016/b978-0-12-801238-3.64349-0
Pession, A., Baronio, F., Togni, M., & Prete, A. (2014) · Springer eBooks · doi:10.1007/978-88-470-5693-0_24
Author's reply to Tripathi et al. and Memon et al.
Prabhash, K., Kapoor, A., Noronha, V., Toshniwal, A., Menon, S. G., Joshi, A., Patil, V. M., Menon, N. S., Prakash, G. J., Murthy, V., et al. (2020) · Cancer Research Statistics and Treatment · doi:10.4103/crst.crst_260_20
(2010) · Springer eBooks · doi:10.1007/978-0-387-88443-1_47
Childhood Adrenocortical Carcinoma
(2011) · Springer eBooks · doi:10.1007/978-3-642-16483-5_1088
Model, L. S., Caty, M. G., & Christison-Lagay, E. R. (2020) · Springer eBooks · doi:10.1007/978-3-642-38482-0_157-1
von Allmen, D. (2016) · Springer eBooks · doi:10.1007/978-3-319-27443-0_98
Stratakis, C. A., & Saloustros, E. S. (2019) · Wiley eBooks · doi:10.1002/9781119152712.ch12
(2009) · Elsevier eBooks · doi:10.1016/b978-0-7216-0645-3.00176-1
Osman, A. A., Abdi, A. O., Abdullahi, I. M., Tahtabaşı, M., & Kaya, V. (2022) · International Medical Case Reports Journal · doi:10.2147/imcrj.s370022
Carcinoma Adrenocortical e a relação genética: uma revisão de literatura
da Paz, J. V. C., Alves, A. A. G., Alves, B. D. C., de Freitas, C. M., Melo, A. D. M., Salgado, D. R. G. B., Silva, A. P. B. M., Restier, V. S. M., Santos, L. H. F., de Barros, M. L. N. M., et al. (2022) · E-Acadêmica · doi:10.52076/eacad-v3i2.204
Pediatric adrenal incidentaloma as a rare and difficult to diagnose finding - review
Pałac, D., Ostrowska, M., Grześk-Kaczyńska, M., & Kaczyński, S. (2022) · Journal of Education Health and Sport · doi:10.12775/jehs.2022.12.08.019
Marinova, L., Vasileva, V., Gabrovski, I., Petrov, V., & Kahchiev, N. (2022) · Journal of Pediatrics Research Reviews & Reports · doi:10.47363/jprrr/2022(4)144
Prenatal presentation of an adrenocortical tumor
Schwartz, J. H., & Smith, E. (2022) · Cancer Reports · doi:10.1002/cnr2.1670
Nebennierentumoren mit Androgen-/Östrogen-Überproduktion
Ladurner, R. (2022) · Springer Reference Medizin · doi:10.1007/978-3-662-63317-5_33
More, C. B. (2022) · Digital Library of Theses and Dissertations (Universidade de São Paulo) · doi:10.11606/t.17.2022.tde-08112022-172105
Fahy, A. S., & Baertschiger, R. M. (2022) · Springer eBooks · doi:10.1007/978-3-031-07524-7_122
Adrenal Tumors and Pheochromocytoma
Mattei, P. (2022) · Springer eBooks · doi:10.1007/978-3-031-07524-7_111
Stecchini, M. F. (2022) · Digital Library of Theses and Dissertations (Universidade de São Paulo) · doi:10.11606/t.17.2022.tde-06022023-112309
Arega, G., Hailu, D., Gidey, A. M., Hailu, A., Nigusie, M., Fikad, G., Yeshiwas, S., Zeray, A., & Sisay, S. (2023) · Mathews Journal of Cancer Science · doi:10.30654/mjcs.10036
Data from Gene Expression Profiling of Childhood Adrenocortical Tumors
West, A. N., Neale, G. A. M., Pounds, S. B., de Figueiredo, B. C., Galindo, C. R., Pianovski, M. A. D., Filho, A. G. O., Malkin, D. M., Lalli, E., Ribeiro, R. C., et al. (2023) · doi:10.1158/0008-5472.c.6495792
Self-citationData from Gene Expression Profiling of Childhood Adrenocortical Tumors
West, A. N., Neale, G. A. M., Pounds, S. B., de Figueiredo, B. C., Galindo, C. R., Pianovski, M. A. D., Filho, A. G. O., Malkin, D. M., Lalli, E., Ribeiro, R. C., et al. (2023) · doi:10.1158/0008-5472.c.6495792.v1
Self-citationPrimary adrenocortical carcinoma: a case report
Neupane, D. P., Khadka, S., Upadhyaya, P., Sah, S. P., Dulal, S., Shah, S., & Shah, U. K. (2023) · Annals of Medicine and Surgery · doi:10.1097/ms9.0000000000000097
PAEDIATRIC ADRENOCORTICAL CARCINOMA: A CASE REPORT
Amir, M. S., Ali, M., Rehman, A., Ghayyour, F., Malik, I., & Khattak, T. G. (2023) · Journal of Postgraduate Medical Institute · doi:10.54079/jpmi.37.2.3131
Zhang, Y., Zhu, Y., & Tang, N. (2023) · Research Square · doi:10.21203/rs.3.rs-3018913/v1
Early-Onset Virilization May Rarely be Due to an Adrenocortical Neoplasm
Nanda, N., Kaur, K., Kadian, K., & Sridharan, K. (2023) · Indian Pediatrics Case Reports · doi:10.4103/ipcares.ipcares_90_23
Pediatric adrenocortical carcinoma revealed by isolated Cushing syndrome: A case report
Chafaaoui, H., Assan, B. R., Andaloussi, S., Dalero, O., & Elmadi, A. (2023) · Journal of Pediatric Surgery Case Reports · doi:10.1016/j.epsc.2023.102720
Głaz, A., Wach, D., Mitek-Palusińska, J., & Woźniak, M. M. (2023) · Journal of Education Health and Sport · doi:10.12775/jehs.2023.39.01.015
Adrenocortical Carcinoma in a 2 Years Old Girl, a Rare Cause of Clitoridomegaly: A Case Report
Léonidas, N., Omid, M., Helle, M. J., Kabirou, M., Diori, A., Issoufou, Y., Efared, B., Aminou, M., & Habibou, A. (2023) · Clinics of Oncology · doi:10.47829/coo.2023.7301
RECURRENT ADRENOCORTICAL CARCINOMA– A CASE REPORT
Devi, S., Kumar, A., Rana, R., & Minakshi, P. (2023) · PARIPEX-INDIAN JOURNAL OF RESEARCH · doi:10.36106/paripex/7101087
Extremely rare spinal tumor in Li-Fraumeni syndrome
Tinka, P., Pavelka, Z., Vejmělková, K., & Ježová, M. (2023) · Onkologie · doi:10.36290/xon.2023.056
Adrenal Multidisipliner Güncel Yaklaşım
Özen, F. Z., Özer, M., Özsoy, Ç., Binnetoğlu, E., Alparslan, A. Ş., Budak, E. S., Kök, E. V., Çetinkaya, G. S., Durmuş, M. E., Köker, G., et al. (2024) · Akademisyen Kitabevi eBooks · doi:10.37609/akya.2992
Patil, P., Monteiro, J., Qureshi, S. S., & Karnik, N. (2024) · Indian Journal of Medical and Paediatric Oncology · doi:10.1055/s-0044-1780522
KASHAMA, V., ANDO, G. O., Bouramdane, S., Elmkaddem, K., HBIBI, H., ABBROURAZAK, S., & Benmiloud, S. (2024) · World Journal of Advanced Research and Reviews · doi:10.30574/wjarr.2024.22.1.1336
Pediatric Endocrine Tumors and Syndromes
Blair, J., & Patócs, A. (2024) · Endocrinology · doi:10.1007/978-3-030-18901-3_13-1
Disorders of the Adrenal Gland in Children and Adolescents
Katugampola, H., & Krone, N. P. (2023) · Endocrinology · doi:10.1007/978-3-030-18901-3_4-1
Functional adrenocortical carcinoma with adrenohepatic fusion: A case report
Escárcega-Fujigaki, P., Hernández-Peredo-Rezk, G., Loeza-Oliva, J. D. J., Luna-Hernández, A., Arreguin-Cortés, B.-N., & López-Cruz, R. (2024) · Journal of Pediatric Surgery Case Reports · doi:10.1016/j.epsc.2024.102841
Kim, S., Khanna, P., Sripada, S., Gaur, R., Lyon, O., Huntress, K., Cheng, A., Dyer, K., Chu, X.-P., Moncure, M., et al. (2024) · SSRN Electronic Journal · doi:10.2139/ssrn.4872850
Virilizing adrenocortical carcinoma in a female child of Li-Fraumeni syndrome
Sankar, K. V. V., Sarkar, D., Pal, D. K., & Chatterjee, U. (2024) · Indian Journal of Pathology and Microbiology · doi:10.4103/ijpm.ijpm_906_23
Mansfield, S. A., Corti, F. D., Aldrink, J. H., Pire, A., Crocoli, A., Dall’Igna, P., Mathyssens, L., & Virgone, C. (2024) · Pediatric Blood & Cancer · doi:10.1002/pbc.31207
Ramanathan, S., Pradhan, N. D., & Chinnaswamy, G. (2024) · Springer eBooks · doi:10.1007/978-981-99-3378-5_66
Orhan, B., Dızdar, Ö., Yalçın, Ş., & Yıldız, Ö. (2024) · Springer eBooks · doi:10.1007/978-3-031-56968-5_24
Hosseini, S. F., Weimin, C., & Nikoofar, P. (2024) · Elsevier eBooks · doi:10.1016/b978-0-443-27302-5.00010-3
Pediatric Endocrine Tumors and Syndromes
Blair, J., & Patócs, A. (2024) · Endocrinology · doi:10.1007/978-3-030-23709-7_13
Disorders of the Adrenal Gland in Children and Adolescents
Katugampola, H., & Krone, N. P. (2024) · Endocrinology · doi:10.1007/978-3-030-23709-7_4
Pädiatrisches adrenokortikales Karzinom – Fallbericht und Überblick
Griss, D., Weber, U., Tatzreiter, A., Morell-Hofert, D., & Steichen‐Gersdorf, E. (2024) · Journal für Endokrinologie Diabetologie und Stoffwechsel · doi:10.1007/s41969-024-00254-2
Pediatric adrenocortical tumor manifesting as Cushing’s syndrome and virilization
Kumar, S., Bishnoi, A., Manayankath, R., Supreeth, C., Kumar, R., & Agrawal, N. K. (2024) · IJEM Case Reports · doi:10.4103/ijemcr.ijemcr_73_24
(2024) · Frontiers research topics · doi:10.3389/978-2-8325-5833-1
Precocious puberty: the unlikely herald of Familial adenomatous polyposis in a young girl
Karthik, V., Jabbar, P. K., Alam, A., & Nair, A. (2025) · BMJ Case Reports · doi:10.1136/bcr-2024-263412
Nutritional support in children treated for advanced adrenocortical carcinoma
Zaghloul, T. M., Pio, L., Mostafa, A. G., Halepota, H. F., Mothi, S. S., Abdelhafeez, A. H., Ribeiro, R. C., & Davidoff, A. M. (2025) · Pediatric Surgery International · doi:10.1007/s00383-025-05974-3
Self-citationLegal, E. F.-D., Ascurra, M., Vega-Paredes, R., Sade, E. R., Monteiro, M. M., Paraizo, M. M., Colman, M., Florentin, A. G., Ojeda, C., Legal-Ayala, H., et al. (2025) · Current Oncology · doi:10.3390/curroncol32060333
Metadata
- Authors
- Michalkiewicz, E., Sandrini, R., Figueiredo, B., Miranda, E. C. M., Caran, E., Oliveira-Filho, A. G., Marques, R., Pianovski, M. A. D., Lacerda, L., Cristofani, L. M., Jenkins, J., Rodriguez-Galindo, C., & Ribeiro, R. C.
- Affiliations
- Universidade Estadual de Campinas (UNICAMP) (BR)
- St. Jude Children's Research Hospital (US)
- From the Oncologic Pediatric Surgery Division, Erasto Gaertner Hospital, Liga Paranaense de Combate ao CÂncer, Curitiba; Division of Pediatric Endocrinology and Center for Molecular Genetics and Childhood Cancer Research (CEGEMPAC), Hospital de Clinicas, Federal University of Paraná, Curitiba, Paraná; the Biostatistics Division, Hemocentro, and The Instituto Domingos Boldrini, Universidade Estadual de Campinas, Campinas; Department of Pediatric Oncology, Universidade Federal de São Paulo, Escola Paulista...
- Corresponding author
- Ribeiro, R.C.
- Venue
- Journal of Clinical Oncology
- Published
- 2004-03-01
- Volume
- 22
- Issue
- 5
- Pages
- 838-845
- ISSN
- 0732-183X (ISSN-L)
- 1527-7755
- OpenAlex
- W2120218419
- Cited by
- 519
- References
- 37
- Citations by year
- 2026: 11 · 2025: 16 · 2024: 29 · 2023: 28 · 2022: 34 · 2021: 35 · 2020: 29 · 2019: 26 · 2018: 24 · 2017: 20 · 2016: 33 · 2015: 27 · 2014: 35 · 2013: 21 · 2012: 22
- FWCI
- 12.67
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Locations
- Journal of Clinical Oncology (publishedVersion)
- PubMed (publishedVersion)
- UNIFESP Institutional Repository (Universidade Federal de São Paulo) (submittedVersion)
- Funders
- U.S. Department of Health and Human Services
- American Lebanese Syrian Associated Charities (CA 21765)
- Conselho Nacional de Desenvolvimento Científico e Tecnológico
- National Institutes of Health (CA21765))
- National Cancer Institute (CA-71907, CA21765, P30CA021765, P01CA071907)
- Topics
- Health Sciences › Medicine › Surgery › Adrenal and Paraganglionic Tumors
- Health Sciences › Medicine › Oncology › Neuroblastoma Research and Treatments
- Health Sciences › Medicine › Oncology › Sarcoma Diagnosis and Treatment
- Keywords
- pediatric adrenocortical tumors, adrenocortical carcinoma, masculinization, Cushing's syndrome, surgical resection, mitotane, chemotherapy, event-free survival, prognosis, disease stage, sex differences, rare pediatric tumors
- MeSH terms
- Adolescent, Adrenal Cortex Neoplasms, Adrenalectomy, Adult, Age Factors, Biopsy, Needle, Child, Child, Preschool, Combined Modality Therapy, Female, Humans, International Cooperation, Male, Neoplasm Staging, Probability, Prognosis, Registries, Retrospective Studies, Sex Factors, Confidence Intervals, Proportional Hazards Models, Survival Analysis, Treatment Outcome, Chemotherapy, Adjuvant, Adrenocortical Carcinoma, Risk Assessment, Disease-Free Survival
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review
