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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1953 1
1971 1
1974 1
1975 4
1976 13
1977 5
1978 8
1979 7
1980 10
1981 6
1982 8
1983 14
1984 15
1985 12
1986 17
1987 15
1988 22
1989 25
1990 25
1991 32
1992 25
1993 47
1994 31
1995 43
1996 42
1997 64
1998 61
1999 54
2000 66
2001 78
2002 57
2003 81
2004 81
2005 98
2006 107
2007 108
2008 122
2009 107
2010 109
2011 133
2012 138
2013 142
2014 165
2015 139
2016 155
2017 143
2018 148
2019 138
2020 158
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2023 149
2024 62

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3,309 results

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Quoted phrase not found in phrase index: "Rare Childhood Malignant Neoplasm"
Page 1
Retinoblastoma.
Rao R, Honavar SG. Rao R, et al. Indian J Pediatr. 2017 Dec;84(12):937-944. doi: 10.1007/s12098-017-2395-0. Epub 2017 Jun 16. Indian J Pediatr. 2017. PMID: 28620731 Review.
Retinoblastoma represents 3% of all childhood cancers, and is the most common intraocular malignancy of childhood. ...The pediatricians have a very important role to play in the diagnosis of this relatively rare, but easily detectable tumor. Early diagnosis y …
Retinoblastoma represents 3% of all childhood cancers, and is the most common intraocular malignancy of childhood. ...The pedi …
Chondroblastoma-like Osteosarcoma.
Hmada YA, Bernieh A, Morris RW, Lewin J, Allen T. Hmada YA, et al. Arch Pathol Lab Med. 2020 Jan;144(1):15-17. doi: 10.5858/arpa.2019-0191-RA. Epub 2019 Aug 7. Arch Pathol Lab Med. 2020. PMID: 31389716 Free article. Review.
CONTEXT.-: Chondroblastoma-like osteosarcoma is an exceedingly rare variant of osteosarcoma, with 22 cases reported in the English-language literature. The tumor is slightly more common in males, with a broad age range (from childhood to elderly). The most commonly …
CONTEXT.-: Chondroblastoma-like osteosarcoma is an exceedingly rare variant of osteosarcoma, with 22 cases reported in the English-la …
Nevus Depigmentosus: An Update.
Kansal NK. Kansal NK. Skinmed. 2019 May 29;17(2):100-104. eCollection 2019. Skinmed. 2019. PMID: 31145059 Review.
Nevus depigmentosus, a disorder of hypopigmentation, occurs in both sexes and all races. It most commonly presents in early infancy and childhood as a nonprogressive hypomelanotic macule. It is considered a form of cutaneous mosaicism due to somatic mutation in pigmentary …
Nevus depigmentosus, a disorder of hypopigmentation, occurs in both sexes and all races. It most commonly presents in early infancy and c …
Lipoblastoma of the extremities.
Rajput S, Alsubaie SA, Singh K, Huang TC, Moran SL. Rajput S, et al. J Plast Reconstr Aesthet Surg. 2022 Oct;75(10):3761-3767. doi: 10.1016/j.bjps.2022.06.077. Epub 2022 Jun 25. J Plast Reconstr Aesthet Surg. 2022. PMID: 36041974
BACKGROUND: Lipoblastoma is a rare benign tumor of infancy and childhood, with similar radiographic imaging findings as malignant liposarcoma. ...Three patients had follow-up imaging, and 11 had follow-up visits between 2 weeks to 15 years. CONCLUSION: Lipobl …
BACKGROUND: Lipoblastoma is a rare benign tumor of infancy and childhood, with similar radiographic imaging findings as mal …
Vascular Anomalies: Other Vascular Tumors.
Atherton K, Hinen H. Atherton K, et al. Dermatol Clin. 2022 Oct;40(4):401-423. doi: 10.1016/j.det.2022.06.011. Epub 2022 Sep 16. Dermatol Clin. 2022. PMID: 36243428 Review.
Vascular tumors are classified into three categories by the International Society for the Study of Vascular Anomalies (ISSVA): benign, locally aggressive/borderline, and malignant. Many of these tumors are rare, cutaneous in nature, and present in childhood. …
Vascular tumors are classified into three categories by the International Society for the Study of Vascular Anomalies (ISSVA): benign, local …
Revived Attention for Adult Craniopharyngioma.
Mende KC, Pantel TF, Flitsch J. Mende KC, et al. Exp Clin Endocrinol Diabetes. 2021 Mar;129(3):172-177. doi: 10.1055/a-1217-7282. Epub 2020 Aug 4. Exp Clin Endocrinol Diabetes. 2021. PMID: 32750720 Review.
Craniopharyngioma as a rare tumor originating from cells of rathke's pouch and representing 2-5% of all intracranial tumors is a rare and generally benign neoplasm of the central nervous system with two incidence peaks one in childhood and one after 40 …
Craniopharyngioma as a rare tumor originating from cells of rathke's pouch and representing 2-5% of all intracranial tumors is a r …
Adrenocortical tumors in children.
Kastenberg ZJ, Scaife ER. Kastenberg ZJ, et al. Semin Pediatr Surg. 2020 Jun;29(3):150927. doi: 10.1016/j.sempedsurg.2020.150927. Epub 2020 May 17. Semin Pediatr Surg. 2020. PMID: 32571512 Review.
Adrenocortical neoplasms are rare in childhood. Unlike their adult counterparts, they are often hormonally active and malignant. ...Furthermore, the clinical overlap between adrenocortical neoplasms, adrenal medullary neoplasms, and funct …
Adrenocortical neoplasms are rare in childhood. Unlike their adult counterparts, they are often hormonally active and …
Pancreatoblastoma.
Saif MW. Saif MW. JOP. 2007 Jan 9;8(1):55-63. JOP. 2007. PMID: 17228135
Pancreatoblastoma (PB), or infantile pancreatic carcinoma, is an extremely rare pancreatic tumor in childhood, comprising 0.5% of pancreatic non-endocrine tumors. Although PB mainly presents during childhood but can also occur in adults. PB tend to be less ag …
Pancreatoblastoma (PB), or infantile pancreatic carcinoma, is an extremely rare pancreatic tumor in childhood, comprising 0.5% …
Challenges and solutions to the study of rare childhood tumors.
Fair D, Potter SL, Venkatramani R. Fair D, et al. Curr Opin Pediatr. 2020 Feb;32(1):7-12. doi: 10.1097/MOP.0000000000000857. Curr Opin Pediatr. 2020. PMID: 31789973 Review.
This focus, along with the progress made in cancer genomics, has changed the landscape for the study and treatment of rare pediatric cancers. This review focuses on the past, present, and future of the study and treatment of rare pediatric cancers. ...SUMMARY: The c …
This focus, along with the progress made in cancer genomics, has changed the landscape for the study and treatment of rare pediatric …
Trichoepithelioma: A Comprehensive Review.
Karimzadeh I, Namazi MR, Karimzadeh A. Karimzadeh I, et al. Acta Dermatovenerol Croat. 2018 Jun;26(2):162-165. Acta Dermatovenerol Croat. 2018. PMID: 29989874 Review.
Trichoepithelioma is an uncommon benign adnexal neoplasm. It can present as a solitary non-familial or multiple familial form. ...The lesions gradually increase in both size and number over time; however, they remain mostly asymptomatic. Although it is rare, trichoe …
Trichoepithelioma is an uncommon benign adnexal neoplasm. It can present as a solitary non-familial or multiple familial form. ...The …
3,309 results