Neuroblastoma

Neuroblastoma is a malignant tumor of neural crest cells, the cells that give rise to the sympathetic nervous system, which is observed in children.

Osteochondroma

A cartilage capped bony outgrowth of a long bone. Osteochondroma arises on the external surface of bone containing a marrow cavity that is continuous with that of the underlying bone.


Total: 10

                       


(per page)
PMID (PMCID)
25728463
(4970322)
 MIXED_SAMPLE Infant, Newborn
Osteochondroma in long-term survivors of high-risk neuroblastoma.
Kushner BH, Roberts SS, Friedman DN, Kuk D, Ostrovnaya I, Modak S, Kramer K, Basu EM, Cheung NK.
Cancer. 2015;121(12):2090-6.
The incidence rate of osteochondroma was determined using the competing risks approach, in which the primary event was osteochondroma calculated from the date of neuroblastoma diagnosis and the competing event was death without osteochondroma.
25728463
(4970322)
 MIXED_SAMPLE Infant, Newborn
Osteochondroma in long-term survivors of high-risk neuroblastoma.
Kushner BH, Roberts SS, Friedman DN, Kuk D, Ostrovnaya I, Modak S, Kramer K, Basu EM, Cheung NK.
Cancer. 2015;121(12):2090-6.
The incidence rate of osteochondroma was determined using the competing risks approach, in which the primary event was osteochondroma calculated from the date of neuroblastoma diagnosis and the competing event was death without osteochondroma.
25728463
(4970322)
 MIXED_SAMPLE Infant, Newborn
Osteochondroma in long-term survivors of high-risk neuroblastoma.
Kushner BH, Roberts SS, Friedman DN, Kuk D, Ostrovnaya I, Modak S, Kramer K, Basu EM, Cheung NK.
Cancer. 2015;121(12):2090-6.
The incidence rate of osteochondroma was determined using the competing risks approach, in which the primary event was osteochondroma calculated from the date of neuroblastoma diagnosis and the competing event was death without osteochondroma.
25728463
(4970322)
 MIXED_SAMPLE Infant, Newborn
Osteochondroma in long-term survivors of high-risk neuroblastoma.
Kushner BH, Roberts SS, Friedman DN, Kuk D, Ostrovnaya I, Modak S, Kramer K, Basu EM, Cheung NK.
Cancer. 2015;121(12):2090-6.
Osteochondroma in long-term survivors of high-risk neuroblastoma.
25728463
(4970322)
 MIXED_SAMPLE Infant, Newborn
Osteochondroma in long-term survivors of high-risk neuroblastoma.
Kushner BH, Roberts SS, Friedman DN, Kuk D, Ostrovnaya I, Modak S, Kramer K, Basu EM, Cheung NK.
Cancer. 2015;121(12):2090-6.
A total of 21 osteochondroma cases were found among 14 patients who were aged 5.7 to 15.3 years (median, 10.4 years) and 3.1 to 11.2 years (median, 8.2 years) from the time of neuroblastoma diagnosis.
26622619
 OTHER
Secondary osteosarcoma arising from osteochondroma following autologous stem cell transplantation with total-body irradiation for neuroblastoma: A case report.
Kawashima H, Ogose A, Hotta T, Imai C, Imamura M, Endo N.
Oncol Lett. 2015;10(2):1026-1030.
Secondary osteosarcoma arising from osteochondroma following autologous stem cell transplantation with total-body irradiation for neuroblastoma: A case report.
8587819
 MALE Child
Simultaneous occurrence of osteosarcoma and osteochondroma following treatment of neuroblastoma with chemotherapy, radiotherapy, and bone marrow transplantation.
Poustchi-Amin M, Leonidas JC, Elkowitz SS.
Pediatr Radiol. 1996;26(2):155-7.
An osteosarcoma of the fourth right rib and an osteochondroma of the left scapula developed in a long-term survivor of abdominal neuroblastoma treated with chemotherapy, local radiation, and bone marrow transplantation.
8587819
 MALE Child
Simultaneous occurrence of osteosarcoma and osteochondroma following treatment of neuroblastoma with chemotherapy, radiotherapy, and bone marrow transplantation.
Poustchi-Amin M, Leonidas JC, Elkowitz SS.
Pediatr Radiol. 1996;26(2):155-7.
Simultaneous occurrence of osteosarcoma and osteochondroma following treatment of neuroblastoma with chemotherapy, radiotherapy, and bone marrow transplantation.
2081362
 MIXED_SAMPLE Infant, Newborn
[Tumors of the ribs in children].
Benz G, Schafer K, Daum R.
Chir Pediatr. 1990;31(3):152-6.
We here present a review of ten pediatric patients with rib tumors that were treated in our hospital since 1970: a juvenile bone cyst, an aneurysmal bone cyst, an eosinophilic granuloma, a Ewing sarcoma, a metastasis of a neuroblastoma, an osteochondroma, a hemangiopericytoma, and a callous tumor at the site of a previous single rib fracture.
7083677
 MIXED_SAMPLE Child
Chondrosarcoma in children and adolescents.
Aprin H, Riseborough EJ, Hall JE.
Clin Orthop Relat Res. 1982;(166):226-32.
Of the latter two, one developed chondrosarcoma in a preexisting osteochondroma and the other had irradiation for neuroblastoma.