Total: 78 |
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PMID (PMCID) | ||
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31005046 |
OTHER | |
A case report of a thymic neuroblastoma associated with syndrome of inappropriate secretion of antidiuretic hormone: Ten-year follow-up results after surgical treatment. | ||
Satoh Y. Int J Surg Case Rep. 2019;58:45-47. |
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Thymic neuroblastoma with syndrome of inappropriate secretion of antidiuretic hormone (SIADH) in adults is an extremely rare and malignant neoplasm. | ||
30067549 |
MALE | Adult |
Ewing-Like Sarcoma: A Case of a Primary Cutaneous Primitive Neuroectodermal Tumor With Atypical Immunohistochemistry and Lack of Fusion Oncogene Detection. | ||
Labadie JG, Florek AG, VandenBoom T, Yazdan P, Krunic AL. Am J Dermatopathol. 2018;40(12):890-893. |
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Differential diagnoses such as rhabdomyosarcoma, desmoplastic small round blue cell tumor, hematolymphoid neoplasm, neuroblastoma, and CIC-DUX round cell sarcoma were ruled out based on immunohistochemistry, genetic studies, and histology. | ||
28208865 |
OTHER | |
Adult Neuroblastoma-Case Report and Literature Review. | ||
Godkhindi VM, Basade MM, Khan K, Thorat K. J Clin Diagn Res. 2016;10(12):ED01-ED02. |
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Neuroblastoma is the most common solid malignant neoplasm in the paediatric age group; accounting for 7% of all childhood malignancies, but neuroblastoma in adult, is a rare occurrence, finding mention in aeons of medical literature with an overall incidence of 1 in 10 million adults/year. | ||
28208865 |
OTHER | |
Adult Neuroblastoma-Case Report and Literature Review. | ||
Godkhindi VM, Basade MM, Khan K, Thorat K. J Clin Diagn Res. 2016;10(12):ED01-ED02. |
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Neuroblastoma is the most common solid malignant neoplasm in the paediatric age group; accounting for 7% of all childhood malignancies, but neuroblastoma in adult, is a rare occurrence, finding mention in aeons of medical literature with an overall incidence of 1 in 10 million adults/year. | ||
27922241 |
MALE | |
An unusual case of neuroblastoma: a 17-year-old adolescent presented with bilateral diffuse lung metastasis at initial diagnosis. | ||
Odek C, Kendirli T, Pekpak E, Yaman A, Adakl-Aksoy B, Dincaslan H, Tacyldz N, Unal E, nce E, Yavuz G. Turk J Pediatr. 2016;58(1):86-89. |
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Neuroblastoma (NB) is the most frequently diagnosed neoplasm during infancy and its incidence declines within the first 3-5 years of life. | ||
24668947 |
MALE | Infant |
Early therapy-related myeloid sarcoma and deletion of 9q22.32 to q31.1. | ||
Brickler MM, Basel DG, Gheorghe G, Margolis DM, Kelly ME, Ehrhardt MJ. Pediatr Blood Cancer. 2014;61(9):1701-3. |
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Survival following childhood neuroblastoma is improving with low rates of secondary myeloid neoplasms. | ||
25386480 |
OTHER | |
Embryonal/Fetal subtype hepatoblastoma: a case report. | ||
Spyridakis I, Kepertis C, Lampropoulos V, Mouravas V, Filippopoulos A. J Clin Diagn Res. 2014;8(9):ND01-2. |
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Hepatoblastoma is the most common primary liver tumor of childhood and after neuroblastoma and nephroblastoma the third most common abdominal neoplasm in this age group. | ||
25291869 |
MIXED_SAMPLE | Adult |
Olfactory neuroblastoma with focal ganglioneuroblastic differentiation: a case report with literature review. | ||
Squillaci S. Pathologica. 2014;106(2):61-6. |
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Neuroblastomas, occurring in the nasal cavity, in analogy to other sites, tend to have an aggressive biologic behaviour and can histologically mimic other undifferentiated malignant neoplasms of the sinonasal tract. | ||
21837482 |
FEMALE | Adult |
Adult pancreatic neuroblastoma, an unusual site and fatal outcome. | ||
Abdou AG, Asaad NY, Elkased A, Said H, Dawoud M. Pathol Oncol Res. 2012;18(2):239-43. |
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The fatal outcome of adult neuroblastoma confirming the independence of age as a prognostic factor in this neoplasm regardless of stage and histology. | ||
22432426 |
FEMALE | Infant, Newborn |
Congenital neuroblastoma: an autopsy report. | ||
Gupta K, Bansal A. Fetal Pediatr Pathol. 2012;31(5):331-5. |
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Neuroblastoma (NB) is the foremost malignant neoplasm of the fetus and neonate. | ||
25343092 |
OTHER | |
Henoch-Schonlein purpura associated with a neuroblastoma: Report of one case and a review of the literature. | ||
Dong Q, Cao S, Zhang H, Geng H. Intractable Rare Dis Res. 2012;1(4):167-9. |
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An imaging study of the abdomen revealed a right retroperitoneal neoplasm that histopathology postoperatively confirmed to be a neuroblastoma. | ||
22540324 (3407001) |
MIXED_SAMPLE | Child |
Three uncommon adrenal incidentalomas: a 13-year surgical pathology review. | ||
Kanthan R, Senger JL, Kanthan S. World J Surg Oncol. 2012;10:64. |
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Metastatic neoplasms were the most common malignant lesions (50%) followed by primary adrenocortical carcinomas (31.8%) and neuroblastoma (13.6%). | ||
21079944 |
MALE | Infant |
Neuroblastoma with primary pleural involvement: an unusual presentation. | ||
Tay M, Kapur J. Pediatr Radiol. 2011;41(4):530-3. |
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Neuroblastomas are the most common neoplasms in infants. | ||
20503331 |
MIXED_SAMPLE | Infant |
Kabuki syndrome and cancer in two patients. | ||
Tumino M, Licciardello M, Sorge G, Cutrupi MC, Di Benedetto F, Amoroso L, Catania R, Pennisi M, D'Amico S, Di Cataldo A. Am J Med Genet A. 2010;152A(6):1536-9. |
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In this paper we present two patients with Kabuki syndrome and a neoplasm: a child of 6 years with hepatoblastoma and an infant, of 6 months affected by neuroblastoma. | ||
20010403 |
FEMALE | Infant |
Melanotic neuroectodermal tumor of infancy presenting in the subcutaneous soft tissue of the thigh. | ||
Lacy SR, Kuhar M. Am J Dermatopathol. 2010;32(3):282-6. |
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The differential diagnosis of soft tissue MNTI can include melanoma, neuroblastoma, rhabdomyosarcoma, desmoplastic small round cell tumor, and other pediatric "small round cell" neoplasms. | ||
19917480 |
FEMALE | Child |
Anaplastic large cell lymphoma: another entity in the differential diagnosis of small round blue cell tumors. | ||
Gustafson S, Medeiros LJ, Kalhor N, Bueso-Ramos CE. Ann Diagn Pathol. 2009;13(6):413-27. |
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The neoplasm was interpreted initially as a neuroblastoma. | ||
18618728 |
FEMALE | Adult |
Imprint cytology of high-grade immature ovarian teratoma: a case report, literature review, and distinction from other ovarian small round cell tumors. | ||
Ramalingam P, Teague D, Reid-Nicholson M. Diagn Cytopathol. 2008;36(8):595-9. |
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Differential diagnoses include other small round cell neoplasms such as ovarian neuroblastoma, small cell carcinoma of hypercalcemic type, primitive neuroectodermal tumor, Wilm's tumor, desmoplastic small round cell tumor, and Non-Hodgkin lymphoma. | ||
17726875 |
MALE | |
[85-years-old patient with paraneoplastic polyneuropathy]. | ||
Pieta M, Boczarska-Jedynak M, Byrski M, Ochudlo S, Pawlas N, Opala G, Hartleb M. Wiad Lek. 2007;60(3-4):189-91. |
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The most common neoplasms inducing PS are oat cell lung carcinoma, ovarian carcinoma, breast carcinoma, neuroblastoma, thymoma and lymphoma. | ||
16630913 |
MIXED_SAMPLE | |
Secondary intracranial neoplasms exhibiting features of astrocytoma and neuroblastoma in 2 children treated for acute lymphoblastic leukemia: report of 2 cases. | ||
Vancura RW, Kepes JJ, Newell KL, Ha TM, Arnold PM. Surg Neurol. 2006;65(5):490-4. |
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Secondary intracranial neoplasms exhibiting features of astrocytoma and neuroblastoma in 2 children treated for acute lymphoblastic leukemia: report of 2 cases. | ||
16338326 |
MIXED_SAMPLE | Infant |
Laparoscopic adrenalectomy for neuroblastoma in children: a report of 6 cases. | ||
Saad DF, Gow KW, Milas Z, Wulkan ML. J Pediatr Surg. 2005;40(12):1948-50. |
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Neuroblastoma, a neoplasm of the sympathetic nervous system, is the most common solid extracranial tumor of childhood. |