|
Total: 54 |
|
| PMID (PMCID) | ||
|---|---|---|
|
27865146 (5120262) |
OTHER | |
| A case report of successful diagnosis of a pulmonary nodule by a survey of oncogenic mutations; primary lung carcinoma or pulmonary metastasis? | ||
|
Haro A, Kuramitsu E, Yamamoto I, Fukuyama Y. Int J Surg Case Rep. 2016;29:176-179. |
||
| Of the some oncogenic mutations investigated, a neuroblastoma RAS viral oncogen homolog (NRAS) codon13 G13D mutation was detected in both the colorectal carcinoma and the pulmonary tumor tissue samples. | ||
|
26712059 |
MALE | |
| Metastatic lung adenocarcinoma related alpha-Fetoprotein elevation in a patient with HBV-related cirrhosis. | ||
|
Hamamci M, Karaahmet F, Akinci H, Kilincalp S, Ackgoz R, Coban S, Yuksel I. Acta Gastroenterol Belg. 2015;78(4):441-2. |
||
| But, increased serum levels of 945-fetoprotein are also seen in acute hepatitis, cirrhosis, and malignancies include yolk sac carcinoma, neuroblastoma, hepatoblastoma, gastric and lung carcinoma. | ||
|
26712059 |
MALE | |
| Metastatic lung adenocarcinoma related alpha-Fetoprotein elevation in a patient with HBV-related cirrhosis. | ||
|
Hamamci M, Karaahmet F, Akinci H, Kilincalp S, Ackgoz R, Coban S, Yuksel I. Acta Gastroenterol Belg. 2015;78(4):441-2. |
||
| But, increased serum levels of 945-fetoprotein are also seen in acute hepatitis, cirrhosis, and malignancies include yolk sac carcinoma, neuroblastoma, hepatoblastoma, gastric and lung carcinoma. | ||
|
25374282 |
MALE | Infant |
| Simultaneous Adrenocortical Carcinoma and Neuroblastoma in an Infant With a Novel Germline p53 Mutation. | ||
|
Courtney R, Ranganathan S. J Pediatr Hematol Oncol. 2015;37(3):215-8. |
||
| The child was found to have a paraspinal neuroblastoma, a concurrent adrenal cortical carcinoma, and an I162F p53 gene mutation. | ||
|
22988357 (3439791) |
OTHER | |
| PNET of kidney: Report of four cases. | ||
|
Mandal PK, Mukherjee S, Roy S, Bhattacharyya NK. Indian J Med Paediatr Oncol. 2012;33(2):130-3. |
||
| In view of its poor prognosis, aggressive nature and different therapeutic approach- renal PNET should be differentiated from other small blue round cell tumors like neuroblastoma, rhabdoid tumor of kidney, nephroblastoma, small cell carcinoma, synovial sarcoma (monophasic, poorly differentiated) and non-Hodgkin lymphoma (NHL) by immunohistochemistry, cytogenetic, and molecular genetics study to see the different gene rearrangements in NHL and 3p deletion in small cell carcinoma. | ||
|
22988357 (3439791) |
OTHER | |
| PNET of kidney: Report of four cases. | ||
|
Mandal PK, Mukherjee S, Roy S, Bhattacharyya NK. Indian J Med Paediatr Oncol. 2012;33(2):130-3. |
||
| In view of its poor prognosis, aggressive nature and different therapeutic approach- renal PNET should be differentiated from other small blue round cell tumors like neuroblastoma, rhabdoid tumor of kidney, nephroblastoma, small cell carcinoma, synovial sarcoma (monophasic, poorly differentiated) and non-Hodgkin lymphoma (NHL) by immunohistochemistry, cytogenetic, and molecular genetics study to see the different gene rearrangements in NHL and 3p deletion in small cell carcinoma. | ||
|
21551110 |
OTHER | Infant |
| The opsoclonus–myoclonus syndrome. | ||
|
Sahu JK, Prasad K. Pract Neurol. 2011;11(3):160-6. |
||
| Sometimes it is due to a self-limiting presumed para-infectious brainstem encephalitis but it may also represent a non-metastatic manifestation of neuroblastoma in children and small cell carcinoma of the lung in adults. | ||
|
19886971 |
MALE | |
| Malignant pilomatricoma in a soft-coated Wheaten Terrier. | ||
|
Jackson K, Boger L, Goldschmidt M, Walton RM. Vet Clin Pathol. 2010;39(2):236-40. |
||
| Given the location, signalment, and cytologic findings, differential interpretations included a primitive embryonal tumor (eg, neuroblastoma or nephroblastoma in an atypical location) or poorly differentiated carcinoma. | ||
|
21085535 (2981762) |
OTHER | |
| Opsoclonus-myoclonus syndrome caused by varicella-zoster virus. | ||
|
Singh D, Sinha M, Kumar R, Shukla R, Ahuja RC. Ann Indian Acad Neurol. 2010;13(3):211-2. |
||
| It is well recognized as a paraneoplastic syndrome in children with neuroblastoma and in adults with small-cell carcinoma of lung and some other cancers. | ||
|
21897800 (3166812) |
OTHER | |
| Idiopathic myenteric ganglionitis underlying acute 'dramatic' intestinal pseudoobstruction: report of an exceptional case. | ||
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Racalbuto A, Magro G, Lanteri R, Aliotta I, Santangelo M, Di Cataldo A. Case Rep Gastroenterol. 2008;2(3):461-8. |
||
| This pathological condition causes atonic gut motor dysfunction and is principally secondary to other diseases, being reported nearly solely as a paraneoplastic phenomenon in neuroendocrine lung tumors, including small cell carcinomas or neuroblastomas. | ||
|
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. |
||
| 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. | ||
|
18577675 |
MIXED_SAMPLE | Infant, Newborn |
| Prenatal sonographic findings of congenital adrenal cortical adenoma. | ||
|
Sherer DM, Dalloul M, Wagreich A, Sokolovski M, Duan H, Zinn H, Abulafia O. J Ultrasound Med. 2008;27(7):1091-3. |
||
| The differential diagnosis of prenatally diagnosed adrenal masses includes neuroblastoma, adrenal hemorrhage, adrenal and cortical renal cysts, adrenal adenoma and carcinoma, subdiaphragmatic pulmonary sequestration, Beckwith-Wiedemann syndrome, duplication of the renal system, Wilms tumors, congenital mesoblastic nephroma, and mesenteric and enteric duplication cysts. | ||
|
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. |
||
| The most common neoplasms inducing PS are oat cell lung carcinoma, ovarian carcinoma, breast carcinoma, neuroblastoma, thymoma and lymphoma. | ||
|
16363772 |
MIXED_SAMPLE | Child |
| Initial experience with laparoscopic adrenal surgery in children: is endoscopic surgery recommended and safe for the treatment of adrenocortical neoplasms? | ||
|
Pampaloni E, Valeri A, Mattei R, Presenti L, Centonze N, Neri AS, Salti R, Noccioli B, Messineo A. Pediatr Med Chir. 2004;26(6):450-9. |
||
| Nineteen pheochromocytomas, 18 neuroblastomas, 15 adenomas, 12 ganglioneuromas, 9 hyperplasias, 2 carcinomas, 1 teratoma and 1 adrenogenital syndrome have been treated with excellent results (follow-up 1 month to 4 years) with no evidence of recurrence. | ||
|
12892556 |
FEMALE | Middle Aged |
| [Opsoclonus-myoclonus syndrome in patient with ovarian cancer]. | ||
|
Rubio Nazabal E, Marey Lopez J, Avarez Perez P, Lopez Facal S, Alonso Magdalena L. An Med Interna. 2003;20(7):370-2. |
||
| The opsoclonus-myoclonus syndrome is a rare entity as a paraneoplastic disorder usually associated to neuroblastoma in children and breast cancer or oat-cell lung carcinoma in adults. | ||
|
11922191 |
MIXED_SAMPLE | Child |
| Cat-scratch disease in children--Texas, September 2000-August 2001. | ||
|
. MMWR Morb Mortal Wkly Rep. 2002;51(10):212-4. |
||
| The findings emphasize that although CSD is generally a mild, self-limited illness, the differential diagnosis often includes more serious conditions (e.g., lymphoma, carcinoma, mycobacterial or fungal infection, or neuroblastoma) that might result in protracted hospital stays and lengthy treatments before diagnosis. | ||
|
11955930 |
MIXED_SAMPLE | Child |
| Hematogenous brain metastasis in children. | ||
|
Curless RG, Toledano SR, Ragheb J, Cleveland WW, Falcone S. Pediatr Neurol. 2002;26(3):219-21. |
||
| The total of 2,040 patients includes our three examples of one neuroblastoma, one hepatoblastoma, and one adrenal carcinoma. | ||
|
12497294 |
MALE | Middle Aged |
| [Paraneoplastic cerebellar degeneration as initial presentation of a pancreatic small-cell carcinoma]. | ||
|
Salmeron-Ato P, Medrano V, Morales-Ortiz A, Martinez-Garcia FA, Villaverde-Gonzalez R, Bas A, Fernandez-Barreiro A, Molto-Jorda JM. Rev Neurol. 2002;35(12):1112-5. |
||
| The association of anti Hu immunity and paraneoplastic encephalomyelitis has been observed in patients with neuroblastoma, seminomas, colorectal, breast and prostate carcinomas and some types of sarcoma. | ||
|
10714067 |
MIXED_SAMPLE | Infant |
| [Evaluation of clinical utility of 123I-MIBG scintigraphy in localization of tumors of sympathetic and adrenomedullary origin--a report of multicenter phase III clinical trials]. | ||
|
Ishii K, Kubo A, Kusakabe K, Murata H, Masaki H, Horiike S, Hayashi A, Hara Y. Kaku Igaku. 2000;37(1):43-59. |
||
| Sixteen patients had pheochromocytoma, 23 had neuroblastoma, 7 had medullary carcinoma of the thyroid, and 2 had Sipple syndrome. | ||
|
9375703 |
FEMALE | |
| Tumor lysis syndrome in small cell carcinoma and other solid tumors. | ||
|
Kalemkerian GP, Darwish B, Varterasian ML. Am J Med. 1997;103(5):363-7. |
||
| Of the 25 reported solid tumor patients who developed TLS, 7 had small cell carcinoma, 5 breast cancer, and 4 neuroblastoma. | ||