[1]
|
Rashidi A, Fisher SI. Primary adrenal lymphoma:a systematic review[J]. Ann Hematol, 2013, 92:1583-1593. doi: 10.1007/s00277-013-1812-3 |
[2]
|
Kumar R, Xiu Y, Mavi A, et al. FDG-PET imaging in primary bilateral adrenal lymphoma:a case report and review of the literature[J]. Clin Nucl Med, 2016, 30:222-230. https://www.ncbi.nlm.nih.gov/pubmed/15764875 |
[3]
|
Kasaliwal R, Goroshi M, Khadilkar K, et al. Primary Adrenal Lymphoma:A Single-center Experience[J].Endocr Pract, 2015, 21:719-724. doi: 10.4158/EP14471.OR |
[4]
|
Martínez-Esteve A, García-Gómez FJ, Madrigal-Toscano MD, et al. Primary bilateral diffuse large B-cell lymphoma of the adrenals[J]. Br J Haematol, 2015, 170:3. doi: 10.1111/bjh.13466 |
[5]
|
Raoofziaee M, Yarmohamadi A, Ahmadnia H.Primary bilateral non-Hodgkin's lymphoma of the adrenal gland[J].Indian J Urol, 2018, 34:300-302. doi: 10.4103/iju.IJU_113_18 |
[6]
|
Ohkura Y, Shindoh J, Haruta S, et al. Primary Adrenal Lymphoma Possibly Associated With Epstein-Barr Virus Reactivation Due to Immunosuppression Under Methotrexate Therapy[J]. Medicine, 2015, 94:e1270. doi: 10.1097/MD.0000000000001270 |
[7]
|
Mozos A, Ye H, Chuang WY, et al. Most primary adrenal lymphomas are diffuse large B-cell lymphomas with non-germinal center B-cell phenotype, BCL6 gene rearrangement and poor prognosis[J]. Mod Pathol, 2009, 22:1210-1217. doi: 10.1038/modpathol.2009.87 |
[8]
|
Grigg AP, Connors JM. Primary adrenal lymphoma[J]. Clin Lymphoma, 2016, 4:154-160. https://www.ncbi.nlm.nih.gov/pubmed/12769357 |
[9]
|
Padhi S, Sahoo J. Primary adrenal non Hodgkin lymphoma:changing trends[J]. Turk J Gastroenterol, 2015, 26:85-86. doi: 10.5152/tjg.2015.4882 |
[10]
|
Erçolak V, Kara O, Günaldi M, et al. Bilateral primary adrenal non-hodgkin lymphoma[J]. Turk J Haematol, 2014, 31:205-206. doi: 10.4274/tjh.2013.0195 |
[11]
|
Robertus JL, Harms G, Blokzijl T, et al. Specific expression of miR-17-5p and miR-127 in testicular and central nervous system diffuse large B-cell lymphoma[J]. Mod Pathol, 2009, 22:547-555. doi: 10.1038/modpathol.2009.10 |
[12]
|
Nakatsuka S, Hongyo T, Syaifudin M, et al. Mutations of p53, c-kit, K-ras, and beta-catenin gene in non-Hodgkin's lymphoma of adrenal gland[J]. Jpn J Cancer Res, 2002, 93:267-274. doi: 10.1111/j.1349-7006.2002.tb02168.x |
[13]
|
Ide M, Fukushima N, Hisatomi T, et al. Non-germinal cell phenotype and Bcl-2 expression in primary adrenal diffuse large B-cell lymphoma[J]. Leuk Lymphoma, 2007, 48:2244-2246. doi: 10.1080/10428190701636450 |
[14]
|
Hong J, Park S, Park J, et al. Evaluation of prognostic values of clinical and histopathologic characteristics in diffuse large B-cell lymphoma treated with rituximab, cyclophosphamide, doxorubicin, vincristine, and prednisolone therapy[J]. Leuk Lymphoma, 2011, 52:1904-1912. doi: 10.3109/10428194.2011.588761 |
[15]
|
Hans CP, Weisenburger DD, Greiner TC, et al. Confirma-tion of the molecular classification of diffuse large B-cell lymphoma by immunohistochemistry using a tissue microarray[J]. Blood, 2004, 103:275-282. doi: 10.1182/blood-2003-05-1545 |
[16]
|
Choi WW, Weisenburger DD, Greiner TC, et al. A new immunostain algorithm classifies diffuse large B-cell lymphoma into molecular subtypes with high accuracy[J]. Clin Cancer Res, 2009, 15:5494-5502. doi: 10.1158/1078-0432.CCR-09-0113 |
[17]
|
Eyden B, Chakrabarty B, Hatimy U. Carcinoma versus cytokeratin-positive lymphoma:a case report emphasizing the diagnostic role of electron microscopy[J]. Ultrastruct Pathol, 2009, 33:33-38. doi: 10.1080/01913120802625830 |
[18]
|
Rashidi A, Bergeron CW, Fisher SI, et al. Primary adrenal de novo CD5-positive diffuse large B-cell lymphoma[J]. Ann Hematol, 2013, 92:1281-1282. doi: 10.1007/s00277-013-1690-8 |
[19]
|
Donner LR, Mott FE, Tafur I. Cytokeratin-positive, CD45-negative primary centroblastic lymphoma of the adrenal gland:a potential for a diagnostic pitfall[J]. Arch Pathol Lab Med, 2001, 125:1104-1106. https://www.ncbi.nlm.nih.gov/pubmed/11473470 |
[20]
|
Chen P, Jin L, Yang Y, et al. Bilateral primary adrenal diffuse large B cell lymphoma without adrenal insufficiency:A case report and review of the literature[J]. Mol Clin Oncol, 2017, 7:145-147. doi: 10.3892/mco.2017.1264 |
[21]
|
Chakrabarti I, Bhowmik S, Sinha MG, et al. Ultrasound-guided aspiration cytology of retroperitoneal masses with histopathological corroboration:A study of 71 cases[J]. J Cytol, 2014, 3115-3119. |
[22]
|
Mehmood S, Jahan A, Loya A, et al. Onsite cytopathology evaluation and ancillary studies beneficial in EUS-FNA of pancreatic, mediastinal, intra-abdominal, and submucosal lesions[J]. Diagn Cytopathol, 2015, 43:278-286. doi: 10.1002/dc.23207 |
[23]
|
Guo AC, Cummings TJ, Dash RC. Lymphomas and high-grade astrocytomas:comparison of water diffusibility and histologic characteristics[J]. Radiology, 2002, 224:177-183. doi: 10.1148/radiol.2241010637 |
[24]
|
Kuritzkes B, Parikh M, Melamed J, et al. False-positive rate of positron emission tomography/computed tomography for presumed solitary metastatic adrenal disease in patients with known malignancy[J]. Ann Surg Oncol, 2015, 22:437-440. doi: 10.1245/s10434-014-4031-9 |
[25]
|
Cistaro A, Niccoli Asabella A, Coppolino P, et al. Diag-nostic and prognostic value of 18F-FDG PET/CT in comparison with morphological imaging in primary adrenal gland malignancies-a multicenter experience[J]. Hell J Nucl Med, 2015, 18:97-102. |
[26]
|
López-Guillermo A, Colomo L, Jiménez M, et al. Diffuse large B-cell lymphoma:clinical and biological characteriza-tion and outcome according to the nodal or extranodal primary origin[J]. J Clin Oncol, 2005, 23:2797-2804. doi: 10.1200/JCO.2005.07.155 |
[27]
|
Abe R, Ogawa K, Maruyama Y, et al. Spontaneous regression of diffuse large B-cell lymphoma harbouring Epstein-Barr virus:a case report and review of the literature[J]. J Clin Exp Hematop, 2007, 47:23-26. doi: 10.3960/jslrt.47.23 |
[28]
|
Marković O, Marisavljević D, Jelić S, et al. Double-hit primary unilateral adrenal lymphoma with good outcome[J]. Vojnosanit Pregl, 2014, 71:689-692. doi: 10.2298/VSP1407689M |
[29]
|
Kim YR, Kim JS, Min YH, et al. Prognostic factors in primary diffuse large B-cell lymphoma of adrenal gland treated with rituximab-CHOP chemotherapy from the Consortium for Improving Survival of Lymphoma (CISL)[J]. J Hematol Oncol, 2012, 5:49. doi: 10.1186/1756-8722-5-49 |
[30]
|
Acker SN, Bruny JL, Garrington TP, et al. Minimally invasive surgical techniques are safe in the diagnosis and treatment of pediatric malignancies[J]. Surg Endosc, 2015, 29:1203-1208. doi: 10.1007/s00464-014-3795-0 |
[31]
|
Coiffier B, Lepage E, Briere J, et al. CHOP chemotherapy plus rituximab compared with CHOP alone in elderly patients with diffuse large-B-cell lymphoma[J]. N Engl J Med, 2002, 346:235-242. doi: 10.1056/NEJMoa011795 |
[32]
|
Hiemcke-Jiwa LS, Leguit RJ, Radersma-van Loon JH, et al.Efficacy of ibrutinib in a patient with transformed lymphoplasmacytic lymphoma and central nervous system involvement[J]. Leuk Lymphoma, 2017, 29:1-4. http://europepmc.org/abstract/MED/28849690 |
[33]
|
Boehme V, Zeynalova S, Kloess M, et al. Incidence and risk factors of central nervous system recurrence in aggressive lymphoma-a survey of 1693 patients treated in protocols of the German High-Grade Non-Hodgkin's Lymphoma Study Group (DSHNHL)[J]. Ann Oncol, 2007, 18:149-157. doi: 10.1093/annonc/mdl327 |
[34]
|
Ferreri AJ, Assanelli A, Crocchiolo R, et al. Central nervous system dissemination in immunocompetent patients with aggressive lymphomas:incidence, risk factors and therapeutic options[J]. Hematol Oncol, 2016, 27:61-70. doi: 10.1002/hon.881 |