Lymphomas of the Mediastinum

References

• Lichtenstein AK, Levine A, Taylor CR, Bos-Well W, Rossman S, Feinstein Dl, Lukes RJ. Primary mediastinal lymphoma in adults. Am J Med. 1980; 68: 509–514
   PubMed Web of Science ®Google Scholar
• Graham M. Non-Hodgkin's lymphomas. PediatrAnn. 1988; 17: 192–203
   Google Scholar
• Van Heerden JA, Harrison EG, Bernatz PE, Kiely JM. Mediastinal malignant lymphoma. Chest 1970; 57: 518–529
   PubMed Web of Science ®Google Scholar
• Dutcher JP, Wiernik PH. Lymphomas involving the mediastinum and lungs. Thoracic Oncology, MM Mfmfmfmfmfm. Saunders, Philadelphia 1989; 448–465
   Google Scholar
• Stea B, Kinsella TJ. Superior vena cava syndrome: an oncologic emergency. Thoracic Oncology, JA Roth, JC Ruckdeschel, TH Weisenburger. Saunders, Philadelphia 1989; 280–290
   Google Scholar
• Olumide AA, Osunkoya BO, Ngu VA. Superior mediastinal compression: a report of five cases caused by malignant lymphoma. Cancer 1971; 27: 193–202
   PubMedGoogle Scholar
• Miller JB, Variakojis D, Bitran JD, et al. Diffuse histiocytic lymphoma with sclerosis: a clinicopathologic entity frequently causing superior vena caval obstruction. Cancer 1981; 47: 748–756
   PubMed Web of Science ®Google Scholar
• Perez-Soler R, McLaughlin P, Velasquez WS, et al. Clinical features and results of management of superior vena cava syndrome secondary to lymphoma. J Clin Oncol. 1984; 2: 260–266
   PubMed Web of Science ®Google Scholar
• Rubush JL, Gardner IR, Boyd WC, Ehrenhaft JL. Mediastinal tumors. Review of 186 cases. J Thorac Cardiovasc Surg. 1973; 65: 216–222
   PubMedGoogle Scholar
• Heimburger IL, Battersby JS. Primary mediastinal tumors of childhood. J Thorac Cardiovasc Surg. 1965; 50: 92–103
   PubMedGoogle Scholar
• Grosfeld JL, Weinberger M, Kilman JW, Clatworthy HW, Jr. Primary mediastinal neoplasms in infants and children. Ann Thorac Surg. 1971; 12: 179–190
   PubMedGoogle Scholar
• Bower RJ, Kiesewetter WB. Mediastinal masses in infants and children. ARch Surg. 1977; 112: 1003–1009
   PubMedGoogle Scholar
• Pokorny WJ, Sherman JO. Mediastinal masses in infants and children. J Thorac Cardiovasc Surg. 1974; 68: 869–875
   PubMedGoogle Scholar
• King RM, Telander RL, Smithson WA, Bands PM, Han M-T. Primary mediastinal tumors in children. J Pediatr Surg. 1982; 17: 512–520
   PubMed Web of Science ®Google Scholar
• Benjamin SP, McCormack LJ, Effler DB, Groves LK. Primary tumors of the mediastinum. Chest 1972; 62: 297–303
   PubMed Web of Science ®Google Scholar
• Silverman NA, Sabiston DC, Jr. Mediastinal masses. Surg Clin North Am. 1980; 60: 757–777
   PubMed Web of Science ®Google Scholar
• Colby TV, Hoppe RT, Warnke RA. Hodgkin's disease: a clinicopathologic study of 659 cases. Cancer 1981; 49: 1848–1858
   Web of Science ®Google Scholar
• Saxe BI, Mandel PR. Hodgkin's disease. Radiotherapeutic management at a cancer oriented community hospital. Cancer 1978; 42: 1046–1056
   PubMedGoogle Scholar
• Null JA, Livolsi VA, Glenn WWL. Hodgkin's disease of the thymus (granulomatous thymoma) and myasthenia gravis. A unique association. Am J Clin Pathol. 1977; 67: 521–525
   PubMed Web of Science ®Google Scholar
• Lee CKK, Bloomfield CD, Goldman Al, Levitt SH. Prognostic significance of mediastinal involvement in Hodgkin's disease treated with curative radiotherapy. Cancer 1980; 46: 2403–2409
   PubMed Web of Science ®Google Scholar
• Mauch P, Goodman R, Hellman S. The significance of mediastinal involvement in early-stage Hodgkin's disease. Cancer 1978; 42: 1039–1045
   PubMed Web of Science ®Google Scholar
• Kjeldsberg CR, Wilson JF, Berard CW. Non-Hodgkin's lymphoma in children. Hum Pathol. 1983; 14: 612–627
   PubMed Web of Science ®Google Scholar
• Yousem SA, Weiss LM, Warnke RA. Primary mediastinal non-Hodgkin's lymphomas: a morphologic and immunologic study of 19 cases. Am J Clin Pathol. 1985; 83: 676–680
   PubMed Web of Science ®Google Scholar
• Addis BJ, Isaacson PG. Large cell lymphoma of the mediastinum: a B-cell tumour of probable thymic origin. Histopathology 1986; 10: 379–390
   PubMed Web of Science ®Google Scholar
• Menestrina F, Chilosi M, Bonetti F, et al. Mediastinal large cell lymphoma of B-type, with sclerosis: histopathological and immunohisto-chemical study of eight cases. Histopathology 1986; 10: 589–600
   PubMed Web of Science ®Google Scholar
• Möller P, Lammler B, Eberlein-Gonska M, et al. Primary mediastinal clear cell lymphoma of B-cell type. Virchows Arch Pathol Anat. 1986; 409: 79–92
   Google Scholar
• Perrone T, Frizzera G, Rosai J. Mediastinal diffuse large-cell lymphoma with sclerosis. A clinicopathologic study of 60 cases. Am J Surg Pathol. 1986; 10: 176–191
   PubMed Web of Science ®Google Scholar
• Möller P, Moldenhauer G, Momburg F, et al. Mediastinal lymphoma of clear cell type is a tumor corresponding to terminal steps of B cell differentiation. Blood 1987; 69: 1087–1095
   PubMed Web of Science ®Google Scholar
• Scarpa A, Bonetti F, Menestrina F, et al. Mediastinal large-cell lymphoma with sclerosis. Genotypic analysis establishes its B nature. Virchows Arch A. 1987; 412: 17–21
   Web of Science ®Google Scholar
• Lamarre L, Jacobson JO, Aisenberg AC, Harris NL. Primary large cell lymphoma of the mediastinum. A histologic and immunopheno-typic study of 29 cases. Am J Surg Pathol. 1989; 13: 730–739
   PubMed Web of Science ®Google Scholar
• Möller P, Matthaei-Maurer DU, Hofmann WJ, Dörken B, Moldenhauer G. Immunophenotypic similarities of mediastinal clear-cell lymphoma and sinusoidal (monocytoid) B cells. Int J Cancer 1989; 43: 10–16
   PubMed Web of Science ®Google Scholar
• Todeschini G, Ambrosetti A, Meneghini V, et al. Mediastinal large-B-cell lymphoma with sclerosis: a clinical study of 21 patients. J Clin Oncol. 1990; 8: 804–808
   PubMed Web of Science ®Google Scholar
• Waldron JA, Jr, Dohring EJ, Farber LR. Primary large cell lymphomas of the mediastinum: an analysis of 20 cases. Semin Diagn Pathol. 1985; 2: 281–295
   PubMedGoogle Scholar
• Grogan TM, Spier CM, Richter LC, Rangel CS. Immunologic approaches to the classification of non-Hodgkin's lymphoma. Immunologic Approaches to the Classification and Management of Lymphomas and Leukemias, JM Bennett, KA Foon. Kluwer Academy Publishers, New York 1988; 31–148
   Google Scholar
• Schuurman H-J, Huppes WIM, Verdonck LF, Van Baarlen J, Van Unnik JAM. Immunophenotyping of non-Hodgkins lymphoma. Correlation with relapse-free survival. Am J Pathol. 1988; 131: 102–111
   PubMed Web of Science ®Google Scholar
• Weiss LM, Strickler JG, Medeiros LJ, Gerdes J, Stein H, Warnke RA. Proliferative rates of non-Hodgkin's lymphomas as assessed by Ki-67 antibody. Hum Pathol. 1977; 18: 1155–1159
   Google Scholar
• Grogan TM, Lippman SM, Spier CM, et al. Independent prognostic significance of a nuclear proliferation antigen in diffuse large cell lymphomas as determined by the monoclonal antibody Ki-67. Blood 1988; 71: 1157–1160
   PubMed Web of Science ®Google Scholar
• Henni T, Gaulard P, Divine M, et al. Comparison of genetic probe with immunophenotype analysis in lymphoproliferative disorders: a study of 87 cases. Blood 1988; 72: 1937–1943
   PubMed Web of Science ®Google Scholar
• Kamat D, Laszewski MJ, Kemp JD, et al. The diagnostic utility of immunophenotyping and immunogenotyping in the pathologic evaluation of lymphoid proliferations. Mod Pathol. 1990; 3: 105–112
   PubMed Web of Science ®Google Scholar
• Mead GM. Malignant lymphoma-a clinician's view. J Pathol. 1987; 151: 179–182
   PubMedGoogle Scholar
• Gerdes J, Schwab U, Lemke H, Stein H. Production of a mouse monoclonal antibody reactive with a human nuclear antigen associated with cell proliferation. Int J Cancer 1983; 31: 13–20
   PubMed Web of Science ®Google Scholar
• Weisenburger DD, Nathwani BN, Diamond LW, Winberg CD, Rappaport H. Malignant lymphoma, intermediate lymphocytic type: a clinicopathologic study of 42 cases. Cancer 1981; 48: 1415–1425
   PubMed Web of Science ®Google Scholar
• Weisenburger DD, Km H, Rappaport H. Mantle zone lymphoma: a follicular variant of intermediate lymphocytic lymphoma. Cancer 1982; 49: 1429–1438
   PubMed Web of Science ®Google Scholar
• Spier CM, Grogan TM, Fielder K, Richter L, Rangel C. Immunophenotypes in ‘well-differentiated’ lymphoproliferative disorders, with emphasis on small lymphocytic lymphoma. Hum Pathol. 1986; 17: 1126–1136
   PubMed Web of Science ®Google Scholar
• Triozzi PL, Borowitz MJ, Gockerman JP. Gastrointestinal involvement and multiple lymphomatous polyposis in mantle-zone lymphoma. J Clin Oncol. 1986; 4: 866–873
   PubMed Web of Science ®Google Scholar
• Van den Oord JJ, de Wolf-Peeters C, Pulford KAF, Mason DY, Desmet VJ. Mantel zone lymphoma. Immuno- and enzymehistochemi-cal studies on the cell of origin. Am J Surg Pathol. 1986; 10: 780–788
   PubMed Web of Science ®Google Scholar
• Grogan TM, Warnke RA, Kaplan HA. A comparative study of Burkitt's and non-Burkitt's undifferentiated malignant lymphoma. Cancer 1982; 49: 1817–1828
   PubMed Web of Science ®Google Scholar
• Pavlova Z, Parker JW, Taylor CR, Levine AM, Feinstein Dl, Lukes RJ. Small noncleaved follicular center cell lymphoma: Burkitt's and non-Burkitt's variants in the US. II. Pathologic and immunologic features. Cancer 1987; 59: 1892–1902
   PubMed Web of Science ®Google Scholar
• Trump DL, Mann RB. Diffuse large cell and undifferentiated lymphomas with prominent mediastinal involvement. A poor prognostic subset of patients with non-Hodgkin's lymphoma. Cancer 1982; 50: 277–282
   PubMed Web of Science ®Google Scholar
• Stroup R, Shebani K, Misset J-L, Szekely AM, Tremblay G, Rappaport H. Surface immunoglobulin-positive lymphoblastic lymphoma. A report of three cases. Cancer 1990; 65: 2559–2563
   PubMedGoogle Scholar
• Grogan T, Spier C, Wirt DP, et al. Immunologic complexity of lymphoblastic lymphoma. Diagn Immunol. 1986; 4: 81–88
   PubMedGoogle Scholar
• Strickler JG, Michie SA, Warnke RA, Dorf-Man RF. The ‘syncytial variant’ of nodular sclerosing Hodgkin's disease. Am J Surg Pathol. 1986; 10: 470–477
   PubMed Web of Science ®Google Scholar
• Grogan TM. Hodgkin's disease. Surgical Pathology of the Lymph Nodes and Related Organs, ES Jaffe. Saunders, Philadelphia 1985; 86–134
   Google Scholar
• Azar HA, Espinoza CG, Richman AV, Saba SR, Wang T. Undifferentiated large cell malignancies: an ultrastructural and immuno-cytochemical study. Hum Pathol. 1982; 13: 323–333
   PubMed Web of Science ®Google Scholar
• Damjanov I, Tuma B, Dominis M. Electron microscopy of large cell undifferentiated and giant cell tumors. Pathol Res Pract. 1989; 184: 137–160
   PubMedGoogle Scholar
• Ghadially FN. Diagnostic Electron Microscopy of Tumours.2nd ed. Butterworths, Boston 1985
   Google Scholar
• Mackay B, Osborne BM. The contribution of electron microscopy to the diagnosis of tumors. Pathobiol Ann 1978; 8: 359–405
   PubMedGoogle Scholar
• Herrera GA, Crofts JL, Roberts CR. Neurosecretory granule-like structures in lymphomas. Hum Pathol. 1980; 11: 449–456
   PubMed Web of Science ®Google Scholar
• Richards JG, Da Prada M. Uranaffin reaction: a new cytochemical technique for the localization of adenine nucleotides in organelles storing biogenic amines. J Histochem Cytochem. 1977; 25: 1322–1336
   PubMed Web of Science ®Google Scholar
• Payne CM, Nagle RB, Borduin VF, Kim A. An ultrastructural evaluation of the cell organelle specificity of the uranaffin reaction in two human endocrine neoplasms. J Submicrosc Cytol. 1983; 15: 833–841
   PubMedGoogle Scholar
• Payne CM, Nagle RB, Borduin VF. An ultrastructural cytochemical stain specific for neuroendocrine neoplasms. Lab Invest. 1984; 51: 350–365
   PubMed Web of Science ®Google Scholar
• Payne CM, Smith WL, Grogan TM, Nagle RB, Paplanus SH, Palmer T. Ultrastructural morphometry distinguishes Burkitt's-like lymphomas from neuroendocrine neoplasms: useful criteria applied to the evaluation of a poorly differentiated neuroendocrine neoplasm of the nasal cavity masquerading as Burkitt's-like lymphoma. Mod Pathol. 1989; 2: 35–45
   PubMedGoogle Scholar
• Said JW, Hargreaves HK, Pinkus GS. Non-Hodgkin's lymphomas: an ultrastructural study correlating morphology with immunologic cell type. Cancer 1979; 44: 504–528
   PubMed Web of Science ®Google Scholar
• Peiper SC, Kahn LB. Ultrastructural comparison of Hodgkin's and non-Hodgkin's lymphomas. Histopathology 1982; 6: 93–109
   PubMed Web of Science ®Google Scholar
• Mackay B. Ultrastructural diagnosis of lymphomas and leukemias. Ultrastruct Pathol. 1985; 9: 209–214
   PubMed Web of Science ®Google Scholar
• Dickersin GR. Electron microscopy of leukemias and lymphomas. Clin Lab Med. 1987; 7: 199–247
   PubMedGoogle Scholar
• Imai Y, Kasajima T, Terashima K, Dobashi M, Matsuda M. Non-Hodgkin malignant lymphoma with special reference to desmosome-like junctions. Acta Pathol Jpn. 1980; 30: 195–217
   PubMedGoogle Scholar
• Eyden BP, Harris M. An immunohistochemically defined non-Hodgkin's lymphoma showing intercellular junctions. Virchows Arch A Pathol Anat. 1989; 415: 297–300
   Google Scholar
• Glick AD, Leech JH, Flexner JM, Collins RD. Ultrastructural study of Reed-Sternberg cells. Am J Pathol. 1976; 85: 195–208
   PubMed Web of Science ®Google Scholar
• Dorfman RF, Rice DF, Mitchell AD, Kempson RL, Levine G. Ultrastructural studies of Hodgkin's disease. Natl Cancer Inst. Monogr. 1973; 36: 221–238
   PubMedGoogle Scholar
• Maksem JA, Hassan MO. The ultrastructurai heterogeneity of the Reed-Sternberg cell and its resemblance to monocyte-macrophage differentiation in vivo. Ultrastruct Pathol. 1983; 4: 379–389
   PubMed Web of Science ®Google Scholar
• Anagnostou D, Parker JW, Taylor CR, Tindle BH, Lukes RJ. Lacunar cells of nodular sclerosing Hodgkin's disease. An ultrastructural and immunohistologic study. Cancer 1977; 39: 1032–1043
   PubMed Web of Science ®Google Scholar
• Kadin ME. Possible origin of the Reed-Sternberg cell from an interdigitating reticulum cell. Cancer Treat Rep. 1982; 66: 601–608
   PubMedGoogle Scholar
• Stein H, Gerdes J, Schwab U, et al. Evidence for the detection of the normal counterpart of Hodgkin and Sternberg-Reed cells. Hematol Oncol. 1983; 1: 21–29
   PubMedGoogle Scholar
• Stein H, Mason DY, Gerdes J, et al. The expression of the Hodgkin's disease associated antigen Ki-1 in reactive and neoplastic lymphoid tissue: evidence that Reed-Sternberg cells and histiocytic malignancies are derived from activated lymphoid cells. Blood 1985; 66: 848–858
   PubMed Web of Science ®Google Scholar
• Drexler HG, Jones DB, Diehl V, Minowada J. Is the Hodgkin cell a T- or B-lymphocyte? Recent evidence from geno- and immuno-phenotypic analysis and in vitro cell lines. Hematol Oncol. 1989; 7: 95–113
   PubMed Web of Science ®Google Scholar
• Schaadt M, Burrichter H, Stein H, Pfreunds-Chuh M, Fonatsch C, Diehl V. The cell of origin in Hodgkin's disease: conclusions from in vivo and in vitro studies. Int Rev Exp Pathol. 1985; 27: 185–202
   PubMedGoogle Scholar
• Kamesaki H, Fukuhara S, Tatsumi E, et al. Cytochemical, immunologic, chromosomal, and molecular genetic analysis of a novel cell line derived from Hodgkin's disease. Blood 1986; 68: 285–292
   PubMed Web of Science ®Google Scholar
• Jones DB. The histogenesis of the Reed-Sternberg cell and its mononuclear counterparts. J Pathol. 1987; 151: 191–195
   PubMed Web of Science ®Google Scholar
• Drexler HG, Leber BF. The nature of the Hodgkin cell. Report of the first international symposium on Hodgkin's lymphoma, Koln, Federal Republic of Germany, October 2–3, 1987. Blut. 1988; 56: 135–137
   PubMedGoogle Scholar
• Payne SV, Newell DG, Jones DB, Wright DH. The Reed-Sternberg cell/lymphocyte interaction. Ultrastructure and characteristics of binding. Am J Pathol. 1980; 100: 7–24
   PubMed Web of Science ®Google Scholar
• Searle J, Kerr JFR, Bishop CJ. Necrosis and apoptosis: distinct modes of cell death with fundamentally different significance. Pathol Annu. 1982; 17: 229–259
   PubMed Web of Science ®Google Scholar
• Koo CH, Mason DY, Miller R, Ben-Ezra J, Sheibani K, Rappaport H. Additional evidence that ‘plasmacytoid T-cell lymphoma’ associated with chronic myeloproliferative disorders is of macrophage/monocyte origin. Am J Clin Pathol. 1990; 93: 822–827
   PubMed Web of Science ®Google Scholar
• Cerezo L. B-cell multilobated lymphoma. Cancer 1984; 52: 2277–2280
   Web of Science ®Google Scholar
• Pinkus GS, Said JW, Hargreaves H. Malignant lymphoma, T-cell type: a distinct morphologic variant with large multi-lobated nuclei, with a report of four cases. Am J Clin Pathol. 1979; 72: 540–550
   PubMed Web of Science ®Google Scholar
• Dardick I, Srinivasan R, Al-Jabi M. Signet-ring cell variant of large cell lymphoma. Ultrastruct Pathol. 1983; 5: 195–200
   PubMed Web of Science ®Google Scholar
• Kim H, Dorfman RF, Rappaport H. Signet ring cell lymphoma: a rare morphologic and functional expression of nodular (follicular) lymphoma. Am J Surg Pathol. 1978; 2: 119–132
   PubMed Web of Science ®Google Scholar
• Grogan TM, Payne CM, Richter LC, Rangel CS. Signet-ring cell lymphoma of T-cell origin. An immunocytochemical and ultrastructural study relating giant vacuole formation to cytoplasmic sequestration of surface membrane. Am J Surg Pathol. 1985; 9: 684–692
   PubMedGoogle Scholar
• Weiss LM, Wood GS, Dorfman RF. T-cell signet-ring cell lymphoma. A histologic, ultrastructural and immunohistochemical study of two cases. Am J Surg Pathol. 1985; 9: 273–280
   PubMed Web of Science ®Google Scholar
• Van der Putte SCJ, Toonstra J, Bruns HM, van Wichen DF, van Unnik JAM, van Vloten WA. T-cell signet-ring cell proliferation in the skin simulating true histiocytic lymphoma. Am J Dermatopathol. 1987; 9: 120–128
   PubMedGoogle Scholar
• Cross PA, Eyden BP, Harris M. Signet ring cell lymphoma of T-cell type. J Clin Pathol. 1989; 42: 239–245
   PubMed Web of Science ®Google Scholar
• Osborne BM, MacKay B, Butler JJ, Ordonez NG. Large cell lymphoma with microvillus-like projections: an ultrastructural study. Am J Clin Pathol. 1983; 79: 443–450
   PubMed Web of Science ®Google Scholar
• Rosen PJ, Feinstein Dl, Pattengale PK, et al. Convoluted lymphocytic lymphoma in adults. A clinicopathologic entity. Ann Intern Med. 1978; 89: 319–324
   PubMed Web of Science ®Google Scholar
• Boucheix C, Diebold J, Bernadou A, et al. Lymphoblastic lymphoma/leukemia with convoluted nuclei. The question of its relation to the T-cell lineage studied in 13 patients. Cancer 1980; 45: 1569–1577
   PubMedGoogle Scholar
• Vezzoni P, Giardini R, Lombardi L, et al. Multienzymatic analyses of human malignant lymphomas. Correlation of enzymatic data with pathologic and ultrastructural findings in Burkitt's and lymphoblastic lymphomas. Cancer 1984; 54: 489–499
   PubMedGoogle Scholar
• Mackay B. Ultrastructural diagnosis of lymphomas and leukemias. Ultrastruct Pathol. 1985; 9: 209–214
   PubMed Web of Science ®Google Scholar
• Long JC, McCaffrey RP, Aisenberg AL, Marks SM, Kung PC. Terminal deoxynucleotidyl transferase positive lymphoblastic lymphoma. A study of 1 5 cases. Cancer 1979; 44: 2127–2139
   PubMedGoogle Scholar
• Levine GD, Rosai J. Thymic hyperplasia and neoplasia: a review of current concepts. Hum Pathol. 1978; 9: 495–515
   PubMed Web of Science ®Google Scholar
• Saab GA, Carloss H. Lymphoblastic lymphoma without TdT. N Engl J Med. 1980; 30(2)969–970
   Google Scholar
• Payne CM, Grogan TM, Cromey DW, Bjore CG, Jr, Kerrigan DP. An ultrastructural mor-phometric and immunophenotypic evaluation of Burkitt's and Burkitt's-like lymphomas. Lab Invest. 1987; 57: 200–218
   PubMed Web of Science ®Google Scholar
• Knowles DM, Chamulak GA, Subar M, et al. Lymphoid neoplasia associated with the acquired immunodeficiency syndrome (AIDS). The New York University Medical Center experience with 105 patients (1981–1986). Ann Intern Med. 1988; 108: 744–753
   PubMed Web of Science ®Google Scholar
• Krikorian JG, Burke JS, Rosenberg SA, Kaplan HS. Occurrence of non-Hodgkin's lymphoma after therapy for Hodgkin's disease. N Engl J Med. 1979; 300: 452–458
   PubMed Web of Science ®Google Scholar
• Dickersin GR. Electron microscopy of leukemias and lymphomas. Clin Lab Med. 1987; 7: 199–247
   PubMedGoogle Scholar
• Maurer R, Taylor CR, Parker JW, Cramer A, Lukes RJ. Immunoblastic sarcoma: morphologic criteria and the distinction of B and T cell types. Oncology 1982; 39: 42–50
   PubMedGoogle Scholar
• Bemier G, Graham RC, Jr. Plasma cell asyn-chrony in myeloma: correlation of light and electron microscopy. Semin Hematol. 1976; 13: 239–245
   PubMedGoogle Scholar
• Ferrer-Roca O. primary gastric plasmacytoma with massive intracytoplasmic crystalline inclusions. A case report. Cancer 1982; 50: 755–759
   PubMed Web of Science ®Google Scholar
• Raz I, Or R, Okou E, Leizerowitz R, Polliack A. Hairy cell leukaemia: report of an unusual case with hepatomegaly due to a large vascular tumour of the liver, mediastinal mass and pleural effusion containing hairy cells. Acta Haematol (Basel) 1984; 71: 393–394
   PubMedGoogle Scholar
• Vardiman JW, Golomb HM. Autopsy findings in hairy cell leukaemia. Semin Oncol. 1984; 11: 370–379
   PubMed Web of Science ®Google Scholar
• Malik STA, Amess J, D'Ardenne AJ, Lister TA. Hairy cell leukemia-mediastinal involvement. A report of two cases and review of the literature. Hematol Oncol. 1989; 7: 303–306
   PubMedGoogle Scholar
• Quesada JR, Hersh EM, Manning J, et al. Treatment of hairy cell leukaemia with recombinant alpha-interferon. Blood 1986; 68: 493–497
   PubMed Web of Science ®Google Scholar
• Zimmerman KG, Payne CM, Nagle RB. Ribosome-lamellae complexes in benign plasma cells accompanying neoplastic infiltrates. J Clin Pathol. 1984; 81: 364–367
   Google Scholar
• Martin JLD, Li C-Y, Banks PM. Blastic variant of hairy-cell leukemia. Am J Clin Pathol. 1987; 87: 576–583
   PubMedGoogle Scholar
• Kubonishi I, Ohtsuki Y, Machida K-l, et al. Granulocytic sarcoma presenting as a mediastinal tumor. Report of a case and cytologi-cal and cytochemical studies of tumor cells in vivo and in vitro. Am J Clin Pathol. 1984; 82: 730–734
   PubMed Web of Science ®Google Scholar
• Banerjee D, Silva E. mediastinal mass with acute leukemia. Myeloblastoma masquerading as lymphoblastic lymphoma. Arch Pathol Lab Med. 1981; 105: 126–129
   PubMed Web of Science ®Google Scholar
• Neely SM. Adult T-cell leukemia-lymphoma. West J Med. 1989; 150: 557–561
   PubMedGoogle Scholar