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Chapter 35 - Lymphoid, myeloid, histiocytic, and dendritic cell proliferations in soft tissues

Published online by Cambridge University Press:  19 October 2016

Markku Miettinen
Affiliation:
National Cancer Institute, Maryland
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Modern Soft Tissue Pathology
Tumors and Non-Neoplastic Conditions
, pp. 941 - 974
Publisher: Cambridge University Press
Print publication year: 2016

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References

Primary Sources

Willemze, R, Jaffe, ES, Burg, G, et al. WHO-EORTC classification of cutaneous lymphomas. Blood 2005;105:37683785.Google Scholar
Swerdlow, SH, Campo, E, Harris, NL, et al. World Health Organization Classification of Tumours of Haematopoietic and Lymphoid Tissues. Lyon: IARC Press; 2008.Google Scholar
LeBoit, PE, Burg, G, Weedon, D, Sarasin, A (eds). World Health Organization Classification of Tumours: Pathology and Genetics of Skin Tumours. Lyon: IARC Press; 2006.Google Scholar
Chu, PG, Chang, KL, Arber, DA, Weiss, LM. Immunophenotyping of hematopoietic neoplasms. Semin Diagn Pathol 2000;17:236256.Google Scholar
Hsi, ED, Yegappan, S. Lymphoma immunophenotyping: a new era in paraffin-section immunohistochemistry. Adv Anat Pathol 2001;8:218239.Google Scholar
Falini, B, Mason, DY. Proteins encoded by genes involved in chromosomal alterations in lymphoma and leukemia: clinical value of their detection by immunocytochemistry. Blood 2002;99:409426.Google Scholar
Travis, WD, Banks, PM, Reiman, HM. Primary extranodal soft tissue lymphoma of the extremities. Am J Surg Pathol 1987;11:359366.CrossRefGoogle ScholarPubMed
Lanham, GR, Weiss, SW, Enzinger, FM. Malignant lymphoma: a study of 75 cases presenting in soft tissue. Am J Surg Pathol 1989;13:110.Google Scholar

Secondary Sources

Utz, GL, Swerdlow, S. Distinction of follicular hyperplasia from follicular lymphoma in B5-fixed tissues: comparison of MT2 and bcl-2 antibodies. Hum Pathol 1993;24:11551158.CrossRefGoogle ScholarPubMed
Leinweber, B, Colli, C, Chott, A, Kerl, H, Cerroni, L. Differential diagnosis of cutaneous infiltrates of B lymphocytes with follicular growth pattern. Am J Dermatopathol 2004;26:413.CrossRefGoogle ScholarPubMed
Goodlad, JR, MacPherson, S, Jackson, R, Batstone, P, White, J; Scotland, Newcastle Lymphoma Group. Extranodal follicular lymphoma: a clinicopathologic and genetic analysis of 15 cases arising at non-cutaneous sites. Histopathology 2004;44:268276.CrossRefGoogle ScholarPubMed
Keller, AR, Hochholzer, L, Castleman, B. Hyaline-vascular and plasma-cell types of giant lymph node hyperplasia of the mediastinum and other locations. Cancer 1972;29:670683.Google Scholar
Kazakov, D, Fanburg-Smith, JC, Suster, S, et al. Castleman disease of the subcutis and underlying skeletal muscle: report of 6 cases. Am J Surg Pathol 2004;28:569577.Google Scholar
Waterston, A, Bower, M. Fifty years of multicentric Castleman’s disease. Acta Oncol 2004;43:698704.Google Scholar
Carbone, A, Gloghini, A. KSHV/HHV8-associated lymphomas. Br J Hematol 2008;140:1324.CrossRefGoogle ScholarPubMed
Cronin, DM, Warnke, RA. Castleman disease: an update on classification and the spectrum of associated lesions. Adv Anat Pathol 2009;16:236246.CrossRefGoogle ScholarPubMed
Ohgami, RS, Zhao, S, Ohgami, JK, et al. TdT+ T-lymphoblastic populations are increased in Castleman disease, in Castleman disease in association with follicular dendritic cell tumors, and in angioimmunoblastic T-cell lymphoma. Am J Surg Pathol 2012;36:16191628.Google Scholar
Kuo, TT, Shih, LY, Chan, HL. Kimura’s disease: involvement of regional lymph nodes and distinction from angiolymphoid hyperplasia with eosinophilia. Am J Surg Pathol 1988;12:843854.CrossRefGoogle ScholarPubMed
Li, TJ, Chen, XM, Wang, SZ, et al. Kimura’s disease: a clinicopathologic study of 54 Chinese patients. Oral Surg Oral Med Oral Pathol Oral Radiol Endod 1996;82:549555.Google Scholar
Chen, H, Thompson, LD, Aguilera, NS, Abbondanzo, SL. Kimura disease: a clinicopathologic study of 21 cases. Am J Surg Pathol 2004;28:505513.CrossRefGoogle ScholarPubMed
Santucci, M, Pimpinelli, N, Arganini, L. Primary cutaneous B-cell lymphoma: a unique type of low-grade lymphoma. clinicopathologic and immunologic study of 83 cases. Cancer 1991;67:23112326.Google Scholar
Aguilera, NSI, Tomaszewski, MM, Moad, JC, et al. Cutaneous follicular center cell lymphoma: clinicopathologic study of 19 cases. Mod Pathol 2001;14:828835.Google Scholar
Senff, NJ, Hoefnagel, JJ, Jansen, PM, et al. Reclassification of 300 primary cutaneous B-cell lymphomas according to the new WHO-EORTC classification for cutaneous lymphomas: comparison with previous classifications and identification of prognostic markers. J Clin Oncol 2007;25:15811587.Google Scholar
Vermeer, MH, Willemze, R. Recent advances in primary cutaneous B-cell lymphomas. Curr Opin Oncol 2014;26:230236.CrossRefGoogle ScholarPubMed
Swerdlow, SH, Quintanilla-Martinez, L, Willemze, R, Kinney, MC. Cutaneous B-cell lymphoproliferative disorders: report of the 2011 Society for Hematopathology/European Association for Haematopathology workshop. Am J Clin Pathol 2013;139:515535.CrossRefGoogle ScholarPubMed
Xie, X, Sundram, U, Natkunam, Y, et al. Expression of HGAL in primary cutaneous large B-cell lymphomas: evidence for germinal center derivation of primary cutaneous follicular lymphoma. Mod Pathol 2008;21:653659.Google Scholar
Cerroni, L, Signoretti, S, Höfler, H, et al. Primary cutaneous marginal zone B-cell lymphoma: a recently described entity of low-grade malignant cutaneous B-cell lymphoma. Am J Surg Pathol 1997;21:13071315.Google Scholar
Tomaszewski, MM, Abbondanzo, SL, Lupton, GP. Extranodal marginal zone B-cell lymphoma of the skin: a morphologic and immunophenotypic study of 11 cases. Am J Dermatopathol 2000;22:205211.Google Scholar
Baldassano, MF, Bailey, EM, Ferry, JA, Harris, NL, Duncan, LM. Cutaneous lymphoid hyperplasia and cutaneous marginal zone lymphoma: comparison of morphologic and immunophenotypic features. Am J Surg Pathol 1999;23:8896.CrossRefGoogle ScholarPubMed
Servitje, O, Gallardo, F, Estrach, T, et al. Primary cutaneous marginal zone B-cell lymphoma: a clinical, histopathological, immunophenotypic and molecular genetic study of 22 cases. Br J Dermatol 2002;147:11471158.CrossRefGoogle Scholar
Cho-Vega, JH, Vega, F, Rassidakis, G, Medeiros, LJ. Primary cutaneous marginal zone B-cell lymphoma. Am J Clin Pathol 2006;125 Suppl:S38–S49.Google Scholar
Dalle, S, Thomas, L, Balme, B, Dumontet, C, Thieblemont, C. Primary cutaneous marginal zone lymphoma. Crit Rev Oncol Hematol 2010;74:156162.CrossRefGoogle ScholarPubMed
Vermeer, MH, Geelen, FA, van Haselen, CW, et al. Primary cutaneous large B-cell lymphomas of the legs: a distinct type of cutaneous B-cell lymphoma with an intermediate prognosis. Arch Dermatol 1996;132:13041308.CrossRefGoogle ScholarPubMed
Kodama, K, Massone, C, Chott, A, et al. Primary cutaneous large B-cell lymphomas: clinicopathologic features, classification, and prognostic factors in a large series of patients. Blood 2005;106:24912497.Google Scholar
Grange, F, Beylot-Barry, M, Courville, P, et al. Primary cutaneous diffuse large B-cell lymphoma, leg type: clinicopathologic features and prognostic analysis of 60 cases. Arch Dermatol 2007;143:11441150.Google Scholar
Tse, CC, Chan, JK, Yuen, RW, Ng, CS. Malignant lymphoma with myxoid stroma: a new pattern in need of recognition. Histopathology 1991;18:3135.Google Scholar
Koo, CH, Shin, SS, Bracho, F, et al. Rosette-forming non-Hodgkin lymphomas. Histopathology 1996;29:557563.Google Scholar
Lin, P, Jones, D, Dorfman, DM, Medeiros, LJ. Precursor B-cell lymphoblastic lymphoma: a predominantly extranodal tumor with low propensity for leukemic involvement. Am J Surg Pathol 2000;24:14801490.Google Scholar
Maitra, A, McKenna, RW, Weinberg, AG, Schneider, NR, Kroft, SH. Precursor B-cell lymphoblastic lymphoma: a study of nine cases lacking blood and bone marrow involvement and review of the literature. Am J Clin Pathol 2001;115:868875.CrossRefGoogle ScholarPubMed
Sheibani, K, Battifora, H, Winberg, CD, et al. Further evidence that “malignant angioendotheliomatosis” is an angiotropic large-cell lymphoma. N Engl J Med 1986;314:943948.Google Scholar
Wick, MR, Mills, SE, Scheithauer, BW, et al. Reassessment of malignant “angioendotheliomatosis”: evidence in favor of its reclassification as “intravascular lymphomatosis.” Am J Surg Pathol 1986;10:112123.Google Scholar
Stroup, RM, Sheibani, K, Moncada, A, Purdy, LJ, Battifora, H. Angiotropic (intravascular) large cell lymphoma: a clinicopathologic study of seven cases with unique clinical presentations. Cancer 1990;66:17811788.Google Scholar
Jalkanen, S, Aho, R, Kallajoki, M, et al. Lymphocyte homing receptors and adhesion molecules in intravascular malignant lymphomatosis. Int J Cancer 1989;44:777782.Google Scholar
Ponzoni, M, Arrigoni, G, Gould, VE, et al. Lack of CD29 (beta integrin) and CD54 (ICAM-1) adhesion molecules in intravascular lymphomatosis. Hum Pathol 2000;31:220226.Google Scholar
Nixon, BK, Kussick, SJ, Carlon, MJ, Rubin, BP. Intravascular large B-cell lymphoma involving hemangiomas: an unusual presentation of a rare neoplasm. Mod Pathol 2005;18:11211126.Google Scholar
Smith, ME, Stamatakos, MD, Neuhauser, TS. Intravascular lymphomatosis presenting within angiolipomas. Ann Diagn Pathol 2001;5:103106.Google Scholar
Matsue, K, Asada, N, Takeuchi, M, et al. A clinicopathological study of 13 cases of intravascular lymphoma: experience in a single institution over a 9-yr period. Eur J Haematol 2008;80:236244.Google Scholar
Samols, MA, Su, A, Ra, S, et al. Intralymphatic cutaneous anaplastic large cell lymphoma/lymphomatoid papulosis: expanding the spectrum of CD30-positive lymphoproliferative disorders. Am J Surg Pathol 2014;38:12031211.Google Scholar
Liu, Y, Zhang, W, An, J, Li, H, Liu, S. Cutaneous intravascular natural killer-cell lymphoma: a case report and review of the literature. Am J Clin Pathol 2014;142:243247.Google Scholar
Crane, GM, Ambinder, RF, Shirley, CM, et al. HHV-8-positive and EBV-positive intravascular lymphoma: an unusual presentation of extracavitary primary effusion lymphoma. Am J Surg Pathol 2014;38:426432.Google Scholar
Wang, MB, Strasnick, B, Zimmerman, MC. Extranodal American Burkitt’s lymphoma of the head and neck. Arch Otolaryngol Head Neck Surg 1992;118:193199.Google Scholar
Wright, D, McKeever, P, Carter, R. Childhood non-Hodgkin lymphomas in the United Kingdom: findings from the UK Children’s Cancer Study Group. J Clin Pathol 1997;50:128134.Google Scholar
Bociek, RG. Adult Burkitt’s lymphoma. Clin Lymphoma 2005;6:1120.Google Scholar
Brady, G, MacArthur, GJ, Farrell, PJ. Epstein-Barr virus and Burkitt lymphoma. J Clin Pathol 2007;60:13971402.Google Scholar
Said, J, Lones, M, Yea, S. Burkitt lymphoma and MYC: what else is new? Adv Anat Pathol 2014;21:160165.Google Scholar
Bladé, J, Fernández de Larrea, C, Rosiñol, L, et al. Soft-tissue plasmacytomas in multiple myeloma: incidence, mechanisms of extramedullary spread, and treatment approach. J Clin Oncol 2011;29:38053812.Google Scholar
Wirk, B, Wingard, JR, Moreb, JS. Extramedullary disease in plasma cell myeloma: the iceberg phenomenon. Bone Marrow Transplant 2013;48:1018.Google Scholar
Delecluse, HJ, Anagnostopoulos, I, Dallenbach, F, et al. Plasmablastic lymphomas of the oral cavity: a new entity associated with the human immunodeficiency virus infection. Blood 1997;89:14131420.Google Scholar
Colomo, L, Loong, F, Rives, S, et al. Diffuse large B-cell lymphomas with plasmablastic differentiation represent a heterogeneous group of disease entities. Am J Surg Pathol 2004;28:736747.Google Scholar
Dong, HY, Scadden, DT, de Leval, T, et al. Plasmablastic lymphoma in HIV-positive patients: an aggressive Epstein-Barr virus-associated extramedullary plasmacytic neoplasm. Am J Surg Pathol 2005;29:16331641.CrossRefGoogle ScholarPubMed
Vega, F, Chang, CC, Medeiros, LJ, et al. Plasmablastic lymphomas and plasmablastic plasma cell myelomas have nearly identical immunophenotypic profiles. Mod Pathol 2005;18:806815.Google Scholar
Salhany, KE, Macon, WR, Choi, JK, et al. Subcutaneous panniculitis-like T-cell lymphoma: clinicopathologic, immunophenotypic, and genotypic analysis of alpha/beta and gamma/delta subtypes. Am J Surg Pathol 1998;22:881893.Google Scholar
Kumar, S, Knenacs, S, Medeiros, J, et al. Subcutaneous panniculitic T-cell lymphoma is a tumor of cytotoxic T lymphocytes. Hum Pathol 1998;29:397403.Google Scholar
Massone, C, Chott, A, Metze, D, et al. Subcutaneous, blastic natural killer cell (NK), NK/T-cell, and other cytotoxic lymphomas of the skin: a morphologic, immunophenotypic, and molecular study of 50 patients. Am J Surg Pathol 2004;28:719735.CrossRefGoogle ScholarPubMed
Kong, YY, Dai, B, Kong, JC, et al. Subcutaneous panniculitis-like T-cell lymphoma: a clinicopathologic, immunophenotypic, and molecular study of 22 Asian cases according to WHO-EORTC classification. Am J Surg Pathol 2008;32:14951502.Google Scholar
Willemze, R, Jansen, PM, Cerroni, L, et al. Subcutaneous panniculitis-like T-cell lymphoma: definition, classification, and prognostic factors: an EORTC cutaneous lymphoma group study of 83 cases. Blood 2008;111:838845.Google Scholar
Huppmann, AR, Xi, L, Raffeld, M, Pittaluga, S, Jaffe, ES. Subcutaneous panniculitis-like T-cell lymphoma in the pediatric age group: a lymphoma of low malignant potential. Pediatr Blood Cancer 2013;60:11651170.Google Scholar
Arps, DP, Patel, RM. Lupus profundus (panniculitis): a potential mimic of subcutaneous panniculitis-like T-cell lymphoma. Arch Pathol Lab Med 2013;137:12111215.Google Scholar
Kempf, W, Kazakov, DV, Kutzner, H. Lobular panniculitis due to Borrelia burgdorferi infection mimicking subcutaneous panniculitis-like T-cell lymphoma. Am J Dermatopathol 2013;35:e30e33.Google Scholar
Chan, JK, Sin, VC, Wong, KF, et al. Nonnasal lymphoma expressing the natural killer cell marker CD56: a clinicopathologic study of 49 cases of an uncommon aggressive neoplasm. Blood 1997;89:45014513.Google Scholar
Ko, YH, Cho, EY, Kim, JE, et al. NK and NK-like T-cell lymphoma in extranasal sites: a comparative clinicopathological study according to the site and EBV status. Histopathology 2004;44:480489.Google Scholar
Stein, H, Foss, HD, Dürkop, H, et al. CD30+ anaplastic large cell lymphoma: a review of its histologic, genetic and clinical features. Blood 2000;96:36813695.Google Scholar
Savage, KJ, Harris, NL, Vose, JM, et al. ALK- anaplastic large-cell lymphoma is clinically and immunophenotypically different from both ALK+ ALCL and peripheral T-cell lymphoma, not otherwise specified: report from the International Peripheral T-cell Lymphoma Project. Blood 2008;111:54965504.Google Scholar
Amin, HN, Lai, R. Pathobiology of ALK+ anaplastic large cell lymphoma. Blood 2007;110:22592267.Google Scholar
Medeiros, LJ, Elenitoba-Johnson, KSJ. Anaplastic large cell lymphoma. Am J Clin Pathol 2007;127:707722.CrossRefGoogle ScholarPubMed
Pant, V, Jambhekar, NA, Madur, P, et al. Anaplastic large cell lymphoma (ALCL) presenting as primary bone and soft tissue sarcoma: a study of 12 cases. Indian J Pathol Microbiol 2007;50:303307.Google Scholar
Kounami, S, Shibuta, K, Yoshiyama, M, et al. Primary anaplastic large cell lymphoma of the psoas muscle: a case report and literature review. Acta Haematol 2012;127:186188.Google Scholar
Gaiser, T, Geissinger, E, Schattenberg, T, et al. Case report: a unique pediatric case of a primary CD8 expressing ALK-1 positive anaplastic large cell lymphoma of skeletal muscle. Diagn Pathol 2012;7:38.CrossRefGoogle ScholarPubMed
Sahoo, S, Rosen, PP, Feddersen, RM, et al. Anaplastic large cell lymphoma arising in a silicone breast implant capsule: a case report and review of the literature. Arch Pathol Lab Med 2003;127:115118.Google Scholar
Gauddet, G, Friedberg, JW, Weng, A, Pinkus, GS, Freedman, AS. Breast lymphoma associated with breast implants: two case reports and review of the literature. Leuk Lymphoma 2002;43:115119.Google Scholar
Fritsche, FR, Pahl, S, Petersen, I, et al. Anaplastic large-cell non-Hodgkin’s lymphoma of the breast in periprosthetic localization 32 years after treatment for primary breast cancer: a case report. Virchows Arch 2006;449:561564.Google Scholar
Roden, AC, Macon, WR, Keeney, GL, et al. Seroma-associated primary anaplastic large-cell lymphoma adjacent to breast implants: an indolent T-cell lymphoproliferative disorder. Mod Pathol 2008;21:455463.CrossRefGoogle ScholarPubMed
Wong, AK, Lopategui, J, Clancy, S, Kulber, D, Bose, S. Anaplastic large cell lymphoma associated with a breast implant capsule: a case report and review of the literature. Am J Surg Pathol 2008;32:12651268.Google Scholar
Ye, X, Shokrollahi, K, Rozen, WM, et al. Anaplastic large cell lymphoma (ALCL) and breast implants: breaking down the evidence. Mutat Res Rev Mutat Res 2014;762C:123132.Google Scholar
Brody, GS, Deapen, D, Taylor, CR, et al. Anaplastic large cell lymphoma (ALCL) occuring in women with breast implants: analysis of 173 cases. Plast Reconstr Surg 2014;135:695705.Google Scholar
Chan, JK, Buchanan, R, Fletcher, CD. Sarcomatoid variant of anaplastic large cell Ki-1 lymphoma. Am J Surg Pathol 1990;14:983988.Google Scholar
Rekhi, B, Sridhar, E, Viswanathan, S, Shet, TM, Jambhekar, NA. ALK+ anaplastic large cell lymphoma with cohesive, perivascular arrangements on cytology, mimicking a soft tissue sarcoma: a report of 2 cases. Acta Cytol 2010;54:7578.Google Scholar
Ten Berge, RL, Snijdewint, FGM, von Mensdorff-Pouilly, S, et al. MUC1 (EMA) is preferentially expressed by ALK positive anaplastic large cell lymphoma, in the normally glycosylated or only partly hypoglycosylated form. J Clin Pathol 2001;54:933939.Google Scholar
Neiman, RS, Barcos, M, Berard, C, et al. Granulocytic sarcoma: a clinicopathologic study of 61 cases. Cancer 1981;48:14261437.Google Scholar
Meis, JM, Butler, JJ, Osborne, BM, Manning, JT. Granulocytic sarcoma in nonleukemic patients. Cancer 1986;58:26972709.3.0.CO;2-R>CrossRefGoogle ScholarPubMed
Remstein, ED, Kurtin, PJ, Nascimento, AG. Sclerosing extramedullary hematopoietic tumor in chronic myeloproliferative disorders. Am J Surg Pathol 2000;24:5155.Google Scholar
Traweek, ST, Arbder, DA, Rappaport, H, Brynes, RK. Extramedullary myeloid tumors: an immunohistochemical and morphological study of 28 cases. Am J Surg Pathol 1993;17:10111019.Google Scholar
Pileri, SA, Ascani, S, Cox, MC, et al. Myeloid sarcoma: clinicopathologic, phenotypic and cytogenetic analysis of 92 adult patients. Leukemia 2007;21:340350.Google Scholar
Paydas, S, Zorludemir, S, Ergin, M. Granulocytic sarcoma: 32 cases and review of the literature. Leuk Lymphoma 2006;47:25272541.Google Scholar
Hudock, J, Chatten, J, Miettinen, M. Immunohistochemical evaluation of myeloid leukemia infiltrates (granulocytic sarcomas) in formaldehyde-fixed and paraffin-embedded tissue. Am J Clin Pathol 1994;102:5560.Google Scholar
Chen, J, Abbondanzo, SL. C-kit (CD117) reactivity in extramedullary myeloid tumor/granulocytic sarcoma. Arch Pathol Lab Med 2001;125:14481452.Google Scholar
Carter, MC, Metcalfe, DD, Komarow, HD. Mastocytosis. Immunol Allergy Clin North Am 2014;34:181196.Google Scholar
Salces, IG, Alfaro, J, Sáenz DE Santamaría, MC, Sanchez, M. Scabies presenting as solitary mastocytoma-like eruption in an infant. Pediatr Dermatol 2009;26:486488.Google Scholar
Longley, BJ, Metcalfe, DD. A proposed classification of mastocytosis incorporating molecular genetics. Hematol Oncol Clin North Am 2000;14:697701.Google Scholar
Ma, D, Stence, AA, Bossler, AB, Hackman, JR, Bellizzi, AM. Identification of KIT activating mutations in paediatric solitary mastocytoma. Histopathology 2014;64:218225.Google Scholar
Foucar, E, Rosai, J, Dorfman, R. Sinus histiocytosis with massive lymphadenopathy (Rosai–Dorfman disease): review of the entity. Semin Diagn Pathol 1990;7:1973.Google Scholar
Foucar, K, Foucar, E. The mononuclear phagocyte and immunoregulatory effector (M-PIRE) system: evolving concepts. Semin Diagn Pathol 1990;7:418.Google ScholarPubMed
Montgomery, EA, Meis, JM, Frizzera, G. Rosai–Dorfman disease of soft tissue. Am J Surg Pathol 1992;16:122129.Google Scholar
Young, PM, Kransdorf, MJ, Temple, HT, Mousavi, F, Robinson, PG. Rosai–Dorfman disease presenting as multiple soft tissue masses. Skeletal Radiol 2005;34:665669.Google Scholar
Kong, Y, Kong, J, Shi, D, et al. Cutaneous Rosai–Dorfman disease: a clinical and histopathologic study of 25 cases in China. Am J Surg Pathol 2007;31:341350.Google Scholar
Bonetti, F, Chilosi, M, Menestrina, F, et al. Immunohistological analysis of Rosai–Dorfman histiocytosis: a disease of S-100 +CD1-histiocytes. Virchows Arch 1987;411:129135.Google Scholar
Miettinen, M, Paljakka, P, Haveri, P, Saxén, E. Sinus histiocytosis with massive lymphadenopathy: a nodal and extranodal proliferation of S-100 protein positive histiocytes. Am J Clin Pathol 1987;88:270277.CrossRefGoogle ScholarPubMed
Eisen, RN, Buckley, PJ, Rosai, J. Immunophenotypic characterization of sinus histiocytosis with massive lymphadenopathy (Rosai–Dorfman disease). Semin Diagn Pathol 1990;7:7482.Google ScholarPubMed
Liu, L, Perry, AM, Cao, W, et al. Relationship between Rosai-Dorfman disease and IgG4-related disease: study of 32 cases. Am J Clin Pathol 2013;140:395402.Google Scholar
Morgan, NV, Morris, MR, Cangul, H, et al. Mutations in SLC29A3, encoding an equilibrative nucleoside transporter ENT3, cause a familial histiocytosis syndrome (Faisalabad histiocytosis) and familial Rosai–Dorfman disease. PLoS Genet 2010;6:e1000833.Google Scholar
Diamond, EL, Dagna, L, Hyman, DM, et al. Consensus guidelines for the diagnosis and clinical management of Erdheim–Chester disease. Blood 2014;124:483492.Google Scholar
Haroche, H, Arnaud, L, Cohen-Aubart, F, et al. Erdheim–Chester disease. Rheum Dis Clin North Am 2013;39:299311.Google Scholar
Munoz, J, Janku, F, Cohen, PR, Kurzrock, R. Erdheim–Chester disease: characteristics and management. Mayo Clin Proc 2014;89:985996.Google Scholar
Veyssier-Belot, C, Cacoub, P, Caparros-Lefebvre, D, et al. Erdheim-Chester disease: clinical and radiologic characteristics of 59 cases. Medicine 1996;75:157169.Google Scholar
Eble, JN, Rosenberg, AE, Young, RH. Retroperitoneal xanthogranuloma in a patient with Erdheim–Chester disease. Am J Surg Pathol 1994;18:843848.Google Scholar
Provenzano, E, Barter, SJ, Wright, PA, et al. Erdheim–Chester disease presenting as bilateral clinically malignant breast masses. Am J Surg Pathol 2010;34:584588.CrossRefGoogle ScholarPubMed
Kenn, W, Eck, M, Allolio, B, et al. Erdheim–Chester disease: evidence for a disease entity different from Langerhans cell histiocytosis? Three cases with a detailed radiological and immunohistochemical analysis. Hum Pathol 2000;31:734739.Google Scholar
Haroche, J, Charlotte, F, Arnaud, L, et al. High prevalence of BRAF V600E mutations in Erdheim–Chester disease but not in other non-Langerhans cell histiocytoses. Blood 2012;120:27002703.Google Scholar
Vencio, EF, Jenkins, RB, Schiller, JL, et al. Clonal cytogenetic abnormalities in Erdheim–Chester disease. Am J Surg Pathol 2007;31:319321.Google Scholar
Chetritt, J, Paradis, V, Dargere, D, et al. Chester-Erdheim disease: a neoplastic disorder. Hum Pathol 1999;30:10931096.Google Scholar
Lieberman, PH, Jones, CR, Steinman, RM, et al. Langerhans cell (eosinophilic) granulomatosis: a clinicopathologic study encompassing 50 years. Am J Surg Pathol 1996;20:519552.Google Scholar
Kapur, P, Erickson, C, Rakheja, D, Carder, KR, Hoang, MP. Congenital self-healing reticulohistiocytosis (Hashimoto-Pritzker disease): ten-year experience at Dallas Children’s Medical Center. J Am Acad Dermatol 2007;56:290294.Google Scholar
O’Malley, DP, Duong, A, Barry, TS, et al. Co-occurrence of Langerhans cell histiocytosis and Rosai–Dorfman disease: possible relationship of two histiocytic disorders in rare cases. Mod Pathol 2010;23:16161623.Google Scholar
Haupt, R, Minkov, M, Astigarraga, I, et al. Langerhans cell histiocytosis (LCH): guidelines for diagnosis, clinical work-up, and treatment for patients till the age of 18 years. Pediatr Blood Cancer 2013;60:175184.Google Scholar
Henck, ME, Simpson, EL, Ochs, RH, Eremus, JL. Extraskeletal soft tissue masses of Langerhans’ cell histiocytosis. Skeletal Radiol 1996;25:409412.Google Scholar
Singhi, AD, Montgomery, EA. Gastrointestinal tract Langerhans cell histiocytosis: a clinicopathologic study of 12 patients. Am J Surg Pathol 2011;35:305310.Google Scholar
Emile, JF, Wechsler, J, Brousse, N, et al. Langerhans’ cell histiocytosis. Definitive diagnosis with the use of monoclonal antibody O10 on routinely paraffin-embedded samples. Am J Surg Pathol 1995;19:636641.Google Scholar
Sholl, LM, Hornick, JL, Pinkus, GS, Padera, RF. Immunohistochemical analysis of langerin in Langerhans’ cell histiocytosis and pulmonary infectious and inflammatory diseases. Am J Surg Pathol 2007;31:947952.Google Scholar
Lau, SK, Chu, PG, Weiss, LM. Immunohistochemical expression of langerin in Langerhans cell histiocytosis and non-Langerhans cell histiocytic disorders. Am J Surg Pathol 2008;32:615619.Google Scholar
Badalian-Very, G, Vergilio, JA, Degar, BA, et al. Recurrent BRAF mutation in Langerhans cell histiocytosis. Blood 2010;116:19191923.Google Scholar
Brown, NA, Furtado, LV, Betz, BL, et al. High prevalence of somatic MAP2K1 mutations in BRAF V600E-negative Langerhans cell histiocytosis. Blood 2014;124:16551658.Google Scholar
Nelson, DS, Quispel, W, Badalian-Very, G, et al. Somatic activating ARAF mutations in Langerhans cell histiocytosis. Blood 2014;123:31523155.Google Scholar
Willman, CL, Busque, L, Griffith, BB, et al. Langerhans’-cell histiocytosis (histiocytosis X): a clonal proliferative disease. N Engl J Med 1994;331(3):154160.Google Scholar
Cohen, BA, Hood, A. Xanthogranuloma: a report on clinical and histologic findings in 64 patients. Pediatr Dermatol 1989;6:262266.Google Scholar
Janney, CG, Hurt, MA, Santa Cruz, DJ. Deep juvenile xanthogranuloma: subcutaneous and intramuscular forms. Am J Surg Pathol 1991;15:150159.Google Scholar
de Graaf, JH, Timens, W, Tamminga, RYJ, Molenaar, WM. Deep juvenile xanthogranuloma: a lesion related to dermal indeterminate cells. Hum Pathol 1992;23:905910.Google Scholar
Zelger, B, Cerio, R, Orchard, G, Wilson-Jones, E. Juvenile and adult xanthogranuloma: a histological and immunohistochemical comparison. Am J Surg Pathol 1994;18:126135.Google Scholar
Janssen, D, Harms, D. Juvenile xanthogranuloma in childhood and adolescence: a clinicopathologic study of 129 patients from the Kiel pediatric tumor registry. Am J Surg Pathol 2005;29:2128.Google Scholar
Dehner, L. Juvenile xanthogranulomas in the first two decades of life: a clinicopathologic study of 174 cases with cutaneous and extracutaneous manifestations. Am J Surg Pathol 2003;27:579593.Google Scholar
Nascimento, AG. A clinicopathologic and immunohistochemical comparative study of cutaneous and intramuscular forms of juvenile xanthogranuloma. Am J Surg Pathol 1997;21:645652.Google Scholar
Zvulunov, A, Barak, Y, Metzker, A. Juvenile xanthogranuloma, neurofibromatosis, and juvenile chronic myelogenous leukemia: world statistical analysis. Arch Dermatol 1995;131(8):904908.Google Scholar
Cambiaghi, S, Restano, L, Caputo, R. Juvenile xanthogranuloma associated with neurofibromatosis. 1: 14 patients without evidence of hematologic malignancies. Pediatr Dermatol 2004;21:97101.Google Scholar
Kraus, MD, Haley, JC, Ruiz, R, et al. “Juvenile” xanthogranuloma: an immunophenotypic study with a reappraisal of its histogenesis. Am J Dermatopathol 2001;23:104111.Google Scholar
Purvis, WE, Helwig, EB. Reticulohistiocytic granuloma (“reticulohistiocytoma”) of the skin. Am J Clin Pathol 1955;24:10051015.Google Scholar
Zelger, B, Cerio, R, Soyer, HP, et al. Reticulohistiocytoma and multicentric reticulohistiocytosis. Am J Surg Pathol 1994;16:577584.Google Scholar
Miettinen, M, Fetsch, JF. Reticulohistiocytoma (solitary epithelioid histiocytoma): a clinicopathologic and immunohistochemical study of 44 cases. Am J Surg Pathol 2006;30:521528.Google Scholar
Barrow, MV, Holubar, K. Multicentric reticulohistiocytosis: a review of 33 patients. Medicine (Baltimore) 1969;48:287305.Google Scholar
Trotta, F, Castellino, G, Lo Monaco, A. Multicentric reticulohistiocytosis. Best Pract Res Clin Rheumatol 2004;18:759772.Google Scholar
Salisbury, JR, Hall, PA, Williams, HC, Mangi, MH, Mufti, GJ. Multicentric reticulohistiocytosis: detailed immunophenotyping confirms macrophage origin. Am J Surg Pathol 1990;14:687693.Google Scholar
Kapadia, SB, Enzinger, FM, Heffner, DK, Hyams, VJ, Frizzera, G. Crystal-storing histiocytosis associated with lymphoplasmacytic neoplasms: report of three cases mimicking adult rhabdomyoma. Am J Surg Pathol 1993;17:461467.Google Scholar
Jones, D, Bhatia, VK, Krausz, T, Pinkus, GS. Crystal-storing histiocytosis: a disorder occurring in plasmacytic tumors expressing immunoglobulin kappa light chain. Hum Pathol 1999;30:14411448.Google Scholar
Friedman, MT, Molho, L, Valderrama, E, et al. Crystal-storing histiocytosis associated with a lymphoplasmacytic neoplasm mimicking adult rhabdomyoma: a case report and review of the literature. Arch Pathol Lab Med 1996;120:11331136.Google Scholar
Wilson, MS, Weiss, LM, Gatter, KC, et al. Malignant histiocytosis: a reassessment of cases previously reported in 1975 based on paraffin section immunophenotyping studies. Cancer 1990;66:530536.Google Scholar
Michgrub, S, Kamel, OW, Wiley, E, et al. Malignant histiocytic neoplasms of the small intestine. Am J Surg Pathol 1992;16:1120.Google Scholar
Miettinen, M, Fletcher, CD, Lasota, J. True histiocytic lymphoma of small intestine: analysis of two S-100 protein positive cases with features of interdigitating reticulum cell sarcoma. Am J Clin Pathol 1993;100:285292.Google Scholar
Soria, C, Orradre, JL, Garcia-Almagro, D, et al. True histiocytic lymphoma (monocytic sarcoma). Am J Dermatopathol 1992;14:511517.Google Scholar
Lauritzen, AF, Delsol, G, Hansen, NE, et al. Histiocytic sarcomas and monoblastic leukemias: a clinical, histologic, and immunophenotypic study. Am J Clin Pathol 1994;102:4554.Google Scholar
Kamel, OW, Gocke, CD, Kell, DL, Cleary, ML, Warnke, RA. True histiocytic lymphoma: a study of 12 cases based on current definition. Leuk Lymphoma 1995;18:8186.Google Scholar
Copie-Bergman, C, Wotherspoon, AC, Norton, AJ, Diss, TC, Isaacson, PG. True histiocytic lymphoma: a morphologic, immunohistochemical, and molecular genetic study of 13 cases. Am J Surg Pathol 1998;22:13861392.Google Scholar
Hornick, JL, Jaffe, ES, Fletcher, CD. Extranodal histiocytic sarcoma: clinicopathologic analysis of 14 cases of a rare epithelioid malignancy. Am J Surg Pathol 2004;28:11331144.Google Scholar
Vos, JA, Abbondanzo, SL, Barekman, CL, et al. Histiocytic sarcoma: a study of five cases including the histiocytic marker CD163. Mod Pathol 2005;18:693704.Google Scholar
Wang, E, Papalas, J, Hutchinson, CB, et al. Sequential development of histiocytic sarcoma and diffuse large B-cell lymphoma in a patient with a remote history of follicular lymphoma with genotypic evidence of a clonal relationship: a divergent (bilineal) neoplastic transformation of an indolent B-cell lymphoma in a single individual. Am J Surg Pathol 2011;35:457463.Google Scholar
Feldman, AL, Arber, DA, Pittaluga, S, et al. Clonally related follicular lymphomas and histiocytic/dendritic cell sarcomas: evidence for transdifferentiation of the follicular lymphoma clone. Blood 2008;111:54335439.Google Scholar
Takahashi, E, Nakamura, S. Histiocytic sarcoma: an updated literature review based on the 2008 WHO classification. J Clin Exp Hematop 2013;53:18.Google Scholar
Venkataraman, G, McClain, KL, Pittaluga, S, Rao, VK, Jaffe, ES. Development of disseminated histiocytic sarcoma in a patient with autoimmune lymphoproliferative syndrome and associated Rosai-Dorfman disease. Am J Surg Pathol 2010;34:589594.Google Scholar
Monda, L, Warnke, R, Rosai, J. A primary lymph node malignancy with features suggestive of dendritic reticulum cell differentiation: a report of 4 cases. Am J Pathol 1986;122:562572.Google Scholar
Chan, JKC, Fletcher, CDM, Nayler, SJ, Cooper, K. Follicular dendritic cell sarcoma: clinicopathologic analysis of 17 cases suggesting a malignant potential higher than currently recognized. Cancer 1997;79:294313.Google Scholar
Chan, JK. Proliferative lesions of follicular dendritic reticulum cells: an overview including a detailed account of follicular dendritic reticulum cell sarcoma, and neoplasm with many faces and uncommon etiologic associations. Adv Anat Pathol 1997;4:387411.Google Scholar
Perez-Ordonez, B, Erlandson, RA, Rosai, J. Follicular dendritic reticulum cell tumor: report of 13 additional cases of a distinctive entity. Am J Surg Pathol 1996;20:944955.Google Scholar
Kairouz, S, Hashash, J, Kabbara, W, McHayleh, W, Tabbara, IA. Dendritic cell neoplasms: an overview. Am J Hematol 2007;82:924928.Google Scholar
Fonseca, R, Yamakawa, M, Nakamura, S, et al. Follicular dendritic reticulum cell sarcoma and interdigitating reticulum cell sarcoma: a review. Am J Hematol 1998;59:161167.Google Scholar
Biddle, DA, Ro, JY, Yonn, GS, et al. Extranodal follicular dendritic cell sarcoma of the head and neck region: three new cases, with a review of the literature. Mod Pathol 2002;15:5058.Google Scholar
Grogg, KL, Lae, ME, Kurtin, PJ, Macon, WR. Clusterin expression distinguishes follicular dendritic cell tumors from other dendritic cell neoplasms: report of a novel follicular dendritic cell marker and clinicopathologic data on 12 additional follicular dendritic cell tumors and 6 additional interdigitating dendritic cell tumors. Am J Surg Pathol 2004;28:988998.Google Scholar
Yu, H, Gibson, JA, Pinkus, GS, Hornick, JL. Podoplanin (D2–40) is a novel marker for follicular dendritic cell tumors. Am J Clin Pathol 2007;128:776782.Google Scholar
Yu, H, Gibson, JA, Pinkus, GS, Hornick, JL. Podoplanin (D2–40) is a novel marker for follicular dendritic cell tumors. Am J Clin Pathol 2007;128:776782.Google Scholar
Weiss, L, Berry, G, Dorfman, RF, et al. Spindle cell neoplasms of lymph nodes of probably reticulum cell lineage: true reticulum cell sarcoma? Am J Surg Pathol 1990;14:405414.Google Scholar
Gaertner, EM, Tsokos, M, Derringer, GA, et al. Interdigitating dendritic cell sarcoma: a report of four cases and review of the literature. Am J Clin Pathol 2001;115:589597.Google Scholar
Andriko, JW, Kaldjian, EP, Tsokos, M, Abbondanzo, SL, Jaffe, ES. Reticulum cell neoplasms of lymph nodes: a clinicopathologic study of 11 cases with recognition of a new subtype derived from fibroblastic reticular cells. Am J Surg Pathol 1998;22:10481058.Google Scholar
Gould, VE, Warren, WH, Faber, LP, Kuhn, C, Franke, WW. Malignant cells of epithelial phenotype limited to thoracic lymph nodes. Eur J Cancer 1990;26:11211126.Google Scholar
Franke, WW, Moll, R. Cytoskeletal components of lymphoid organs. I. Synthesis of cytokeratins 8 and 18 and desmin in subpopulations of extrafollicular reticulum cells of human lymph nodes, tonsils, and spleen. Differentiation 1987;36:145163.Google Scholar

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