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Chapter 9 - Non-Neoplastic Diseases of Salivary Glands

Published online by Cambridge University Press:  26 June 2017

Robert O. Greer ,
Robert E. Marx ,
Sherif Said  and
Lori D. Prok
By
Sherif Said ,
Robert O. Greer  and
Robert E. Marx
Robert O. Greer
Affiliation:
University of Colorado, Denver
Robert E. Marx
Affiliation:
University of Miami
Sherif Said
Affiliation:
University of Colorado, Denver
Lori D. Prok
Affiliation:
University of Colorado, Denver
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Pediatric Head and Neck Pathology , pp. 225 - 245
Publisher: Cambridge University Press
Print publication year: 2016

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Reuter, J, Hausamen, JE. Sialolithiasis der glandula submandibularis im kindesalter. Klin Padiatr 1976; 188: 285–288.Google Scholar
Zenk, J, Constantinidis, J, Kydles, S, et al. Klinische und diagnostische befund bei der sialolthiasis. HNO 1999; 47: 963–969.Google Scholar
Blatt, I. Chronic and recurrent inflammations about the salivary glands with reference to children. Laryngoscope 1966; 76: 917–921.Google Scholar
Nahlieli, O, Shacham, R, Shlesinger, M, Eliav, E. Juvenile recurrent parotitis: a new method of diagnosis and treatment. Pediatrics 2004; 114: 9–12.Google Scholar
Galili, D, Mammary, Y. Juvenile recurrent parotitis: clinicoradiological follow up study and the beneficial effect of sialography. Oral Surg Oral Med Oral Pathol 1986; 61: 550–556.Google Scholar
Seifert, G. Aetiological and histological classification of Sialadenitis. Pathologica 1997; 89(1): 7–17.Google Scholar
Roby, BB, Mattingly, J, Jensen, EL, et al. Treatment of juvenile recurrent parotitis of childhood: an analysis of effectiveness. JAMA Otolaryngol Head and Neck Surg, 2015; 141: 126–129.Google Scholar
Harrison, JD. Histology and pathology of sialolithiasis. In: Witt, RL, ed. Salivary Gland Diseases: Surgical and Medical Management. New York: Thieme Medical Publishers, Inc., 2005: 71–78.Google Scholar
Bodner, L, Azaz, B: Submandibular sialolithiasis in children. J Oral Maxillofac Surg 1982; 40: 551–554.Google Scholar
Marchal, F, Dulguerov, P. Sialolithiasis management: the state of the art. Arch Otolaryngol Head Neck Surg 2003; 129(9): 951–956.Google Scholar
Iro, H, Dlugaiczyk, J, Zenk, J. Current concepts in the diagnosis and treatment of sialolithiasis. Br J Hosp Med (Lond) 2006; 67(1): 24–28.Google Scholar
Reimers, M, Varvina, J, Schlegel, C. Results after shock wave lithotripsy for salivary gland stones. Schweiz Med Wochenschr 2000; suppl 125: 12s–126s.Google Scholar
Iro, H, Zen, KJ. Salivary gland diseases in children. GMS Current Top Otorhinolaryngol Head and Neck Surg 2014 December; 13: 1–30.Google Scholar
Küttner, H. Uber entzundliche tumeron der submaxillar-speicheldruse. Burns Beitr Klin Chir 1896; 15: 815–828.Google Scholar
Kitagawa, S, Zen, Y, Harada, K, et al. Abundant IgG4 positive plasma cell infiltration characterizes chronic sialadenitis (Kuttner tumor). Am J Surg Pathol 2005; 29: 783–791.Google Scholar
Kamisawa, T, Nakajima, H, Egawa, N, et al. IgG-related sclerosing disease incorporating sclerosing pancreatitis, cholangitis, sialadenitis and retroperitoneal fibrosis with lymphadenopathy. Pancreatology 2006; 6: 132–137.Google Scholar
Shin, Y, Oh, Y, and Lee, Y. Unusual involvement of IgG-4 related sclerosing disease in lacrimal and submandibular glands and extraocular muscles. Korean J Ophthalmol 2012; 26: 216–221.Google Scholar
Blanco, M, Mesko, T, Cura, M, et al. Chronic sclerosing sialadenitis (Kuttner tumor): unusual presentation with bilateral involvement of the major and minor salivary glands. Ann Diagn Pathol 2003; 7: 25–30.Google Scholar
Melo, JC, Kitsko, D, Reyes-Mugaica, M. Pediatric chronic sclerosing sialadenitis: Kuttner tumor. Pediatr Dev Pathol 2012 Mar–Apr; 15: 165–169.Google Scholar
Seifert, G, Donath, K. On the pathogenesis of the Kuttner tumor of the submandibular gland: analysis of 349 cases with chronic sialadenitis of the submandibular gland HNO 1977; 25: 81–92.Google Scholar
Kojima, M, Nakamura, S, Itoh, H, et al. Kuttner tumor of the salivary glands resembling marginal zone B-cell lymphoma of the MALT type: a histopathologic and immunohistochemical study of 7 cases. Int J Surg Pathol 2004; 12: 389–393.Google Scholar
Kojima, M, Nakamura, S, Itoh, H. Sclerosing variant of follicular lymphoma arising from the submandibular glands and resembling Kuttner tumor: a report of 3 patients. Int J Surg Pathol 2003; 11: 303–307.Google Scholar
Ochoa, ER, Harris, NL, Pilch, BZ. Marginal B-cell lymphoma of the salivary glands arising in chronic sclerosing sialadenitis (Kuttner tumor). Am J Surg Pathol 2001; 25: 1546–1550.Google Scholar
Culver, EL, Hunt, A, Crewe, E, et al. Immunoglobulin G4 related chronic sclerosing sialadenitis. J Laryngolotol 2015; 129: 226–231.Google Scholar
McQuone, SJ. Acute viral and bacterial infections of the salivary glands. Otolaryngol Clin North Am 1999; 32: 793–811.Google Scholar
Mehta, D, Willging, JP. Pediatric salivary gland lesions. Semin Ped Surg 2006 May; 15: 76–84.Google Scholar
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Basis, K, Toib, D, Cooper, M, et al. Recurrent parotitis as a presentation of primary pediatric Sjögren syndrome. Pediatrics 2012; 129: e179–e182.Google Scholar
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McQuone, SJ. Acute viral and bacterial infections of the salivary glands. Otolaryngol Clin North Am 1999; 32: 793–811.Google Scholar
Mehta, D, Willging, JP. Pediatric salivary gland lesions. Semin Ped Surg 2006 May; 15: 76–84.Google Scholar
Hviid, A, Rubin, S, Muhlemann, K. Mumps. Lancet 2008; 371: 931–944.Google Scholar
Morimoto, T. Otolaryngolological infections in children and vaccines. Nihon Jibiinkoka Gakkai Kaiho 2012 Mar; 115: 206–208.Google Scholar
Hendriksz, T, Malouf, P, Foy, JE; Vaccines for measles, mumps, rubella, varicella, and herpes zoster: immunization guidelines for adults. J Am Osteopath Assoc 2011; 111(10 Suppl 6): S10–12.Google Scholar
Xiao, H, Wei, Y, Tan, M, et al. Epidemic parotitis being accompanied by acute pancreatitis and sensorineural hearing loss: case report and literature review. Lin Chung Er Bi Yan Hou Tou Jing Wai Ke Za Zhi 2007; 21: 548–549.Google Scholar
Ayadi, L, Khabir, A, Boudawara, T, et al. Cellular hemangioma of the parotid gland associated with an infection by cytomegalovirus. Rev Stomatol Chir Maxillofac 2003; 104: 290–293.Google Scholar
Yoshida, M, Ueda, S, Harano, H, et al. Chronic myelocytic leukemia associated with cytomegalovirus induced sialoadenitis after unrelated allogeneic bone marrow transplantation]. Rinsho Ketsueki 1996; 37: 46–52.Google Scholar
Boppana, SB, Ross, SA, Novak, Z, et al. Dried blood spot real-time polymerase chain reaction assays to screen newborns for congenital cytomegalovirus infection. JAMA 2010; 303: 1375–1382.Google Scholar
Variend, S, O’Neill, D, Arnold, P. The possible significance of cytomegaloviral parotitis in infant and early childhood deaths. Arch Pathol Lab Med 1997; 121: 1272–1276.Google Scholar
Melnick, M, Sedghizadeh, PP, Allen, CM, Jaskoll, T. Human cytomegalovirus and mucoepidermoid carcinoma of salivary glands: cell-specific localization of active viral and oncogenic signaling proteins is confirmatory of a causal relationship. Exp Mol Pathol 2012; 92: 118–125.Google Scholar
Dave, S, Pernas, F, Roy, S. The benign lymphoepithelial cyst and a classification system for lymphocytic parotid gland enlargement in pediatric HIV population. Laryngoscope 2007; 117: 106–113.Google Scholar
Morris, MR, Moore, DW, Shearer, GL. Bilateral multiple benign lymphoepithelial cysts of the parotid gland. Otolaryngol Head Neck Surg 1987; 97: 87–90.Google Scholar
Morales-Aguirre, JJ, Patino-nino, AP, Mendoza-Azpiri, M, et al. Parotid cysts in children infected with human immunodeficiency virus. Arch Otolaryngol Head Neck Surg 2005; 131: 353–355.Google Scholar
Shugar, JM, Som, PM, Jacobson, Al, et al. Multicentric parotid cysts and cervical adenopathy in AIDS patients. A newly recognized entity: CT and MR manifestations. Laryngoscope 1988; 98: 772–775.Google Scholar
Echavez, MI, Lee, KC, Sooy, CD. Tetracycline sclerosis for Treatment of benign lymphoepithelial cyst of the parotid gland in patients infected with human immunodefiency virus. Laryngoscope 1994; 104: 1499–1502.Google Scholar
Lustig, LR, Lee, KC, Murr, A, et al. Doxycycline sclerosis of benign lymphoepithelial cysts in patients infected with HIV. Laryngoscope 1988; 108: 1199–1205.Google Scholar
Abrams, AM, Melrose, RJ, Howell, FV. Necrotizing sialometaplasia. A disease simulating malignancy. Cancer 1973; 32: 130–135.Google Scholar
Penner, CR, Thompson, LD. Necrotizing sialometaplasia. Ear Nose Throat J 2003; 82: 483–494.Google Scholar
Brannon, RB, Fowler, CB, Hartman, KS. Necrotizing sialometaplasia. A clinicopathologic study of sixty nine cases and review of the literature. Oral Surg Oral Med Oral Pathol 1991; 72: 317–325.Google Scholar
Ylikontiola, L, Siponen, M, Sandor, G. Sialometaplasia of the soft palate in a 2 year old girl. JCDA May 2007; 73: 333–336.Google Scholar
Sandmeier, D, Bouzourene, H. Necrotizing sialometaplasia: a potential diagnostic pitfall. Histopathology 2002; 40: 200–201.Google Scholar
Imbrey, TA, Edwards, PA. Necrotizing sialometaplasia: literature review and case reports. J Am Dent Assoc 1996; 127: 1087–1092.Google Scholar
Rizkalla, H, Toner, M. Necrotizing sialometaplasia versus invasive carcinoma of the head and neck: the use of myoepithelial markers and keratin subtype as an adjunct to diagnosis. Histopathology 2007; 51: 184–189.Google Scholar
Werning, J, Waterhouse, J, Mooney, J. Subacute necrotizing sialadenitis. Oral Surg Oral Med Oral Pathol 1990; 70: 756–759.Google Scholar
Suresh, L, Aguire, A. Subacute necrotizing sialadenitis: a clinicopathologic study. Oral Med Oral Pathol Oral radiol Endod 2007; 104: 385–390.Google Scholar
Fowler, C, Brannon, R. Subacute necrotizing sialadenitis: report of 7 cases and a review of the literature. Oral Med Oral Pathol Oral Radiol Endod 2000; 89: 600–609.Google Scholar
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Andrade, E, Sorbal, A, Santos, M, Camarago, I. Cheilitis glandularis and actinic cheilitis: differential diagnosis – report of three unusual cases. Dermatology Online Journal 2009; 15: 5.Google Scholar
Yacobi, R, Brown, DA. Cheilitis glandularis: a pediatric case report. J Am Dent Assoc 1989; 118: 317–318.Google Scholar
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Leao, JC, Ferriera, AMC, Martins, S, et al. Cheilitis glandularis: an unusual presentation in patient with HIV infection. Oral Med Oral Pathol Oral Radiol Endod 2003; 95: 142–144.Google Scholar
Winchester, L, Scully, C, Prime, SS, et al. Cheilitis glandularis. Oral Surg Oral Med Oral Pathol 1986; 62: 654–656.Google Scholar
Carrington, PR, Horn, TD. Cheilitis glandularis: a clinical marker for both malignancy and /or severe inflammatory disease of the oral cavity. J Am Acad Dermatol 2006; 54: 336–337.Google Scholar
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Bansal, M, Mohanti, BK, Shah, N, et al. Head and neck cancer. Radiation related morbidities and their impact on quality of life in head and neck cancer patients receiving radical radiotherapy. Qual Life Res 2004; 13: 481–488.Google Scholar
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Mikulicz, J. Uber ein eigenartige symmetrische erkrankung der trannen – und mundspeicheldrusen. Beitr Z Chir Festschr Theodore Billroth 1982; 2: 610–630.Google Scholar
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Sjögren, H. Zur kennetnis der keratoconjunctivitis sicca (Keratitis filiformis bei hypofunction trannendrussen). Acta Ophthalmol (suppl) 1933; 2: 1–151.Google Scholar
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Bartunkova, J, Sediva, A, Vencovsky, J, Tesar, V. Primary Sjögren syndrome in children and adolescents: proposal for diagnostic criteria. Clin Exp Rheumatol 1999; 17: 381–386.Google Scholar
Singer, NG, Tomanova-Soltys, I, Lowe, R. Sjögren syndrome in childhood. Curr Rheumatol Rep 2008; 10: 147–155.Google Scholar
Basis, K, Toib, D, Cooper, M, et al. Recurrent parotitis as a presentation of primary pediatric Sjögren syndrome. Pediatrics 2012; 129: e179–e182.Google Scholar
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