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Published in: Head and Neck Pathology 1/2017

01-03-2017 | Original Paper

Update from the 4th Edition of the World Health Organization of Head and Neck Tumours: Tumours of the Oral Cavity and Mobile Tongue

Author: Susan Müller

Published in: Head and Neck Pathology | Issue 1/2017

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Abstract

There have been several additions and deletions in Chapter 4 on Tumours of the oral cavity and mobile tongue in the 2017 fourth edition of the World Health Organization Classification of Tumours of the Head and Neck. This chapter excludes the oropharynx, which now is a stand-alone chapter acknowledging the uniqueness of the oropharynx from the oral cavity. New entries in Chapter 4 include rhabdomyoma, haemangioma, schwannoma, neurofibroma and myofibroblastic sarcoma in the section titled Soft tissue and neural tumours. Discussion of salivary gland entities have been reduced and includes mucoepidermoid carcinoma and pleomorphic adenoma as the other salivary gland types are discussed elsewhere. In the Haematolymphoid tumours section, like the salivary gland section, only tumors that commonly present in the oral cavity are discussed in Chapter 4. Excluded entities in the updated classification include papillary hyperplasia, median rhomboid glossitis, keratoacanthoma, focal oral mucinosis, and secondary tumors. This article will summarize the changes in the new classification since the 2005 edition focusing on selected entities that have had significant changes along with new entries.
Literature
1.
go back to reference Tumours of the oral cavity and mobile tongue. In: el-Naggar AK, Chan JKC, Grandis JR, Takata T, Slootweg PJ, editors, WHO classification of tumours of the head and neck. 4th ed. Lyon: IARC Press; 2017. Tumours of the oral cavity and mobile tongue. In: el-Naggar AK, Chan JKC, Grandis JR, Takata T, Slootweg PJ, editors, WHO classification of tumours of the head and neck. 4th ed. Lyon: IARC Press; 2017.
2.
go back to reference Sloan P, Gale N, Hunter K, et al. Malignant surface epithelial tumours: Squamous cell carcinoma. In: el-Naggar AK, Chan JKC, Grandis JR, Takata T, Slootweg PJ, editors. WHO classification of tumours of the head and neck. 4th ed. Lyon: IARC Press, 2017. Sloan P, Gale N, Hunter K, et al. Malignant surface epithelial tumours: Squamous cell carcinoma. In: el-Naggar AK, Chan JKC, Grandis JR, Takata T, Slootweg PJ, editors. WHO classification of tumours of the head and neck. 4th ed. Lyon: IARC Press, 2017.
3.
go back to reference Dahlgren L, Dahlstrand HM, Lindquist D, et al. Human papillomavirus is more common in base of tongue than in mobile tongue cancer and is a favorable prognostic factor in base of tongue cancer patients. Int J Cancer. 2004;112:1015–9.CrossRefPubMed Dahlgren L, Dahlstrand HM, Lindquist D, et al. Human papillomavirus is more common in base of tongue than in mobile tongue cancer and is a favorable prognostic factor in base of tongue cancer patients. Int J Cancer. 2004;112:1015–9.CrossRefPubMed
4.
go back to reference Gillison ML, Chaturvedi AK, Anderson WF, Fakhry C. Epidemiology of human papillomavirus-positive head and neck squamous cell carcinoma. J Clin Oncol. 2015;33:3235–42.CrossRefPubMedPubMedCentral Gillison ML, Chaturvedi AK, Anderson WF, Fakhry C. Epidemiology of human papillomavirus-positive head and neck squamous cell carcinoma. J Clin Oncol. 2015;33:3235–42.CrossRefPubMedPubMedCentral
5.
go back to reference Lingen MW, Xiao W, Schmitt A, et al. Low etiologic fraction for high-risk human papillomavirus in oral cavity squamous cell carcinomas. Oral Oncol. 2013;49:1–8.CrossRefPubMed Lingen MW, Xiao W, Schmitt A, et al. Low etiologic fraction for high-risk human papillomavirus in oral cavity squamous cell carcinomas. Oral Oncol. 2013;49:1–8.CrossRefPubMed
6.
go back to reference Sgaramella N, Coates PJ, Strindlund K, et al. Expression of p16 in squamous cell carcinoma of the mobile tongue is independent of HPV infection despite presence of the HPV-receptor syndecan-1. Br J Cancer. 2015;113:321–6.CrossRefPubMedPubMedCentral Sgaramella N, Coates PJ, Strindlund K, et al. Expression of p16 in squamous cell carcinoma of the mobile tongue is independent of HPV infection despite presence of the HPV-receptor syndecan-1. Br J Cancer. 2015;113:321–6.CrossRefPubMedPubMedCentral
7.
go back to reference Zafereo ME, Xu L, Dahlstrom KR, Viamonte CA, et al. Squamous cell carcinoma of the oral cavity often overexpresses p16 but is rarely driven by human papillomavirus. Oral Oncol. 2016;56:47–53.CrossRefPubMed Zafereo ME, Xu L, Dahlstrom KR, Viamonte CA, et al. Squamous cell carcinoma of the oral cavity often overexpresses p16 but is rarely driven by human papillomavirus. Oral Oncol. 2016;56:47–53.CrossRefPubMed
8.
go back to reference Reuschenbach M, Kansy K, Garbe K, et al. Lack of evidence of human papillomavirus-induced squamous cell carcinomas of the oral cavity in southern Germany. Oral Oncol. 2013;49(9):937–42.CrossRefPubMed Reuschenbach M, Kansy K, Garbe K, et al. Lack of evidence of human papillomavirus-induced squamous cell carcinomas of the oral cavity in southern Germany. Oral Oncol. 2013;49(9):937–42.CrossRefPubMed
9.
go back to reference Bagnardi V, Rota M, Botteri E, et al. Alcohol consumption and site-specific cancer risk: a comprehensive dose-response meta-analysis. Br J Cancer. 2015;112:580–93.CrossRefPubMed Bagnardi V, Rota M, Botteri E, et al. Alcohol consumption and site-specific cancer risk: a comprehensive dose-response meta-analysis. Br J Cancer. 2015;112:580–93.CrossRefPubMed
10.
go back to reference Goldstein BY, Chang SC, Hashibe M, et al. Alcohol consumption and cancers of the oral cavity and pharynx from 1988 to 2009: an update. Eur J Cancer Prev. 2010;19:431–65.CrossRefPubMedPubMedCentral Goldstein BY, Chang SC, Hashibe M, et al. Alcohol consumption and cancers of the oral cavity and pharynx from 1988 to 2009: an update. Eur J Cancer Prev. 2010;19:431–65.CrossRefPubMedPubMedCentral
11.
go back to reference IARC. (2010). Alcohol consumption and ethyl carbamate. IARC Monogr Eval Carcinog Risks Hum. 96:1–1428. IARC. (2010). Alcohol consumption and ethyl carbamate. IARC Monogr Eval Carcinog Risks Hum. 96:1–1428.
12.
go back to reference Llewellyn CD, Johnson NW, Warnakulasuriya KA. Risk factors for squamous cell carcinoma of the oral cavity in young people–a comprehensive literature review. Oral Oncol. 2001;37:401–18.CrossRefPubMed Llewellyn CD, Johnson NW, Warnakulasuriya KA. Risk factors for squamous cell carcinoma of the oral cavity in young people–a comprehensive literature review. Oral Oncol. 2001;37:401–18.CrossRefPubMed
13.
go back to reference Shiboski CH, Schmidt BL, Jordan RC. Tongue and tonsil carcinoma: increasing trends in the U.S. population ages 20–44 years. Cancer. 2005;103:1843–9.CrossRefPubMed Shiboski CH, Schmidt BL, Jordan RC. Tongue and tonsil carcinoma: increasing trends in the U.S. population ages 20–44 years. Cancer. 2005;103:1843–9.CrossRefPubMed
14.
15.
go back to reference Fritsch VA, Gerry DR, Lentsch EJ. Basaloid squamous cell carcinoma of the oral cavity: an analysis of 92 cases. Laryngoscope. 2014;124:1573–8.CrossRefPubMed Fritsch VA, Gerry DR, Lentsch EJ. Basaloid squamous cell carcinoma of the oral cavity: an analysis of 92 cases. Laryngoscope. 2014;124:1573–8.CrossRefPubMed
16.
go back to reference Bice TC, Tran V, Merkley MA, et al. Disease-Specific survival with spindle cell carcinoma of the head and neck. Otolaryngol Head Neck Surg. 2015;153:973–80.CrossRefPubMed Bice TC, Tran V, Merkley MA, et al. Disease-Specific survival with spindle cell carcinoma of the head and neck. Otolaryngol Head Neck Surg. 2015;153:973–80.CrossRefPubMed
17.
go back to reference Kass JI, Lee SC, Abberbock S, et al. Adenosquamous carcinoma of the head and neck: Molecular analysis using CRTC-MAML FISH and survival comparison with paired conventional squamous cell carcinoma. Laryngoscope. 2015;125:E371–E6.CrossRefPubMed Kass JI, Lee SC, Abberbock S, et al. Adenosquamous carcinoma of the head and neck: Molecular analysis using CRTC-MAML FISH and survival comparison with paired conventional squamous cell carcinoma. Laryngoscope. 2015;125:E371–E6.CrossRefPubMed
18.
go back to reference Sun Y, Kuyama K, Burkhardt A, Yamamoto H. Clinicopathological evaluation of carcinoma cuniculatum: a variant of oral squamous cell carcinoma. J Oral Pathol Med. 2012;41:303–8.CrossRefPubMed Sun Y, Kuyama K, Burkhardt A, Yamamoto H. Clinicopathological evaluation of carcinoma cuniculatum: a variant of oral squamous cell carcinoma. J Oral Pathol Med. 2012;41:303–8.CrossRefPubMed
19.
go back to reference Mallick S, Breta M, Gupta SD, et al. Angiogenesis, proliferative activity and DNA ploidy in oral verrucous carcinoma: a comparative study including verrucous hyperplasia and squamous cell carcinoma. Pathol Oncol Res. 2015;21:1249–57.CrossRefPubMed Mallick S, Breta M, Gupta SD, et al. Angiogenesis, proliferative activity and DNA ploidy in oral verrucous carcinoma: a comparative study including verrucous hyperplasia and squamous cell carcinoma. Pathol Oncol Res. 2015;21:1249–57.CrossRefPubMed
20.
go back to reference Samman M, Wood HM, Conway C, et al. A novel genomic signature reclassifies an oral cancer subtype. Int J Cancer. 2015;137:2364–73.CrossRefPubMed Samman M, Wood HM, Conway C, et al. A novel genomic signature reclassifies an oral cancer subtype. Int J Cancer. 2015;137:2364–73.CrossRefPubMed
21.
go back to reference Garcia C, Crowson AN. Acantholytic squamous cell carcinoma: is it really a more aggressive tumor? Dermatol Surg. 2011;37:353–6.CrossRefPubMed Garcia C, Crowson AN. Acantholytic squamous cell carcinoma: is it really a more aggressive tumor? Dermatol Surg. 2011;37:353–6.CrossRefPubMed
22.
go back to reference Rytkönen AE, Hirvikoski PP, Salo TA. Lymphoepithelial carcinoma: two case reports and a systematic review of oral and sinonasal cases. Head Neck Pathol. 2011;5:327–34.CrossRefPubMedPubMedCentral Rytkönen AE, Hirvikoski PP, Salo TA. Lymphoepithelial carcinoma: two case reports and a systematic review of oral and sinonasal cases. Head Neck Pathol. 2011;5:327–34.CrossRefPubMedPubMedCentral
23.
go back to reference Brandwein-Gensler M, Teixeira MS, Lewis CM, et al. Oral squamous cell carcinoma: histologic risk assessment, but not margin status, is strongly predictive of local disease-free and overall survival. Am J Surg Pathol. 2005;29:167–78.CrossRefPubMed Brandwein-Gensler M, Teixeira MS, Lewis CM, et al. Oral squamous cell carcinoma: histologic risk assessment, but not margin status, is strongly predictive of local disease-free and overall survival. Am J Surg Pathol. 2005;29:167–78.CrossRefPubMed
24.
go back to reference Li Y, Bai S, Carroll W, Dayan D, et al. Validation of the risk model: high-risk classification and tumor pattern of invasion predict outcome for patients with low-stage oral cavity squamous cell carcinoma. Head Neck Pathol. 2013;7:211–23.CrossRefPubMed Li Y, Bai S, Carroll W, Dayan D, et al. Validation of the risk model: high-risk classification and tumor pattern of invasion predict outcome for patients with low-stage oral cavity squamous cell carcinoma. Head Neck Pathol. 2013;7:211–23.CrossRefPubMed
25.
go back to reference Woolgar JA. Histopathological prognosticators in oral and oropharyngeal squamous cell carcinoma. Oral Oncol. 2006;42:229–39. Woolgar JA. Histopathological prognosticators in oral and oropharyngeal squamous cell carcinoma. Oral Oncol. 2006;42:229–39.
26.
go back to reference Woolgar JA, Triantafyllou A. Squamous cell carcinoma and precursor lesions: clinical pathology. Periodontol 2000. 2011;57:51–72.CrossRef Woolgar JA, Triantafyllou A. Squamous cell carcinoma and precursor lesions: clinical pathology. Periodontol 2000. 2011;57:51–72.CrossRef
27.
go back to reference Almangush A, Bello IO, Coletta RD, et al. For early-stage oral tongue cancer, depth of invasion and worst pattern of invasion are the strongest pathological predictors for locoregional recurrence and mortality. Virchows Arch. 2015;467:39–46.CrossRefPubMed Almangush A, Bello IO, Coletta RD, et al. For early-stage oral tongue cancer, depth of invasion and worst pattern of invasion are the strongest pathological predictors for locoregional recurrence and mortality. Virchows Arch. 2015;467:39–46.CrossRefPubMed
28.
go back to reference Ridge JA, Lydiatt WM, Patel SG, et al. Head and Neck In: Amin MB, Edge S, Greene FL, Byrd DR, Brookland RK, Washington MK, Gershenwald JE, Compton CC, Hess KR, Sullivan DC, Jessup JM, Brierley JD, Gaspar LE, Schilsky RL, Balch CM, Winchester DP, Asare EA, Madera M, Gress DM, Meyer LR, editors. AJCC cancer staging manual. 8th ed. New York: Springer; 2017:79–94.CrossRef Ridge JA, Lydiatt WM, Patel SG, et al. Head and Neck In: Amin MB, Edge S, Greene FL, Byrd DR, Brookland RK, Washington MK, Gershenwald JE, Compton CC, Hess KR, Sullivan DC, Jessup JM, Brierley JD, Gaspar LE, Schilsky RL, Balch CM, Winchester DP, Asare EA, Madera M, Gress DM, Meyer LR, editors. AJCC cancer staging manual. 8th ed. New York: Springer; 2017:79–94.CrossRef
29.
go back to reference Reibel J, Gale N, Hille J, et al. Oral potentially malignant disorders and oral epithelial dysplasia. In: el-Naggar AK, Chan JKC, Grandis JR, Takata T, Slootweg PJ, editors, WHO classification of tumours of the head and neck. 4th ed. Lyon: IARC Press; 2017. Reibel J, Gale N, Hille J, et al. Oral potentially malignant disorders and oral epithelial dysplasia. In: el-Naggar AK, Chan JKC, Grandis JR, Takata T, Slootweg PJ, editors, WHO classification of tumours of the head and neck. 4th ed. Lyon: IARC Press; 2017.
30.
go back to reference Kuribayashi Y, Tsushima F, Morita K, et al. Long-term outcome of non-surgical treatment in patients with oral leukoplakia. Oral Oncol. 2015;51:1020–5.CrossRefPubMed Kuribayashi Y, Tsushima F, Morita K, et al. Long-term outcome of non-surgical treatment in patients with oral leukoplakia. Oral Oncol. 2015;51:1020–5.CrossRefPubMed
31.
go back to reference Petti S. Pooled estimate of world leukoplakia prevalence: a systematic review. Oral Oncol. 2003;39:770–80.CrossRefPubMed Petti S. Pooled estimate of world leukoplakia prevalence: a systematic review. Oral Oncol. 2003;39:770–80.CrossRefPubMed
32.
go back to reference Gale N, Blagus R, El-Mofty SK, et al. Evaluation of a new grading system for laryngeal squamous intraepithelial lesions—a proposed unified classification. Histopathology. 2014;65:456–64.CrossRefPubMed Gale N, Blagus R, El-Mofty SK, et al. Evaluation of a new grading system for laryngeal squamous intraepithelial lesions—a proposed unified classification. Histopathology. 2014;65:456–64.CrossRefPubMed
33.
go back to reference Woo SB, Cashman EC, Lerman MA. Human papillomavirus-associated oral intraepithelial neoplasia. Mod Pathol. 2013;26:1288–97.CrossRefPubMed Woo SB, Cashman EC, Lerman MA. Human papillomavirus-associated oral intraepithelial neoplasia. Mod Pathol. 2013;26:1288–97.CrossRefPubMed
34.
go back to reference Vigneswaran N, Carlos R, Lippman S, et al. Multifocal epithelial hyperplasia. In: el-Naggar AK, Chan JKC, Grandis JR, Takata T, Slootweg PJ, edotors. WHO classification of tumours of the head and neck. 4th ed. Lyon: IARC Press; 2017. Vigneswaran N, Carlos R, Lippman S, et al. Multifocal epithelial hyperplasia. In: el-Naggar AK, Chan JKC, Grandis JR, Takata T, Slootweg PJ, edotors. WHO classification of tumours of the head and neck. 4th ed. Lyon: IARC Press; 2017.
35.
go back to reference Carlos R, Sedano HO. Multifocal papilloma virus epithelial hyperplasia. Oral Surg Oral Med Oral Pathol. 1994;77:631–5.CrossRefPubMed Carlos R, Sedano HO. Multifocal papilloma virus epithelial hyperplasia. Oral Surg Oral Med Oral Pathol. 1994;77:631–5.CrossRefPubMed
36.
go back to reference King MD, Reznik DA, O’Daniels CM, et al. Human papillomavirus-associated oral warts among human immunodeficiency virus-seropositive patients in the era of highly active antiretroviral therapy: an emerging infection. Clin Infect Dis. 2002;34:641–8.CrossRefPubMed King MD, Reznik DA, O’Daniels CM, et al. Human papillomavirus-associated oral warts among human immunodeficiency virus-seropositive patients in the era of highly active antiretroviral therapy: an emerging infection. Clin Infect Dis. 2002;34:641–8.CrossRefPubMed
37.
go back to reference Said AK, Leao JC, Fedele S, Porter SR. Focal epithelial hyperplasia—an update. J Oral Pathol Med. 2013;42:435–42.CrossRefPubMed Said AK, Leao JC, Fedele S, Porter SR. Focal epithelial hyperplasia—an update. J Oral Pathol Med. 2013;42:435–42.CrossRefPubMed
38.
go back to reference Archard HO, Heck JW, Stanley HR. Focal epithelial hyperplasia: an unusual oral mucosal lesion found in Indian children. Oral Surg Oral Med Oral Pathol. 1965;20:201–12.CrossRefPubMed Archard HO, Heck JW, Stanley HR. Focal epithelial hyperplasia: an unusual oral mucosal lesion found in Indian children. Oral Surg Oral Med Oral Pathol. 1965;20:201–12.CrossRefPubMed
39.
go back to reference Henke RP, Guèrin-Reverchon I, Milde-Langosch K, et al. In situ detection of human papillomavirus types 13 and 32 in focal epithelial hyperplasia of the oral mucosa. J Oral Pathol Med. 1989;18:419–21.CrossRefPubMed Henke RP, Guèrin-Reverchon I, Milde-Langosch K, et al. In situ detection of human papillomavirus types 13 and 32 in focal epithelial hyperplasia of the oral mucosa. J Oral Pathol Med. 1989;18:419–21.CrossRefPubMed
40.
go back to reference Bishop J, Gnepp DR, Ro JY. Ectomesenchymal chondromyxoid tumour. In: el-Naggar AK, Chan JKC, Grandis JR, Takata T, Slootweg PJ, editors. WHO classification of tumours of the head and neck. 4th ed. Lyon: IARC Press; 2017. Bishop J, Gnepp DR, Ro JY. Ectomesenchymal chondromyxoid tumour. In: el-Naggar AK, Chan JKC, Grandis JR, Takata T, Slootweg PJ, editors. WHO classification of tumours of the head and neck. 4th ed. Lyon: IARC Press; 2017.
41.
go back to reference Aldojain A, Jaradat J, Summersgill K, Bilodeau EA. Ectomesenchymal chondromyxoid tumor: a series of seven cases and review of the literature. Head Neck Pathol. 2015;9:315–22.CrossRefPubMed Aldojain A, Jaradat J, Summersgill K, Bilodeau EA. Ectomesenchymal chondromyxoid tumor: a series of seven cases and review of the literature. Head Neck Pathol. 2015;9:315–22.CrossRefPubMed
42.
go back to reference Nigam S, Dhingra KK, Gulati A. Ectomesenchymal chondromyxoid tumor of the hard palate–a case report. J Oral Pathol Med. 2006;35:126–8.CrossRefPubMed Nigam S, Dhingra KK, Gulati A. Ectomesenchymal chondromyxoid tumor of the hard palate–a case report. J Oral Pathol Med. 2006;35:126–8.CrossRefPubMed
43.
go back to reference Goveas N, Ethunandan M, Cowlishaw D, Flood TR. Ectomesenchymal chondromyxoid tumour of the tongue: unlikely to originate from myoepithelial cells. Oral Oncol. 2006;42:1026–8.CrossRefPubMed Goveas N, Ethunandan M, Cowlishaw D, Flood TR. Ectomesenchymal chondromyxoid tumour of the tongue: unlikely to originate from myoepithelial cells. Oral Oncol. 2006;42:1026–8.CrossRefPubMed
44.
go back to reference Smith BC, Ellis GL, Meis-Kindblom JM, Williams SB. Ectomesenchymal chondromyxoid tumor of the anterior tongue. Nineteen cases of a new clinicopathologic entity. Am J Surg Pathol. 1995;19:519–30.CrossRefPubMed Smith BC, Ellis GL, Meis-Kindblom JM, Williams SB. Ectomesenchymal chondromyxoid tumor of the anterior tongue. Nineteen cases of a new clinicopathologic entity. Am J Surg Pathol. 1995;19:519–30.CrossRefPubMed
45.
go back to reference Bullerdiek J, Ro JY. Thompson LDR. rhabdomyoma. In: el-Naggar AK, Chan JKC, Grandis JR, Takata T, Slootweg PJ, editors. WHO classification of tumours of the head and neck. 4th ed. Lyon: IARC Press; 2017. Bullerdiek J, Ro JY. Thompson LDR. rhabdomyoma. In: el-Naggar AK, Chan JKC, Grandis JR, Takata T, Slootweg PJ, editors. WHO classification of tumours of the head and neck. 4th ed. Lyon: IARC Press; 2017.
46.
go back to reference Hettmer S, Teot LA, van Hummelen P, et al. Mutations in Hedgehog pathway genes in fetal rhabdomyomas. J Pathol. 2013;231:44–52.CrossRefPubMed Hettmer S, Teot LA, van Hummelen P, et al. Mutations in Hedgehog pathway genes in fetal rhabdomyomas. J Pathol. 2013;231:44–52.CrossRefPubMed
47.
go back to reference Bullerdiek J, Flucke U. Lymphangioma. In: el-Naggar AK, Chan JKC, Grandis JR, Takata T, Slootweg PJ, editors. WHO classification of tumours of the head and neck. 4th ed. Lyon: IARC Press; 2017. Bullerdiek J, Flucke U. Lymphangioma. In: el-Naggar AK, Chan JKC, Grandis JR, Takata T, Slootweg PJ, editors. WHO classification of tumours of the head and neck. 4th ed. Lyon: IARC Press; 2017.
48.
go back to reference Kardon DE, Wenig BM, Heffner DK, Thompson LD. Tonsillar lymphangiomatous polyps: a clinicopathologic series of 26 cases. Mod Pathol. 2000;13:1128–33.CrossRefPubMed Kardon DE, Wenig BM, Heffner DK, Thompson LD. Tonsillar lymphangiomatous polyps: a clinicopathologic series of 26 cases. Mod Pathol. 2000;13:1128–33.CrossRefPubMed
49.
go back to reference Bruder E, Alaggio R, Kozakewich HP, et al. Vascular and perivascular lesions of skin and soft tissues in children and adolescents. Pediatr Dev Pathol. 2012;15:26–61. Bruder E, Alaggio R, Kozakewich HP, et al. Vascular and perivascular lesions of skin and soft tissues in children and adolescents. Pediatr Dev Pathol. 2012;15:26–61.
50.
51.
go back to reference Mardekian S, Karp JK. Lymphangioma of the palatine tonsil. Arch Pathol Lab Med. 2013;137:1837–42.CrossRefPubMed Mardekian S, Karp JK. Lymphangioma of the palatine tonsil. Arch Pathol Lab Med. 2013;137:1837–42.CrossRefPubMed
52.
go back to reference Rekhi B, Sethi S, Kulkarni SS, Jambhekar NA. Kaposiform hemangioendothelioma in tonsil of a child associated with cervical lymphangioma: a rare case report. World J Surg Oncol. 2011;9:57.CrossRefPubMedPubMedCentral Rekhi B, Sethi S, Kulkarni SS, Jambhekar NA. Kaposiform hemangioendothelioma in tonsil of a child associated with cervical lymphangioma: a rare case report. World J Surg Oncol. 2011;9:57.CrossRefPubMedPubMedCentral
53.
54.
go back to reference Bullerdiek J, Flucke U. Haemangioma. In: el-Naggar AK, Chan JKC, Grandis JR, Takata T, Slootweg PJ, editors. WHO classification of tumours of the head and neck. 4th ed. Lyon: IARC Press; 2017. Bullerdiek J, Flucke U. Haemangioma. In: el-Naggar AK, Chan JKC, Grandis JR, Takata T, Slootweg PJ, editors. WHO classification of tumours of the head and neck. 4th ed. Lyon: IARC Press; 2017.
55.
go back to reference Açikgöz A, Sakallioglu U, Ozdamar S, Uysal A. Rare benign tumours of oral cavity–capillary haemangioma of palatal mucosa: a case report. Int J Paediatr Dent. 2000;10:161–5.PubMed Açikgöz A, Sakallioglu U, Ozdamar S, Uysal A. Rare benign tumours of oral cavity–capillary haemangioma of palatal mucosa: a case report. Int J Paediatr Dent. 2000;10:161–5.PubMed
56.
go back to reference Bonet-Coloma C, Mínguez-Martínez I, Palma-Carrió C, et al. Clinical characteristics, treatment and outcome of 28 oral haemangiomas in pediatric patients. Med Oral Patol Oral Cir Bucal. 2011;16:e19–e22.CrossRefPubMed Bonet-Coloma C, Mínguez-Martínez I, Palma-Carrió C, et al. Clinical characteristics, treatment and outcome of 28 oral haemangiomas in pediatric patients. Med Oral Patol Oral Cir Bucal. 2011;16:e19–e22.CrossRefPubMed
57.
go back to reference Maaita JK. Oral tumors in child- ren: a review. J Clin Pediatr Dent. 2000;24:133–5.PubMed Maaita JK. Oral tumors in child- ren: a review. J Clin Pediatr Dent. 2000;24:133–5.PubMed
58.
go back to reference Sato M, Tanaka N, Sato T, Amagasa T. Oral and maxillofacial tumours in children: a review. Br J Oral Maxillofac Surg. 1997;35:92–5.CrossRefPubMed Sato M, Tanaka N, Sato T, Amagasa T. Oral and maxillofacial tumours in children: a review. Br J Oral Maxillofac Surg. 1997;35:92–5.CrossRefPubMed
59.
go back to reference Flucke U, Franchi A. Myofibroblastic sarcoma. In: el-Naggar AK, Chan JKC, Grandis JR, Takata T, Slootweg PJ, editors. WHO classification of tumours of the head and neck. 4th ed. Lyon: IARC Press; 2017. Flucke U, Franchi A. Myofibroblastic sarcoma. In: el-Naggar AK, Chan JKC, Grandis JR, Takata T, Slootweg PJ, editors. WHO classification of tumours of the head and neck. 4th ed. Lyon: IARC Press; 2017.
60.
go back to reference Fisher C. Low-grade sarcomas with CD34-positive fibroblasts and low-grade myofibroblastic sarcomas. Ultrastruct Pathol. 2003;428:291–305. Fisher C. Low-grade sarcomas with CD34-positive fibroblasts and low-grade myofibroblastic sarcomas. Ultrastruct Pathol. 2003;428:291–305.
61.
go back to reference Mentzel T, Dry S, Katenkamp D, Fletcher CD. Low-grade myofibroblastic sarcoma: analysis of 18 cases in the spectrum of myofibroblastic tumors. Am J Surg Pathol. 1998;22:1228–38.CrossRefPubMed Mentzel T, Dry S, Katenkamp D, Fletcher CD. Low-grade myofibroblastic sarcoma: analysis of 18 cases in the spectrum of myofibroblastic tumors. Am J Surg Pathol. 1998;22:1228–38.CrossRefPubMed
62.
go back to reference Inagaki H, Bell D, Brandwein-Gensler M. Mucoepidermoid Carcinoma. In: el-Naggar AK, Chan JKC, Grandis JR, Takata T, Slootweg PJ, editors. WHO classification of tumours of the head and neck. 4th ed. Lyon: IARC Press; 2017. Inagaki H, Bell D, Brandwein-Gensler M. Mucoepidermoid Carcinoma. In: el-Naggar AK, Chan JKC, Grandis JR, Takata T, Slootweg PJ, editors. WHO classification of tumours of the head and neck. 4th ed. Lyon: IARC Press; 2017.
63.
go back to reference Bell D, Brandwein-Gensler M, Chiosea S. Pleomorphic Adenoma. In: el-Naggar AK, Chan JKC, Grandis JR, Takata T, Slootweg PJ, editors. WHO classification of tumours of the head and neck. 4th ed. Lyon: IARC Press; 2017. Bell D, Brandwein-Gensler M, Chiosea S. Pleomorphic Adenoma. In: el-Naggar AK, Chan JKC, Grandis JR, Takata T, Slootweg PJ, editors. WHO classification of tumours of the head and neck. 4th ed. Lyon: IARC Press; 2017.
64.
go back to reference Feldman AL, Boy S, Ferry JA, et al. CD30-positive T-cell lymphoproliferative disorder. In: el-Naggar AK, Chan JKC, Grandis JR, Takata T, Slootweg PJ, editors. WHO classification of tumours of the head and neck. 4th ed. Lyon: IARC Press, 2017. Feldman AL, Boy S, Ferry JA, et al. CD30-positive T-cell lymphoproliferative disorder. In: el-Naggar AK, Chan JKC, Grandis JR, Takata T, Slootweg PJ, editors. WHO classification of tumours of the head and neck. 4th ed. Lyon: IARC Press, 2017.
65.
go back to reference Rosenberg A, Biesma DH, Sie-Go DM, Slootweg PJ. Primary extranodal CD30-positive T-cell non-Hodgkins lymphoma of the oral mucosa. Report of two cases. Int J Oral Maxillofac Surg. 1996;25:57–9.CrossRefPubMed Rosenberg A, Biesma DH, Sie-Go DM, Slootweg PJ. Primary extranodal CD30-positive T-cell non-Hodgkins lymphoma of the oral mucosa. Report of two cases. Int J Oral Maxillofac Surg. 1996;25:57–9.CrossRefPubMed
66.
go back to reference Sciallis AP, Law ME, Inwards DJ, et al. Mucosal CD30-positive T-cell lymphoproliferations of the head and neck show a clinicopathologic spectrum similar to cutaneous CD30-positive T-cell lymphoproliferative disorders. Mod Pathol. 2012;25:983–92.CrossRefPubMed Sciallis AP, Law ME, Inwards DJ, et al. Mucosal CD30-positive T-cell lymphoproliferations of the head and neck show a clinicopathologic spectrum similar to cutaneous CD30-positive T-cell lymphoproliferative disorders. Mod Pathol. 2012;25:983–92.CrossRefPubMed
67.
go back to reference Wang W, Cai Y, Sheng W, Lu H, Li X. The spectrum of primary mucosal CD30-positive T-cell lymphoproliferative disorders of the head and neck. Oral Surg Oral Med Oral Pathol Oral Radiol. 2014;117:96–104.CrossRefPubMed Wang W, Cai Y, Sheng W, Lu H, Li X. The spectrum of primary mucosal CD30-positive T-cell lymphoproliferative disorders of the head and neck. Oral Surg Oral Med Oral Pathol Oral Radiol. 2014;117:96–104.CrossRefPubMed
68.
go back to reference Alobeid B, Pan LX, Milligan L, et al. Eosinophil-rich CD30+ lymphoproliferative disorder of the oral mucosa. A form of “traumatic eosinophilic granuloma”. Am J Clin Pathol. 2004;121:43–50.CrossRefPubMed Alobeid B, Pan LX, Milligan L, et al. Eosinophil-rich CD30+ lymphoproliferative disorder of the oral mucosa. A form of “traumatic eosinophilic granuloma”. Am J Clin Pathol. 2004;121:43–50.CrossRefPubMed
69.
go back to reference Hirshberg A, Amariglio N, Akrish S, et al. Traumatic ulcerative granuloma with stromal eosinophilia: a reactive lesion of the oral mucosa. Am J Clin Pathol. 2006;126:522–9.CrossRefPubMed Hirshberg A, Amariglio N, Akrish S, et al. Traumatic ulcerative granuloma with stromal eosinophilia: a reactive lesion of the oral mucosa. Am J Clin Pathol. 2006;126:522–9.CrossRefPubMed
70.
go back to reference Boy S, Ferry JA. Plasmablastic lymphoma. In: el-Naggar AK, Chan JKC, Grandis JR, Takata T, Slootweg PJ, editors. WHO classification of tumours of the head and neck. 4th ed. Lyon: IARC Press, 2017. Boy S, Ferry JA. Plasmablastic lymphoma. In: el-Naggar AK, Chan JKC, Grandis JR, Takata T, Slootweg PJ, editors. WHO classification of tumours of the head and neck. 4th ed. Lyon: IARC Press, 2017.
71.
go back to reference Castillo JJ, Bibas M, Miranda RN. The biology and treatment of plasmablastic lymphoma. Blood. 2015;125:2323–30.CrossRefPubMed Castillo JJ, Bibas M, Miranda RN. The biology and treatment of plasmablastic lymphoma. Blood. 2015;125:2323–30.CrossRefPubMed
72.
go back to reference Castillo J, Pantanowitz L, Dezube BJ. HIV-associated plasmablastic lymphoma: lessons learned from 112 published cases. Am J Hematol. 2008;83:804–9.CrossRefPubMed Castillo J, Pantanowitz L, Dezube BJ. HIV-associated plasmablastic lymphoma: lessons learned from 112 published cases. Am J Hematol. 2008;83:804–9.CrossRefPubMed
73.
go back to reference 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;89:1413–20.PubMed 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;89:1413–20.PubMed
74.
go back to reference Boy S, van Heerden M, Pool R, et al. Plasmablastic lymphoma versus diffuse large B-cell lymphoma with plasmablastic differentiation: proposal for a novel diagnostic scoring system. J Hematop. 2015;8:3–11.CrossRef Boy S, van Heerden M, Pool R, et al. Plasmablastic lymphoma versus diffuse large B-cell lymphoma with plasmablastic differentiation: proposal for a novel diagnostic scoring system. J Hematop. 2015;8:3–11.CrossRef
75.
go back to reference Loghavi S, Alayed K, Aladily TN, et al. Stage, age, and EBV status impact outcomes of plasmablastic lymphoma patients: a clinicopathologic analysis of 61 patients. J Hematol Oncol. 2015;8:65.CrossRefPubMedPubMedCentral Loghavi S, Alayed K, Aladily TN, et al. Stage, age, and EBV status impact outcomes of plasmablastic lymphoma patients: a clinicopathologic analysis of 61 patients. J Hematol Oncol. 2015;8:65.CrossRefPubMedPubMedCentral
Metadata
Title
Update from the 4th Edition of the World Health Organization of Head and Neck Tumours: Tumours of the Oral Cavity and Mobile Tongue
Author
Susan Müller
Publication date
01-03-2017
Publisher
Springer US
Published in
Head and Neck Pathology / Issue 1/2017
Electronic ISSN: 1936-0568
DOI
https://doi.org/10.1007/s12105-017-0792-3

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