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Primary hematologic malignancies with the onset of involvement of the major salivary glands in rheumatologic practice

https://doi.org/10.14412/1996-7012-2019-1-44-51

Abstract

Objective: to identify the main types of lymphoma with the onset of involvement of the major salivary glands (MSGs), which are encountered in rheumatologic practice, and to evaluate the efficiency of minimally invasive incisional biopsies of the MSGs/lacrimal glands in the diagnosis of different diseases affecting the parotid, submandibular, sublingual, and lacrimal glands.

Patients and methods. A total of339patients (291 women and 48 men) aged 18 to 78 years (median age, 55 years) with MSG involvement were examined at the V.A. Nasonova Research Institute of Rheumatology in 2004 to 2017. Minimally invasive incisional biopsies of the parotid, submandibular salivary (SMSG), and lacrimal glands were carried out to verify the diagnosis.

Results and discussion. Different variants of hematological malignancies with MSG involvement were diagnosed in 187 (55%) patients; nonneoplastic diseases were in 152 (45%) patients. Primary tumors with the onset of MSG involvement were detected in 52 (15.3%) patients. Hematologic malignancies were diagnosed in 32 (61.5%) cases and 20 (38.5%) patients had various benign neoplastic or infectious diseases with MSG involvement. The prevailing hematologic malignances with MSG involvement were non-Hodgkin lymphomas (NHL), indolent MALT-lymphomas in 12 (23%) patients, follicular lymphomas in 6 (11.5%), and AL-amyloidosis affecting the SMSG in 9 (17.3%). The diagnosis was morphologically verified using minimally invasive incisional biopsy of the salivary/lacrimal glands; in all cases, the biopsy was informative for full morphopathological examination and diagnosis verification.

Conclusion. Minimally invasive incisional biopsy of the MSG/lacrimal glands should be actively used in dentistry, rheumatology and blood oncology hospitals for verification of nosological diagnoses when the MSG and lacrimal glands are involved. A sufficient number of tissues obtained using these techniques allows one to abandon severe surgical interventions (partial and complete parotidectomy, SMSG removal, and orbitotomy) currently used for diagnostic purposes in various types of hospitals.

About the Authors

V. I. Vasilyev
V.A. Nasonova Research Institute of Rheumatology
Russian Federation

34A, Kashirskoe Shosse, Moscow 115522



I. V. Gaiduk
A.I. Evdokimov Moscow State University of Medicine and Dentistry, Ministry of Health of Russia
Russian Federation

20, Delegatskaya St., Build. 1, Moscow 127473



S. G. Palshina
V.A. Nasonova Research Institute of Rheumatology
Russian Federation

34A, Kashirskoe Shosse, Moscow 115522



V. R. Gorodetsky
V.A. Nasonova Research Institute of Rheumatology
Russian Federation

34A, Kashirskoe Shosse, Moscow 115522



E. V. Sokol
V.A. Nasonova Research Institute of Rheumatology
Russian Federation

34A, Kashirskoe Shosse, Moscow 115522



E. B. Rodionova
V.A. Nasonova Research Institute of Rheumatology
Russian Federation

34A, Kashirskoe Shosse, Moscow 115522



M. V. Burtseva
V.A. Nasonova Research Institute of Rheumatology
Russian Federation

34A, Kashirskoe Shosse, Moscow 115522



N. S. Shornikova
V.A. Nasonova Research Institute of Rheumatology
Russian Federation

Natalia Sergeevna Shornikova

34A, Kashirskoe Shosse, Moscow 115522



N. A. Probatova
N.N. Blokhin National Medical Research Center of Oncology, Ministry of Health of Russia
Russian Federation

23, Kashirskoe Shosse, Moscow 115478



N. V. Kokosadze
N.N. Blokhin National Medical Research Center of Oncology, Ministry of Health of Russia
Russian Federation

23, Kashirskoe Shosse, Moscow 115478



A. I. Pavlovskaya
N.N. Blokhin National Medical Research Center of Oncology, Ministry of Health of Russia
Russian Federation

23, Kashirskoe Shosse, Moscow 115478



N. A. Kupryshina
N.N. Blokhin National Medical Research Center of Oncology, Ministry of Health of Russia
Russian Federation

23, Kashirskoe Shosse, Moscow 115478



T. N. Safonova
Research Institute of Eye Diseases
Russian Federation

11A,B, Rossolomo St., Moscow 119021



References

1. Marx RE, Stern D, editors. Oral and Maxillofacial Pathology. A Rationale for Diagnosis and Treatment. Second Edition. Quintessence Publishing Co; 2012. 980 p.

2. Myers EN, Ferris RL, editors. Salivary Gland Disorders. Springer; 2007. 518 p.

3. Васильев ВИ, Сокол ЕВ, Родионова ЕБ и др. Связанные с IgG-4 поражения слюнных желёз. Терапевтический архив. 2015;(8):92-102. [Vasilev VI, Sokol EV, Rodionova EB, et al. IgG-4-related lesions of the salivary glands. Terapevticheskii arkhiv. 2015;(8):92-102. (In Russ.)].

4. Jackson AE, Mian M, Kalpadakis C, et al. Extranodal Marginal Zone Lymphoma of Mucosa-Associated Lymphoid Tissue of the Salyvary Glands: A Multicenter International Experience of 248 Patients (IELSG 41). Oncologist. 2015 Oct;20(10):1149-53. doi: 10.1634/theoncologist.2015-0180. Epub 2015 Aug 12.

5. Mitrikov BV. Features of lymphoproliferative lesions of salivary glands in patients with Sjogren's disease. Autoref. dis. cand. med. sci. Moscow; 2008.

6. Sedyshev SKh. Diseases, manifested by symmetrical increase n salivary glands and tissues of the orbits in rheumatological practice. Autoref. dis. cand. med. sci. Moscow; 2012.

7. Swerdlow SH, Campo E, Harris NL, et al, editors. WHO Classification of Tumours of Haematopoietic and Lymphoid Tissues. Lyon: International Agency for Research on Cancer; 2017.

8. Barnes L, Eveson JW, Reichart P, Sidransky D, editors. WHO Classification of Tumours. Pathology&Genetics Head and Neck Tumours. Lyon: IARC Press; 2005.

9. Bertoni F, Zucca E. MALT Lymphomas. Medical Intelligence Unit. Kluwer Academic/Plenum Publishers; 2004. 133 p.

10. Guzzo M, Locati LD, Prott FJ, et al. Major and minor salivary gland tumors. Crit Rev Oncol Hematol. 2010 May;74(2):134-48. doi: 10.1016/j.critrevonc.2009.10.004. Epub 2009 Nov 24.

11. His ED, Martin P. Indolent mantle cell lymphoma. LeukLymphoma. 2014 Apr;55(4): 761-7. doi: 10.3109/10428194.2013.815353. Epub 2013 Sep 24.

12. You MJ, Medeiros LJ, Hsi ED. T-lymphoblastic Leukemia/Lymphoma. Am J Clin Pathol. 2015 Sep;144(3):411-22. doi: 10.1309/AJCPMF03LVSBLHPJ.

13. Shankland KR, Armitage JO, Hancock BW. Non-Hodgkin lymphoma. Lancet. 2012 Sep 1;380(9844):848-57. doi: 10.1016/S0140-6736(12)60605-9. Epub 2012 Jul 25.

14. Morel P, Lepage E, Brice P, et al. Prognosis and treatment of lymhoblastic lymphoma in adults: a report on 80 patients. JClin Oncol. 1992 Jul;10(7):1078-85.

15. Pohar S, Gay H, Rosenbaum P, et al. Malignant parotid tumors: Presentation, clinical/pathologic prognostic factors, and treatment outcomes. Int J Radiat Oncol Biol Phys. 2005 Jan 1;61(1):112-8.

16. Vasil'ev VI, Gorodetskii VR, Radenska-Lopovok SG, et al. New approaches to the determination of organ lesions in AL-amyloidosis. Nauchno-prakticheskaya revmatologiya = Rheumatology Science and Practice. 2012;50(1):83-90. (In Russ.). Doi: 10.14412/1995-4484-2012-510

17. Mehle ME, Kraus DH, Wood BG, et al. Lymphoma of the Parotid Gland. Laryngoscope. 1993 Jan;103(1 Pt 1):17-21.

18. Shine NP, Blake SP, O’Leary G. Extranodal Lymphoma: clinical presentation and diagnostic pitfalls. Hosp Med. 2005 Jun; 66(6):341-5.

19. Vasil'ev VI, Logvinenko OA, Probatova NA, et al. The role of biopsy of the parotid salivary gland in the early diagnosis of lymphomas in Sjogren's disease. Tarapevticheskii arkhiv. 2009;(6): 20-7. (In Russ.).


Review

For citations:


Vasilyev VI, Gaiduk IV, Palshina SG, Gorodetsky VR, Sokol EV, Rodionova EB, Burtseva MV, Shornikova NS, Probatova NA, Kokosadze NV, Pavlovskaya AI, Kupryshina NA, Safonova TN. Primary hematologic malignancies with the onset of involvement of the major salivary glands in rheumatologic practice. Sovremennaya Revmatologiya=Modern Rheumatology Journal. 2019;13(1):44-51. (In Russ.) https://doi.org/10.14412/1996-7012-2019-1-44-51

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ISSN 1996-7012 (Print)
ISSN 2310-158X (Online)