Dental and Medical Problems

Dent Med Probl
Index Copernicus (ICV 2021) – 132.50
MEiN – 70 pts
CiteScore (2021) – 2.0
JCI (2021) – 0.5
Average rejection rate (2022) – 79.69%
ISSN 1644-387X (print)
ISSN 2300-9020 (online)
Periodicity – quarterly

Download PDF

Dental and Medical Problems

2017, vol. 54, nr 3, July-September, p. 291–295

doi: 10.17219/dmp/74144

Publication type: clinical case

Language: English

Download citation:

  • BIBTEX (JabRef, Mendeley)
  • RIS (Papers, Reference Manager, RefWorks, Zotero)

Creative Commons BY-NC-ND 3.0 Open Access

Severe alveolar bone loss and internal root resorption in linear IgA disease and eosinophilic granulomatosis with polyangiitis: A rare case report

Nasilony ubytek kości wyrostka zębodołowego i wewnętrzna resorpcja korzeni zębów w przebiegu linijnej IgA dermatozy oraz eozynofilowej ziarniniakowatości z zapaleniem naczyń – opis rzadkiego przypadku

Phisut Amnuaiphanit1,A,B,C,D,E,F, Sarinthon Pariyawathee1,A,B,C,D,E,F, Kobkan Thongprasom1,A,B,C,D,E,F

1 Department of Oral Medicine, Faculty of Dentistry, Chulalongkorn University, Bangkok, Thailand

Abstract

Linear IgA disease (LAD) is rare and there are only a few cases reported where its lesions were limited to the oral mucosa. Eosinophilic granulomatosis with polyangiitis (EGPA) is also a rare multisystemic disease. Therefore, the occurrence of LAD and EGPA in the same patient is very rare. Here we report the oral manifestations of a case of a 24-year-old female who first presented with idiopathic thrombocytopenic purpura (ITP) and was treated with dapsone, with LAD occurring later. Over the next 6 years, this patient developed hypothyroidism, asthma, eosinophilia, glaucoma, abnormal menstruation, arthritis, glomerulonephritis and respiratory tract involvement. Finally, EGPA was diagnosed by her physicians. This is the first case report of LAD and EGPA that radiographically showed the development of generalized severe alveolar bone loss and internal root resorption of the maxillary right second premolar between the first visit and a 2-year follow-up.

Key words

linear IgA disease, eosinophilic granulomatosis with polyangiitis, alveolar bone loss, internal root resorption,

Słowa kluczowe

linijna IgA dermatoza, ziarniniakowatość eozynofilowa z zapaleniem naczyń, ubytek kości wyrostka zębodołowego, wewnętrzna resorpcja korzeni

References (32)

  1. Eguia del VA, Aguirre UJM, Martínez SA. Oral manifestations caused by the linear IgA disease. Med Oral, 2004;9:39–44.
  2. Neville BW, Damm DD, Allen CM, Chi AC. Oral and maxillofacial pathology. 4th edition, St. Louis: Saunders Elsevier; 2016:721.
  3. Angiero F, Benedicenti S, Crippa R, Magistro S, Farronato D, Stefani M. A rare case of desquamative gingivitis due to linear IgA disease: morphological and immunofluorescence features. In Vivo, 2007; 21:1093–1098.
  4. Godfrey K, Wojnarowska F, Leonard J. Linear IgA disease of adults: Association with lymphoproliferative malignancy and possible role of other triggering factors. Br J Dermatol. 1990;123:447–452.
  5. Wakelin SH, Allen J, Zhou S, Wojnarowska F. Drug-induced linear IgA disease with antibodies to collagen VII. Br J Dermatol. 1998;138:310–314.
  6. Gabrielsen TO, Staerfelt F, Thune PO. Drug induced linear IgA deposits along the basement membrane. Acta Derm Venereol. 1981;61:439–441.
  7. Mc Whirter JD, Hashimoto K, Fayne S, Ito K. Linear IgA bullous dermatosis related to lithium. Arch Dermatol. 1987;123:1120–1122.
  8. König C, Eickert A, Scharfetter-Kochanek K, Krieg T, Hunzelmann N. Linear bullous IgA dermatosis induced by atorvastin. J Am Acad Dermatol. 2001;44:689–692.
  9. Plunkett RW, Chiarello SE, Beutner EH. Linear bullous dermatosis in one of two piroxicam induced eruptions: A distinct immunofluorescence trend revealed by the literature. J Am Acad Dermatol. 2001;45:691–696.
  10. Avci O, Okmen M, Cetiner S. Acetaminophen induced linear IgA bullous dermatosis. J Am Acad Dematol. 2003;48:299–301.
  11. Bachot N, Wechsler J, Demoule A, Roujeau JC. Amiodarone related linear IgA bullous dermatosis. J Am Acad Dermatol. 2003;49:e2.
  12. Shimanovich I, Rose C, Sitaru C, Bröcker EB, Zillikens D. Localized linear IgA disease induced by ampicillin/sulbactam. J Am Acad Dermatol. 2004;51:95–98.
  13. Rashid Dar N, Raza N. Drug induced linear IgA disease with unusual features: Koebner phenomenon, local insulin sensitivity and annular blister of the nipples. Acta Dermatovenerol Croat. 2008;16:215–217.
  14. Panasiti V, Rossi M, Devirgiliis V, Curzio M, Bottoni U, Calvieri S. Amoxicillin-clavulanic acid-induced linear immunoglobulin A bullous dermatosis: Case report and review of the literature. Int J Dermatol. 2009;48:1006–1010.
  15. Kocyigit P, Akay BN, Karaosmanoglu N. Linear IgA bullous dermatosis induced by interferon-alpha 2a. Clin Exp Dermatol. 2009;34:e123–124.
  16. Nantel-Battista M, Al Dhaybi RA, Hatami A, Marcoux D, DesRoches A, Kokta V. Childhood linear IgA bullous disease induced by trimethoprim-sulfamethoxazole. J Dermatol Case Rep. 2010;4:33–35.
  17. Choudhry SZ, Kashat M, Lim HW. Vancomycin-induced linear IgA bullous dermatosis demonstrating the isomorphic phenomenon. Int J Dermatol. 2015;54:1211–1213.
  18. Porter SR, Scully C, Midda M, Eveson JW. Adult linear immunoglobulin A disease manifesting as desquamative gingivitis. Oral Surg Oral Med Oral Pathol. 1990;70:450–453.
  19. Gioffredi A, Maritati F, Oliva E, Buzio C. Eosinophilic granulomatosis with polyangiitis: An overview. Front Immunol. 2014;5:549.
  20. Mouthon L, Dunogue B, Guillevin L. Diagnosis and classification of eosinophilic granulomatosis with polyangiitis (formerly named Churg-Strauss syndrome). J Autoimmun. 2014;48–49:99–103.
  21. Alberici F, Martorana D, Bonatti F, Gioffredi A, Lyons PA, Vaglio A. Genetics of ANCA-Associated vasculitides: HLA and beyond. Clin Exp Rheumatol. 2014;32:90–97.
  22. del Valle AE, Martínez-Sahuquillo A, Padrón JR, Urizar JM. Two cases of linear IgA disease with clinical manifestations limited to the gingiva. J Periodontol. 2003;74:879–882.
  23. Joseph TI, Sathyan P, Goma Kumar KU. Linear IgA dermatosis adult variant with oral manifestation: A rare case report. J Oral Maxillofac Pathol. 2015;19:83–87.
  24. Mahévas M, Michel M, Godeau B. How we manage immune thrombocytopenia in the elderly. Br J Haematol. 2016;173:844–856.
  25. Chanal J, Ingen-Housz-Oro S, Ortonne N, Duong TA, Thomas ML. Linear IgA bullous dermatosis: Comparison between the drug-induced and spontaneous forms. Br J Dermatol. 2013;169:1041–1048.
  26. Greco A, Rizzo MI, De Virgilio A, Gallo A, Fusconi M, Ruoppolo G. Churg-Strauss syndrome. Autoimmun Rev. 2015;14:341–348.
  27. Gambari PF, Ostuni PA, Lazzarin P, Fassina A, Todesco S. Eosinophilic granuloma and necrotizing vasculitis (Churg-Strauss syndrome?) involving a parotid gland, lymph nodes, liver and spleen. Scand J Rheumatol. 1989;18:171–175.
  28. Boin F, Sciubba JJ, Stone JH. Churg-Strauss syndrome presenting with salivary gland enlargement and respiratory distress. Arthritis Rheum. 2006;55;167–170.
  29. Tovoli F, Vannini A, Masi C, Balbi T, Bolondi L, Cavazza M. Eosinophilic granulomatosis with polyangiitis of the major salivary glands: A case of sialadenitis in a young patient. Intern Med. 2013;52:2131–2134.
  30. Mazzantini M, Fattori B, Matteucci F, Gaeta P, Ursino F. Neuro-laryngeal involvement in Churg-Strauss syndrome. Eur Arch Otorhinolaryngol. 1998;255:302–306.
  31. Proffit WR, Fields HW, Sarver DM, Ackerman JL. Contemporary orthodontics. 5th edition, St. Louis: Elsevier Mosby; 2013:303.
  32. Zahrowski J, Jeske A. Apical root resorption is associated with comprehensive orthodontic treatment but not clearly dependent on prior tooth characteristics or orthodontic techniques. J Am Dent Assoc. 2011;142:66–68.