The histopathological spectrum ofMelkersson-Rosenthalsyndrome: Analysis of 47 cases

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Citações na Scopus
7
Tipo de produção
article
Data de publicação
2020
Título da Revista
ISSN da Revista
Título do Volume
Editora
WILEY
Autores
FLOREZI, Giovanna Piacenza
LOURENCO, Silvia Vanessa
Citação
JOURNAL OF CUTANEOUS PATHOLOGY, v.47, n.11, p.1010-1017, 2020
Projetos de Pesquisa
Unidades Organizacionais
Fascículo
Resumo
Background Melkersson-Rosenthal syndrome (MRS) is a rare disease characterized by the triad of recurrent orofacial edema, relapsing facial paralysis and plicated tongue. Histopathological features of MRS have not been extensively analyzed. Methods This study investigated the histopathological aspects of oral lesions from 47 MRS patients. Results The most common biopsy site was the upper lip, followed by the lower lip, gingiva and palate. The most important findings were ill-defined and well-formed granulomas. Lymphoplasmacytic inflammatory infiltrate was seen in early and late stages of MRS. Edema, fibrosis, vasodilatation and congestion were the most common finding in the lamina propria. Gingival and palate exams also demonstrated granulomatous infiltrates. Regarding the evolution time of the disease, we demonstrated that, in initial phases, there is a lymphoplasmacytic inflammatory infiltrates, followed by a granulomatous infiltrate and, subsequently, fibrosis. Conclusion Histopathological examination of oral lesions is helpful for the diagnosis of MRS; the absence of granulomatous inflammation does not exclude the diagnosis of syndrome. Clinical and histopathological analysis of the rare gingival and palate lesions is important, since all histopathological findings of the disease were detected in these sites.
Palavras-chave
facial paralysis, granulomatosis, orofacial, Melkersson-Rosenthal syndrome, pathology, cheilitis granulomatosa, orofacial granulomatosis, tongue, fissured
Referências
  1. Feng S, 2014, ACTA OTO-LARYNGOL, V134, P977, DOI 10.3109/00016489.2014.927587
  2. Gavioli CFB, 2020, EUR J MED GENET, V63, DOI 10.1016/j.ejmg.2020.103879
  3. Gibson J, 2000, BRIT J DERMATOL, V143, P1119, DOI 10.1046/j.1365-2133.2000.03877.x
  4. Goto A, 1999, Rinsho Shinkeigaku, V39, P1020
  5. Grave B, 2009, ORAL DIS, V15, P46, DOI 10.1111/j.1601-0825.2008.01500.x
  6. GREENE RM, 1989, J AM ACAD DERMATOL, V21, P1263, DOI 10.1016/S0190-9622(89)70341-8
  7. Hornstein Otto P., 1997, Journal of Dermatology (Tokyo), V24, P281
  8. Kaminagakura E, 2011, J CUTAN PATHOL, V38, P241, DOI 10.1111/j.1600-0560.2009.01446.x
  9. Liu RZ, 2013, J CLIN NEUROSCI, V20, P993, DOI 10.1016/j.jocn.2012.10.009
  10. McCartan BE, 2011, ORAL DIS, V17, P696, DOI 10.1111/j.1601-0825.2011.01826.x
  11. MEISELSTOSIEK M, 1990, ACTA DERM-VENEREOL, V70, P221
  12. Pagan AJ, 2018, ANNU REV IMMUNOL, V36, P639, DOI 10.1146/annurev-immunol-032712-100022
  13. PATTON DW, 1985, BRIT J ORAL MAX SURG, V23, P235, DOI 10.1016/0266-4356(85)90038-5
  14. Ratzinger G, 2007, J EUR ACAD DERMATOL, V21, P1065, DOI 10.1111/j.1468-3083.2007.02194.x
  15. Sciubba JJ, 2003, J ORAL PATHOL MED, V32, P576, DOI 10.1034/j.1600-0714.2003.t01-1-00056.x
  16. Tan ZL, 2015, AM J OTOLARYNG, V36, P334, DOI 10.1016/j.amjoto.2014.12.001
  17. van der Waal RIF, 2002, INT J DERMATOL, V41, P225, DOI 10.1046/j.1365-4362.2002.01466.x
  18. van der Waal RIF, 2001, J EUR ACAD DERMATOL, V15, P519, DOI 10.1046/j.1468-3083.2001.00353.x
  19. WIESENFELD D, 1985, Q J MED, V54, P101
  20. WORSAAE N, 1982, ORAL SURG ORAL MED O, V54, P404, DOI 10.1016/0030-4220(82)90387-5
  21. ZIMMER WM, 1992, ORAL SURG ORAL MED O, V74, P610, DOI 10.1016/0030-4220(92)90354-S