Delia Urdea https://orcid.org/0009-0003-6590-1889 Florentina Severin https://orcid.org/0000-0002-9362-2030 Victor V. Costan https://orcid.org/0000-0002-3978-5103 Deniss V. Mereuta https://orcid.org/0009-0006-7339-0443

Abstract

Melkersson-Rosenthal syndrome (MRS) is a rare and often challenging condition of unknown etiology, typically defined by a clinical triad of peripheral facial nerve palsy, recurrent orofacial edema, and fissured tongue. Its variable presentation and overlap with allergic reactions, mast cell-mediated disorders, and drug hypersensitivity reactions can delay diagnosis and appropriate management. We report the case of a 43-year-old man with a personal long-standing history of recurrent hemifacial and lip swelling associated with facial nerve palsy and a plicated tongue, fulfilling the complete clinical triad of MRS. Extensive laboratory, immunological, infectious, and allergological investigations ruled out alternative diagnoses, including hereditary angioedema and drug hypersensitivity. Histopathological examination of a lip biopsy did not reveal granulomatous inflammation. The disease was refractory to multiple standard therapies, including antihistamines, corticosteroids, epinephrine, antibiotics, and immunomodulatory agents. Administration of fresh frozen plasma at a dose of 10 ml/kg resulted in a rapid and marked clinical improvement within 6 hours. This case highlights a rare complete presentation of MRS and underscores the challenges in diagnosis and management. The favorable response to fresh frozen plasma suggests a potential therapeutic option in refractory cases; however, further studies are required to clarify its role and mechanism of action in Melkersson-Rosenthal syndrome.​

##plugins.themes.bootstrap3.article.details##

Keywords

allergy, angioedema, fresh frozen plasma, Melkersson-Rosenthal Syndrome, hypersensitivity

References
[1] Wang S, Wang H, Shi X, et al. A case of Melkersson-Rosenthal syndrome with endocrine disorders: Extraordinary efficiency of hydroxychloroquine and mechanism hypothesis. Eur J Neurol. 2021 Mar;28(3):928-933. doi: 10.1111/ene.14615. PMID: 33270950.
[2] Aoun G, Skandri N, Ghattas H, Maksoud C. Melkersson-Rosenthal Syndrome in a 38-Year-Old Female Patient: A Rare Case With Complete Triad. Cureus. 2022 Jul 28;14(7):e27427. doi: 10.7759/cureus.27427. PMID: 36051736; PMCID: PMC9420175.
[3] Dhawan SR, Saini AG, Singhi PD. Management Strategies of Melkersson-Rosenthal Syndrome: A Review. Int J Gen Med. 2020 Feb 26;13:61-65. doi: 10.2147/IJGM.S186315. PMID: 32161488; PMCID: PMC7049838.
[4] Gavioli CFB, Nico MMS, Panajotopoulos N, Rodrigues H, Rosales CB, Valente NYS, Florezi GP, Lourenço SV. A case-control study of HLA alleles in Brazilian patients with Melkersson-Rosenthal syndrome. Eur J Med Genet. 2020 Jul;63(7):103879. doi: 10.1016/j.ejmg.2020.103879. PMID: 32045706.
[5] Xu XG, Guan LP, Lv Y, et al. Exome sequencing identifies FATP1 mutation in Melkersson-Rosenthal syndrome. J Eur Acad Dermatol Venereol. 2017 May;31(5):e230-e232. doi: 10.1111/jdv.14042. PMID: 27862329.
[6] Wu A, Zhang Y, Cao W, et al. A case of Melkersson-Rosenthal syndrome with temporomandibular joint osteoarthritis: multidisciplinary treatment and autoimmune etiological hypothesis. BMC Oral Health. 2024 Aug 13;24(1):935. doi: 10.1186/s12903-024-04723-7. PMID: 39135018; PMCID: PMC11320842.
[7] Lee YJ, Cheon CK, Yeon GM, Kim YM, Nam SO. Melkersson-Rosenthal syndrome with Hashimoto thyroiditis in a 9-year-old girl: an autoimmune disorder. Pediatr Neurol. 2014 May;50(5):503-6. doi: 10.1016/j.pediatrneurol.2014.01.010. PMID: 24656464.
[8] Apaydin R, Bahadir S, Kaklikkaya N, Bilen N, Bayramgürler D. Possible role of Mycobacterium tuberculosis complex in Melkersson-Rosenthal syndrome demonstrated with Gen-Probe amplified Mycobacterium tuberculosis direct test. Australas J Dermatol. 2004 May;45(2):94-9. doi: 10.1111/j.1440-0960.2004.00071.x. Erratum in: Australas J Dermatol. 2005 Aug;46(3):209. Kakklikkaya, N [corrected to Kaklikkaya, N]. PMID: 15068454.
[9] Zhang W, Yan Z. A case of complete Melkersson-Rosenthal syndrome: Possibly associated with Mycolicibacterium fortuitum from odontogenic origin. J Dermatol. 2023 Jul;50(7):935-937. doi: 10.1111/1346-8138.16751. PMID: 36815397.
[10] Martins JA, Azenha A, Almeida R, Pinheiro JP. Melkersson-Rosenthal syndrome with coeliac and allergic diseases. BMJ Case Rep. 2019 Aug 28;12(8):e229857. doi: 10.1136/bcr-2019-229857. PMID: 31466978; PMCID: PMC6721715.
[11] Cockerham KP, Hidayat AA, Cockerham GC, et al. Melkersson-Rosenthal syndrome: new clinicopathologic findings in 4 cases. Arch Ophthalmol. 2000 Feb;118(2):227-32. doi: 10.1001/archopht.118.2.227. PMID: 10676788.
[12] Casper J, Mohammad-Khani S, Schmidt JJ, et al. Melkersson-Rosenthal syndrome in the context of sarcoidosis: a case report. J Med Case Rep. 2021 Oct 4;15(1):488. doi: 10.1186/s13256-021-03044-5. PMID: 34602094; PMCID: PMC8489098.
[13] Savasta S, Rossi A, Foiadelli T, et al. Melkersson⁻Rosenthal Syndrome in Childhood: Report of Three Paediatric Cases and a Review of the Literature. Int J Environ Res Public Health. 2019 Apr 10;16(7):1289. doi: 10.3390/ijerph16071289. PMID: 30974872; PMCID: PMC6479526.
[14] Pavuluri A, Smith S, Narsinghani U. Rare diagnosis of Melkersson-Rosenthal syndrome in a paediatric patient. BMJ Case Rep. 2021 Jun 11;14(6):e238431. doi: 10.1136/bcr-2020-238431. PMID: 34116987; PMCID: PMC8201983.
[15] Banks T, Gada S. A comprehensive review of current treatments for granulomatous cheilitis. Br J Dermatol. 2012 May;166(5):934-7. doi: 10.1111/j.1365-2133.2011.10794.x. PMID: 22187977.
[16] Cancian M, Giovannini S, Angelini A, et al. Melkersson-Rosenthal syndrome: a case report of a rare disease with overlapping features. Allergy Asthma Clin Immunol. 2019 Jan 5;15:1. doi: 10.1186/s13223-018-0316-z. PMID: 30622569; PMCID: PMC6320604.
[17] Alessi DM, Azhdam AM, Borrelli M. A Case of Melkersson-Rosenthal Syndrome Treated With 5-FU. Ear Nose Throat J. 2021 Sep;100(6_suppl):873S-875S. doi: 10.1177/01455613211038391. PMID: 34448401.
[18] Błochowiak K, Kraiz A, Bowszyc-Dmochowska M, Paszyńska E, Jenerowicz D. Miescher's Cheilitis as a Diagnostic and Therapeutic Challenge-A Case Report. Medicina (Kaunas). 2025 Feb 9;61(2):299. doi: 10.3390/medicina61020299. PMID: 40005416; PMCID: PMC11857799.
[19] Mishra S, Badouriya SKS, Vaidya S. Early Onset Melkersson–Rosenthal Syndrome: A Case Managed Conservatively in an ENT Outpatient Clinic. Indian J Otolaryngol Head Neck Surg 2006; 78:1238–1240. https://doi.org/10.1007/s12070-025-06242-5
[20] Oudrhiri L, Chiheb S, Marnissi F, Zamiati S, Benchikhi H. Successful treatment of Miescher's cheilitis in Melkersson-Rosenthal syndrome with betamethasone injections and doxycycline. Pan Afr Med J. 2012;13:75. PMID: 23397029; PMCID: PMC3567407.
How to Cite
Urdea, D., Severin, F. ., Costan, V. V., & Mereuta, D. V. (2026). Melkersson-Rosenthal syndrome in an allergic patient successfully treated with fresh frozen plasma. Archive of Clinical Cases, 13(2), 26-29. https://doi.org/10.22551/2026.51.1302.10337
Section
Case Reports

How to Cite

Urdea, D., Severin, F. ., Costan, V. V., & Mereuta, D. V. (2026). Melkersson-Rosenthal syndrome in an allergic patient successfully treated with fresh frozen plasma. Archive of Clinical Cases, 13(2), 26-29. https://doi.org/10.22551/2026.51.1302.10337