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Journal of Dermatological Treatment Volume 34, 2023 - Issue 1
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Case Report

An 8-year follow-up of IgG4-related skin disease presented with generalized ALHE-like eruptions: successful treatment of glucocorticoid and cyclophosphamide

Guanyu Wanga Department of Dermatology, Peking University Third Hospital, Beijing, ChinaORCID Iconhttps://orcid.org/0000-0002-6723-8158View further author information
ORCID Icon,
Ping Tub Department of Dermatology, Peking University First Hospital, Beijing, ChinaView further author information
,
Jing Suc Department of Pathology, Peking University Third Hospital, Beijing, ChinaView further author information
,
Wenting Wua Department of Dermatology, Peking University Third Hospital, Beijing, ChinaView further author information
,
Chunlei Zhanga Department of Dermatology, Peking University Third Hospital, Beijing, ChinaView further author information
,
Wenhui Wanga Department of Dermatology, Peking University Third Hospital, Beijing, ChinaView further author information
&
Weiwei Lia Department of Dermatology, Peking University Third Hospital, Beijing, ChinaCorrespondence[email protected]
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Article: 2279899 | Received 15 Oct 2023, Accepted 01 Nov 2023, Published online: 27 Nov 2023

References

  • Adler BL, Krausz AE, Minuti A, et al. Epidemiology and treatment of angiolymphoid hyperplasia with eosinophilia (ALHE): a systematic review. J Am Acad Dermatol. 2016;74(3):1–4. doi:10.1016/j.jaad.2015.10.011.
  • Umehara H, Okazaki K, Kawa S, et al. The 2020 revised comprehensive diagnostic (RCD) criteria for IgG4-RD. Mod Rheumatol. 2021;31(3):529–533. doi:10.1080/14397595.2020.1859710.
  • Bennett AE, Fenske NA, Rodriguez-Waitkus P, et al. IgG4-related skin disease may have distinct systemic manifestations: a systematic review. Int J Dermatol. 2016;55(11):1184–1195. doi:10.1111/ijd.13369.
  • Umehara H, Okazaki K, Kawano M, et al. How to diagnose IgG4-related disease. Ann Rheum Dis. 2017;76(11):e46–e46. doi:10.1136/annrheumdis-2017-211330.
  • Ingen-Housz-Oro S, Ortonne N, Elhai M, et al. IgG4-related skin disease successfully treated by thalidomide: a report of 2 cases with emphasis on pathological aspects. JAMA Dermatol. 2013;149(6):742–747. doi:10.1001/jamadermatol.2013.2625.
  • Hegde P, Relhan V, Tomar R. IgG4-related disease: a rare case of isolated cutaneous involvement. Clin Exp Dermatol. 2021;46(2):343–345. doi:10.1111/ced.14334.
  • Tokura Y, Yagi H, Yanaguchi H, et al. IgG4-related skin disease. Br J Dermatol. 2014;171(5):959–967. doi:10.1111/bjd.13296.
  • Lanzillotta M, Mancuso G, Della-Torre E. Advances in the diagnosis and management of IgG4 related disease. BMJ. 2020;369:m1067. doi:10.1136/bmj.m1067.
  • Liu Z, Nie Y, Peng Y, et al. The external validation of the 2019 ACR/EULAR classification criteria for IgG4-related disease in a large cohort from China. Semin Arthritis Rheum. 2023;61:152202. doi:10.1016/j.semarthrit.2023.152202.
  • Hamaguchi Y, Fujimoto M, Matsushita Y, et al. IgG4-related skin disease, a mimic of angiolymphoid hyperplasia with eosinophilia. Dermatology. 2011;223(4):301–305. doi:10.1159/000335372.
  • Fernandez-Flores A, Cassarino DS. Three unusual histopathological presentations of angiolymphoid hyperplasia with eosinophilia. J Cutan Pathol. 2017;44(3):300–306. doi:10.1111/cup.12886.
  • Sato Y, Takeuchi M, Takata K, et al. Clinicopathologic analysis of IgG4-related skin disease. Mod Pathol. 2013;26(4):523–532. doi:10.1038/modpathol.2012.196.
  • Yunyun F, Yu C, Panpan Z, et al. Efficacy of cyclophosphamide treatment for immunoglobulin G4-related disease with addition of glucocorticoids. Sci Rep. 2017;7(1):6195. doi:10.1038/s41598-017-06520-5.

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