Citation: | HU Zhonghui, YANG Lu, LIU Yuehua, JIN Hongzhong, XU Qiang, LIU Wenjing, LUO Yaping, YANG Hongbo, WANG Tao. Necrolytic Migratory Erythema—A Case Report of Pancreatic Occupying Lesion[J]. Journal of Rare Diseases, 2023, 2(3): 427-431. DOI: 10.12376/j.issn.2097-0501.2023.03.014 |
Glucagonoma is a rare neuroendocrine tumor of α cells of the pancreas. The tumor excessively secretes glucagon and causes glucagonoma syndrome.70%-90% of patients with glucagonoma will develop necrolytic migratory erythema (NME). We reported a patient of glucagonoma syndrome who was presented to the dermatology outpatient clinic with a 2-year-history of recurrent erythema and scaling on the skin migrating throughout the body. A skin biopsy was performed and resulting features matched with NME, whilst imaging examinations suggested a soft tissue density tumor present in the tail of the pancreas with somatostatin receptor expression and laboratory tests found an elevated levels of serum glucagon. After the diagnosis was confirmed, the patient was treated with surgical resection of the glucagonoma and the skin eruptions resolved rapidly in 4 days. Meanwhile, we reviewed relevant literature published in recent years and summarized its clinical characteristics in order to improve its understanding by clinicians, including clinical manifestations, laboratory and imaging examinations, diagnosis and treatments.
[1] |
Luber AJ, Ackerman LS, Culpepper KS, et al. Paediatric necrolytic migratory erythema as a presenting sign of glucagonoma syndrome[J]. Br J Dermatol, 2016, 174(5): 1092-1095. doi: 10.1111/bjd.14298
|
[2] |
Al-Faouri A, Ajarma K, Alghazawi S, et al. Glucagonoma and glucagonoma syndrome: a case report with review of recent advances in management[J]. Case Rep Surg, 2016, 2016: 1484089.
|
[3] |
Wermers RA, Fatourechi V, Wynne AG, et al. The glucagonoma syndrome. Clinical and pathologic features in 21 patients[J]. Medicine (Baltimore), 1996, 75(2): 53-63. doi: 10.1097/00005792-199603000-00002
|
[4] |
Tolliver S, Graham J, Kaffenberger BH. A review of cutaneous manifestations within glucagonoma syndrome: necrolytic migratory erythema[J]. Int J Dermatol, 2018, 57(6): 642-645. doi: 10.1111/ijd.13947
|
[5] |
Daly DM, Thompson B, Low J, et al. Emergency pancreatic resection for glucagonoma associated with severe necrolytic migratory erythema[J]. ANZ J Surg, 2019, 89(5): 599-602. doi: 10.1111/ans.14186
|
[6] |
Remes-Troche JM, García-de-Acevedo B, Zuñiga-Varga J, et al. Necrolytic migratory erythema: a cutaneous clue to glucagonoma syndrome[J]. J Eur Acad Dermatol Venereol, 2004, 18(5): 591-595. doi: 10.1111/j.1468-3083.2004.00981.x
|
[7] |
Liu JW, Qian YT, Ma DL. Necrolytic migratory erythema[J]. JAMA Dermatol, 2019, 155(10): 1180. doi: 10.1001/jamadermatol.2019.1658
|
[8] |
John AM, Schwartz RA. Glucagonoma syndrome: a review and update on treatment[J]. J Eur Acad Dermatol Venereol, 2016, 30(12): 2016-2022. doi: 10.1111/jdv.13752
|
[9] |
Compton NL, Chien AJ. A rare but revealing sign: necrolytic migratory erythema[J]. Am J Med, 2013, 126(5): 387-389. doi: 10.1016/j.amjmed.2013.01.012
|
[10] |
Gracia-Darder I, Ramos D, Boix-Vilanova J, et al. Necrolytic migratory erythema associated with painful plantar keratoderma. A new diagnostic clue for this paraneoplastic syndrome?[J]. An Bras Dermatol, 2020, 95(5): 666-668. doi: 10.1016/j.abd.2020.02.011
|
[11] |
Kitamura Y, Sato M, Hatamochi A, et al. Necrolytic migratory erythema without glucagonoma associated with hepatitis B[J]. Eur J Dermatol, 2005, 15(1): 49-51.
|
[12] |
Chiyomaru K, Takai T, Ohashi A, et al. Necrolytic migratory erythema with cholangiocarcinoma: pseudoglucagonoma syndrome[J]. Eur J Dermatol, 2010, 20(2): 238-239. doi: 10.1684/ejd.2010.0878
|
[13] |
Technau K, Renkl A, Norgauer J, et al. Necrolytic migratory erythema with myelodysplastic syndrome without glucagonoma[J]. Eur J Dermatol, 2005, 15(2): 110-112.
|
[14] |
Lobo I, Carvalho A, Amaral C, et al. Glucagonoma syndrome and necrolytic migratory erythema[J]. Int J Dermatol, 2010, 49(1): 24-29. doi: 10.1111/j.1365-4632.2009.04220.x
|
[15] |
Ramage JK, Ahmed A, Ardill J, et al. Guidelines for the management of gastroenteropancreatic neuroendocrine (including carcinoid) tumours (NETs)[J]. Gut, 2012, 61(1): 6-32. doi: 10.1136/gutjnl-2011-300831
|
[16] |
Zhu WF, Zheng SS. Glucagonoma syndrome with necrolytic migratory erythema as initial manifestation[J]. Hepatobiliary Pancreat Dis Int, 2021, 20(6): 598-600. doi: 10.1016/j.hbpd.2021.09.005
|
[17] |
Wu SL, Bai JG, Xu J, et al. Necrolytic migratory erythema as the first manifestation of pancreatic neuroendocrine tumor[J]. World J Surg Oncol, 2014, 12: 220. doi: 10.1186/1477-7819-12-220
|
[18] |
Jiménez-Gallo D, Ossorio-García L, de la Varga-Martínez R, et al. Necrolytic migratory erythema associated with glucagonoma treated successfully with cyclosporine[J]. Dermatol Ther, 2017, 30(4). 10.1111/dth. 12498.
|
[19] |
Tremblay C, Marcil I. Necrolytic migratory erythema: a forgotten paraneoplastic condition[J]. J Cutan Med Surg, 2017, 21(6): 559-561. doi: 10.1177/1203475417719051
|