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Insights Into the Characteristics of Sweet Syndrome in Patients With and Without Hematologic Malignancy

Background: Sweet syndrome is a neutrophilic dermatosis that could be associated with malignancy, especially hematologic malignancy. Few studies have systematically elaborated on this disorder and its features related with hematologic malignancy. Objective: This study aimed to describe the clinicopa...

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Autores principales: Zheng, Siting, Li, Sheng, Tang, Shunli, Pan, Yunlei, Ding, Yuwei, Qiao, Jianjun, Fang, Hong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7039821/
https://www.ncbi.nlm.nih.gov/pubmed/32133363
http://dx.doi.org/10.3389/fmed.2020.00020
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author Zheng, Siting
Li, Sheng
Tang, Shunli
Pan, Yunlei
Ding, Yuwei
Qiao, Jianjun
Fang, Hong
author_facet Zheng, Siting
Li, Sheng
Tang, Shunli
Pan, Yunlei
Ding, Yuwei
Qiao, Jianjun
Fang, Hong
author_sort Zheng, Siting
collection PubMed
description Background: Sweet syndrome is a neutrophilic dermatosis that could be associated with malignancy, especially hematologic malignancy. Few studies have systematically elaborated on this disorder and its features related with hematologic malignancy. Objective: This study aimed to describe the clinicopathological characteristics, treatment, and outcome of Sweet syndrome and to evaluate patient characteristics associated with hematologic malignancy. Methods: We retrospectively reviewed patients with Sweet syndrome at the Department of Dermatology, the First Affiliated Hospital of Zhejiang University from October 2010 to February 2019. Results: The study included 37 patients (16 men and 21 women), with a mean age of 53 years. Ten patients (27%) were classified as having malignancy-associated Sweet syndrome: nine with a hematologic malignancy including acute myeloid leukemia (4/9, 44%), myelodysplastic syndrome (4/9, 44%), and multiple myeloma (1/9, 11%) and one with a solid tumor diagnosed with liver carcinoma. The mean hemoglobin and platelet levels (P = 0.007 and P = 0.013, respectively), were significantly lower in patients with hematologic malignancy than in those with Sweet syndrome only. No significant difference in histopathology was found between patients with and without hematologic malignancy. Systemic corticosteroids were the most frequently used treatment (24/37, 65%). Higher mortality was found in patients with hematologic malignancy. Conclusion: It is important to assess Sweet syndrome patients who have laboratory evidence of lower hemoglobin and platelet levels for a hematologic malignancy.
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spelling pubmed-70398212020-03-04 Insights Into the Characteristics of Sweet Syndrome in Patients With and Without Hematologic Malignancy Zheng, Siting Li, Sheng Tang, Shunli Pan, Yunlei Ding, Yuwei Qiao, Jianjun Fang, Hong Front Med (Lausanne) Medicine Background: Sweet syndrome is a neutrophilic dermatosis that could be associated with malignancy, especially hematologic malignancy. Few studies have systematically elaborated on this disorder and its features related with hematologic malignancy. Objective: This study aimed to describe the clinicopathological characteristics, treatment, and outcome of Sweet syndrome and to evaluate patient characteristics associated with hematologic malignancy. Methods: We retrospectively reviewed patients with Sweet syndrome at the Department of Dermatology, the First Affiliated Hospital of Zhejiang University from October 2010 to February 2019. Results: The study included 37 patients (16 men and 21 women), with a mean age of 53 years. Ten patients (27%) were classified as having malignancy-associated Sweet syndrome: nine with a hematologic malignancy including acute myeloid leukemia (4/9, 44%), myelodysplastic syndrome (4/9, 44%), and multiple myeloma (1/9, 11%) and one with a solid tumor diagnosed with liver carcinoma. The mean hemoglobin and platelet levels (P = 0.007 and P = 0.013, respectively), were significantly lower in patients with hematologic malignancy than in those with Sweet syndrome only. No significant difference in histopathology was found between patients with and without hematologic malignancy. Systemic corticosteroids were the most frequently used treatment (24/37, 65%). Higher mortality was found in patients with hematologic malignancy. Conclusion: It is important to assess Sweet syndrome patients who have laboratory evidence of lower hemoglobin and platelet levels for a hematologic malignancy. Frontiers Media S.A. 2020-02-18 /pmc/articles/PMC7039821/ /pubmed/32133363 http://dx.doi.org/10.3389/fmed.2020.00020 Text en Copyright © 2020 Zheng, Li, Tang, Pan, Ding, Qiao and Fang. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Medicine
Zheng, Siting
Li, Sheng
Tang, Shunli
Pan, Yunlei
Ding, Yuwei
Qiao, Jianjun
Fang, Hong
Insights Into the Characteristics of Sweet Syndrome in Patients With and Without Hematologic Malignancy
title Insights Into the Characteristics of Sweet Syndrome in Patients With and Without Hematologic Malignancy
title_full Insights Into the Characteristics of Sweet Syndrome in Patients With and Without Hematologic Malignancy
title_fullStr Insights Into the Characteristics of Sweet Syndrome in Patients With and Without Hematologic Malignancy
title_full_unstemmed Insights Into the Characteristics of Sweet Syndrome in Patients With and Without Hematologic Malignancy
title_short Insights Into the Characteristics of Sweet Syndrome in Patients With and Without Hematologic Malignancy
title_sort insights into the characteristics of sweet syndrome in patients with and without hematologic malignancy
topic Medicine
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7039821/
https://www.ncbi.nlm.nih.gov/pubmed/32133363
http://dx.doi.org/10.3389/fmed.2020.00020
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