Kamimura Anna, Yanagisawa Hiroto, Tsunemi Yuichiro, Kusano Takeru, Arai Eiichi, Tsuchida Tetsuya, Nakamura Koichiro
Department of Dermatology, Saitama Medical University, Iruma-gun, Japan.
Department of General Internal Medicine, Saitama Medical University, Iruma-gun, Japan.
J Dermatol. 2021 May;48(5):695-698. doi: 10.1111/1346-8138.15781. Epub 2021 Feb 13.
We report a rare case of xanthomatized Sweet's syndrome with myelodysplastic syndrome (MDS) in a patient who presented with erythematous plaques on his chest that were elevated and became yellowish. A diagnosis of MDS with single lineage dysplasia was made during the development of the eruption. Bone marrow biopsy showed an increased number of megakaryoblasts. Histopathologically, there was neutrophil infiltration with leukocytoclasia and the infiltration of xanthomatous cells. Immunohistochemical analysis revealed that the xanthomatized cells were predominantly CD163 positive. We propose that our case of xanthomatized neutrophilic dermatosis is a rare clinicopathological variant of Sweet's syndrome associated with a hematologic disorder.
我们报告了一例罕见的伴有骨髓增生异常综合征(MDS)的黄瘤化Sweet综合征病例,患者胸部出现红斑性斑块,斑块隆起并变黄。在皮疹发展过程中诊断为单系发育异常的MDS。骨髓活检显示巨核母细胞数量增加。组织病理学检查发现有中性粒细胞浸润伴核碎裂以及黄瘤细胞浸润。免疫组织化学分析显示,黄瘤化细胞主要为CD163阳性。我们认为,我们的黄瘤化嗜中性皮病病例是与血液系统疾病相关的Sweet综合征的一种罕见临床病理变体。