组织细胞样甜证样表现为成熟浆细胞样树突状细胞增生。

Q3 Medicine
Katelyn Rypka, John Meisenheimer, Rob Shaver, Adarsh Ravishankar, Justin Peltola, Hector Mesa, Erick Jacobson-Dunlop, Sigrid Collier, Kevin Gaddis, Noah Goldfarb
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引用次数: 0

摘要

成熟浆细胞样树突状细胞增生与髓系肿瘤有关,最常见的是慢性髓单细胞白血病。浆细胞样树突状细胞在形态和免疫表型上与淋巴细胞和组织细胞相似。成熟浆细胞样树突状细胞增殖可能因此无法识别,如果不怀疑诊断和浆细胞样树突状细胞不进行适当的染色。在此,我们报告一例成熟浆细胞样树突状细胞增生,在临床和组织学上伪装成组织细胞样Sweet综合征。该患者先前被诊断为成熟浆细胞样树突状细胞增生,表现为粉红色、水肿、瘙痒丘疹和斑块,在急性髓单细胞白血病诱导化疗后最初消退。然而,在服用非格拉西汀治疗中性粒细胞减少症后的几周内,他在躯干出现了硬化的紫癜斑块。活组织检查显示明显的真皮水肿,间质性,浅表性和深部浸润,组织细胞样细胞出现与组织细胞样Sweet综合征有关的细胞。进一步检查表明,浸润主要由CD3-、CD4+、CD34-、CD123+、CD56-、CD68-、髓过氧化物酶阴性的单核细胞组成,与成熟浆细胞样树突状细胞增殖一致。本病例表明MPDCP在临床和组织学上表现为组织细胞样Sweet综合征,但髓过氧化物酶染色阴性的皮疹鉴别诊断中应予以考虑。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Histiocytoid Sweet syndrome-like presentation of mature plasmacytoid dendritic cell proliferation.

Mature plasmacytoid dendritic cell proliferation is a condition associated with myeloid neoplasms, most commonly chronic myelomonocytic leukemia. Plasmacytoid dendritic cells can resemble lymphocytes and histiocytes morphologically and immunophenotypically. Mature plasmacytoid dendritic cell proliferation may therefore go unrecognized if the diagnosis is not suspected and appropriate stains for plasmacytoid dendritic cells are not performed. Herein, we present a case of mature plasmacytoid dendritic cell proliferation masquerading clinically and histologically as histiocytoid Sweet syndrome. The patient, who had previously been diagnosed with mature plasmacytoid dendritic cell proliferation that presented as pink, edematous, pruritic papules and plaques, had initially resolved following induction chemotherapy for acute myelomonocytic leukemia. However, he presented later with indurated purpuric plaques on the trunk within weeks of receiving filgrastim for neutropenia. Biopsies demonstrated marked dermal edema, interstitial, superficial, and deep infiltrate with histiocytoid appearing cells concerning for histiocytoid Sweet syndrome. Further work-up demonstrated that the infiltrate was predominantly composed of CD3-, CD4+, CD34-, CD123+, CD56-, CD68-, myeloperoxidase negative mononuclear cells consistent with mature plasmacytoid dendritic cell proliferation. This case demonstrates that MPDCP should be considered in the differential diagnosis of eruptions that clinically and histologically look like histiocytoid Sweet syndrome but stain negatively for myeloperoxidase.

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来源期刊
Dermatology online journal
Dermatology online journal Medicine-Dermatology
CiteScore
1.70
自引率
0.00%
发文量
200
审稿时长
6 weeks
期刊介绍: An open-access, refereed publication intended to meet reference and education needs of the international dermatology community since 1995. Dermatology Online Journal is supported by the Department of Dermatology UC Davis, and by the Northern California Veterans Administration.
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