Department of Pathology and Immunology, Washington University School of Medicine, St. Louis, Missouri, USA.
Dermatology Associates of Macomb-Oakland, Novi, Michigan, USA.
J Cutan Pathol. 2021 Mar;48(3):439-450. doi: 10.1111/cup.13932. Epub 2020 Dec 18.
Within the literature, there is overlap in the histopathological features described in eosinophilic folliculitis associated with chronic lymphocytic leukemia (CLL), eosinophilic dermatosis of hematologic malignancy, and acneiform follicular mucinosis. These disorders are described with varying degrees of superficial and deep lymphocytic and eosinophilic inflammation demonstrating perivascular, perifollicular, and folliculocentric involvement with or without follicular mucin deposition. Given significant histopathological overlap, these diagnoses may represent a continuum on a spectrum of dermatoses. Here, we present two cases with histopathological elements that reflect components of this clinicopathological spectrum and compare our findings with previously reported cases to compare and contrast reported features. Our first case is a 71-year-old African American man with long-standing CLL who developed a pruritic erythematous papular eruption on the face and chest with biopsy revealing a dense folliculotropic lymphocytic infiltrate with conspicuous eosinophils and follicular mucinosis. Our second case is a 70-year-old Caucasian man recently diagnosed with CLL/small lymphocytic lymphoma who developed an erythematous papular rash on the neck and face with biopsy revealing superficial and deep perivascular and periadnexal lymphocytic inflammation with scattered eosinophils. Characterization of our two cases and comparison with available literature suggest that these disorders may represent a continuum of dermatoses.
在文献中,与慢性淋巴细胞白血病(CLL)相关的嗜酸性毛囊炎、血液恶性肿瘤嗜酸性皮肤病和痤疮样滤泡黏蛋白病的组织病理学特征存在重叠。这些疾病的描述具有不同程度的浅表和深层淋巴细胞和嗜酸性炎症,表现为血管周围、毛囊周围和滤泡中心受累,伴有或不伴有滤泡黏蛋白沉积。鉴于显著的组织病理学重叠,这些诊断可能代表皮肤病谱上的一个连续体。在这里,我们介绍了两例具有反映该临床病理谱成分的组织病理学特征的病例,并将我们的发现与以前报道的病例进行比较,以比较和对比报告的特征。我们的第一个病例是一名 71 岁的非裔美国男性,患有长期 CLL,他的面部和胸部出现瘙痒性红斑丘疹性皮疹,活检显示密集的滤泡性淋巴细胞浸润,伴有明显的嗜酸性粒细胞和滤泡黏蛋白病。我们的第二个病例是一名 70 岁的白人男性,最近被诊断为 CLL/小淋巴细胞淋巴瘤,他的颈部和面部出现红斑丘疹性皮疹,活检显示浅表和深层血管周围和附属器周围淋巴细胞炎症,伴有散在的嗜酸性粒细胞。我们的两个病例的特征描述并与可用文献进行比较表明,这些疾病可能代表皮肤病的一个连续体。