首页> 外文期刊>American Journal of Dermatopathology >Treated Whipple disease with erythema nodosum leprosum-like lesions: Cutaneous PAS-positive macrophages slowly decrease with time and are associated with lymphangiectases: A case report
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Treated Whipple disease with erythema nodosum leprosum-like lesions: Cutaneous PAS-positive macrophages slowly decrease with time and are associated with lymphangiectases: A case report

机译:结节性红斑样麻风样病变治疗的Whipple病:皮肤PAS阳性巨噬细胞随时间缓慢减少,并与淋巴管扩张酶相关:一例报告

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Pathologically, Whipple disease (WD) is characterized by the accumulation of myriad macrophages parasitized by Tropheryma whipplei (TW) bacilli denoted by periodic acid-Schiff (PAS) positivity. These PAS+ macrophages are typically found in the duodenum associated with lymphangiectasia. Recently, we reported the presence of PAS+ macrophages and free TW in erythema nodosum leprosum (ENL)-like lesions and normal skin in a patient with WD who suffered from the immune reconstitution inflammatory syndrome (IRIS). We extend that report by describing the clinical and pathologic findings over 5 years of follow-up. First, the IRIS gradually diminished and abated over 18-month time. Second, at no point did WD recur, and all duodenal and skin biopsies tested by polymerase chain reaction were negative for TW DNA. Third, PAS+ macrophages were identified in 26 of 27 skin biopsies (96%) and decreased along with free TW over time. Fourth, ENL-like lesions had significantly greater numbers of PAS+ macrophages than normal skin. Moreover, normal abdominal skin (region of ENL-like lesions) had greater PAS+ counts than arm skin (not a site of IRIS). Last, lymphangiectases, a histologic sign of lymphostasis, was found in all skin biopsies. Overall, these findings implicate bacillary burden as a factor in the immune tolerance to live TW in active WD and the initiation of ENL-like nodules against deadonreplicative TW in treated WD. In addition, poor lymphatic drainage is likely responsible for the gradual clearance of TW from the skin and the impaired delayed-type hypersensitivity reaction (absence of activated macrophages) against TW found in WD, presumptively due to reduced/absent immune cell trafficking necessary for lymphocyte-macrophage interactions and induction of adaptive immunity.
机译:病理上,Whipple病(WD)的特征在于无数巨噬细胞的积累,而巨噬细胞是由高碘酸希夫(PAS)阳性表示的特发性疟原虫(TW)细菌所寄生。这些PAS +巨噬细胞通常在与淋巴管扩张相关的十二指肠中发现。最近,我们报道了患有免疫重建性炎症综合症(IRIS)的WD患者中,结节性红斑(ENL)样病变和正常皮肤中存在PAS +巨噬细胞和游离TW。我们通过描述5年随访的临床和病理发现来扩展该报告。首先,在18个月的时间内,IRIS逐渐减少并减弱。其次,WD完全没有复发,并且通过聚合酶链反应测试的所有十二指肠和皮肤活检对TW DNA均为阴性。第三,在27例皮肤活检中有26例(96%)识别出PAS +巨噬细胞,并且随着时间的推移,PAS +巨噬细胞随游离TW下降。第四,ENL样病变的PAS +巨噬细胞数量明显多于正常皮肤。此外,正常的腹部皮肤(ENL样病变区域)比手臂皮肤(不是IRIS部位)具有更高的PAS +计数。最后,在所有皮肤活检组织中都发现了淋巴管扩张酶(一种淋巴结的组织学标志)。总体而言,这些发现暗示细菌负担是活动性WD对活TW免疫耐受的因素,也是治疗的WD中针对死/非复制性TW的ENL样结节的起始。此外,不良的淋巴引流可能是皮肤中TW逐渐清除和WD中发现的针对TW的针对TW的迟发型迟发型超敏反应(无活化巨噬细胞)受损的原因,推测是由于淋巴细胞所需的免疫细胞运输减少/缺乏-巨噬细胞相互作用和适应性免疫的诱导。

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