Naraghi Zahra Safee, Seirafi Hassan, Valikhani Mahin, Farnaghi Forshad, Kavusi Susan, Dowlati Yahya
Razi Hospital, Tehran University of Medical Sciences, Tehran, Iran.
Int J Dermatol. 2003 Jan;42(1):45-52. doi: 10.1046/j.1365-4362.2003.01566.x.
The histologic diagnosis of early mycosis fungoides (MF) can be difficult to establish in many instances because the subtle changes observed in patches of MF are also present in many inflammatory dermatoses.
To assess the frequency and significance of many of these histologic parameters, we retrospectively reviewed 50 slides from patients with documented MF in patch, plaque, and tumor stages. The diagnosis of MF was unequivocally established either by the progression of patients to advanced stages of the disease or by indubitable histologic findings. In the second phase of the study, we compared the histologic parameters observed in 24 patch stage MF patients with those in 24 non-MF patients. The non-MF group were patients whose pathologic pattern was suspicious for MF, but who definitely did not have MF on clinical grounds. The two groups were matched by histologic pattern. Two different observers evaluated the slides and the intensities of 32 histologic parameters were graded on a four-point scale to minimize the subjective variability in the histologic reports.
On univariate analysis, the following parameters achieved significance in distinguishing MF from non-MF: Pautrier's microabscesses, haloed lymphocytes, disproportionate epidermotropism, epidermal lymphocytes larger than dermal lymphocytes, hyperconvoluted lymphocytes in the epidermis and dermis, absence of dyskeratosis, and papillary dermal fibrosis. None of these features proved to have additional discriminating power on multivariate analysis.
The efficacy of single histologic features in the diagnosis of early MF is generally poor and, to discriminate MF from its inflammatory simulators, a combination of cytologic and architectural features must be used.
在许多情况下,早期蕈样肉芽肿(MF)的组织学诊断可能难以确立,因为在MF斑块中观察到的细微变化在许多炎症性皮肤病中也存在。
为了评估许多这些组织学参数的频率和意义,我们回顾性地分析了50例记录在案的处于斑块期、斑块期和肿瘤期的MF患者的玻片。MF的诊断通过患者病情进展至疾病晚期或明确的组织学发现得以明确确立。在研究的第二阶段,我们将24例斑块期MF患者的组织学参数与24例非MF患者的进行了比较。非MF组患者的病理模式可疑为MF,但基于临床理由肯定没有MF。两组按组织学模式进行匹配。两名不同的观察者评估玻片,并对32个组织学参数的强度按四点量表进行分级,以尽量减少组织学报告中的主观变异性。
单因素分析显示,以下参数在区分MF与非MF方面具有显著意义:Pautrier微脓肿、晕状淋巴细胞、不成比例的亲表皮现象、表皮淋巴细胞大于真皮淋巴细胞、表皮和真皮中的高度卷曲淋巴细胞、无角化不良以及乳头真皮纤维化。在多因素分析中,这些特征均未显示出额外的鉴别能力。
单一组织学特征在早期MF诊断中的效果通常较差,为了将MF与其炎症性模拟物区分开来,必须结合细胞学和结构特征。