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Early-stage mycosis fungoides variants: case-based review.早期蕈样肉芽肿变异型:基于病例的综述。
Ann Diagn Pathol. 2010 Oct;14(5):369-85. doi: 10.1016/j.anndiagpath.2010.06.003.
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Cutaneous T cell lymphoma-mycosis fungoides and Sezary syndrome: an update.皮肤 T 细胞淋巴瘤-蕈样肉芽肿和塞扎里综合征:最新进展。
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Early mycosis fungoides vs. inflammatory mimics: how reliable is histology?
Indian J Dermatol Venereol Leprol. 2008 Sep-Oct;74(5):462-6. doi: 10.4103/0378-6323.42644.
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Lesional gene expression profiling in cutaneous T-cell lymphoma reveals natural clusters associated with disease outcome.皮肤T细胞淋巴瘤的病灶基因表达谱分析揭示了与疾病预后相关的自然聚类。
Blood. 2007 Oct 15;110(8):3015-27. doi: 10.1182/blood-2006-12-061507. Epub 2007 Jul 16.
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Incidence of cutaneous T-cell lymphoma in the United States, 1973-2002.1973 - 2002年美国皮肤T细胞淋巴瘤的发病率
Arch Dermatol. 2007 Jul;143(7):854-9. doi: 10.1001/archderm.143.7.854.
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Mycosis fungoides: a dermatological masquerader.蕈样肉芽肿:一种皮肤伪装者。
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7
Biological insights into the pathogenesis of cutaneous T-cell lymphomas (CTCL).皮肤T细胞淋巴瘤(CTCL)发病机制的生物学见解。
Semin Oncol. 2006 Feb;33(1 Suppl 3):S3-6. doi: 10.1053/j.seminoncol.2005.12.015.
8
Defining early mycosis fungoides.蕈样肉芽肿早期的定义。
J Am Acad Dermatol. 2005 Dec;53(6):1053-63. doi: 10.1016/j.jaad.2005.08.057.
9
Histopathologic features of early (patch) lesions of mycosis fungoides: a morphologic study on 745 biopsy specimens from 427 patients.蕈样肉芽肿早期(斑片)损害的组织病理学特征:对427例患者的745份活检标本的形态学研究
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Familial mycosis fungoides: report of 6 kindreds and a study of the HLA system.家族性蕈样肉芽肿:6个家族的报告及HLA系统研究
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蕈样肉芽肿早期的组织学谱:对58例沙特阿拉伯患者的研究

The Histological Spectrum of Early Mycosis Fungoides: A Study of 58 Saudi Arab patients.

作者信息

Arafah Maha, Zaidi Shaesta Naseem, Kfoury Hala Kassouf, Al Rikabi Ammar, Al Ghamdi Khalid

出版信息

Oman Med J. 2012 Mar;27(2):134-9. doi: 10.5001/omj.2012.28.

DOI:10.5001/omj.2012.28
PMID:22496939
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3321345/
Abstract

OBJECTIVES

The histopathological diagnosis of Mycosis Fungoides (MF) is challenging in its early stages and can easily be confused with inflammatory dermatoses. This study aims to; (i) assess the frequency and significance of different histopathological parameters in early MF, seen in Saudi patients, and (ii) to study the utility of these parameters in differentiating between early MF and inflammatory dermatoses.

METHODS

This is a five years study of 66 skin biopsies generated from 58 patients with clinically suspicious MF lesions or early patch stage MF. These cases were retrieved from the archives of the Department of Pathology, King Khalid University Hospital, Riyadh from the year 2002 to 2006. Histological criteria were assessed and graded semi-quantitatively on a four-point scale by a dermatopathologist and two pathologists independently.

RESULTS

The histological parameters suggesting the diagnosis in early stages MF include epidermotropism, dermal fibrosis, Pautrier's micro abscesses, Basal alignment of neoplastic lymphocytes, hyperconvoluted dermal and epidermal lymphocytes and grandiosity sign (size of lymphocytes becoming larger as they migrate towards granular layer of epidermis). These parameters on univariate analysis achieved statistical significance (p<0.05) in differentiating MF from non-MF cases. In addition, hyperconvoluted dermal and epidermal lymphocytes proved to be highly reliable with high specificity and sensitivity.

CONCLUSION

The histopathological diagnosis of early MF lesions and their discrimination from inflammatory simulators can be achieved by carefully observing the hyperconvoluted dermal and epidermal lymphocytes along with the constellation of the other parameters.

摘要

目的

蕈样肉芽肿(MF)的组织病理学诊断在早期具有挑战性,容易与炎症性皮肤病混淆。本研究旨在:(i)评估沙特患者早期MF中不同组织病理学参数的频率和意义,以及(ii)研究这些参数在区分早期MF和炎症性皮肤病中的效用。

方法

这是一项为期五年的研究,对58例临床疑似MF病变或早期斑块期MF患者的66份皮肤活检样本进行分析。这些病例取自利雅得国王哈立德大学医院病理科2002年至2006年的存档。由一名皮肤病理学家和两名病理学家独立地根据四点量表对组织学标准进行半定量评估和分级。

结果

提示早期MF诊断的组织学参数包括亲表皮现象、真皮纤维化、Pautrier微脓肿、肿瘤性淋巴细胞的基底排列、真皮和表皮淋巴细胞高度卷曲以及夸张征(淋巴细胞在向表皮颗粒层迁移时变大)。在单变量分析中,这些参数在区分MF与非MF病例方面具有统计学意义(p<0.05)。此外,真皮和表皮淋巴细胞高度卷曲被证明具有高度可靠性,特异性和敏感性都很高。

结论

通过仔细观察真皮和表皮淋巴细胞高度卷曲以及其他参数的组合,可以实现早期MF病变的组织病理学诊断及其与炎症性模拟病变的鉴别。