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蕈样肉芽肿和原发性皮肤边缘区淋巴瘤同时发生:4 例临床病理研究及文献复习。

Concurrent Presentation of Mycosis Fungoides and Primary Cutaneous Marginal Zone LPD: Clinicopathological Study of 4 Cases and Literature Review.

机构信息

Department of Dermatology, Hospital Clínico Universitario Lozano Blesa, Universidad de Zaragoza, Zaragoza, Spain.

Department of Dermatology, Fundación Jiménez Díaz, Universidad Autónoma, Madrid, Spain.

出版信息

Am J Dermatopathol. 2023 Mar 1;45(3):163-169. doi: 10.1097/DAD.0000000000002378. Epub 2023 Jan 10.

Abstract

BACKGROUND

Mycosis fungoides is rarely associated to B-cell malignancies, and the few reported cases are mainly internal lymphomas involving secondarily the skin (ie, chronic lymphocytic leukemia).

OBJECTIVES

The aim of our study is to describe the clinical and histopathological features of 4 patients presenting with 2 concurrent primary cutaneous lymphomas and review the pertinent literature.

METHODS

We identified 4 cases of concurrent primary cutaneous lymphomas in our institutions. An extracutaneous lymphoma was ruled out on the basis of a complete work out. We performed a PubMed search to identify reported cases of primary cutaneous composite or concurrent lymphomas.

RESULTS

Eleven cases of primary cutaneous concurrent lymphomas have been described in the literature. Counting all together (our cases and the cases previously described in the literature), mycosis fungoides was the most frequent primary cutaneous T-cell lymphoma (TCL) (13/15), followed by 1 case of peripheral TCL-NOS and 1 case of subcutaneous panniculitis-like TCL. Regarding the associated primary cutaneous B-cell lymphomas, 8/15 cases consisted of low-grade B-cell lymphomas [that is, 5 marginal zone lymphoma (in the most recent classification reclassified as marginal zone lymphoproliferative disorder, MZLD, 2 follicular-center B-cell lymphoma (primary cutaneous follicle-center lymphoma) and 1 low-grade NOS B-cell lymphoma]; 4/15 were associated to Epstein-Barr virus; 1 case consisted of a methotrexate-associated lymphoproliferative disease, and 2 cases consisted of primary cutaneous diffuse large B-cell lymphoma-leg type.

CONCLUSIONS

Primary cutaneous concurrent lymphomas are exceptional. Clinicopathological correlation and a complete workout to reach the correct diagnosis may guide the appropriate treatment in each case.

摘要

背景

蕈样肉芽肿很少与 B 细胞恶性肿瘤相关,少数报道的病例主要为累及皮肤的继发性内部淋巴瘤(即慢性淋巴细胞白血病)。

目的

我们研究的目的是描述 4 例同时患有 2 种原发性皮肤淋巴瘤的患者的临床和组织病理学特征,并回顾相关文献。

方法

我们在机构中确定了 4 例同时患有原发性皮肤淋巴瘤的病例。根据全面检查排除了皮肤外淋巴瘤。我们在 PubMed 上进行了搜索,以确定报告的原发性皮肤复合或同时性淋巴瘤病例。

结果

文献中描述了 11 例原发性皮肤同时性淋巴瘤。将所有病例(包括我们的病例和文献中以前描述的病例)一起计算,蕈样肉芽肿是最常见的原发性皮肤 T 细胞淋巴瘤(TCL)(13/15),其次是 1 例外周 TCL-NOS 和 1 例皮下脂膜炎样 TCL。关于相关的原发性皮肤 B 细胞淋巴瘤,15 例中有 8 例为低级别 B 细胞淋巴瘤[即 5 例边缘区淋巴瘤(在最新分类中重新归类为边缘区淋巴增生性疾病,MZLD,2 例滤泡中心 B 细胞淋巴瘤(原发性皮肤滤泡中心淋巴瘤)和 1 例低级别NOS B 细胞淋巴瘤];4/15 例与 Epstein-Barr 病毒相关;1 例为甲氨蝶呤相关性淋巴增生性疾病,2 例为原发性皮肤弥漫性大 B 细胞淋巴瘤-腿型。

结论

原发性皮肤同时性淋巴瘤非常罕见。临床病理相关性和全面检查以达到正确诊断可以指导每个病例的适当治疗。

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