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皮肤滤泡性淋巴瘤

Cutaneous follicular lymphoma.

作者信息

Garcia C F, Weiss L M, Warnke R A, Wood G S

出版信息

Am J Surg Pathol. 1986 Jul;10(7):454-63. doi: 10.1097/00000478-198607000-00002.

Abstract

Fifteen cases of cutaneous follicular lymphoma were evaluated clinically, histologically, and immunologically. Nine of the patients presented with skin disease alone, which showed a predilection for the scalp and forehead. The six remaining cases had either concurrent or secondary cutaneous involvement. All of the cases had a nodular configuration which was evident histologically or immunologically. In many cases, the diagnostic microscopic fields were in the deep dermis or subcutis, with nonspecific inflammation in the superficial dermis. The cases consisted of five small cleaved, seven mixed, and three large cell follicular lymphomas. A senior dermatopathologist diagnosed four of the 15 cases as benign, indicating the difficulty of diagnosis by morphology alone when the biopsy is small or the inflammatory component is prominent. This underscores the importance of large, deep biopsies for accurate histologic diagnosis. Immunological studies confirmed the B cell lineage of these lesions. An unexpectedly high proportion of immunoglobulin-negative cases (eight cases) was found, especially among the primary cutaneous follicular lymphomas (six of nine cases). Immunoglobulin-expressing cases exhibited monotypic immunoglobulin light-chain staining of tumor cells. In all cases, the dendritic reticulum cell network within lymphoma follicles lacked the polytypic immunoglobulin complexes characteristic of reactive follicles. As described previously for follicular lymphomas in lymph nodes, many cases exhibited polytypic follicular mantle zones similar to reactive follicles. The low-grade nature of these lymphomas was supported by clinical follow-up. We conclude that given adequate sampling, cutaneous follicular lymphomas can usually be diagnosed by histologic criteria similar to those used for lymph nodes; however, immunohistologic studies are an important adjunct.

摘要

对15例皮肤滤泡性淋巴瘤进行了临床、组织学和免疫学评估。其中9例患者仅表现为皮肤疾病,病变多累及头皮和前额。其余6例患者同时存在或继发皮肤受累。所有病例均呈结节状,在组织学或免疫学上表现明显。在许多病例中,诊断性显微镜视野位于真皮深层或皮下组织,而浅表真皮有非特异性炎症。这些病例包括5例小裂细胞型、7例混合型和3例大细胞型滤泡性淋巴瘤。一位资深皮肤病理学家将15例中的4例诊断为良性,这表明当活检组织小或炎症成分突出时,仅靠形态学诊断存在困难。这凸显了进行大面积、深部活检以获得准确组织学诊断的重要性。免疫学研究证实了这些病变的B细胞谱系。发现免疫球蛋白阴性病例的比例出乎意料地高(8例),尤其是在原发性皮肤滤泡性淋巴瘤中(9例中有6例)。表达免疫球蛋白的病例显示肿瘤细胞呈单型免疫球蛋白轻链染色。在所有病例中,淋巴瘤滤泡内的树突状网状细胞网络缺乏反应性滤泡特有的多型免疫球蛋白复合物。如先前关于淋巴结滤泡性淋巴瘤的描述,许多病例表现出与反应性滤泡相似的多型滤泡套区。临床随访支持了这些淋巴瘤的低级别性质。我们得出结论,在进行充分取材的情况下,皮肤滤泡性淋巴瘤通常可通过与用于淋巴结相同的组织学标准进行诊断;然而,免疫组织学研究是一项重要的辅助手段。

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