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系统性滤泡性淋巴瘤皮肤表现的临床病理谱。11例患者的研究。

Clinicopathologic spectrum of cutaneous manifestations in systemic follicular lymphoma. A study of 11 patients.

作者信息

Dabski K, Banks P M, Winkelmann R K

机构信息

Department of Dermatology, Mayo Clinic, Rochester, Minnesota 55905.

出版信息

Cancer. 1989 Oct 1;64(7):1480-5. doi: 10.1002/1097-0142(19891001)64:7<1480::aid-cncr2820640720>3.0.co;2-s.

Abstract

Follicular lymphoma is rarely diagnosed on the basis of only a cutaneous biopsy. Eleven patients with primary follicular lymphoma of lymph nodes who developed skin lesions were studied. Skin lesions involved the scalp, head and neck, trunk, and buttocks and were small cleaved cell type in four cases, large cell type in three cases, and mixed type in four cases. The follicular pattern with a bottom-heavy distribution was identified in only six of the 11 cases. One case showed a nodular, perivascular pattern in the deep dermis and subcutaneous tissue. Four cases were characterized by a diffuse pattern of lymphocytic infiltrate. One patient with a diffuse pattern had an isolated subepidermal band of lymphoma cells representing primary cutaneous T-cell lymphoma. Cutaneous involvement by lymphoma previously diagnosed as low-grade (follicular growth pattern) transformed to higher grade disease in five of ten asynchronous cases. The 5-year survival rate was 60% among the transformed cases and 100% among the nontransformed cases. Extranodal cutaneous involvement in follicular lymphoma occurred in 3.8% of cases. The correct histologic diagnosis in a skin biopsy specimen can be established in cases with a follicular pattern (60%) with conventional histologic criteria such as redundancy of follicles, uniformity of follicular center cell composition, lack of interspersed phagocytic histiocytes, and absence of immunosecretory cellular elements such as plasma cells and immunoblasts.

摘要

滤泡性淋巴瘤很少仅根据皮肤活检确诊。对11例出现皮肤病变的原发性淋巴结滤泡性淋巴瘤患者进行了研究。皮肤病变累及头皮、头颈部、躯干和臀部,其中4例为小裂细胞型,3例为大细胞型,4例为混合型。11例中仅6例发现滤泡模式呈底部密集分布。1例在真皮深层和皮下组织表现为结节状、血管周围模式。4例以淋巴细胞浸润的弥漫性模式为特征。1例弥漫性模式患者有一条孤立的淋巴瘤细胞表皮下带,代表原发性皮肤T细胞淋巴瘤。在10例不同时发生的病例中,先前诊断为低级别(滤泡生长模式)的淋巴瘤皮肤受累有5例转变为更高级别疾病。转变病例的5年生存率为60%,未转变病例为100%。滤泡性淋巴瘤结外皮肤受累发生率为3.8%。对于具有滤泡模式(60%)的病例,通过传统组织学标准,如滤泡冗余、滤泡中心细胞组成均匀、缺乏散在的吞噬性组织细胞以及不存在免疫分泌性细胞成分(如浆细胞和免疫母细胞),可在皮肤活检标本中确立正确的组织学诊断。

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