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T细胞淋巴瘤累及皮下组织。2例报告。

Subcutaneous tissue involvement by T-cell lymphoma. A report of 2 cases.

作者信息

Monterroso V, Bujan W, Jaramillo O, Medeiros L J

机构信息

Department of Pathology, Mexico Hospital, San Jose, Costa Rica.

出版信息

Arch Dermatol. 1996 Nov;132(11):1345-50.

PMID:8915313
Abstract

BACKGROUND

T-cell lymphomas may involve the subcutaneous tissue as a manifestation of generalized disease. However, T-cell lymphomas rarely present with extensive involvement of the subcutaneous fat without other sites of disease.

OBSERVATIONS

We describe 2 women who presented with fever and subcutaneous nodules or masses. In case 1, the nodules were generalized and did not respond to chemotherapy. The patient died 2 months after diagnosis. In case 2, the mass was large but localized and responded to chemotherapy. The tumor subsequently recurred in a cervical lymph node 9 months later, and the patient was being treated with chemotherapy 15 months after initial diagnosis. Histologically, biopsy specimens from both patients revealed malignant lymphoma involving the subcutaneous tissue. The dermis and epidermis were not involved. At low power the lesions resembled panniculitis, but high-power examination revealed cytologic atypia of the malignant lymphoid cells. Immunohistochemical studies revealed T-cell lineage. In case 2, the neoplastic cells also expressed the CD30 antigen, were positive for Epstein-Barr virus RNA, and carried the t(2;5) (p23;q35) chromosomal translocation. We interpreted case 1 as an example of subcutaneous panniculitic T-cell lymphoma. We believe that case 2 is best classified as anaplastic large cell lymphoma of T-cell lineage.

CONCLUSIONS

A variety of T-cell lymphomas rarely present with only subcutaneous tissue involvement. Knowledge of this phenomenon and recognition of the cytologic atypia of the lymphoid cells will help to prevent misdiagnosis.

摘要

背景

T细胞淋巴瘤可累及皮下组织,作为全身性疾病的一种表现。然而,T细胞淋巴瘤很少仅表现为皮下脂肪广泛受累而无其他疾病部位。

观察结果

我们描述了2名出现发热及皮下结节或肿块的女性。病例1中,结节为全身性,对化疗无反应。患者在诊断后2个月死亡。病例2中,肿块较大但局限,对化疗有反应。肿瘤随后在9个月后于颈部淋巴结复发,患者在初次诊断后15个月正在接受化疗。组织学上,两名患者的活检标本均显示为累及皮下组织的恶性淋巴瘤。真皮和表皮未受累。低倍镜下病变类似脂膜炎,但高倍镜检查显示恶性淋巴细胞有细胞学异型性。免疫组织化学研究显示为T细胞谱系。病例2中,肿瘤细胞还表达CD30抗原,爱泼斯坦 - 巴尔病毒RNA阳性,并携带t(2;5)(p23;q35)染色体易位。我们将病例1解释为皮下脂膜炎样T细胞淋巴瘤的一个例子。我们认为病例2最好归类为T细胞谱系间变性大细胞淋巴瘤。

结论

多种T细胞淋巴瘤很少仅表现为皮下组织受累。了解这一现象并认识淋巴细胞的细胞学异型性将有助于防止误诊。

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