Burke J S
Semin Diagn Pathol. 1985 Aug;2(3):169-82.
Malignant lymphomas of the skin, excluding mycosis fungoides, are pathologically, immunologically, and clinically heterogeneous. Varying patterns and degrees of cutaneous infiltration are encountered in all histologic subtypes of non-Hodgkin's lymphomas. Immunologic studies have shown relatively equal numbers of cases with B and T cell phenotypes, but true histiocytic lymphomas of the skin also occur. Patients may be of any age, and they may have lymphoma in any clinical stage. A low clinical stage and a low-grade histologic subtype are significant factors for long survival. The differential diagnosis includes a variety of lymphoid infiltrates that are referred to as a group as cutaneous lymphoid hyperplasia; it also includes lymphomatoid papulosis as well as nonlymphoid cutaneous infiltrates such as myeloid leukemias, histiocytosis X, malignant histiocytosis, regressing atypical histiocytosis, and neuroendocrine (Merkel) cell carcinoma. Distinction of cutaneous lymphomas from these entities requires comprehension of multiple variables, including immunologic as well as morphologic and clinical factors.
皮肤恶性淋巴瘤,不包括蕈样肉芽肿,在病理、免疫和临床方面具有异质性。在非霍奇金淋巴瘤的所有组织学亚型中,均可出现不同的皮肤浸润模式和程度。免疫研究表明,B细胞表型和T细胞表型的病例数量相对相等,但皮肤真性组织细胞淋巴瘤也会发生。患者可处于任何年龄,且淋巴瘤可处于任何临床分期。临床分期低和组织学亚型分级低是长期生存的重要因素。鉴别诊断包括多种被统称为皮肤淋巴样增生的淋巴样浸润;还包括淋巴瘤样丘疹病以及非淋巴样皮肤浸润,如髓性白血病、组织细胞增多症X、恶性组织细胞增多症、消退性非典型组织细胞增多症和神经内分泌(默克尔)细胞癌。将皮肤淋巴瘤与这些疾病区分开来需要综合考虑多个变量,包括免疫、形态学和临床因素。