Disseminated lymphocytoma cutis in a patient with B-cell non-hodgkin's lymphoma

D. Parmar, J. Tandel, Rutoo V. Polra, J. Patel, P. Nair
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Abstract

Lymphocytoma cutis (LC) is one of the pseudolymphomas. It clinically and histopathologically resembles to cutaneous lymphomas due to the accumulation of lymphocytes. LC can be solitary characterized by only one nodule or disseminated, presenting as extensive lesions. It presents with soft and doughy or firm nodules, skin color, reddish brown, or reddish purple mainly on exposed area, such as the face. It has to be differentiated from Jessner's lymphocytic infiltrate of skin by histopathological and immunohistochemical examinations. Apart from treatment, follow-up of patients is crucial, as the condition can evolve into cutaneous lymphoma. We present a case of 54-year-old male, with lesions over the face, trunk, and both extremities diagnosed with disseminated LC.
一例B细胞非霍奇金淋巴瘤患者的皮肤播散性淋巴细胞瘤
皮肤淋巴细胞瘤(LC)是一种假淋巴瘤。由于淋巴细胞的积聚,它在临床和组织病理学上类似于皮肤淋巴瘤。LC可以是孤立的,其特征是只有一个结节或播散,表现为广泛的病变。主要在面部等暴露部位表现为柔软、粘稠或坚硬的结节、肤色、红棕色或红紫色。必须通过组织病理学和免疫组织化学检查将其与皮肤的Jessner淋巴细胞浸润区分开来。除了治疗之外,患者的随访也是至关重要的,因为这种情况可能会演变成皮肤淋巴瘤。我们报告一例54岁男性,面部、躯干和四肢病变,诊断为弥漫性LC。
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