Mercer Stephen E, Vidal Claudia I, Grummer Sarah E, Strauchen James A, Gordon Marsha L, Birge Miriam B
Division of Dermatopathology, Mount Sinai School of Medicine, New York, NY 10029, USA.
Am J Dermatopathol. 2010 Feb;32(1):79-82. doi: 10.1097/DAD.0b013e3181b15a8a.
We describe a 60-year-old man with a history of primary cutaneous anaplastic large cell lymphoma on the chest, who presented with a new scaly red plaque on the same site 11 years after radiation therapy. Histological examination revealed a dense epidermotropic infiltrate of atypical mononuclear cells consistent with pagetoid reticulosis. Immunohistochemistry revealed the infiltrate to be CD4, CD8, and CD30. Remarkably, all the atypical cells were strongly CD30, and furthermore, the CD30 cells were found exclusively in the epidermis. In the initial cutaneous anaplastic large cell lymphoma lesion, the CD4, CD8, and focally CD30 atypical cells were well confined within the dermis with no epidermal component. To our knowledge, the present case seems to be the first description of pagetoid reticulosis presenting at the site of a previously treated dermal anaplastic large cell lymphoma. This case also represents an extreme presentation of epidermotropism and CD30 expression in pagetoid reticulosis.
我们描述了一名60岁男性,有胸部原发性皮肤间变性大细胞淋巴瘤病史,在放疗11年后,同一部位出现了一个新的鳞屑性红色斑块。组织学检查显示,有密集的向表皮性浸润的非典型单核细胞,符合蕈样网状细胞增生症。免疫组化显示浸润细胞为CD4、CD8和CD30阳性。值得注意的是,所有非典型细胞均为强CD30阳性,此外,CD30阳性细胞仅见于表皮。在最初的皮肤间变性大细胞淋巴瘤病变中,CD4、CD8以及局灶性CD30阳性的非典型细胞很好地局限于真皮内,无表皮成分。据我们所知,本病例似乎是首例关于蕈样网状细胞增生症出现在先前治疗过的皮肤间变性大细胞淋巴瘤部位的描述。该病例也代表了蕈样网状细胞增生症中向表皮性和CD30表达的一种极端表现。