Int J Gynecol Pathol. 2021 May 1;40(3):229-233. doi: 10.1097/PGP.0000000000000648.
Cutaneous T-cell lymphomas may present with a clinical course that is incongruent with the associated histologic findings. Primary cutaneous CD8+ aggressive epidermotropic cytotoxic T-cell lymphoma classically presents as an abrupt eruption of disseminated ulcerated annular plaques with aggressive behavior and a poor prognosis. Herein we describe a vulvar primary cutaneous CD8+ aggressive epidermotropic cytotoxic T-cell lymphoma with a locally aggressive clinical course that was strikingly responsive to radiation therapy. As aggressive therapy involving systemic chemotherapy is indicated for primary cutaneous CD8+ aggressive epidermotropic cytotoxic T-cell lymphoma, appropriate clinico-pathologic correlation is crucial for preventing potentially excessive or insufficient therapeutic intervention. Our case also highlights the pivotal role of both radiation therapy and infection control in the management of aggressive cutaneous vulvar lymphomas.
皮肤 T 细胞淋巴瘤的临床表现可能与相关的组织学发现不一致。原发性皮肤 CD8+侵袭性表皮亲细胞细胞毒性 T 细胞淋巴瘤通常表现为突然出现播散性溃疡性环状斑块,具有侵袭性和不良预后。在此,我们描述了一例外阴原发性皮肤 CD8+侵袭性表皮亲细胞细胞毒性 T 细胞淋巴瘤,其临床表现具有局部侵袭性,对放射治疗反应明显。由于原发性皮肤 CD8+侵袭性表皮亲细胞细胞毒性 T 细胞淋巴瘤需要进行全身性化疗的侵袭性治疗,因此恰当的临床病理相关性对于防止潜在的过度或不足的治疗干预至关重要。我们的病例还强调了放射治疗和感染控制在侵袭性皮肤外阴淋巴瘤治疗中的关键作用。