Melanoma and Skin Cancer Unit, Facultad de Medicina, Pontificia Universidad Católica de Chile, Santiago, Chile.
Department of Dermatology, Facultad de Medicina, Pontificia Universidad Católica de Chile, Santiago, Chile.
Int J Dermatol. 2019 Nov;58(11):1270-1276. doi: 10.1111/ijd.14590. Epub 2019 Jul 26.
Primary cutaneous lymphomas (PCLs) and pseudolymphomas presenting as single pink-red nodules/tumors are highly unspecific and include a wide differential diagnosis.
To describe the dermoscopic characteristics of PCL/pseudolymphoma.
In this retrospective, case-control study, we evaluated the dermoscopic features of patients with solitary PCL/pseudolymphoma tumors and compared them to a control group of non-lymphomatous, nonpigmented, solitary tumors (e.g., basal cell carcinoma, amelanotic melanoma, etc).
We included 14 patients with PCL/pseudolymphomas and 35 controls. T-cell and B-cell lymphoma proportions were 28.6% (n = 4) and 71.4% (n = 10), respectively. Compared to controls, most lymphomas presented dermoscopically with orange color (71.4% vs. 14.2%, P < 0.001), follicular plugs (85% vs. 2.8%, P < 0.001), and as organized lesions (85% vs. 31.4%, P = 0.001). Coexistence of orange color and follicular plugs had an odds ratio (OR) of 2.8 (P < 0.001), highly suggestive of PCL . The kappa index for independent observers was 0.66, 0.49, 0.43 for orange background, follicular plugs, and organized lesion, respectively. Histopathologic correlation was performed in six PCL cases and showed dense diffuse and perifollicular lymphocytic infiltrate in all cases and keratin plugs in five of six cases, possibly correlating with the orange color and the follicular plugs, respectively.
Primary cutaneous lymphomas/pseudolymphomas present with characteristic dermoscopic findings irrespective of immunohistochemical subtype.
表现为单一粉红色结节/肿瘤的原发性皮肤淋巴瘤(PCL)和假性淋巴瘤高度不特异,包括广泛的鉴别诊断。
描述 PCL/假性淋巴瘤的皮肤镜特征。
在这项回顾性病例对照研究中,我们评估了患有单发 PCL/假性淋巴瘤肿瘤的患者的皮肤镜特征,并将其与非淋巴瘤性、非色素性、单发肿瘤(例如基底细胞癌、无黑色素瘤等)的对照组进行比较。
我们纳入了 14 例 PCL/假性淋巴瘤患者和 35 例对照组。T 细胞和 B 细胞淋巴瘤的比例分别为 28.6%(n=4)和 71.4%(n=10)。与对照组相比,大多数淋巴瘤的皮肤镜表现为橙色(71.4% vs. 14.2%,P<0.001)、毛囊塞(85% vs. 2.8%,P<0.001)和组织病变(85% vs. 31.4%,P=0.001)。橙色和毛囊塞共存的优势比(OR)为 2.8(P<0.001),高度提示为 PCL。独立观察者的kappa 指数分别为 0.66、0.49 和 0.43,用于橙色背景、毛囊塞和组织病变。在 6 例 PCL 病例中进行了组织病理学相关性研究,所有病例均显示密集弥漫性和滤泡周围淋巴细胞浸润,6 例中有 5 例可见角蛋白塞,这可能分别与橙色和毛囊塞相关。
原发性皮肤淋巴瘤/假性淋巴瘤具有特征性的皮肤镜表现,与免疫组织化学亚型无关。