Bains Anupama, Vedant Deepak, Shanker Vinay, Tegta G R
Department of Dermatology, Venereology and Leprosy, AIIMS, Jodhpur, Rajasthan, India.
Department of Pathology, AIIMS, Jodhpur, Rajasthan, India.
Indian Dermatol Online J. 2016 Nov-Dec;7(6):526-528. doi: 10.4103/2229-5178.193896.
Primary cutaneous anaplastic large cell lymphoma (pcALCL) forms 9% of the cutaneous T-cell lymphomas. It usually presents as solitary reddish brown ulcerating nodule or indurated plaque. Sometimes, it mimics other dermatological diseases such as eczema, pyoderma gangrenosum, pyogenic granuloma, morphea, and squamous cell carcinoma. Our case presented with large pyogenic granuloma like lesion with regional lymphadenopathy. Since pcALCL is rare, one can misdiagnose such cases and therefore high index of suspicion is necessary.
原发性皮肤间变性大细胞淋巴瘤(pcALCL)占皮肤T细胞淋巴瘤的9%。它通常表现为孤立的红棕色溃疡性结节或硬结性斑块。有时,它会模仿其他皮肤病,如湿疹、坏疽性脓皮病、化脓性肉芽肿、硬斑病和鳞状细胞癌。我们的病例表现为类似化脓性肉芽肿的大病变并伴有局部淋巴结病。由于pcALCL很罕见,可能会误诊此类病例,因此需要高度怀疑。