Bagheri Farshad, Cervellione Kelly L, Delgado Belkis, Abrante Luis, Cervantes Jose, Patel Jitendra, Roth Alan
Departments of Internal Medicine, Clinical Research and Family Practice, Jamaica Hospital Medical Center, 8900 Van Wyck Expressway, Jamaica, NY 11418, USA.
J Skin Cancer. 2011;2011:824528. doi: 10.1155/2011/824528. Epub 2011 Mar 3.
Subcutaneous panniculitis-like T-cell lymphoma (SPTCL) is a very rare form of skin lymphoma that is localized primarily to the subcutaneous adipose tissue without palpable involvement of the lymph nodes. Diagnosis of SPTCL is a challenge, especially during its early phases when symptoms mimic other, more common conditions, such as benign panniculitis, eczema, dermatitis, psoriasis and cellulitis. Clinical and systemic features are nonspecific and can include fever, chills, and weight loss. Further complicating diagnosis is the high number of false negatives provided by biopsy. Here we present a case of SPTCL that illustrates the full course of the disease, from presentation and multiple misdiagnoses to correct disease recognition and successful treatment. A review of the challenges of diagnosis is provided with recommendations for more accurate and timely recognition of SPTCL.
皮下脂膜炎样T细胞淋巴瘤(SPTCL)是一种非常罕见的皮肤淋巴瘤形式,主要局限于皮下脂肪组织,无明显的淋巴结受累。SPTCL的诊断具有挑战性,尤其是在疾病早期,其症状类似其他更常见的病症,如良性脂膜炎、湿疹、皮炎、银屑病和蜂窝织炎。临床和全身特征不具有特异性,可能包括发热、寒战和体重减轻。活检出现大量假阴性结果使诊断进一步复杂化。在此,我们报告一例SPTCL病例,该病例展示了疾病的全过程,从发病、多次误诊到正确识别疾病并成功治疗。本文还对诊断挑战进行了综述,并给出了更准确、及时识别SPTCL的建议。