A Case of Adult T-cell Leukemia Masquerading as Mycosis Fungoides

L. Pinter-Brown
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Abstract

INTRODUCTION AND INITIAL PRESENTATION This 81 year old Japanese American male presented 9 years ago with a rash that was diagnosed as psoriasis and was treated with 14 weeks of light therapy. Shortly after this therapy a skin biopsy of the right buttock revealed an atypical T-cell infiltrate consistent with mycosis fungoides with the malignant cells positive for CD 2,3,4, and 5 but negative for CD7 and 8. The epidermis showed hyperkeratosis, hyperparakeratosis, and acanthosis and there was a band-like lymphocytic infiltrate in the superficial dermis. Epidermotropism and Pautrier microabscesses with atypical lymphocytes with convoluted nuclei and occasional large cells were noted. T-cell gene rearrangement and HTLV-1 serology were positive. Bone marrow examination was unrevealing. While the patient had not ever been in Japan, his father came from Kyushu. The patient received therapy with PUVA with an initial response, then experienced progression in skin. Treatment with topical BCNU and extracorporeal photopheresis were also rendered; again with initial short-lived responses, then progression of the skin rash. Two years after the initial diagnostic skin biopsy, the patient had a PET scan showing right hilar, axillary, and inguinal adenopathy. The patient began therapy with bexarotene with a complete response in skin and continued on bexarotene in good health for 3 years. He then presented with a hemoglobin of 8.9 and white blood cells of 12,800. CT scanning showed bilateral perihilar alveolar infiltrates, a 1.5 cm density at the right apex of the lung, mediastinal and right hilar adenopathy and splenomegaly with peripheral hypodensities.
成人t细胞白血病伪装成蕈样真菌病1例
介绍和初步表现:81岁的日裔美国男性,9年前出现皮疹,诊断为牛皮癣,接受了14周的光疗治疗。治疗后不久,右臀部皮肤活检显示非典型t细胞浸润,与真菌样霉菌病一致,恶性细胞cd2、3、4和5阳性,但CD7和8阴性。表皮表现为角化过度、角化过度和棘层增生,真皮浅层有带状淋巴细胞浸润。嗜表皮性和鲍特里微脓肿伴非典型淋巴细胞,核卷曲,偶见大细胞。t细胞基因重排、HTLV-1血清学阳性。骨髓检查未见异常。虽然患者从未去过日本,但他的父亲来自九州。患者接受了PUVA治疗,最初有反应,然后皮肤出现进展。局部BCNU和体外光疗治疗也进行了报道;最初的反应是短暂的,然后是皮疹的进展。在最初诊断性皮肤活检两年后,患者进行PET扫描显示右侧肺门、腋窝和腹股沟腺病。患者开始使用贝萨罗汀治疗,皮肤完全缓解,并持续使用贝萨罗汀3年,健康状况良好。他的血红蛋白为8.9,白细胞为12800。CT示双侧肺门周围肺泡浸润,右肺尖1.5 cm密度,纵隔和右肺门淋巴结病变,脾肿大伴周围低密度。
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