Lo H-C, Yu D-S, Lee C-T, Chen A, Chang S-Y, Sun G-H
Division of Urology, Department of Surgery, Tri-Service General Hospital, National Defense Medical Center, National Defense University, No. 325, Section 2 Cheng-Gung Road, Neihu 114, Taipei, Taiwan, ROC.
Arch Androl. 2003 Nov-Dec;49(6):467-70. doi: 10.1080/01485010390219953.
Malignant lymphoma uncommonly manifests in the genitourinary tract. Primary penile lymphoma is extremely rare. A 77-year-old male presented with primary malignant B-cell lymphoma of the penis with the chief complaint of a painless and itching nodule on the penile glans for more than 2 months. The pathologic examination with immunohistochemical stain of penile biopsy revealed malignant B cell lymphoma, mixed cellular type. The physical examination and the computed tomography scan of chest, abdomen, and pelvis showed no evidence of superficial, thoracic, abdominal, or pelvic lymphadenopathy. This case was treated with local excision and systemic chemotherapy with good cosmetic and functional results. There was absence of recurrence 16 months after therapy.
恶性淋巴瘤很少在泌尿生殖道表现。原发性阴茎淋巴瘤极为罕见。一名77岁男性因阴茎头出现无痛性瘙痒结节2个多月为主诉，被诊断为原发性阴茎恶性B细胞淋巴瘤。阴茎活检的病理检查及免疫组化染色显示为恶性B细胞淋巴瘤，混合细胞型。体格检查以及胸部、腹部和骨盆的计算机断层扫描未发现浅表、胸部、腹部或盆腔淋巴结病的证据。该病例接受了局部切除和全身化疗，取得了良好的美容和功能效果。治疗后16个月无复发。
